Structure of PDB 1icu Chain B Binding Site BS02
Receptor Information
>1icu Chain B (length=217) Species:
562
(Escherichia coli) [
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MDIISVALKRHSTKAFDASKKLTPEQAEQIKTLLQYSPSSTNSQPWHFIV
ASTEEGKARVAKSAAGNYVFNERKMLDASHVVVFCAKTAMDDVWLKLVVD
QEDADGRFATPEAKAANDKGRKFFADMHRKDLHDDAEWMAKQVYLNVGNF
LLGVAALGLDAVPIEGFDAAILDAEFGLKEKGYTSLVVVPVGHHSVEDFN
ATLPKSRLPQNITLTEV
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
1icu Chain A Residue 221 [
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Receptor-Ligand Complex Structure
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PDB
1icu
The structure of Escherichia coli nitroreductase complexed with nicotinic acid: three crystal forms at 1.7 A, 1.8 A and 2.4 A resolution.
Resolution
1.8 Å
Binding residue
(original residue number in PDB)
F70 G166
Binding residue
(residue number reindexed from 1)
F70 G166
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
K14 K74 E165
Catalytic site (residue number reindexed from 1)
K14 K74 E165
Enzyme Commision number
1.-.-.-
1.5.1.34
: 6,7-dihydropteridine reductase.
Gene Ontology
Molecular Function
GO:0003955
NAD(P)H dehydrogenase (quinone) activity
GO:0004155
6,7-dihydropteridine reductase activity
GO:0010181
FMN binding
GO:0016491
oxidoreductase activity
GO:0042802
identical protein binding
GO:0042803
protein homodimerization activity
GO:0046857
oxidoreductase activity, acting on other nitrogenous compounds as donors, with NAD or NADP as acceptor
Biological Process
GO:0046256
2,4,6-trinitrotoluene catabolic process
Cellular Component
GO:0005829
cytosol
GO:0016020
membrane
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1icu
,
PDBe:1icu
,
PDBj:1icu
PDBsum
1icu
PubMed
11491290
UniProt
P38489
|NFSB_ECOLI Oxygen-insensitive NAD(P)H nitroreductase (Gene Name=nfsB)
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