Structural biology of the thioester-dependent degradation and synthesis of fatty acids

被引:30
作者
Bhaumik, P
Koski, MK
Glumoff, T
Hiltunen, JK
Wierenga, RK
机构
[1] Univ Oulu, Bioctr, FIN-90014 Oulu, Finland
[2] Univ Oulu, Dept Biochem, FIN-90014 Oulu, Finland
基金
芬兰科学院;
关键词
D O I
10.1016/j.sbi.2005.10.010
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The fatty acid degradation and synthesis pathways consist of the same four chemical transformations. These transformations are facilitated by conjugating the fatty acid, via a thioester bond, to coenzyme A or acyl carrier protein in, respectively, the degradation and synthesis pathways. These pathways are compartmentalized in the peroxisomes, mitochondria and cytosol of eukaryotic cells. Current structural knowledge of the enzymes comprising these pathways shows that the approximately 130 entries in the RCSB Protein Data Bank can be grouped into seven superfamilies. Multifunctional enzymes are important in both pathways.
引用
收藏
页码:621 / 628
页数:8
相关论文
共 48 条
  • [11] Crystal structure of the liganded SCP-2-like domain of human peroxisomal multifunctional enzyme type 2 at 1.75 A resolution
    Haapalainen, AM
    van Aalten, DMF
    Meriläinen, G
    Jalonen, JE
    Pirilä, P
    Wierengal, RK
    Hiltunen, JK
    Glumoff, T
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 2001, 313 (05) : 1127 - 1138
  • [12] Heath Richard J, 2004, Curr Opin Investig Drugs, V5, P146
  • [13] The Claisen condensation in biology
    Heath, RJ
    Rock, CO
    [J]. NATURAL PRODUCT REPORTS, 2002, 19 (05) : 581 - 596
  • [14] β-Oxidation -: strategies for the metabolism of a wide variety of acyl-CoA esters
    Hiltunen, JK
    Qin, YM
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS, 2000, 1484 (2-3): : 117 - 128
  • [15] The biochemistry of peroxisomal β-oxidation in the yeast Saccharomyces cerevisiae
    Hiltunen, JK
    Mursula, AM
    Rottensteiner, H
    Wierenga, RK
    Kastaniotis, AJ
    Gurvitz, A
    [J]. FEMS MICROBIOLOGY REVIEWS, 2003, 27 (01) : 35 - 64
  • [16] The crotonase superfamily: Divergently related enzymes that catalyze different reactions involving acyl coenzyme A thioesters
    Holden, HM
    Benning, MM
    Haller, T
    Gerlt, JA
    [J]. ACCOUNTS OF CHEMICAL RESEARCH, 2001, 34 (02) : 145 - 157
  • [17] Domain swapping in the low-similarity isomerase/hydratase superfamily:: The crystal structure of rat mitochondrial Δ3,Δ2-enoyl-CoA isomerase
    Hubbard, PA
    Yu, WF
    Schulz, H
    Kim, JJP
    [J]. PROTEIN SCIENCE, 2005, 14 (06) : 1545 - 1555
  • [18] The crystal structure and reaction mechanism of Escherichia coli 2,4-dienoyl-CoA reductase
    Hubbard, PA
    Liang, XQ
    Schulz, H
    Kim, JJP
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (39) : 37553 - 37560
  • [19] Structural basis for channelling mechanism of a fatty acid β-oxidation multienzyme complex
    Ishikawa, M
    Tsuchiya, D
    Oyama, T
    Tsunaka, Y
    Morikawa, K
    [J]. EMBO JOURNAL, 2004, 23 (14) : 2745 - 2754
  • [20] Multiplicity of eukaryotic ADH and other MDR forms
    Jörnvall, H
    Nordling, E
    Persson, B
    [J]. CHEMICO-BIOLOGICAL INTERACTIONS, 2003, 143 : 255 - 261