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  2. Missense mutation - Wikipedia

    en.wikipedia.org/wiki/Missense_mutation

    Missense mutation is a type of nonsynonymous substitution in a DNA sequence. Two other types of nonsynonymous substitution are the nonsense mutations, in which a codon is changed to a premature stop codon that results in truncation of the resulting protein, and the nonstop mutations, in which a stop codon erasement results in a longer ...

  3. Missense mRNA - Wikipedia

    en.wikipedia.org/wiki/Missense_mRNA

    Site-directed mutagenesis is a technique often employed to create knock-in and knock-out models that express missense mRNAs. For example, in knock-in studies, human orthologs are identified in model organisms to introduce missense mutations, [7] or a human gene with a substitution mutation is integrated into the genome of the model organism. [8]

  4. 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. Notable mutations

  5. Nonsynonymous substitution - Wikipedia

    en.wikipedia.org/wiki/Nonsynonymous_substitution

    Nonsense mutations are nonsynonymous substitutions that arise when a mutation in the DNA sequence causes a protein to terminate prematurely by changing the original amino acid to a stop codon. Another type of mutation that deals with stop codons is known as a nonstop mutation or readthrough mutation, which occurs when a stop codon is exchanged ...

  6. Nonsense-mediated decay - Wikipedia

    en.wikipedia.org/wiki/Nonsense-mediated_decay

    They collected his DNA and amplified it using PCR. Sequencing analysis revealed a homozygous single substitution determining a stop codon. This caused an aberrant protein and the corresponding amino acid sequence indicated the exact position of the homozygous nucleotide. The substitution was localized in exon 3 and nonsense mutation at codon 68.

  7. Ka/Ks ratio - Wikipedia

    en.wikipedia.org/wiki/Ka/Ks_ratio

    A point mutation causing a nonsynonymous substitution; Type of structure Before Change After Result Codon in a DNA sequence: GAG: Missense mutation; Nonsynonymous substitution: GTG: ↓ codes for: ↓ codes for ↓ codes for: Amino acid in a Protein: Glutamic acid structural change: Valine Altered protein may or may not cause harm

  8. Glossary of cellular and molecular biology (M–Z) - Wikipedia

    en.wikipedia.org/wiki/Glossary_of_cellular_and...

    For example, a guanine paired with a thymine would be a mismatch, as guanine normally pairs with cytosine. [12] mismatch repair (MMR) missense mutation A type of point mutation which results in a codon that codes for a different amino acid than in the unmutated sequence. Compare nonsense mutation. mistranslation

  9. Nonsense mutation - Wikipedia

    en.wikipedia.org/wiki/Nonsense_mutation

    In other words, this means that the mutation does not positively or negatively affect the organism. As this effect is unnoticed, there is a lack of papers describing such mutations. An example of this type of nonsense mutation is one that occurs directly before the original stop codon for that given protein. [8]