ライフサイエンスコーパス: phosphoglucomutase

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

3 Recent studies have identified phosphoglucomutase 1 (PGM1) deficiency as an inherited m

4 used to identify a mutation in the gene for phosphoglucomutase 1 (PGM1) in two siblings.

5 Human phosphoglucomutase 1 (PGM1) plays a central role in cell

6 Phosphoglucomutase 1 deficiency, previously identified a

7 Phosphoglucomutase 1 enzyme activity was assayed on cell

8 Phosphoglucomutase 1 enzyme activity was markedly dimini

9 ta-enolase and triosephosphate isomerase and phosphoglucomutase-1.

10 Human phosphoglucomutase 3 (PGM3) catalyzes the conversion of

11 ucial enzyme in the glycosylation pathway is phosphoglucomutase 3 (PGM3), which catalyzes a key step

12 osomal recessive mutations in a single gene, phosphoglucomutase 3 (PGM3).

13 s a sole carbon source and was defective for phosphoglucomutase activity, suggesting functional ident

14 Two classes of phosphoglucomutases (alpha-PGM and beta-PGM) are disting

15 eficient in leaf starch and lacked plastidic phosphoglucomutase, an enzyme critical for gluconeogenes

16 nnose and appears to be generated in part by phosphoglucomutase, an enzyme important for lipooligosac

17 irect determination of kinetic constants for phosphoglucomutase and its phosphorylated products is de

18 reading frames: a partial pgm gene (encoding phosphoglucomutase) and a complete qor gene (encoding NA

19 potential inhibitors of phosphomannomutase/ phosphoglucomutase, and one compound, the anthraquinone-

20 variation in glycogen synthase, hexokinase, phosphoglucomutase, and trehalase activity.

21 librium reactions, phosphoglucose isomerase, phosphoglucomutase, and triosephosphate isomerase fail t

22 (a mutation in the starch-biosynthetic gene PHOSPHOGLUCOMUTASE) at the homozygous state display a mo

23 Lactococcus lactis beta-phosphoglucomutase (beta-PGM) catalyzes the interconvers

24 of the Mg(II) complex of phosphorylated beta-phosphoglucomutase (beta-PGM) from Lactococcus lactis ha

25 nesate and fluoroaluminate complexes of beta-phosphoglucomutase (beta-PGM) have demonstrated the impo

26 Tauhe beta-phosphoglucomutase (beta-PGM) of the haloacid dehalogena

27 beta-Phosphoglucomutase (betaPGM) catalyzes isomerization of

28 Activated Lactococcus lactis beta-phosphoglucomutase (betaPGM) catalyzes the conversion of

29 Phosphoglucomutases catalyze the interconversion of D-gl

30 e dual-specificity enzyme phosphomannomutase/phosphoglucomutase catalyzes the transfer of a phosphory

31 ce of BT2127 and its closest homologue, beta-phosphoglucomutase, control the leaving group size (phos

32 structure obtained only in the debated beta-phosphoglucomutase crystal.

33 se synthase, UDP-glucopyrophosphorylase, and phosphoglucomutase during expansion, thus suggesting an

34 gene with high sequence identity to the pgm (phosphoglucomutase) gene of Escherichia coli, which enco

35 by Pseudomonas aeruginosa phosphomannomutase/phosphoglucomutase, has been studied by transient-state

36 Given the previously defined role for phosphoglucomutase in antimicrobial peptide resistance i

37 Crystallization of phosphorylated beta-phosphoglucomutase in the presence of the Mg(II) cofacto

38 form of 52 kDa bacterial phosphomannomutase/phosphoglucomutase is less accessible to dye or protease

39 ene is cotranscribed with pgm (which encodes phosphoglucomutase), it is likely to be polar on the exp

40 In the starchless phosphoglucomutase mutant at night, protein synthesis wa

41 Phosphomannomutase/phosphoglucomutase occupies a central position in the pa

42 we present evidence that the S. aureus alpha-phosphoglucomutase (PgcA) and UTP:alpha-glucose 1-phosph

43 P to Glc-1-P to UDP-Glc and is mediated by a phosphoglucomutase (PGM) and a Glc-1-P uridylyltransfera

44 The phosphoglucomutase (PGM) and Glc-1-P uridylyltransferase

45 examined two additional gravitropic mutants, phosphoglucomutase (pgm) and sgr9, which show abnormal a

46 The other two proteins, phosphoglucomutase (Pgm) and transketolase (TktA), are e

47 Phosphoglucomutase (PGM) catalyzes the interconversion o

48 Loss of the major isoform of phosphoglucomutase (PGM) causes an accumulation of gluco

49 Using in vivo complementation of PMM and phosphoglucomutase (PGM) deficient strains of Pseudomona

50 n, and show that it is a novel member of the phosphoglucomutase (PGM) family of proteins.

51 mutant disrupted an S. iniae homologue of a phosphoglucomutase (pgm) gene.

52 Phosphoglucomutase (PGM) is a key enzyme in glucose meta

53 Phosphoglucomutase (PGM) is a ubiquitous highly conserve

54 iana) Columbia (Col-0) and in the starchless phosphoglucomutase (pgm) mutant.

55 Although the enzyme phosphoglucomutase (PGM) possesses several allozyme poly

56 hospho-N-acetylglucosamine mutase (PAGM) and phosphoglucomutase (PGM) reversibly catalyse the transfe

57 strain 2019 with mutations in genes encoding phosphoglucomutase (pgm), UDP-galactose-4-epimerase, and

58 Human phosphoglucomutase (PGM1) is a highly poly-morphic prote

59 , by introducing mutations in the plastidial phosphoglucomutase (pgm1) or the small subunit of ADP-Gl

60 a yeast strain lacking the major isoform of phosphoglucomutase (pgm2Delta) accumulates a high level

61 different position within the gene encoding phosphoglucomutase (pgmA; y1258).

62 The enzyme phosphoglucomutase plays a key role in cellular metaboli

63 The enzyme phosphomannomutase/phosphoglucomutase (PMM/PGM) from Pseudomonas aeruginosa

64 The enzyme phosphomannomutase/phosphoglucomutase (PMM/PGM) from Pseudomonas aeruginosa

65 The enzyme phosphomannomutase/phosphoglucomutase (PMM/PGM) from the bacterium Pseudomo

66 Phosphomannomutase/phosphoglucomutase (PMM/PGM) is a ubiquitous four-domain

67 at the PGM-RP promoter evolved from the main phosphoglucomutase promoter which is active in wide rang

68 ently characterised a 60-kDa muscle-specific phosphoglucomutase-related protein (PGM-RP) which is exp

69 ers phosphonoacetaldehyde hydrolase and beta-phosphoglucomutase, the Gly was mutated to Pro, Val, or

70 enic candidates, phosphoglycerate mutase and phosphoglucomutase, were identified in all the three pol