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Crystal structure of a putative dipeptidyl-peptidase VI (BT_1314) from bacteroides thetaiotaomicron vpi-5482 at 2.10 a resolution

Analyse Crystal structure of a putative dipeptidyl-peptidase VI (BT_1314) from… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3PVQ
Type
protein
Length
594 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Dipeptidyl-peptidase VI
UniProt
Q8A860
Ligands
CL
Pockets
5 · best druggability 0.63

Structure

x-ray diffraction · 1 distinct chain · 19% helix, 41% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BDipeptidyl-peptidase VIprotein29719% helix, 41% strandQ8A860

Ligands and binding sites

  • CL · Chloride ion · ion · 2 copies · chains A, B
  • GOL · Glycerol · additive · 5 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, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16540.630.7465empty
21580.540.8036GOL, CL
31360.410.7531GOL
41040.360.7417empty
51130.350.7321empty

Interfaces

1 interface between chains.

  • A–B · 1454 Ų buried · 8 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 20 modified (engineered, oxidation).

Compared structures

  • 3PVQ · Crystal structure of a putative dipeptidyl-peptidase VI (BT_1314) from BACTEROIDES… · the same entry in another collection · chain A against A, TM-score 1.00

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