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NITROGEN-CONTAINING BIOLOGICAL COMPOUNDS THAT FORM NUCLEOSIDES
Nitrogeneous bases; Nitrogenous bases; Nitrogenous base; Nucleobases; N-base; N-Base; N-Bases; N-bases; Nucleobase transport proteins; DNA base; RNA base; ACGT; ACGU; DNA bases; Nucleotide bases; Nitrogen base; Nucleotide base; Nucleic base; Base (genetics)
  • Chemical structure of 5-methylcytidine
  • Chemical structure of 5-methylcytosine
  • Chemical structure of 7-methylguanosine
  • Chemical structure of 7-methylguanine
  • Base pairing: Two [[base pair]]s are produced by four nucleotide monomers, nucleobases are ''in blue''. Guanine (G) is paired with cytosine (C) via ''three'' [[hydrogen bond]]s, ''in red''. Adenine (A) is paired with uracil (U) via ''two'' hydrogen bonds, ''in red''.
  • Purine nucleobases are fused-ring molecules.
  • Pyrimidine nucleobases are simple ring molecules.
  • directionality]] of each of the two phosphate-deoxyribose backbones, or strands. The 5' to 3' (''read'' "5 prime to 3 prime") directions are: ''down'' the strand on the left, and ''up'' the strand on the right. The strands twist around each other to form a double helix structure.
  • Chemical structure of dihydrouracil
  • Chemical structure of dihydrouridine
  • Chemical structure of 5-hydroxymethylcytosine
  • Chemical structure of hypoxanthine
  • Chemical structure of inosine
  • 87px
  • Chemical structure of xanthine
  • Chemical structure of xanthosine

nitrogenous      
adj. αζωτούχος

Definitie

nitrogen
Nitrogen is a colourless element that has no smell and is usually found as a gas. It forms about 78% of the earth's atmosphere, and is found in all living things.
N-UNCOUNT

Wikipedia

Nucleobase

Nucleobases (nitrogenous bases or simply bases) are nitrogen-containing biological compounds that form nucleosides, which, in turn, are components of nucleotides, with all of these monomers constituting the basic building blocks of nucleic acids. The ability of nucleobases to form base pairs and to stack one upon another leads directly to long-chain helical structures such as ribonucleic acid (RNA) and deoxyribonucleic acid (DNA). Five nucleobases—adenine (A), cytosine (C), guanine (G), thymine (T), and uracil (U)—are called primary or canonical. They function as the fundamental units of the genetic code, with the bases A, G, C, and T being found in DNA while A, G, C, and U are found in RNA. Thymine and uracil are distinguished by merely the presence or absence of a methyl group on the fifth carbon (C5) of these heterocyclic six-membered rings. In addition, some viruses have aminoadenine (Z) instead of adenine. It differs in having an extra amine group, creating a more stable bond to thymine.

Adenine and guanine have a fused-ring skeletal structure derived of purine, hence they are called purine bases. The purine nitrogenous bases are characterized by their single amino group (−NH2), at the C6 carbon in adenine and C2 in guanine. Similarly, the simple-ring structure of cytosine, uracil, and thymine is derived of pyrimidine, so those three bases are called the pyrimidine bases.

Each of the base pairs in a typical double-helix DNA comprises a purine and a pyrimidine: either an A paired with a T or a C paired with a G. These purine-pyrimidine pairs, which are called base complements, connect the two strands of the helix and are often compared to the rungs of a ladder. Only pairing purine with pyrimidine ensures a constant width for the DNA. The A–T pairing is based on two hydrogen bonds, while the C–G pairing is based on three. In both cases, the hydrogen bonds are between the amine and carbonyl groups on the complementary bases.

Nucleobases such as adenine, guanine, xanthine, hypoxanthine, purine, 2,6-diaminopurine, and 6,8-diaminopurine may have formed in outer space as well as on earth.

The origin of the term base reflects these compounds' chemical properties in acid–base reactions, but those properties are not especially important for understanding most of the biological functions of nucleobases.