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Ligand thiocholine

Basic Ligand Information

Molecular Structure

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Roles as Enzyme Ligand

In Vivo Product in Enzyme-catalyzed Reactions (17 results)

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Show Natural Product (17 entries)

EC NUMBER

PROVEN IN VIVO REACTION

REACTION DIAGRAM

LITERATURE

ENZYME 3D STRUCTURE

3.1.1.7

acetylcholine + H2O = thiocholine + acetate

-

2c58, 3D-view

3.1.1.7

acetylcholine + H2O = thiocholine + acetate

-

2c5g, 3D-view

3.1.1.7

acetylcholine + H2O = thiocholine + acetate

-

2ha5, 3D-view

3.1.1.7

acetylcholine + H2O = thiocholine + acetate

-

2ha7, 3D-view

3.1.1.7

acetylthiocholine + H2O = acetate + thiocholine

-

2c58, 3D-view

3.1.1.7

acetylthiocholine + H2O = acetate + thiocholine

-

2c5g, 3D-view

3.1.1.7

acetylthiocholine + H2O = acetate + thiocholine

-

2ha5, 3D-view

3.1.1.7

acetylthiocholine + H2O = acetate + thiocholine

-

2ha7, 3D-view

3.1.1.7

acetylthiocholine + H2O = thiocholine + acetate

-

2c58, 3D-view

3.1.1.7

acetylthiocholine + H2O = thiocholine + acetate

-

2c5g, 3D-view

3.1.1.7

acetylthiocholine + H2O = thiocholine + acetate

-

2ha5, 3D-view

3.1.1.7

acetylthiocholine + H2O = thiocholine + acetate

-

2ha7, 3D-view

3.1.1.8

acetylthiocholine + H2O = acetate + thiocholine

-

-

3.1.1.8

acetylthiocholine + H2O = thiocholine + acetate

-

-

3.1.1.8

butyrylthiocholine + H2O = butyrate + thiocholine

-

-

3.1.1.8

butyrylthiocholine + H2O = thiocholine + butyrate

-

-

3.1.1.8

propionylthiocholine + H2O = thiocholine + propionate

-

-

3.1.1.7

12 entries

3.1.1.8

5 entries

Product in Enzyme-catalyzed Reactions (118 results)

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Show Product (118 entries)

EC NUMBER

REACTION

REACTION DIAGRAM

LITERATURE

ENZYME 3D STRUCTURE

3.1.1.1

butyrylthiocholine + H2O = butyric acid + thiocholine

-

-

3.1.1.7

2-methoxyacetylthiocholine + H2O = thiocholine + 2-methoxyacetate

-

2c58, 3D-view

3.1.1.7

2-methoxyacetylthiocholine + H2O = thiocholine + 2-methoxyacetate

-

2c5g, 3D-view

3.1.1.7

2-methoxyacetylthiocholine + H2O = thiocholine + 2-methoxyacetate

-

2ha5, 3D-view

3.1.1.7

2-methoxyacetylthiocholine + H2O = thiocholine + 2-methoxyacetate

-

2ha7, 3D-view

3.1.1.7

3-methylbutyrylthiocholine + H2O = thiocholine + 3-methylbutyrate

-

2c58, 3D-view

3.1.1.7

3-methylbutyrylthiocholine + H2O = thiocholine + 3-methylbutyrate

-

2c5g, 3D-view

3.1.1.7

3-methylbutyrylthiocholine + H2O = thiocholine + 3-methylbutyrate

-

2ha5, 3D-view

3.1.1.7

3-methylbutyrylthiocholine + H2O = thiocholine + 3-methylbutyrate

-

2ha7, 3D-view

3.1.1.7

acetylcholine + H2O = thiocholine + acetate

-

2c58, 3D-view

3.1.1.7

acetylcholine + H2O = thiocholine + acetate

-

2c5g, 3D-view

3.1.1.7

acetylcholine + H2O = thiocholine + acetate

-

2ha5, 3D-view

3.1.1.7

acetylcholine + H2O = thiocholine + acetate

-

2ha7, 3D-view

3.1.1.7

acetylthiocholine + H2O = acetate + thiocholine

650742,

2c58, 3D-view

3.1.1.7

acetylthiocholine + H2O = acetate + thiocholine

650742,

2c5g, 3D-view

3.1.1.7

acetylthiocholine + H2O = acetate + thiocholine

650742,

2ha5, 3D-view

3.1.1.7

acetylthiocholine + H2O = acetate + thiocholine

650742,

2ha7, 3D-view

3.1.1.7

acetylthiocholine + H2O = thiocholine + acetate

, 650141, 653710, 650246, 649716, 649772, 650215, 652645, 653806, 653349, 651163, 651505, 651202, 649795, 653108, 650832

2c58, 3D-view

3.1.1.7

acetylthiocholine + H2O = thiocholine + acetate

, 650141, 653710, 650246, 649716, 649772, 650215, 652645, 653806, 653349, 651163, 651505, 651202, 649795, 653108, 650832

2c5g, 3D-view

3.1.1.7

acetylthiocholine + H2O = thiocholine + acetate

, 650141, 653710, 650246, 649716, 649772, 650215, 652645, 653806, 653349, 651163, 651505, 651202, 649795, 653108, 650832

2ha5, 3D-view

3.1.1.7

acetylthiocholine + H2O = thiocholine + acetate

, 650141, 653710, 650246, 649716, 649772, 650215, 652645, 653806, 653349, 651163, 651505, 651202, 649795, 653108, 650832

2ha7, 3D-view

3.1.1.7

acetylthiocholine iodide + H2O = thiocholine + acetate

-

2c58, 3D-view

3.1.1.7

acetylthiocholine iodide + H2O = thiocholine + acetate

-

2c5g, 3D-view

3.1.1.7

acetylthiocholine iodide + H2O = thiocholine + acetate

-

2ha5, 3D-view

3.1.1.7

acetylthiocholine iodide + H2O = thiocholine + acetate

-

2ha7, 3D-view

3.1.1.7

benzoylthiocholine + H2O = thiocholine + benzoate

-

2c58, 3D-view

3.1.1.7

benzoylthiocholine + H2O = thiocholine + benzoate

-

2c5g, 3D-view

3.1.1.7

benzoylthiocholine + H2O = thiocholine + benzoate

-

2ha5, 3D-view

3.1.1.7

benzoylthiocholine + H2O = thiocholine + benzoate

-

2ha7, 3D-view

3.1.1.7

butylthiocholine + H2O = thiocholine + butanol

-

2c58, 3D-view

3.1.1.7

butylthiocholine + H2O = thiocholine + butanol

-

2c5g, 3D-view

3.1.1.7

butylthiocholine + H2O = thiocholine + butanol

-

2ha5, 3D-view

3.1.1.7

butylthiocholine + H2O = thiocholine + butanol

-

2ha7, 3D-view

3.1.1.7

butyrylthiocholine + H2O = butyrate + thiocholine

-

2c58, 3D-view

3.1.1.7

butyrylthiocholine + H2O = butyrate + thiocholine

-

2c5g, 3D-view

3.1.1.7

butyrylthiocholine + H2O = butyrate + thiocholine

-

2ha5, 3D-view

3.1.1.7

butyrylthiocholine + H2O = butyrate + thiocholine

-

2ha7, 3D-view

3.1.1.7

butyrylthiocholine + H2O = thiocholine + butanoate

-

2c58, 3D-view

3.1.1.7

butyrylthiocholine + H2O = thiocholine + butanoate

-

2c5g, 3D-view

3.1.1.7

butyrylthiocholine + H2O = thiocholine + butanoate

-

2ha5, 3D-view

3.1.1.7

butyrylthiocholine + H2O = thiocholine + butanoate

-

2ha7, 3D-view

3.1.1.7

butyrylthiocholine + H2O = thiocholine + butyrate

651163, 651202, 653108,

2c58, 3D-view

3.1.1.7

butyrylthiocholine + H2O = thiocholine + butyrate

651163, 651202, 653108,

2c5g, 3D-view

3.1.1.7

butyrylthiocholine + H2O = thiocholine + butyrate

651163, 651202, 653108,

2ha5, 3D-view

3.1.1.7

butyrylthiocholine + H2O = thiocholine + butyrate

651163, 651202, 653108,

2ha7, 3D-view

3.1.1.7

cyclopentylcarbonylthiocholine + H2O = thiocholine + cyclopentanecarboxylate

-

2c58, 3D-view

3.1.1.7

cyclopentylcarbonylthiocholine + H2O = thiocholine + cyclopentanecarboxylate

-

2c5g, 3D-view

3.1.1.7

cyclopentylcarbonylthiocholine + H2O = thiocholine + cyclopentanecarboxylate

-

2ha5, 3D-view

3.1.1.7

cyclopentylcarbonylthiocholine + H2O = thiocholine + cyclopentanecarboxylate

-

2ha7, 3D-view

3.1.1.7

cyclopropylcarbonylthiocholine + H2O = thiocholine + cyclopropanecarboxylate

-

2c58, 3D-view

3.1.1.7

cyclopropylcarbonylthiocholine + H2O = thiocholine + cyclopropanecarboxylate

-

2c5g, 3D-view

3.1.1.7

cyclopropylcarbonylthiocholine + H2O = thiocholine + cyclopropanecarboxylate

-

2ha5, 3D-view

3.1.1.7

cyclopropylcarbonylthiocholine + H2O = thiocholine + cyclopropanecarboxylate

-

2ha7, 3D-view

3.1.1.7

hexanoylthiocholine + H2O = thiocholine + hexanoate

-

2c58, 3D-view

3.1.1.7

hexanoylthiocholine + H2O = thiocholine + hexanoate

-

2c5g, 3D-view

3.1.1.7

hexanoylthiocholine + H2O = thiocholine + hexanoate

-

2ha5, 3D-view

3.1.1.7

hexanoylthiocholine + H2O = thiocholine + hexanoate

-

2ha7, 3D-view

3.1.1.7

isobutyrylthiocholine + H2O = thiocholine + isobutyrate

-

2c58, 3D-view

3.1.1.7

isobutyrylthiocholine + H2O = thiocholine + isobutyrate

-

2c5g, 3D-view

3.1.1.7

isobutyrylthiocholine + H2O = thiocholine + isobutyrate

-

2ha5, 3D-view

3.1.1.7

isobutyrylthiocholine + H2O = thiocholine + isobutyrate

-

2ha7, 3D-view

3.1.1.7

methylthiocholine + H2O = thiocholine + methanol

-

2c58, 3D-view

3.1.1.7

methylthiocholine + H2O = thiocholine + methanol

-

2c5g, 3D-view

3.1.1.7

methylthiocholine + H2O = thiocholine + methanol

-

2ha5, 3D-view

3.1.1.7

methylthiocholine + H2O = thiocholine + methanol

-

2ha7, 3D-view

3.1.1.7

pentanoylthiocholine + H2O = thiocholine + pentanoate

-

2c58, 3D-view

3.1.1.7

pentanoylthiocholine + H2O = thiocholine + pentanoate

-

2c5g, 3D-view

3.1.1.7

pentanoylthiocholine + H2O = thiocholine + pentanoate

-

2ha5, 3D-view

3.1.1.7

pentanoylthiocholine + H2O = thiocholine + pentanoate

-

2ha7, 3D-view

3.1.1.7

phenylacetylthiocholine + H2O = thiocholine + phenylacetate

-

2c58, 3D-view

3.1.1.7

phenylacetylthiocholine + H2O = thiocholine + phenylacetate

-

2c5g, 3D-view

3.1.1.7

phenylacetylthiocholine + H2O = thiocholine + phenylacetate

-

2ha5, 3D-view

3.1.1.7

phenylacetylthiocholine + H2O = thiocholine + phenylacetate

-

2ha7, 3D-view

3.1.1.7

pivaloylthiocholine + H2O = thiocholine + pivalate

-

2c58, 3D-view

3.1.1.7

pivaloylthiocholine + H2O = thiocholine + pivalate

-

2c5g, 3D-view

3.1.1.7

pivaloylthiocholine + H2O = thiocholine + pivalate

-

2ha5, 3D-view

3.1.1.7

pivaloylthiocholine + H2O = thiocholine + pivalate

-

2ha7, 3D-view

3.1.1.7

propionylthiocholine + H2O = propanoate + thiocholine

-

2c58, 3D-view

3.1.1.7

propionylthiocholine + H2O = propanoate + thiocholine

-

2c5g, 3D-view

3.1.1.7

propionylthiocholine + H2O = propanoate + thiocholine

-

2ha5, 3D-view

3.1.1.7

propionylthiocholine + H2O = propanoate + thiocholine

-

2ha7, 3D-view

3.1.1.7

propionylthiocholine + H2O = thiocholine + propanoate

-

2c58, 3D-view

3.1.1.7

propionylthiocholine + H2O = thiocholine + propanoate

-

2c5g, 3D-view

3.1.1.7

propionylthiocholine + H2O = thiocholine + propanoate

-

2ha5, 3D-view

3.1.1.7

propionylthiocholine + H2O = thiocholine + propanoate

-

2ha7, 3D-view

3.1.1.7

propionylthiocholine + H2O = thiocholine + propionate

651202, 653108, , 651505, 650832

2c58, 3D-view

3.1.1.7

propionylthiocholine + H2O = thiocholine + propionate

651202, 653108, , 651505, 650832

2c5g, 3D-view

3.1.1.7

propionylthiocholine + H2O = thiocholine + propionate

651202, 653108, , 651505, 650832

2ha5, 3D-view

3.1.1.7

propionylthiocholine + H2O = thiocholine + propionate

651202, 653108, , 651505, 650832

2ha7, 3D-view

3.1.1.7

propylthiocholine + H2O = thiocholine + propanol

-

2c58, 3D-view

3.1.1.7

propylthiocholine + H2O = thiocholine + propanol

-

2c5g, 3D-view

3.1.1.7

propylthiocholine + H2O = thiocholine + propanol

-

2ha5, 3D-view

3.1.1.7

propylthiocholine + H2O = thiocholine + propanol

-

2ha7, 3D-view

3.1.1.7

S-acetylthiocholine + H2O = acetate + thiocholine

-

2c58, 3D-view

3.1.1.7

S-acetylthiocholine + H2O = acetate + thiocholine

-

2c5g, 3D-view

3.1.1.7

S-acetylthiocholine + H2O = acetate + thiocholine

-

2ha5, 3D-view

3.1.1.7

S-acetylthiocholine + H2O = acetate + thiocholine

-

2ha7, 3D-view

3.1.1.7

S-butyrylthiocholine + H2O = thiocholine + butyrate

651505,

2c58, 3D-view

3.1.1.7

S-butyrylthiocholine + H2O = thiocholine + butyrate

651505,

2c5g, 3D-view

3.1.1.7

S-butyrylthiocholine + H2O = thiocholine + butyrate

651505,

2ha5, 3D-view

3.1.1.7

S-butyrylthiocholine + H2O = thiocholine + butyrate

651505,

2ha7, 3D-view

3.1.1.8

(S)-butyrylthiocholine + H2O = thiocholine + butyrate

-

-

3.1.1.8

acetylthiocholine + H2O = acetate + thiocholine

-

-

3.1.1.8

acetylthiocholine + H2O = thiocholine + acetate

, 650659, 649795, 653775

-

3.1.1.8

acetylthiocholine iodide + H2O = thiocholine + acetate

-

-

3.1.1.8

benzoylthiocholine + H2O = thiocholine + benzoate

651173,

-

3.1.1.8

butyrylthiocholine + H2O = butyrate + thiocholine

-

-

3.1.1.8

butyrylthiocholine + H2O = thiocholine + butyrate

650246, , 649707, 650141, 650347, 650381, 650659, 650809, 651156, 651163, 651173, 652971, 653036, 653355, 651187, 649772, 653108, 650956, 649786, 652467, 653283, 653775

-

3.1.1.8

butyrylthiocholine iodide + H2O = thiocholine + butyrate

-

-

3.1.1.8

bytyrylhiocholine + H2O = thiocholine + butyrate

649795

-

3.1.1.8

formylthiocholine + H2O = thiocholine + formate

-

-

3.1.1.8

propionylthiocholine + H2O = propanoate + thiocholine

-

-

3.1.1.8

propionylthiocholine + H2O = thiocholine + propanoate

-

-

3.1.1.8

propionylthiocholine + H2O = thiocholine + propionate

, 649786, 649795, 653775

-

3.1.1.8

propionylthiocholine iodide + H2O = thiocholine + propionate

-

-

3.1.1.8

S-butyrylthiocholine + H2O = butyrate + thiocholine

-

-

3.1.1.8

succinylthiocholine + H2O = thiocholine + succinate

650347

-

3.1.1.8

valerylthiocholine + H2O = pentanoate + thiocholine

-

-

3.1.1.7

100 entries

3.1.1.8

17 entries

Inhibitor in Enzyme-catalyzed Reactions (4 results)

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Show Inhibitors (4 entries)

EC NUMBER

COMMENTARY

LITERATURE

ENZYME 3D STRUCTURE

2.8.2.6

-

643827

-

2.8.2.6

linear mixed type inhibitor with respect to PAPS

643829

-

2.8.2.6

2 entries

3.1.4.38

inhibitory effect is greater on the Co2+ -enzyme

95160

-

3.4.22.B63

-

718001

-

3D Structure of Enzyme-Ligand-Complex (PDB) (8 results)

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Show 3D Structure of Enzyme-Ligand-Complex (PDB) (8 entries)

EC NUMBER

ENZYME 3D STRUCTURE

3.1.1.7

2c58, 3D-view

3.1.1.7

2c5g, 3D-view

3.1.1.7

2ha5, 3D-view

3.1.1.7

2ha7, 3D-view

3.1.1.7

2c58, 3D-view

3.1.1.7

2c5g, 3D-view

3.1.1.7

2ha5, 3D-view

3.1.1.7

2ha7, 3D-view

3.1.1.7

8 entries

Enzyme Kinetic Parameters

K_i Value (1 result)

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Show KI Value (1 entry)

EC NUMBER

KI VALUE [MM]

KI VALUE MAXIMUM [MM]

COMMENTARY

LITERATURE

2.8.2.6

5.8

-

pH 7.8, 37°C

643829

References & Links

Literature References (36)

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Show Reference (36 entries)

BRENDA REFERENCE ID

PUBMED ID

TITLE

YEAR

AUTHORS

JOURNAL

VOLUME

PAGES

95160

9357012

Interaction of divalent metal ions with Zn(2+)-glycerophosphocholine cholinephosphodiesterase from ox brain

1997

Lee, J.Y.; Kim, M.R.; Kim, Y.B.; Myung, P.K.; Sok, D.E.

Neurochem. Res.

22

1471-1476

643827

14202240

Choline sulphokinase (sulfotransferase)

1964

Orsi, B.A.; Spencer, B.

J. Biochem.

56

81-91

643829

18095

Choline sulfokinase of Penicillium chrysogenum: partial purification and kinetic mechanism

1977

Renosto, F.; Segel, I.H.

Arch. Biochem. Biophys.

180

416-428

649707

11368776

Pressure- and heat-induced inactivation of butyrylcholinesterase: evidence for multiple intermediates and the remnant inactivation process

2001

Weingand-Ziade, A.; Ribes, F.; Renault, F.; Masson, P.

Biochem. J.

356

487-493

649716

11463350

Effect of chemical modification of recombinant human acetylcholinesterase by polyethylene glycol on its circulatory longevity

2001

Cohen, O.; Kronman, C.; Chitlaru, T.; Ordentlich, A.; Velan, B.; Shafferman, A.

Biochem. J.

357

795-802

649772

14575524

Amino acid domains control the circulatory residence time of primate acetylcholinesterases in rhesus macaques (Macaca mulatta)

2004

Cohen, O.; Kronman, C.; Velan, B.; Shafferman, A.

Biochem. J.

378

117-128

649786

10718335

Isolation and characterization of a cDNA encoding a horse liver butyrylcholinesterase: evidence for CPT-11 drug activation

2000

Wierdl, M.; Morton, C.L.; Danks, M.K.; Potter, P.M.

Biochem. Pharmacol.

59

773-781

649795

12110369

DNA sequence of butyrylcholinesterase from the rat: expression of the protein and characterization of the properties of rat butyrylcholinesterase

2002

Boeck, A.T.; Schopfer, L.M.; Lockridge, O.

Biochem. Pharmacol.

63

2101-2110

650141

11888271

Kinetic and structural studies on the interaction of cholinesterases with the anti-Alzheimer drug Rivastigmine

2002

Bar-On, P.; Millard, C.B.; Harel, M.; Dvir, H.; Enz, A.; Sussman, J.L.; Silman, I.

Biochemistry

41

3555-3564

650215

12731886

Unmasking tandem site interaction in human acetylcholinesterase. Substrate activation with a cationic acetanilide substrate

2003

Johnson, J.L.; Cusack, B.; Davies, M.P.; Fauq, A.; Rosenberry, T.L.

Biochemistry

42

5438-5452

650246

15023072

Mutant cholinesterases possessing enhanced capacity for reactivation of their phosphonylated conjugates

2004

Kovarik, Z.; Radic, Z.; Berman, H.A.; Simeon-Rudolf, V.; Reiner, E.; Taylor, P.

Biochemistry

43

3222-3229

650347

11341926

Effects of mutations of active site residues and amino acids interacting with the W loop on substrate activation of butyrylcholinesterase

2001

Masson, P.; Xie, W.; Froment, M.T.; Lockridge, O.

Biochim. Biophys. Acta

1544

166-176

650381

12044901

Butyrylcholinesterase-catalyzed hydrolysis of N-methylindoxyl acetate: analysis of volume changes upon reaction and hysteretic behavior

2002

Masson, P.; Froment, M.T.; Fort, S.; Ribes, F.; Bec, N.; Balny, C.; Schopfer, L.M.

Biochim. Biophys. Acta

1597

229-243

650659

-

Expression of biologically active human butyrylcholinesterase in the cabbage looper (Trichoplusia ni)

2000

Platteborze, P.L.; Broomfield, C.A.

Biotechnol. Appl. Biochem.

31

225-229

650742

12372547

In vivo and in vitro effects of aluminum on the activity of mouse brain acetylcholinesterase

2002

Zatta, P.; Ibn-Lkhayat-Idrissi, M.; Zambenedetti, P.; Kilyen, M.; Kiss, T.

Brain Res. Bull.

59

41-45

650809

11569538

Butyrylcholinesterase-mediated enhancement of the enzymatic activity of trypsin

2001

Darvesh, S.; Kumar, R.; Roberts, S.; Walsh, R.; Martin, E.

Cell. Mol. Neurobiol.

21

285-296

650832

11311211

Soluble and membrane-bound acetylcholinesterases in Mytilus galloprovincialis (Pelecypoda: Filibranchia) from the northern Adriatic sea

2001

Talesa, V.; Romani, R.; Antognelli, C.; Giovannini, E.; Rosi, G.

Chem. Biol. Interact.

134

151-166

650956

12019201

Characterization of equine butyrylcholinesterase disposition in the mouse

2002

Koetzner, L.; Woods, J.H.

Drug Metab. Dispos.

30

724-730

651156

12605682

High activity of human butyrylcholinesterase at low pH in the presence of excess butyrylthiocholine

2003

Masson, P.; Nachon, F.; Bartels, C.F.; Froment, M.T.; Ribes, F.; Matthews, C.; Lockridge, O.

Eur. J. Biochem.

270

315-324

651163

14622273

Aromatic amino-acid residues at the active and peripheral anionic sites control the binding of E2020 (Aricept) to cholinesterases

2003

Saxena, A.; Fedorko, J.M.; Vinayaka, C.R.; Medhekar, R.; Radic, Z.; Taylor, P.; Lockridge, O.; Doctor, B.P.

Eur. J. Biochem.

270

4447-4458

651173

14686935

Damped oscillatory hysteretic behaviour of butyrylcholinesterase with benzoylcholine as substrate

2004

Masson, P.; Goldstein, B.N.; Debouzy, J.C.; Froment, M.T.; Lockridge, O.; Schopfer, L.M.

Eur. J. Biochem.

271

220-234

651187

-

Stereoselective hydrolysis of quaternary quinuclidinium benzoates catalyzed by butyrylcholinesterase

2003

Primozic, I.; Hrenar, T.; Tomic, S.; Meic, Z.

Eur. J. Org. Chem.

2003

295-301

651202

12094012

Characterization of acetylcholinesterase in Caco-2 cells

2002

Plageman, L.R.; Pauletti, G.M.; Skau, K.A.

Exp. Biol. Med.

227

480-486

651505

11520688

An acetylcholinesterase purified from the greenbug (Schizaphis graminum) with some unique enzymological and pharmacological characteristics

2001

Gao, J.R.; Zhu, K.Y.

Insect Biochem. Mol. Biol.

31

1095-1104

652467

12869558

Crystal structure of human butyrylcholinesterase and of its complexes with substrate and products

2003

Nicolet, Y.; Lockridge, O.; Masson, P.; Fontecilla-Camps, J.C.; Nachon, F.

J. Biol. Chem.

278

41141-41147

652645

-

Indophenol chromogenic substrates of cholinesterases of different origin

2002

Rozengart, E.V.; Basova, N.E.; Suvorov, A.A.; Khovanskikh, A.E.

J. Evol. Biochem. Physiol.

38

16-23

652971

10646540

The butyrylcholinesterase K-variant shows similar cellular protein turnover and quaternary interaction to the wild-type enzyme

2000

Altamirano, C.V.; Bartels, C.F.; Lockridge, O.

J. Neurochem.

74

869-877

653036

12018615

A new perspective on thermal inactivation kinetics of human serum butyrylcholinesterase

2002

Cengiz, D.; Cokugras, A.N.; Tezcan, E.F.

J. Protein Chem.

21

145-149

653108

14580806

Characterization of choline esterases and their tissue and subcellular distribution in mussel (Mytilus edulis)

2003

Brown, M.; Davies, I.M.; Moffat, C.F.; Redshaw, J.; Craft, J.A.

Mar. Environ. Res.

57

155-169

653283

12130672

Re-engineering butyrylcholinesterase as a cocaine hydrolase

2002

Sun, H.; Pang, Y.P.; Lockridge, O.; Brimijoin, S.

Mol. Pharmacol.

62

220-224

653349

10823579

Changes of acetylcholinesterase activity in brain areas and liver of sucrose- and ethanol-fed rats

2000

Ruano, M.J.; Sanchez-Martin, M.M.; Alonso, J.M.; Hueso, P.

Neurochem. Res.

25

461-470

653355

12675140

Cholinesterases: New roles in brain function and in Alzheimer's disease

2003

Giacobini, E.

Neurochem. Res.

28

515-522

653710

11842237

Acetylcholinesterase engineering for detection of insecticide residues

2002

Boublik, Y.; Saint-Aguet, P.; Lougarre, A.; Arnaud, M.; Villatte, F.; Estrada-Mondaca, S.; Fournier, D.

Protein Eng.

15

43-50

653775

15106880

Partial purification and characterization of soluble isoform of butyrylcholinesterase from rat intestine

2004

Yildiz, O.; Bodur, E.; Cokugras, A.N.; Ozer, N.

Protein J.

23

143-151

653806

14627729

Studying the roles of W86, E202, and Y337 in binding of acetylcholine to acetylcholinesterase using a combined molecular dynamics and multiple docking approach

2003

Kua, J.; Zhang, Y.; Eslami, A.C.; Butler, J.R.; McCammon, J.A.

Protein Sci.

12

2675-2684

718001

22033482

The crystal structure analysis of group B Streptococcus sortase C1: a model for the "lid" movement upon substrate binding

2011

Khare, B.; Fu, Z.Q.; Huang, I.H.; Ton-That, H.; Narayana, S.V.

J. Mol. Biol.

414

563-577

Links to other databases for thiocholine

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ChEBI

PubChem

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