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MolNFT v1 · #82778 · protein

X/N joint refinement of human alpha-thrombin-bivalirudin complex PD5

3VXF · Thrombin light chain: “X/N joint refinement of human alpha-thrombin-bivalirudin complex PD5”. X-ray diffraction; neutron diffraction, 1 ligand (NAG), 3 pockets (best druggability 0.33). MolNFT v1 #82778 on GenesisL1: 3D structure…

PDB
3VXF
Type
protein
Length
297 residues
Chains
4
Method
x-ray diffraction; neutron diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Thrombin light chain; Thrombin heavy chain; Bivalirudin
EC
3.4.21.5
UniProt
P00734
Ligands
NAG
Pockets
3 · best druggability 0.33

Structure

x-ray diffraction; neutron diffraction · 4 distinct chains · 16% helix, 30% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
LThrombin light chain (EC 3.4.21.5)protein2737% helix, 0% strandP00734
HThrombin heavy chain (EC 3.4.21.5)protein25715% helix, 34% strandP00734
JBivalirudinprotein100% helix, 0% strand—
IBivalirudinprotein30% helix, 33% strand—

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · chains H

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

Pockets

3 pockets found on a 1 Å grid, 0 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1880.330.7320empty
2600.330.7618empty
3510.260.7412empty

Interfaces

3 interfaces between chains.

  • L–H · 1137 Ų buried · 24 hydrogen bonds · protein-protein
  • H–J · 549 Ų buried · 3 hydrogen bonds · protein-protein
  • H–I · 466 Ų buried · 15 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 disulfide, 1 d-amino, 1 glycan (disulfide, D-amino acid, N-glycosylation).

Compared structures

  • 3VXF · X/N Joint refinement of Human alpha-thrombin-Bivalirudin complex PD5 · the same entry in another collection · chain L against L, TM-score 1.00

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