Structure of PDB 6jd1 Chain B Binding Site BS01
Receptor Information
>6jd1 Chain B (length=331) Species:
273057
(Saccharolobus solfataricus P2) [
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DKTVLDANLDPLKGKTIGVIGYGNQGRVQATIMRENGLNVIVGNVKDKYY
ELAKKEGFEVYEIDEAVRRSDVALLLIPDEVMKEVYEKKIAPVLQGKKEF
VLDFASGYNVAFGLIRPPKSVDTIMVAPRMVGEGIMDLHKQGKGYPVLLG
VKQDASGKAWDYAKAIAKGIGAIPGGIAVISSFEEEALLDLMSEHTWVPI
LFGAIKACYDIAVKEYGVSPEAALLEFYASGELAEIARLIAEEGIFNQMV
HHSTTSQYGTLTRMFKYYDVVRRIVENEAKYIWDGSFAKEWSLEQQAGYP
VFYRLWELATQSEMAKAEKELYKLLGRKVKN
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
6jd1 Chain B Residue 401 [
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Receptor-Ligand Complex Structure
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PDB
6jd1
Use of Cryo-EM To Uncover Structural Bases of pH Effect and Cofactor Bispecificity of Ketol-Acid Reductoisomerase.
Resolution
3.38 Å
Binding residue
(original residue number in PDB)
D191 L192 E195
Binding residue
(residue number reindexed from 1)
D190 L191 E194
Annotation score
1
Enzymatic activity
Enzyme Commision number
1.1.1.86
: ketol-acid reductoisomerase (NADP(+)).
Gene Ontology
Molecular Function
GO:0004455
ketol-acid reductoisomerase activity
GO:0016491
oxidoreductase activity
Biological Process
GO:0008652
amino acid biosynthetic process
GO:0009082
branched-chain amino acid biosynthetic process
GO:0009097
isoleucine biosynthetic process
GO:0009099
L-valine biosynthetic process
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Molecular Function
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Biological Process
External links
PDB
RCSB:6jd1
,
PDBe:6jd1
,
PDBj:6jd1
PDBsum
6jd1
PubMed
30921515
UniProt
Q97YJ9
|ILVC2_SACS2 Putative ketol-acid reductoisomerase 2 (Gene Name=ilvC2)
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