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  2. Amino acid replacement - Wikipedia

    en.wikipedia.org/wiki/Amino_acid_replacement

    Amino acid replacement is a change from one amino acid to a different amino acid in a protein due to point mutation in the corresponding DNA sequence. It is caused by nonsynonymous missense mutation which changes the codon sequence to code other amino acid instead of the original.

  3. Point mutation - Wikipedia

    en.wikipedia.org/wiki/Point_mutation

    At times, a change to one amino acid in the protein is not detrimental to the organism as a whole. Most proteins can withstand one or two point mutations before their function changes. Non-conservative mutations result in an amino acid change that has different properties than the wild type. The protein may lose its function, which can result ...

  4. Conservative replacement - Wikipedia

    en.wikipedia.org/wiki/Conservative_replacement

    A conservative replacement (also called a conservative mutation or a conservative substitution or a homologous replacement) is an amino acid replacement in a protein that changes a given amino acid to a different amino acid with similar biochemical properties (e.g. charge, hydrophobicity and size). [1] [2]

  5. Missense mutation - Wikipedia

    en.wikipedia.org/wiki/Missense_mutation

    This results in an incorrect amino acid (proline) being incorporated into the protein sequence. Missense mutation refers to a change in one amino acid in a protein, arising from a point mutation in a single nucleotide. Missense mutation is a type of nonsynonymous substitution in a DNA sequence.

  6. Mutation - Wikipedia

    en.wikipedia.org/wiki/Mutation

    Amino acid substitution (e.g., D111E) – The first letter is the one letter code of the wild-type amino acid, the number is the position of the amino acid from the N-terminus, and the second letter is the one letter code of the amino acid present in the mutation. Nonsense mutations are represented with an X for the second amino acid (e.g. D111X).

  7. Frameshift mutation - Wikipedia

    en.wikipedia.org/wiki/Frameshift_mutation

    A codon is a set of three nucleotides, a triplet that codes for a certain amino acid. The first codon establishes the reading frame, whereby a new codon begins. A protein's amino acid backbone sequence is defined by contiguous triplets. [6] Codons are key to translation of genetic information for the synthesis of proteins.

  8. Synonymous substitution - Wikipedia

    en.wikipedia.org/wiki/Synonymous_substitution

    Protein translation involves a set of twenty amino acids.Each of these amino acids is coded for by a sequence of three DNA base pairs called a codon.Because there are 64 possible codons, but only 20-22 encoded amino acids (in nature) and a stop signal (i.e. up to three codons that do not code for any amino acid and are known as stop codons, indicating that translation should stop), some amino ...

  9. Molecular lesion - Wikipedia

    en.wikipedia.org/wiki/Molecular_lesion

    Tautomerization is a chemical reaction that is primarily relevant in the behavior of amino acids and nucleic acids. Both of which are correlated to DNA and RNA. The process of tautomerization of DNA bases occurs during DNA replication. The ability for the wrong tautomer of one of the standard nucleic bases to mispair causes a mutation during ...