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1 - thymine

As a ubiquitous ROS, OH is known to react efficiently with the main purine and pyrimidine bases by its addition to unsaturated bonds. There is, however, a major exception - the hydrogen abstraction reaction from the methyl group of thymine 9. [Pg.58]


In RNA the sugar is ribose and uracil replaces thymine. Different varieties of RNA exist with widely different molecular weights. Messenger RNA conveys information in the form of the sequence of bases from DNA to RNA on the ribosomes, where proteins are... [Pg.283]

It is the parent substance of a group of compounds which includes cytosine, thymine and uracil, which are constituents of nucleic acids and barbituric acid and its derivatives, which are important medicinally. [Pg.335]

Allen M J, Baloooh M, Subbiah S, Tenoh R J, Balhorn R and Siekhaus W 1991 Soanning tunnelling miorosoope images of adenine and thymine at atomio resolution Scanning Microsc. 5 625... [Pg.1722]

The DNA base pairs guanine (G), cytosine (C), adenine (A) and thymine (T). The uracil-2,6-diaminopyridine pair can also form three hydrogen bonds but has a much lower association constant than G-C. [Pg.245]

A,G,CT, (U) Adenine, guanine, cytosine, thymine - the four bases present in DNA. Urac replaces thymine in RNA... [Pg.569]

Uracil occurs only m RNA thymine occurs only m DNA... [Pg.1158]

Avery s paper prompted other biochemists to rethink their ideas about DNA One of them Erwin Chargaff of Columbia University soon discovered that the distribution of adenine thymine cytosine and guanine differed from species to species but was the same within a species and within all the cells of a species Perhaps DNA did have the capacity to carry genetic information after all Chargaff also found that regardless of the source of the DNA half the bases were purines and the other half were pyrimidines Significantly the ratio of the purine adenine (A) to the pyrimidine thymine (T) was always close to 1 1 Likewise the ratio of the purine guanine (G) to the pyrimidine cyto sine (C) was also close to 1 1 For human DNA the values are... [Pg.1166]

Base pair (Section 28 7) Term given to the punne of a nu cleotide and its complementary pyrimidine Adenine (A) is complementary to thymine (T) and guanine (G) is comple mentary to cytosine (C)... [Pg.1277]

Fig. 21. (a) Diagrammatical representation of an allosteric receptor mechanism (b) allosteric binding of a thymine derivative promoted on uptake (34). [Pg.186]

The mode of action has been a subject for research for a number of years. While it was originally thought that maleic hydrazide replaced uracil in the RNA sequence, it has been deterrnined that the molecule may be a pyrimidine or purine analogue and therefore base-pair formation is possible with uracil and thymine and there exists the probabiHty of base-pair formation with adenine however, if maleic hydrazide occurs in an in vivo system as the diketo species, then there remains the possibiHty of base-pairing with guanine (50). Whatever the mechanism, it is apparent that the inhibitory effects are the result of a shutdown of the de novo synthesis of protein. [Pg.425]

The primary stmcture of DNA is based on repeating nucleotide units, where each nucleotide is made up of the sugar, ie, 2 -deoxyribose, a phosphate, and a heterocycHc base, N. The most common DNA bases are the purines, adenine (A) and guanine (G), and the pyrimidines, thymine (T) and cytosine (C) (Fig. 1). The base, N, is bound at the I -position of the ribose unit through a heterocycHc nitrogen. [Pg.248]

Fig. 11. The amidite method for synthesizing oligodeoxynucleotides, where B and represent one of the protected bases thymine, A/ -benzoylcytosine,... Fig. 11. The amidite method for synthesizing oligodeoxynucleotides, where B and represent one of the protected bases thymine, A/ -benzoylcytosine,...
Modified oligonucleotides can be used to cross-link DNA sequences via a reactive group tethered to an oligonucleotide. When irradiated with uv light, psoralens (31) reacts with thymine bases, and the reaction yields a cross-link if the thymine residues are adjacent to each other on opposite strands. Psoralen linked to oligonucleotides have been shown to induce site-specific cross-links in vitro (51). [Pg.266]

Cellular Protein Biosynthesis. The process of cellular protein biosynthesis is virtually the same in all organisms. The information which defines the amino acid sequence of a protein is encoded by its corresponding sequence of DNA (the gene). The DNA is composed of two strands of polynucleotides, each comprising some arrangement (sequence) of the four nucleotide building blocks of the nucleic acids adenine (A), thymine (T),... [Pg.196]

The sugars are typically ribose (ribonucleic acids, RNA), or 2-deoxyribose (deoxyribonucleic acids, DNA). There are five common bases in nucleic acids adenine (A) thymine (T) uracil (U) cytosine (C) and guanine (G). DNA polymers incorporate the four bases. A, T, C, and G, and RNA, the set A, U, C, and G. [Pg.94]


See other pages where 1 - thymine is mentioned: [Pg.52]    [Pg.283]    [Pg.284]    [Pg.397]    [Pg.397]    [Pg.397]    [Pg.1722]    [Pg.245]    [Pg.343]    [Pg.1157]    [Pg.1164]    [Pg.1165]    [Pg.1166]    [Pg.1166]    [Pg.1167]    [Pg.1168]    [Pg.1175]    [Pg.577]    [Pg.327]    [Pg.21]    [Pg.992]    [Pg.992]    [Pg.186]    [Pg.210]    [Pg.228]    [Pg.248]    [Pg.254]    [Pg.467]    [Pg.199]    [Pg.227]    [Pg.127]   
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1- thymine biological activity

1- thymine synthesis

2,6-diamino-triazine/thymine

5-Fluorouracil thymine nucleotide synthesis

5-methyluracil. thymine

Adenine base pairing with thymine

Adenine thymine ratio

Adenine, pairing with thymine

Adenine, pairing with thymine deoxyribonucleic acid

Adenine, tautomerism base pair with thymine and uracil

Adenine-thymine base pair

Adenine-thymine interactions

Adenine-thymine pairing

Adenine-thymine radical cations, proton

Adenine-thymine radical cations, proton transfer

Adenine.. .thymine Watson-Crick base pair

Adenine/thymine, hydrogen bonding

Adsorption thymine

Binding thymine

Biosynthesis of thymine deoxyribonucleotides

Bromine Activation of Thymine, Guanine, and Cytosine

Cycloaddition reactions thymine dimers

DNA thymine

Deoxyribonucleic acid thymine

Dipole moments thymine

Electron addition, thymine hydroperoxides

Hydrogen addition, thymine hydroperoxides

Hydrogen bonding adenine-thymine pairs

Hydroxyl radical thymine oxidation

In thymine

Intrastrand thymine dimer

L- thymine

Morse Potential Energy Curves Cytosine, Thymine

Morse Potential Energy Curves for Thymine and Cytosine

Oligo thymine

Ozonolysis thymine

Photochemical substitution thymine

Photodimerization of thymine

Photophysics thymine

Photoreactions of Thymines and Related Compounds

Photoreactions of Thymines, etc

Photostimulated Degenerate Ring Transformations of Thymines

Polynucleotides adenine-thymine base pairs

Products Derived from the Thymine Moiety

Pyrimidine Thymine

Pyrimidine bases thymine

Quantum chemical calculations thymine

Radical anion thymine

Ring-saturated thymine derivatives

Rotational constants thymine

SUBJECTS thymin

SUBJECTS thymine

Serine thymine

Solvated electron addition, thymine

Solvated electron addition, thymine hydroperoxide formation

Surfaces thymine

Tautomerism of Uracil and Thymine

Tautomerism thymine

Thio thymine

Three- thymine

Thymin

Thymine 1 - conjugate

Thymine 1-methyl

Thymine 2,3 -imino-1 -

Thymine 5 -phosphate

Thymine 5-methyl cytosine

Thymine 6-4 photoproduct

Thymine 6-amino

Thymine Crosslinks

Thymine DNA glycosylases

Thymine Raman spectra

Thymine Tautomer energy

Thymine activity

Thymine analogs

Thymine analysis

Thymine atom

Thymine bacterial synthesis

Thymine base damage, distortions

Thymine base pairing and

Thymine bases

Thymine canonical forms

Thymine catabolism

Thymine chromatography

Thymine conical intersections

Thymine cycloaddition

Thymine definition

Thymine degradation

Thymine deoxyriboside

Thymine derivatives

Thymine detection

Thymine dimer

Thymine dimer formation

Thymine dimer scission

Thymine dimerization, quantum

Thymine dimers excision

Thymine dimers, long-range repair

Thymine dimers, monomerization

Thymine dioxygenase

Thymine dipeptide

Thymine discovery

Thymine excision

Thymine formation

Thymine formation from uracil

Thymine glycol

Thymine hydrates

Thymine hydrogen bonding

Thymine hydroperoxides

Thymine hydroperoxides characterization

Thymine hydroperoxides decomposition

Thymine hydroperoxides nucleoside

Thymine hydroxyl radical-mediated oxidation

Thymine in DNA

Thymine in Water

Thymine lesions, ring-saturated

Thymine metal complexes

Thymine moieties

Thymine nucleoside phosphorylase

Thymine nucleosides containing

Thymine nucleotide

Thymine orientation

Thymine oxidation

Thymine oxidation potential

Thymine oxidation, bacterial

Thymine pairs

Thymine parameters

Thymine pentofuranosyl)

Thymine phosphonate

Thymine photochemistry

Thymine polyoxin

Thymine preparation

Thymine production blocking

Thymine psoralen photoreaction

Thymine pyrimidine structure

Thymine quantum mechanical studies

Thymine reaction

Thymine reaction with

Thymine reaction with psoralen

Thymine repair

Thymine structural formula

Thymine structure

Thymine structure and reactivity

Thymine tautomeric forms

Thymine tautomers

Thymine vibrational structure

Thymine, 1 - , antitumor activity

Thymine, 1-methyl-, structure

Thymine, and Uracil

Thymine, configuration

Thymine, dimerisation

Thymine, dimerization

Thymine, electrostatic potential

Thymine, electrostatic potential structure

Thymine, from desoxyribosenucleic acid desoxyribose nucleoside

Thymine, methylation

Thymine, molecular orbitals, energy

Thymine, nucleosides

Thymine, photodimerization

Thymine, reversible

Thymine, reversible photodimerization

Thymine-3-propenal

Thymine-7-hydroxylase

Thymine-DNA glycosylase

Thymine-containing polymers

Thymine-cytosine base pair

Thymine-guanine

Thymine-uraciluria

Thymine/adenine

Thymine/triazine

Uracil (U) and Thymine (T)

Uracil-thymine oxidase

Why DNA Contains Thymine Instead of Uracil

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