Structure of PDB 4knu Chain E Binding Site BS01
Receptor Information
>4knu Chain E (length=285) Species:
228410
(Nitrosomonas europaea ATCC 19718) [
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KTVQVTLHAVETDVAYDNKGSTYRAWTFDGKVPGPVVRVTEGDTVEFTLI
NDKNSKNSHSMDFHAARLDVVEDFESIKPGETKKYTFTADNPGVFFYHCG
SDPMIQHIARGMYGVIIVDPKDANALPKADREYVLIQAEHYENPDDKTAM
MQNKWSNVVFNGGVFKYDPVHDSEATSWLQAKPGERVRIYFVNAGPNELS
SLHPIAGIWDRVYPSGNPKNVQYALQSYLIGAGDAATLDLISPVEGANAI
VDHSMRHAHSGAIAVIMFTNDADPEAGRGENILIR
Ligand information
Ligand ID
CU
InChI
InChI=1S/Cu/q+2
InChIKey
JPVYNHNXODAKFH-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Cu+2]
CACTVS 3.341
[Cu++]
Formula
Cu
Name
COPPER (II) ION
ChEMBL
DrugBank
DB14552
ZINC
PDB chain
4knu Chain E Residue 401 [
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Receptor-Ligand Complex Structure
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PDB
4knu
Characterization of a nitrite reductase involved in nitrifier denitrification.
Resolution
1.8 Å
Binding residue
(original residue number in PDB)
H83 C123 H131 M136
Binding residue
(residue number reindexed from 1)
H59 C99 H107 M112
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
H83 D86 H88 H122 C123 H131 M136 H227 Q250 S251 H277
Catalytic site (residue number reindexed from 1)
H59 D62 H64 H98 C99 H107 M112 H203 Q226 S227 H253
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
View graph for
Molecular Function
External links
PDB
RCSB:4knu
,
PDBe:4knu
,
PDBj:4knu
PDBsum
4knu
PubMed
23857587
UniProt
Q82VX5
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