Results 251 to 260 of about 496,088 (311)

Cyclic transformation of stable/metastable nucleic acid structures enables dynamic monitoring of ATP in living cells. [PDF]

Chem Sci
Su ML, Yang J, Yang WG, Ye ZX, Wang RW, Qin JM, Song DQ, Yuan R, Ma PY, Zhuo Y, Yang C, Liang WB.   +11 more
europepmc   +1 more source

Temperature-Dependent Conformational Dynamics of Substrate Entrance Loops in β-Glucosidase: Insights from Molecular Dynamics Simulations. [PDF]

Int J Mol Sci
Nam KH.
europepmc   +1 more source

Multimerization interactions between protein-inspired single-chain random heteropolymers. [PDF]

PLoS One
Hilburg SL, Jin T, Ganesh P, Alexander-Katz A.   +3 more
europepmc   +1 more source

Some of the next articles are maybe not open access.

Related searches:

Molecular Conformation of Inosine

Nature, 1969
INOSINE is one of the rare nucleosides found in nucleic acids. It occurs especially in transfer ribonucleic acid where it appears to form part of a number of anticodons1,2. It can form a base pair with any one of the bases adenine, uracil or cytidine in the third codon1,2 position, and the possibility of atypical base pairs is part of the “wobble ...
P, Tollin, A R, Munns
openaire   +2 more sources

Molecular Conformation of GABA

Nature New Biology, 1971
CURTIS et al.1,2 have described evidence suggesting that the alkaloid bicuculline is a specific antagonist to the action of γ-aminobutyric acid (GABA), a possible inhibitory transmitter in the mammalian brain3,4. By considering structural models, they suggested3 as a stereochemical basis for this antagonism a geometrical configuration in which the N ...
E G, Steward, R, Player, J P, Quilliam, D A, Brown, M J, Pringle   +4 more
openaire   +2 more sources

Molecular Conformation of Deoxyuridine

Nature, 1971
THE structure determination of deoxyuridine was undertaken as part of a series of conformational studies of nucleic acid components. Such studies give information about the preferred conformation of nucleosides and nucleotides1,2, and may clarify the conformational differences and changes that occur in nucleic acids.
A, Rahman, H R, Wilson
openaire   +2 more sources

Molecular Conformation and Crystallization: The Case of Ethenzamide

Crystal Growth & Design, 2012
Ethenzamide is a small, conformationally labile pharmaceutical molecule which crystallizes in an unusual conformation relative to both its co-crystals and to similar molecules found in the Cambridge Structural Database. Relative to its co-crystals, large ethenzamide crystals are challenging to grow, a property which may be linked to the crystal ...
Back, Kevin R., Davey, Roger J., Grecu, Tudor, Hunter, Christopher A., Taylor, Lynne S.   +4 more
openaire   +2 more sources

Molecular Conformations of 5-Iodouridine

Nature, 1970
THE structure of unusual nucleic acid components is of importance in relation to conformational and model building studies on nucleic acids in general and those concerning tRNA in particular. In the case of 5-iodouridine (Fig. 1) it is particularly desirable to know the crystal structure in order to compare the effects of ionizing radiation on single ...
A, Rahman, H R, Wilson
openaire   +2 more sources

Molecular conformation of prostaglandin A1

Prostaglandins, 1973
Abstract The crystal and molecular structure of prostaglandin A1 (PGA1) has been determined by X-ray diffraction. (Space group P212121, a = 18.10 A A , b = 21.09 A A , c = 5.42, Z = 4) . Comparison of the structure of PGA1 with that of PGF1β (determined previously as the tribromobenzoate) indicates significant ...
W L, Duax, J W, Edmonds
openaire   +2 more sources

Molecular Structure and Conformation of Dinitrosylheme

Journal of the American Chemical Society, 2003
DFT calculations indicate a surprisingly strong cis orientational preference of the two NO ligands of dinitrosylheme, a unique reactive species of potential biological relevance that has been recently generated and spectroscopically characterized at low temperature.
Jeanet, Conradie, Tebikie, Wondimagegn, Abhik, Ghosh   +2 more
openaire   +2 more sources