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2z9s

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{{STRUCTURE_2z9s| PDB=2z9s | SCENE= }}
{{STRUCTURE_2z9s| PDB=2z9s | SCENE= }}
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'''Crystal Structure Analysis of rat HBP23/Peroxiredoxin I, Cys52Ser mutant'''
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===Crystal Structure Analysis of rat HBP23/Peroxiredoxin I, Cys52Ser mutant===
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==Overview==
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Rat heme-binding protein 23 (HBP23)/peroxiredoxin (Prx I) belongs to the 2-Cys peroxiredoxin type I family and exhibits peroxidase activity coupled with reduced thioredoxin (Trx) as an electron donor. We analyzed the dimer-oligomer interconversion of wild-type and mutant HBP23/Prx I by gel filtration and found that the C52S and C173S mutants existed mostly as decamers, whereas the wild type was a mixture of various forms, favoring the decamer at higher protein concentration and lower ionic salt concentration and in the presence of dithiothreitol. The C83S mutant was predominantly dimeric, in agreement with a previous crystallographic analysis (Hirotsu, S., Abe, Y., Okada, K., Nagahara, N., Hori, H., Nishino, T., and Hakoshima, T. (1999) Proc. Natl. Acad. Sci. U. S. A. 96, 12333-12338). X-ray diffraction analysis of the decameric C52S mutant revealed a toroidal structure (diameter, approximately 130A; inside diameter, approximately 55A; thickness, approximately 45A). In contrast to human Prx I, which was recently reported to exist predominantly as the decamer with Cys(83)-Cys(83) disulfide bonds at all dimer-dimer interfaces, rat HBP23/Prx I has a Cys(83)-Cys(83) disulfide bond at only one dimer-dimer interface (S-S separation of approximately 2.1A), whereas the interactions at the other interfaces (mean S-S separation of 3.6A) appear to involve hydrophobic and van der Waals forces. This finding is consistent with gel filtration analyses showing that the protein readily interconverts between dimer and oligomeric forms. The C83S mutant exhibited similar peroxidase activity to the wild type, which is exclusively dimeric, in the Trx/Trx reductase system. At higher concentrations, where the protein was mostly decameric, less efficient attack of reduced Trx was observed in a [(14)C]iodoacetamide incorporation experiment. We suggest that the dimerdecamer interconversion may have a regulatory role.
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{{ABSTRACT_PUBMED_17974571}}
==About this Structure==
==About this Structure==
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==Reference==
==Reference==
Dimer-oligomer interconversion of wild-type and mutant rat 2-Cys peroxiredoxin: disulfide formation at dimer-dimer interfaces is not essential for decamerization., Matsumura T, Okamoto K, Iwahara S, Hori H, Takahashi Y, Nishino T, Abe Y, J Biol Chem. 2008 Jan 4;283(1):284-93. Epub 2007 Nov 1. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/17974571 17974571]
Dimer-oligomer interconversion of wild-type and mutant rat 2-Cys peroxiredoxin: disulfide formation at dimer-dimer interfaces is not essential for decamerization., Matsumura T, Okamoto K, Iwahara S, Hori H, Takahashi Y, Nishino T, Abe Y, J Biol Chem. 2008 Jan 4;283(1):284-93. Epub 2007 Nov 1. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/17974571 17974571]
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Crystal structure of a multifunctional 2-Cys peroxiredoxin heme-binding protein 23 kDa/proliferation-associated gene product., Hirotsu S, Abe Y, Okada K, Nagahara N, Hori H, Nishino T, Hakoshima T, Proc Natl Acad Sci U S A. 1999 Oct 26;96(22):12333-8. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/10535922 10535922]
[[Category: Peroxiredoxin]]
[[Category: Peroxiredoxin]]
[[Category: Rattus norvegicus]]
[[Category: Rattus norvegicus]]
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[[Category: Redox-active center]]
[[Category: Redox-active center]]
[[Category: Thiol-specific antioxidant protein]]
[[Category: Thiol-specific antioxidant protein]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Jul 27 23:01:52 2008''

Revision as of 20:01, 27 July 2008

Image:2z9s.png

Template:STRUCTURE 2z9s

Crystal Structure Analysis of rat HBP23/Peroxiredoxin I, Cys52Ser mutant

Template:ABSTRACT PUBMED 17974571

About this Structure

2Z9S is a Single protein structure of sequence from Rattus norvegicus. Full crystallographic information is available from OCA.

Reference

Dimer-oligomer interconversion of wild-type and mutant rat 2-Cys peroxiredoxin: disulfide formation at dimer-dimer interfaces is not essential for decamerization., Matsumura T, Okamoto K, Iwahara S, Hori H, Takahashi Y, Nishino T, Abe Y, J Biol Chem. 2008 Jan 4;283(1):284-93. Epub 2007 Nov 1. PMID:17974571

Crystal structure of a multifunctional 2-Cys peroxiredoxin heme-binding protein 23 kDa/proliferation-associated gene product., Hirotsu S, Abe Y, Okada K, Nagahara N, Hori H, Nishino T, Hakoshima T, Proc Natl Acad Sci U S A. 1999 Oct 26;96(22):12333-8. PMID:10535922

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