Literature DB >> 2969753

Processing reactions in the later stages of hormone activation.

A Bleakman1, A F Bradbury, N J Darby, K Maruthainar, D G Smyth.   

Abstract

Three tiers of processing have been investigated in the reactions that transform prohormones into their mature end products. Evidence is presented that the proteolytic reactions that convert lipotropin into shortened forms of beta-endorphin take place in individually distinct stages. After these cleavages have occurred, the removal of basic residues by carboxypeptidase H and amidation of the products are effected by independent reactions which do not synergise. Experiments are also described which show that the amidating enzyme can accept certain imino acids as substrates and utilises a mechanism that involves hydroxylation; it is implicit that peptide amidation proceeds by a similar mechanism. These results point to a general concept that pro-hormone processing involves consecutive reactions which take place in a predetermined order.

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Year:  1988        PMID: 2969753     DOI: 10.1016/0300-9084(88)90152-6

Source DB:  PubMed          Journal:  Biochimie        ISSN: 0300-9084            Impact factor:   4.079


  2 in total

1.  Functional redundancy of FMRFamide-related peptides at the Drosophila larval neuromuscular junction.

Authors:  R S Hewes; E C Snowdeal; M Saitoe; P H Taghert
Journal:  J Neurosci       Date:  1998-09-15       Impact factor: 6.167

Review 2.  Diversity of Neuropeptide Cell-Cell Signaling Molecules Generated by Proteolytic Processing Revealed by Neuropeptidomics Mass Spectrometry.

Authors:  Vivian Hook; Christopher B Lietz; Sonia Podvin; Tomas Cajka; Oliver Fiehn
Journal:  J Am Soc Mass Spectrom       Date:  2018-04-17       Impact factor: 3.109

  2 in total

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