Structure of PDB 1ycg Chain A Binding Site BS02
Receptor Information
>1ycg Chain A (length=398) Species:
1525
(Moorella thermoacetica) [
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SQPVAITDGIYWVGAVDWNIRYFHGPAFSTHRGTTYNAYLIVDDKTALVD
TVYEPFKEELIAKLKQIKDPVKLDYLVVNHTESDHAGAFPAIMELCPDAH
VLCTQRAFDSLKAHYSHIDFNYTIVKTGTSVSLGKRSLTFIEAPMLHWPD
SMFTYVPEEALLLPNDAFGQHIATSVRFDDQVDAGLIMDEAAKYYANILM
PFSNLITKKLDEIQKINLAIKTIAPSHGIIWRKDPGRIIEAYARWAEGQG
KAKAVIAYDTMWLSTEKMAHALMDGLVAGGCEVKLFKLSVSDRNDVIKEI
LDARAVLVGSPTINNDILPVVSPLLDDLVGLRPKNKVGLAFGAYGWGGGA
QKILEERLKAAKIELIAEPGPTVQWVPRGEDLQRCYELGRKIAARIAD
Ligand information
Ligand ID
FEO
InChI
InChI=1S/2Fe.O
InChIKey
NPMYUMBHPJGBFA-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
[Fe]O[Fe]
OpenEye OEToolkits 1.5.0
O([Fe])[Fe]
Formula
Fe2 O
Name
MU-OXO-DIIRON
ChEMBL
DrugBank
ZINC
PDB chain
1ycg Chain A Residue 501 [
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Receptor-Ligand Complex Structure
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PDB
1ycg
X-ray crystal structures of Moorella thermoacetica FprA. Novel diiron site structure and mechanistic insights into a scavenging nitric oxide reductase.
Resolution
2.8 Å
Binding residue
(original residue number in PDB)
H81 E83 D85 H86 H148 D167 H228
Binding residue
(residue number reindexed from 1)
H80 E82 D84 H85 H147 D166 H227
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
H25 H81 E83 D85 H148 D167 Y195 H228
Catalytic site (residue number reindexed from 1)
H24 H80 E82 D84 H147 D166 Y194 H227
Enzyme Commision number
1.-.-.-
Gene Ontology
Molecular Function
GO:0009055
electron transfer activity
GO:0010181
FMN binding
GO:0016491
oxidoreductase activity
GO:0046872
metal ion binding
View graph for
Molecular Function
External links
PDB
RCSB:1ycg
,
PDBe:1ycg
,
PDBj:1ycg
PDBsum
1ycg
PubMed
15850383
UniProt
Q9FDN7
|FPRA_MOOTA Nitric oxide reductase (Gene Name=fprA)
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