1xsh

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[[Image:1xsh.gif|left|200px]]
[[Image:1xsh.gif|left|200px]]
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{{Structure
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<!--
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|PDB= 1xsh |SIZE=350|CAPTION= <scene name='initialview01'>1xsh</scene>
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The line below this paragraph, containing "STRUCTURE_1xsh", 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=A:ADENOSINE-5&#39;-MONOPHOSPHATE'>A</scene>, <scene name='pdbligand=C:CYTIDINE-5&#39;-MONOPHOSPHATE'>C</scene>, <scene name='pdbligand=G:GUANOSINE-5&#39;-MONOPHOSPHATE'>G</scene>, <scene name='pdbligand=U:URIDINE-5&#39;-MONOPHOSPHATE'>U</scene>
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or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
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|GENE=
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|DOMAIN=
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{{STRUCTURE_1xsh| PDB=1xsh | SCENE= }}
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|RELATEDENTRY=[[1f6z|1F6Z]], [[1f6x|1F6X]], [[1xsg|1XSG]]
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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1xsh FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1xsh OCA], [http://www.ebi.ac.uk/pdbsum/1xsh PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1xsh RCSB]</span>
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}}
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'''Solution structure of E.coli RNase P RNA P4 stem oligoribonucleotide, U69C/C70U mutation'''
'''Solution structure of E.coli RNase P RNA P4 stem oligoribonucleotide, U69C/C70U mutation'''
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==About this Structure==
==About this Structure==
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1XSH is a [[Protein complex]] structure of sequences from [http://en.wikipedia.org/wiki/ ]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1XSH OCA].
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Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1XSH OCA].
==Reference==
==Reference==
Change of RNase P RNA function by single base mutation correlates with perturbation of metal ion binding in P4 as determined by NMR spectroscopy., Schmitz M, Nucleic Acids Res. 2004 Dec 2;32(21):6358-66. Print 2004. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/15576680 15576680]
Change of RNase P RNA function by single base mutation correlates with perturbation of metal ion binding in P4 as determined by NMR spectroscopy., Schmitz M, Nucleic Acids Res. 2004 Dec 2;32(21):6358-66. Print 2004. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/15576680 15576680]
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[[Category: Protein complex]]
 
[[Category: Schmitz, M.]]
[[Category: Schmitz, M.]]
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[[Category: metal binding site]]
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[[Category: Metal binding site]]
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[[Category: p4 stem]]
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[[Category: P4 stem]]
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[[Category: ribonuclease p rna]]
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[[Category: Ribonuclease p rna]]
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[[Category: ribozyme]]
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[[Category: Ribozyme]]
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[[Category: transfer rna processing]]
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[[Category: Transfer rna processing]]
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[[Category: u69c/c70u mutant]]
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[[Category: U69c/c70u mutant]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sat May 3 15:27:28 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Mar 31 00:54:05 2008''
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Revision as of 12:27, 3 May 2008

Template:STRUCTURE 1xsh

Solution structure of E.coli RNase P RNA P4 stem oligoribonucleotide, U69C/C70U mutation


Overview

The solution structures of two 27 nt RNA hairpins and their complexes with cobalt(III)-hexammine [Co(NH(3))(6)(3+)] were determined by NMR spectroscopy. The RNA hairpins are variants of the P4 region from Escherichia coli RNase P RNA: a U-to-A mutant changing the identity of the bulged nucleotide, and a U-to-C, C-to-U double mutant changing only the bulge position. Structures calculated from NMR constraints show that the RNA hairpins adopt different conformations. In the U-to-C, C-to-U double mutant, the conserved bulged uridine in the P4 wild-type stem is found to be shifted in the 3'-direction by one nucleotide when compared with the wild-type structure. Co(NH(3))(6)(3+) is used as a spectroscopic probe for Mg(H(2)O)(6)(2+) binding sites because both complexes have octahedral symmetry and have similar radii. Intermolecular NOE crosspeaks between Co(NH(3))(6)(3+) and RNA protons were used to locate the site of Co(NH(3))(6)(3+) binding to both RNA hairpins. The metal ion binds in the major groove near a bulge loop in both mutants, but is shifted 3' by about one base pair in the double mutant. The change of the metal ion binding site is compared with results obtained on corresponding mutant RNase P RNA molecules as reported by Harris and co-workers (RNA, 1, 210-218).

About this Structure

Full crystallographic information is available from OCA.

Reference

Change of RNase P RNA function by single base mutation correlates with perturbation of metal ion binding in P4 as determined by NMR spectroscopy., Schmitz M, Nucleic Acids Res. 2004 Dec 2;32(21):6358-66. Print 2004. PMID:15576680 Page seeded by OCA on Sat May 3 15:27:28 2008

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