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  2. Disulfide - Wikipedia

    en.wikipedia.org/wiki/Disulfide

    The structure of a disulfide bond can be described by its χ ss dihedral angle between the C β −S γ −S γ −C β atoms, which is usually close to ±90°. The disulfide bond stabilizes the folded form of a protein in several ways: It holds two portions of the protein together, biasing the protein towards the folded topology.

  3. Peptide synthesis - Wikipedia

    en.wikipedia.org/wiki/Peptide_synthesis

    The formation of multiple native disulfides remains challenging of native peptide synthesis by solid-phase methods. Random chain combination typically results in several products with nonnative disulfide bonds. [41] Stepwise formation of disulfide bonds is typically the preferred method, and performed with thiol protecting groups. [42]

  4. DsbC protein family - Wikipedia

    en.wikipedia.org/wiki/DsbC_protein_family

    DsbC (Disulfide bond C) is a prokaryotic disulfide bond isomerase. The formation of native disulfide bonds play an important role in the proper folding of proteins and stabilize tertiary structures of the protein. [1] [2] [3] DsbC is one of 6 proteins in the Dsb family in prokaryotes. The other proteins are DsbA, DsbB, DsbD, DsbE and DsbG. [4]

  5. TCEP - Wikipedia

    en.wikipedia.org/wiki/TCEP

    TCEP is often used as a reducing agent to break disulfide bonds within and between proteins as a preparatory step for gel electrophoresis.. Compared to the other two most common agents used for this purpose (dithiothreitol and β-mercaptoethanol), TCEP has the advantages of being odorless, a more powerful reducing agent, an irreversible reducing agent (in the sense that TCEP does not ...

  6. DsbA - Wikipedia

    en.wikipedia.org/wiki/DsbA

    DsbA is a bacterial thiol disulfide oxidoreductase (TDOR). DsbA is a key component of the Dsb (disulfide bond) family of enzymes. DsbA catalyzes intrachain disulfide bond formation as peptides emerge into the cell's periplasm. [2] Structurally, DsbA contains a thioredoxin domain with an inserted helical domain of unknown function. [3]

  7. Thioredoxin - Wikipedia

    en.wikipedia.org/wiki/Thioredoxin

    The primary function of thioredoxin (Trx) is the reduction of oxidized cysteine residues and the cleavage of disulfide bonds. [10] Multiple in vitro substrates for thioredoxin have been identified, including ribonuclease, choriogonadotropins, coagulation factors, glucocorticoid receptor, and insulin.

  8. Thiuram disulfide - Wikipedia

    en.wikipedia.org/wiki/Thiuram_disulfide

    The C(S)−N bond is short (1.33 Å), indicative of multiple bonding. The dihedral angle between the two dithiocarbamate subunits approaches 90°. [3] Structure of tetramethylthiuram disulfide, emphasizing the 90º dihedral angle between the two planar subunits. Thiuram disulfides are weak oxidants. They can be reduced to dithiocarbamates.

  9. 2,2'-Dipyridyldisulfide - Wikipedia

    en.wikipedia.org/wiki/2,2'-Dipyridyldisulfide

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