2f9j

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(New page: 200px<br /> <applet load="2f9j" size="450" color="white" frame="true" align="right" spinBox="true" caption="2f9j, resolution 3.00&Aring;" /> '''3.0 angstrom resolu...)
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<applet load="2f9j" size="450" color="white" frame="true" align="right" spinBox="true"
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caption="2f9j, resolution 3.00&Aring;" />
caption="2f9j, resolution 3.00&Aring;" />
'''3.0 angstrom resolution structure of a Y22M mutant of the spliceosomal protein p14 bound to a region of SF3b155'''<br />
'''3.0 angstrom resolution structure of a Y22M mutant of the spliceosomal protein p14 bound to a region of SF3b155'''<br />
==Overview==
==Overview==
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The precise excision of introns from precursor mRNAs (pre-mRNAs) in, eukaryotes is accomplished by the spliceosome, a complex assembly, containing five small nuclear ribonucleoprotein (snRNP) particles. Human, p14, a component of the spliceosomal U2 and U11/U12 snRNPs, has been shown, to associate directly with the pre-mRNA branch adenosine early in, spliceosome assembly and within the fully assembled spliceosome. Here we, report the 2.5-A crystal structure of a complex containing p14 and a, peptide derived from the p14-associated U2 snRNP component SF3b155. p14, contains an RNA recognition motif (RRM), the surface of which is largely, occluded by a C-terminal alpha-helix and a portion of the SF3b155 peptide., An analysis of RNA.protein crosslinking to wild-type and mutant p14 shows, that the branch adenosine directly interacts with a conserved aromatic, within a pocket on the surface of the complex. This result, combined with, a comparison of the structure with known RRMs and pseudoRRMs as well as, model-building by using the electron cryomicroscopy structure of a, spliceosomal U11/U12 di-snRNP, suggests that p14.SF3b155 presents a, noncanonical surface for RNA recognition at the heart of the mammalian, spliceosome.
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The precise excision of introns from precursor mRNAs (pre-mRNAs) in eukaryotes is accomplished by the spliceosome, a complex assembly containing five small nuclear ribonucleoprotein (snRNP) particles. Human p14, a component of the spliceosomal U2 and U11/U12 snRNPs, has been shown to associate directly with the pre-mRNA branch adenosine early in spliceosome assembly and within the fully assembled spliceosome. Here we report the 2.5-A crystal structure of a complex containing p14 and a peptide derived from the p14-associated U2 snRNP component SF3b155. p14 contains an RNA recognition motif (RRM), the surface of which is largely occluded by a C-terminal alpha-helix and a portion of the SF3b155 peptide. An analysis of RNA.protein crosslinking to wild-type and mutant p14 shows that the branch adenosine directly interacts with a conserved aromatic within a pocket on the surface of the complex. This result, combined with a comparison of the structure with known RRMs and pseudoRRMs as well as model-building by using the electron cryomicroscopy structure of a spliceosomal U11/U12 di-snRNP, suggests that p14.SF3b155 presents a noncanonical surface for RNA recognition at the heart of the mammalian spliceosome.
==About this Structure==
==About this Structure==
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2F9J is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=2F9J OCA].
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2F9J is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2F9J OCA].
==Reference==
==Reference==
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[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Protein complex]]
[[Category: Protein complex]]
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[[Category: MacMillan, A.M.]]
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[[Category: MacMillan, A M.]]
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[[Category: Schellenberg, M.J.]]
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[[Category: Schellenberg, M J.]]
[[Category: sf3bp14 sf3b155 sap155 p14y22m rrm]]
[[Category: sf3bp14 sf3b155 sap155 p14y22m rrm]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Mon Nov 12 22:01:54 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 17:19:06 2008''

Revision as of 15:19, 21 February 2008


2f9j, resolution 3.00Å

Drag the structure with the mouse to rotate

3.0 angstrom resolution structure of a Y22M mutant of the spliceosomal protein p14 bound to a region of SF3b155

Overview

The precise excision of introns from precursor mRNAs (pre-mRNAs) in eukaryotes is accomplished by the spliceosome, a complex assembly containing five small nuclear ribonucleoprotein (snRNP) particles. Human p14, a component of the spliceosomal U2 and U11/U12 snRNPs, has been shown to associate directly with the pre-mRNA branch adenosine early in spliceosome assembly and within the fully assembled spliceosome. Here we report the 2.5-A crystal structure of a complex containing p14 and a peptide derived from the p14-associated U2 snRNP component SF3b155. p14 contains an RNA recognition motif (RRM), the surface of which is largely occluded by a C-terminal alpha-helix and a portion of the SF3b155 peptide. An analysis of RNA.protein crosslinking to wild-type and mutant p14 shows that the branch adenosine directly interacts with a conserved aromatic within a pocket on the surface of the complex. This result, combined with a comparison of the structure with known RRMs and pseudoRRMs as well as model-building by using the electron cryomicroscopy structure of a spliceosomal U11/U12 di-snRNP, suggests that p14.SF3b155 presents a noncanonical surface for RNA recognition at the heart of the mammalian spliceosome.

About this Structure

2F9J is a Protein complex structure of sequences from Homo sapiens. Full crystallographic information is available from OCA.

Reference

Crystal structure of a core spliceosomal protein interface., Schellenberg MJ, Edwards RA, Ritchie DB, Kent OA, Golas MM, Stark H, Luhrmann R, Glover JN, MacMillan AM, Proc Natl Acad Sci U S A. 2006 Jan 31;103(5):1266-71. Epub 2006 Jan 23. PMID:16432215

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