2pqy

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[[Image:2pqy.jpg|left|200px]]
[[Image:2pqy.jpg|left|200px]]
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{{Structure
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<!--
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|PDB= 2pqy |SIZE=350|CAPTION= <scene name='initialview01'>2pqy</scene>, resolution 2.30&Aring;
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The line below this paragraph, containing "STRUCTURE_2pqy", creates the "Structure Box" on the page.
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|SITE=
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You may change the PDB parameter (which sets the PDB file loaded into the applet)
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|LIGAND= <scene name='pdbligand=CA:CALCIUM+ION'>CA</scene>, <scene name='pdbligand=MES:2-(N-MORPHOLINO)-ETHANESULFONIC+ACID'>MES</scene>
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or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
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|ACTIVITY= <span class='plainlinks'>[http://en.wikipedia.org/wiki/Enterobacter_ribonuclease Enterobacter ribonuclease], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.1.27.6 3.1.27.6] </span>
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or leave the SCENE parameter empty for the default display.
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|GENE= rna, rnsA ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=562 Escherichia coli])
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-->
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|DOMAIN=
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{{STRUCTURE_2pqy| PDB=2pqy | SCENE= }}
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|RELATEDENTRY=[[2pqx|2PQX]]
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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2pqy FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2pqy OCA], [http://www.ebi.ac.uk/pdbsum/2pqy PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=2pqy RCSB]</span>
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}}
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'''E. coli RNase 1 (in vitro refolded with DsbA only)'''
'''E. coli RNase 1 (in vitro refolded with DsbA only)'''
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[[Category: Loris, R.]]
[[Category: Loris, R.]]
[[Category: Messens, J.]]
[[Category: Messens, J.]]
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[[Category: hydrolase]]
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[[Category: Hydrolase]]
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[[Category: ribonuclease]]
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[[Category: Ribonuclease]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun May 4 13:39:25 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Mar 31 04:39:36 2008''
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Revision as of 10:39, 4 May 2008

Image:2pqy.jpg

Template:STRUCTURE 2pqy

E. coli RNase 1 (in vitro refolded with DsbA only)


Overview

One of the last unsolved problems of molecular biology is how the sequential amino acid information leads to a functional protein. Correct disulfide formation within a protein is hereby essential. We present periplasmic ribonuclease I (RNase I) from Escherichia coli as a new endogenous substrate for the study of oxidative protein folding. One of its four disulfides is between nonconsecutive cysteines. In general view, the folding of proteins with nonconsecutive disulfides requires the protein disulfide isomerase DsbC. In contrast, our study with RNase I shows that DsbA is a sufficient catalyst for correct disulfide formation in vivo and in vitro. DsbA is therefore more specific than generally assumed. Further, we show that the redox potential of the periplasm depends on the presence of glutathione and the Dsb proteins to maintain it at-165 mV. We determined the influence of this redox potential on the folding of RNase I. Under the more oxidizing conditions of dsb(-) strains, DsbC becomes necessary to correct non-native disulfides, but it cannot substitute for DsbA. Altogether, DsbA folds a protein with a nonconsecutive disulfide as long as no incorrect disulfides are formed.

About this Structure

2PQY is a Single protein structure of sequence from Escherichia coli. Full crystallographic information is available from OCA.

Reference

The oxidase DsbA folds a protein with a nonconsecutive disulfide., Messens J, Collet JF, Van Belle K, Brosens E, Loris R, Wyns L, J Biol Chem. 2007 Oct 26;282(43):31302-7. Epub 2007 Aug 16. PMID:17702751 Page seeded by OCA on Sun May 4 13:39:25 2008

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