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1 ilar to that of the alpha-chain of mammalian propionyl-CoA carboxylase.
2 ants in PCCA and PCCB impair the activity of propionyl-CoA carboxylase.
3 ferase domain of the Streptomyces coelicolor propionyl-CoA carboxylase.
4 dy was the identification of a high level of propionyl-CoA carboxylase activity and a lesser amount o
5                                              Propionyl-CoA carboxylase activity was undetectable in t
6 e POD-2/acetyl-CoA carboxylase alpha, PCCA-1/propionyl-CoA carboxylase alpha, PYC-1/pyruvate carboxyl
7 lphosphate synthetase, pyruvate carboxylase, propionyl-CoA carboxylase and 3-methylcrotonyl-CoA carbo
8 it in the mammalian biotin-dependent enzymes propionyl-CoA carboxylase and 3-methylcrotonyl-CoA carbo
9 emia (MMA), arise from deficient activity of propionyl-CoA carboxylase and methylmalonyl-CoA mutase a
10 nd fatty acid synthase polypeptides, but not propionyl-CoA carboxylase and mitochondrial pyruvate car
11 disease-causing mutations M204K and R374Q of propionyl-CoA carboxylase and R385S of 3-methylcrotonyl-
12 rboxyltransferase subunits of acetyl-CoA and propionyl-CoA carboxylases and of methylmalonyl-CoA deca
13 iotin carboxylase subunits of acetyl-CoA and propionyl-CoA carboxylases and of pyruvate carboxylase.
14  carboxylase (anaplerosis, gluconeogenesis), propionyl-CoA carboxylase, and 3-methylcrotonyl-CoA carb
15 indicate that pccB encodes the beta-chain of propionyl-CoA carboxylases, and suggest that the alpha-c
16           To identify the mouse cDNA for the propionyl CoA carboxylase beta-subunit (pccb), we have s
17                      A homology model of the propionyl-CoA carboxylase beta-subunit, based on this 12
18 y of beta-methylcrotonyl-CoA carboxylase and propionyl-CoA carboxylase in the islet.
19 tal structure, provides new insight into the propionyl-CoA carboxylase mechanism, its oligomeric stru
20                                              Propionyl CoA carboxylase (PCC) is a mitochondrial, biot
21        Mutations in the mitochondrial enzyme propionyl-CoA carboxylase (PCC) cause propionic aciduria
22 d by deficiency of the mitochondrial enzyme, propionyl-CoA carboxylase (PCC) composed of six alpha (P
23                                              Propionyl-CoA carboxylase (PCC) is a biotin-dependent mi
24    MCC has strong sequence conservation with propionyl-CoA carboxylase (PCC), and their holoenzymes a
25 tabolism caused by the genetic deficiency of propionyl-CoA carboxylase (PCC).
26 s 3-methylcrotonyl-CoA carboxylase (MCC) and propionyl-CoA carboxylase (PCC).
27 system for the human alpha and beta cDNAs of propionyl-CoA carboxylase (PCC).
28  fragments of the mitochondrial carboxylases propionyl-CoA carboxylase, pyruvate carboxylase, and met
29 d that, in intact livers and hearts, (i) the propionyl-CoA carboxylase reaction is slightly reversibl
30            The result shows that deletion of propionyl-CoA carboxylase subunit B gene (Pccb) in alpha
31              Convergent evidence prioritized Propionyl-CoA Carboxylase Subunit Beta (PCCB), a nuclear
32 rror of metabolism caused by a deficiency of propionyl CoA carboxylase which often manifests with fre
33 The 12S reaction is similar to that of human propionyl-CoA carboxylase, whose beta-subunit has 50% se