Structure of PDB 1o68 Chain D Binding Site BS01
Receptor Information
>1o68 Chain D (length=262) Species:
491
(Neisseria meningitidis serogroup B) [
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SLITVNTLQKMKAAGEKIAMLTAYESSFAALMDDAGVEMLLVGDSLGMAV
QGRKSTLPVSLRDMCYHTECVARGAKNAMIVSDLPFGAYQQSKEQAFAAA
AELMAAGAHMVKLEGGVWMAETTEFLQMRGIPVCAHIGLTPQSVFAFGGY
KVQGRGGKAQALLNDAKAHDDAGAAVVLMECVLAELAKKVTETVSCPTIG
IGAGADCDGQVLVMHDMLGIFPGKTAKFVKNFMQGHDSVQAAVRAYVAEV
KAKTFPAAEHIF
Ligand information
Ligand ID
KIV
InChI
InChI=1S/C5H8O3/c1-3(2)4(6)5(7)8/h3H,1-2H3,(H,7,8)
InChIKey
QHKABHOOEWYVLI-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
O=C(C(=O)O)C(C)C
CACTVS 3.341
CC(C)C(=O)C(O)=O
OpenEye OEToolkits 1.5.0
CC(C)C(=O)C(=O)O
Formula
C5 H8 O3
Name
3-METHYL-2-OXOBUTANOIC ACID;
ALPHA-KETOISOVALERIC ACID;
KETOVALINE
ChEMBL
CHEMBL146554
DrugBank
DB04074
ZINC
ZINC000001532553
PDB chain
1o68 Chain D Residue 275 [
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Receptor-Ligand Complex Structure
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PDB
1o68
Structural analysis of a set of proteins resulting from a bacterial genomics project
Resolution
2.1 Å
Binding residue
(original residue number in PDB)
L40 G42 D43 S44
Binding residue
(residue number reindexed from 1)
L41 G43 D44 S45
Annotation score
5
Enzymatic activity
Enzyme Commision number
2.1.2.11
: 3-methyl-2-oxobutanoate hydroxymethyltransferase.
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0003824
catalytic activity
GO:0003864
3-methyl-2-oxobutanoate hydroxymethyltransferase activity
GO:0016740
transferase activity
GO:0046872
metal ion binding
Biological Process
GO:0015940
pantothenate 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:1o68
,
PDBe:1o68
,
PDBj:1o68
PDBsum
1o68
PubMed
16021622
UniProt
Q9JZW6
|PANB_NEIMB 3-methyl-2-oxobutanoate hydroxymethyltransferase (Gene Name=panB)
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