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Human coagulation factor xa in complex with M55532

Analyse Human coagulation factor xa in complex with M55532 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1IOE
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
XMA, CA
Pockets
2 · best druggability 0.49

Structure

x-ray diffraction · 2 distinct chains · 12% helix, 33% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ACoagulation factor xa (EC 3.4.21.6)protein23511% helix, 34% strandP00742
LCoagulation factor xa (EC 3.4.21.6)protein5114% helix, 27% strandP00742

Ligands and binding sites

  • XMA · (-)-7-[(6-chloro-2-naphthalenyl)sulfonyl]tetrahydro-8A-(methoxymethyl)-1'-(4-pyridinyl)-spiro[5h-oxazolo[3,2-a]pyrazine-2(3H),4'-piperidin]-5-one · 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

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11360.490.7927XMA
2770.310.7322empty

Interfaces

1 interface between chains.

  • A–L · 903 Ų buried · 14 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 8 disulfide (disulfide).

Compared structures

  • 1IOE · Human coagulation factor Xa in complex with M55532 · 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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