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USP15 catalytic domain in complex with small molecule

Analyse USP15 catalytic domain in complex with small molecule in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6GH9
Type
protein
Length
640 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Ubiquitin carboxyl-terminal hydrolase 15
EC
3.4.19.12
UniProt
Q9Y4E8
Ligands
MIX, ZN
Pockets
9 · best druggability 0.55

Structure

x-ray diffraction · 2 distinct chains · 29% helix, 28% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AUbiquitin carboxyl-terminal hydrolase 15 (EC 3.4.19.12)protein33128% helix, 28% strandQ9Y4E8
BUbiquitin carboxyl-terminal hydrolase 15 (EC 3.4.19.12)protein30929% helix, 27% strandQ9Y4E8

Ligands and binding sites

  • MIX · 1,4-dihydroxy-5,8-bis({2-[(2-hydroxyethyl) amino]ethyl}amino)-9,10-anthracenedione · ligand · chains A
  • ZN · Zinc ion · metal · chains A
  • DMS · Dimethyl sulfoxide · additive · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12850.550.7637empty
21640.470.7630empty
3890.420.7922empty
41180.400.7532empty
5820.370.7618empty

Interfaces

1 interface between chains.

  • A–B · 696 Ų buried · 11 hydrogen bonds · protein-protein

Compared structures

  • 6GH9 · USP15 catalytic domain in complex with small molecule · the same entry in another collection · chain A against A, TM-score 1.00
  • Q9Y4E8 · AlphaFold monomer V2.0 prediction for ubiquitin carboxyl-terminal hydrolase 15 (Q9Y4E8) · a predicted model of the same protein · chain B against A, TM-score 0.98

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