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Crystal structure of the human alpha-thrombin-haemadin complex: an exosite II-binding inhibitor

Analyse Crystal structure of the human alpha-thrombin-haemadin complex: an exosite… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1E0F
Type
protein
Length
1,048 residues
Chains
9
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Thrombin; Haemadin
EC
3.4.21.5
UniProt
P00734, Q25163
Pockets
16 · best druggability 0.72

Structure

x-ray diffraction · 7 distinct chains · 13% helix, 31% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BThrombinprotein3625% helix, 0% strandP00734
CThrombinprotein3531% helix, 0% strandP00734
DThrombin (EC 3.4.21.5)protein25713% helix, 35% strandP00734
EThrombin (EC 3.4.21.5)protein25612% helix, 36% strandP00734
FThrombin (EC 3.4.21.5)protein25915% helix, 35% strandP00734
I, KHaemadinprotein570% helix, 16% strandQ25163
JHaemadinprotein550% helix, 24% strandQ25163

Pockets

16 pockets found on a 1 Å grid, 4 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13670.720.8449empty
21240.550.8319empty
32950.550.7627empty
41950.500.7736empty
51840.460.7520empty

Interfaces

13 interfaces between chains.

  • C–F · 1347 Ų buried · 25 hydrogen bonds · protein-protein
  • D–I · 1272 Ų buried · 23 hydrogen bonds · protein-protein
  • B–E · 1218 Ų buried · 25 hydrogen bonds · protein-protein
  • F–K · 1197 Ų buried · 19 hydrogen bonds · protein-protein
  • A–D · 1184 Ų buried · 27 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 21 disulfide (disulfide).

Compared structures

  • 1E0F · Crystal structure of the human alpha-thrombin-haemadin complex: an exosite II-binding… · the same entry in another collection · chain A against A, TM-score 1.00

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