메뉴 건너뛰기




Volumn 61, Issue 3-6, 1997, Pages 127-132

The impact of aromatase mechanism on other P450s

Author keywords

[No Author keywords available]

Indexed keywords

AROMATASE; CYTOCHROME P450;

EID: 0031120090     PISSN: 09600760     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0960-0760(96)00218-X     Document Type: Conference Paper
Times cited : (46)

References (23)
  • 1
    • 0006656956 scopus 로고
    • Isolation of a full length cDNA insert encoding human aromatase system cytochrome P-450 and its expression in non-steroidogenic cells
    • Corbin C.J., Graham-Lorence S., McPhaul M., Mason J.I., Mendelson C.R., Simpson E.R. Isolation of a full length cDNA insert encoding human aromatase system cytochrome P-450 and its expression in non-steroidogenic cells. Proc. Natn. Acad. Sci. U.S.A. 85:1988;8948-8952.
    • (1988) Proc. Natn. Acad. Sci. U.S.A. , vol.85 , pp. 8948-8952
    • Corbin, C.J.1    Graham-Lorence, S.2    McPhaul, M.3    Mason, J.I.4    Mendelson, C.R.5    Simpson, E.R.6
  • 2
    • 0014327584 scopus 로고
    • The intermediary role of a 19-oxoandrogen in the biosynthesis of oestrogen
    • Akhtar M., Skinner S.J.M. The intermediary role of a 19-oxoandrogen in the biosynthesis of oestrogen. Biochem. J. 109:1968;318-321.
    • (1968) Biochem. J. , vol.109 , pp. 318-321
    • Akhtar, M.1    Skinner, S.J.M.2
  • 3
    • 0014556069 scopus 로고
    • The stereospecific removal of a C-19 hydrogen atom in oestrogen biosynthesis
    • Skinner S.J.M., Akhtar M. The stereospecific removal of a C-19 hydrogen atom in oestrogen biosynthesis. Biochem. J. 114:1969;75-81.
    • (1969) Biochem. J. , vol.114 , pp. 75-81
    • Skinner, S.J.M.1    Akhtar, M.2
  • 4
    • 0016293443 scopus 로고
    • Utilisation of oxygen and reduced nicotinamide adenine dinucleotide phosphate by human placental microsomes during aromatisation of androstenedione
    • Thompson E.A., Siiteri P.K. Utilisation of oxygen and reduced nicotinamide adenine dinucleotide phosphate by human placental microsomes during aromatisation of androstenedione. J. Biol. Chem. 249:1974;5364-5374.
    • (1974) J. Biol. Chem. , vol.249 , pp. 5364-5374
    • Thompson, E.A.1    Siiteri, P.K.2
  • 5
    • 0020073188 scopus 로고
    • Mechanistic studies on C-19 demethylation in oestrogen biosynthesis
    • Akhtar M., Calder M.R., Corina D.L., Wright J.N. Mechanistic studies on C-19 demethylation in oestrogen biosynthesis. Biochem. J. 201:1982;569-580.
    • (1982) Biochem. J. , vol.201 , pp. 569-580
    • Akhtar, M.1    Calder, M.R.2    Corina, D.L.3    Wright, J.N.4
  • 6
    • 37049080904 scopus 로고
    • Mechanistic consideration of P-450-dependent enzymic reactions: Studies on oestriol biosynthesis
    • Stevenson D.E., Wright J.N., Akhtar M. Mechanistic consideration of P-450-dependent enzymic reactions: studies on oestriol biosynthesis. J. Chem. Soc. Perkin Trans. 1:1988;2043-2052.
    • (1988) J. Chem. Soc. Perkin Trans. , vol.1 , pp. 2043-2052
    • Stevenson, D.E.1    Wright, J.N.2    Akhtar, M.3
  • 7
    • 0027273894 scopus 로고
    • Mechanism of human placental aromatase: A new active site model
    • Oh S.S., Robinson C.H. Mechanism of human placental aromatase: a new active site model. J. Steroid Biochem. Molec. Biol. 44:1993;389-397.
    • (1993) J. Steroid Biochem. Molec. Biol. , vol.44 , pp. 389-397
    • Oh, S.S.1    Robinson, C.H.2
  • 8
    • 0025955439 scopus 로고
    • Structure-function relationships of human aromatase, cytochrome P-450 using molecular modelling and site-directed mutagenesis
    • Graham-Lorence S., Khalil M.W., Lorence M.C., Mendelson C.R., Simpson E.R. Structure-function relationships of human aromatase, cytochrome P-450 using molecular modelling and site-directed mutagenesis. J. Biol. Chem. 266:1991;11939-11946.
    • (1991) J. Biol. Chem. , vol.266 , pp. 11939-11946
    • Graham-Lorence, S.1    Khalil, M.W.2    Lorence, M.C.3    Mendelson, C.R.4    Simpson, E.R.5
  • 9
    • 0017841564 scopus 로고
    • Chemical and enzymic studies on the characterisation of intermediates during the removal of the 14α-methyl group in cholesterol biosynthesis
    • Akhtar M., Alexander K., Boar R.B., McGhie J.F., Barton D.H.R. Chemical and enzymic studies on the characterisation of intermediates during the removal of the 14α-methyl group in cholesterol biosynthesis. Biochem. J. 169:1978;449-463.
    • (1978) Biochem. J. , vol.169 , pp. 449-463
    • Akhtar, M.1    Alexander, K.2    Boar, R.B.3    McGhie, J.F.4    Barton, D.H.R.5
  • 13
    • 0027198401 scopus 로고
    • Expression and purification of functional human 17 alpha-hydroxylase/17,20-lyase (P450c 17) in Escherichia coli. Use of this system for study of a novel for of combined 17 alpha-hydroxylase/17,20-lyase deficiency
    • Imai T., Globerman H., Gertner J.M., Kagawa N., Waterman M.R. Expression and purification of functional human 17 alpha-hydroxylase/17,20-lyase (P450c 17) in Escherichia coli. Use of this system for study of a novel for of combined 17 alpha-hydroxylase/17,20-lyase deficiency. J. Biol. Chem. 268:1993;19681-19689.
    • (1993) J. Biol. Chem. , vol.268 , pp. 19681-19689
    • Imai, T.1    Globerman, H.2    Gertner, J.M.3    Kagawa, N.4    Waterman, M.R.5
  • 17
    • 0023873225 scopus 로고
    • A peroxide model reaction for placental aromatase
    • Cole P.A., Robinson C.H. A peroxide model reaction for placental aromatase. J. Am. Chem. Soc. 110:1988;1284-1285.
    • (1988) J. Am. Chem. Soc. , vol.110 , pp. 1284-1285
    • Cole, P.A.1    Robinson, C.H.2
  • 18
    • 0025990208 scopus 로고
    • Catalysis by cytochrome P-450 of an oxidative reaction in xenobiotic aldehyde metabolism: Deformylation with olefin formation
    • Roberts E.S., Vaz A.D.N., Coon M.J. Catalysis by cytochrome P-450 of an oxidative reaction in xenobiotic aldehyde metabolism: deformylation with olefin formation. Proc. Natn. Acad. Sci. U.S.A. 88:1991;8963-8966.
    • (1991) Proc. Natn. Acad. Sci. U.S.A. , vol.88 , pp. 8963-8966
    • Roberts, E.S.1    Vaz, A.D.N.2    Coon, M.J.3
  • 19
    • 0025822136 scopus 로고
    • Lanosterol 14α-methyl demethylase: Isolation and characterisation of the third metabolically generated oxidative demethylation intermediate
    • Fischer R.T., Trzaskos J.M., Magolda R.L., Ko S.S., Brosz C.S., Larsen B. Lanosterol 14α-methyl demethylase: isolation and characterisation of the third metabolically generated oxidative demethylation intermediate. J. Biol. Chem. 266:1991;6124-6132.
    • (1991) J. Biol. Chem. , vol.266 , pp. 6124-6132
    • Fischer, R.T.1    Trzaskos, J.M.2    Magolda, R.L.3    Ko, S.S.4    Brosz, C.S.5    Larsen, B.6
  • 20
    • 0026737886 scopus 로고
    • 17-O-Acetyltestosterone formation from progesterone in microsomes from pig testes: Evidence for the Baeyer-Villiger rearrangement in androgen formation catalysed by CYP17
    • Mak A.Y., Swinney D.C. 17-O-Acetyltestosterone formation from progesterone in microsomes from pig testes: evidence for the Baeyer-Villiger rearrangement in androgen formation catalysed by CYP17. J. Am. Chem. Soc. 114:1992;8309-8310.
    • (1992) J. Am. Chem. Soc. , vol.114 , pp. 8309-8310
    • Mak, A.Y.1    Swinney, D.C.2
  • 21
    • 0026270378 scopus 로고
    • A unified mechanistic view of oxidative reactions catalysed by P-450 and related Fe-containing enzymes
    • Akhtar M., Wright J.N. A unified mechanistic view of oxidative reactions catalysed by P-450 and related Fe-containing enzymes. Natn. Prod. Rep. 1991;527-551.
    • (1991) Natn. Prod. Rep. , pp. 527-551
    • Akhtar, M.1    Wright, J.N.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.