Structure of PDB 1oqu Chain B Binding Site BS01
Receptor Information
>1oqu Chain B (length=296) Species:
1697
(Corynebacterium ammoniagenes) [
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SNEYDEYIANHTDPVKAINWNVIPDEKDLEVWDRLTGNFWLPEKIPVSND
IQSWNKMTPQEQLATMRVFTGLTLLDTIQGTVGAISLLPDAETMHEEAVY
TNIAFMESVHAKSYSNIFMTLASTPQINEAFRWSEENENLQRKAKIIMSY
YNGDDPLKKKVASTLLESFLFYSGFYLPMYLSSRAKLTNTADIIRLIIRD
ESVHGYYIGYKYQQGVKKLSEAEQEEYKAYTFDLMYDLYENEIEYTEDIY
DDLGWTEDVKRFLRYNANKALNNLGYEGLFPTDETKVSPAILSSLS
Ligand information
Ligand ID
FE
InChI
InChI=1S/Fe/q+3
InChIKey
VTLYFUHAOXGGBS-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
CACTVS 3.341
OpenEye OEToolkits 1.5.0
[Fe+3]
Formula
Fe
Name
FE (III) ION
ChEMBL
DrugBank
DB13949
ZINC
PDB chain
1oqu Chain B Residue 1003 [
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Receptor-Ligand Complex Structure
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PDB
1oqu
A protein carboxylate coordinated oxo-centered tri-nuclear iron complex with possible implications for ferritin mineralization
Resolution
2.0 Å
Binding residue
(original residue number in PDB)
D77 E108 H111 E202
Binding residue
(residue number reindexed from 1)
D76 E107 H110 E201
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
Y115 D201
Catalytic site (residue number reindexed from 1)
Y114 D200
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:0016491
oxidoreductase activity
GO:0046872
metal ion binding
Biological Process
GO:0009263
deoxyribonucleotide biosynthetic process
Cellular Component
GO:0005971
ribonucleoside-diphosphate reductase complex
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Cellular Component
External links
PDB
RCSB:1oqu
,
PDBe:1oqu
,
PDBj:1oqu
PDBsum
1oqu
PubMed
15178319
UniProt
O69274
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