5hwi

Crystal structure of selenomethionine labelled gama glutamyl cyclotransferease specific to glutathione from yeast

spinqualitylabelsall models 5hwi, resolution 1.75Å Show:Asymmetric Unit Biological Assembly Drag the structure with the mouse to rotate   Export Animated Image   Print3D Structural highlights 5hwi is a 1 chain structure with sequence from Saccharomyces cerevisiae S288C. Full crystallographic information is available from OCA. For a guided tour on the structure components use FirstGlance. Method: X-ray diffraction, Resolution 1.755Å Ligands: GOL, MSE, SIN Resources: FirstGlance, OCA, PDBe, RCSB, PDBsum, ProSAT Function CHAC_YEAST Catalyzes the cleavage glutathione into 5-oxoproline and a Cys-Gly dipeptide. Acts specifically on glutathione, but not on other gamma-glutamyl peptides. Allows utilization of gluthathione through subsequent cleavage of the Cys-Gly dipeptide by Cys-Gly metallodipeptidase DUG1. Publication Abstract from PubMed Glutathione degradation plays an important role in glutathione and redox homeostasis and thus it is imperative to understand the enzymes and the mechanisms involved in glutathione degradation in detail. We describe here ChaC2, a member of the ChaC family of gamma-glutamylcyclotransferases, as an enzyme that degrades glutathione in the cytosol of mammalian cells. ChaC2 is distinct from the previously described ChaC1, to which ChaC2 shows about 50% sequence identity. Human and mouse ChaC2 proteins, purified in vitro, show 10-20 fold lower catalytic efficiency than ChaC1, although they showed comparable Km values (Km of 3.7+/-0.4 mM and kcat of 15.9+/-1.0 min-1 towards glutathione for human ChaC2; Km of 2.2+/-0.4 mM and kcat of 225.2+/-15 min-1 towards glutathione for human ChaC1). The ChaC1 and ChaC2 proteins also shared the same specificity for reduced glutathione, with no activity against either gamma-glutamyl amino acids or oxidized glutathione. The ChaC2 proteins were found to be expressed constitutively in cells, unlike the tightly regulated ChaC1. Moreover, lower eukaryotes have a single member of the ChaC family that appears to be orthologous to ChaC2. In addition, we determined the crystal structure of yeast ChaC2 homologue, GCG1 at 1.34 A resolution which represents the first structure of the ChaC family of proteins. The catalytic site is defined by a fortuitous benzoic acid molecule bound to the crystal structure. The mechanism for binding and catalytic activity of this new enzyme of glutathione degradation, which is involved in continuous, but basal turnover of cytosolic glutathione, is proposed. ChaC2: An Enzyme for Slow Turnover of Cytosolic Glutathione.,Kaur A, Gautam R, Srivastava R, Chandel A, Kumar A, Karthikeyan S, Bachhawat AK J Biol Chem. 2016 Dec 2. pii: jbc.M116.727479. PMID:27913623 From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

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