Structure of PDB 2icj Chain A Binding Site BS01
Receptor Information
>2icj Chain A (length=219) Species:
9606
(Homo sapiens) [
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LDKQQVQLLAEMCILIDENDNKIGAETKKNCHLNENIEKGLLHRAFSVFL
FNTENKLLLQQRSDAKITFPGCFTNTCCSHPLSNPAELEESDALGVRRAA
QRRLKAELGIPLEEVPPEEINYLTRIHYKAQSDGIWGEHEIDYILLVRKN
VTLNPDPNEIKSYCYVSKEELKELLKKAASGEIKITPWFKIIAATFLFKW
WDNLNHLNQFVDHEKIYRM
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
2icj Chain A Residue 400 [
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Receptor-Ligand Complex Structure
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PDB
2icj
The crystal structure of human isopentenyl diphosphate isomerase at 1.7 A resolution reveals its catalytic mechanism in isoprenoid biosynthesis
Resolution
1.7 Å
Binding residue
(original residue number in PDB)
H41 H52 E147 E149
Binding residue
(residue number reindexed from 1)
H32 H43 E138 E140
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
H52 C87 H89 E116 Y137 E147 E149 W197
Catalytic site (residue number reindexed from 1)
H43 C78 H80 E107 Y128 E138 E140 W188
Enzyme Commision number
5.3.3.2
: isopentenyl-diphosphate Delta-isomerase.
Gene Ontology
Molecular Function
GO:0004452
isopentenyl-diphosphate delta-isomerase activity
GO:0016853
isomerase activity
GO:0046872
metal ion binding
Biological Process
GO:0006695
cholesterol biosynthetic process
GO:0008299
isoprenoid biosynthetic process
GO:0009240
isopentenyl diphosphate biosynthetic process
GO:0050992
dimethylallyl diphosphate biosynthetic process
Cellular Component
GO:0005737
cytoplasm
GO:0005777
peroxisome
GO:0005829
cytosol
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:2icj
,
PDBe:2icj
,
PDBj:2icj
PDBsum
2icj
PubMed
17250851
UniProt
Q13907
|IDI1_HUMAN Isopentenyl-diphosphate Delta-isomerase 1 (Gene Name=IDI1)
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