Crystal Structure of type II inhibitor NG25 bound to TAK1-TAB1. Determined by X-ray diffraction at 2.39 Å resolution. Released 30 Jul 2014.
Explore 4O91 in 3D Show helices and sheets RCSB PDB PDBe
4O91 contains 20 α-helices and 14 β-strands across 1 chain. Residue ranges use author residue numbering, as in the PDB file, from PDBe. To see them in 3D, choose the Cartoon representation with Secondary structure coloring: helices, sheets and coils get different colors.
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 29-30 | 2 | 1 |
| α-helix | 33-35 | 3 | |
| β-strand | 36-43 | 8 | 1 |
| β-strand | 49-55 | 7 | 1 |
| β-strand | 58-64 | 7 | 1 |
| α-helix | 68-70 | 3 | |
| α-helix | 71-83 | 13 | |
| β-strand | 89 | 1 | 2 |
| β-strand | 92-97 | 6 | 1 |
| β-strand | 100-105 | 6 | 1 |
| β-strand | 111 | 1 | 2 |
| α-helix | 112-117 | 6 | |
| β-strand | 122-123 | 2 | 3 |
| α-helix | 124 | 1 | |
| α-helix | 127-146 | 20 | |
| α-helix | 151-153 | 3 | |
| α-helix | 159-161 | 3 | |
| β-strand | 162-165 | 4 | 2 |
| β-strand | 170-173 | 4 | 2 |
| α-helix | 193-195 | 3 | |
| α-helix | 198-201 | 4 | |
| α-helix | 209-224 | 16 | |
| α-helix | 236-244 | 9 | |
| α-helix | 249-250 | 2 | |
| β-strand | 251-252 | 2 | 4 |
| α-helix | 257-267 | 11 | |
| α-helix | 271-273 | 3 | |
| α-helix | 275-276 | 2 | |
| α-helix | 277-287 | 11 | |
| α-helix | 288-290 | 3 | |
| α-helix | 297-298 | 2 | |
| β-strand | 301-302 | 2 | 3 |
| β-strand | 477-478 | 2 | 4 |
| α-helix | 485-494 | 10 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Mitogen-activated protein kinase kinase kinase 7/TGF-beta-activated kinase 1 and MAP3K7-binding… | A | protein | 314 | Homo sapiens | O43318 (AlphaFold model), Q15750 (AlphaFold model) |
>4O91_1 Mitogen-activated protein kinase kinase kinase 7/TGF-beta-activated kinase 1 and MAP3K7-binding protein 1 chimera (chains A) SLHMIDYKEIEVEEVVGRGAFGVVCKAKWRAKDVAIKQIESESERKAFIVELRQLSRVNH PNIVKLYGACLNPVCLVMEYAEGGSLYNVLHGAEPLPYYTAAHAMSWCLQCSQGVAYLHS MQPKALIHRDLKPPNLLLVAGGTVLKICDFGTACDIQTHMTNNKGSAAWMAPEVFEGSNY SEKCDVFSWGIILWEVITRRKPFDEIGGPAFRIMWAVHNGTRPPLIKNLPKPIESLMTRC WSKDPSQRPSMEEIVKIMTHLMRYFPGADEPLQYPCQHSLPPGEDGRVEPYVDFAEFYRL WSVDHGEQSVVTAP
| ID | Name | Formula | Copies |
|---|---|---|---|
| NG2 | N-{4-[(4-ethylpiperazin-1-yl)methyl]-3-(trifluoromethyl)phenyl}-4-methyl-3-(1H-… | C29 H30 F3 N5 O2 | 1 |
Discovery of Type II Inhibitors of TGF beta-Activated Kinase 1 (TAK1) and Mitogen-Activated Protein Kinase Kinase Kinase Kinase 2 (MAP4K2). Tan, L., Nomanbhoy, T., Gurbani, D. et al. J Med Chem (2015) 58:183-196. DOI 10.1021/jm500480k · PubMed
Other PDB entries of the same protein (UniProt O43318 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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