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InterPro: IPR000997 Cholinesterase
Protein matches
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UniProtKB Matches: 487 proteins |
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Accession
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IPR000997 Cholinesterase |
Type
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Family |
Signatures
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InterPro Relationships
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Children
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IPR000908 Acetylcholinesterase, fish/snake
IPR001445 Acetylcholinesterase, insect
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Contains
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IPR002018 Carboxylesterase, type B
IPR019819 Carboxylesterase type B, conserved site
IPR019826 Carboxylesterase type B, active site
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GO Term annotation
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Function
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GO:0004104 cholinesterase activity
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InterPro annotation
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Entry Details in BioMart
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Abstract
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Cholinesterase enzymes are members of the broader alpha/beta hydrolase family and can be dividied into two distinct groups: those that catalyse the hydrolysis of acetylcholine to choline and acetate (acetylcholinesterases EC:3.1.1.7)
acetylcholine + H2O -> choline + acetate
and those that catalyse the conversion of other acylcholines to a choline and a weak acid (cholinesterases EC:3.1.1.8)
an acylcholine + H2O -> choline + a carboxylate
Acetylcholinesterase also acts on a variety of acetic esters and catalyses transacetylations. It is the most intensively studied of the cholinesterase enzymes due to its key physiological role in the turnover of the neurotransmitter acylcholine [1]. This enzyme is found in, or attached to, cellular or basement membranes of presynaptic cholinergic neurons and postsynaptic cholinoceptive cells within the neuromuscular junction. Signal transmission at the neuromuscular junction involves the release of acylcholine, its interaction with the acycholine receptor and hydrolysis, all occuring in a period of a few milliseconds. Rapid hydrolysis of the newly released aceytlcholine is vital in order to prevent continuous firing of the nerve impulses [2]. Consistent with its role in this process, acetylcholinesterase has an unusually high turnover number, ensuring that acetylcholine is broken down quickly. There is evidence to suggest that acetylcholinesterase has additional important roles including involvement in neuronal adhesion, the formation of Alzheimer fibrils, and neurite growth [3, 4, 5].
The 3D structure of acetylcholinesterase and a cholinesterase have been determined [6, 7]. These proteins share the 3-layer alpha-beta-alpha sandwich fold common to members of the alpha/beta hydrolase family. Surprisingly, given the high turnover number of acetylcholinesterase, the active site of these enzymes is located at the bottom of a deep and narrow cleft, named the active-site gorge. Some of the proteins in this group are responsible for the molecular basis of the blood group antigens, surface markers on the outside of the red blood cell membrane. Most of these markers are proteins, but some are carbohydrates attached to lipids or proteins [Reid M.E., Lomas-Francis C. The Blood Group Antigen FactsBook Academic Press, London / San Diego, (1997)]. Acetylcholinesterase (EC:3.1.1.7) belongs to the Yt blood group system and is associated with Yt(a/b) antigen.
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Structural links
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Database links
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Publications
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1.
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Silman I, Sussman JL.
Acetylcholinesterase: 'classical' and 'non-classical' functions and pharmacology.
5 293-302 2005
[PubMed: 15907917]
http://dx.doi.org/10.1016/j.coph.2005.01.014
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2.
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Anglister L, Stiles JR, Salpeter MM.
Acetylcholinesterase density and turnover number at frog neuromuscular junctions, with modeling of their role in synaptic function.
Neuron 12 783-94 1994
[PubMed: 8161450]
http://dx.doi.org/10.1016/0896-6273(94)90331-X
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3.
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Darboux I, Barthalay Y, Piovant M, Hipeau-Jacquotte R.
The structure-function relationships in Drosophila neurotactin show that cholinesterasic domains may have adhesive properties.
EMBO J. 15 4835-43 1996
[PubMed: 8890157]
http://ukpmc.ac.uk/articlerender.cgi?tool=EBI&pubmedid=8890157
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4.
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Inestrosa NC, Alvarez A, Perez CA, Moreno RD, Vicente M, Linker C, Casanueva OI, Soto C, Garrido J.
Acetylcholinesterase accelerates assembly of amyloid-beta-peptides into Alzheimer's fibrils: possible role of the peripheral site of the enzyme.
Neuron 16 881-91 1996
[PubMed: 8608006]
http://dx.doi.org/10.1016/S0896-6273(00)80108-7
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5.
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Sharma KV, Koenigsberger C, Brimijoin S, Bigbee JW.
Direct evidence for an adhesive function in the noncholinergic role of acetylcholinesterase in neurite outgrowth.
J. Neurosci. Res. 63 165-75 2001
[PubMed: 11169626]
http://dx.doi.org/10.1002/1097-4547(20010115)63:2<165::AID-JNR1008>3.3.CO;2-F
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6.
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Sussman JL, Harel M, Frolow F, Oefner C, Goldman A, Toker L, Silman I.
Atomic structure of acetylcholinesterase from Torpedo californica: a prototypic acetylcholine-binding protein.
Science 253 872-9 1991
[PubMed: 1678899]
http://www.sciencemag.org/cgi/content/abstract/253/5022/872
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7.
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Nicolet Y, Lockridge O, Masson P, Fontecilla-Camps JC, Nachon F.
Crystal structure of human butyrylcholinesterase and of its complexes with substrate and products.
J. Biol. Chem. 278 41141-7 2003
[PubMed: 12869558]
http://dx.doi.org/10.1074/jbc.M210241200
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Additional Reading
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Ekstrom FJ, Astot C, Pang YP.
Novel nerve-agent antidote design based on crystallographic and mass spectrometric analyses of tabun-conjugated acetylcholinesterase in complex with antidotes.
Clin. Pharmacol. Ther. 82 2007 282-93
[PubMed: 17443135]
http://dx.doi.org/10.1038/sj.clpt.6100151
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Ngamelue MN, Homma K, Lockridge O, Asojo OA.
Crystallization and X-ray structure of full-length recombinant human butyrylcholinesterase.
Acta Crystallogr. Sect. F Struct. Biol. Cryst. Commun. 63 2007 723-7
[PubMed: 17768338]
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Harel M, Sonoda LK, Silman I, Sussman JL, Rosenberry TL.
Crystal structure of thioflavin T bound to the peripheral site of Torpedo californica acetylcholinesterase reveals how thioflavin T acts as a sensitive fluorescent reporter of ligand binding to the acylation site.
J. Am. Chem. Soc. 130 2008 7856-61
[PubMed: 18512913]
http://dx.doi.org/10.1021/ja7109822
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Cousin X, Hotelier T, Giles K, Toutant JP, Chatonnet A.
aCHEdb: the database system for ESTHER, the alpha/beta fold family of proteins and the Cholinesterase gene server.
Nucleic Acids Res. 26 1998 226-8
[PubMed: 9399841]
http://dx.doi.org/10.1093/nar/26.1.226
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Colletier JP, Bourgeois D, Sanson B, Fournier D, Sussman JL, Silman I, Weik M.
Shoot-and-Trap: use of specific x-ray damage to study structural protein dynamics by temperature-controlled cryo-crystallography.
Proc. Natl. Acad. Sci. U.S.A. 105 2008 11742-7
[PubMed: 18701720]
http://dx.doi.org/10.1073/pnas.0804828105
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Colletier JP, Royant A, Specht A, Sanson B, Nachon F, Masson P, Zaccai G, Sussman JL, Goeldner M, Silman I, Bourgeois D, Weik M.
Use of a 'caged' analogue to study the traffic of choline within acetylcholinesterase by kinetic crystallography.
Acta Crystallogr. D Biol. Crystallogr. 63 2007 1115-28
[PubMed: 18007027]
http://dx.doi.org/10.1107/S0907444907044472
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InterPro 23.1
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