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Crystal structure of human PCNA in complex with three P15 peptides

Analyse Crystal structure of human PCNA in complex with three P15 peptides in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6GWS
Type
protein
Length
831 residues
Chains
6
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Proliferating cell nuclear antigen; PCNA-associated factor
UniProt
P12004, Q15004
Pockets
5 · best druggability 0.46

Structure

x-ray diffraction · 4 distinct chains · 17% helix, 38% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, CProliferating cell nuclear antigenprotein25518% helix, 46% strandP12004
DPCNA-associated factorprotein2114% helix, 5% strandQ15004
EPCNA-associated factorprotein2214% helix, 9% strandQ15004
FPCNA-associated factorprotein2313% helix, 4% strandQ15004

Pockets

5 pockets found on a 1 Å grid, 0 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11210.460.7820empty
21220.420.7623empty
31010.420.7721empty
4810.390.7819empty
5530.290.7617empty

Interfaces

9 interfaces between chains.

  • B–E · 1212 Ų buried · 13 hydrogen bonds · protein-protein
  • C–D · 1188 Ų buried · 14 hydrogen bonds · protein-protein
  • A–F · 1177 Ų buried · 19 hydrogen bonds · protein-protein
  • A–B · 750 Ų buried · 14 hydrogen bonds · protein-protein
  • A–C · 697 Ų buried · 11 hydrogen bonds · protein-protein

Compared structures

  • 6GWS · Crystal structure of human PCNA in complex with three p15 peptides · the same entry in another collection · chain F against F, TM-score 1.00
  • Q15004 · AlphaFold monomer V2.0 prediction for PCNA-associated factor (Q15004) · a predicted model of the same protein · chain F against A, TM-score 0.40

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