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Human 14-3-3 isoform zeta in complex with a diphoyphorylated C-RAF peptide and cotylenin a
Analyse Human 14-3-3 isoform zeta in complex with a diphoyphorylated C-RAF peptide and… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 4IHL
- Type
- protein
- Length
- 474 residues
- Chains
- 3
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- 14-3-3 protein ZETA/DELTA; RAF proto-oncogene SERINE/THREONINE-protein kinase
- EC
- 2.7.11.1
- UniProt
- P63104, P04049
- Ligands
- 1F5, K
- Pockets
- 4 · best druggability 0.66
Structure
x-ray diffraction · 3 distinct chains · 80% helix, 0% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | 14-3-3 protein ZETA/DELTA | protein | 230 | 83% helix, 0% strand | P63104 |
| B | 14-3-3 protein ZETA/DELTA | protein | 227 | 82% helix, 0% strand | P63104 |
| P | RAF proto-oncogene SERINE/THREONINE-protein kinase (EC 2.7.11.1) | protein | 17 | 0% helix, 0% strand | P04049 |
Ligands and binding sites
- 1F5 · (1R,3aS,4R,5R,6R,9aR,10E)-6-({(1S,2R,4S,5R,6R,8S,9S)-5-hydroxy-2-(methoxymethyl)-9-methyl-9-[(2S)-oxiran-2-yl]-3,7,10,1 1-tetraoxatricyclo[6.2.1.0~1,6~]undec-4-yl}oxy)-1-(methoxymethyl)-4,9a-dimethyl-7-(propan-2-yl)-1,2,3,3a,4,5,6,8,9,9a-de cahydrodicyclopenta[a,d][8]annulene-1,5-diol · ligand · 2 copies · chains A, P, B
- K · Potassium ion · metal · 2 copies · chains A, B
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
4 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 311 | 0.66 | 0.82 | 36 | K, 1F5 |
| 2 | 249 | 0.66 | 0.83 | 27 | K, 1F5 |
| 3 | 336 | 0.55 | 0.75 | 26 | empty |
| 4 | 66 | 0.33 | 0.76 | 16 | empty |
Interfaces
3 interfaces between chains.
- A–B · 985 Ų buried · 13 hydrogen bonds · protein-protein
- B–P · 585 Ų buried · 13 hydrogen bonds · protein-protein
- A–P · 577 Ų buried · 16 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 2 modified (phosphorylation).
Compared structures
- 4IHL · Human 14-3-3 isoform zeta in complex with a diphoyphorylated C-RAF peptide and Cotylenin A · the same entry in another collection · chain A against A, TM-score 1.00
- P63104 · AlphaFold monomer V2.0 prediction for 14-3-3 protein ZETA/DELTA (P63104) · a predicted model of the same protein · chain A against A, TM-score 0.99
- P04049 · AlphaFold monomer V2.0 prediction for RAF proto-oncogene SERINE/THREONINE-protein kinase… · a predicted model of the same protein · chain P against A, TM-score 0.25
Analyse
- Open in the research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides and crosslinks on the 3D structure
- Every structure of UniProt P63104
- Every structure of UniProt P04049
- Elsewhere: RCSB PDB 4IHL · PDBe 4IHL · UniProt P63104 · UniProt P04049
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