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The intact and cleaved human antithrombin III complex as a model for serpin-proteinase interactions

Analyse The intact and cleaved human antithrombin III complex as a model for… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1ATH
Type
protein
Length
751 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Antithrombin III
UniProt
P01008
Pockets
5 · best druggability 0.76

Structure

x-ray diffraction · 2 distinct chains · 31% helix, 34% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AAntithrombin IIIprotein38929% helix, 33% strandP01008
BAntithrombin IIIprotein36233% helix, 35% strandP01008

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15150.760.8450empty
2850.510.8413empty
3830.440.8015empty
4790.390.7816empty
5600.310.7516empty

Interfaces

1 interface between chains.

  • A–B · 990 Ų buried · 16 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 5 disulfide (disulfide).

Compared structures

  • 1ATH · The intact and cleaved human antithrombin III complex as a model for serpin-proteinase… · the same entry in another collection · chain A against A, TM-score 1.00
  • P01008 · AlphaFold monomer V2.0 prediction for antithrombin-III (P01008) · a predicted model of the same protein · chain A against A, TM-score 0.92

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