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Crystal structure of bovine thrombin complex with protease inhibitor ecotin

Analyse Crystal structure of bovine thrombin complex with protease inhibitor ecotin in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1ID5
Type
protein
Length
424 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Thrombin; Ecotin
EC
3.4.21.5
UniProt
P00735, P23827
Ligands
CA
Pockets
6 · best druggability 0.57

Structure

x-ray diffraction · 3 distinct chains · 12% helix, 35% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
LThrombin (EC 3.4.21.5)protein3037% helix, 0% strandP00735
HThrombin (EC 3.4.21.5)protein25612% helix, 32% strandP00735
IEcotinprotein1387% helix, 49% strandP23827

Ligands and binding sites

  • CA · Calcium ion · metal · chains H
  • TRS · 2-amino-2-hydroxymethyl-propane-1,3-diol · additive · chains H

Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11370.570.8322empty
22500.530.7635empty
3540.380.8019empty
4750.380.7715TRS
5560.360.7912empty

Interfaces

2 interfaces between chains.

  • L–H · 1182 Ų buried · 24 hydrogen bonds · protein-protein
  • H–I · 1179 Ų buried · 18 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 5 disulfide (disulfide).

Compared structures

  • 1ID5 · Crystal structure of bovine thrombin complex with protease inhibitor ecotin · the same entry in another collection · chain L against L, TM-score 1.00
  • P23827 · AlphaFold monomer V2.0 prediction for ecotin (P23827) · a predicted model of the same protein · chain I against A, TM-score 0.97
  • P00735 · AlphaFold monomer V2.0 prediction for prothrombin (P00735) · a predicted model of the same protein · chain H against A, TM-score 0.96

Analyse

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