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1S9S

SOLUTION STRUCTURE OF MLV PSI SITE

Summary for 1S9S
Entry DOI10.2210/pdb1s9s/pdb
DescriptorMLV Psi encapsidation site (1 entity in total)
Functional Keywordsmlv, a-minor k-turn, stem loop, bulge, g-u mismatch, g-a mismatch, u-u mismatch, a-c mismatch, rna
Total number of polymer chains1
Total formula weight32703.43
Authors
D'Souza, V.,Dey, A.,Habib, D.,Summers, M.F. (deposition date: 2004-02-05, release date: 2004-04-06, Last modification date: 2024-05-22)
Primary citationD'Souza, V.,Dey, A.,Habib, D.,Summers, M.F.
NMR structure of the 101-nucleotide core encapsidation signal of the Moloney Murine Leukemia Virus.
J.Mol.Biol., 337:427-442, 2004
Cited by
PubMed Abstract: The full length, positive-strand genome of the Moloney Murine Leukemia Virus contains a "core encapsidation signal" that is essential for efficient genome packaging during virus assembly. We have determined the structure of a 101-nucleotide RNA that contains this signal (called mPsi) using a novel isotope-edited NMR approach. The method is robust and should be generally applicable to larger RNAs. mPsi folds into three stem loops, two of which (SL-C and SL-D) co-stack to form an extended helix. The third stem loop (SL-B) is connected to SL-C by a flexible, four-nucleotide linker. The structure contains five mismatched base-pairs, an unusual C.CG base-triple platform, and a novel "A-minor K-turn," in which unpaired adenosine bases A340 and A341 of a GGAA bulge pack in the minor groove of a proximal stem, and a bulged distal uridine (U319) forms a hydrogen bond with the phosphodiester of A341. Phylogenetic analyses indicate that these essential structural elements are conserved among the murine C-type retroviruses.
PubMed: 15003457
DOI: 10.1016/j.jmb.2004.01.037
PDB entries with the same primary citation
Experimental method
SOLUTION NMR
Structure validation

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