Structure of PDB 1haw Chain A Binding Site BS01
Receptor Information
>1haw Chain A (length=336) Species:
85698
(Achromobacter xylosoxidans) [
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QDADKLPHTKVTLVAPPQVHPHEQATKSGPKVVEFTMTIEEKKMVIDDKG
TTLQAMTFNGSMPGPTLVVHEGDYVQLTLVNPATNAMPHNVDFHGATGAL
GGAKLTNVNPGEQATLRFKADRSGTFVYHCAPEGMVPWHVVSGMSGTLMV
LPRDGLKDPQGKPLHYDRAYTIGEFDLYIPKGPDGKYKDYATLAESYGDT
VQVMRTLTPSHIVFNGKVGALTGANALTAKVGETVLLIHSQANRDTRPHL
IGGHGDWVWETGKFANPPQRDLETWFIRGGSAGAALYTFKQPGVYAYLNH
NLIEAFELGAAGHIKVEGKWNDDLMKQIKAPAPIPR
Ligand information
Ligand ID
CU1
InChI
InChI=1S/Cu/q+1
InChIKey
VMQMZMRVKUZKQL-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
CACTVS 3.341
OpenEye OEToolkits 1.5.0
[Cu+]
Formula
Cu
Name
COPPER (I) ION
ChEMBL
DrugBank
ZINC
PDB chain
1haw Chain A Residue 501 [
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Receptor-Ligand Complex Structure
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PDB
1haw
X-Ray Structure of a Blue Copper Nitrite Reductase at High Ph and in Copper-Free Form at 1.9 A Resolution
Resolution
1.9 Å
Binding residue
(original residue number in PDB)
H89 C130 H139 M144
Binding residue
(residue number reindexed from 1)
H89 C130 H139 M144
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
H89 D92 H94 H129 C130 H139 M144 H249 E273 T274 H300
Catalytic site (residue number reindexed from 1)
H89 D92 H94 H129 C130 H139 M144 H249 E273 T274 H300
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:1haw
,
PDBe:1haw
,
PDBj:1haw
PDBsum
1haw
PubMed
11468394
UniProt
O68601
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