The function of a protein can be explored in several different ways. Genetic approaches are used to suppress the expression of the respective gene/protein, for example using gene editing methods such as siRNA or shRNA or by CRISPR/Cas9 (Mali et al., 2013). However, in drug discovery, these methods have some deficiencies: they commonly remove or suppress the entire protein and thus cannot easily reveal the function of a specific druggable protein domain – although domain-based CRISPR is becoming a more widely used method; they are not reversible; their effects are not instantaneous; and they not only disrupt the protein, but also the protein interactome around the targeted protein. Selective small molecule modulators (‘chemical probes’), in contrast, can probe the particular function of a targeted domain and can, therefore, be used to study its role in biological processes and in human disease in a dose and time-dependent manner across a wide range of cell and animal models. These probes can also be modified to enhance the degradation of the protein(s) they bind to (Mali et al., 2013; Toure and Crews, 2016).

Small molecules can be used in a broad panel of assay systems comprising primary cells, tissues and also in vivo models, and other systems not easily amenable even for state-of-the-art genetic target validation methods. Despite the fact that non-selective compounds cast a wide net and can be used to uncover interesting polypharmacologies, having a panel of selective probes that can be used in combination will facilitate data deconvolution and target identification. These properties, together with the possibility of further development of probes into drug candidates, make them among the most versatile tools to explore the relevance of a protein for therapeutic development. However, the necessary characterization data is often missing for chemical compounds, and inhibitors are announced as being ‘selective’ despite missing a comprehensive profile. Tool compounds, which are chemically unstable or not comprehensively characterized are therefore limited in their utility (Arrowsmith et al., 2015). Moreover, poorly characterized chemical modulators generate misleading results and litter the literature with contradicting data on a target’s function and its role in biology. This is also true for probes that are used improperly, e.g. at higher than appropriate concentration thus inhibiting other proteins in addition to the target or resulting in non-specific cellular toxicity. Unfortunately, reactive and non-specific inhibitors are widely used in the academic research community, often resulting in incorrect functional annotation (Baell and Walters, 2014).

The ideal chemical probes need to be selective, active in cells and chemically stable. The recent discussion on best practice within the chemical biology community suggested a number of stringent quality criteria for chemical probes (Arrowsmith et al., 2015; Blagg and Workman, 2017; Edwards et al., 2009; Bunnage et al., 2013). Typical criteria as applied by the Structural Genomics Consortium (SGC) are shown in Figure 1, although these may vary slightly depending on the specific protein.

Figure 1

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A diverse set of chemical tool compounds is available to cell biologists. However, characterization data associated with these compounds are often either incomplete or buried in patents or supplemental data files of publications. Thus, scientists face a challenge to decide which tools to use for their research. Help is provided for example by the Chemical Probes Portal (Baell and Walters, 2014; Blagg and Workman, 2017), which was established in 2015 to provide a comprehensive overview of published and newly released tool compounds that are annotated with a simple star-rating system. All compounds submitted to the portal are reviewed by at least three members of an independent expert scientific advisory board. Only probes that receive three stars (‘Best available probe for this target, or a high-quality probe that is a useful orthogonal tool’) or four stars (‘Recommended as a probe for this target’) are recommended to be used. Of all the compounds submitted to the probe portal so far (about 400), 125 have achieved a rating of three stars or better, thereby showing that there is an urgent need for more high-quality tool compounds to foster reproducible research.

Like drug discovery, probe development is a multi-disciplinary effort involving experts from several areas including protein chemistry, biochemistry, cell biology, pharmacology and medicinal chemistry (Dahlin and Walters, 2014; Garbaccio and Parmee, 2016). Once a target has been selected, the first step is the design of a project-specific screening cascade. The screening procedure needs to reflect target-related probe criteria as well as the desired compound properties.

A typical screening cascade for a kinase probe discovery project is shown in Figure 2. The screening cascade consists of a primary assay – usually a biochemical activity assay – plus an assay with an orthogonal readout, e.g., a biophysical assay, a number of selectivity assays for the target and a cell-based assay to demonstrate on-target activity in the cellular environment. If possible, a crystallization system should be established to elucidate the binding modes of selected compounds enabling the rational design of better inhibitors. In silico analyses to exclude undesired events such as frequent hitters and pan-assay interference compounds (PAINs), and assays characterizing the physical and chemical properties of the identified hits (Hughes et al., 2011) complement the analysis (Baell and Walters, 2014). Medicinal chemistry optimization is then started for selected compound classes. For a typical project, multiple rounds of the Design – Make – Test – Analyze circle (Plowright et al., 2012) are needed before a suitable probe candidate is identified. Importantly, cross-correlating results from different assays within a compound class (e.g. tracking of cellular read-outs with biochemical potency and cellular target engagement data) provide a continuing consistency check if observed effects are truly a function of inhibiting the target of interest. Experience within the SGC shows that approximately 1–2 years and €2 million are needed to generate one chemical probe fulfilling these stringent criteria (Donner, 2014). This observation is in line with the experience of many medicinal chemists at pharmaceutical companies.

Figure 2

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As there may be similarities among binding sites on both related and unrelated proteins, unwanted binding to proteins other than the original target is regularly observed. This selectivity challenge can never be completely avoided, and thus the end users should be aware of unknown cross-reactivity challenges. A way to reduce the risk of non-specific effects is the use of a suitable control compound having a chemical structure closely related to that of the probe but lacking activity on the target. A wider profiling against a panel of pharmacologically active targets or proteomics analysis of the compound provides additional information about compound selectivity. Having access to multiple probes from structurally different chemical series further reduces the risk that unknown off-target activities give rise to incorrect conclusions about target functions.

Many quality probe compounds are buried in the chemical vaults of the pharmaceutical industry, depriving the scientific community of useful tools and limiting the impact of the original research. In some cases, particular compounds, their properties and some structure–activity relationships (SAR) have been published (Nara et al., 2014; Siebeneicher et al., 2016; Takahashi et al., 2015; Wu-Wong et al., 1999). However, often only selected data are published and the proprietary compounds are not made available to the researchers except via restrictive contractual agreements, and this impedes their use and their impact. Indeed, in the nuclear hormone receptor field, we showed that any legal encumbrances to compound access reduced the subsequent use of the compound in the literature significantly (Isserlin, 2011). Thus, the open access/open science approach is the fastest route to reach the end users and thereby to have a positive effect on research.

This evidence, as well as impact from the SGC epigenetics probes project, has convinced the SGC partner companies that the release of previously hidden compounds and data to the public will provide value to science and to the companies (Lee, 2015). To this end, seven pharmaceutical companies associated with the SGC have each agreed to donate 10 of these valuable compounds, stemming from their research pipelines, for a total of 70 high-quality small molecules, thus providing a major boost to the chemical biology toolbox. The compounds have been selected based on a variety of criteria, which are different for each participating company. These include profiling available for the compound, feasibility of generating a control compound, availability of physical compound, target class, intellectual property considerations, and other factors.

This is an exciting development, but many of the compounds will require wider profiling to meet today’s more stringent quality criteria. As the primary focus of the pharmaceutical industry is not to generate chemical probes, but to develop new drugs, not all donated probes have been profiled to the same depth that is required of a high-quality chemical probe. Moreover, specificity for a particular target is not a requirement for an effective drug. Thus, although most of the pharma-donated probes have been extensively characterized, they often need to be better adapted for use as a single chemical tool (Figure 1). In particular, no bespoke control compounds have been generated as the progress of the probe compounds within the company is usually followed by extensive SAR across a series of analogues. Selection and characterization of the control compound is needed to complete a probe package. In addition, control compounds also have to be carefully characterized to weed out promiscuous compounds.

The aim of our partnership is to provide this comprehensive characterization. We believe this to be a valuable contribution to the community. Once broadly characterized and accompanied by relevant control compounds, the initial set of 70 probes reflect a collective contribution of at least €140 million to the public domain (Figure 3). These donated probes cover a broad array of targets from different protein families relevant for a number of disease indications (see Table 1).

Table 1

Family	Target	Mode of action	Company	Structure
	D4 Dopamine receptor	Agonist	AbbVie ABT-724
GPCR	ETA Endothelin receptor	Antagonist	AbbVie ABT-546
	Par1/F2R (F2R) Protease activated receptor	Antagonist	Bayer BAY-386
	CRTH2 (Prostaglandin DP2 receptor)	Antagonist	MSD CRTH2i
	CB1 Cannabinoid receptor	Inverse Agonist	MSD MRL-650
	EP2Prostaglandin receptor	Antagonist	Pfizer PF-04418948
	α1D Adrenoceptor	Antagonist	Takeda (R)-9s
	KISS1 Receptor (GPR54)	Agonist	Takeda KISS1-305	D-Tyr-D-Pya(4)-Asn-Ser-Phe-azaGly-Leu-Arg(Me)-Phe-NH2
Hydrolase	sEH (Soluble epoxide hydrolase)	Inhibitor	Boehringer Ingelheim BI-1935
	FAAH (Fatty acid amide hydrolase)	Inhibitor	Pfizer PF-04457845
Ion channel	TRPM8 (Cold and menthol receptor 1)	Antagonist	Pfizer PF-05105679
Kinase	c-MET (Tyrosine-protein Kinase Met)	Inhibitor	Bayer BAY-474
	TIE (Tyrosine kinase with Ig and EGF homology domains 1), DDR (Discoidin domain receptor family)	Inhibitor	Bayer BAY-826
	ERK1/2 (Extracellular signal-regulated kinase)	Inhibitor	MSD MRK-ERKi
	SYK (Spleen tyrosine kinase)	Inhibitor	MSD MRL-SYKi
	FAK/PYK2(focal adhesion kinase/proline-rich tyrosine kinase 2)	Inhibitor	Pfizer PF-04554878
Other	FLAP (5-Lipoxygenase-activating protein)	Inhibitor	Boehringer Ingelheim BI 665915
	FASN (Fatty acid synthase)	Inhibitor	Boehringer Ingelheim BI 99179
	MIF (Macrophage migration inhibitory factor)	Activator	Takeda BTZO-1
	Farnesyltransferase	Inhibitor	AbbVie ABT-100
	P300/CBP(E1A binding protein/CREB binding protein)	Inhibitor	AbbVie A-485
	NHE1, SLC9A1	Antagonist	Boehringer Ingelheim BI-9267
	MTH1 (MutT homolog 1)	Inhibitor	Bayer BAY-707
Protease	MMP12 (Matrix metallopeptidase 12)	Inhibitor	Bayer BAY-7598
	Gamma secretase	Inhibitor	MSD MRK-560
	Gamma secretase	Modulator	MSD GSM1
	METAP2 (Methionine aminopeptidase-2)	Inhibitor	Takeda TP-004

Figure 3

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In order to guarantee the quality of the compounds, the donated probe candidates and control compounds are subjected to a two-tier scientific review process: the first review takes place internally, including partners who have not been involved in the probe project, and the second review is performed by a panel of renowned scientists, who have agreed to act as independent reviewers. The first 30 proposals were presented to the internal review committee during a two-day meeting in June 2017 in Frankfurt am Main, Germany, where a process for their release to the public was also established. At this ‘historic’ meeting scientists from eight pharmaceutical companies scrutinized the quality of the probes proposed by the other partners and made constructive suggestions on improvement of the associated data packages (Figure 4A).

In the initial set, most targets are uniquely addressed by only one chemical compound, but a maximum of two chemical probes for the same target will be accepted if they represent different chemotypes as judged by the review panels. The remaining probe sets will be provided during the course of 2018/2019. All approved probes are measured against the same quality criteria (Figure 1) and will be profiled in assay panels comprising of >500 assays, including broad panels of pharmacologically active targets such as GPCRs, kinases, ion channels and proteases to identify off-target activities (Table 2). Disease-specific phenotypic panels such as assays in primary tissues established by SGC partners will provide an initial characterization of their biological effects (Edwards et al., 2015).

The proposed probes range from completely novel ‘best in class’, to probes that have been selected because they are provided as a complete set, with control compounds. Although some of the proposed compounds themselves are already commercially available, for most there is no widely characterized partner control compound (Figure 4B).

Figure 4

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The current probe proposals cover proteins from many different families such as GPCRs, kinases and proteases as well as other protein targets implicated in a variety of therapeutic areas ranging from oncology to inflammatory diseases and neurodegenerative disorders. An excellent example of a donated probe is the recently published p300/CBP histone acetyltransferase (HAT) inhibitor (A-485), which was shown to have efficacy in several cell models of malignancies (Lasko et al., 2017). This probe, including its control compound, has been approved by both internal as well as external reviewers and is now available to the scientific community. In contrast, other donated probes are not published or only mentioned in patents and therefore have not been accessible at all. Examples include a novel coagulation factor II thrombin receptor (F2R/PAR-1) inhibitor, which has potential for thrombosis management, and an inhibitor for focal adhesion kinase (FAK) and proline-rich tyrosine kinase 2 (PYK2), which has been in clinical trials for advanced non-haematologic malignancies, but for which profiling data have not yet been available. Even previously published probes are not always widely accessible. For example, the set includes a probe for the solute carrier NHE1, a target associated with ischemia/reperfusion-induced cell death, a peptidomimetic agonist for the KISS1 receptor, which plays a crucial role in cellular hormone function and puberty, and the inhibitor for a gamma secretase (GSI) protease, which may have potential in targeting Alzheimer’s disease.

Using the infrastructure and established processes of past SGC probe projects, a non-bureaucratic and simple distribution process is implemented. This process involves distribution in bespoke probe libraries under a simple web-accessible Open Science Trust Agreement (http://www.thesgc.org/click-trust) as well as through trusted commercial vendors. To the best of our knowledge, our initiative is unique in enabling open access to well-validated probes including controls generated in the pharmaceutical industry for diverse target families.

All supporting potency and selectivity data, as well as advice for the appropriate use of the compounds for cellular assays and – if applicable – in vivo assays, will be easily accessible via the public database (https://openscienceprobes.sgc-frankfurt.de/). The launch for the first version is planned for the beginning of 2018. The database supports the data needs of both biologists and chemists. The first version focusses on a search for the target proteins, probes, control compounds and recommendations on use. For the second version, additional features such as chemical substructure searches will be accessible. Full assay details will be provided and reagents used will be listed so that scientists using the probes are enabled to judge the quality of the data provided as well as to reproduce key data in their own lab. For example, it is important to know if a protein kinase has been screened in a binding or activity assay, and which ATP concentration has been used. Further, the protein construct used to perform certain assays is of significance.

As both the probes and the negative controls will be characterized in more than 500 assays, we will generate more than 70,000 biological data sets within the next 1–2 years: a rich and easily accessible source for future analyses. By providing the data in a comprehensive way we hope to extend our understanding of this particular mechanism or protein in a way that leads to new therapeutic approaches.

The new tool compounds and the corresponding data will help to improve the quality of research and will deepen our understanding of the target biology. However, comprehensive characterization, which ideally should be consistent to make data comparable and facilitate data mining, comes at a cost, and in many cases also requires resources for the (re-)synthesis of the chemical probe. The biggest problem is in the availability and characterization of the control compounds. Not all candidate probes will have a suitable similar analogue that does not inhibit/activate the target of interest. Funding will be necessary in order to fill such gaps, but financing such a project and the resources to synthesize and characterize compounds is no easy task. It does not usually fit into the remit of the major funding agencies and help is needed by relevant translational organizations and individual labs to support the project. Organizations like the Division of Pre-Clinical Innovation of the National Center for Advancing Translational Sciences (NCATS; https://ncats.nih.gov/) and the National Institute of Mental Health (NIMH) Psychoactive Drug Screening Program (https://pdspdb.unc.edu/pdspWeb/) housed at the laboratory of Dr Bryan Roth at UNC are generously supporting this crucial endeavour by synthesizing negative controls and conducting probe profiling experiments.

The distribution of probes will occur via commercial vendors, but it is no trivial task to make the well-characterized control compounds available to the user. Due to reduced revenues from the control compounds, vendors are often reluctant to offer these important controls. Regrettably, researchers often perform experiments without the appropriate control compound due to cost reasons or because initial experiments have already been performed without the control. A trial kit, which we will offer, including both probe and control compound, and/or sets of pre-diluted compounds may aid researchers to perform properly controlled experiments from the start. It is up to the combined efforts of researchers, vendors, journal editors and referees to make use of the chemical probes in combination with their available control standard practice in biomedical research.

While in the past almost all aspects of pharmaceutical research and development (R&D) were seen as competitive, the thinking in the field has shifted remarkably over the last decade. More and more challenges in the R&D process are seen as precompetitive, resulting in public–private partnerships and multilateral, critical mass consortia jointly addressing overarching issues. Many pharmaceutical companies have initiated open innovation projects interacting with the academic community. A key success factor for these endeavours is the easy access to know-how and reagents without complicated contractual arrangements (Nilsson and Felding, 2015; Ehrismann and Patel, 2015). We hope that the project initiated here will entice other companies and academics to follow suit and join us in the quest to increase the availability of well-validated probes meeting stringent quality criteria for the scientific community and decide to make some of their assets openly available. Whilst ultimately, the success of the project will depend on the willingness and support of the scientific community, additional pharmaceutical companies and funding bodies to engage, we believe this is an exciting first step in uncovering and delivering high–quality chemical probes to unlock new biology and ultimately new high-quality targets for drug discovery.

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Thank you for submitting your article "Donated Chemical Probes For Open Science" to eLife for consideration as a Feature Article. Your article has been reviewed by two peer reviewers, and the evaluation has been overseen by Emma Pewsey (as Associate Features Editor for eLife) and Peter Rodgers (the eLife Features Editor) as the Senior Editor. The reviewers have opted to remain anonymous.

The reviewers have discussed the reviews with one another and I have drafted this decision to help you prepare a revised submission.

Summary:

The manuscript describes an important initiative that has the potential to significantly improve the quality of pharmacological agents available and further strengthen the use of chemical probes in many areas of biology. Importantly, probe-associated data generated internally, best use practices and inactive control compounds will also be shared. Thus, it will be of wide interest to the readers of eLife.

Essential revisions:

1) Please describe clearly how novel the donated probes are. No structures or names are provided for the probes listed in Table 1. Therefore, it is unclear in what way the current initiative is merely a repurposing/rebranding of other similar efforts or provides truly novel compounds. For example, the AbbVie P300/CBP inhibitor appears to be compound A-485, published in Nature 2017 and is currently available as an SGC probe and from several vendors. What constitutes the donation in that case, given that the compound is available, and data are already published? Similarly, are the Pfizer compounds those already currently available from Sigma for the same targets? Are the Boehringer Ingelheim compounds a subset of the ones made available in the opnMe initiative? Or are all these novel additional compounds?

2) High-quality probes already exist for several of the targets listed. Please include an analysis of the superiority of the new donated probes, indicating:

i) Targets for which there are currently no high-quality probes available;

ii) Targets for which the donated probe promises a significant (e.g. 10-fold) benefit in potency or selectivity;

iii) Cases in which the new donated probe has similar potency/selectivity as currently available probes but an entirely different chemotype;

iv) Cases where none of the above points apply (but there might still be a benefit in availability/control compounds/data annotation).

3) The purpose of the manuscript needs to be defined more clearly. Currently it is not clear whether the manuscript is primarily about defining chemical probes or about bringing awareness to the new resource.

4) Please provide more discussion about how the probes have been selected. It also needs to be made clear that the standards used for selection are not a definition of what a chemical probe is. Although having potent and selective inhibitor probes is ideal, non-selective chemical probes can also provide powerful information and should also be mentioned as good chemical probes.

Essential revisions:

1) Please describe clearly how novel the donated probes are. No structures or names are provided for the probes listed in Table 1. Therefore, it is unclear in what way the current initiative is merely a repurposing/rebranding of other similar efforts or provides truly novel compounds. For example, the AbbVie P300/CBP inhibitor appears to be compound A-485, published in Nature 2017 and is currently available as an SGC probe and from several vendors. What constitutes the donation in that case, given that the compound is available, and data are already published? Similarly, are the Pfizer compounds those already currently available from Sigma for the same targets? Are the Boehringer Ingelheim compounds a subset of the ones made available in the opnMe initiative? Or are all these novel additional compounds?

The donated compounds of this initial wave are a mixture of novel, already published, and commercially available compounds. However, even though some of the compounds themselves might be available from other sources, for none is available a comprehensive and standard dataset comprising potency, selectivity, and often pharmacology, and for none is available an inactive negative control. Our collecting and organizing these underlying data is what differentiates a “compound that is commercially available” and a donated probe. For all compounds, the distinction compared to other initiatives will be that they are peer-reviewed by a 2-Tier process by an internal committee comprising all participating industry partners and independent external referees to be suitable as probes i.e. fulfilling selectivity and specificity criteria. This quality bar is a distinct feature of the donated probe set. Indeed, during the course of the review process, some probes were found no longer to be the ‘best in class’ compounds and the external referees rejected these compounds as part of the probe set.

Our selection of these specific donated probes was deliberate. Characterization data for these compounds were already fairly complete, which enabled a set of about 30 compounds to be proposed in a relatively short time-frame. An excellent example is A-485, which has a complete dataset and a negative control compound, something that is missing from most compounds provided by vendors. A-485 has been donated to the community and the associated data will be made more easily searchable in the database. For example, currently the selectivity data are buried in the supplements of the Nature publication, which describes this probe. For other compounds, like the ones from Pfizer, no negative control compound had been available before. Full profiling data (such as kinome wide selectivity screens) will also be made available through this initiative.

To facilitate uptake and proper use by the biology community, each probe characterization package also contains clear instructions on use (e.g. suggested concentration ranges) and a matching control compound accompanies each probe molecule. The Boehringer Ingelheim compounds are also available via the complementary opnMe initiative. However, the opnMe platform also contains compounds that have not been through the mentioned 2-Tier approval process, which is a quality factor missing for compounds that are available, but that have not been evaluated against quality criteria.

We have introduced Figure 4A to explain the process better and added the probe compound structures to Table 1.

We believe therefore that by this process the best available chemical probes will be made available for each target.

2) High-quality probes already exist for several of the targets listed. Please include an analysis of the superiority of the new donated probes, indicating:

i) Targets for which there are currently no high-quality probes available;

ii) Targets for which the donated probe promises a significant (e.g. 10-fold) benefit in potency or selectivity;

iii) Cases in which the new donated probe has similar potency/selectivity as currently available probes but an entirely different chemotype;

iv) Cases where none of the above points apply (but there might still be a benefit in availability/control compounds/data annotation).

We thank the referee for this suggestion. An analysis grouping the probes into the suggested categories has been added as Figure 4B.

3) The purpose of the manuscript needs to be defined more clearly. Currently it is not clear whether the manuscript is primarily about defining chemical probes or about bringing awareness to the new resource.

While the main point of the manuscript is to make researchers – notably our bioscience colleagues, who are the most common probe user community – aware of the new resource, we would like at the same time to point out why the resource is necessary and useful: despite the efforts of other initiatives the basic problem remains that chemical probes are difficult to find among the large number of chemical modulators that are currently available, which are often less specific or poorly characterized. In order to achieve easier access to the most suitable chemical probes and their negative control compounds, we introduce a definition of quality criteria for each target family. We also would like to highlight that the project involves more than just making some of the already available compounds accessible and adding new ones. The characterization of each probe against homogenous sets of screening assays within and outside the target family, synthesis of control compounds, the two-step approval process and additional phenotypic data contributed from probe users in an open database is a considerable extension to the current policy of making published compounds available by chemical vendors.

4) Please provide more discussion about how the probes have been selected. It also needs to be made clear that the standards used for selection are not a definition of what a chemical probe is. Although having potent and selective inhibitor probes is ideal, non-selective chemical probes can also provide powerful information and should also be mentioned as good chemical probes.

The probes have been selected based on a variety of factors: characterization level of the compounds, availability of material, novelty, availability of control compound. We have added a discussion of the selection criteria to the manuscript.

We agree with the reviewer that well characterized non-selective chemical compounds can unravel interesting pharmacologies and be useful tool compounds. However, we would like to reserve the term ‘chemical probe’ for potent and selective, cell active chemical modulators and distinguish them from non-selective tool compounds/modulators. The probe project, in the definition of the manuscript, aims to make available compounds that are optimized to connect a phenotype to one or very few target(s) the compound modulates. It should not be mistaken with a compound that has been optimized for a phenotypic effect in a given assay. We have amended the manuscript using the term ‘probes’ consistently only for selective chemical modulators to reflect this better. Additionally, wording has been added to reflect that non-specific chemical modulators can also be valuable.

Author details

1. Susanne Müller

   Susanne Müller is in the Structural Genomics Consortium, Buchmann Institute for Molecular Life Sciences, Goethe University Frankfurt, Frankfurt am Main, Germany

   For correspondence

   susanne.mueller-knapp@bmls.de

   Competing interests

   No competing interests declared

   "This ORCID iD identifies the author of this article:" 0000-0003-2402-4157

2. Suzanne Ackloo

   Suzanne Ackloo is in the Structural Genomics Consortium, University of Toronto, Toronto, Ontario, Canada

   Competing interests

   No competing interests declared

3. Cheryl H Arrowsmith

   Cheryl H Arrowsmith is in the Structural Genomics Consortium and the Princess Margret Cancer Centre, Department of Medical Biophysics, University of Toronto, Toronto, Ontario, Canada

   Competing interests

   No competing interests declared

4. Marcus Bauser

   Marcus Bauser is at Bayer AG, Drug Discovery Pharmaceuticals, Berlin, Germany

   Competing interests

   employee of Bayer AG

5. Jeremy L Baryza

   Jeremy L Baryza is at Vertex Pharmaceuticals, Boston, Massachusetts, United States

   Competing interests

   employee of Vertex Pharmaceuticals

6. Julian Blagg

   Julian Blagg is in the Cancer Research UK Cancer Therapeutics Unit, The Institute of Cancer Research, London, United Kingdom

   Competing interests

   No competing interests declared

7. Jark Böttcher

   Jark Böttcher is at Boehringer Ingelheim, Discovery Research, Vienna, Austria

   Competing interests

   employee of Boehringer Ingelheim

8. Chas Bountra

   Chas Bountra is in the Structural Genomics Consortium, Nuffield Departmentof Medicine, University of Oxford, Oxford, United Kingdom

   Competing interests

   No competing interests declared

9. Peter J Brown

   Peter J Brown is in the Structural Genomics Consortium, University of Toronto, Toronto, Ontario, Canada

   Competing interests

   No competing interests declared

10. Mark E Bunnage

    Mark E Bunnage is at Vertex Pharmaceuticals, Boston, Massachusetts, United States

    Competing interests

    Mark E Bunnage: employee of Vertex Pharmaceuticals

11. Adrian J Carter

    Adrian J Carter is at Boehringer Ingelheim, Discovery Research, Ingelheim am Rhein, Germany

    Competing interests

    Adrian J Carter: employee of Boehringer Ingelheim

12. David Damerell

    David Damerell is in the Structural Genomics Consortium, Nuffield Department of Medicine, University of Oxford, Oxford, United Kingdom

    Competing interests

    No competing interests declared

13. Volker Dötsch

    Volker Dötsch is a Reviewing Editor of eLife and is in the Institute of Biophysical Chemistry and Center for Biomolecular Magnetic Resonance, Goethe University, Frankfurt am Main, Germany

    Competing interests

    Reviewing editor, eLife

    "This ORCID iD identifies the author of this article:" 0000-0001-5720-212X

14. David H Drewry

    David H Drewry is in the Structural Genomics Consortium, UNC Eshelman School of Pharmacy, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States

    Competing interests

    No competing interests declared

15. Aled M Edwards

    Aled M Edwards is in the Structural Genomics Consortium, University of Toronto, Toronto, Ontario, Canada

    Competing interests

    No competing interests declared

16. James Edwards

    James Edwards is at Janssen Pharmaceutical Research and Development LLC, Spring House, Pennsylvania, United States

    Competing interests

    employee of Janssen Pharmaceutical Research and Development LLC

17. Jon M Elkins

    Jon M Elkins is in the Structural Genomics Consortium, Nuffield Department of Medicine, University of Oxford, Oxford, United Kingdom and the Structural Genomics Consortium, Universidade Estadual de Campinas — UNICAMP, Campinas, Brazil

    Competing interests

    No competing interests declared

    "This ORCID iD identifies the author of this article:" 0000-0003-2858-8929

18. Christian Fischer

    Christian Fischer is at Merck & Co., Inc., Boston, Massachusetts, United States

    Competing interests

    employee of Merck & Co., Inc.

19. Stephen V Frye

    Stephen V Frye is in the Center for Integrative Chemical Biology and Drug Discovery, Division of Chemical Biology and Medicinal Chemistry, UNC Eshelman School of Pharmacy, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States

    Competing interests

    No competing interests declared

20. Andreas Gollner

    Andreas Gollner is at Boehringer Ingelheim, Discovery Research, Biberach an der Riss, Germany

    Competing interests

    Andreas Gollner: employee of Boehringer Ingelheim

21. Charles E Grimshaw

    Charles E Grimshaw is a Pharma and Biotech Consultant at Ched Grimshaw Consulting, LLC, Poway, San Diego, California, United States

    Competing interests

    employee of Ched Grimshaw Consulting, LLC

    "This ORCID iD identifies the author of this article:" 0000-0002-2897-3483

22. Adriaan IJzerman

    Adriaan IJzerman is in the Division of Medicinal Chemistry, LACDR, Leiden University, Leiden, The Netherlands

    Competing interests

    No competing interests declared

23. Thomas Hanke

    Thomas Hanke is in the Structural Genomics Consortium, Buchmann Institute for Molecular Life Sciences, Goethe University Frankfurt, Frankfurt am Main, Germany

    Competing interests

    No competing interests declared

    "This ORCID iD identifies the author of this article:" 0000-0001-7202-9468

24. Ingo V Hartung

    Ingo V Hartung is at Bayer AG, Drug Discovery Pharmaceuticals, Berlin, Germany

    Competing interests

    Ingo V Hartung: employee of Bayer AG

25. Steve Hitchcock

    Steve Hitchcock is at Takeda California Inc., San Diego, California, United States

    Competing interests

    employee of Takeda California Inc.

26. Trevor Howe

    Trevor Howe is at J&J Innovation Centre, London, United Kingdom

    Competing interests

    employee of J&J Innovation Centre

27. Terry V Hughes

    Terry V Hughes is at J&J Innovation Centre, London, United Kingdom

    Competing interests

    Terry V Hughes: employee of J&J Innovation Centre

28. Stefan Laufer

    Stefan Laufer is in the Department of Pharmaceutical Chemistry, Eberhard Karls Universität Tübingen, Tübingen, Germany

    Competing interests

    No competing interests declared

29. Volkhart MJ Li

    Volkhart MJ Li is at Bayer AG, Drug Discovery Pharmaceuticals, Wuppertal, Germany

    Competing interests

    Volkhart MJ Li: employee of Bayer AG

30. Spiros Liras

    Spiros Liras is at Worldwide Medicinal Chemistry, Pfizer, Cambridge, Massachusetts, United States

    Competing interests

    employee of Pfizer

31. Brian D Marsden

    Brian D Marsden is in the Structural Genomics Consortium, Nuffield Department of Medicine, and the Kennedy Institute of Rheumatology, Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences University of Oxford, Oxford, United Kingdom

    Competing interests

    No competing interests declared

32. Hisanori Matsui

    Hisanori Matsui is at Research Takeda Pharmaceutical Company Ltd., Fujisawa, Japan

    Competing interests

    employee of Takeda Pharmaceutical Company Ltd

33. John Mathias

    John Mathias is at Worldwide Medicinal Chemistry, Pfizer, Cambridge, Massachusetts, United States

    Competing interests

    John Mathias: employee of Pfizer

34. Ronan C O'Hagan

    Ronan C O'Hagan is at Merck & Co., Inc., Boston, Massachusets, United States

    Competing interests

    Ronan C O'Hagan: employee of Merck & Co., Inc.,

35. Dafydd R Owen

    Dafydd R Owen is at Worldwide Medicinal Chemistry, Pfizer, Cambridge, Massachusets, United States

    Competing interests

    Dafydd R Owen: employee of Pfizer

36. Vineet Pande

    Vineet Pande is at Discovery Sciences, Janssen-Pharmaceutical Companies of Johnson & Johnson, Beerse, Belgium

    Competing interests

    employee of Janssen-Pharmaceutical Companies of Johnson & Johnson

37. Daniel Rauh

    Daniel Rauh is in the Fakultät für Chemie und Chemische Biologie, Technische Universität Dortmund, Dortmund, Germany

    Competing interests

    Daniel Rauh received consulting and lecture fees (Sanofi-Aventis, Takeda, Novartis, Pfizer, LDC) as well as research support (Novartis, J&J, Bayer, Merck, MSD).

38. Saul H Rosenberg

    Saul H Rosenberg is at AbbVie, North Chicago, Illinois, United States

    Competing interests

    employee of AbbVie

39. Bryan L Roth

    Bryan L Roth is in The National Institute of Mental Health Psychoactive Active Drug Screening Program and the Department of Pharmacology, University of North Carolina Chapel Hill School of Medicine, Chapel Hill, North Carolina, United States

    Competing interests

    No competing interests declared

40. Natalie S Schneider

    Natalie S Schneider is in the Structural Genomics Consortium, Buchmann Institute for Molecular Life Sciences, Goethe University Frankfurt, Frankfurt am Main, Germany

    Competing interests

    No competing interests declared

41. Cora Scholten

    Cora Scholten is at Bayer AG, Drug Discovery Pharmaceuticals, Berlin, Germany

    Competing interests

    Cora Scholten: employee of Bayer AG

42. Kumar Singh Saikatendu

    Kumar Singh Saikatendu is at Takeda California Inc., San Diego, California, United States

    Competing interests

    Kumar Singh Saikatendu: employee of Takeda California Inc

43. Anton Simeonov

    Anton Simeonov is in the National Center for Advancing Translational Sciences, National Institutes of Health, Bethesda, Maryland, United States

    Competing interests

    No competing interests declared

44. Masayuki Takizawa

    Masayuki Takizawa is at Research Takeda Pharmaceutical Company Ltd., Fujisawa, Kanagawa, Japan

    Competing interests

    Masayuki Takizawa: employee of Takeda Pharmaceutical Company Ltd.

45. Chris Tse

    Chris Tse is at AbbVie, North Chicago, Illinois, United States

    Competing interests

    Chris Tse: employee of AbbVie

46. Paul R Thompson

    Paul R Thompson is in the Department of Biochemistry and Pharmacology and the Program in Chemical Biology, University of Massachusetts Medical School, Worcester, United States

    Competing interests

    No competing interests declared

47. Daniel K Treiber

    Daniel K Treiber is at Eurofins DiscoverX, San Diego, California, United States

    Competing interests

    employee of Eurofins DiscoverX

48. Amélia YI Viana

    Amélia YI Viana is at Boehringer Ingelheim, Ingelheim am Rhein, Germany

    Competing interests

    Amélia YI Viana: employee of Boehringer Ingelheim

49. Carrow I Wells

    Carrow I Wells is in the Structural Genomics Consortium, UNC Eshelman School of Pharmacy, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States

    Competing interests

    No competing interests declared

50. Timothy M Willson

    Timothy M Willson is in the Structural Genomics Consortium, UNC Eshelman School of Pharmacy, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States

    Competing interests

    No competing interests declared

51. William J Zuercher

    William J Zuercher is in the Structural Genomics Consortium, UNC Eshelman School of Pharmacy, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States

    Competing interests

    No competing interests declared

52. Stefan Knapp

    Stefan Knapp is in the Structural Genomics Consortium, Buchmann Institute for Molecular Life Sciences, Goethe University Frankfurt, Frankfurt am Main, Germany

    Competing interests

    No competing interests declared

53. Anke Mueller-Fahrnow

    Anke Mueller-Fahrnow is at Bayer AG, Berlin, Germany

    For correspondence

    anke.mueller-fahrnow@bayer.com

    Competing interests

    Anke Mueller-Fahrnow: employee of Bayer AG

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