Literature DB >> 3753747

Primary structure of Torpedo californica acetylcholinesterase deduced from its cDNA sequence.

M Schumacher, S Camp, Y Maulet, M Newton, K MacPhee-Quigley, S S Taylor, T Friedmann, P Taylor.   

Abstract

Acetylcholinesterase, an essential enzyme of the nervous system, rapidly terminates the action of acetylcholine released into the synapse. Acetylcholinesterase is also found (in lower abundance) in extrajunctional areas of muscle and nerve and on erythrocyte membranes. Hydrodynamic analyses of the native enzyme and characterization of its dissociated subunits have revealed multiple enzyme forms which can be divided into two classes: dimensionally asymmetric forms which are usually found within the synapse and contain a collagen-like structural subunit disulphide-linked to the catalytic subunits; and globular forms which appear to be widely distributed on the outer surface of cell membranes. Both forms have been characterized in the ray Torpedo californica and, although their catalytic behaviours seem to be identical, they differ slightly in amino-acid composition, peptide maps and reactivity with certain monoclonal antibodies. Here, we report the complete amino-acid sequence of an acetylcholinesterase inferred from the sequence of a complementary DNA clone. The 575-residue protein shows significant homology with the C-terminal portion of thyroglobulin.

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Year:  1986        PMID: 3753747     DOI: 10.1038/319407a0

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


  80 in total

Review 1.  Thyroglobulin as autoantigen: structure-function relationships.

Authors:  M Vali; N R Rose; P Caturegli
Journal:  Rev Endocr Metab Disord       Date:  2000-01       Impact factor: 6.514

Review 2.  Processing of cholinesterase-like α/β-hydrolase fold proteins: alterations associated with congenital disorders.

Authors:  Antonella De Jaco; Davide Comoletti; Noga Dubi; Shelley Camp; Palmer Taylor
Journal:  Protein Pept Lett       Date:  2012-02       Impact factor: 1.890

Review 3.  Comparison of butyrylcholinesterase and acetylcholinesterase.

Authors:  A Chatonnet; O Lockridge
Journal:  Biochem J       Date:  1989-06-15       Impact factor: 3.857

Review 4.  Autoimmunity in Graves' ophthalmopathy: a review.

Authors:  A P Weetman
Journal:  J R Soc Med       Date:  1989-03       Impact factor: 5.344

5.  Molecular cloning and construction of the coding region for human acetylcholinesterase reveals a G + C-rich attenuating structure.

Authors:  H Soreq; R Ben-Aziz; C A Prody; S Seidman; A Gnatt; L Neville; J Lieman-Hurwitz; E Lev-Lehman; D Ginzberg; Y Lipidot-Lifson
Journal:  Proc Natl Acad Sci U S A       Date:  1990-12       Impact factor: 11.205

6.  Naturally occurring variations in the human cholinesterase genes: heritability and association with cardiovascular and metabolic traits.

Authors:  Anne M Valle; Zoran Radic; Brinda K Rana; Vafa Mahboubi; Jennifer Wessel; Pei-an Betty Shih; Fangwen Rao; Daniel T O'Connor; Palmer Taylor
Journal:  J Pharmacol Exp Ther       Date:  2011-04-14       Impact factor: 4.030

7.  Structural analysis of the synaptic protein neuroligin and its beta-neurexin complex: determinants for folding and cell adhesion.

Authors:  Igor P Fabrichny; Philippe Leone; Gerlind Sulzenbacher; Davide Comoletti; Meghan T Miller; Palmer Taylor; Yves Bourne; Pascale Marchot
Journal:  Neuron       Date:  2007-12-20       Impact factor: 17.173

8.  Congenital hypothyroidism mutations affect common folding and trafficking in the α/β-hydrolase fold proteins.

Authors:  Antonella De Jaco; Noga Dubi; Shelley Camp; Palmer Taylor
Journal:  FEBS J       Date:  2012-11-01       Impact factor: 5.542

9.  Recombinant human acetylcholinesterase is secreted from transiently transfected 293 cells as a soluble globular enzyme.

Authors:  B Velan; C Kronman; H Grosfeld; M Leitner; Y Gozes; Y Flashner; T Sery; S Cohen; R Ben-Aziz; S Seidman
Journal:  Cell Mol Neurobiol       Date:  1991-02       Impact factor: 5.046

10.  A single amino acid change in the acetylcholinesterase-like domain of thyroglobulin causes congenital goiter with hypothyroidism in the cog/cog mouse: a model of human endoplasmic reticulum storage diseases.

Authors:  P S Kim; S A Hossain; Y N Park; I Lee; S E Yoo; P Arvan
Journal:  Proc Natl Acad Sci U S A       Date:  1998-08-18       Impact factor: 11.205

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