Structure of PDB 7s5g Chain B Binding Site BS01
Receptor Information
>7s5g Chain B (length=287) Species:
9606
(Homo sapiens) [
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SIPWNLERITPPQPPDGGSLVEVYLLDTSIQSDHREIEGRVMVTDFENVP
EEDGTRFHRQASKCDSHGTHLAGVVSGRDAGVAKGASMRSLRVLNCQGKG
TVSGTLIGLEFIRKSQLVQPVGPLVVLLPLAGGYSRVLNAACQRLARAGV
VLVTAAGNFRDDACLYSPASAPEVITVGATNAQDQPVTLGTLGTNFGRCV
DLFAPGEDIIGASSDCSTCFVSQSGTSQAAAHVAGIAAMMLSAEPELTLA
ELRQRLIHFSAKDVINEAWFPEDQRVLTPNLVAALPP
Ligand information
>7s5g Chain C (length=10) Species:
32630
(synthetic construct) [
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FAAFWPTYPC
Receptor-Ligand Complex Structure
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PDB
7s5g
A Series of Novel, Highly Potent, and Orally Bioavailable Next-Generation Tricyclic Peptide PCSK9 Inhibitors.
Resolution
2.041 Å
Binding residue
(original residue number in PDB)
P155 W156 D238 D367 I369 T377 C378 F379 V380 S381
Binding residue
(residue number reindexed from 1)
P3 W4 D79 D208 I210 T218 C219 F220 V221 S222
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:7s5g
,
PDBe:7s5g
,
PDBj:7s5g
PDBsum
7s5g
PubMed
34704436
UniProt
Q8NBP7
|PCSK9_HUMAN Proprotein convertase subtilisin/kexin type 9 (Gene Name=PCSK9)
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