Structure of PDB 5lf0 Chain V Binding Site BS02
Receptor Information
>5lf0 Chain V (length=220) Species:
9606
(Homo sapiens) [
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TTIAGVVYKDGIVLGADTRATEGMVVADKNCSKIHFISPNIYCCGAGTAA
DTDMTTQLISSNLELHSLSTGRLPRVVTANRMLKQMLFRYQGYIGAALVL
GGVDVTGPHLYSIYPHGSTDKLPYVTMGSGSLAAMAVFEDKFRPDMEEEE
AKNLVSEAIAAGIFNDLGSGSNIDLCVISKNKLDFLRPYTVPNKKGTRLG
RYRCEKGTTAVLTEKITPLE
Ligand information
>5lf0 Chain h (length=4) Species:
32630
(synthetic construct) [
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IITg
Receptor-Ligand Complex Structure
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PDB
5lf0
The inhibition mechanism of human 20S proteasomes enables next-generation inhibitor design.
Resolution
2.41 Å
Binding residue
(original residue number in PDB)
Y114 S118
Binding residue
(residue number reindexed from 1)
Y114 S118
Enzymatic activity
Catalytic site (original residue number in PDB)
T1 D17 R19 K33 G47 S129 D166 S169
Catalytic site (residue number reindexed from 1)
T1 D17 R19 K33 G47 S129 D166 S169
Enzyme Commision number
3.4.25.1
: proteasome endopeptidase complex.
Gene Ontology
Molecular Function
GO:0004298
threonine-type endopeptidase activity
Biological Process
GO:0051603
proteolysis involved in protein catabolic process
Cellular Component
GO:0005839
proteasome core complex
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:5lf0
,
PDBe:5lf0
,
PDBj:5lf0
PDBsum
5lf0
PubMed
27493187
UniProt
Q99436
|PSB7_HUMAN Proteasome subunit beta type-7 (Gene Name=PSMB7)
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