Structure of PDB 2afw Chain B Binding Site BS01
Receptor Information
>2afw Chain B (length=323) Species:
9606
(Homo sapiens) [
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ASAWPEEKNYHQPAILNSSALRQIAEGTSISEMWQNDLQPLLIERYPGSP
GSYAARQHIMQRIQRLQADWVLEIDTFLSQTPYGYRSFSNIISTLNPTAK
RHLVLACHYDSKYFSHWNNRVFVGATDSAVPCAMMLELARALDKKLLSLK
PDLSLQLIFFDGEEAFLHWSPQDSLYGSRHLAAKMASTPHPPGARGTSQL
HGMDLLVLLDLIGAPNPTFPNFFPNSARWFERLQAIEHELHELGLLKDHS
LEGRYFQNYSYGGVIQDDHIPFLRRGVPVLHLIPSPFPEVWHTMDDNEEN
LDESTIDNLNKILQVFVLEYLHL
Ligand information
Ligand ID
ZN
InChI
InChI=1S/Zn/q+2
InChIKey
PTFCDOFLOPIGGS-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
[Zn++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Zn+2]
Formula
Zn
Name
ZINC ION
ChEMBL
CHEMBL1236970
DrugBank
DB14532
ZINC
PDB chain
2afw Chain B Residue 997 [
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Receptor-Ligand Complex Structure
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PDB
2afw
Crystal structures of human glutaminyl cyclase, an enzyme responsible for protein N-terminal pyroglutamate formation
Resolution
1.56 Å
Binding residue
(original residue number in PDB)
D159 E202 H330
Binding residue
(residue number reindexed from 1)
D127 E164 H292
Annotation score
1
Enzymatic activity
Enzyme Commision number
2.3.2.5
: glutaminyl-peptide cyclotransferase.
Gene Ontology
Molecular Function
GO:0005515
protein binding
GO:0008270
zinc ion binding
GO:0016603
glutaminyl-peptide cyclotransferase activity
GO:0016746
acyltransferase activity
GO:0046872
metal ion binding
Biological Process
GO:0017186
peptidyl-pyroglutamic acid biosynthetic process, using glutaminyl-peptide cyclotransferase
GO:0036211
protein modification process
Cellular Component
GO:0005576
extracellular region
GO:0035580
specific granule lumen
GO:0070062
extracellular exosome
GO:1904724
tertiary granule lumen
GO:1904813
ficolin-1-rich granule lumen
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:2afw
,
PDBe:2afw
,
PDBj:2afw
PDBsum
2afw
PubMed
16135565
UniProt
Q16769
|QPCT_HUMAN Glutaminyl-peptide cyclotransferase (Gene Name=QPCT)
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