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Structure of DUP1 mutant H67A:UBIQUITIN complex

Analyse Structure of DUP1 mutant H67A:UBIQUITIN complex in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6RYA
Type
protein
Length
1,152 residues
Chains
6
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Septation initiation protein; Polyubiquitin-C
UniProt
A0A3A6VNK6, P0CG48
Pockets
13 · best druggability 0.67

Structure

x-ray diffraction · 2 distinct chains · 47% helix, 10% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, C, ESeptation initiation proteinprotein30853% helix, 5% strandA0A3A6VNK6
B, D, FPolyubiquitin-Cprotein7624% helix, 30% strandP0CG48

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15540.670.7748empty
23950.650.7937empty
34160.650.7840empty
43660.600.7753empty
5500.590.9217empty

Interfaces

6 interfaces between chains.

  • C–D · 1440 Ų buried · 16 hydrogen bonds · protein-protein
  • E–F · 1432 Ų buried · 17 hydrogen bonds · protein-protein
  • A–B · 1415 Ų buried · 14 hydrogen bonds · protein-protein
  • A–E · 446 Ų buried · 1 hydrogen bond · protein-protein
  • A–D · 175 Ų buried · 1 hydrogen bond · protein-protein

Compared structures

  • 6RYA · Structure of Dup1 mutant H67A:Ubiquitin complex · the same entry in another collection · chain A against A, TM-score 1.00

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