Structure of PDB 1mhw Chain A Binding Site BS02
Receptor Information
>1mhw Chain A (length=174) Species:
9606
(Homo sapiens) [
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APRSVDWREKGYVTPVKNQGQCGSCWAFSATGALEGQMFRKTGRLISLSE
QNLVDCSGPQGNEGCNGGLMDYAFQYVQDNGGLDSEESYPYEATEESCKY
NPKYSVANDTGFVDIPKQEKALMKAVATVGPISVAIDAGHESFLFYKEGI
YFEPDCSSEDMDHGVLVVGYGFES
Ligand information
>1mhw Chain F (length=3) [
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GCR
Receptor-Ligand Complex Structure
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PDB
1mhw
Design of non-covalent inhibitors of human cathepsin L. From the 96-residue proregion to optimized tripeptides
Resolution
1.9 Å
Binding residue
(original residue number in PDB)
N18 L144
Binding residue
(residue number reindexed from 1)
N18 L144
Enzymatic activity
Catalytic site (original residue number in PDB)
V16 Q19 C25 H163
Catalytic site (residue number reindexed from 1)
V16 Q19 C25 H163
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:1mhw
,
PDBe:1mhw
,
PDBj:1mhw
PDBsum
1mhw
PubMed
12431059
UniProt
P07711
|CATL1_HUMAN Procathepsin L (Gene Name=CTSL)
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