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  2. Dihydrolipoyl transacetylase - Wikipedia

    en.wikipedia.org/wiki/Dihydrolipoyl_transacetylase

    Because dihydrolipoyl transacetylase is the second of the three enzyme components participating in the reaction mechanism for conversion of pyruvate into acetyl CoA, it is sometimes referred to as E2. In humans, dihydrolipoyl transacetylase enzymatic activity resides in the pyruvate dehydrogenase complex component E2 (PDCE2) that is encoded by ...

  3. Elimination reaction - Wikipedia

    en.wikipedia.org/wiki/Elimination_reaction

    An elimination reaction is a type of organic reaction in which two substituents are removed from a molecule in either a one- or two-step mechanism. [2] The one-step mechanism is known as the E2 reaction, and the two-step mechanism is known as the E1 reaction. The numbers refer not to the number of steps in the mechanism, but rather to the ...

  4. Dehydration - Wikipedia

    en.wikipedia.org/wiki/Dehydration

    The term "dehydration" has sometimes been used incorrectly as a proxy for the separate, related condition of hypovolemia, which specifically refers to a decrease in volume of blood plasma. [3] The two are regulated through independent mechanisms in humans; [3] the distinction is important in guiding treatment. [25]

  5. Evelyn effect - Wikipedia

    en.wikipedia.org/wiki/Evelyn_effect

    A kinetic and regional chemical study of the Evelyn effect has been described. The results, in the Journal of Chemical Education, made claims involving the mechanism by which the dehydrations occurred. The article looks into the claim of having E1 and E2 mechanisms occur in the reaction.

  6. Dehydration reaction - Wikipedia

    en.wikipedia.org/wiki/Dehydration_reaction

    The classic example of a dehydration reaction is the Fischer esterification, which involves treating a carboxylic acid with an alcohol to give an ester RCO 2 H + R′OH ⇌ RCO 2 R′ + H 2 O Often such reactions require the presence of a dehydrating agent, i.e. a substance that reacts with water.

  7. Pyruvate dehydrogenase complex - Wikipedia

    en.wikipedia.org/wiki/Pyruvate_dehydrogenase_complex

    In a ring-opening S N 2-like mechanism, S2 is displaced as a sulfide or sulfhydryl moiety. Subsequent collapse of the tetrahedral intermediate ejects thiazole, releasing the TPP cofactor and generating a thioacetate on S1 of lipoate. The E1-catalyzed process is the rate-limiting step of the whole pyruvate dehydrogenase complex.

  8. Fumarase - Wikipedia

    en.wikipedia.org/wiki/Fumarase

    Figure 1 depicts the fumarase reaction mechanism. Two residues catalyze proton transfer and the ionization state of these residues is in part defined by two forms of the enzyme, E 1 and E 2. In E 1, the groups exist in an internally neutralized AH/B: state, while in E 2, they occur in a zwitterionic A − /BH + state.

  9. Ubiquitin-activating enzyme - Wikipedia

    en.wikipedia.org/wiki/Ubiquitin-activating_enzyme

    However, the transthioesterification process is very complicated, as both E1 and E2 enzymes form an intermediate complex wherein both enzymes undergo a series of conformational changes in order to bind with one another. [5] Throughout this mechanism, the E1 enzyme is bound to two ubiquitin molecules.