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Crystal structure of the extracellular segment of integrin ALPHAVBETA3

Analyse Crystal structure of the extracellular segment of integrin ALPHAVBETA3 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1JV2
Type
protein
Length
1,466 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Integrin, alpha V; Platelet membrane glycoprotein iiia beta subunit
Ligands
NAG, NDG, CA
Pockets
17 · best druggability 0.80

Structure

x-ray diffraction · 2 distinct chains · 8% helix, 33% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AIntegrin, alpha Vprotein9273% helix, 39% strand—
BPlatelet membrane glycoprotein iiia beta subunitprotein53916% helix, 23% strand—

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 15 copies · chains A, B
  • NDG · 2-acetamido-2-deoxy-alpha-D-glucopyranose · sugar · 3 copies · chains A, B
  • CA · Calcium ion · metal · 6 copies · chains A, B

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

Pockets

17 pockets found on a 1 Å grid, 4 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110420.800.8298empty
26610.780.8456empty
35990.680.7749NAG
4860.510.8324empty
51460.430.7524empty

Interfaces

1 interface between chains.

  • A–B · 2960 Ų buried · 18 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 25 disulfide, 11 glycan (disulfide, N-glycosylation).

Compared structures

  • 1JV2 · Crystal structure of the extracellular segment of integrin ALPHAVBETA3 · the same entry in another collection · chain A against A, TM-score 1.00

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