Structure of PDB 5kto Chain A Binding Site BS01
Receptor Information
>5kto Chain A (length=298) Species:
70601
(Pyrococcus horikoshii OT3) [
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DLVEEILRLKEERNAIILAHNYQLPEVQDIADFIGDSLELARRATRVDAD
VIVFAGVDFMAETAKILNPDKVVLIPSREATCAMANMLKVEHILEAKRKY
PNAPVVLYVNSTAEAKAYADVTVTSANAVEVVKKLDSDVVIFGPDKNLAH
YVAKMTGKKIIPVPSKGHCYVHQKFTLDDVERAKKLHPNAKLMIHPECIP
EVQEKADIIASTGGMIKRACEWDEWVVFTEREMVYRLRKLYPQKKFYPAR
EDAFCIGMKAITLKNIYESLKDMKYKVEVPEEIARKARKAIERMLEMS
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
5kto Chain A Residue 401 [
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Receptor-Ligand Complex Structure
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PDB
5kto
Crystal Structures of the Iron-Sulfur Cluster-Dependent Quinolinate Synthase in Complex with Dihydroxyacetone Phosphate, Iminoaspartate Analogues, and Quinolinate.
Resolution
1.442 Å
Binding residue
(original residue number in PDB)
Y23 C83 C170 C256
Binding residue
(residue number reindexed from 1)
Y22 C82 C169 C255
Annotation score
1
Enzymatic activity
Enzyme Commision number
2.5.1.72
: quinolinate synthase.
Gene Ontology
Molecular Function
GO:0008987
quinolinate synthetase A activity
GO:0016740
transferase activity
GO:0016765
transferase activity, transferring alkyl or aryl (other than methyl) groups
GO:0046872
metal ion binding
GO:0051539
4 iron, 4 sulfur cluster binding
Biological Process
GO:0009435
NAD biosynthetic process
GO:0019363
pyridine nucleotide biosynthetic process
GO:0019805
quinolinate biosynthetic process
GO:0034628
'de novo' NAD biosynthetic process from aspartate
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:5kto
,
PDBe:5kto
,
PDBj:5kto
PDBsum
5kto
PubMed
27404889
UniProt
O57767
|NADA_PYRHO Quinolinate synthase (Gene Name=nadA)
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