Crystal structure of JNK1 in complex with ATF2(19-58). Determined by X-ray diffraction at 2.7 Å resolution. Released 18 Nov 2020.
Explore 6ZR5 in 3D Show helices and sheets RCSB PDB PDBe
6ZR5 contains 47 α-helices and 26 β-strands across 4 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 | 6-9 | 4 | |
| β-strand | 10-15 | 6 | 1 |
| β-strand | 18-23 | 6 | 1 |
| β-strand | 26-35 | 10 | 2 |
| β-strand | 38-45 | 8 | 2 |
| β-strand | 50-58 | 9 | 2 |
| α-helix | 64-79 | 16 | |
| β-strand | 85 | 1 | 3 |
| β-strand | 88-92 | 5 | 2 |
| β-strand | 103-108 | 6 | 2 |
| β-strand | 113-114 | 2 | 3 |
| α-helix | 116-119 | 4 | |
| α-helix | 125-144 | 20 | |
| α-helix | 154-156 | 3 | |
| β-strand | 157-159 | 3 | 3 |
| β-strand | 165-167 | 3 | 3 |
| α-helix | 194-197 | 4 | |
| α-helix | 206-220 | 15 | |
| α-helix | 232-241 | 10 | |
| α-helix | 243-245 | 3 | |
| α-helix | 246-248 | 3 | |
| α-helix | 253-257 | 5 | |
| α-helix | 264-265 | 2 | |
| α-helix | 271-274 | 4 | |
| α-helix | 285-301 | 17 | |
| α-helix | 306-308 | 3 | |
| α-helix | 310-311 | 2 | |
| α-helix | 312-316 | 5 | |
| α-helix | 322-324 | 3 | |
| α-helix | 327-330 | 4 | |
| α-helix | 332-335 | 4 | |
| α-helix | 341-343 | 3 | |
| α-helix | 349-360 | 12 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 7-9 | 3 | |
| β-strand | 10-15 | 6 | 5 |
| β-strand | 18-23 | 6 | 5 |
| β-strand | 26-35 | 10 | 6 |
| β-strand | 38-45 | 8 | 6 |
| β-strand | 50-58 | 9 | 6 |
| α-helix | 64-79 | 16 | |
| β-strand | 85 | 1 | 7 |
| α-helix | 86-87 | 2 | |
| β-strand | 88-92 | 5 | 6 |
| β-strand | 103-108 | 6 | 6 |
| β-strand | 113-114 | 2 | 7 |
| α-helix | 115-119 | 5 | |
| α-helix | 125-144 | 20 | |
| α-helix | 154-156 | 3 | |
| β-strand | 157-159 | 3 | 7 |
| β-strand | 165-167 | 3 | 7 |
| α-helix | 194-197 | 4 | |
| α-helix | 206-220 | 15 | |
| α-helix | 230-241 | 12 | |
| α-helix | 243-245 | 3 | |
| α-helix | 248-250 | 3 | |
| α-helix | 254-261 | 8 | |
| α-helix | 264-265 | 2 | |
| α-helix | 271-274 | 4 | |
| α-helix | 281-282 | 2 | |
| α-helix | 285-301 | 17 | |
| α-helix | 306-308 | 3 | |
| α-helix | 310-311 | 2 | |
| α-helix | 312-316 | 5 | |
| α-helix | 322-324 | 3 | |
| α-helix | 327-330 | 4 | |
| α-helix | 341-343 | 3 | |
| α-helix | 349-360 | 12 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 25-26 | 2 | 4 |
| β-strand | 35-36 | 2 | 4 |
| α-helix | 39-49 | 11 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 26 | 1 | 8 |
| β-strand | 35 | 1 | 8 |
| α-helix | 39-49 | 11 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Mitogen-activated protein kinase 8 | A, B | protein | 366 | Homo sapiens | P45983 (AlphaFold model) |
| Cyclic AMP-dependent transcription factor ATF-2 | C, D | protein | 40 | Homo sapiens | P15336 (AlphaFold model) |
>6ZR5_1 Mitogen-activated protein kinase 8 (chains A, B) GSMSRSKRDNNFYSVEIGDSTFTVLKRYQNLKPIGSGAQGIVCAAYDAILERNVAIKKLS RPFQNQTHAKRAYRELVLMKCVNHKNIIGLLNVFTPQKSLEEFQDVYIVMELMDANLCQV IQMELDHERMSYLLYQMLCGIKHLHSAGIIHRDLKPSNIVVKSDCTLKILDFGLARTAGT SFMMTPYVVTRYYRAPEVILGMGYKENVDIWSVGCIMGEMIKGGVLFPGTDHIDQWNKVI EQLGTPCPEFMKKLQPTVRTYVENRPKYAGYSFEKLFPDVLFPADSEHNKLKASQARDLL SKMLVIDASKRISVDEALQHPYINVWYDPSEAEAPPPKIPDKQLDEREHTIEEWKELIYK EVMDLE
>6ZR5_2 Cyclic AMP-dependent transcription factor ATF-2 (chains C, D) YSDDKPFLCTAPGCGRRFTNEDHLAVHKRKHEMTLKFGPA
| ID | Name | Formula | Copies |
|---|---|---|---|
| ZN | Zinc ion | Zn | 2 |
| ANP | Phosphoaminophosphonic acid-adenylate ester | C10 H17 N6 O12 P3 | 2 |
| MG | Magnesium ion | Mg | 4 |
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 P45983 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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