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Ligands
Code Name Style Show Link
NA Sodium ion
Non-standard Residues
Code Name Show
0BN 4-carbamimidoyl-L-phenylalanine
CHG Cyclohexyl-glycine
PRR 3-(methyl-pyridinium)alanine
TYS O-sulfo-L-tyrosine
Glycosylation
Code Name Emphasize
Modification
Code Name Show
ACE Acetyl group
NH2 Amino group
Code : 7KME   PDBj   RCSB PDB   PDBe
Header : HYDROLASE/HYDROLASE INHIBITOR
Title : CRYSTAL STRUCTURE OF HUMAN ALPHA-THROMBIN INHIBITED WITH SEL2711.
Release Data : 1999-03-09
Compound :
mol_id molecule chains
1 THROMBIN L-CHAIN L
ec: 3.4.21.5
mol_id molecule chains
2 THROMBIN H-CHAIN H
ec: 3.4.21.5
mol_id molecule chains
3 HIRUGEN I
mol_id molecule chains
4 SEL2711 J
Source :
mol_id organism_scientific organism_common
1 Homo sapiens  (taxid:9606) Human
mol_id organism_scientific organism_common
2 Homo sapiens  (taxid:9606) Human
mol_id organism_scientific
3
synthetic: yes
mol_id organism_scientific
4
synthetic: yes
Authors : Mochalkin, I., Tulinsky, A.
Keywords : SELECTIDE INHIBITOR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
Exp. method : X-RAY DIFFRACTION ( 2.10 Å )
Citation :

Structures of thrombin retro-inhibited with SEL2711 and SEL2770 as they relate to factor Xa binding.

Mochalkin, I.,Tulinsky, A.
(1999)  Acta Crystallogr.,Sect.D  55 : 785 - 793

PubMed: 10089309
DOI: 10.1107/S0907444999000359

Chain : H
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 -
-