Proteins have properties that could either be global or local, that is, wholistic protein properties (e.g. stability of a protein) or regional protein properties (e.g. phosphorylation of an amino acid residue by a protein kinase). These different protein properties are usually determined through wet lab experiments, which can be challenging, time-consuming, and costly. The change in protein stability based on changes in protein sequence, for example, requires measuring the change in Gibbs free energy of folding of the purified wild-type and mutant proteins (Walls and Loughran, 2017). Even though this experimental procedure provides direct understanding of protein stability, much time and high costs are involved, especially when multiple mutations in a sequence need to be analysed. This has driven interest into computational methods to guide mutation analysis and design (Pan et al., 2022). Employing a computational approach can also aid the experimental approach by providing a ranked list of predictions for a property (e.g. to predict the likelihood of interaction between two given protein sequences) that can be experimentally verified or refuted by scientists in focused experimental testing, which can save much time and other resources (Ehrenberger et al., 2015).

There has been an exponential growth in the number of protein sequences collected in public repositories using high-throughput technologies. However, the gap between the number of sequenced proteins and the number of protein property annotations continues to widen (UniProt Consortium, 2019; Varadi et al., 2022). Recently, machine learning (ML) methods, in general, and large-scale deep learning (DL) methods, in particular, have gained much attention due to their ability to extract complex patterns from large collections of protein data (Shi et al., 2021; Li et al., 2022) to automatically predict protein properties. There is now a vast and growing number of applications of DL methods used in the proteomic field that assist in building knowledge about various protein properties.

Since recent large-scale DL models have played a crucial role in computational protein property prediction (Bileschi et al., 2022), we describe in this review the most common DL architectures in use today. DL methods, especially those coming from the field of natural language processing (NLP), are gaining popularity, and we therefore discuss DL methods in the context of NLP. We denote such models as language models. Further, we explain how language models relate and have been adopted to analyse protein sequences. Various language models have been developed in the protein area, and we highlight some recent examples where they have been used to predict protein properties in the life sciences. In particular, we discuss and explain the Transformer model, which has managed to overcome several of the shortcomings of previous methods. We further provide a proof-of-principle example, where we predict a post-translational modification (PTM) in proteins. PTMs are a common way of changing a protein’s functionality and are often associated with regulatory cascades and cellular signaling. PTMs can be determined in wet lab settings, for example, with mass spectrometry, but can also be predicted using computational approaches. In our proof-of-principle example, we set out to predict whether lysine residues in proteins are phosphoglycerylated or not. To do this, we compared the prediction performance when using traditional protein features, determined by the analyst, to the performance when using features automatically found using two types of Transformer models. By feature here, we mean, for instance, some description of a protein, a statistic, or a measurement. Finally, we discuss the future of protein property prediction and predict that Transformer-like models will be the standard approach for many computational biology and bioinformatics tasks in the near future.

ML is a subarea of artificial intelligence (AI), and much of the recent developments within the field of AI come from progress made within ML. The aim of ML is to use data to solve a task, for instance, to predict a specific protein property based on measurements, that is, data, from other proteins where those properties are known. Most of the recent ML developments have been made within DL, a subarea of ML. However, NLP is also a subfield of AI, where the aim is to use computers to analyse and understand natural language, which is naturally evolved human language, and often uses ML to process and analyse text data. There is an overlap between ML/DL and NLP, however, and ideas flow both ways between the fields. Recently, developments in NLP have been driving much of the development within all of ML and DL.

DL methods are often based on deep artificial neural network models, a class of ML models that are very flexible in the sense that they are able to model very complicated relationships between the measurements (the input data, such as amino acid sequences) and the quantities to be predicted (such as a protein property). The main advantage of neural network models is that they can automatically learn rich feature representations, and they do that directly from large unstructured input data. This means, for instance, that they can take variable-length protein sequences as inputs and automatically find a way to represent them as a fixed-length real (floating-point) vector, where the learned representations contain all the relevant information from the protein sequences that is necessary to solve a particular prediction problem. Having found such a representation, these models also automatically perform a traditional machine learning tasks in the newly learnt representation, such as classification or regression (Charte et al., 2019). Some examples of machine learning tasks are illustrated in Figure 1. In contrast, traditional ML models typically rely on input features determined by the analyst, which are computed from the raw unstructured data, after which a model is determined using those features in a second step. DL models are instead end-to-end systems, meaning that there is only a single step where they automatically learn to map directly from the input data, through an internal learned representation, the automatically determined features, to the target quantities that we want to predict, and they do this with unprecedented accuracy (Khan et al., 2019).

Figure 1

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The architecture of a neural network model is the network layout and its components, such as the number of artificial neurons in each layer (the number of computational units in the layer), the number of layers (the number of levels of abstractions it can learn), and the type of connections between these layers (which layers are connected to which). The architecture of the network governs the overall behaviour of the neural network, what it can learn, and what assumptions about the data are built in.

There are many types of neural network models that are made for analysing different types of data. Some of the most well-known and successful types of neural network models include multilayer perceptrons (MLPs), convolutional neural networks (CNNs), and recurrent neural networks (RNNs) (Koumakis, 2020; see illustrations in Figure 2). These models have been used by themselves, as well as in combination as hybrid models. Examples include work on protein fold recognition, which used a CNN for feature extraction together with an RNN model (Liu et al., 2020), and the popularly used Word2Vec model that can provide embeddings for words to be used in language processing by neural networks, as in the continuous bag-of-words model and the continuous skip-gram model (Mikolov et al., 2013a). MLPs are characterized by an input layer that accepts any type of inputs, for instance, features computed from proteins, several possible interconnected so-called hidden layers, and an output layer with the predicted value, such as a protein property. CNNs use convolution operations, or, technically, they use what is called linear spatial operation, in at least one of their layers. The convolution layers learn filters that detect features, or patterns, in the input signals. The filters automatically capture features in a local region, called the receptive field, and in order to capture feature more distantly, CNNs learn a hierarchy of features. The pooling operation after the convolution layer reduces the dimensionality of the captured features. CNNs have been very successful when analysing image and audio input data, and are very common in computer vision for analysing images, but have also been used to analyse protein sequence data (for instance, DNA-protein binding; Zeng et al., 2016). RNN models have gained much attention since they were first introduced (Elman, 1990) and have been applied widely in many NLP tasks, such as speech recognition (Mikolov et al., 2011). They are suitable for modelling sequential data such as text or time series data, but can also model DNA and protein sequences. The elements in the sequence, for example, words or amino acids, are processed step-by-step one at a time using so-called recurrent connection units, where the output of each step depends on both the current and the previous steps. Common RNN models include the long short-term memory (LSTM) model (Hochreiter and Schmidhuber, 1997) and the gated recurrent units (GRUs) (Chung et al., 2014). There are also models that learn both forwards and backwards, such as the bidirectional LSTM model, BiLSTM (Huang et al., 2015), which uses two LSTM models to capture information from a sequence in both directions. RNNs can model the contextual dependencies in language and were preferred over MLPs and CNNs for most NLP tasks for a long time (Yin et al., 2017).

Figure 2

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The field of NLP was founded in the 1950s and today covers a wide range of applications, such as sentiment analysis (extracting subjective qualities, like emotions, from text), named entity recognition (classify named entities from text, such as places or person names), machine translation, or question answering. Early NLP systems comprised hand-coded and rule-based assessments (grammar rules) by humans that were then encoded into special-purpose algorithms to predict some property of the sentence. This, however, produced unsatisfactory results and generally failed to deliver when applied to larger text volumes. More recent NLP systems often utilize DL models to automatically learn to solve natural language tasks based on very large volumes of raw, unstructured, and unlabelled text datasets.

To perform an NLP task, the input text data must be pre-processed to be in a form suitable for automation. The first steps in this process involve splitting the text up into either sentences, words, or parts of words. This process includes a step called tokenization, and the units the text is broken down into are called tokens. These tokens are translated into numerical representations called input embeddings, such as one-hot encoding, count vectors, or word embeddings (Wang et al., 2018), as illustrated in Figure 3A. Word embeddings are the most common real-valued vector representations of the tokens (Levy and Goldberg, 2014) and are often automatically learned (Turian and Ratinov, 2010).

Figure 3

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The ability of DL methods to automatically learn feature representations of the input data significantly reduces the need for manual specification or extraction of features by natural language experts. Meaningful information can be extracted from unstructured data using DL methods at a fraction of the time and cost and also often considerably better than human experts (Young et al., 2018; Nauman et al., 2019). The most recent NLP methods, based on a particular model called the Transformer, learn feature representations automatically through the process of unsupervised learning, often called self-supervised learning (Devlin et al., 2018; Peters et al., 2018).

Most NLP tasks today are solved using DL methods based on the Transformer, with existing methods constantly being improved and new methods proposed (Raffel et al., 2019; Brown et al., 2020; Heinzinger et al., 2021). Recent models are also trained on text data of ever-increasing sizes, which have made them perform even better.

The Transformer model was introduced in 2017 by Vaswani et al., 2017 and achieved state-of-the-art results in language translation using only a fraction of the previous training times. It is an encoder–decoder type of model (see Figure 4A for the general idea of an encoder–decoder model), where the encoder maps the vector representations of the tokens from an input text (the input embeddings) to an internal representation. The decoder then uses the internal representation and maps it to the output sequences (the target language, for instance). Compared to contemporary models at the time, the Transformer model did not use recurrent layers, nor did it use convolution layers—instead, it used an architecture component called attention. The attention module enables a model to consider the interactions among every pair of tokens in a sequence and automatically learn the relationships between tokens in a sequence that are relevant for the task at hand (Cheng et al., 2021). There are many kinds of attention modules, but most of them, and the one used by Vaswani et al., automatically learn an interaction pattern between pairs of tokens. These interaction patterns give an importance weight to each input token for the prediction task at hand and allows the model to learn dependencies between tokens far apart in the input sequence. In most cases, not just one but several such attention modules are used in parallel, allowing the model to learn multiple different aspects of the relationships between input tokens—this is called multihead attention.

Figure 4

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The Transformer model by Vaswani et al. comprises multihead attention (eight parallel attention heads) and fully connected feed-forward networks (these networks are in fact MLP models, used as intermediate components in the overall Transformer model) in six layers of both the encoder and decoder blocks. To generate the input embeddings to the model, the authors used two schemes: encoding the sentences using byte-pair encoding (Britz et al., 2017) or splitting tokens into word-piece vocabulary (Wu et al., 2016), based on the training dataset. The model’s embedding layers produce contextualized embeddings (the internal representations) of size 512 (per token). The multihead attention in the different layers of each block of the network enabled the model to learn rich and useful representation by considering information from tokens at different positions in the input sequence.

The procedure used to train such models is called self-supervision and is typically one of the following two approaches: (1) to predict the next token in a sequence, given the previous tokens (Peters et al., 2018) (this is called autoregressive language modelling), or (2) predict 'masked' tokens, where certain tokens are removed (typically 15% in an input sequence), and the model is made to predict them using the information available in the unmasked tokens in the sequence (this is called masked language modelling [MLM]) (Devlin et al., 2018). These two types of training approaches are illustrated in Figure 3B. The approach originally employed, already before the Transformer models, was to predict the next token in the input sequence. Transformers trained using the MLM approach have become very popular and successful, likely because it allows the model to consider the whole input sequence directly instead of everything up until the present point in the sequence (Nambiar et al., 2020; Elnaggar et al., 2020a; Rives et al., 2021; Brandes et al., 2021; Rao et al., 2021; He et al., 2021).

Many other models, based on the Transformer model, have been proposed after the introduction of the original Transformer. These models all have attention modules as their core components. An example is the BERT model (Devlin et al., 2018), which is an encoder model that has achieved outstanding performance compared with other language models on many NLP tasks, such as machine translation, question answering, etc. (Chung et al., 2014; Cheng et al., 2021). The BERT model attained new state-of-the-art results on 11 NLP tasks. The work demonstrated that bidirectional pre-training is important for language representations and that the pre-trained model can be adapted to many other specific tasks, which is relatively inexpensive compared to building separate models for each individual task. There were two primary models developed: BERT_BASE (with 12 layers, 12 attention heads, and 768-dimensional contextual embeddings) and BERT_LARGE (24 layers, 16 attention heads, and 1024-dimensional contextual embeddings). The authors found that the BERT_LARGE results surpassed the results of BERT_BASE on all the tasks, which indicates the importance of the model size for the performance.

Because of the recent successes of DL-based language models in a myriad of NLP tasks, and particularly so when using the Transformer model, there has been an increased interest in such models for applications in other fields, such as in computational biology and bioinformatics. In these fields, NLP models can be applied to sequences of, for example, genomic or proteomic data, and recent results indicate that this is a highly successful approach for protein prediction applications (Choromanski et al., 2020).

DL models are known to be computationally expensive and to take considerable amount of time to train. The Transformer models, however, avoid some of the challenges associated with traditional DL methods for sequence modelling.

For instance, RNN models capture information from previous positions in an input sequence, advancing from the beginning of the sequence (forward). But in doing so, they do not capture any input sequence context from the other side of the current position in the sequence. They also suffer from some fundamental problems (called the vanishing and exploding gradient problems) (Bengio et al., 1994; Pascanu et al., 2013; Hanin, 2018), which makes them difficult to train (Dai et al., 2018). The effect of this is that RNN models have problems to learn relationships between distant tokens in an input sequence (Bengio et al., 1994; Pascanu et al., 2013; Hanin, 2018). Also, since the data is processed one token at a time, it is not possible to parallelize the computations, making the training slow (Wang et al., 2019).

For a CNN to capture distant features in the input, they need to learn a hierarchy of features. It may take many such hierarchy levels to extract meaningful information from a larger part of an input sequence (Raghu et al., 2021), which can make CNNs slow. CNNs are also invariant to spatial translations and do therefore not utilize the positional information that may be relevant in an input sequence (Albawi et al., 2017). While CNNs have had a remarkable success on, for example., image data, they have not been as successful in sequence modelling.

The Transformer models solve many of the hurdles faced by conventional DL approaches, some of which were described above. The Transformer model’s attention module allows each token to influence weights for every other token in the sequence. This allows the Transformer model to attend to long-range dependencies between input tokens, a very beneficial property since it enables Transformers to consider the whole context of an input sequence (Dehghani et al., 2018). As a result, they obtain superior results and sequence embeddings (Väth et al., 2022). The direct connections between distant tokens also help when training the Transformer models, making it easy to train them (Dai et al., 2018). The Transformer models are also highly parallelizable, and only have simple components such as attention modules and fully connected layers, which makes them computationally attractive (Wang et al., 2019).

The models used in the field of NLP can thus also be used to learn and understand protein sequences and in this context, they are commonly referred to as protein language models (Heinzinger et al., 2019). While there are abstract similarities between sentences and protein sequences, there are of course major differences in their properties, syntax, and semantics (Ofer et al., 2021). When handling proteins, a word can be one of the individual twenty canonical amino acids (excluding unconventional and rare amino acids) Lopez and Mohiuddin, 2020 found in the genetic code or it could be a number of these amino acids grouped together, while a protein sequence would correspond to a sentence (Ferruz et al., 2022; ElAbd et al., 2020). A word being individual amino acids is the most common approach, and other alternatives do not appear to have been explored much (Ofer et al., 2021). Just like with natural language, protein sequences contain long-range dependencies, making them excellent candidates for analysis by recent NLP models such as Transformers (Ofer et al., 2021).

Figure 4B illustrates how a Transformer language model can be applied to protein sequences. The encoder maps the amino acid tokens of an input protein sequence to an internal representation (the model’s embedding of the protein sequence). This internal representation is then used as a feature vector that represents the protein sequence and is passed on to a conventional machine learning model for classification or regression, for instance. For clarity, we will denote this internal representation the representation of a protein sequence in a given protein language model.

For properties of proteins, such as their 3D structure, the mapping from a sequence of amino acids to the corresponding 3D structure is quite challenging (Kuhlman and Bradley, 2019; Jiang et al., 2017), but there is typically an abundance of sequenced proteins openly available that a DL model can make use of. The largest open sources of protein sequence information and data are the Universal Protein Resource (UniProt) (UniProt, 2021), Pfam (Mistry et al., 2021), and the Big Fantastic Database (BFD) (BFD, 2022). UniProt contains around 0.567M sequences that are reviewed and manually annotated and more than 230M sequences that are automatically annotated. The Pfam is a database containing protein families, where a family is determined by similar functional domains. Pfam currently has 19,632 families and clans (higher-level groupings), as per Pfam 35.0, and contains a total of 61M sequences (Pfam 35.0, 2021). BFD is a very large collection of protein families publicly available. It comprises 65.9M families covering more than 2B protein sequences and was built using UniProt, and a reference protein catalogue (Steinegger et al., 2019), clustered to 30% sequence identity. Protein language models are typically trained on such large open collections of protein data. The table in Supplementary file 1 gives an overview of some of the pre-trained Transformer language models available in the literature.

Using self-supervised training procedures on large databases of proteins, protein language models are able to learn very complex relationships and patterns in protein sequences through the global biome and across time.

Large protein language models, trained using one of the two approaches described above (Figure 3B) on very large databases of protein sequences, are used for downstream applications using one of two common approaches (Laskar et al., 2020). The first, called feature-based, is where a model is trained in a self-supervised manner, for instance, using one of the two approaches illustrated in Figure 3B, without any labels. The trained model’s representation of each protein sequence is then considered a feature vector for a protein that can directly be used for downstream protein prediction tasks. This is called pre-training and is what we used in the post-translational modification example in the section ‘A proof-of-principle example’ below. The second, called fine-tuning, is where a model is trained first in a self-supervised manner without any labels for the protein sequences, and then updated, or fine-tuned, using protein sequences with labels of interest. After that, the model’s fine-tuned protein sequence representations are used for downstream prediction tasks.

Protein prediction tasks for which the Transformer has been used include predictions of protein structure, protein residue contact, protein–protein interactions (PPI), drug–target interactions (DTI), PTMs, and homology studies. The task can either be local (sites of interest within the sequence) or global (entire sequence). The fixed size Transformer representation for the local task can be obtained by taking a fixed window around the sites of interest, while the fixed size representation of a protein for a global task is achieved, for instance, by averaging the residue vectors to yield the protein sequence vector (Väth et al., 2022). It remains to be seen on which protein problems the Transformer models do not perform so well since the use of Transformer models is still spreading, and they are being used to solve more and more protein prediction tasks. Most of the state-of-the-art techniques for such predictions have been based on features from profile-to-profile comparison created from multiple sequence alignments (MSAs) of proteins using tools such as PSI-BLAST (Altschul et al., 1997) and HMMER (Finn et al., 2011). A protein profile is built by converting MSAs into a scoring system of amino acid positions based on their frequency of occurrence and is used to model protein families and domains. However, such techniques have limitations due to the existence of gaps in the protein sequences stemming from deletions and insertions (Golubchik et al., 2007) and work unsatisfactory for sequences having few to no homologs to generate MSA and profiles (Phuong et al., 2006). Moreover, predicted structural features, such as secondary structure, have also been popular when developing predictive models, but they suffer a limitation since the structural information problem is yet to be solved, which results in imperfect features (Sułkowska et al., 2012; Schmiedel and Lehner, 2019).

The results obtained using Transformer models on such tasks have been quite promising, and without the use of MSA tools that require homologous sequences, and also without structural information. A recent framework introduced by Chowdhury et al., 2022, which has a Transformer-based language model at its core, outperformed AlphaFold2 (Jumper et al., 2021), an MSA-based approach, in structure prediction for sequences that lack homologs. There are Transformer models that utilize evolutionary information extracted from MSAs during the pre-training stage, but pre-training is mostly done as a one-off process, and representation for new proteins is extracted using only the pretrained hidden states of the Transformer models. MSA tools generate alignment by searching homologs from the entire UniProt database, time-consuming (Hong et al., 2021) process, whereby generating embeddings using protein language models is less cumbersome but it also builds richer and more complete features for low homologous proteins (Wang et al., 2022).

In the following, we summarize typical problems from different fields of the life sciences, for which Transformer models have been used to aid in the prediction of protein properties. Most of these works employ pre-trained Transformer models to generate protein representations that can be used in downstream tasks for predictions.

Apart from the ground-breaking performance of Transformer models, they also offer possibilities for visualization and interpretation of their attention weights. In addition to traditional approaches such as using scatter plots (Van der Maaten and Hinton, 2008; Abdi and Williams, 2010) to visualize the learned representations (Nambiar et al., 2020; Elnaggar et al., 2020a; Rives et al., 2021; Rao et al., 2019), Transformers offer other prospects for interpretation, allowing a researcher to look inside their model to better understand its function rather than using the model as a black box. The analysis of attention heads reveal the weight assignments between pairs of input tokens, and these weights can be used to draw conclusions about the interactions between tokens that contributed to a model’s decision (Hao et al., 2021). Note, however, that such an analysis does not necessarily point out the feature importance in the representation of the Transformer. Examples of some commonly used Transformer model visualizations include assessments of both the attention mechanism and the embeddings using, for example, attention weights (Elnaggar et al., 2020a) and heatmaps (Brandes et al., 2021; Zhang et al., 2021; Yamaguchi and Saito, 2021; Vig et al., 2020). Attention weight visualization allows the portrayal of attention weights between an amino acid to the other amino acids in the form of intensity of line connections. Heatmaps can be used to show the colour shades for the different attention heads across the different layers for each amino acid, amino acid to amino acid maps using averaged weights of the heads across the network layers, etc. Transformer visualizations are not limited to the only ones listed here as new techniques are continually suggested in scientific publications which shows how versatile Transformer models are (Chefer et al., 2021). Moreover, the intricacy in the existing ways of interpreting Transformer models, especially its multihead attention, is also being improved so that model’s internal learnings can be made more easy for analysis (Hao et al., 2021; Vig, 2019b).

Figure 5A illustrates attention weights in an example using the BERT model. The model identifies dependencies in the sentence by showing which words attend to the word 'sick' in an attention head of a layer of the model. The model clearly connects the words 'tom' and 'he' to the word 'sick', indicating that the model has learnt to identify context in the sentence.

Figure 5

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Attention weight visualization was utilized by Elnaggar et al., 2020a, who visualized the attention weights of each amino acid residue onto the other residues in the protein sequence, where a darker line represented a higher attention weight, as in Figure 5B. Specifically, they analysed the residue contacts (protein structural motifs) crucial for zinc-binding and found that the model had learned to put more weight from one residue onto three other residues in one layer, and all these residues collectively were involved in the ground truth binding coordination. Heatmaps were used by Yamaguchi and Saito, 2021, who analysed effects of fine-tuning Transformer model with the use of evolutionary properties of proteins. The pre-trained and fine-tuned maps of a protein from the final layer were compared to the contact maps computed from its tertiary structure. It was observed that the fine-tuned model’s maps resembled that of contact maps and this pattern was absent from the map prior to fine-tuning. The visualization indicated that the structural information was captured by the model after fine-tuning on evolutionary related sequences. Heatmaps were also used by Zhang et al., 2021, where they proposed an evolutionary information-based attention (co-evolution attention). They visualized the maps with and without the evolutionary information-based attention and concluded that their attention component was effective in extracting contact patterns.

Such visualizations can thus be used to understand biological aspects of different protein properties, and by visualizing a Transformer model’s internal state we can gather and present deeper biological insights.

There has been a steady increase in the volume of scientific publications relating to Transformer-based models since their introduction in 2017 (Vaswani et al., 2017). This is evident in the progresses of both NLP and in computational biology and bioinformatics research. Figure 6A illustrates the yearly count of publications from 2017 to 2021 for the query 'Transformer Language Model' in Google Scholar, 2022. This resulted in a total number of publications of 1388. The plot has been extended to include the year 2022 by extrapolating the counts for 2022 (counts of scientific publications were until 2022-07-01 at the time of writing this article) until the end of the year. There is clearly an increase in how often Transformer-type of models are mentioned in the literature.

Figure 6

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In Figure 6B, the number of publications per year is illustrated for scientific publications related to Transformer-based models which were identified by searching within articles in Google Scholar citing the 'Attention is all you need' paper by Vaswani et al., 2017. The search was based on the query 'Life Science' and included all scientific research papers from 2017 to 2022 (cut-off on 2022-06-23). We excluded review papers and theses from the analysis. Articles focusing solely on method developments were excluded from the query results as well, leaving us with a total of 87 publications. The results were sorted by three main disciplines: medicine, pharmacology, and biology, as shown in Figure 7. Within the main disciplines, articles were sorted by their sub-categories. The increased use of Transformer models in the different areas of bioinformatics indicates that it is an effective model to use when studying different protein properties.

Figure 7

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To illustrate how the features learned by the Transformer model can be used to directly improve results over traditional protein features, we have conducted a pilot study in phosphoglycerylation prediction. Phosphoglycerylation is a type of PTM discovered in human cells and mouse liver which occurs when the amino acid lysine in a protein sequence is covalently modified by a primary glycolytic intermediate (1,3-BPG) to form 3-phosphoglyceryl-lysine. This PTM has been found to be associated with cardiovascular diseases like heart failure (Bulcun et al., 2012).

The task was to predict phosphoglycerylation, and for this we used the dataset from Chandra et al., 2019 which was originally obtained from the Protein Lysine Modification Database (PLMD, available at http://plmd.biocuckoo.org). The features used by Chandra et al., 2019 were based on position-specific scoring matrices that were obtained using the PSI-BLAST toolbox (Altschul et al., 1997), which is an MSA tool, and then they calculated its profile bigrams (Sharma et al., 2013) (a type of feature extraction) to produce the final feature set. We used this feature set, denoted BigramPGK, and compared the results to results when using features extracted from two pre-trained Transformer models. Additionally, we also used a second baseline feature set that composed of 10 commonly used physicochemical/biochemical properties of each amino acid (Yu et al., 2017; Chen et al., 2020; Cortés and Aguilar-Ruiz, 2011; Liu et al., 2012). We denote this feature set as Phy + Bio. The features were length of side chain, molecular weight, free energy of solution in water, melting point, hydrostatic pressure asymmetry index, isoelectric point, hydrophobicity index, ionization equilibrium constant (pK-a), pK (-COOH), and net charge. The Transformer models were the ESM-1b (Rives et al., 2021) and the ProtT5-XL-UniRef50 (Elnaggar et al., 2020a). We used two aggregation techniques for the ESM-1b model since it has a restriction on the length of the protein sequence that can be processed. First, the protein sequence was split into multiple parts by using 878 consecutive amino acids at a time, starting at each amino acid in the sequence. The ESM-1b model was used to extract a feature vector for each such subsequence of length 878, and the feature vectors were averaged to obtain a single feature vector for the entire protein sequence. We denote this approach ESM1b-avg. The second approach was to again split the protein sequence up into subparts of length 878, but this time splitting from where the last split ended and finally concatenating to get the resulting feature vector of the protein sequence. We denote this approach ESM1b-concate. We denote the features extracted from the ProtT5-XL-UniRef50 model as T5, and this model accepts variable-length input sequences so there was no need to aggregate multiple feature vectors manually.

After obtaining the representation of the protein sequences from the Transformer models, the feature of each sample was extracted by examining the sites of interest in the protein sequences and selecting the window size around those sites. The samples were extracted based on the standard practices, as outlined, for example, by Ramazi and Zahiri, 2021, which include to consider a window size of 15 amino acid residues upstream and 15 amino acid residues downstream of the lysine sites (López et al., 2017; Jia et al., 2016; Xu et al., 2018), to disregard the sites which did not have enough residues to make up the full upstream and downstream window (Wang et al., 2017; Saethang et al., 2016), and to take unlabelled sites as non-phosphoglycerylated samples only if the protein has two or more confirmed PTM sites in its sequence (Khalili et al., 2022; Trost and Kusalik, 2013). These conditions were applied to all the feature sets. The resultant dataset had a total of 526 samples (relating to each lysine) containing 101 phosphoglycerylated samples (positive labels) and 425 non-phosphoglycerylated samples (negative labels). We used random under-sampling to resolve the class imbalance ratio from 1:4 to 1:1.5 by randomly selecting the negative labels (Ramazi and Zahiri, 2021). The final number of samples used in the experiment was 253 (with 101 phosphoglycerylated and 152 non-phosphoglycerylated samples).

We used and compared five classifiers: logistic regression with ridge regularization (denoted LR), a support vector machine with a polynomial kernel (denoted SVM (poly)), a support vector machine with a radial basis function kernel (denoted SVM (RBF)), random forest (denoted RF), and finally a light gradient-boosting machine (denoted LightGBM). We set aside 51 samples for final test of each model (maintaining the same ratio between the positive and negative labels, i.e., 1:1.5) and performed fivefold cross-validation on the remaining 202 samples to select the models’ hyper-parameters with standard scaling of the data, based on the training set in each cross-validation round. The hyper-parameters were tuned using Hyperopt (Bergstra et al., 2013) with 15 evaluations.

We thus had five datasets (Phy + Bio, BigramPGK, T5, ESM1b-avg, and ESM1b-concate) and five classification models (LR, SVM (poly), SVM (RBF), RF, and LightGBM). We evaluated each model on all datasets using accuracy (ACC) and the area under the receiver operating characteristic curve (AUC), reporting both the fivefold cross-validation (CV) scores (those used to select the hyper-parameters) and the score obtained on the held-out test set (the 51 set-aside samples mentioned above). The results are presented in Table 1.

The Transformer models perform better in general than the BigramPGK protein features (based on MSAs) and the Phy + Bio features on the accuracy and AUC metrics across all the classifiers, except for the RF classifier where BigramPGK attained the highest accuracy on the fivefold cross-validation. Out of the five features, Phy + Bio had the lowest performance. We see that the concatenated features from the ESM-1b Transformer model generally perform better than all of the other feature sets, including the Transformer features (averaged features from ESM-1b, and the T5 features). While the differences are not always significant, it is clear that the trend is that the Transformer features perform better.

The Transformer family of models has shown large improvements over RNNs and other DL-based models. In just a few years, they have been used for many different prediction tasks and their representations have been used with very promising results. In contrast, it took decades for conventional features based on MSAs to reach their current performances. The Transformer models have their own set of limitations, and future improvements in their architecture will likely give further boosts in their performance.

For instance, the standard attention mechanisms can only process fixed-length input sequences. For longer sequences, they need to be split into smaller fragments before being fed to a model. However, splitting a sequence up means context is being lost beyond the split boundary. Recent developments have attempted to overcome the fixed-length issue, where, for instance, some variants allow hidden states from previous fragments to be used as inputs for the current fragment (Elnaggar et al., 2020a; Dai et al., 2019). ProtT5-XL-UniRef50 model used in the section ‘A proof-of-principle example’ uses the same technique to pass information from one fragment to the other in the protein sequence. This allows a Transformer model to consider very long dependencies and at least in theory handle unlimited-length contexts since the information from one segment can be passed on to the next infinitely (Wang et al., 2019). Furthermore, some transformer models need the users to pre-process the sequences to adhere to a sequence length limit. This was apparent with the ESM-1b model in the ‘A proof-of-principle example’. The workaround was to break the longer sequences into fragments (maximum lengths of 878 in this work) to get the Transformer representations, which was then concatenated to produce a representation for the entire sequence. That approach worked out as the best-performing features in this study out of the features compared. Fragmenting the sequence of course results in loss of some contexts, and future improvements to the sequence length limit can lead to more robust performances.

The attention mechanism, which is an integral part of Transformer models, also brings a limitation when it comes to long sequences. Since each token attends to every other token, the memory and computational complexity of the model increases quadratically in the attention layers with respect to the sequence length. A solution using sparse attention mechanism was proposed by Zaheer et al., 2020 that changed the complexity from quadratic to linear and allowed up to eight times longer sequences to be handled on similar hardware. Their proposed attention mechanism consisted of three parts: (1) making some tokens global which attend to the entire sequence, (2) all tokens attend to a set of local neighbouring tokens, and (3) all tokens attend to a set of random tokens. This technique also allows the Transformer to handle longer contexts. Moreover, the memory requirements and the complexity of Transformer models was also addressed by Kitaev et al., 2020, who introduced two techniques: (1) they replaced the dot-product attention with a locality-sensitive hashing which deals with a subset of nearest neighbours in high-dimensional spaces for the attention computation which saw the reduction of complexity from quadratic to log linear, and (2) they utilized reversible residual layers in place of standard residuals, thereby allowing the storage of activations only once instead of in every layer, which makes it much more memory efficient. Furthermore, Sourkov, 2018 proposed to replace pairwise dot-product attention mechanism with an IGLOO-base block to a get computational advantage. This new block did not require the computation of the full self-attention matrix, but rather a constant number of elements from distant parts of the sequence. This is particularly useful for bioinformatics tasks since these tasks often comprise long sequences.

The Transformer models, even though emerging as the new workhorse for NLP, were found not to perform well in comparison to LSTM in some tasks. For instance, Tran et al., 2018 compared LSTMs and Transformers in their ability to model the hierarchical structure in sentences. The tasks that were performed were subject–verb agreement and logical inference. They observed that the LSTMs consistently outperformed Transformers and the performance gap increased with the distance between the subject and the verb in a sentence. The task of logical inference, which is to predict logical relations between pairs of sentences, was also found to be modelled better with the LSTM architecture, especially in longer sequences. Work by Hahn, 2020 also showed that Transformers had problems to accurately evaluate logical formulas and to model hierarchical structures. Moreover, regarding linguistics, a Transformer model called GPT-2 had problems to learn poetry and rhyming (Wang et al., 2021). Its successor, called GTP-3, did a bit better on this task, but not as much improvement as was seen in tasks like arithmetic. These shortcomings of the Transformer models are important to be aware of since they could also be considerable factors in protein prediction tasks for which these or similar properties are critical.

A better performance on downstream task can usually be achieved by increasing the Transformer model’s size (adding more layers and more parameters). Such high-capacity models face both memory limitation and longer training times. Lan et al., 2019 managed to limit these issues by employing techniques in their framework that lowers the memory consumption and increases training speed. These include projecting the word embeddings into a lower dimensional embedding, thereby resulting in parameter reduction, parameter sharing in feed-forward network and attention across the layers to improve parameter efficiency and employed a sentence prediction loss that helped improve downstream task performance.

In the MLM approach, where some of the tokens are masked, the model neglects dependency between these masked positions. One way of overcoming this limitation is to utilize the benefits of autoregressive language modelling and to combine it with bidirectional context capturing used in MLM, instead of the original MLM (Yang et al., 2019). Moreover, the standard MLM approach is computationally expensive because it learns from only about 15% of the tokens at a time in most models (Wettig et al., 2022). In recent developments, Clark et al., 2020 proposed a sample-efficient pre-training method called replaced token detection that allows the model to learn from all the input tokens, unlike the masked subset approach in MLM.

The recent improvements to the Transformer model architectures indicate that this model class is still in its infancy, is clearly under fast development, and shows much promise as the architecture continues to enhance and expand. Many developments are coming in from multiple directions, such as from ML in general, from NLP, from computer vision, and from computational biology and bioinformatics, among other areas. These developments are crucial since the original Transformer architecture was designed and optimized for natural language tasks; the application of these models to biological data such as protein sequences, which are usually longer, has the possibility of running into high computational costs and memory limitation as well as suboptimally capturing very long-range dependencies. We can expect many more improvements in the years to come, and we can suppose that whatever limitations exist today will be addressed tomorrow.

A trend in the development of large Transformer models in NLP has been to build larger and larger models. 'Standard' models in NLP today have hundreds of billions of model parameters, such as Openai’s GPT-3 model with 175 billion model parameters (Brown et al., 2020) or Microsoft and Nvidia’s Megatron-Turing NLG model with 530 billion model parameters (Smith et al., 2022), but the very latest models have over a trillion model parameters (Fedus et al., 2021; Narayanan et al., 2021). This trend with ever larger models is unlikely to be sustainable since they require enormous amounts of memory and compute resources, and therefore severely limit who can build and train such models. But the trend is nevertheless clear that larger and larger models are built and are more successful. These models are also trained on ever larger sets of data. We can expect both trends to follow into computational biology and bioinformatics, with larger models trained on larger sets of data. Such a trend might limit future protein research to resource rich research institutes and companies and prevent such research to be performed at universities with limited resources.

1. 1. Abdi H
   2. Williams LJ

   (2010) Principal component analysis

   Wiley Interdisciplinary Reviews: Computational Statistics 2:433–459.

   https://doi.org/10.1098/rsta.2015.0202

   • Google Scholar
2. 1. Alanis-Lobato G
   2. Andrade-Navarro MA
   3. Schaefer MH

   (2016) HIPPIE v2. 0: enhancing meaningfulness and reliability of protein–protein interaction networks

   Nucleic Acids Research 45:D408–D414.

   https://doi.org/10.1093/nar/gkw985

   • Google Scholar
3. Conference

   1. Albawi S
   2. Mohammed TA
   3. Al-Zawi S

   (2017) Understanding of a convolutional neural network

   2017 International Conference on Engineering and Technology (ICET.

   https://doi.org/10.1109/ICEngTechnol.2017.8308186

   • Google Scholar
4. 1. Altschul SF
   2. Madden TL
   3. Schäffer AA
   4. Zhang J
   5. Zhang Z
   6. Miller W
   7. Lipman DJ

   (1997) Gapped blast and PSI-BLAST: a new generation of protein database search programs

   Nucleic Acids Research 25:3389–3402.

   https://doi.org/10.1093/nar/25.17.3389

   • PubMed
   • Google Scholar
5. Software

   1. Ammari MG
   2. Gresham CR
   3. McCarthy FM
   4. Nanduri B

   (2016)

   HPIDB 2.0: a curated database for host–pathogen interactions

   Database.
6. 1. Behjati A
   2. Zare-Mirakabad F
   3. Arab SS
   4. Nowzari-Dalini A

   (2022) Protein sequence profile prediction using protalbert transformer

   Computational Biology and Chemistry 99:107717.

   https://doi.org/10.1016/j.compbiolchem.2022.107717

   • PubMed
   • Google Scholar
7. 1. Bengio Y
   2. Simard P
   3. Frasconi P

   (1994) Learning long-term dependencies with gradient descent is difficult

   IEEE Transactions on Neural Networks 5:157–166.

   https://doi.org/10.1109/72.279181

   • PubMed
   • Google Scholar
8. 1. Bepler T
   2. Berger B

   (2021) Learning the protein language: evolution, structure, and function

   Cell Systems 12:654–669.

   https://doi.org/10.1016/j.cels.2021.05.017

   • Google Scholar
9. Conference

   1. Bergstra J
   2. Yamins D
   3. Cox D

   (2013)

   Making a science of model search: Hyperparameter optimization in hundreds of dimensions for vision architectures

   International conference on machine learning; 2013: PMLR.

   • Google Scholar
10. Website

    1. BFD

    (2022) BFD

    Accessed July 1, 2022.

    https://bfd.mmseqs.com
11. 1. Bileschi ML
    2. Belanger D
    3. Bryant DH
    4. Sanderson T
    5. Carter B
    6. Sculley D
    7. Bateman A
    8. DePristo MA
    9. Colwell LJ

    (2022) Using deep learning to annotate the protein universe

    Nature Biotechnology 40:932–937.

    https://doi.org/10.1038/s41587-021-01179-w

    • Google Scholar
12. Preprint

    1. Brandes N
    2. Ofer D
    3. Peleg Y
    4. Rappoport N
    5. Linial M

    (2021) ProteinBERT: A Universal Deep-Learning Model of Protein Sequence and Function

    bioRxiv.

    https://doi.org/10.1101/2021.05.24.445464

    • Google Scholar
13. Conference

    1. Britz D
    2. Goldie A
    3. Luong MT
    4. Le Q

    (2017) Massive Exploration of Neural Machine Translation Architectures

    Proceedings of the 2017 Conference on Empirical Methods in Natural Language Processing.

    https://doi.org/10.18653/v1/D17-1151

    • Google Scholar
14. Conference

    1. Brown T
    2. Mann B
    3. Ryder N
    4. Subbiah M
    5. Kaplan JD
    6. Dhariwal P

    (2020)

    Language models are few-shot learners

    Advances in Neural Information Processing Systems. pp. 1877–1901.

    • Google Scholar
15. 1. Bulcun E
    2. Ekici M
    3. Ekici A

    (2012) Disorders of glucose metabolism and insulin resistance in patients with obstructive sleep apnoea syndrome

    International Journal of Clinical Practice 66:91–97.

    https://doi.org/10.1111/j.1742-1241.2011.02795.x

    • PubMed
    • Google Scholar
16. 1. Cai T
    2. Lim H
    3. Abbu KA
    4. Qiu Y
    5. Nussinov R
    6. Xie L

    (2021) MSA-regularized protein sequence transformer toward predicting genome-wide chemical-protein interactions: application to gpcrome deorphanization

    Journal of Chemical Information and Modeling 61:1570–1582.

    https://doi.org/10.1021/acs.jcim.0c01285

    • PubMed
    • Google Scholar
17. 1. Chan WKB
    2. Zhang H
    3. Yang J
    4. Brender JR
    5. Hur J
    6. Özgür A
    7. Zhang Y

    (2015) Glass: a comprehensive database for experimentally validated GPCR-ligand associations

    Bioinformatics 31:3035–3042.

    https://doi.org/10.1093/bioinformatics/btv302

    • PubMed
    • Google Scholar
18. 1. Chandra A
    2. Sharma A
    3. Dehzangi A
    4. Shigemizu D
    5. Tsunoda T

    (2019) Bigram-PGK: phosphoglycerylation prediction using the technique of bigram probabilities of position specific scoring matrix

    BMC Molecular and Cell Biology 20:57.

    https://doi.org/10.1186/s12860-019-0240-1

    • PubMed
    • Google Scholar
19. 1. Chandra AA
    2. Sharma A
    3. Dehzangi A
    4. Tsunoda T

    (2020) RAM-PGK: prediction of lysine phosphoglycerylation based on residue adjacency matrix

    Genes 11:1524.

    https://doi.org/10.3390/genes11121524

    • PubMed
    • Google Scholar
20. 1. Charte D
    2. Charte F
    3. García S
    4. Herrera F

    (2019) A snapshot on nonstandard supervised learning problems: taxonomy, relationships, problem transformations and algorithm adaptations

    Progress in Artificial Intelligence 8:1–14.

    https://doi.org/10.1007/s13748-018-00167-7

    • Google Scholar
21. Conference

    1. Chefer H
    2. Gur S
    3. Wolf L

    (2021)

    Transformer interpretability beyond attention visualization

    Proceedings of the IEEE/CVF Conference on Computer Vision and Pattern Recognition.

    • Google Scholar
22. 1. Chen X
    2. Lin Y
    3. Liu M
    4. Gilson MK

    (2002) The binding database: data management and interface design

    Bioinformatics 18:130–139.

    https://doi.org/10.1093/bioinformatics/18.1.130

    • PubMed
    • Google Scholar
23. 1. Chen CW
    2. Lin MH
    3. Liao CC
    4. Chang HP
    5. Chu YW

    (2020) IStable 2.0: predicting protein thermal stability changes by integrating various characteristic modules

    Computational and Structural Biotechnology Journal 18:622–630.

    https://doi.org/10.1016/j.csbj.2020.02.021

    • PubMed
    • Google Scholar
24. 1. Cheng J
    2. Bendjama K
    3. Rittner K
    4. Malone B

    (2021) BERTMHC: improved MHC-peptide class II interaction prediction with transformer and multiple instance learning

    Bioinformatics 37:4172–4179.

    https://doi.org/10.1093/bioinformatics/btab422

    • PubMed
    • Google Scholar
25. Preprint

    1. Choromanski K
    2. Likhosherstov V
    3. Dohan D
    4. Song X
    5. Gane A
    6. Sarlos T

    (2020) Masked Language Modeling for Proteins via Linearly Scalable Long-Context Transformers

    arXiv.

    https://arxiv.org/abs/2006.03555

    • Google Scholar
26. 1. Chou KC
    2. Zhang CT

    (1995) Prediction of protein structural classes

    Critical Reviews in Biochemistry and Molecular Biology 30:275–349.

    https://doi.org/10.3109/10409239509083488

    • PubMed
    • Google Scholar
27. 1. Chou KC

    (2020) Progresses in predicting post-translational modification

    International Journal of Peptide Research and Therapeutics 26:873–888.

    https://doi.org/10.1007/s10989-019-09893-5

    • Google Scholar
28. 1. Chowdhury R
    2. Bouatta N
    3. Biswas S
    4. Floristean C
    5. Kharkare A
    6. Roye K

    (2022) Single-sequence protein structure prediction using a language model and deep learning

    Nature Biotechnology 22:1–7.

    https://doi.org/10.1038/s41587-022-01432-w

    • Google Scholar
29. Preprint

    1. Chung J
    2. Gulcehre C
    3. Cho K
    4. Bengio Y

    (2014) Empirical Evaluation of Gated Recurrent Neural Networks on Sequence Modeling

    arXiv.

    https://arxiv.org/abs/1412.3555

    • Google Scholar
30. Preprint

    1. Clark K
    2. Luong MT
    3. Le QV

    (2020) ELECTRA: Pre-Training Text Encoders as Discriminators Rather Than Generators

    arXiv.

    https://arxiv.org/abs/2003.10555

    • Google Scholar
31. 1. Cortés GA
    2. Aguilar-Ruiz JA

    (2011) Predicting protein distance maps according to physicochemical properties

    Journal of Integrative Bioinformatics 8:158–175.

    https://doi.org/10.1515/jib-2011-181

    • Google Scholar
32. Software

    1. Dai Z
    2. Yang Z
    3. Yang Y
    4. Cohen WW
    5. Carbonell J
    6. Le QV

    (2018)

    Transformer-xl: language modeling with longer-term dependency

    Transformer-Xl.
33. Preprint

    1. Dai Z
    2. Yang Z
    3. Yang Y
    4. Carbonell J
    5. Le QV
    6. Salakhutdinov R

    (2019) Transformer-Xl: Attentive Language Models beyond a Fixed-Length Context

    arXiv.

    https://arxiv.org/abs/1901.02860

    • Google Scholar
34. 1. Davis MI
    2. Hunt JP
    3. Herrgard S
    4. Ciceri P
    5. Wodicka LM
    6. Pallares G

    (2011) Comprehensive analysis of kinase inhibitor selectivity

    Nature Biotechnology 29:1046–1051.

    https://doi.org/10.1038/nbt.1990

    • Google Scholar
35. Preprint

    1. Dehghani M
    2. Gouws S
    3. Vinyals O
    4. Uszkoreit J
    5. Kaiser Ł

    (2018) Universal Transformers

    arXiv.

    https://arxiv.org/abs/1807.03819

    • Google Scholar
36. Preprint

    1. Devlin J
    2. Chang MW
    3. Lee K
    4. Toutanova K

    (2018) Bert: Pre-Training of Deep Bidirectional Transformers for Language Understanding

    arXiv.

    https://arxiv.org/abs/1810.04805

    • Google Scholar
37. 1. Dick K
    2. Green JR

    (2018) Reciprocal perspective for improved protein-protein interaction prediction

    Scientific Reports 8:1–12.

    https://doi.org/10.1038/s41598-018-30044-1

    • Google Scholar
38. 1. Dodge C
    2. Schneider R
    3. Sander C

    (1998) The HSSP database of protein structure-sequence alignments and family profiles

    Nucleic Acids Research 26:313–315.

    https://doi.org/10.1093/nar/26.1.313

    • PubMed
    • Google Scholar
39. 1. Du Z
    2. Su H
    3. Wang W
    4. Ye L
    5. Wei H
    6. Peng Z
    7. Anishchenko I
    8. Baker D
    9. Yang J

    (2021) The trrosetta server for fast and accurate protein structure prediction

    Nature Protocols 16:5634–5651.

    https://doi.org/10.1038/s41596-021-00628-9

    • PubMed
    • Google Scholar
40. 1. Ehrenberger T
    2. Cantley LC
    3. Yaffe MB

    (2015) Computational prediction of protein-protein interactions

    Methods in Molecular Biology 1278:57–75.

    https://doi.org/10.1007/978-1-4939-2425-7_4

    • PubMed
    • Google Scholar
41. 1. ElAbd H
    2. Bromberg Y
    3. Hoarfrost A
    4. Lenz T
    5. Franke A
    6. Wendorff M

    (2020) Amino acid encoding for deep learning applications

    BMC Bioinformatics 21:235.

    https://doi.org/10.1186/s12859-020-03546-x

    • PubMed
    • Google Scholar
42. 1. ElGebali S
    2. Mistry J
    3. Bateman A
    4. Eddy SR
    5. Luciani A
    6. Potter SC
    7. Qureshi M
    8. Richardson LJ
    9. Salazar GA
    10. Smart A
    11. Sonnhammer ELL
    12. Hirsh L
    13. Paladin L
    14. Piovesan D
    15. Tosatto SCE
    16. Finn RD

    (2019) The pfam protein families database in 2019

    Nucleic Acids Research 47:D427–D432.

    https://doi.org/10.1093/nar/gky995

    • Google Scholar
43. 1. Elman JL

    (1990) Finding structure in time

    Cognitive Science 14:179–211.

    https://doi.org/10.1207/s15516709cog1402_1

    • Google Scholar
44. Preprint

    1. Elnaggar A
    2. Heinzinger M
    3. Dallago C
    4. Rehawi G
    5. Wang Y
    6. Jones L
    7. Gibbs T
    8. Feher T
    9. Angerer C
    10. Steinegger M
    11. Bhowmik D
    12. Rost B

    (2020a) ProtTrans: Towards Cracking the Language of Life’s Code Through Self-Supervised Learning

    bioRxiv.

    https://doi.org/10.1101/2020.07.12.199554

    • Google Scholar
45. Preprint

    1. Elnaggar A
    2. Heinzinger M
    3. Dallago C
    4. Rehawi G
    5. Wang Y
    6. Jones L
    7. Gibbs T
    8. Feher T
    9. Angerer C
    10. Steinegger M
    11. Bhowmik D
    12. Rost B

    (2020b) ProtTrans: Towards Cracking the Language of Life’s Code through Self-Supervised Deep Learning and High Performance Computing

    arXiv.

    https://arxiv.org/abs/2007.06225

    • Google Scholar
46. 1. Fang J

    (2020) A critical review of five machine learning-based algorithms for predicting protein stability changes upon mutation

    Briefings in Bioinformatics 21:1285–1292.

    https://doi.org/10.1093/bib/bbz071

    • PubMed
    • Google Scholar
47. Preprint

    1. Fedus W
    2. Zoph B
    3. Shazeer N

    (2021) Switch Transformers: Scaling to Trillion Parameter Models with Simple and Efficient Sparsity

    arXiv.

    https://arxiv.org/abs/2101.03961

    • Google Scholar
48. 1. Ferruz N
    2. Schmidt S
    3. Höcker B

    (2022) ProtGPT2 is a deep unsupervised language model for protein design

    Nature Communications 13:4348.

    https://doi.org/10.1038/s41467-022-32007-7

    • PubMed
    • Google Scholar
49. 1. Finn RD
    2. Clements J
    3. Eddy SR

    (2011) HMMER web server: interactive sequence similarity searching

    Nucleic Acids Research 39:W29–W37.

    https://doi.org/10.1093/nar/gkr367

    • Google Scholar
50. 1. Gaulton A
    2. Bellis LJ
    3. Bento AP
    4. Chambers J
    5. Davies M
    6. Hersey A
    7. Light Y
    8. McGlinchey S
    9. Michalovich D
    10. Al-Lazikani B
    11. Overington JP

    (2012) ChEMBL: a large-scale bioactivity database for drug discovery

    Nucleic Acids Research 40:D1100–D1107.

    https://doi.org/10.1093/nar/gkr777

    • Google Scholar
51. 1. Golubchik T
    2. Wise MJ
    3. Easteal S
    4. Jermiin LS

    (2007) Mind the gaps: evidence of bias in estimates of multiple sequence alignments

    Molecular Biology and Evolution 24:2433–2442.

    https://doi.org/10.1093/molbev/msm176

    • PubMed
    • Google Scholar
52. Website

    1. Google Scholar

    (2022) Google Scholar

    Accessed July 1, 2022.

    https://scholar.google.com/scholar?q=transformer+language+model+transformer+language+model&hl=en&as_sdt=0,5
53. Software

    1. Gromiha MM
    2. Nagarajan R
    3. Selvaraj S

    (2019)

    Protein structural bioinformatics: an overview

    Protein Structural Bioinformatics.
54. 1. Guerler A
    2. Govindarajoo B
    3. Zhang Y

    (2013) Mapping monomeric threading to protein-protein structure prediction

    Journal of Chemical Information and Modeling 53:717–725.

    https://doi.org/10.1021/ci300579r

    • PubMed
    • Google Scholar
55. 1. Hahn M

    (2020) Theoretical limitations of self-attention in neural sequence models

    Transactions of the Association for Computational Linguistics 8:156–171.

    https://doi.org/10.1162/tacl_a_00306

    • Google Scholar
56. Conference

    1. Hanin B

    (2018)

    Which neural net architectures give rise to exploding and vanishing gradients?

    Advances in Neural Information Processing Systems.

    • Google Scholar
57. Conference

    1. Hao Y
    2. Dong L
    3. Wei F
    4. Xu K

    (2021) Self-attention attribution: interpreting information interactions inside transformer

    Proceedings of the AAAI Conference on Artificial Intelligence. pp. 12963–12971.

    https://doi.org/10.1609/aaai.v35i14.17533

    • Google Scholar
58. Preprint

    1. He L
    2. Zhang S
    3. Wu L
    4. Xia H
    5. Ju F
    6. Zhang H

    (2021) Pre-Training Co-Evolutionary Protein Representation via A Pairwise Masked Language Model

    arXiv.

    https://arxiv.org/abs/2110.15527

    • Google Scholar
59. Preprint

    1. Heinzinger M
    2. Elnaggar A
    3. Wang Y
    4. Dallago C
    5. Nechaev D
    6. Matthes F

    (2019) Modeling the Language of Life–Deep Learning Protein Sequences

    bioRxiv.

    https://doi.org/10.1101/614313

    • Google Scholar
60. Preprint

    1. Heinzinger M
    2. Littmann M
    3. Sillitoe I
    4. Bordin N
    5. Orengo C
    6. Rost B

    (2021) Contrastive Learning on Protein Embeddings Enlightens Midnight Zone at Lightning Speed

    bioRxiv.

    https://doi.org/10.1101/2021.11.14.468528

    • Google Scholar
61. 1. Heinzinger M
    2. Littmann M
    3. Sillitoe I
    4. Bordin N
    5. Orengo C
    6. Rost B

    (2022) Contrastive learning on protein embeddings enlightens midnight zone

    NAR Genomics and Bioinformatics 4:lqac043.

    https://doi.org/10.1093/nargab/lqac043

    • PubMed
    • Google Scholar
62. 1. Hochreiter S
    2. Schmidhuber J

    (1997) Long short-term memory

    Neural Computation 9:1735–1780.

    https://doi.org/10.1162/neco.1997.9.8.1735

    • PubMed
    • Google Scholar
63. Preprint

    1. Hong L
    2. Sun S
    3. Zheng L
    4. Tan Q
    5. Li Y

    (2021) FastMSA: Accelerating Multiple Sequence Alignment with Dense Retrieval on Protein Language

    bioRxiv.

    https://doi.org/10.1101/2021.12.20.473431

    • Google Scholar
64. Preprint

    1. Huang Z
    2. Xu W
    3. Yu K

    (2015) Bidirectional LSTM-CRF Models for Sequence Tagging

    arXiv.

    https://arxiv.org/abs/1508.01991

    • Google Scholar
65. 1. Jia J
    2. Liu Z
    3. Xiao X
    4. Liu B
    5. Chou KC

    (2016) ISuc-pseopt: identifying lysine succinylation sites in proteins by incorporating sequence-coupling effects into pseudo components and optimizing imbalanced training dataset

    Analytical Biochemistry 497:48–56.

    https://doi.org/10.1016/j.ab.2015.12.009

    • PubMed
    • Google Scholar
66. 1. Jiang Q
    2. Jin X
    3. Lee SJ
    4. Yao S

    (2017) Protein secondary structure prediction: A survey of the state of the art

    Journal of Molecular Graphics & Modelling 76:379–402.

    https://doi.org/10.1016/j.jmgm.2017.07.015

    • PubMed
    • Google Scholar
67. Preprint

    1. Jiang T
    2. Fang L
    3. Wang K

    (2021) MutFormer: A Context-Dependent Transformer-Based Model to Predict Pathogenic Missense Mutations

    arXiv.

    https://arxiv.org/abs/2110.14746

    • Google Scholar
68. 1. Jones DT

    (1999) Protein secondary structure prediction based on position-specific scoring matrices

    Journal of Molecular Biology 292:195–202.

    https://doi.org/10.1006/jmbi.1999.3091

    • PubMed
    • Google Scholar
69. 1. Jumper J
    2. Evans R
    3. Pritzel A
    4. Green T
    5. Figurnov M
    6. Ronneberger O
    7. Tunyasuvunakool K
    8. Bates R
    9. Žídek A
    10. Potapenko A
    11. Bridgland A
    12. Meyer C
    13. Kohl SAA
    14. Ballard AJ
    15. Cowie A
    16. Romera-Paredes B
    17. Nikolov S
    18. Jain R
    19. Adler J
    20. Back T
    21. Petersen S
    22. Reiman D
    23. Clancy E
    24. Zielinski M
    25. Steinegger M
    26. Pacholska M
    27. Berghammer T
    28. Bodenstein S
    29. Silver D
    30. Vinyals O
    31. Senior AW
    32. Kavukcuoglu K
    33. Kohli P
    34. Hassabis D

    (2021) Highly accurate protein structure prediction with alphafold

    Nature 596:583–589.

    https://doi.org/10.1038/s41586-021-03819-2

    • PubMed
    • Google Scholar
70. 1. Katchalski-Katzir E
    2. Shariv I
    3. Eisenstein M
    4. Friesem AA
    5. Aflalo C
    6. Vakser IA

    (1992) Molecular surface recognition: determination of geometric fit between proteins and their ligands by correlation techniques

    PNAS 89:2195–2199.

    https://doi.org/10.1073/pnas.89.6.2195

    • PubMed
    • Google Scholar
71. 1. Khalili E
    2. Ramazi S
    3. Ghanati F
    4. Kouchaki S

    (2022) Predicting protein phosphorylation sites in soybean using interpretable deep tabular learning network

    Briefings in Bioinformatics 23:bbac015.

    https://doi.org/10.1093/bib/bbac015

    • Google Scholar
72. Conference

    1. Khan M
    2. Jan B
    3. Farman H

    (2019) Deep learning: convergence to big data analytics

    Deep Learning Methods and Applications. pp. 31–42.

    https://doi.org/10.1007/978-981-13-3459-7

    • Google Scholar
73. Preprint

    1. Kitaev N
    2. Kaiser Ł
    3. Levskaya A

    (2020) Reformer: The Efficient Transformer

    arXiv.

    https://arxiv.org/abs/2001.04451

    • Google Scholar
74. Preprint

    1. Ko J
    2. Lee J

    (2021) Can AlphaFold2 Predict Protein-Peptide Complex Structures Accurately?

    bioRxiv.

    https://doi.org/10.1101/2021.07.27.453972

    • Google Scholar
75. 1. Koumakis L

    (2020) Deep learning models in genomics; are we there yet?

    Computational and Structural Biotechnology Journal 18:1466–1473.

    https://doi.org/10.1016/j.csbj.2020.06.017

    • PubMed
    • Google Scholar
76. 1. Kryshtafovych A
    2. Schwede T
    3. Topf M
    4. Fidelis K
    5. Moult J

    (2019) Critical assessment of methods of protein structure prediction (CASP)-round XIII

    Proteins 87:1011–1020.

    https://doi.org/10.1002/prot.25823

    • PubMed
    • Google Scholar
77. 1. Kuhlman B
    2. Bradley P

    (2019) Advances in protein structure prediction and design

    Nature Reviews. Molecular Cell Biology 20:681–697.

    https://doi.org/10.1038/s41580-019-0163-x

    • PubMed
    • Google Scholar
78. Preprint

    1. Lan Z
    2. Chen M
    3. Goodman S
    4. Gimpel K
    5. Sharma P
    6. Soricut R

    (2019) Albert: A Lite Bert for Self-Supervised Learning of Language Representations

    arXiv.

    https://arxiv.org/abs/1909.11942

    • Google Scholar
79. Conference

    1. Lanchantin J
    2. Weingarten T
    3. Sekhon A
    4. Miller C
    5. Qi Y

    (2021) Transfer learning for predicting virus-host protein interactions for novel virus sequences

    BCB ’21: Proceedings of the 12th ACM Conference on Bioinformatics, Computational Biology, and Health Informatics. pp. 1–10.

    https://doi.org/10.1145/3459930.3469527

    • Google Scholar
80. Conference

    1. Laskar MTR
    2. Huang X
    3. Hoque E

    (2020)

    Contextualized embeddings based transformer encoder for sentence similarity modeling in answer selection task

    Proceedings of The 12th Language Resources and Evaluation Conference. pp. 5505–5514.

    • Google Scholar
81. Conference

    1. Levy O
    2. Goldberg Y

    (2014)

    Dependency-based word embeddings

    Proceedings of the 52nd Annual Meeting of the Association for Computational Linguistics.

    • Google Scholar
82. 1. Li F
    2. Dong S
    3. Leier A
    4. Han M
    5. Guo X
    6. Xu J
    7. Wang X
    8. Pan S
    9. Jia C
    10. Zhang Y
    11. Webb GI
    12. Coin LJM
    13. Li C
    14. Song J

    (2022) Positive-unlabeled learning in bioinformatics and computational biology: a brief review

    Briefings in Bioinformatics 23:bbab461.

    https://doi.org/10.1093/bib/bbab461

    • Google Scholar
83. 1. Liu T
    2. Lin Y
    3. Wen X
    4. Jorissen RN
    5. Gilson MK

    (2007) BindingDB: a web-accessible database of experimentally determined protein-ligand binding affinities

    Nucleic Acids Research 35:D198–D201.

    https://doi.org/10.1093/nar/gkl999

    • PubMed
    • Google Scholar
84. 1. Liu B
    2. Wang X
    3. Chen Q
    4. Dong Q
    5. Lan X

    (2012) Using amino acid physicochemical distance transformation for fast protein remote homology detection

    PLOS ONE 7:e46633.

    https://doi.org/10.1371/journal.pone.0046633

    • PubMed
    • Google Scholar
85. 1. Liu B
    2. Li CC
    3. Yan K

    (2020) DeepSVM-fold: protein fold recognition by combining support vector machines and pairwise sequence similarity scores generated by deep learning networks

    Briefings in Bioinformatics 21:1733–1741.

    https://doi.org/10.1093/bib/bbz098

    • PubMed
    • Google Scholar
86. 1. López Y
    2. Dehzangi A
    3. Lal SP
    4. Taherzadeh G
    5. Michaelson J
    6. Sattar A
    7. Tsunoda T
    8. Sharma A

    (2017) SucStruct: prediction of succinylated lysine residues by using structural properties of amino acids

    Analytical Biochemistry 527:24–32.

    https://doi.org/10.1016/j.ab.2017.03.021

    • PubMed
    • Google Scholar
87. Software

    1. Lopez MJ
    2. Mohiuddin SS

    (2020)

    Biochemistry, essential amino acids

    Biochemistry.
88. Preprint

    1. Lu T
    2. Lu AX
    3. Moses AM

    (2021) Random Embeddings and Linear Regression Can Predict Protein Function

    arXiv.

    https://arxiv.org/abs/2104.14661

    • Google Scholar
89. 1. McDowall MD
    2. Scott MS
    3. Barton GJ

    (2009) Pips: human protein-protein interaction prediction database

    Nucleic Acids Research 37:D651–D656.

    https://doi.org/10.1093/nar/gkn870

    • Google Scholar
90. Conference

    1. Mikolov T
    2. Kombrink S
    3. Burget L
    4. Černocký J

    (2011) Extensions of recurrent neural network language model

    2011 IEEE international conference on acoustics, speech and signal processing (ICASSP); 2011: IEEE.

    https://doi.org/10.1109/ICASSP.2011.5947611

    • Google Scholar
91. Conference

    1. Mikolov T
    2. Chen K
    3. Corrado GS

    (2013a)

    International Conference on Learning Representations

    Efficient Estimation of Word Representations in Vector Space.

    • Google Scholar
92. Preprint

    1. Mikolov T
    2. Chen K
    3. Corrado G
    4. Dean J

    (2013b) Efficient Estimation of Word Representations in Vector Space

    arXiv.

    https://arxiv.org/abs/1301.3781

    • Google Scholar
93. 1. Mirdita M
    2. Schütze K
    3. Moriwaki Y
    4. Heo L
    5. Ovchinnikov S
    6. Steinegger M

    (2022) ColabFold: making protein folding accessible to all

    Nature Methods 19:679–682.

    https://doi.org/10.1038/s41592-022-01488-1

    • PubMed
    • Google Scholar
94. 1. Mistry J
    2. Chuguransky S
    3. Williams L
    4. Qureshi M
    5. Salazar GA
    6. Sonnhammer EL

    (2021) Pfam: the protein families database in 2021

    Nucleic Acids Research 49:D412–D419.

    https://doi.org/10.1093/nar/gkaa913

    • Google Scholar
95. Conference

    1. Nambiar A
    2. Heflin M
    3. Liu S
    4. Maslov S
    5. Hopkins M
    6. Ritz A

    (2020) Transforming the Language of Life: Transformer Neural Networks for Protein Prediction Tasks

    BCB ’20: Proceedings of the 11th ACM International Conference on Bioinformatics, Computational Biology and Health Informatics. pp. 1–8.

    https://doi.org/10.1145/3388440.3412467

    • Google Scholar
96. Conference

    1. Narayanan D
    2. Shoeybi M
    3. Casper J
    4. LeGresley P
    5. Patwary M
    6. Korthikanti V

    (2021)

    Efficient large-scale language model training on gpu clusters using megatron-lm

    Proceedings of the International Conference for High Performance Computing, Networking, Storage and Analysis.

    • Google Scholar
97. 1. Nauman M
    2. Ur Rehman H
    3. Politano G
    4. Benso A

    (2019) Beyond homology transfer: deep learning for automated annotation of proteins

    Journal of Grid Computing 17:225–237.

    https://doi.org/10.1007/s10723-018-9450-6

    • Google Scholar
98. 1. Ofer D
    2. Brandes N
    3. Linial M

    (2021) The language of proteins: Nlp, machine learning & protein sequences

    Computational and Structural Biotechnology Journal 19:1750–1758.

    https://doi.org/10.1016/j.csbj.2021.03.022

    • PubMed
    • Google Scholar
99. 1. Öztürk H
    2. Özgür A
    3. Ozkirimli E

    (2018) DeepDTA: deep drug-target binding affinity prediction

    Bioinformatics 34:i821–i829.

    https://doi.org/10.1093/bioinformatics/bty593

    • PubMed
    • Google Scholar
100. 1. Pan Q
     2. Nguyen TB
     3. Ascher DB
     4. Pires DEV

     (2022) Systematic evaluation of computational tools to predict the effects of mutations on protein stability in the absence of experimental structures

     Briefings in Bioinformatics 23:bbac025.

     https://doi.org/10.1093/bib/bbac025

     • PubMed
     • Google Scholar
101. Conference

     1. Pascanu R
     2. Mikolov T
     3. Bengio Y

     (2013)

     On the difficulty of training recurrent neural networks

     International conference on machine learning; 2013: PMLR.

     • Google Scholar
102. Conference

     1. Peters M
     2. Neumann M
     3. Iyyer M
     4. Gardner M
     5. Clark C
     6. Lee K
     7. Zettlemoyer L

     (2018) Deep Contextualized Word Representations

     Proceedings of the 2018 Conference of the North American Chapter of the Association for Computational Linguistics: Human Language Technologies.

     https://doi.org/10.18653/v1/N18-1202

     • Google Scholar
103. Website

     1. Pfam 35.0

     (2021) Pfam 35.0 is released 2021

     Accessed July 1, 2022.

     https://xfam.wordpress.com/2021/11/19/pfam-35-0-is-released
104. 1. Phuong TM
     2. Do CB
     3. Edgar RC
     4. Batzoglou S

     (2006) Multiple alignment of protein sequences with repeats and rearrangements

     Nucleic Acids Research 34:5932–5942.

     https://doi.org/10.1093/nar/gkl511

     • PubMed
     • Google Scholar
105. 1. Qiao Y
     2. Zhu X
     3. Gong H
     4. Xu J

     (2022) BERT-kcr: prediction of lysine crotonylation sites by a transfer learning method with pre-trained BERT models

     Bioinformatics 38:648–654.

     https://doi.org/10.1093/bioinformatics/btab712

     • Google Scholar
106. Preprint

     1. Raffel C
     2. Shazeer N
     3. Roberts A
     4. Lee K
     5. Narang S
     6. Matena M

     (2019) Exploring the Limits of Transfer Learning with a Unified Text-to-Text Transformer

     arXiv.

     https://arxiv.org/abs/1910.10683

     • Google Scholar
107. Conference

     1. Raghu M
     2. Unterthiner T
     3. Kornblith S
     4. Zhang C
     5. Dosovitskiy A

     (2021)

     Do vision transformers see like convolutional neural networks

     Advances in Neural Information Processing Systems.

     • Google Scholar
108. 1. Ramazi S
     2. Zahiri J

     (2021) Posttranslational modifications in proteins: resources, tools and prediction methods

     Database 2021:baab012.

     https://doi.org/10.1093/database/baab012

     • PubMed
     • Google Scholar
109. Conference

     1. Rao R
     2. Bhattacharya N
     3. Thomas N
     4. Duan Y
     5. Chen X
     6. Canny J
     7. Abbeel P
     8. Song YS

     (2019)

     Evaluating protein transfer learning with TAPE

     Advances in Neural Information Processing Systems. pp. 9689–9701.

     • Google Scholar
110. Conference

     1. Rao RM
     2. Liu J
     3. Verkuil R
     4. Meier J
     5. Canny J

     (2021)

     MSA transformer

     International Conference on Machine Learning; 2021: PMLR.

     • Google Scholar
111. 1. Rives A
     2. Meier J
     3. Sercu T
     4. Goyal S
     5. Lin Z
     6. Liu J
     7. Guo D
     8. Ott M
     9. Zitnick CL
     10. Ma J
     11. Fergus R

     (2021) Biological structure and function emerge from scaling unsupervised learning to 250 million protein sequences

     PNAS 118:e2016239118.

     https://doi.org/10.1073/pnas.2016239118

     • PubMed
     • Google Scholar
112. 1. Saethang T
     2. Payne DM
     3. Avihingsanon Y
     4. Pisitkun T

     (2016) A machine learning strategy for predicting localization of post-translational modification sites in protein-protein interacting regions

     BMC Bioinformatics 17:307.

     https://doi.org/10.1186/s12859-016-1165-8

     • PubMed
     • Google Scholar
113. 1. Schmiedel JM
     2. Lehner B

     (2019) Determining protein structures using deep mutagenesis

     Nature Genetics 51:1177–1186.

     https://doi.org/10.1038/s41588-019-0431-x

     • PubMed
     • Google Scholar
114. 1. Sharma A
     2. Lyons J
     3. Dehzangi A
     4. Paliwal KK

     (2013) A feature extraction technique using bi-gram probabilities of position specific scoring matrix for protein fold recognition

     Journal of Theoretical Biology 320:41–46.

     https://doi.org/10.1016/j.jtbi.2012.12.008

     • PubMed
     • Google Scholar
115. 1. Shi Q
     2. Chen W
     3. Huang S
     4. Wang Y
     5. Xue Z

     (2021) Deep learning for mining protein data

     Briefings in Bioinformatics 22:194–218.

     https://doi.org/10.1093/bib/bbz156

     • PubMed
     • Google Scholar
116. 1. Singh J
     2. Litfin T
     3. Paliwal K
     4. Singh J
     5. Hanumanthappa AK
     6. Zhou Y
     7. Martelli D

     (2021) SPOT-1D-single: improving the single-sequence-based prediction of protein secondary structure, backbone angles, solvent accessibility and half-sphere exposures using a large training set and ensembled deep learning

     Bioinformatics 37:3464–3472.

     https://doi.org/10.1093/bioinformatics/btab316

     • Google Scholar
117. 1. Singh J
     2. Litfin T
     3. Singh J
     4. Paliwal K
     5. Zhou Y

     (2022) SPOT-contact-LM: improving single-sequence-based prediction of protein contact MAP using a transformer language model

     Bioinformatics 38:1888–1894.

     https://doi.org/10.1093/bioinformatics/btac053

     • PubMed
     • Google Scholar
118. Preprint

     1. Smith S
     2. Patwary M
     3. Norick B
     4. LeGresley P
     5. Rajbhandari S
     6. Casper J

     (2022) Using Deepspeed and Megatron to Train Megatron-Turing Nlg 530b, a Large-Scale Generative Language Model

     arXiv.

     https://arxiv.org/abs/2201.11990

     • Google Scholar
119. Preprint

     1. Sourkov V

     (2018) Igloo: Slicing the Features Space to Represent Sequences

     arXiv.

     https://arxiv.org/abs/1807.03402

     • Google Scholar
120. 1. Steinegger M
     2. Söding J

     (2017) MMseqs2 enables sensitive protein sequence searching for the analysis of massive data sets

     Nature Biotechnology 35:1026–1028.

     https://doi.org/10.1038/nbt.3988

     • PubMed
     • Google Scholar
121. 1. Steinegger M
     2. Mirdita M
     3. Söding J

     (2019) Protein-level assembly increases protein sequence recovery from metagenomic samples manyfold

     Nature Methods 16:603–606.

     https://doi.org/10.1038/s41592-019-0437-4

     • PubMed
     • Google Scholar
122. Preprint

     1. Sturmfels P
     2. Vig J
     3. Madani A
     4. Rajani NF

     (2020) Profile Prediction: An Alignment-Based Pre-Training Task for Protein Sequence Models

     arXiv.

     https://arxiv.org/abs/2012.00195

     • Google Scholar
123. 1. Sułkowska JI
     2. Morcos F
     3. Weigt M
     4. Hwa T
     5. Onuchic JN

     (2012) Genomics-aided structure prediction

     PNAS 109:10340–10345.

     https://doi.org/10.1073/pnas.1207864109

     • Google Scholar
124. 1. Tang J
     2. Szwajda A
     3. Shakyawar S
     4. Xu T
     5. Hintsanen P
     6. Wennerberg K
     7. Aittokallio T

     (2014) Making sense of large-scale kinase inhibitor bioactivity data sets: a comparative and integrative analysis

     Journal of Chemical Information and Modeling 54:735–743.

     https://doi.org/10.1021/ci400709d

     • PubMed
     • Google Scholar
125. 1. Tavares LS
     2. Silva CSF
     3. de Souza VC
     4. da Silva VL
     5. Diniz CG
     6. Santos MO

     (2013) Strategies and molecular tools to fight antimicrobial resistance: resistome, transcriptome, and antimicrobial peptides

     Frontiers in Microbiology 4:412.

     https://doi.org/10.3389/fmicb.2013.00412

     • PubMed
     • Google Scholar
126. Conference

     1. Tran K
     2. Bisazza A
     3. Monz C

     (2018) The Importance of Being Recurrent for Modeling Hierarchical Structure

     Proceedings of the 2018 Conference on Empirical Methods in Natural Language Processing.

     https://doi.org/10.18653/v1/D18-1503

     • Google Scholar
127. 1. Trost B
     2. Kusalik A

     (2013) Computational phosphorylation site prediction in plants using random forests and organism-specific instance weights

     Bioinformatics 29:686–694.

     https://doi.org/10.1093/bioinformatics/btt031

     • PubMed
     • Google Scholar
128. Conference

     1. Turian J
     2. Ratinov L

     (2010)

     Word representations: a simple and general method for semi-supervised learning

     Proceedings of the 48th annual meeting of the association for computational linguistics.

     • Google Scholar
129. 1. UniProt

     (2021) UniProt: the universal protein knowledgebase in 2021

     Nucleic Acids Research 49:D480–D489.

     https://doi.org/10.1093/nar/gkaa1100

     • Google Scholar
130. 1. UniProt Consortium

     (2019) UniProt: a worldwide hub of protein knowledge

     Nucleic Acids Research 47:D506–D515.

     https://doi.org/10.1093/nar/gky1049

     • PubMed
     • Google Scholar
131. 1. Vakser IA

     (2014) Protein-Protein docking: from interaction to interactome

     Biophysical Journal 107:1785–1793.

     https://doi.org/10.1016/j.bpj.2014.08.033

     • PubMed
     • Google Scholar
132. 1. Van der Maaten L
     2. Hinton G

     (2008)

     Visualizing data using t-SNE

     Journal of Machine Learning Research 9:11.

     • Google Scholar
133. 1. Varadi M
     2. Anyango S
     3. Deshpande M
     4. Nair S
     5. Natassia C
     6. Yordanova G
     7. Yuan D
     8. Stroe O
     9. Wood G
     10. Laydon A
     11. Žídek A
     12. Green T
     13. Tunyasuvunakool K
     14. Petersen S
     15. Jumper J
     16. Clancy E
     17. Green R
     18. Vora A
     19. Lutfi M
     20. Figurnov M
     21. Cowie A
     22. Hobbs N
     23. Kohli P
     24. Kleywegt G
     25. Birney E
     26. Hassabis D
     27. Velankar S

     (2022) AlphaFold protein structure database: massively expanding the structural coverage of protein-sequence space with high-accuracy models

     Nucleic Acids Research 50:D439–D444.

     https://doi.org/10.1093/nar/gkab1061

     • PubMed
     • Google Scholar
134. Conference

     1. Vaswani A
     2. Shazeer N
     3. Parmar N
     4. Uszkoreit J
     5. Jones L
     6. Gomez AN

     (2017)

     Attention is all you need

     Advances in Neural Information Processing Systems.

     • Google Scholar
135. 1. Väth P
     2. Münch M
     3. Raab C
     4. Schleif FM

     (2022) PROVAL: A framework for comparison of protein sequence embeddings

     Journal of Computational Mathematics and Data Science 2022:100044.

     https://doi.org/10.1016/j.jcmds.2022.100044

     • Google Scholar
136. Conference

     1. Vig J

     (2019a)

     BertViz: A tool for visualizing multihead self-attention in the BERT model

     ICLR Workshop: Debugging Machine Learning Models.

     • Google Scholar
137. Preprint

     1. Vig J

     (2019b) A Multiscale Visualization of Attention in the Transformer Model

     arXiv.

     https://arxiv.org/abs/1906.05714

     • Google Scholar
138. Preprint

     1. Vig J
     2. Madani A
     3. Varshney LR
     4. Xiong C
     5. Socher R
     6. Rajani NF

     (2020) Bertology Meets Biology: Interpreting Attention in Protein Language Models

     arXiv.

     https://arxiv.org/abs/2006.15222

     • Google Scholar
139. Software

     1. Vig J

     (2022) Bertviz, version 04755ef

     GitHub.

     https://github.com/jessevig/bertviz
140. Book

     1. Walls D
     2. Loughran ST

     (2017) Protein chromatography

     In: Walls D, editors. Protein Stability: Enhancement and Measurement. Springer. pp. 101–129.

     https://doi.org/10.1007/978-1-4939-6412-3

     • Google Scholar
141. 1. Wang X
     2. Xu ML
     3. Li BQ
     4. Zhai HL
     5. Liu JJ
     6. Li SY

     (2017) Prediction of phosphorylation sites based on krawtchouk image moments

     Proteins 85:2231–2238.

     https://doi.org/10.1002/prot.25388

     • PubMed
     • Google Scholar
142. 1. Wang Y
     2. Liu S
     3. Afzal N
     4. Rastegar-Mojarad M
     5. Wang L
     6. Shen F
     7. Kingsbury P
     8. Liu H

     (2018) A comparison of word embeddings for the biomedical natural language processing

     Journal of Biomedical Informatics 87:12–20.

     https://doi.org/10.1016/j.jbi.2018.09.008

     • PubMed
     • Google Scholar
143. Preprint

     1. Wang C
     2. Li M
     3. Smola AJ

     (2019) Language Models with Transformers

     arXiv.

     https://arxiv.org/abs/1904.09408

     • Google Scholar
144. 1. Wang D
     2. Liu D
     3. Yuchi J
     4. He F
     5. Jiang Y
     6. Cai S
     7. Li J
     8. Xu D

     (2020) MusiteDeep: a deep-learning based Webserver for protein post-translational modification site prediction and visualization

     Nucleic Acids Research 48:W140–W146.

     https://doi.org/10.1093/nar/gkaa275

     • PubMed
     • Google Scholar
145. 1. wang J
     2. Wen N
     3. Wang C
     4. Zhao L
     5. Cheng L

     (2021) ELECTRA-DTA: A new compound-protein binding affinity prediction model based on the contextualized sequence encoding

     Journal of Cheminformatics 14:14.

     https://doi.org/10.1186/s13321-022-00591-x

     • Google Scholar
146. 1. Wang J
     2. Zhang X
     3. Zhou Y
     4. Suh C
     5. Rudin C

     (2021) There once was a really bad poet, it was automated but you did ’'t know it

     Transactions of the Association for Computational Linguistics 9:605–620.

     https://doi.org/10.1162/tacl_a_00387

     • Google Scholar
147. 1. Wang Q
     2. Wei J
     3. Zhou Y
     4. Lin M
     5. Ren R
     6. Wang S
     7. Cui S
     8. Li Z
     9. Cowen L

     (2022) Prior knowledge facilitates low homologous protein secondary structure prediction with DSM distillation

     Bioinformatics 38:3574–3581.

     https://doi.org/10.1093/bioinformatics/btac351

     • Google Scholar
148. Preprint

     1. Wettig A
     2. Gao T
     3. Zhong Z
     4. Mask C

     (2022) Should You Mask 15% in Masked Language Modeling?

     arXiv.

     https://arxiv.org/abs/2202.08005

     • Google Scholar
149. 1. Wilburn GW
     2. Eddy SR

     (2020) Remote homology search with hidden Potts models

     PLOS Computational Biology 16:e1008085.

     https://doi.org/10.1371/journal.pcbi.1008085

     • PubMed
     • Google Scholar
150. 1. Wishart DS
     2. Knox C
     3. Guo AC
     4. Shrivastava S
     5. Hassanali M
     6. Stothard P
     7. Chang Z
     8. Woolsey J

     (2006) DrugBank: a comprehensive resource for in silico drug discovery and exploration

     Nucleic Acids Research 34:D668–D672.

     https://doi.org/10.1093/nar/gkj067

     • PubMed
     • Google Scholar
151. Preprint

     1. Wu Y
     2. Schuster M
     3. Chen Z
     4. Le QV
     5. Norouzi M
     6. Macherey W

     (2016) Google’s Neural Machine Translation System: Bridging the Gap between Human and Machine Translation

     arXiv.

     https://arxiv.org/abs/1609.08144

     • Google Scholar
152. 1. Xu Y
     2. Song J
     3. Wilson C
     4. Whisstock JC

     (2018) PhosContext2vec: a distributed representation of residue-level sequence contexts and its application to general and kinase-specific phosphorylation site prediction

     Scientific Reports 8:8240.

     https://doi.org/10.1038/s41598-018-26392-7

     • PubMed
     • Google Scholar
153. Conference

     1. Xue Y
     2. Liu Z
     3. Fang X

     (2022)

     Multimodal Pre-Training Model for Sequence-based Prediction of Protein-Protein Interaction

     Machine Learning in Computational Biology; 2022: PMLR.

     • Google Scholar
154. 1. Yamaguchi H
     2. Saito Y

     (2021) Evotuning protocols for transformer-based variant effect prediction on multi-domain proteins

     Briefings in Bioinformatics 22:bbab234.

     https://doi.org/10.1093/bib/bbab234

     • Google Scholar
155. Conference

     1. Yang Z
     2. Dai Z
     3. Yang Y
     4. Carbonell J
     5. Salakhutdinov RR
     6. Le QV

     (2019)

     Xlnet: generalized autoregressive pretraining for language understanding

     Advances in Neural Information Processing Systems.

     • Google Scholar
156. Preprint

     1. Yang KK
     2. Lu AX
     3. Fusi NK

     (2022) Convolutions Are Competitive with Transformers for Protein Sequence Pretraining

     bioRxiv.

     https://doi.org/10.1101/2022.05.19.492714

     • Google Scholar
157. Preprint

     1. Yin W
     2. Kann K
     3. Yu M
     4. Schütze H

     (2017) Comparative Study of CNN and RNN for Natural Language Processing

     arXiv.

     https://arxiv.org/abs/1702.01923

     • Google Scholar
158. 1. Young T
     2. Hazarika D
     3. Poria S
     4. Cambria E

     (2018) Recent trends in deep learning based natural language processing [review article]

     IEEE Computational Intelligence Magazine 13:55–75.

     https://doi.org/10.1109/MCI.2018.2840738

     • Google Scholar
159. 1. Yu L
     2. Zhang Y
     3. Gutman I
     4. Shi Y
     5. Dehmer M

     (2017) Protein sequence comparison based on physicochemical properties and the position-feature energy matrix

     Scientific Reports 7:46237.

     https://doi.org/10.1038/srep46237

     • PubMed
     • Google Scholar
160. Conference

     1. Zaheer M
     2. Guruganesh G
     3. Dubey KA
     4. Ainslie J
     5. Alberti C
     6. Ontanon S

     (2020)

     Big bird: transformers for longer sequences

     Advances in Neural Information Processing Systems. pp. 17283–17297.

     • Google Scholar
161. Preprint

     1. Zare-Mirakabad F
     2. Behjati A
     3. Arab SS
     4. Nowzari-Dalini A

     (2021) Protein Sequence Profile Prediction Using Protalbert Transformer1

     bioRxiv.

     https://doi.org/10.1101/2021.09.23.461475

     • Google Scholar
162. 1. Zeng H
     2. Edwards MD
     3. Liu G
     4. Gifford DK

     (2016) Convolutional neural network architectures for predicting DNA-protein binding

     Bioinformatics 32:i121–i127.

     https://doi.org/10.1093/bioinformatics/btw255

     • PubMed
     • Google Scholar
163. Conference

     1. Zhang H
     2. Ju F
     3. Zhu J
     4. He L
     5. Shao B
     6. Zheng N

     (2021)

     Co-evolution Transformer for Protein Contact Prediction

     Advances in Neural Information Processing Systems.

     • Google Scholar
164. Conference

     1. Zhao Q
     2. Ma J
     3. Wang Y
     4. Xie F
     5. Lv Z
     6. Xu Y

     (2021) Mul-SNO: A novel prediction tool for S-nitrosylation sites based on deep learning methods

     IEEE Journal of Biomedical and Health Informatics.

     https://doi.org/10.1109/JBHI.2021.3123503

     • Google Scholar

Author details

1. Abel Chandra

   Department of Computing Science, Umeå University, Umeå, Sweden

   Contribution

   Conceptualization, Data curation, Software, Formal analysis, Validation, Investigation, Visualization, Methodology, Writing - original draft, Writing - review and editing

   Competing interests

   No competing interests declared

   "This ORCID iD identifies the author of this article:" 0000-0001-8497-028X

2. Laura Tünnermann

   Umeå Plant Science Centre (UPSC), Department of Forest Genetics and Plant Physiology, Swedish University of Agricultural Sciences, Umeå, Sweden

   Contribution

   Data curation, Investigation, Visualization, Writing - review and editing

   Competing interests

   No competing interests declared

3. Tommy Löfstedt

   Department of Computing Science, Umeå University, Umeå, Sweden

   Contribution

   Conceptualization, Resources, Data curation, Software, Formal analysis, Supervision, Funding acquisition, Investigation, Methodology, Project administration, Writing - review and editing

   Competing interests

   No competing interests declared

4. Regina Gratz

   1. Umeå Plant Science Centre (UPSC), Department of Forest Genetics and Plant Physiology, Swedish University of Agricultural Sciences, Umeå, Sweden
   2. Department of Forest Ecology and Management, Swedish University of Agricultural Sciences, Umeå, Sweden

   Contribution

   Conceptualization, Data curation, Supervision, Funding acquisition, Investigation, Visualization, Project administration, Writing - review and editing

   For correspondence

   regina.gratz@slu.se

   Competing interests

   No competing interests declared

   "This ORCID iD identifies the author of this article:" 0000-0002-8820-7211

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