Structure of PDB 1ep3 Chain B Binding Site BS02
Receptor Information
>1ep3 Chain B (length=261) Species:
1358
(Lactococcus lactis) [
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SQLQEMMTVVSQREVAYNIFEMVLKGTLVDEMDLPGQFLHLAVPNGAMLL
RRPISISSWDKRAKTCTILYRIGDETTGTYKLSKLESGAKVDVMGPLGNG
FPVAEVTSTDKILIIGGGIGVPPLYELAKQLEKTGCQMTILLGFASENVK
ILENEFSNLKNVTLKIATDDGSYGTKGHVGMLMNEIDFEVDALYTCGAPA
MLKAVAKKYDQLERLYISMESRMACGIGACYACVEHDKEDESHALKVCED
GPVFLGKQLSL
Ligand information
Ligand ID
FES
InChI
InChI=1S/2Fe.2S
InChIKey
NIXDOXVAJZFRNF-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
[Fe]1S[Fe]S1
CACTVS 3.341
OpenEye OEToolkits 1.5.0
S1[Fe]S[Fe]1
Formula
Fe2 S2
Name
FE2/S2 (INORGANIC) CLUSTER
ChEMBL
DrugBank
ZINC
PDB chain
1ep3 Chain B Residue 503 [
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Receptor-Ligand Complex Structure
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PDB
1ep3
Structure of dihydroorotate dehydrogenase B: electron transfer between two flavin groups bridged by an iron-sulphur cluster.
Resolution
2.1 Å
Binding residue
(original residue number in PDB)
M224 C226 G227 G229 C231 Y232 C234 C249
Binding residue
(residue number reindexed from 1)
M223 C225 G226 G228 C230 Y231 C233 C248
Annotation score
4
Enzymatic activity
Enzyme Commision number
1.3.3.1
: Transferred entry: 1.3.98.1.
Gene Ontology
Molecular Function
GO:0005515
protein binding
GO:0009055
electron transfer activity
GO:0016491
oxidoreductase activity
GO:0046872
metal ion binding
GO:0050660
flavin adenine dinucleotide binding
GO:0051537
2 iron, 2 sulfur cluster binding
Biological Process
GO:0006221
pyrimidine nucleotide biosynthetic process
GO:0044205
'de novo' UMP biosynthetic process
Cellular Component
GO:0005737
cytoplasm
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1ep3
,
PDBe:1ep3
,
PDBj:1ep3
PDBsum
1ep3
PubMed
11188687
UniProt
P56968
|PYRK_LACLM Dihydroorotate dehydrogenase B (NAD(+)), electron transfer subunit (Gene Name=pyrK)
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