Figures and data
Performance of the PPI-HotspotID vs. FTMap and SPOTONEa
Performance of AlphaFold-Multimer, PPI-HotspotID, and their combination for 48 “unsolved” complex structures
(Top left) The X-ray structure (PDB: 1IAR) of interleukin-4 (grey) in complex with interleukin-4 receptor subunit alpha (wheat) with five PPI-hot spots; interface PPI-hot spots (E13, R92, and N93) are in blue and the non-interface ones (K127 and Y128) are in green. The PPI-hot spot numberings are based on the interleukin-4 free structure (PDB: 1BBN). The correct predictions of PPI-hotspotID (top right), FTMap (bottom left) and SPOTONE (bottom right) are mapped to the corresponding residues of the complex structure.
Evaluation of the predicted CPEB2-interacting amino acid residues in eEF2. (a) Salient features of mouse eEF2, showing the various domains and the mutated amino acids in domain V. mut 1, G778A, T779A, and P780A; mut 2, F794A; mut 3, D815A. (b) Reciprocal co-IP. The 293T cells expressing myc-CPEB2 along with wt or mutant flag-eEF2 or control GFP were harvested and then precipitated with flag or myc IgG. The precipitated substances were used for western blotting with myc and flag antibodies. IP, immunoprecipitation; IB, immunoblotting; IgG H.C., IgG heavy chain. (c) HeLa cells transfected with the plasmid expressing shRNA against human eEF2 (siheEF2) were harvested after 4-day puromycin selection for western blotting. HeLa cells transfected with the eEF2 knockdown plasmid along with flag-tagged wt or mutant mouse eEF2 after 4-day selection with puromycin and G418 were used for (d) S35-met/cys-labeling of synthesized proteins or (e) western blotting with the denoted antibodies. The normalized HIF-1α protein level (HIF-1α/β-actin signal) was calculated and expressed as mean ± SEM from three independent experiments. 2-tailed Student’s t-test, * < 0.05.
(Top) The structure (PDB 2N73)84 of GCP60 (green) in complex with PI4K-b (cyan) with the GCP60—PI4K-b interface encircled. (Bottom) The four experimentally known PPI-hot spots of GCP60 are shown in red. H45 and Y49 form hydrogen bonds across the interface with PI4K-b. Although F19 and Y46 do not directly contact PI4K-b, F19 is in vdW contact with Q42, which in turn forms vdW contacts with H45, whereas Y46 is in vdW contact with both H45 and Y49.
(Left) The structure (PDB 2OF5)68 of 7 CRADD proteins in complex with 5 PIDD proteins. The circle shows the CRADD—CRADD interface between chains C (cyan) and G (orange), whereas the other 5 CRADD chains are in gray, and the 5 PIDD proteins are in green. (Right) G128 (red) in CRADD (chain C) participates indirectly in CRADD—CRADD interactions via a backbone—side chain hydrogen bond between its neighbor, L127, and R147 in another CRADD (chain G).
Uncropped immunoblot images. The uncropped images for Figures 2b, 2c, and 2e are shown with indicated molecular weight marker.
Uncropped immunoblot images of the entire membranes for Figure 2b.
Uncropped images of the entire membrane for Figure 2c and phosphoimager file for 2d.
Uncropped immunoblot images of the cut membranes for Figure 2e.
