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Structure of ovarian tumor (otu) domain in complex with ubiquitin

Analyse Structure of ovarian tumor (otu) domain in complex with ubiquitin in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3C0R
Type
protein
Length
500 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Ubiquitin thioesterase OTU1; Ubiquitin
EC
3.4.19.12
UniProt
P43558, P62988
Ligands
3CN
Pockets
6 · best druggability 0.70

Structure

x-ray diffraction · 2 distinct chains · 33% helix, 23% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, CUbiquitin thioesterase OTU1 (EC 3.4.19.12)protein17537% helix, 20% strandP43558
B, DUbiquitinprotein7524% helix, 29% strandP62988

Ligands and binding sites

  • 3CN · 3-aminopropane · ligand · 2 copies · chains A, B, C, D

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1580.700.9727empty
21020.690.9223empty
3730.620.9018empty
42450.510.7530empty
52290.500.7529empty

Interfaces

3 interfaces between chains.

  • C–D · 1113 Ų buried · 18 hydrogen bonds · protein-protein
  • A–B · 1108 Ų buried · 16 hydrogen bonds · protein-protein
  • A–C · 757 Ų buried · 9 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 8 modified, 4 covalent (engineered, covalent ligand).

Compared structures

  • 3C0R · Structure of Ovarian Tumor (OTU) domain in complex with Ubiquitin · the same entry in another collection · chain A against A, TM-score 1.00
  • P43558 · AlphaFold monomer V2.0 prediction for ubiquitin thioesterase OTU1 (P43558) · a predicted model of the same protein · chain A against A, TM-score 0.99

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