Structure of PDB 1ylu Chain A Binding Site BS01
Receptor Information
>1ylu Chain A (length=216) Species:
562
(Escherichia coli) [
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DIISVALKRHSTKAFDASKKLTPEQAEQIKTLLQYSPSSTNSQPWHFIVA
STEEGKARVAKSAAGNYVFNERKMLDASHVVVFCAKTAMDDVWLKLVVDQ
EDADGRFATPEAKAANDKGRKFFADMHRKDLHDDAEWMAKQVYLNVGNFL
LGVAALGLDAVPIEGFDAAILDAEFGLKEKGYTSLVVVPVGHHSVEDFNA
TLPKSRLPQNITLTEV
Ligand information
Ligand ID
ACT
InChI
InChI=1S/C2H4O2/c1-2(3)4/h1H3,(H,3,4)/p-1
InChIKey
QTBSBXVTEAMEQO-UHFFFAOYSA-M
SMILES
Software
SMILES
ACDLabs 10.04
[O-]C(=O)C
OpenEye OEToolkits 1.5.0
CC(=O)[O-]
CACTVS 3.341
CC([O-])=O
Formula
C2 H3 O2
Name
ACETATE ION
ChEMBL
DrugBank
DB14511
ZINC
PDB chain
1ylu Chain A Residue 2219 [
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Receptor-Ligand Complex Structure
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PDB
1ylu
Structural and mechanistic studies of Escherichia coli nitroreductase with the antibiotic nitrofurazone. Reversed binding orientations in different redox states of the enzyme.
Resolution
2.0 Å
Binding residue
(original residue number in PDB)
T41 F124
Binding residue
(residue number reindexed from 1)
T40 F123
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
K14 K74 E165
Catalytic site (residue number reindexed from 1)
K13 K73 E164
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
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1ylu
,
PDBe:1ylu
,
PDBj:1ylu
PDBsum
1ylu
PubMed
15684426
UniProt
P38489
|NFSB_ECOLI Oxygen-insensitive NAD(P)H nitroreductase (Gene Name=nfsB)
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