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Ligands
Code Name Style Show Link
00P (5s)-N-[(trans-4-aminocyclohexyl)methyl]-1,3-dioxo-2-[2-(phenylsulfonyl)ethyl]-2,3,5,8-tetrahydro-1h-[1,2,4]triazolo[1,2-a]pyridazine-5-carboxamide
NA Sodium ion
Non-standard Residues
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TYS O-sulfo-L-tyrosine
Glycosylation
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Modification
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Code : 1D9I   PDBj   RCSB PDB   PDBe
Header : HYDROLASE/HYDROLASE INHIBITOR
Title : STRUCTURE OF THROMBIN COMPLEXED WITH SELECTIVE NON-ELECTOPHILIC INHIBITORS HAVING CYCLOHEXYL MOIETIES AT P1
Release Data : 2000-10-30
Compound :
mol_id molecule chains
1 THROMBIN A
ec: 3.4.21.5
mol_id molecule chains
2 HIRUGEN I
Source :
mol_id organism_scientific organism_common
1 Homo sapiens  (taxid:9606) Human
mol_id organism_scientific
2 Hirudo medicinalis  (taxid:6421)
synthetic: yes
other_details: THIS SEQUENCE WAS CHEMICALLY SYNTHESIZED
Authors : Krishnan, R., Mochalkin, I., Arni, R., Tulinsky, A.
Keywords : GLOBULAR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
Exp. method : X-RAY DIFFRACTION ( 2.3 Å )
Citation :

Structure of thrombin complexed with selective non-electrophilic inhibitors having cyclohexyl moieties at P1.

Krishnan, R.,Mochalkin, I.,Arni, R.  et al.
(2000)  Acta Crystallogr.,Sect.D  56 : 294 - 303

PubMed: 10713516
DOI: 10.1107/S0907444900000068

Chain : A
UniProt : P00734 (THRB_HUMAN)
Reaction: EC: Evidence:
Physiological Direction:
Selective cleavage of Arg-|-Gly bonds in fibrinogen to form fibrin and release fibrinopeptides A and B. 3.4.21.5 -
-
Chain : I
UniProt : P28504 (HIR2_HIRME)
Reaction : -