GL1X · GenesisL1 explorer

Research workbench

Factor xa - cation inhibitor complex

Analyse Factor xa - cation inhibitor complex in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2Y5F
Type
protein
Length
287 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Activated factor xa heavy chain; Factor X light chain
EC
3.4.21.6
UniProt
P00742
Ligands
XWG, NA
Pockets
2 · best druggability 0.49

Structure

x-ray diffraction · 2 distinct chains · 12% helix, 34% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AActivated factor xa heavy chain (EC 3.4.21.6)protein23313% helix, 36% strandP00742
LFactor X light chain (EC 3.4.21.6)protein547% helix, 26% strandP00742

Ligands and binding sites

  • XWG · (3as,4r,5s,8as,8br)-4-[5-(5-chlorothiophen-2-yl)-1,2-oxazol-3-yl]-2-[3-[1-(2-hydroxyethyl)pyrrolidin-1-ium-1-yl]propyl]-4,6,7,8,8A,8B-hexahydro-3AH-pyrrolo[3,4-a]pyrrolizine-1,3-dione · ligand · chains A
  • NA · Sodium ion · metal · 2 copies · 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
11290.490.7924XWG
21170.420.7625empty

Interfaces

1 interface between chains.

  • A–L · 925 Ų buried · 11 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 8 disulfide (disulfide).

Compared structures

  • 2Y5F · Factor xa - cation inhibitor complex · 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 0.99

Analyse

GL1X is a live explorer of the GenesisL1 blockchain. Turn on JavaScript for search, charts and interactive views.