enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Protein phosphorylation - Wikipedia

    en.wikipedia.org/wiki/Protein_phosphorylation

    It was found that an enzyme, named phosphorylase kinase and Mg-ATP were required to phosphorylate glycogen phosphorylase by assisting in the transfer of the γ-phosphoryl group of ATP to a serine residue on phosphorylase b. Protein phosphatase 1 is able to catalyze the dephosphorylation of phosphorylated enzymes by removing the phosphate group.

  3. Protein kinase inhibitor - Wikipedia

    en.wikipedia.org/wiki/Protein_kinase_inhibitor

    A protein kinase inhibitor (PKI) is a type of enzyme inhibitor that blocks the action of one or more protein kinases. [1] Protein kinases are enzymes that phosphorylate (add a phosphate , or PO 4 , group) to a protein and can modulate its function.

  4. Phosphorylase kinase - Wikipedia

    en.wikipedia.org/wiki/Phosphorylase_kinase

    Phosphorylase kinase (PhK) is a serine/threonine-specific protein kinase which activates glycogen phosphorylase to release glucose-1-phosphate from glycogen.PhK phosphorylates glycogen phosphorylase at two serine residues, triggering a conformational shift which favors the more active glycogen phosphorylase "a" form over the less active glycogen phosphorylase b.

  5. Phosphorylase - Wikipedia

    en.wikipedia.org/wiki/Phosphorylase

    Phosphorylase a is the more active R form of glycogen phosphorylase that is derived from the phosphorylation of the less active R form, phosphorylase b with associated AMP. The inactive T form is either phosphorylated by phosphoylase kinase and inhibited by glucose, or dephosphorylated by phosphoprotein phosphatase with inhibition by ATP and/or ...

  6. Protein kinase - Wikipedia

    en.wikipedia.org/wiki/Protein_kinase

    Above is a ball-and-stick model of the inorganic phosphate molecule (H PO 4 2−).Colour coding: P (orange); O (red); H (white). The chemical activity of a protein kinase involves removing a phosphate group from ATP and covalently attaching it to one of three amino acids that have a free hydroxyl group.

  7. Pyruvate dehydrogenase kinase - Wikipedia

    en.wikipedia.org/wiki/Pyruvate_dehydrogenase_kinase

    The primary sequencing between the four isozymes are conserved with 70% identity. The greatest differences occur near the N-terminus. [2] PDK1 is the largest of the four with 436 residues while PDK2, PDK3 and PDK4 have 407, 406, and 411 residues respectively. The isozymes have different activity and phosphorylation rates at each site.

  8. Protein kinase C - Wikipedia

    en.wikipedia.org/wiki/Protein_kinase_C

    Protein kinase C inhibitors, such as ruboxistaurin, may potentially be beneficial in peripheral diabetic nephropathy. [26] Chelerythrine is a natural selective PKC inhibitor. Other naturally occurring PKCIs are miyabenol C, myricitrin, gossypol. Bryostatin 1 can act as a PKC inhibitor; It was investigated for cancer.

  9. Protein phosphatase - Wikipedia

    en.wikipedia.org/wiki/Protein_phosphatase

    A protein phosphatase is a phosphatase enzyme that removes a phosphate group from the phosphorylated amino acid residue of its substrate protein. Protein phosphorylation is one of the most common forms of reversible protein posttranslational modification (), with up to 30% of all proteins being phosphorylated at any given time.