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PDBsum entry 1dgo
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DOI no:
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Nucleic Acids Res
28:1906-1912
(2000)
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PubMed id:
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Structural basis for uracil DNA glycosylase interaction with uracil: NMR study.
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M.Ghosh,
N.Vinay Kumar,
U.Varshney,
K.V.Chary.
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ABSTRACT
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Two dimensional (2D) NMR and molecular dynamics simulations have been used to
determine the three dimensional (3D) structure of a hairpin DNA,
d-CTA-GAGGATCC-TUTT-GGATCCT (22mer; abbreviated as U2-hairpin), which has uracil
at the second position from the 5' end of the tetraloop. The(1)H resonances of
this hairpin have been assigned almost completely. NMR restrained molecular
dynamics and energy minimization procedures have been used to describe the 3D
structure of U2-hairpin. This study establishes that the stem of the hairpin
adopts a right-handed B-DNA conformation, while the T(12)and T(15)nucleotides
stack upon 3' and 5' ends of the stem, respectively. Further, T(14)stacks upon
both T(12)and T(15). Though U(13)partially stacks upon T(14), no stacking
interaction is observed between U(13)and T(12). All the individual nucleotide
bases belonging to the stem and T(12)and T(15)of the loop adopt ' anti '
conformation with respect to their sugar moiety, while the U(13)and T(14)of the
loop are in ' syn ' conformation. The turning phosphate in the loop is located
between T(13)and T(14). This study and a concurrent NMR structural study on yet
another hairpin DNA d-CTAGAGGAATAA-TTTU-GGATCCT (22mer; abbreviated as
U4-hairpin), with uracil at the fourth position from the 5' end of the tetraloop
throw light upon various interactions which have been reported between
Escherichia coli uracil DNA glycosylase (UDG) and uracil containing DNA. The
epsilon of T(12)and alpha, beta, gamma, epsilon and zeta of U(13)and gamma of
T(14), which partially influence the local conformation of U(13)in U2-hairpin
are all locked in ' trans ' conformation. Such stretched out backbone
conformation in the vicinity of U(13)could be the reason as to why the
U2-hairpin is found to be the poor substrate for its interaction with UDG
compared to the other substrates in which the uracil is at first, third and
fourth positions of the tetraloop from its 5' end, as reported earlier by Vinay
and Varshney. This study shows that UDG actively promotes the flipping of uracil
from a stacked conformation and rules out the possibility of UDG recognizing the
flipped out uracil bases.
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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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C.Dupouy,
P.Millard,
A.Boissonnet,
and
J.M.Escudier
(2010).
Alpha,beta-D-CNA preorganization of unpaired loop moiety stabilizes DNA hairpin.
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Chem Commun (Camb),
46,
5142-5144.
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M.N.Kinde-Carson,
C.Ferguson,
N.A.Oyler,
G.S.Harbison,
and
G.A.Meints
(2010).
Solid state 2H NMR analysis of furanose ring dynamics in DNA containing uracil.
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J Phys Chem B,
114,
3285-3293.
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D.J.Wilton,
M.Ghosh,
K.V.Chary,
K.Akasaka,
and
M.P.Williamson
(2008).
Structural change in a B-DNA helix with hydrostatic pressure.
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Nucleic Acids Res,
36,
4032-4037.
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PDB codes:
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S.R.Bellamy,
K.Krusong,
and
G.S.Baldwin
(2007).
A rapid reaction analysis of uracil DNA glycosylase indicates an active mechanism of base flipping.
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Nucleic Acids Res,
35,
1478-1487.
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M.Ghosh,
N.Rumpal,
U.Varshney,
and
K.V.Chary
(2002).
Structural basis for poor uracil excision from hairpin DNA. An NMR study.
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Eur J Biochem,
269,
1886-1894.
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PDB codes:
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The most recent references are shown first.
Citation data come partly from CiteXplore and partly
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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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