Structure of PDB 2iv0 Chain A Binding Site BS02
Receptor Information
>2iv0 Chain A (length=412) Species:
2234
(Archaeoglobus fulgidus) [
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MQYEKVKPPENGEKIRYENGKLIVPDNPIIPYFEGDGIGKDVVPAAIRVL
DAAADKIGKEVVWFQVYAGEDAYKLYGNYLPDDTLNAIKEFRVALKGPLT
TPVGGGYRSLNVTIRQVLDLYANVRPVYYLKGVPSPIKHPEKVNFVIFRE
NTEDVYAGIEWPRGSEEALKLIRFLKNEFGVTIREDSGIGIKPISEFATK
RLVRMAIRYAIENNRKSVTLVHKGNIMKYTEGAFRDWGYEVAKQEFGEYC
ITEDELWDKYGGKQPEGKIVVKDRIADNMFQQILTRTDEYDVIALPNLNG
DYLSDAAAALIGGLGIAPGSNIGDGIGVFEPVHGSAPKYAGQNKVNPTAE
ILTGALMFEYIGWKDASEMIKKAVEMTISSGIVTYDIHRHMGGTKVGTRE
FAEAVVENLQSL
Ligand information
Ligand ID
ZN
InChI
InChI=1S/Zn/q+2
InChIKey
PTFCDOFLOPIGGS-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
[Zn++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Zn+2]
Formula
Zn
Name
ZINC ION
ChEMBL
CHEMBL1236970
DrugBank
DB14532
ZINC
PDB chain
2iv0 Chain A Residue 1415 [
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Receptor-Ligand Complex Structure
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PDB
2iv0
Thermal Stability of Isocitrate Dehydrogenase from Archaeoglobus Fulgidus Studied by Crystal Structure Analysis and Engineering of Chimers
Resolution
2.5 Å
Binding residue
(original residue number in PDB)
D301 D305
Binding residue
(residue number reindexed from 1)
D301 D305
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
Y156 K223 D277 D301 D305
Catalytic site (residue number reindexed from 1)
Y156 K223 D277 D301 D305
Enzyme Commision number
1.1.1.42
: isocitrate dehydrogenase (NADP(+)).
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0004450
isocitrate dehydrogenase (NADP+) activity
GO:0016491
oxidoreductase activity
GO:0016616
oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
GO:0046872
metal ion binding
GO:0051287
NAD binding
Biological Process
GO:0006097
glyoxylate cycle
GO:0006099
tricarboxylic acid cycle
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:2iv0
,
PDBe:2iv0
,
PDBj:2iv0
PDBsum
2iv0
PubMed
17401542
UniProt
O29610
|IDH_ARCFU Isocitrate dehydrogenase [NADP] (Gene Name=icd)
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