Structure of PDB 6e1j Chain B Binding Site BS03
Receptor Information
>6e1j Chain B (length=408) Species:
3707
(Brassica juncea) [
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ERWPEYIPNKLPDKNYVRVFDTTLRDGEQSPGAALTPPQKIEIARQLAKL
RVDIMEVGFPVSSEEEFETIQTIAKTVGNEVDEETGYIPVICVIARSKER
DIKAAWESVKYAKRPRIVIFTSTSDIHLKYKLKMTREEVVDMVASSIRFA
KSLGFEDIEFGCEDGGRSDKDYICTVFEEAIKAGATTLACPDTVGINMPH
EYGKLVRYIKANTPGIDDVIFSAHCHNDLGVATANTIAGICAGARQVEVT
INGIGERSGNAPLEEVVMALKCRGAFVMGGVYTRIDTRQIMATSKMVQEY
TGLYVQPHKPIVGANCFVHESGIHQDGILKNRSTYEIISPEDVGVVKSQN
SGIVLGKLSGRHAVKGRLKELGYEISDEKLNEVFSRFRDLTKQKKRVTDD
DLKALVTC
Ligand information
Ligand ID
KMT
InChI
InChI=1S/C5H8O3S/c1-9-3-2-4(6)5(7)8/h2-3H2,1H3,(H,7,8)
InChIKey
SXFSQZDSUWACKX-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
O=C(O)C(=O)CCSC
CACTVS 3.341
CSCCC(=O)C(O)=O
OpenEye OEToolkits 1.5.0
CSCCC(=O)C(=O)O
Formula
C5 H8 O3 S
Name
4-(METHYLSULFANYL)-2-OXOBUTANOIC ACID
ChEMBL
CHEMBL1233860
DrugBank
DB02238
ZINC
ZINC000001532883
PDB chain
6e1j Chain B Residue 602 [
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Receptor-Ligand Complex Structure
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PDB
6e1j
Molecular Basis of the Evolution of Methylthioalkylmalate Synthase and the Diversity of Methionine-Derived Glucosinolates.
Resolution
2.096 Å
Binding residue
(original residue number in PDB)
R89 P255 T257 H288 H290
Binding residue
(residue number reindexed from 1)
R25 P191 T193 H224 H226
Annotation score
1
Enzymatic activity
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0003824
catalytic activity
GO:0003852
2-isopropylmalate synthase activity
GO:0016740
transferase activity
GO:0046872
metal ion binding
GO:0046912
acyltransferase activity, acyl groups converted into alkyl on transfer
Biological Process
GO:0009098
L-leucine biosynthetic process
GO:0019752
carboxylic acid metabolic process
GO:0043436
oxoacid metabolic process
Cellular Component
GO:0009507
chloroplast
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:6e1j
,
PDBe:6e1j
,
PDBj:6e1j
PDBsum
6e1j
PubMed
31023839
UniProt
C5J4P1
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