Structure of PDB 6tfo Chain C Binding Site BS02
Receptor Information
>6tfo Chain C (length=424) Species:
670307
(Hyphomicrobium denitrificans 1NES1) [
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SHAPVVFTLRTGIAEGRMVYIGVGGDIDRQVNPKLVVHEGETVQINLING
EGAQHDAVIDQYAARSAIVSGKNASSTFSFIASKVGQFDYYCSLPGHRQA
GMQGVLQVVPGNRAEMPSTAADITRDPADLPGPIGARQAKTVRIDLETVE
LKGQLDDKTTYTYWTFNGKVPGPFLRVRVGDTVELHLKNAKDSLMIHSVD
FHGATGPGGAAAYTQTDPGAETVVTFKALVPGIFVYHCATPSVPNHITNG
MYGLLLVEPEGGLPQVDREFYVMQGEIYTVKPFGTSGEQEMDYEKLISEK
PEYFLFNGSVGALTRTHPLYANVGETVRIFFGVGGPNFTSSFHVIGEIFD
HVYALGSVTSPPLTGVQTVSVPPGGATIVDFKLDRGGRYVLVDHALSRLD
HGLVGFLNVDGPKNDAIMHEGPPK
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
6tfo Chain C Residue 502 [
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Receptor-Ligand Complex Structure
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PDB
6tfo
Structures of substrate- and product-bound forms of a multi-domain copper nitrite reductase shed light on the role of domain tethering in protein complexes.
Resolution
2.05 Å
Binding residue
(original residue number in PDB)
H227 H262
Binding residue
(residue number reindexed from 1)
H202 H237
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
H222 D225 H227 H262 C263 H271 M276 H368 Q392 T393 H419
Catalytic site (residue number reindexed from 1)
H197 D200 H202 H237 C238 H246 M251 H343 Q367 T368 H394
Enzyme Commision number
1.7.2.1
: nitrite reductase (NO-forming).
Gene Ontology
Molecular Function
GO:0005507
copper ion binding
GO:0009055
electron transfer activity
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:6tfo
,
PDBe:6tfo
,
PDBj:6tfo
PDBsum
6tfo
PubMed
32431838
UniProt
N0B9M5
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