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  2. Sirtuin 4 - Wikipedia

    en.wikipedia.org/wiki/Sirtuin_4

    75387 Ensembl ENSG00000089163 ENSMUSG00000029524 UniProt Q9Y6E7 Q8R216 RefSeq (mRNA) NM_012240 NM_001385733 NM_001385734 NM_001385735 NM_001167691 NM_133760 RefSeq (protein) NP_036372 NP_001161163 NP_598521 Location (UCSC) Chr 12: 120.3 – 120.31 Mb Chr 5: 115.48 – 115.48 Mb PubMed search Wikidata View/Edit Human View/Edit Mouse Sirtuin 4, also known as SIRT4, is a mitochondrial protein ...

  3. Apamin - Wikipedia

    en.wikipedia.org/wiki/Apamin

    Apamin selectively blocks SK channels, a type of Ca 2+-activated K + channel expressed in the central nervous system. Toxicity is caused by only a few amino acids, in particular cysteine 1, lysine 4, arginine 13, arginine 14 and histidine 18. These amino acids are involved in the binding of apamin to the Ca 2+-activated K + channel.

  4. Sirtuin - Wikipedia

    en.wikipedia.org/wiki/Sirtuin

    [2] [3] They are ancient in animal evolution and appear to possess a highly conserved structure throughout all kingdoms of life. [2] Chemically, sirtuins are a class of proteins that possess either mono- ADP-ribosyltransferase or deacylase activity, including deacetylase, desuccinylase , demalonylase , demyristoylase and depalmitoylase activity.

  5. Pleckstrin homology domain - Wikipedia

    en.wikipedia.org/wiki/Pleckstrin_homology_domain

    Pleckstrin homology domain (PH domain) or (PHIP) is a protein domain of approximately 120 amino acids that occurs in a wide range of proteins involved in intracellular signaling or as constituents of the cytoskeleton.

  6. Amino acid - Wikipedia

    en.wikipedia.org/wiki/Amino_acid

    Amino acids with the structure NH + 3 −CXY−CXY−CO − 2, such as β-alanine, a component of carnosine and a few other peptides, are β-amino acids. Ones with the structure NH + 3 −CXY−CXY−CXY−CO − 2 are γ-amino acids, and so on, where X and Y are two substituents (one of which is normally H). [7]

  7. S-Aminoethyl-L-cysteine - Wikipedia

    en.wikipedia.org/wiki/S-Aminoethyl-L-cysteine

    S-Aminoethyl-l-cysteine, also known as thialysine, is a toxic analog of the amino acid lysine in which the second carbon of the amino acid's R-group (side chain) has been replaced with a sulfur atom. Strictly speaking, L-thialysine is actually considered an S-(2-aminoethyl) analogue of L-cysteine.

  8. ADDA (amino acid) - Wikipedia

    en.wikipedia.org/wiki/ADDA_(amino_acid)

    ADDA ((all-S,all-E)-3-amino-9-methoxy-2,6,8-trimethyl-10-phenyldeca-4,6-dienoic acid) is a non-proteinogenic amino acid found in toxins made by cyanobacteria. Toxins which include this amino acid include microcystins [1] and nodularins. Along with leucine and arginine, it is found in microcystin-LR, an extremely toxic compound produced by ...

  9. Stable isotope labeling by amino acids in cell culture

    en.wikipedia.org/wiki/Stable_isotope_labeling_by...

    One of the cell populations is fed with growth medium containing normal amino acids. In contrast, the second population is fed with growth medium containing amino acids labeled with stable (non-radioactive) heavy isotopes. For example, the medium can contain arginine labeled with six carbon-13 atoms (13 C) instead of the normal carbon-12 (12 C ...