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Crystal structure of porcine dipeptidyl peptidase IV (CD26)

Analyse Crystal structure of porcine dipeptidyl peptidase IV (CD26) in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1ORV
Type
protein
Length
2,912 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Dipeptidyl peptidase IV
EC
3.4.14.5
Ligands
NAG, BMA, SO4
Pockets
20 · best druggability 0.74

Structure

x-ray diffraction · 1 distinct chain · 18% helix, 38% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, DDipeptidyl peptidase IV (EC 3.4.14.5)protein72818% helix, 38% strand—

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 33 copies · chains A, B, C, D
  • BMA · beta-D-mannopyranose · sugar · 2 copies · chains B
  • SO4 · Sulfate ion · ion · 4 copies · chains A, B, C, D

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

Pockets

20 pockets found on a 1 Å grid, 14 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1630.740.9922empty
2670.740.9822empty
38940.720.76113SO4
46180.680.7779empty
55480.670.7770empty

Interfaces

4 interfaces between chains.

  • A–B · 2298 Ų buried · 44 hydrogen bonds · protein-protein
  • C–D · 2276 Ų buried · 41 hydrogen bonds · protein-protein
  • B–D · 599 Ų buried · 10 hydrogen bonds · protein-protein
  • A–C · 595 Ų buried · 11 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 24 glycan, 16 disulfide (N-glycosylation, disulfide).

Compared structures

  • 1ORV · Crystal Structure of Porcine Dipeptidyl Peptidase IV (CD26) · the same entry in another collection · chain A against A, TM-score 1.00

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