Structure of PDB 5og5 Chain A Binding Site BS04
Receptor Information
>5og5 Chain A (length=332) Species:
223
(Achromobacter cycloclastes) [
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DISTLPRVKVDLVKPPFVHAHDQVAKTGPRVVEFTMTIEEKKLVIDREGT
EIHAMTFNGSVPGPLMVVHENDYVELRLINPDTNTLLHNIDFHAATGALG
GGALTQVNPGEETTLRFKATKPGVFVYHCAPEGMVPWHVTSGMNGAIMVL
PRDGLKDEKGQPLTYDKIYYVGEQDFYVPKDEAGNYKKYETPGEAYEDAV
KAMRTLTPTHIVFNGAVGALTGDHALTAAVGERVLVVHSQANRDTRPHLI
GGHGDYVWATGKFRNPPDLDQETWLIPGGTAGAAFYTFRQPGVYAYVNHN
LIEAFELGAAGHFKVTGEWNDDLMTSVVKPAS
Ligand information
Ligand ID
NO2
InChI
InChI=1S/HNO2/c2-1-3/h(H,2,3)/p-1
InChIKey
IOVCWXUNBOPUCH-UHFFFAOYSA-M
SMILES
Software
SMILES
ACDLabs 10.04
CACTVS 3.341
[O-]N=O
OpenEye OEToolkits 1.5.0
N(=O)[O-]
Formula
N O2
Name
NITRITE ION
ChEMBL
DrugBank
DB12529
ZINC
PDB chain
5og5 Chain A Residue 505 [
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Receptor-Ligand Complex Structure
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PDB
5og5
Enzyme catalysis captured using multiple structures from one crystal at varying temperatures.
Resolution
1.82 Å
Binding residue
(original residue number in PDB)
D251 R253 E310
Binding residue
(residue number reindexed from 1)
D244 R246 E303
Annotation score
5
Enzymatic activity
Catalytic site (original residue number in PDB)
H95 D98 H100 H135 C136 H145 M150 H255 E279 T280 H306
Catalytic site (residue number reindexed from 1)
H88 D91 H93 H128 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: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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Cellular Component
External links
PDB
RCSB:5og5
,
PDBe:5og5
,
PDBj:5og5
PDBsum
5og5
PubMed
29755744
UniProt
P25006
|NIR_ACHCY Copper-containing nitrite reductase (Gene Name=nirK)
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