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  2. Codon degeneracy - Wikipedia

    en.wikipedia.org/wiki/Codon_degeneracy

    A less degenerate site would produce a nonsynonymous mutation on some of the substitutions. An example (and the only) 3-fold degenerate site is the third position of an isoleucine codon. AUU, AUC, or AUA all encode isoleucine, but AUG encodes methionine. In computation, this position is often treated as a twofold degenerate site.

  3. Saturation mutagenesis - Wikipedia

    en.wikipedia.org/wiki/Saturation_mutagenesis

    Saturation mutagenesis is commonly achieved by site-directed mutagenesis PCR with a randomised codon in the primers (e.g. SeSaM) [2] or by artificial gene synthesis, with a mixture of synthesis nucleotides used at the codons to be randomised. [3] Different degenerate codons can be used to encode sets of amino acids. [1]

  4. Synonymous substitution - Wikipedia

    en.wikipedia.org/wiki/Synonymous_substitution

    This is possible because the genetic code is "degenerate", meaning that some amino acids are coded for by more than one three-base-pair codon; since some of the codons for a given amino acid differ by just one base pair from others coding for the same amino acid, a mutation that replaces the "normal" base by one of the alternatives will result ...

  5. Codon usage bias - Wikipedia

    en.wikipedia.org/wiki/Codon_usage_bias

    Codon usage bias in Physcomitrella patens. Codon usage bias refers to differences in the frequency of occurrence of synonymous codons in coding DNA. A codon is a series of three nucleotides (a triplet) that encodes a specific amino acid residue in a polypeptide chain or for the termination of translation (stop codons).

  6. Missense mutation - Wikipedia

    en.wikipedia.org/wiki/Missense_mutation

    In the most common variant of sickle-cell disease, the 20th nucleotide of the gene for the beta chain of hemoglobin is altered from the codon GAG to GTG. Thus, the 6th amino acid glutamic acid is substituted by valine—notated as an "E6V" mutation—and the protein is sufficiently altered to cause the sickle-cell disease. [5]

  7. Silent mutation - Wikipedia

    en.wikipedia.org/wiki/Silent_mutation

    The premature insertion of a stop codon, a nonsense mutation, can alter the primary structure of a protein. [12] In this case, a truncated protein is produced. Protein function and folding is dependent on the position in which the stop codon was inserted and the amount and composition of the sequence lost.

  8. 3-Base Periodicity Property - Wikipedia

    en.wikipedia.org/wiki/3-Base_Periodicity_Property

    However, in a protein-coding sequence, the DNA sequence is made up of a string of codons which correspond to amino acids. Because the genetic code is degenerate (more than one codon map to a single amino acid) and samples from the amino acids rather than the codons, the codons are not sampled uniformly thus leading to differences in the PCFs.

  9. Degeneracy (biology) - Wikipedia

    en.wikipedia.org/wiki/Degeneracy_(biology)

    Examples of degeneracy are found in the genetic code, when many different nucleotide sequences encode the same polypeptide; in protein folding, when different polypeptides fold to be structurally and functionally equivalent; in protein functions, when overlapping binding functions and similar catalytic specificities are observed; in metabolism, when multiple, parallel biosynthetic and ...