Brand  (β version)

PDB ID: 6EZP

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Ligands
Code Name Style Show Link
C3E (3~{S},14~{E})-19-chloranyl-~{N}-(1-cyanocyclopropyl)-5-oxidanylidene-12,17-dioxa-4-azatricyclo[16.2.2.0^{6,11}]docosa-1(21),6(11),7,9,14,18(22),19-heptaene-3-carboxamide PoSSuM
GOL Glycerol PoSSuM
Non-standard Residues
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Glycosylation
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Structure summary

Code : 6EZP   PDBj   RCSB PDB   PDBe
Header : HYDROLASE
Title : CATHEPSIN L IN COMPLEX WITH (3S,14E)-19-chloro-N-(1-cyanocyclopropyl)-5-oxo-12,17-dioxa-4-azatricyclo[16.2.2.06,11]docosa-1(21),6(11),7,9,14,18(22),19-heptaene-3-carboxamide
Release Data : 2018-04-11
Compound :
mol_id molecule chains synonym
1 Cathepsin L1 A Cathepsin L,Major excreted protein,MEP
ec: 3.4.22.15
Source :
mol_id organism_scientific organism_common expression_system
1 Homo sapiens  (taxid:9606) Human Escherichia coli  (taxid:562)
gene: CTSL, CTSL1
Authors : Banner, D.W., Benz, J., Kuglstatter, A.
Keywords : PROTEASE INHIBITOR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX, HYDROLASE
Exp. method : X-RAY DIFFRACTION ( 1.37 Å )
Citation :

Repurposing a Library of Human Cathepsin L Ligands: Identification of Macrocyclic Lactams as Potent Rhodesain and Trypanosoma brucei Inhibitors.

Giroud, M.,Dietzel, U.,Anselm, L.  et al.
(2018)  J. Med. Chem.  61 : 3350 - 3369

PubMed: 29590750
DOI: 10.1021/acs.jmedchem.7b01869

Reaction

Chain : A
UniProt : P07711 (CATL1_HUMAN)
Reaction: EC: Evidence:
Physiological Direction:
Specificity close to that of papain. As compared to cathepsin B, cathepsin L exhibits higher activity toward protein substrates, but has little activity on Z-Arg-Arg-NHMec, and no peptidyl- dipeptidase activity. 3.4.22.15 PubMed:9468501
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