コーパス検索結果 (1語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 e from hydrolysis than the HADSF member beta-phosphoglucomutase.
2 lates and enhances the enzymatic activity of phosphoglucomutase 1 (PGM), an important regulatory enzy
12 ucial enzyme in the glycosylation pathway is phosphoglucomutase 3 (PGM3), which catalyzes a key step
14 S patients: Autosomal recessive mutations in phosphoglucomutase-3 (PGM3); Autosomal dominant negative
16 nfolded protein response (UPR) by inhibiting phosphoglucomutase activity and causing the accumulation
17 s a sole carbon source and was defective for phosphoglucomutase activity, suggesting functional ident
20 eficient in leaf starch and lacked plastidic phosphoglucomutase, an enzyme critical for gluconeogenes
21 nnose and appears to be generated in part by phosphoglucomutase, an enzyme important for lipooligosac
22 irect determination of kinetic constants for phosphoglucomutase and its phosphorylated products is de
23 reading frames: a partial pgm gene (encoding phosphoglucomutase) and a complete qor gene (encoding NA
24 potential inhibitors of phosphomannomutase/ phosphoglucomutase, and one compound, the anthraquinone-
26 librium reactions, phosphoglucose isomerase, phosphoglucomutase, and triosephosphate isomerase fail t
27 ibuted to loss of glycogen phosphorylase and phosphoglucomutase at the protein level in both C9orf72
28 (a mutation in the starch-biosynthetic gene PHOSPHOGLUCOMUTASE) at the homozygous state display a mo
30 of the Mg(II) complex of phosphorylated beta-phosphoglucomutase (beta-PGM) from Lactococcus lactis ha
31 nesate and fluoroaluminate complexes of beta-phosphoglucomutase (beta-PGM) have demonstrated the impo
37 e dual-specificity enzyme phosphomannomutase/phosphoglucomutase catalyzes the transfer of a phosphory
38 ce of BT2127 and its closest homologue, beta-phosphoglucomutase, control the leaving group size (phos
40 se synthase, UDP-glucopyrophosphorylase, and phosphoglucomutase during expansion, thus suggesting an
41 xible domain 4, we show that the cyclase and phosphoglucomutase form a stable complex in vitro and th
42 gene with high sequence identity to the pgm (phosphoglucomutase) gene of Escherichia coli, which enco
43 of the B. subtilis CdaA is regulated by the phosphoglucomutase GlmM, which has been shown to interac
44 by Pseudomonas aeruginosa phosphomannomutase/phosphoglucomutase, has been studied by transient-state
48 form of 52 kDa bacterial phosphomannomutase/phosphoglucomutase is less accessible to dye or protease
49 ene is cotranscribed with pgm (which encodes phosphoglucomutase), it is likely to be polar on the exp
52 we present evidence that the S. aureus alpha-phosphoglucomutase (PgcA) and UTP:alpha-glucose 1-phosph
53 P to Glc-1-P to UDP-Glc and is mediated by a phosphoglucomutase (PGM) and a Glc-1-P uridylyltransfera
55 examined two additional gravitropic mutants, phosphoglucomutase (pgm) and sgr9, which show abnormal a
59 Using in vivo complementation of PMM and phosphoglucomutase (PGM) deficient strains of Pseudomona
66 hospho-N-acetylglucosamine mutase (PAGM) and phosphoglucomutase (PGM) reversibly catalyse the transfe
67 strain 2019 with mutations in genes encoding phosphoglucomutase (pgm), UDP-galactose-4-epimerase, and
69 , by introducing mutations in the plastidial phosphoglucomutase (pgm1) or the small subunit of ADP-Gl
70 ctose utilization genes GAL2, GAL1/10/7, and phosphoglucomutase (PGM1), and that the reference allele
71 a yeast strain lacking the major isoform of phosphoglucomutase (pgm2Delta) accumulates a high level
79 at the PGM-RP promoter evolved from the main phosphoglucomutase promoter which is active in wide rang
80 ently characterised a 60-kDa muscle-specific phosphoglucomutase-related protein (PGM-RP) which is exp
81 ers phosphonoacetaldehyde hydrolase and beta-phosphoglucomutase, the Gly was mutated to Pro, Val, or
82 These and earlier results from studies on B-phosphoglucomutase, triosephosphate isomerase, and glyce
83 enic candidates, phosphoglycerate mutase and phosphoglucomutase, were identified in all the three pol