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 DOI | 10.2210/pdb6qw6/pdb |
EMDB information | 4658 |
Descriptor | U4/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 Keywords | rnp complex, splicing, rna, protein, spliceosome |
Biological source | Homo sapiens (Human) More |
Total number of polymer chains | 39 |
Total formula weight | 1683428.27 |
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 citation | Charenton, 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: 30975767DOI: 10.1126/science.aax3289 PDB entries with the same primary citation |
Experimental method | ELECTRON MICROSCOPY (2.92 Å) |
Structure validation
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