2f9d: Difference between revisions

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[[Image:2f9d.gif|left|200px]]
{{Seed}}
[[Image:2f9d.png|left|200px]]


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{{STRUCTURE_2f9d|  PDB=2f9d  |  SCENE=  }}  
{{STRUCTURE_2f9d|  PDB=2f9d  |  SCENE=  }}  


'''2.5 angstrom resolution structure of the spliceosomal protein p14 bound to region of SF3b155'''
===2.5 angstrom resolution structure of the spliceosomal protein p14 bound to region of SF3b155===




==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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{{ABSTRACT_PUBMED_16432215}}


==About this Structure==
==About this Structure==
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[[Category: Schellenberg, M J.]]
[[Category: Schellenberg, M J.]]
[[Category: P14 sf3bp14 sf3b155 sap155 rrm]]
[[Category: P14 sf3bp14 sf3b155 sap155 rrm]]
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