Structure of PDB 8a7d Chain Q Binding Site BS01
Receptor Information
>8a7d Chain Q (length=273) Species:
9606
(Homo sapiens) [
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PVDCSIPDHHQVYAASFSCPEGTTFGSQCSFQCRHPAQLKGNNSLLTCME
DGLWSFPEALCELMCLAPPPVPNADLQTARCRENKHKVGSFCKYKCKPGY
HVPGSSRKSKKRAFKTQCTQDGSWQEGACVPGQCSVPNELNSNLKLQCPD
GYAIGSECATSCLDHNSESIILPMNVTVRDIPHWLNPTRVERVVCTAGLK
WYPHPALIHCVKGCEPFMGDNYCDAINNRAFCNYDGGDCCTSTVKTKKVT
PFPMSCDLQGDCACRDPQAQEHS
Ligand information
Ligand ID
CA
InChI
InChI=1S/Ca/q+2
InChIKey
BHPQYMZQTOCNFJ-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
[Ca++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Ca+2]
Formula
Ca
Name
CALCIUM ION
ChEMBL
DrugBank
DB14577
ZINC
PDB chain
8a7d Chain Q Residue 1702 [
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Receptor-Ligand Complex Structure
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PDB
8a7d
Structure of the proteolytic enzyme PAPP-A with the endogenous inhibitor stanniocalcin-2 reveals its inhibitory mechanism.
Resolution
3.06 Å
Binding residue
(original residue number in PDB)
F1561 M1562 D1564 Y1566 D1568 D1579 D1582
Binding residue
(residue number reindexed from 1)
F217 M218 D220 Y222 D224 D235 D238
Annotation score
4
Enzymatic activity
Enzyme Commision number
3.4.24.79
: pappalysin-1.
Gene Ontology
Molecular Function
GO:0004175
endopeptidase activity
GO:0004222
metalloendopeptidase activity
GO:0005515
protein binding
GO:0008237
metallopeptidase activity
GO:0008270
zinc ion binding
GO:0046872
metal ion binding
Biological Process
GO:0006508
proteolysis
GO:0007166
cell surface receptor signaling pathway
GO:0007565
female pregnancy
GO:0030163
protein catabolic process
GO:0032354
response to follicle-stimulating hormone
GO:0071548
response to dexamethasone
Cellular Component
GO:0005576
extracellular region
GO:0005615
extracellular space
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:8a7d
,
PDBe:8a7d
,
PDBj:8a7d
PDBsum
8a7d
PubMed
36257932
UniProt
Q13219
|PAPP1_HUMAN Pappalysin-1 (Gene Name=PAPPA)
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