Literature DB >> 2068091

Anionic subsites of the catalytic center of acetylcholinesterase from Torpedo and from cobra venom.

H J Kreienkamp1, C Weise, R Raba, A Aaviksaar, F Hucho.   

Abstract

A peptide of acetylcholinesterase (AcChoEase; acetylcholine acetylhydrolase, EC 3.1.1.7) from the venom of the cobra Naja naja oxiana labeled by the affinity reagent N,N-dimethyl-2-phenylaziridinium (DPA) has been identified. The sequence is Gly-Ala-Glu-Met-Trp-Asn-Pro-Asn. In AcChoEase from Torpedo californica, a homologous peptide was labeled and isolated. Its sequence is Ser-Gly-Ser-Glu-Met-Trp-Asn-Pro-Asn, representing positions 79 through 87. In both cases labeling can be prevented by 0.1 mM edrophonium, indicating that the respective peptides form part of the anionic subsite of the catalytic center. The modified residue was tryptophan (Trp-84 in Torpedo AcChoEase) in both enzymes. In contrast to AcChoEase from Torpedo, the enzyme from cobra venom does not contain a peripheral anionic binding site.

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Year:  1991        PMID: 2068091      PMCID: PMC52033          DOI: 10.1073/pnas.88.14.6117

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  42 in total

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Authors:  D NACHMANSOHN; I B WILSON
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4.  Cobra venom acetylcholinesterase. Purification and molecular properties.

Authors:  R Raba; A Aaviksaar; M Raba; J Siigur
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5.  Mutagenesis of essential functional residues in acetylcholinesterase.

Authors:  G Gibney; S Camp; M Dionne; K MacPhee-Quigley; P Taylor
Journal:  Proc Natl Acad Sci U S A       Date:  1990-10       Impact factor: 11.205

6.  A novel irreversible inhibitor of acetylcholinesterase specifically directed at the anionic binding site: structure-activity relationships.

Authors:  B Belleau; H Tani
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Authors:  J P Changeux
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8.  Cloning of the bovine pancreatic cholesterol esterase/lysophospholipase.

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5.  Proteomic Investigations of Two Pakistani Naja Snake Venoms Species Unravel the Venom Complexity, Posttranslational Modifications, and Presence of Extracellular Vesicles.

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