Molecular cloning of neuropathy target esterase (NTE).

Abstract:

:Covalent modification of NTE, a neuronal protein with serine esterase activity, by certain organophosphates (OP) initiates degeneration of long axons in the peripheral and central nervous system. Simple inhibition of NTE esterase activity does not initiate neuropathy; the latter requires aging of the OP bound to the catalytic serine residue so that a negatively-charged species is left attached to the active site. This may indicate that a non-esterase function of NTE is important for axonal maintenance. We have recently cloned NTE and shown that it is unrelated to any known serine hydrolases but contains a novel C-terminal domain which is conserved from bacteria to man. Furthermore, the catalytic serine is located within this domain at the centre of a helical hydrophobic segment of the polypeptide's secondary structure. The integrity of NTE would be severely compromised by the presence of a negatively-charged organophosphate moiety at this site. Implications for possible higher-order structures and functions for NTE are discussed.

journal_name

Chem Biol Interact

authors

Glynn P,Read DJ,Lush MJ,Li Y,Atkins J

doi

10.1016/s0009-2797(99)00065-4

subject

Has Abstract

pub_date

1999-05-14 00:00:00

pages

513-7

eissn

0009-2797

issn

1872-7786

pii

S0009-2797(99)00065-4

journal_volume

119-120

pub_type

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