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6QW6

Structure of the human U5.U4/U6 tri-snRNP at 2.9A resolution.

This is a non-PDB format compatible entry.
Summary for 6QW6
Entry DOI10.2210/pdb6qw6/pdb
EMDB information4658
DescriptorU4/U6.U5 small nuclear ribonucleoprotein 27 kDa protein, Small nuclear ribonucleoprotein-associated proteins B and B', Small nuclear ribonucleoprotein E, ... (36 entities in total)
Functional Keywordsrnp complex, splicing, rna, protein, spliceosome
Biological sourceHomo sapiens (Human)
More
Total number of polymer chains39
Total formula weight1683428.27
Authors
Charenton, C.,Wilkinson, M.E.,Nagai, K. (deposition date: 2019-03-05, release date: 2019-04-17, Last modification date: 2020-10-07)
Primary citationCharenton, C.,Wilkinson, M.E.,Nagai, K.
Mechanism of 5' splice site transfer for human spliceosome activation.
Science, 364:362-367, 2019
Cited by
PubMed Abstract: The prespliceosome, comprising U1 and U2 small nuclear ribonucleoproteins (snRNPs) bound to the precursor messenger RNA 5' splice site (5'SS) and branch point sequence, associates with the U4/U6.U5 tri-snRNP to form the fully assembled precatalytic pre-B spliceosome. Here, we report cryo-electron microscopy structures of the human pre-B complex captured before U1 snRNP dissociation at 3.3-angstrom core resolution and the human tri-snRNP at 2.9-angstrom resolution. U1 snRNP inserts the 5'SS-U1 snRNA helix between the two RecA domains of the Prp28 DEAD-box helicase. Adenosine 5'-triphosphate-dependent closure of the Prp28 RecA domains releases the 5'SS to pair with the nearby U6 ACAGAGA-box sequence presented as a mobile loop. The structures suggest that formation of the 5'SS-ACAGAGA helix triggers remodeling of an intricate protein-RNA network to induce Brr2 helicase relocation to its loading sequence in U4 snRNA, enabling Brr2 to unwind the U4/U6 snRNA duplex to allow U6 snRNA to form the catalytic center of the spliceosome.
PubMed: 30975767
DOI: 10.1126/science.aax3289
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (2.92 Å)
Structure validation

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数据于2024-10-30公开中

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