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1LPW

Solution structure of the yeast spliceosomal U2 snRNA-intron branch site helix featuring a conserved pseudouridine

Summary for 1LPW
Entry DOI10.2210/pdb1lpw/pdb
Related1LMV
NMR InformationBMRB: 5394
Descriptor5'-R(*GP*GP*UP*GP*(PSU)P*AP*GP*UP*A)-3', 5'-R(*UP*AP*CP*UP*AP*AP*CP*AP*CP*C)-3' (2 entities in total)
Functional Keywordsu2 snrna, branch site, pseudouridine, rna
Biological sourceSaccharomyces cerevisiae (baker's yeast)
More
Total number of polymer chains2
Total formula weight6017.70
Authors
Newby, M.I.,Greenbaum, N.L. (deposition date: 2002-05-08, release date: 2002-11-27, Last modification date: 2024-05-22)
Primary citationNewby, M.I.,Greenbaum, N.L.
Sculpting of the Spliceosomal Branch Site Recognition Motif by a Conserved Pseudouridine
Nat.Struct.Biol., 12:958-965, 2002
Cited by
PubMed Abstract: Pairing of a consensus sequence of the precursor (pre)-mRNA intron with a short region of the U2 small nuclear (sn)RNA during assembly of the eukaryotic spliceosome results in formation of a complementary helix of seven base pairs with a single unpaired adenosine residue. The 2' OH of this adenosine, called the branch site, brings about nucleophilic attack at the pre-mRNA 5' splice site in the first step of splicing. Another feature of this pairing is the phylogenetic conservation of a pseudouridine (psi) residue in U2 snRNA nearly opposite the branch site. We show that the presence of this psi in the pre-mRNA branch-site helix of Saccharomyces cerevisiae induces a dramatically altered architectural landscape compared with that of its unmodified counterpart. The psi-induced structure places the nucleophile in an accessible position for the first step of splicing.
PubMed: 12426583
DOI: 10.1038/nsb873
PDB entries with the same primary citation
Experimental method
SOLUTION NMR
Structure validation

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