Structure of PDB 1kqg Chain B Binding Site BS04
Receptor Information
>1kqg Chain B (length=289) Species:
562
(Escherichia coli) [
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AMETQDIIKRSATNSITPPSQVRDYKAEVAKLIDVSTCIGCKACQVACSE
WNDIRDEVGHCVGVYDNPADLSAKSWTVMRFSETEQNGKLEWLIRKDGCM
HCEDPGCLKACPSAGAIIQYANGIVDFQSENCIGCGYCIAGCPFNIPRLN
KEDNRVYKCTLCVDRVSVGQEPACVKTCPTGAIHFGTKKEMLELAEQRVA
KLKARGYEHAGVYNPEGVGGTHVMYVLHHADQPELYHGLPKDPKIDTSVS
LWKGALKPLAAAGFIATFAGLIFHYIGIGPNKEVDDDEE
Ligand information
Ligand ID
SF4
InChI
InChI=1S/4Fe.4S
InChIKey
LJBDFODJNLIPKO-UHFFFAOYSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 2.0.7
[S]12[Fe]3[S]4[Fe]1[S]5[Fe]2[S]3[Fe]45
CACTVS 3.385
S1[Fe]S[Fe]1.S2[Fe]S[Fe]2
Formula
Fe4 S4
Name
IRON/SULFUR CLUSTER
ChEMBL
DrugBank
ZINC
PDB chain
1kqg Chain B Residue 808 [
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Receptor-Ligand Complex Structure
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PDB
1kqg
Molecular basis of proton motive force generation: structure of formate dehydrogenase-N.
Resolution
2.8 Å
Binding residue
(original residue number in PDB)
C112 P113 I118 C133 I134 G135 C136 G137 Y138 C139 V157
Binding residue
(residue number reindexed from 1)
C111 P112 I117 C132 I133 G134 C135 G136 Y137 C138 V156
Annotation score
1
Enzymatic activity
Enzyme Commision number
1.2.1.2
: Transferred entry: 1.17.1.9.
Gene Ontology
Molecular Function
GO:0009055
electron transfer activity
GO:0036397
formate dehydrogenase (quinone) activity
GO:0046872
metal ion binding
GO:0051539
4 iron, 4 sulfur cluster binding
Biological Process
GO:0006788
heme oxidation
GO:0009061
anaerobic respiration
GO:0015944
formate oxidation
GO:0019645
anaerobic electron transport chain
GO:0045333
cellular respiration
Cellular Component
GO:0005886
plasma membrane
GO:0009326
formate dehydrogenase complex
GO:0016020
membrane
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1kqg
,
PDBe:1kqg
,
PDBj:1kqg
PDBsum
1kqg
PubMed
11884747
UniProt
P0AAJ3
|FDNH_ECOLI Formate dehydrogenase, nitrate-inducible, iron-sulfur subunit (Gene Name=fdnH)
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