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  2. Iodoacetamide - Wikipedia

    en.wikipedia.org/wiki/Iodoacetamide

    Iodoacetamide (IAA) is an organic compound with the chemical formula I C H 2 CO NH 2. It is an alkylating agent used for peptide mapping purposes. Its actions are similar to those of iodoacetate. It is commonly used to bind covalently with the thiol group of cysteine so the protein cannot form disulfide bonds.

  3. In-gel digestion - Wikipedia

    en.wikipedia.org/wiki/In-gel_digestion

    In course of the subsequent irreversible alkylation of the SH groups with iodoacetamide the cysteines are transformed to the stable S-carboxyamidomethylcysteine (CAM; adduct: -CH 2-CONH 2). The molecular weight of the cysteine amino-acid residue is thereby increased from 103.01 Da to 160.03 Da.

  4. Iodoacetic acid - Wikipedia

    en.wikipedia.org/wiki/Iodoacetic_acid

    It is often used to modify −SH groups to prevent the re-formation of disulfide bonds after the reduction of cystine residues to cysteine during protein sequencing. In 1929, Dr. Einar Lundsgaard (1899-1968) discovered that muscle poisoned in vitro with iodoacetic acid is unable to produce lactate as glycolysis from muscle glycogen is blocked ...

  5. Isotope-coded affinity tag - Wikipedia

    en.wikipedia.org/wiki/Isotope-coded_affinity_tag

    An isotope-coded affinity tag (ICAT) is an in-vitro isotopic labeling method used for quantitative proteomics by mass spectrometry that uses chemical labeling reagents. [1] [2] [3] These chemical probes consist of three elements: a reactive group for labeling an amino acid side chain (e.g., iodoacetamide to modify cysteine residues), an isotopically coded linker, and a tag (e.g., biotin) for ...

  6. Acetaldehyde dehydrogenase - Wikipedia

    en.wikipedia.org/wiki/Acetaldehyde_dehydrogenase

    Cysteine-302 is one of three consecutive Cys residues and is crucial to the enzyme's catalytic function. The residue is alkylated by iodoacetamide in both the cytosolic and mitochondrial isozymes, with modifications to Cys-302 indicative of catalytic activity with other residues.

  7. N-Ethylmaleimide - Wikipedia

    en.wikipedia.org/wiki/N-Ethylmaleimide

    It contains the amide functional group, but more importantly it is an alkene that is reactive toward thiols and is commonly used to modify cysteine residues in proteins and peptides. [ 2 ] Organic chemistry

  8. Cystinuria - Wikipedia

    en.wikipedia.org/wiki/Cystinuria

    Initial treatment is with adequate hydration, alkalization of the urine with citrate supplementation or acetazolamide, and dietary modification to reduce salt and protein intake (especially methionine). If this fails then patients are usually started on chelation therapy with an agent such as penicillamine. [8] [9] Tiopronin is another agent ...

  9. Cysteine protease - Wikipedia

    en.wikipedia.org/wiki/Cysteine_protease

    The activity of cysteine proteases is regulated by a few general mechanisms, which includes the production of zymogens, selective expression, pH modification, cellular compartmentalization, and regulation of their enzymatic activity by endogenous inhibitors, which seemingly is the most efficient mechanism associated with the regulation of the ...