지방산산 과산화효소

Fatty-acid peroxygenase
지방산산 과산화효소
식별자
EC 번호1.11.2.4
데이터베이스
인텐츠IntEnz 뷰
브렌다브렌다 입력
엑스퍼시나이스자이메 뷰
케그KEG 입력
메타사이크대사통로
프리암프로필
PDB 구조RCSB PDB PDBe PDBsum

지방산산 과산화효소(EC 1.11.2.4, 지방산 하이드록실라제(주변), P450 과산화효소, CYP152A1, P450BS, P450SP알파)는 체계적인 이름지방산:하이드로페산화산화효소(RH-hydroxylating)가진 효소.[1][2][3][4][5][6][7][8]이 효소는 다음과 같은 화학 반응을 촉진한다.

지방산 + H2O2 3- 또는 2-hydroxy 지방산 + H2O

지방산성 과산화지질효소는 세포질 헤메-티올레이트 단백질이다.

참조

  1. ^ Matsunaga I, Yamada M, Kusunose E, Nishiuchi Y, Yano I, Ichihara K (May 1996). "Direct involvement of hydrogen peroxide in bacterial alpha-hydroxylation of fatty acid". FEBS Letters. 386 (2–3): 252–4. doi:10.1016/0014-5793(96)00451-6. PMID 8647293.
  2. ^ Matsunaga I, Yamada M, Kusunose E, Miki T, Ichihara K (July 1998). "Further characterization of hydrogen peroxide-dependent fatty acid alpha-hydroxylase from Sphingomonas paucimobilis". Journal of Biochemistry. 124 (1): 105–10. doi:10.1093/oxfordjournals.jbchem.a022068. PMID 9644252.
  3. ^ Matsunaga I, Ueda A, Fujiwara N, Sumimoto T, Ichihara K (August 1999). "Characterization of the ybdT gene product of Bacillus subtilis: novel fatty acid beta-hydroxylating cytochrome P450". Lipids. 34 (8): 841–6. doi:10.1007/s11745-999-0431-3. PMID 10529095.
  4. ^ Imai Y, Matsunaga I, Kusunose E, Ichihara K (August 2000). "Unique heme environment at the putative distal region of hydrogen peroxide-dependent fatty acid alpha-hydroxylase from Sphingomonas paucimobilis (peroxygenase P450(SPalpha)". Journal of Biochemistry. 128 (2): 189–94. doi:10.1093/oxfordjournals.jbchem.a022740. PMID 10920253.
  5. ^ Matsunaga I, Yamada A, Lee DS, Obayashi E, Fujiwara N, Kobayashi K, Ogura H, Shiro Y (February 2002). "Enzymatic reaction of hydrogen peroxide-dependent peroxygenase cytochrome P450s: kinetic deuterium isotope effects and analyses by resonance Raman spectroscopy". Biochemistry. 41 (6): 1886–92. doi:10.1021/bi011883p. PMID 11827534.
  6. ^ Lee DS, Yamada A, Sugimoto H, Matsunaga I, Ogura H, Ichihara K, Adachi S, Park SY, Shiro Y (March 2003). "Substrate recognition and molecular mechanism of fatty acid hydroxylation by cytochrome P450 from Bacillus subtilis. Crystallographic, spectroscopic, and mutational studies". The Journal of Biological Chemistry. 278 (11): 9761–7. doi:10.1074/jbc.M211575200. PMID 12519760.
  7. ^ Matsunaga I, Shiro Y (April 2004). "Peroxide-utilizing biocatalysts: structural and functional diversity of heme-containing enzymes". Current Opinion in Chemical Biology. 8 (2): 127–32. doi:10.1016/j.cbpa.2004.01.001. PMID 15062772.
  8. ^ Shoji O, Wiese C, Fujishiro T, Shirataki C, Wünsch B, Watanabe Y (September 2010). "Aromatic C-H bond hydroxylation by P450 peroxygenases: a facile colorimetric assay for monooxygenation activities of enzymes based on Russig's blue formation". Journal of Biological Inorganic Chemistry. 15 (7): 1109–15. doi:10.1007/s00775-010-0671-9. PMID 20490877.

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