Structure of PDB 1nfs Chain B Binding Site BS02
Receptor Information
>1nfs Chain B (length=180) Species:
562
(Escherichia coli) [
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EHVILLNAQGVPTGTLEKYAAHTADTRLHLAFSSWLFNAKGQLLVTRRAL
SKKAWPGVWTNSVCGHPQLGESNEDAVIRRCRYELGVEITPPESIYPDFR
YRATDPSGIVENEVCPVFAARTTSALQINDDEVMDYQWCDLADVLHGIDA
TPWAFSPWMVMQATNREARKRLSAFTQLKL
Ligand information
Ligand ID
MG
InChI
InChI=1S/Mg/q+2
InChIKey
JLVVSXFLKOJNIY-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Mg+2]
CACTVS 3.341
[Mg++]
Formula
Mg
Name
MAGNESIUM ION
ChEMBL
DrugBank
DB01378
ZINC
PDB chain
1nfs Chain B Residue 401 [
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Receptor-Ligand Complex Structure
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PDB
1nfs
Catalytic Mechanism of Escherichia coli Isopentenyl Diphosphate Isomerase Involves Cys-67, Glu-116, and Tyr-104 as Suggested by Crystal Structures of Complexes with Transition State Analogues and Irreversible Inhibitors
Resolution
1.96 Å
Binding residue
(original residue number in PDB)
C67 E87
Binding residue
(residue number reindexed from 1)
C64 E84
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
H25 H32 C67 H69 E87 Y104 E114 E116 W161
Catalytic site (residue number reindexed from 1)
H22 H29 C64 H66 E84 Y101 E111 E113 W158
Enzyme Commision number
5.3.3.2
: isopentenyl-diphosphate Delta-isomerase.
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0003824
catalytic activity
GO:0004452
isopentenyl-diphosphate delta-isomerase activity
GO:0008270
zinc ion binding
GO:0016853
isomerase activity
GO:0046872
metal ion binding
Biological Process
GO:0006974
DNA damage response
GO:0008299
isoprenoid biosynthetic process
GO:0050992
dimethylallyl diphosphate biosynthetic process
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:1nfs
,
PDBe:1nfs
,
PDBj:1nfs
PDBsum
1nfs
PubMed
12540835
UniProt
Q46822
|IDI_ECOLI Isopentenyl-diphosphate Delta-isomerase (Gene Name=idi)
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