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Thrombin inhibition

Analyse Thrombin inhibition in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2ZI2
Type
protein
Length
287 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Thrombin light chain; Thrombin heavy chain; Hirudin variant-1
EC
3.4.21.5
UniProt
P00734, P01050
Ligands
24U, BEN, NA
Pockets
1 · best druggability 0.56

Structure

x-ray diffraction · 3 distinct chains · 16% helix, 31% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
LThrombin light chain (EC 3.4.21.5)protein2737% helix, 0% strandP00734
HThrombin heavy chain (EC 3.4.21.5)protein25015% helix, 36% strandP00734
IHirudin variant-1protein100% helix, 0% strandP01050

Ligands and binding sites

  • 24U · 1-butanoyl-N-(4-carbamimidoylbenzyl)-L-prolinamide · ligand · chains H
  • BEN · Benzamidine · ligand · chains H
  • NA · Sodium ion · metal · 2 copies · chains H

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

Pockets

1 pocket found on a 1 Å grid, 1 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12870.560.763824U

Interfaces

2 interfaces between chains.

  • L–H · 1093 Ų buried · 30 hydrogen bonds · protein-protein
  • H–I · 573 Ų buried · 6 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 disulfide, 1 modified (disulfide, sulfation).

Compared structures

  • 2ZI2 · Thrombin Inhibition · the same entry in another collection · chain L against L, TM-score 1.00
  • P01050 · AlphaFold monomer V2.0 prediction for hirudin variant-1 (P01050) · a predicted model of the same protein · chain I against A, TM-score 0.50

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