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MolNFT v1 · #33513 · protein

Complex of recombinant human thrombin with a designed inhibitor

2CN0 · Prothrombin precursor: “Complex of recombinant human thrombin with a designed inhibitor”. X-ray diffraction, 3 ligands (F25, NA, CA), 1 pocket (best druggability 0.57). MolNFT v1 #33513 on GenesisL1: 3D structure, binding sites and…

PDB
2CN0
Type
protein
Length
283 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Prothrombin precursor; Hirudin iia
EC
3.4.21.5
UniProt
P00734, P28503
Ligands
F25, NA, CA
Pockets
1 · best druggability 0.57

Structure

x-ray diffraction · 3 distinct chains · 17% helix, 32% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
HProthrombin precursor (EC 3.4.21.5)protein25015% helix, 36% strandP00734
IHirudin iiaprotein50% helix, 0% strandP28503
LProthrombin precursor (EC 3.4.21.5)protein2836% helix, 0% strandP00734

Ligands and binding sites

  • F25 · 4-(1r,3as,4r,8as,8br)-[1-difluoromethyl-2-(4-fluorobenzyl)-3-oxodecahydropyrrolo[3,4-a]pyrrolizin-4-yl]benzamidine · ligand · chains H
  • NA · Sodium ion · metal · chains H
  • CA · Calcium ion · metal · chains H
  • SIN · Succinic acid · additive · chains H, I

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
12760.570.7736F25

Interfaces

2 interfaces between chains.

  • H–L · 1132 Ų buried · 28 hydrogen bonds · protein-protein
  • H–I · 402 Ų buried · 2 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 disulfide, 1 covalent (disulfide, additive adduct).

Compared structures

  • 2CN0 · Complex of Recombinant Human Thrombin with a Designed Inhibitor · the same entry in another collection · chain H against H, TM-score 1.00
  • P28503 · AlphaFold monomer V2.0 prediction for hirudin-2A (P28503) · a predicted model of the same protein · chain I against A, TM-score 0.72

Analyse

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