Structure of PDB 7s5h Chain B Binding Site BS01
Receptor Information
>7s5h Chain B (length=230) Species:
9606
(Homo sapiens) [
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VEVYLLDTSIQSDHREIEGRVMVTDFENVPEETRFHRQASKCDSHGTHLA
GVVSGRDAGVAKGASMRSLRVLNCQGKGTVSGTLIGLEFIRKSQLVGPLV
VLLPLAGGYSRVLNAACQRLARAGVVLVTAAGNFRDDACLYSPASAPEVI
TVGATNAQDQPVGTNFGRCVDLFAPGEDIIGASSDCSTCFVSQSGTSQAA
AHVAGIAAMMLSAEPELTLAELRQRLIHFS
Ligand information
>7s5h Chain C (length=11) Species:
32630
(synthetic construct) [
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cCAAFWPTYPC
Receptor-Ligand Complex Structure
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PDB
7s5h
A Series of Novel, Highly Potent, and Orally Bioavailable Next-Generation Tricyclic Peptide PCSK9 Inhibitors.
Resolution
1.272 Å
Binding residue
(original residue number in PDB)
D238 D367 I369 D374 T377 C378 F379 V380 S381
Binding residue
(residue number reindexed from 1)
D57 D178 I180 D185 T188 C189 F190 V191 S192
Enzymatic activity
Enzyme Commision number
3.4.21.-
Gene Ontology
Molecular Function
GO:0004252
serine-type endopeptidase activity
GO:0008236
serine-type peptidase activity
Biological Process
GO:0006508
proteolysis
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Molecular Function
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Biological Process
External links
PDB
RCSB:7s5h
,
PDBe:7s5h
,
PDBj:7s5h
PDBsum
7s5h
PubMed
34704436
UniProt
Q8NBP7
|PCSK9_HUMAN Proprotein convertase subtilisin/kexin type 9 (Gene Name=PCSK9)
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