ライフサイエンスコーパス: phosphomannomutase

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1 CDG-Ib have mutations in the genes encoding phosphomannomutase 2 (PMM2) and phosphomannose isomerase

2 congenital disorder of glycosylation (CDG), phosphomannomutase 2 (PMM2)-CDG, is caused by mutations

3 ients a promoter mutation (c.-167G>T) in the phosphomannomutase 2 gene (PMM2), either homozygous or i

4 cid/base residue Asp(21) suggests that alpha-phosphomannomutase (alpha-PMM) uses a different method o

5 ich includes the sarcoplasmic Ca(2+)-ATPase, phosphomannomutase, and phosphoserine phosphatase.

6 esis of the O-antigen) and ManBcoreproteins (phosphomannomutase involved in the biosynthesis of a man

7 It is caused by mutations in alpha-phosphomannomutase (of which there are two isozymes, alp

8 was used to identify potential inhibitors of phosphomannomutase/ phosphoglucomutase, and one compound

9 The enzyme phosphomannomutase/phosphoglucomutase (PMM/PGM) from Pse

10 The enzyme phosphomannomutase/phosphoglucomutase (PMM/PGM) from Pse

11 The enzyme phosphomannomutase/phosphoglucomutase (PMM/PGM) from the

12 Phosphomannomutase/phosphoglucomutase (PMM/PGM) is a ubi

13 onas aeruginosa, the dual-specificity enzyme phosphomannomutase/phosphoglucomutase catalyzes the tran

14 The phosphorylated form of 52 kDa bacterial phosphomannomutase/phosphoglucomutase is less accessible

15 Phosphomannomutase/phosphoglucomutase occupies a central

16 osphate, catalyzed by Pseudomonas aeruginosa phosphomannomutase/phosphoglucomutase, has been studied

17 B. melitensis 16M by removing genes encoding phosphomannomutase/phosphomannoisomerase (delta manBA) a

18 key enzymes: phosphomannose isomerase (PMI), phosphomannomutase (PMM) and GDP-mannose pyrophosphoryla

19 spectrometry (ACESI-MS) to assay the enzymes phosphomannomutase (PMM) and phosphomannose isomerase (P

20 Phosphomannomutase (PMM) deficiency causes congenital di

21 ts from mutations in pmm2, which encodes the phosphomannomutase (Pmm) that converts mannose-6-phospha

22 The enzymes phosphomannomutase (PMM), phospho-N-acetylglucosamine mu

23 transposon interruption in the gene encoding phosphomannomutase (pmm), suggesting that this activity

24 ose-6-phosphate to mannose-1-phosphate, by a phosphomannomutase (PMM), to produce GDP-mannose, the pr

25 Ia), results from a deficiency of the enzyme phosphomannomutase (PMM).

26 s of the ure1 operon, virB2, or pmm encoding phosphomannomutase were constructed and compared to the

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