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PDBsum entry 1kpy
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DOI no:
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J Mol Biol
322:621-633
(2002)
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PubMed id:
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Solution structure of a luteoviral P1-P2 frameshifting mRNA pseudoknot.
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P.L.Nixon,
A.Rangan,
Y.G.Kim,
A.Rich,
D.W.Hoffman,
M.Hennig,
D.P.Giedroc.
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ABSTRACT
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A hairpin-type messenger RNA pseudoknot from pea enation mosaic virus RNA1
(PEMV-1) regulates the efficiency of programmed -1 ribosomal frameshifting. The
solution structure and 15N relaxation rates reveal that the PEMV-1 pseudoknot is
a compact-folded structure composed almost entirely of RNA triple helix. A three
nucleotide reverse turn in loop 1 positions a protonated cytidine, C(10), in the
correct orientation to form an A((n-1)).C(+).G-C(n) major groove base quadruple,
like that found in the beet western yellows virus pseudoknot and the hepatitis
delta virus ribozyme, despite distinct structural contexts. A novel loop 2-loop
1 A.U Hoogsteen base-pair stacks on the C(10)(+).G(28) base-pair of the
A(12).C(10)(+).G(28)-C(13) quadruple and forms a wedge between the pseudoknot
stems stabilizing a bent and over-rotated global conformation. Substitution of
key nucleotides that stabilize the unique conformation of the PEMV-1 pseudoknot
greatly reduces ribosomal frameshifting efficacy.
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Selected figure(s)
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Figure 6.
Figure 6. (a) Stereo view of the A[(n
-1)]·C^+·G-C[n] base quadruple in the average
structure of the PEMV-1 pseudoknot formed by loop 1 and stem 2
(A[12]·C[10]^+·G[28]-C[13]). C[10] is shown in
red, the accepting Watson-Crick pair in blue, and A[12] of stem
2 which forms the third hydrogen bond to C[10]^+. (b) The
three-base reverse turn places C[10] in the proper orientation
to form the A[(n -1)]·C^+·G-C[n] base quadruple.
C[10] is shown in red, U[9] from the Hoogsteen wedge pair in
yellow and G[11], which forms the closing base-pair of stem 2,
in blue. (c) Superposition of the bases from the A[(n
-1)]·C^+·G-C[n] quadruples from the BWYV
pseudoknot (white, 437D),[9.] the HDV ribozyme (red, 1CX0) [22.]
and the average structure of the PEMV-1 pseudoknot (blue). (d)
Overlay of the heavy atoms of the base quadruples and
intervening nucleotide from the HDV ribozyme (red, residues
141-144, 161 of 1CX0) [22.] and the PEMV-1 pseudoknot (blue,
residues 10-13, 28).
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Figure 8.
Figure 8. (a) Overlay of the 15 lowest energy structures of
the PEMV-1 pseudoknot with loop 2 (green) and U[14] (purple)
highlighted. (b) Details of the A[25], A[26], and A[27]
non-canonical base-pairings between loop 2 (green) and stem 1
(blue) nucleotides. A[25] forms an N1-2' OH hydrogen bond with
the sugar of C[16], A[27] forms the analogous interaction with
the sugar of C[15], and A[26] forms a pair of reciprocal
hydrogen bonds with G[8] from stem 1 (A[26] amino to G[8] N3,
G[8] amino to A[26] N1, shown with donors in red, acceptors in
blue).
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The above figures are
reprinted
by permission from Elsevier:
J Mol Biol
(2002,
322,
621-633)
copyright 2002.
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Figures were
selected
by an automated process.
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Literature references that cite this PDB file's key reference
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PubMed id
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Reference
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B.Liu,
D.H.Mathews,
and
D.H.Turner
(2010).
RNA pseudoknots: folding and finding.
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F1000 Biol Rep,
2,
8.
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M.Y.Chou,
and
K.Y.Chang
(2010).
An intermolecular RNA triplex provides insight into structural determinants for the pseudoknot stimulator of -1 ribosomal frameshifting.
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Nucleic Acids Res,
38,
1676-1685.
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R.C.Olsthoorn,
R.Reumerman,
C.W.Hilbers,
C.W.Pleij,
and
H.A.Heus
(2010).
Functional analysis of the SRV-1 RNA frameshifting pseudoknot.
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Nucleic Acids Res,
38,
7665-7672.
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S.Cao,
D.P.Giedroc,
and
S.J.Chen
(2010).
Predicting loop-helix tertiary structural contacts in RNA pseudoknots.
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RNA,
16,
538-552.
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D.P.Giedroc,
and
P.V.Cornish
(2009).
Frameshifting RNA pseudoknots: structure and mechanism.
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Virus Res,
139,
193-208.
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PDB codes:
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G.Chen,
K.Y.Chang,
M.Y.Chou,
C.Bustamante,
and
I.Tinoco
(2009).
Triplex structures in an RNA pseudoknot enhance mechanical stability and increase efficiency of -1 ribosomal frameshifting.
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Proc Natl Acad Sci U S A,
106,
12706-12711.
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L.Zhang,
P.Bao,
M.J.Leibowitz,
and
Y.Zhang
(2009).
Slow formation of a pseudoknot structure is rate limiting in the productive co-transcriptional folding of the self-splicing Candida intron.
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RNA,
15,
1986-1992.
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M.H.Mazauric,
J.L.Leroy,
K.Visscher,
S.Yoshizawa,
and
D.Fourmy
(2009).
Footprinting analysis of BWYV pseudoknot-ribosome complexes.
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RNA,
15,
1775-1786.
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N.E.Grossoehme,
L.Li,
S.C.Keane,
P.Liu,
C.E.Dann,
J.L.Leibowitz,
and
D.P.Giedroc
(2009).
Coronavirus N protein N-terminal domain (NTD) specifically binds the transcriptional regulatory sequence (TRS) and melts TRS-cTRS RNA duplexes.
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J Mol Biol,
394,
544-557.
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PDB code:
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P.Liu,
L.Li,
S.C.Keane,
D.Yang,
J.L.Leibowitz,
and
D.P.Giedroc
(2009).
Mouse hepatitis virus stem-loop 2 adopts a uYNMG(U)a-like tetraloop structure that is highly functionally tolerant of base substitutions.
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J Virol,
83,
12084-12093.
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B.Han,
B.Dost,
V.Bafna,
and
S.Zhang
(2008).
Structural alignment of pseudoknotted RNA.
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J Comput Biol,
15,
489-504.
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J.M.Hart,
S.D.Kennedy,
D.H.Mathews,
and
D.H.Turner
(2008).
NMR-assisted prediction of RNA secondary structure: identification of a probable pseudoknot in the coding region of an R2 retrotransposon.
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J Am Chem Soc,
130,
10233-10239.
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S.Pennell,
E.Manktelow,
A.Flatt,
G.Kelly,
S.J.Smerdon,
and
I.Brierley
(2008).
The stimulatory RNA of the Visna-Maedi retrovirus ribosomal frameshifting signal is an unusual pseudoknot with an interstem element.
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RNA,
14,
1366-1377.
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P.C.Bevilacqua,
A.L.Cerrone-Szakal,
and
N.A.Siegfried
(2007).
Insight into the functional versatility of RNA through model-making with applications to data fitting.
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Q Rev Biophys,
40,
55-85.
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P.Liu,
L.Li,
J.J.Millership,
H.Kang,
J.L.Leibowitz,
and
D.P.Giedroc
(2007).
A U-turn motif-containing stem-loop in the coronavirus 5' untranslated region plays a functional role in replication.
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RNA,
13,
763-780.
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S.V.Steinberg,
and
Y.I.Boutorine
(2007).
G-ribo motif favors the formation of pseudoknots in ribosomal RNA.
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RNA,
13,
1036-1042.
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A.T.Perrotta,
T.S.Wadkins,
and
M.D.Been
(2006).
Chemical rescue, multiple ionizable groups, and general acid-base catalysis in the HDV genomic ribozyme.
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RNA,
12,
1282-1291.
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P.V.Cornish,
D.P.Giedroc,
and
M.Hennig
(2006).
Dissecting non-canonical interactions in frameshift-stimulating mRNA pseudoknots.
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J Biomol NMR,
35,
209-223.
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P.V.Cornish,
and
D.P.Giedroc
(2006).
Pairwise coupling analysis of helical junction hydrogen bonding interactions in luteoviral RNA pseudoknots.
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Biochemistry,
45,
11162-11171.
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P.V.Cornish,
S.N.Stammler,
and
D.P.Giedroc
(2006).
The global structures of a wild-type and poorly functional plant luteoviral mRNA pseudoknot are essentially identical.
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RNA,
12,
1959-1969.
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PDB codes:
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D.W.Staple,
and
S.E.Butcher
(2005).
Pseudoknots: RNA structures with diverse functions.
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PLoS Biol,
3,
e213.
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E.P.Plant,
G.C.Pérez-Alvarado,
J.L.Jacobs,
B.Mukhopadhyay,
M.Hennig,
and
J.D.Dinman
(2005).
A three-stemmed mRNA pseudoknot in the SARS coronavirus frameshift signal.
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PLoS Biol,
3,
e172.
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F.R.Schmidt
(2005).
About the nature of RNA interference.
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Appl Microbiol Biotechnol,
67,
429-435.
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P.V.Cornish,
M.Hennig,
and
D.P.Giedroc
(2005).
A loop 2 cytidine-stem 1 minor groove interaction as a positive determinant for pseudoknot-stimulated -1 ribosomal frameshifting.
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Proc Natl Acad Sci U S A,
102,
12694-12699.
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PDB codes:
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E.P.Plant,
K.L.Jacobs,
J.W.Harger,
A.Meskauskas,
J.L.Jacobs,
J.L.Baxter,
A.N.Petrov,
and
J.D.Dinman
(2003).
The 9-A solution: how mRNA pseudoknots promote efficient programmed -1 ribosomal frameshifting.
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RNA,
9,
168-174.
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The most recent references are shown first.
Citation data come partly from CiteXplore and partly
from an automated harvesting procedure. Note that this is likely to be
only a partial list as not all journals are covered by
either method. However, we are continually building up the citation data
so more and more references will be included with time.
Where a reference describes a PDB structure, the PDB
codes are
shown on the right.
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