Structure of PDB 2d33 Chain B Binding Site BS02

Receptor Information
>2d33 Chain B (length=503) Species: 562 (Escherichia coli) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
MIPDVSQALAWLEKHPQALKGIQRGLERETLRVNADGTLATTGHPEALGS
ALTHKWITTDFAEALLEFITPVDGDIEHMLTFMRDLHRYTARNMGDERMW
PLSMPSYIAEGQDIELAQYGTSNTGRFKTLYREGLKNRYGALMQTISGVH
YNFSLPMAFWQAKSAKEKISAGYFRVIRNYYRFGWVIPYLFGASPAISSS
FLSLPFEKTESGMYYLPYATSLRLSDLGYTNSNLGITFNDLYEYVAGLKQ
AIKTPSEEYAKIGIEKDGKRLQINSNVLQIENELYAPIRPKRVTRSGESP
SDALLRGGIEYIEVRSLDINPFSPIGVDEQQVRFLDLFMVWCALADAPEM
SSSELACTRVNWNRVILEGRKPGLTLGIGCETAQFPLPQVGKDLFRDLKR
VAQTLDSINGGEAYQKVCDELVACFDNPDLTFSARILRSMIDTGIGGTGK
AFAEAYRNLLREEPLEILREEDFVAEREASERRQQEMEAADTEPFAVWLE
KHA
Ligand information
Ligand IDMG
InChIInChI=1S/Mg/q+2
InChIKeyJLVVSXFLKOJNIY-UHFFFAOYSA-N
SMILES
SoftwareSMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Mg+2]
CACTVS 3.341[Mg++]
FormulaMg
NameMAGNESIUM ION
ChEMBL
DrugBankDB01378
ZINC
PDB chain2d33 Chain B Residue 1524 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
Global viewLocal viewStructure summary

[Spin on] [Spin off] [Reset]
[High quality] [Low quality]
[White background] [Black background]

[Spin on] [Spin off] [Reset]
[High quality] [Low quality]
[White background] [Black background]
PDB2d33 Crystal structure of gamma-glutamylcysteine synthetase: insights into the mechanism of catalysis by a key enzyme for glutathione homeostasis.
Resolution2.6 Å
Binding residue
(original residue number in PDB)
E27 H150 E328
Binding residue
(residue number reindexed from 1)
E27 H150 E313
Annotation score1
Enzymatic activity
Enzyme Commision number 6.3.2.2: glutamate--cysteine ligase.
Gene Ontology
Molecular Function
GO:0003824 catalytic activity
GO:0004357 glutamate-cysteine ligase activity
GO:0005524 ATP binding
GO:0016874 ligase activity
GO:0016879 ligase activity, forming carbon-nitrogen bonds
GO:0046872 metal ion binding
Biological Process
GO:0006750 glutathione biosynthetic process
GO:0006972 hyperosmotic response
GO:0071243 cellular response to arsenic-containing substance
GO:0071288 cellular response to mercury ion
Cellular Component
GO:0005829 cytosol

View graph for
Molecular Function

View graph for
Biological Process

View graph for
Cellular Component
External links
PDB RCSB:2d33, PDBe:2d33, PDBj:2d33
PDBsum2d33
PubMed
UniProtP0A6W9|GSH1_ECOLI Glutamate--cysteine ligase (Gene Name=gshA)

[Back to BioLiP]