Crystal structure of double-phosphorylated p38alpha with ATF2(83-102). Determined by X-ray diffraction at 1.95 Å resolution. Released 18 Nov 2020.
Explore 6ZQS in 3D Show helices and sheets RCSB PDB PDBe
6ZQS contains 25 α-helices and 13 β-strands across 2 chains. 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 |
|---|---|---|---|
| α-helix | 5-7 | 3 | |
| β-strand | 8-12 | 5 | 1 |
| β-strand | 17-21 | 5 | 1 |
| β-strand | 24-29 | 6 | 2 |
| α-helix | 30-33 | 4 | |
| β-strand | 38-43 | 6 | 2 |
| β-strand | 48-54 | 7 | 2 |
| α-helix | 62-77 | 16 | |
| β-strand | 83 | 1 | 3 |
| β-strand | 88-90 | 3 | 2 |
| α-helix | 96-98 | 3 | |
| β-strand | 103-107 | 5 | 2 |
| β-strand | 112 | 1 | 3 |
| α-helix | 113-117 | 5 | |
| α-helix | 124-143 | 20 | |
| β-strand | 146-147 | 2 | 4 |
| α-helix | 153-155 | 3 | |
| β-strand | 156-158 | 3 | 3 |
| β-strand | 164-166 | 3 | 3 |
| β-strand | 173-174 | 2 | 4 |
| α-helix | 186-188 | 3 | |
| α-helix | 191-195 | 5 | |
| α-helix | 203-218 | 16 | |
| α-helix | 228-239 | 12 | |
| α-helix | 244-247 | 4 | |
| α-helix | 253-260 | 8 | |
| α-helix | 263-264 | 2 | |
| α-helix | 266-268 | 3 | |
| α-helix | 270-272 | 3 | |
| α-helix | 279-288 | 10 | |
| α-helix | 293-295 | 3 | |
| α-helix | 297-298 | 2 | |
| α-helix | 299-303 | 5 | |
| α-helix | 306-308 | 3 | |
| α-helix | 320-324 | 5 | |
| α-helix | 334-346 | 13 | |
| α-helix | 350-352 | 3 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 91-100 | 10 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Mitogen-activated protein kinase 14 | A | protein | 362 | Homo sapiens | Q16539 (AlphaFold model) |
| Cyclic AMP-dependent transcription factor ATF-2 | B | protein | 20 | Homo sapiens | P15336 (AlphaFold model) |
>6ZQS_1 Mitogen-activated protein kinase 14 (chains A) GSMSQERPTFYRQELNKTIWEVPERYQNLSPVGSGAYGSVCAAFDTKTGLRVAVKKLSRP FQSIIHAKRTYRELRLLKHMKHENVIGLLDVFTPARSLEEFNDVYLVTHLMGADLNNIVK CQKLTDDHVQFLIYQILRGLKYIHSADIIHRDLKPSNLAVNEDCELKILDFGLARHTDDE MTGYVATRWYRAPEIMLNWMHYNQTVDIWSVGCIMAELLTGRTLFPGTDHIDQLKLILRL VGTPGAELLKKISSESARNYIQSLTQMPKMNFANVFIGANPLAVDLLEKMLVLDSDKRIT AAQALAHAYFAQYHDPDDEPVADPYDQSFESRDLLIDEWKSLTYDEVISFVPPPLDQEEM ES
>6ZQS_2 Cyclic AMP-dependent transcription factor ATF-2 (chains B) GLFNELANPFENEFKKASED
| ID | Name | Formula | Copies |
|---|---|---|---|
| 3FF | 2-[(2,4-difluorophenyl)amino]-7-{[(2R)-2,3-dihydroxypropyl]oxy}-10,11-dihydro-5… | C24 H21 F2 N O4 | 1 |
Co-regulation of the transcription controlling ATF2 phosphoswitch by JNK and p38. Kirsch, K., Zeke, A., Toke, O. et al. Nat Commun (2020) 11:5769-5769. DOI 10.1038/s41467-020-19582-3 · PubMed
Other PDB entries of the same protein (UniProt Q16539 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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