메뉴 건너뛰기




Volumn 49, Issue 5, 2006, Pages 1499-1502

Selective irreversible inhibition of fructose 1,6-bisphosphate aldolase from Trypanosoma brucei

Author keywords

[No Author keywords available]

Indexed keywords

ALDEHYDE DERIVATIVE; ANTITRYPANOSOMAL AGENT; ENZYME INHIBITOR; FRUCTOSE 1,6 BISPHOSPHATE ALDOLASE INHIBITOR; FRUCTOSE BISPHOSPHATE ALDOLASE; HYDROXYNAPHTHALDEHYDE PHOSPHATE; ISOENZYME; LYSINE; SCHIFF BASE; SERINE; TBK 1; UNCLASSIFIED DRUG;

EID: 33644869449     PISSN: 00222623     EISSN: None     Source Type: Journal    
DOI: 10.1021/jm050237b     Document Type: Article
Times cited : (35)

References (25)
  • 2
    • 0022259097 scopus 로고
    • The modes of action of anti-protozoal drugs
    • (a) Howells, R. E. The modes of action of anti-protozoal drugs. Parasitology 1985, 90, 687-703.
    • (1985) Parasitology , vol.90 , pp. 687-703
    • Howells, R.E.1
  • 3
    • 0039413877 scopus 로고
    • Chemotherapy and chemoprophylaxis of sleeping sickness caused by Trypanosoma gambiense
    • (b) Neujean, G. Chemotherapy and chemoprophylaxis of sleeping sickness caused by Trypanosoma gambiense. Rev. Med. Liege 1959, 14, 5-13.
    • (1959) Rev. Med. Liege , vol.14 , pp. 5-13
    • Neujean, G.1
  • 4
    • 0026660462 scopus 로고
    • Efficacy and toxicity of eflornithine for treatment of Trypanosoma brucei gambiense sleeping sickness
    • Milord, F.; Pepin, J.; Loko, L.; Ethier, L.: Mpia, B. Efficacy and toxicity of eflornithine for treatment of Trypanosoma brucei gambiense sleeping sickness. Lancet 1992, 340, 652-655.
    • (1992) Lancet , vol.340 , pp. 652-655
    • Milord, F.1    Pepin, J.2    Loko, L.3    Ethier, L.4    Mpia, B.5
  • 5
    • 0021344078 scopus 로고
    • Chemotherapeutic implication of polyamine biosynthesis inhibition
    • Sjoerdsma, A.; Schechter, P. J. Chemotherapeutic implication of polyamine biosynthesis inhibition. Clin. Pharmacol. Ther. 1984, 35, 287-300.
    • (1984) Clin. Pharmacol. Ther. , vol.35 , pp. 287-300
    • Sjoerdsma, A.1    Schechter, P.J.2
  • 6
    • 33644855659 scopus 로고
    • Clinical evaluation of eflornithine in Trypanosomiasis
    • Van Nieuwenhove, S. Clinical evaluation of eflornithine in Trypanosomiasis. Trans. R. Soc. Trop. Med. Hyg. 1985, 79, 692-696.
    • (1985) Trans. R. Soc. Trop. Med. Hyg. , vol.79 , pp. 692-696
    • Van Nieuwenhove, S.1
  • 7
    • 0018977225 scopus 로고
    • Glycolysis in Trypanosoma brucei
    • (a) Visser, N.; Opperdoes, F. R. Glycolysis in Trypanosoma brucei. Eur. J. Biochem. 1980, 103, 623-632.
    • (1980) Eur. J. Biochem. , vol.103 , pp. 623-632
    • Visser, N.1    Opperdoes, F.R.2
  • 9
    • 0021142570 scopus 로고
    • Purification, morphometric analysis and characterization of the glycosomes of the protozoan hemoflagallate Trypanosoma brucei
    • Opperdoes, F. R.; Baudhuin, P.; Coppens, J.; De Roe, C.; Edwards, S. W.; Weijers, P. J.; Misset, O. Purification, morphometric analysis and characterization of the glycosomes of the protozoan hemoflagallate Trypanosoma brucei. J. Cell Biol. 1984, 98, 1178-1184.
    • (1984) J. Cell Biol. , vol.98 , pp. 1178-1184
    • Opperdoes, F.R.1    Baudhuin, P.2    Coppens, J.3    De Roe, C.4    Edwards, S.W.5    Weijers, P.J.6    Misset, O.7
  • 10
    • 0015240396 scopus 로고
    • Fluorescence studies of the binding of alkyls and aryl phosphates to rat muscle aldolase
    • Shu, B.; Barker, R. Fluorescence studies of the binding of alkyls and aryl phosphates to rat muscle aldolase. J. Biol. Chem. 1971, 246, 7041-7045.
    • (1971) J. Biol. Chem. , vol.246 , pp. 7041-7045
    • Shu, B.1    Barker, R.2
  • 11
    • 0029093932 scopus 로고
    • Effects of chirality and substituents at carbon 3 in dihydroxyacetone- phosphate analogues on their binding to rabbit muscle aldolase
    • (a) Blonski, C.; Gefflaut, T.; Périé, J. Effects of chirality and substituents at carbon 3 in dihydroxyacetone-phosphate analogues on their binding to rabbit muscle aldolase. Bioorg. Med. Chem. 1995, 3, 1247-1253.
    • (1995) Bioorg. Med. Chem. , vol.3 , pp. 1247-1253
    • Blonski, C.1    Gefflaut, T.2    Périé, J.3
  • 12
    • 0030453226 scopus 로고    scopus 로고
    • Slow reversible inhibitions of rabbit muscle aldolase with substrate analogues: Synthesis, enzymatic kinetics and UV difference spectroscopy studies
    • (b) Gefflaut, T.; Blonski, C.; Perie, J. Slow reversible inhibitions of rabbit muscle aldolase with substrate analogues: synthesis, enzymatic kinetics and UV difference spectroscopy studies. Bioorg. Med. Chem. 1996, 4, 2043-2054.
    • (1996) Bioorg. Med. Chem. , vol.4 , pp. 2043-2054
    • Gefflaut, T.1    Blonski, C.2    Perie, J.3
  • 13
    • 0029444684 scopus 로고
    • Class 1 aldolases: Substrate specificity, mechanism, inhibitors and structural aspects
    • (c) Gefflaut, T.; Blonski, C.; Périé, J.; Willson, M. Class 1 aldolases: substrate specificity, mechanism, inhibitors and structural aspects. Prog. Biophys. Mol. Biol. 1995, 63, 301-340.
    • (1995) Prog. Biophys. Mol. Biol. , vol.63 , pp. 301-340
    • Gefflaut, T.1    Blonski, C.2    Périé, J.3    Willson, M.4
  • 14
    • 0030949759 scopus 로고    scopus 로고
    • Inhibition of rabbit muscle aldolase by phosphorylated aromatic compounds
    • (a) Blonski, C.; Moissac, D.; Perie, J.; Sygusch, J. Inhibition of rabbit muscle aldolase by phosphorylated aromatic compounds. Biochem. J. 1997, 323, 11-77.
    • (1997) Biochem. J. , vol.323 , pp. 11-77
    • Blonski, C.1    Moissac, D.2    Perie, J.3    Sygusch, J.4
  • 15
    • 16844384600 scopus 로고    scopus 로고
    • Hydroxynaphthaldehyde phosphate derivatives as potent covalent Schiff base inhibitors of fructose-1,6-bisphosphate aldolase
    • (b) Dax, C.; Coincon, M.; Sygusch, J.; Blonski, C. Hydroxynaphthaldehyde phosphate derivatives as potent covalent Schiff base inhibitors of fructose-1,6-bisphosphate aldolase. Biochemistry 2005, 44, 5430-5443.
    • (2005) Biochemistry , vol.44 , pp. 5430-5443
    • Dax, C.1    Coincon, M.2    Sygusch, J.3    Blonski, C.4
  • 16
    • 37049176132 scopus 로고
    • Condensation of diphenyl formamidine with phenol. Part 1. A new synthesis of β-resorcy-aldehyde
    • (a) Shoesmith, J. B.; Haldane, J. Condensation of diphenyl formamidine with phenol. Part 1. A new synthesis of β-resorcy-aldehyde. J. Chem. Soc. 1923, 123, 2704-2707.
    • (1923) J. Chem. Soc. , vol.123 , pp. 2704-2707
    • Shoesmith, J.B.1    Haldane, J.2
  • 17
    • 33644850471 scopus 로고
    • Condensation of diphenyl formamidine with phenol. Part II. The general nature of the reaction
    • (b) Shoesmith, J. B.; Aldane, J. Condensation of diphenyl formamidine with phenol. Part II. The general nature of the reaction. J. Chem. Soc. 1924, 125, 2405-2407.
    • (1924) J. Chem. Soc. , vol.125 , pp. 2405-2407
    • Shoesmith, J.B.1    Aldane, J.2
  • 18
    • 0028920229 scopus 로고
    • A new method for the phosphorylation of alcohols and phenols
    • (a) Stowell, J. K.; Wildlanski, T. S. A new method for the phosphorylation of alcohols and phenols. Tetrahedron Lett. 1995, 36, 1825.
    • (1995) Tetrahedron Lett. , vol.36 , pp. 1825
    • Stowell, J.K.1    Wildlanski, T.S.2
  • 20
    • 0013936228 scopus 로고
    • Specific anion binding to fructose bisphosphate aldolase from rabbit muscle
    • Ginsburg, A.; Mehler, A. H. Specific anion binding to fructose bisphosphate aldolase from rabbit muscle. Biochemistry 1966, 5, 2623-2634.
    • (1966) Biochemistry , vol.5 , pp. 2623-2634
    • Ginsburg, A.1    Mehler, A.H.2
  • 21
    • 0037019276 scopus 로고    scopus 로고
    • Naphthalene dicarboxaldehyde as an electrophilic fluorogenic moiety for affinity labelling: Application to opioid receptor affinity labels with greatly improved fluorogenic properties
    • McCurdy, C. R.; Le Bourdonnec, B.; Metzger, T. G.; El Kouhen, R.; Zhang, Y.; Law, P. Y.; Portoghese, P. S. Naphthalene dicarboxaldehyde as an electrophilic fluorogenic moiety for affinity labelling: application to opioid receptor affinity labels with greatly improved fluorogenic properties. J. Med. Chem. 2002, 45, 2887-2890.
    • (2002) J. Med. Chem. , vol.45 , pp. 2887-2890
    • McCurdy, C.R.1    Le Bourdonnec, B.2    Metzger, T.G.3    El Kouhen, R.4    Zhang, Y.5    Law, P.Y.6    Portoghese, P.S.7
  • 22
    • 0001540702 scopus 로고
    • Kinetics and equilibria of the reaction of pyridoxal 5′-phosphate with ethylenediamine to form Schiff bases and cyclic geminal diamines: Evidence for kinetically competent geminal diamine intermediates in transimination sequences
    • (a) Tobias, P. S.; Kallen, R. G. Kinetics and equilibria of the reaction of pyridoxal 5′-phosphate with ethylenediamine to form Schiff bases and cyclic geminal diamines: evidence for kinetically competent geminal diamine intermediates in transimination sequences. J. Am. Chem. Soc. 1975, 97, 6530-6539.
    • (1975) J. Am. Chem. Soc. , vol.97 , pp. 6530-6539
    • Tobias, P.S.1    Kallen, R.G.2
  • 23
    • 0000450328 scopus 로고
    • Kinetic and equilibrium studies on the formation of zinc(II) salicylaldehyde Schiff base derived from ethylenediamine and 1,3-diaminopropane
    • (b) McQuate, R. S.; Leussing, D. L. Kinetic and equilibrium studies on the formation of zinc(II) salicylaldehyde Schiff base derived from ethylenediamine and 1,3-diaminopropane. J. Am. Chem. Soc. 1975, 97, 5117-5125.
    • (1975) J. Am. Chem. Soc. , vol.97 , pp. 5117-5125
    • McQuate, R.S.1    Leussing, D.L.2
  • 25
    • 84988053694 scopus 로고
    • An all atom force field for simulation of proteins and nucleic acids
    • (b) Weiner, S. J.; Kollman, P. A.; Nguyen, D. T.; Case, D. A. An all atom force field for simulation of proteins and nucleic acids. J. Comput. Chem. 1986, 7, 230-252.
    • (1986) J. Comput. Chem. , vol.7 , pp. 230-252
    • Weiner, S.J.1    Kollman, P.A.2    Nguyen, D.T.3    Case, D.A.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.