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Structure of chlamydia trachomatis effector protein CHLADUB1 bound to ubiquitin

Analyse Structure of chlamydia trachomatis effector protein CHLADUB1 bound to ubiquitin in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6GZS
Type
protein
Length
325 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Deubiquitinase and deneddylase DUB1; Polyubiquitin-B
EC
3.4.22.-
UniProt
B0B9A0, P0CG47
Ligands
AYE, SO4
Pockets
3 · best druggability 0.67

Structure

x-ray diffraction · 2 distinct chains · 42% helix, 15% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ADeubiquitinase and deneddylase DUB1 (EC 3.4.22.-)protein25048% helix, 11% strandB0B9A0
BPolyubiquitin-Bprotein7524% helix, 29% strandP0CG47

Ligands and binding sites

  • AYE · prop-2-en-1-amine · ligand · chains A, B
  • SO4 · Sulfate ion · ion · chains A
  • GOL · Glycerol · additive · chains A

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

Pockets

3 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1990.670.9130empty
22740.640.8129empty
3570.410.8114empty

Interfaces

1 interface between chains.

  • A–B · 927 Ų buried · 11 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 covalent (covalent ligand).

Compared structures

  • 6GZS · Structure of Chlamydia trachomatis effector protein ChlaDUB1 bound to ubiquitin · the same entry in another collection · chain A against A, TM-score 1.00
  • B0B9A0 · AlphaFold monomer V2.0 prediction for deubiquitinase and deneddylase DUB1 (B0B9A0) · a predicted model of the same protein · chain A against A, TM-score 0.99

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