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PDBsum entry 1zf7
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PDB id:
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DNA
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Title:
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Gac duplex b-DNA
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Structure:
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5'-d( Cp Cp Gp Tp Cp Gp Ap Cp Gp G)-3'. Chain: a, b. Engineered: yes
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Source:
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Synthetic: yes. Other_details: DNA was synthesized on an applied biosystems DNA synthesizer using phosphoramidite chemistry, with the trityl- protecting group left intact at the 5'-terminal nucleotide then deprotected by treatment with 3% acetic acid for fifteen minutes, neutralized with ammonium hydroxide, and desalted on a sigma g-25 sephadex column.
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Resolution:
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1.05Å
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R-factor:
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0.276
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R-free:
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0.288
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Authors:
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F.A.Hays,A.T.Teegarden,Z.J.R.Jones,M.Harms,D.Raup,J.Watson, E.Cavaliere,P.S.Ho
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Key ref:
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F.A.Hays
et al.
(2005).
How sequence defines structure: a crystallographic map of DNA structure and conformation.
Proc Natl Acad Sci U S A,
102,
7157-7162.
PubMed id:
DOI:
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Date:
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20-Apr-05
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Release date:
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10-May-05
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Headers
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References
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C-C-G-T-C-G-A-C-G-G
10 bases
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C-C-G-T-C-G-A-C-G-G
10 bases
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DOI no:
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Proc Natl Acad Sci U S A
102:7157-7162
(2005)
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PubMed id:
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How sequence defines structure: a crystallographic map of DNA structure and conformation.
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F.A.Hays,
A.Teegarden,
Z.J.Jones,
M.Harms,
D.Raup,
J.Watson,
E.Cavaliere,
P.S.Ho.
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ABSTRACT
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The fundamental question of how sequence defines conformation is explicitly
answered if the structures of all possible sequences of a macromolecule are
determined. We present here a crystallographic screen of all permutations of the
inverted repeat DNA sequence d(CCnnnN6N7N8GG), where N6, N7, and N8 are any of
the four naturally occurring nucleotides. At this point, 63 of the 64 possible
permutations have been crystallized from a defined set of solutions. When
combined with previous work, we have assembled a data set of 37 single-crystal
structures from 29 of the sequences in this motif, representing three structural
classes of DNA (B-DNA, A-DNA, and four-stranded Holliday junctions). This data
set includes a unique set of amphimorphic sequence, those that crystallize in
two different conformations and serve to bridge the three structural phases. We
have thus constructed a map of DNA structures that can be walked through in
single nucleotide steps. Finally, the resulting data set allows us to dissect in
detail the stabilization of and conformational variations within structural
classes and identify significant conformational deviations within a particular
structural class that result from sequence rather than crystal or
crystallization effects.
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Selected figure(s)
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Figure 2.
Fig. 2. Map of DNA structure space sampled by crystals of
d(CCnnnN[6]N[7]N[8]GG). The map is divided into three specific
structural classes (labeled B for B-DNA, A for A-DNA, and J for
junctions) and the interfaces between each conformational phase.
The sequences in uppercase letters define those that have been
uniquely solved or reproduced in the current study, while those
in lowercase letters are structures from previous studies, but
not reproduced here. The rectangle around GCC indicates that the
structure is induced by a change in divalent cations (from Ca^2+
to Mg2+). Similarly, the oval around GGC indicates that the A
form is induced by alcohol. Arrows trace paths through the
conformational map as the N[6]N[7]N[8] trinucleotide undergoes
single-nucleotide transitions or transversions. These are not
unique paths, but show one set of consistent single-nucleotide
steps through the conformational space.
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Figure 3.
Fig. 3. Correlating sequence effects to atomic interactions
in junctions. The interactions that are identified as being
important for fixing the junction in ACC are shown in the
insets. General rules for junction-forming sequences are noted
in green, red, and blue for the nucleotides N[6], N[7], and
N[8], respectively. The inset for the cytosine C[8] to phosphate
of N[7] is rotated relative to the orientation of the overall
structure.
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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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S.Venkadesh,
P.K.Mandal,
and
N.Gautham
(2011).
The sequence d(CGGCGGCCGC) self-assembles into a two dimensional rhombic DNA lattice.
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Biochem Biophys Res Commun,
407,
548-551.
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PDB code:
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B.Heddi,
C.Oguey,
C.Lavelle,
N.Foloppe,
and
B.Hartmann
(2010).
Intrinsic flexibility of B-DNA: the experimental TRX scale.
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Nucleic Acids Res,
38,
1034-1047.
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R.Lavery,
K.Zakrzewska,
D.Beveridge,
T.C.Bishop,
D.A.Case,
T.Cheatham,
S.Dixit,
B.Jayaram,
F.Lankas,
C.Laughton,
J.H.Maddocks,
A.Michon,
R.Osman,
M.Orozco,
A.Perez,
T.Singh,
N.Spackova,
and
J.Sponer
(2010).
A systematic molecular dynamics study of nearest-neighbor effects on base pair and base pair step conformations and fluctuations in B-DNA.
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Nucleic Acids Res,
38,
299-313.
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T.Yamamoto,
T.Uda,
T.Yamasaki,
and
T.Ohno
(2010).
Hydration effect on the optical property of a DNA fiber: first-principles and molecular dynamics studies.
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Phys Chem Chem Phys,
12,
9300-9311.
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A.G.Tsai,
A.E.Engelhart,
M.M.Hatmal,
S.I.Houston,
N.V.Hud,
I.S.Haworth,
and
M.R.Lieber
(2009).
Conformational variants of duplex DNA correlated with cytosine-rich chromosomal fragile sites.
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J Biol Chem,
284,
7157-7164.
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A.Marathe,
D.Karandur,
and
M.Bansal
(2009).
Small local variations in B-form DNA lead to a large variety of global geometries which can accommodate most DNA-binding protein motifs.
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BMC Struct Biol,
9,
24.
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C.Batchelor-McAuley,
G.G.Wildgoose,
and
R.G.Compton
(2009).
The physicochemical aspects of DNA sensing using electrochemical methods.
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Biosens Bioelectron,
24,
3183-3190.
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P.Khuu,
and
P.S.Ho
(2009).
A rare nucleotide base tautomer in the structure of an asymmetric DNA junction.
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Biochemistry,
48,
7824-7832.
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PDB code:
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P.S.Ho
(2009).
Detailed mechanism for transposition by TnpA transposase involves DNA shape rather than direct protein-DNA recognition to generate an active nucleoprotein complex.
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F1000 Biol Rep,
1,
0.
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D.Svozil,
J.Kalina,
M.Omelka,
and
B.Schneider
(2008).
DNA conformations and their sequence preferences.
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Nucleic Acids Res,
36,
3690-3706.
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M.A.Karymov,
M.Chinnaraj,
A.Bogdanov,
A.R.Srinivasan,
G.Zheng,
W.K.Olson,
and
Y.L.Lyubchenko
(2008).
Structure, dynamics, and branch migration of a DNA Holliday junction: a single-molecule fluorescence and modeling study.
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Biophys J,
95,
4372-4383.
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P.Singhal,
B.Jayaram,
S.B.Dixit,
and
D.L.Beveridge
(2008).
Prokaryotic gene finding based on physicochemical characteristics of codons calculated from molecular dynamics simulations.
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Biophys J,
94,
4173-4183.
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A.R.Voth,
F.A.Hays,
and
P.S.Ho
(2007).
Directing macromolecular conformation through halogen bonds.
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Proc Natl Acad Sci U S A,
104,
6188-6193.
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PDB codes:
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J.A.Greenbaum,
B.Pang,
and
T.D.Tullius
(2007).
Construction of a genome-scale structural map at single-nucleotide resolution.
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Genome Res,
17,
947-953.
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M.Egli,
and
P.S.Pallan
(2007).
Insights from crystallographic studies into the structural and pairing properties of nucleic acid analogs and chemically modified DNA and RNA oligonucleotides.
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Annu Rev Biophys Biomol Struct,
36,
281-305.
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S.N.Richter,
G.Giaretta,
V.Comuzzi,
E.Leo,
L.A.Mitchenall,
L.M.Fisher,
A.Maxwell,
and
M.Palumbo
(2007).
Hot-spot consensus of fluoroquinolone-mediated DNA cleavage by Gram-negative and Gram-positive type II DNA topoisomerases.
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Nucleic Acids Res,
35,
6075-6085.
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V.I.Poltev,
E.Gonzalez,
A.Deriabina,
A.Martinez,
A.Furmanchuk,
L.Gorb,
and
J.Leszczynski
(2007).
Electron correlated ab initio study of amino group flexibility for improvement of molecular mechanics simulations on nucleic Acid conformations and interactions.
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J Biol Phys,
33,
499-514.
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F.A.Hays,
V.Schirf,
P.S.Ho,
and
B.Demeler
(2006).
Solution formation of Holliday junctions in inverted-repeat DNA sequences.
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Biochemistry,
45,
2467-2471.
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G.Kudla,
L.Lipinski,
F.Caffin,
A.Helwak,
and
M.Zylicz
(2006).
High guanine and cytosine content increases mRNA levels in mammalian cells.
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PLoS Biol,
4,
e180.
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P.A.Khuu,
A.R.Voth,
F.A.Hays,
and
P.S.Ho
(2006).
The stacked-X DNA Holliday junction and protein recognition.
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J Mol Recognit,
19,
234-242.
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R.M.Doss,
M.A.Marques,
S.Foister,
D.M.Chenoweth,
and
P.B.Dervan
(2006).
Programmable oligomers for minor groove DNA recognition.
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J Am Chem Soc,
128,
9074-9079.
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S.B.Dixit,
and
D.L.Beveridge
(2006).
Structural bioinformatics of DNA: a web-based tool for the analysis of molecular dynamics results and structure prediction.
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Bioinformatics,
22,
1007-1009.
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S.Winters-Hilt,
M.Landry,
M.Akeson,
M.Tanase,
I.Amin,
A.Coombs,
E.Morales,
J.Millet,
C.Baribault,
and
S.Sendamangalam
(2006).
Cheminformatics methods for novel nanopore analysis of HIV DNA termini.
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BMC Bioinformatics,
7,
S22.
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J.Hihath,
B.Xu,
P.Zhang,
and
N.Tao
(2005).
Study of single-nucleotide polymorphisms by means of electrical conductance measurements.
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Proc Natl Acad Sci U S A,
102,
16979-16983.
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S.B.Dixit,
D.L.Beveridge,
D.A.Case,
T.E.Cheatham,
E.Giudice,
F.Lankas,
R.Lavery,
J.H.Maddocks,
R.Osman,
H.Sklenar,
K.M.Thayer,
and
P.Varnai
(2005).
Molecular dynamics simulations of the 136 unique tetranucleotide sequences of DNA oligonucleotides. II: sequence context effects on the dynamical structures of the 10 unique dinucleotide steps.
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Biophys J,
89,
3721-3740.
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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
code is
shown on the right.
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