Structure of PDB 4axm Chain L Binding Site BS01
Receptor Information
>4axm Chain L (length=216) Species:
9606
(Homo sapiens) [
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APRSVDWREKGYVTPVKNQGQCGSCWAFSATGALEGQMFRKTGRLISLSE
QNLVDCSGPQGNEGCNGGLMDYAFQYVQDNGGLDSEESYPYEATEESCKY
NPKYSVANDTGFVDIPKQEKALMKAVATVGPISVAIDAGHESFLFYKEGI
YFEPDCSSEDMDHGVLVVGYGFESNNKYWLVKNSWGEEWGMGGYVKMAKD
RRNHCGIASAASYPTV
Ligand information
Ligand ID
V65
InChI
InChI=1S/C21H27ClN6O2/c22-16-8-6-15(7-9-16)14-28(17-4-2-1-3-5-17)21-25-19(18(23)29)24-20(26-21)27-10-12-30-13-11-27/h6-9,17H,1-5,10-14H2,(H2,23,29)
InChIKey
WEJFTJFUONLSMW-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 12.01
Clc1ccc(cc1)CN(c2nc(nc(n2)C(=O)N)N3CCOCC3)C4CCCCC4
CACTVS 3.385
NC(=O)c1nc(nc(n1)N(Cc2ccc(Cl)cc2)C3CCCCC3)N4CCOCC4
OpenEye OEToolkits 1.9.2
c1cc(ccc1CN(c2nc(nc(n2)N3CCOCC3)C(=O)N)C4CCCCC4)Cl
Formula
C21 H27 Cl N6 O2
Name
4-[(4-chlorobenzyl)(cyclohexyl)amino]-6-morpholin-4-yl-1,3,5-triazine-2-carboxamide
ChEMBL
DrugBank
ZINC
ZINC000098209519
PDB chain
4axm Chain L Residue 1222 [
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Receptor-Ligand Complex Structure
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PDB
4axm
Optimization of Triazine Nitriles as Rhodesain Inhibitors: Structure-Activity Relationships, Bioisosteric Imidazopyridine Nitriles, and X-Ray Crystal Structure Analysis with Human Cathepsin L
Resolution
2.8 Å
Binding residue
(original residue number in PDB)
G23 C25 N66 G67 G68 A135 D162
Binding residue
(residue number reindexed from 1)
G23 C25 N66 G67 G68 A135 D162
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
Q19
Catalytic site (residue number reindexed from 1)
Q19
Enzyme Commision number
3.4.22.15
: cathepsin L.
Gene Ontology
Molecular Function
GO:0008234
cysteine-type peptidase activity
Biological Process
GO:0006508
proteolysis
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Molecular Function
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Biological Process
External links
PDB
RCSB:4axm
,
PDBe:4axm
,
PDBj:4axm
PDBsum
4axm
PubMed
23658062
UniProt
P07711
|CATL1_HUMAN Procathepsin L (Gene Name=CTSL)
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