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  2. Click chemistry - Wikipedia

    en.wikipedia.org/wiki/Click_chemistry

    The synthesis of luciferin exemplifies another strategy of isolating reaction partners, which is to take advantage of rarely-occurring, natural groups such as the 1,2-aminothiol, which appears only when a cysteine is the final N' amino acid in a protein. Their natural selectivity and relative bioorthogonality is thus valuable in developing ...

  3. Food Wars! Shokugeki no Soma season 3 - Wikipedia

    en.wikipedia.org/wiki/Food_Wars!_Shokugeki_no...

    Day 3 passes without much improvement. Soma notices that though Kuga is getting steady business, the long wait time and the need for quick eating at peak times frustrates the diners. On Day 4, Soma adds tables and chairs to his booth, and a remade version of his Yukihira-style mapo tofu by adding noodles and a giant mystery meatball with curry ...

  4. Cystine - Wikipedia

    en.wikipedia.org/wiki/Cystine

    Cystine is the oxidized derivative of the amino acid cysteine and has the formula (SCH 2 CH(NH 2)CO 2 H) 2.It is a white solid that is poorly soluble in water. As a residue in proteins, cystine serves two functions: a site of redox reactions and a mechanical linkage that allows proteins to retain their three-dimensional structure.

  5. List of Food Wars!: Shokugeki no Soma chapters - Wikipedia

    en.wikipedia.org/wiki/List_of_Food_Wars...

    The Food Wars!:Shokugeki no Soma manga is written by Yūto Tsukuda and published by Shueisha in Weekly Shōnen Jump and Jump Giga! for its 3-part epilogue. It began as a one-shot in April 2012 and then began as a series in November 2012 and then ended in June 2019.

  6. Sulfur assimilation - Wikipedia

    en.wikipedia.org/wiki/Sulfur_assimilation

    The synthesis of O-acetylserine is catalyzed by serine acetyltransferase and together with O-acetylserine (thiol)lyase it is associated as enzyme complex named cysteine synthase. The formation of cysteine is the direct coupling step between sulfur (sulfur metabolism) and nitrogen assimilation in plants.

  7. Cystamine - Wikipedia

    en.wikipedia.org/wiki/Cystamine

    Cystamine (2,2'-dithiobisethanamine) is an organic disulfide.It is formed when cystine is heated, the result of decarboxylation.Cystamine is an unstable liquid and is generally handled as the dihydrochloride salt, C 4 H 12 N 2 S 2 ·2HCl, which is stable to 203-214 °C at which point it decomposes.

  8. Cystathionine beta synthase - Wikipedia

    en.wikipedia.org/wiki/Cystathionine_beta_synthase

    The lack of CBS in these tissues implies that these tissues are unable to synthesize cysteine and that cysteine must be supplied from extracellular sources. It also suggests that these tissues might have increased sensitivity to homocysteine toxicity because they cannot catabolize excess homocysteine via transsulfuration. [13]

  9. Cystathionine - Wikipedia

    en.wikipedia.org/wiki/Cystathionine

    Cystathionine is an intermediate in the synthesis of cysteine from homocysteine. It is produced by the transsulfuration pathway and is converted into cysteine by cystathionine gamma-lyase (CTH). Biosynthetically, cystathionine is generated from homocysteine and serine by cystathionine beta synthase (upper reaction in the diagram below).