Structure of PDB 1wae Chain A Binding Site BS02
Receptor Information
>1wae Chain A (length=334) Species:
85698
(Achromobacter xylosoxidans) [
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DADKLPHTKVTLVAPPQVHPHEQATKSGPKVVEFTMTIEEKKMVIDDKGT
TLQAMTFNGSMPGPTLVVHEGDYVQLTLVNPATNAMPHNVDFHGATGALG
GAKLTNVNPGEQATLRFKADRSGTFVYVCAPEGMVPWHVVSGMSGTLMVL
PRDGLKDPQGKPLHYDRAYTIGEFDLYIPKGPDGKYKDYATLAESYGDTV
QVMRTLTPSHIVFNGKVGALTGANALTAKVGETVLLIHSQANRDTRPHLI
GGHGDWVWETGKFANPPQRDLETWFIRGGSAGAALYTFKQPGVYAYLNHN
LIEAFELGAAGHIKVEGKWNDDLMKQIKAPAPIP
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
1wae Chain A Residue 503 [
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Receptor-Ligand Complex Structure
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PDB
1wae
Observation of an Unprecedented Cu Bis-His Site: Crystal Structure of the H129V Mutant of Nitrite Reductase
Resolution
1.95 Å
Binding residue
(original residue number in PDB)
H165 D167
Binding residue
(residue number reindexed from 1)
H164 D166
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
H89 D92 H94 V129 C130 H139 M144 H249 E273 T274 H300
Catalytic site (residue number reindexed from 1)
H88 D91 H93 V128 C129 H138 M143 H248 E272 T273 H299
Enzyme Commision number
1.7.2.1
: nitrite reductase (NO-forming).
Gene Ontology
Molecular Function
GO:0005507
copper ion binding
GO:0005515
protein binding
GO:0016491
oxidoreductase activity
GO:0046872
metal ion binding
GO:0050421
nitrite reductase (NO-forming) activity
Biological Process
GO:0019333
denitrification pathway
GO:0042128
nitrate assimilation
Cellular Component
GO:0042597
periplasmic space
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1wae
,
PDBe:1wae
,
PDBj:1wae
PDBsum
1wae
PubMed
15554622
UniProt
O68601
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