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Human ubiquitin-activating enzyme 5 in complex with amppnp

Analyse Human ubiquitin-activating enzyme 5 in complex with amppnp in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3GUC
Type
protein
Length
463 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Ubiquitin-like modifier-activating enzyme 5
EC
2.7.7.-
UniProt
Q9GZZ9
Ligands
ANP, ZN
Pockets
5 · best druggability 0.64

Structure

x-ray diffraction · 2 distinct chains · 41% helix, 19% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AUbiquitin-like modifier-activating enzyme 5 (EC 2.7.7.-)protein24242% helix, 18% strandQ9GZZ9
BUbiquitin-like modifier-activating enzyme 5 (EC 2.7.7.-)protein22140% helix, 19% strandQ9GZZ9

Ligands and binding sites

  • ANP · Phosphoaminophosphonic acid-adenylate ester · ligand · chains A
  • ZN · Zinc ion · metal · 2 copies · chains A, B

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

Pockets

5 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14270.640.7742empty
22340.610.8034empty
31380.510.8028ANP
4900.460.8124empty
51110.420.7727empty

Interfaces

1 interface between chains.

  • A–B · 1188 Ų buried · 25 hydrogen bonds · protein-protein

Compared structures

  • 3GUC · Human Ubiquitin-activating Enzyme 5 in Complex with AMPPNP · the same entry in another collection · chain A against A, TM-score 1.00
  • Q9GZZ9 · AlphaFold monomer V2.0 prediction for ubiquitin-like modifier- activating enzyme 5… · a predicted model of the same protein · chain B against A, TM-score 0.95

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