Structure of PDB 6w4x Chain D Binding Site BS01
Receptor Information
>6w4x Chain D (length=341) Species:
83333
(Escherichia coli K-12) [
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AYTTFSQTKNDQLKEPMFFGQPVNVARYDQQKYDIFEKLIEKQLSFFWRP
EQVDVSRDRIDYQALPEHEKHIFISNLKYQTLLDSIQGRSPNVALLPLIS
IPELETWVETWAFSETIHSRSYTHIIRNIVNDPSVVFDDIVTNEQIQKRA
EGISSYYDELIEMTSYWHLLGEGTHTVNGKTVTVSLRELKKKLYLCLMSV
NALEAIRFYVSFACSFAFAERELMEGNAKIIRLIARDEALHLTGTQHMLN
LLRSGADDPEMAEIAEECKQECYDLFVQAAQQEKDWADYLFRDGSMIGLN
KDILCQYVEYITNIRMQAVGLDLPFQTRSNPIPWINTWLVS
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
6w4x Chain D Residue 501 [
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Receptor-Ligand Complex Structure
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PDB
6w4x
Structure of a trapped radical transfer pathway within a ribonucleotide reductase holocomplex.
Resolution
3.6 Å
Binding residue
(original residue number in PDB)
D84 E115 H118 E204 E238 H241
Binding residue
(residue number reindexed from 1)
D84 E115 H118 E204 E238 H241
Annotation score
1
Enzymatic activity
Enzyme Commision number
1.17.4.1
: ribonucleoside-diphosphate reductase.
Gene Ontology
Molecular Function
GO:0004748
ribonucleoside-diphosphate reductase activity, thioredoxin disulfide as acceptor
GO:0005506
iron ion binding
GO:0005515
protein binding
GO:0016491
oxidoreductase activity
GO:0042802
identical protein binding
GO:0046872
metal ion binding
Biological Process
GO:0009185
ribonucleoside diphosphate metabolic process
GO:0009263
deoxyribonucleotide biosynthetic process
GO:0009265
2'-deoxyribonucleotide biosynthetic process
GO:0015949
nucleobase-containing small molecule interconversion
Cellular Component
GO:0005737
cytoplasm
GO:0005829
cytosol
GO:0005971
ribonucleoside-diphosphate reductase complex
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:6w4x
,
PDBe:6w4x
,
PDBj:6w4x
PDBsum
6w4x
PubMed
32217749
UniProt
P69924
|RIR2_ECOLI Ribonucleoside-diphosphate reductase 1 subunit beta (Gene Name=nrdB)
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