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Structure of an ubiquitin complex

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

PDB
4NQK
Type
protein
Length
1,187 residues
Chains
10
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Probable ATP-dependent RNA helicase DDX58; Ubiquitin
EC
3.6.4.13
UniProt
O95786, P0CG48
Pockets
15 · best druggability 0.90

Structure

x-ray diffraction · 5 distinct chains · 40% helix, 19% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, DProbable ATP-dependent RNA helicase DDX58 (EC 3.6.4.13)protein18872% helix, 0% strandO95786
EUbiquitinprotein7221% helix, 32% strandP0CG48
F, JUbiquitinprotein7321% helix, 30% strandP0CG48
G, IUbiquitinprotein7117% helix, 32% strandP0CG48
HUbiquitinprotein7516% helix, 31% strandP0CG48

Pockets

15 pockets found on a 1 Å grid, 8 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110580.900.92124empty
22560.770.9032empty
33630.760.8648empty
4930.740.9622empty
5840.730.9618empty

Interfaces

17 interfaces between chains.

  • A–B · 1087 Ų buried · 10 hydrogen bonds · protein-protein
  • C–D · 1076 Ų buried · 14 hydrogen bonds · protein-protein
  • B–C · 1022 Ų buried · 10 hydrogen bonds · protein-protein
  • A–D · 941 Ų buried · 8 hydrogen bonds · protein-protein
  • C–H · 708 Ų buried · 8 hydrogen bonds · protein-protein

Compared structures

  • 4NQK · Structure of an Ubiquitin complex · the same entry in another collection · chain D against D, TM-score 1.00
  • O95786 · AlphaFold monomer V2.0 prediction for antiviral innate immune response receptor rig-I… · a predicted model of the same protein · chain C against A, TM-score 0.96

Analyse

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