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Structure of E6AP-E6 complex in Att1 state

Analyse Structure of E6AP-E6 complex in Att1 state in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
8JRN
Type
protein
Length
1,660 residues
Chains
4
Method
electron microscopy
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
2.6
Source
Homo sapiens; Human papillomavirus 16
Molecule
Protein E6; Ubiquitin-protein ligase E3A
EC
2.3.2.26
UniProt
P03126, Q05086
Ligands
ZN
Pockets
20 · best druggability 0.79

Structure

electron microscopy · resolution 2.6 · 2 distinct chains · 52% helix, 10% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
D, BProtein E6protein14139% helix, 17% strandP03126
C, AUbiquitin-protein ligase E3A (EC 2.3.2.26)protein68955% helix, 8% strandQ05086

Ligands and binding sites

  • ZN · Zinc ion · metal · 4 copies · chains D, B

Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.

Pockets

20 pockets found on a 1 Å grid, 9 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14770.790.8776empty
26140.770.8380empty
311640.740.77106empty
48360.730.7868empty
54800.710.8156empty

Interfaces

5 interfaces between chains.

  • D–C · 1646 Ų buried · 26 hydrogen bonds · protein-protein
  • B–A · 1642 Ų buried · 26 hydrogen bonds · protein-protein
  • C–B · 517 Ų buried · 6 hydrogen bonds · protein-protein
  • D–A · 517 Ų buried · 6 hydrogen bonds · protein-protein
  • C–A · 230 Ų buried · 0 hydrogen bonds · protein-protein

Compared structures

  • Q05086 · AlphaFold monomer V2.0 prediction for ubiquitin-protein ligase E3A (Q05086) · a predicted model of the same protein · chain C against A, TM-score 0.93

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