GL1X · GenesisL1 explorer

MolNFT v1 · #10407 · protein

Human coagulation factor xa in complex with M54471

1IQM: “Human coagulation factor xa in complex with M54471”. X-ray diffraction, 2 ligands (XMK, CA), 3 pockets (best druggability 0.42). MolNFT v1 #10407 on GenesisL1: 3D structure, binding sites and pockets in GL1X.

PDB
1IQM
Type
protein
Length
286 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Coagulation factor xa
EC
3.4.21.6
UniProt
P00742
Ligands
XMK, CA
Pockets
3 · best druggability 0.42

Structure

x-ray diffraction · 2 distinct chains · 13% helix, 34% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ACoagulation factor xa (EC 3.4.21.6)protein23513% helix, 36% strandP00742
LCoagulation factor xa (EC 3.4.21.6)protein5114% helix, 25% strandP00742

Ligands and binding sites

  • XMK · 1-[[(1E)-2-(4-chlorophenyl)ethenyl]sulfonyl]-4-[[1-(4-pyridinyl)-4-piperidinyl]methyl]piperazine · ligand · chains A
  • CA · Calcium ion · metal · chains A

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
11000.420.7824XMK
2570.300.7411empty
3610.290.7415empty

Interfaces

1 interface between chains.

  • A–L · 909 Ų buried · 10 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 8 disulfide (disulfide).

Compared structures

  • 1IQM · Human coagulation factor Xa in complex with M54471 · the same entry in another collection · chain A against A, TM-score 1.00
  • P00742 · AlphaFold monomer V2.0 prediction for coagulation factor X (P00742) · a predicted model of the same protein · chain A against A, TM-score 0.98

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