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   2 terial cell growth through inhibition of the beta-ketoacyl-ACP synthase activity of type II fatty aci
     3 iosynthesis, pfKASIII exhibited typical KAS (beta-ketoacyl ACP synthase) activity using acetyl-CoA as
     4 al production, with fatty-acid biosynthesis (beta-ketoacyl-ACP synthases) attracting the most attenti
  
     6 teins: an acyl carrier protein (ACP) and two beta-ketoacyl ACP synthase components known as KSalpha a
     7 contribution to chain length regulation of a beta-ketoacyl-ACP synthase, Cw KAS A1, derived from Cuph
     8  This enzyme, along with the M. tuberculosis beta-ketoacyl ACP synthase I mtKasA, catalyzes the Clais
  
    10 ne by regulating the expression of the fabB (beta-ketoacyl-ACP synthase I) and fabA (beta-hydroxydeca
    11 petition for 16:0-ACP by down-regulating the beta-ketoacyl-ACP synthase II 16:0 elongase further incr
    12 se), acpP (encoding ACP), and fabF (encoding beta-ketoacyl-ACP synthase II) genes was cloned and sequ
    13 e residues in Streptococcus pneumoniae FabF (beta-ketoacyl-ACP synthase II; SpFabF) were investigated
    14 tified initiation of fatty acid synthesis by beta-ketoacyl-ACP synthase III (fabH) and enoyl-ACP redu
    15 ructure of ACP with the crystal structure of beta-ketoacyl-ACP synthase III (FabH) and experimentally
    16 at the inhibition of chain initiation at the beta-ketoacyl-ACP synthase III step contributes to the a
  
  
  
    20 c deletion of acyl carrier protein (ACP) and beta-ketoacyl-ACP synthase indicated that this pathway i
    21 etreatment of the wild-type protein with the beta-ketoacyl-ACP synthase inhibitor cerulenin also bloc
    22 racterization of purified KasA and KasB, two beta-ketoacyl-ACP synthase (KAS) enzymes of the M. tuber
  
    24 encoding beta-ketoacyl-acyl carrier protein (beta-ketoacyl-ACP) synthase (KAS) III (FabH), was overex
  
  
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