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Structural and biochemical studies of human PCNA complexes provide the basis for association with CDK/CYCLIN and rationale for inhibitor design

Analyse Structural and biochemical studies of human PCNA complexes provide the basis… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1VYJ
Type
protein
Length
1,641 residues
Chains
12
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Proliferating cell nuclear antigen; Small peptide savlqkkitdyfhpkk
UniProt
P12004
Pockets
14 · best druggability 0.68

Structure

x-ray diffraction · 3 distinct chains · 18% helix, 45% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, C, E, I, KProliferating cell nuclear antigenprotein25719% helix, 46% strandP12004
B, D, F, H, J, LSmall peptide savlqkkitdyfhpkkprotein1619% helix, 25% strand—
GProliferating cell nuclear antigenprotein26017% helix, 45% strandP12004

Pockets

14 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
17800.680.7580empty
24740.600.7551empty
3980.420.7818empty
4840.380.7723empty
5770.380.7817empty

Interfaces

16 interfaces between chains.

  • C–D · 922 Ų buried · 10 hydrogen bonds · protein-protein
  • G–H · 898 Ų buried · 8 hydrogen bonds · protein-protein
  • K–L · 894 Ų buried · 8 hydrogen bonds · protein-protein
  • I–J · 859 Ų buried · 10 hydrogen bonds · protein-protein
  • E–F · 857 Ų buried · 9 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 5 disulfide (disulfide).

Compared structures

  • 1VYJ · Structural and biochemical studies of human PCNA complexes provide the basis for… · the same entry in another collection · chain A against A, TM-score 1.00

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