Structure of PDB 3hrd Chain A Binding Site BS05
Receptor Information
>3hrd Chain A (length=420) Species:
1528
(Eubacterium barkeri) [
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GKDYQVLGKNKVKVDSLEKVMGTAKFAADYSFPDMLYAGVFRSTVPHARI
VSLDLSKARAIDGVEAVLDYHAIPGKNRFGIIIKDEPCLVDDKVRRYGDA
IAVVAAQTPDLVQEALDAITIEYEELEGIFTMERALEEDSPAIHGDTNIH
QVKHLEYGDVDAAFKQCDIVVEDTYSTHRLTHMFIEPDAGVSYYDNEGML
TVVVSTQNPHYDRGEVAGMLALPNSKVRIIQATTGGGFGGKLDLSVQCHC
ALLTYHTKKPVKMVRSREESTTVSSKRHPMTMHCKTGATKDGRLQAVQVE
MFGDTGAYASYGPAVITRATVHCMGPYVVPNVRVDAKFVYTNNPMSGAFR
GFGVPQASVCHEGQMNALAKALGMDPIDIRILNAHQVGAKLATGQVLENS
VGLIETLEKAREKAVEVMGY
Ligand information
Ligand ID
NIO
InChI
InChI=1S/C6H5NO2/c8-6(9)5-2-1-3-7-4-5/h1-4H,(H,8,9)
InChIKey
PVNIIMVLHYAWGP-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
O=C(O)c1cccnc1
OpenEye OEToolkits 1.5.0
c1cc(cnc1)C(=O)O
CACTVS 3.341
OC(=O)c1cccnc1
Formula
C6 H5 N O2
Name
NICOTINIC ACID
ChEMBL
CHEMBL573
DrugBank
DB00627
ZINC
ZINC000000001795
PDB chain
3hrd Chain B Residue 5661 [
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Receptor-Ligand Complex Structure
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PDB
3hrd
The Mo-Se active site of nicotinate dehydrogenase
Resolution
2.2 Å
Binding residue
(original residue number in PDB)
A315 R319 F353
Binding residue
(residue number reindexed from 1)
A314 R318 F352
Annotation score
5
Enzymatic activity
Catalytic site (original residue number in PDB)
Q208 L243 R319 H323 R351
Catalytic site (residue number reindexed from 1)
Q207 L242 R318 H322 R350
Enzyme Commision number
1.17.1.5
: nicotinate dehydrogenase.
Gene Ontology
Molecular Function
GO:0005506
iron ion binding
GO:0016491
oxidoreductase activity
GO:0046872
metal ion binding
GO:0050138
nicotinate dehydrogenase activity
Biological Process
GO:1901848
nicotinate catabolic process
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Molecular Function
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Biological Process
External links
PDB
RCSB:3hrd
,
PDBe:3hrd
,
PDBj:3hrd
PDBsum
3hrd
PubMed
19549881
UniProt
Q0QLF2
|NDLMS_EUBBA Nicotinate dehydrogenase large molybdopterin subunit (Gene Name=ndhL)
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