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| - | [[Image:1v4g.gif|left|200px]] | + | {{Seed}} |
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| | {{STRUCTURE_1v4g| PDB=1v4g | SCENE= }} | | {{STRUCTURE_1v4g| PDB=1v4g | SCENE= }} |
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| - | '''Crystal Structure of gamma-Glutamylcysteine Synthetase from Escherichia coli B'''
| + | ===Crystal Structure of gamma-Glutamylcysteine Synthetase from Escherichia coli B=== |
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| - | ==Overview==
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| - | Gamma-glutamylcysteine synthetase (gammaGCS), a rate-limiting enzyme in glutathione biosynthesis, plays a central role in glutathione homeostasis and is a target for development of potential therapeutic agents against parasites and cancer. We have determined the crystal structures of Escherichia coli gammaGCS unliganded and complexed with a sulfoximine-based transition-state analog inhibitor at resolutions of 2.5 and 2.1 A, respectively. In the crystal structure of the complex, the bound inhibitor is phosphorylated at the sulfoximido nitrogen and is coordinated to three Mg2+ ions. The cysteine-binding site was identified; it is formed inductively at the transition state. In the unliganded structure, an open space exists around the representative cysteine-binding site and is probably responsible for the competitive binding of glutathione. Upon inhibitor binding, the side chains of Tyr-241 and Tyr-300 turn, forming a hydrogen-bonding triad with the carboxyl group of the inhibitor's cysteine moiety, allowing this moiety to fit tightly into the cysteine-binding site with concomitant accommodation of its side chain into a shallow pocket. This movement is caused by a conformational change of a switch loop (residues 240-249). Based on this crystal structure, the cysteine-binding sites of mammalian and parasitic gammaGCSs were predicted by multiple sequence alignment, although no significant sequence identity exists between the E. coli gammaGCS and its eukaryotic homologues. The identification of this cysteine-binding site provides important information for the rational design of novel gammaGCS inhibitors.
| + | The line below this paragraph, {{ABSTRACT_PUBMED_15477603}}, adds the Publication Abstract to the page |
| | + | (as it appears on PubMed at http://www.pubmed.gov), where 15477603 is the PubMed ID number. |
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| | + | {{ABSTRACT_PUBMED_15477603}} |
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| | ==About this Structure== | | ==About this Structure== |
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| | [[Category: Glutathione regulation]] | | [[Category: Glutathione regulation]] |
| | [[Category: Peptide synthesis]] | | [[Category: Peptide synthesis]] |
| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sat May 3 12:03:54 2008'' | + | |
| | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Jul 27 20:30:59 2008'' |
Revision as of 17:31, 27 July 2008
Template:STRUCTURE 1v4g
Crystal Structure of gamma-Glutamylcysteine Synthetase from Escherichia coli B
Template:ABSTRACT PUBMED 15477603
About this Structure
1V4G is a Single protein structure of sequence from Escherichia coli. Full crystallographic information is available from OCA.
Reference
Crystal structure of gamma-glutamylcysteine synthetase: insights into the mechanism of catalysis by a key enzyme for glutathione homeostasis., Hibi T, Nii H, Nakatsu T, Kimura A, Kato H, Hiratake J, Oda J, Proc Natl Acad Sci U S A. 2004 Oct 19;101(42):15052-7. Epub 2004 Oct 11. PMID:15477603
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