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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 sylation protein 6)-deficiency CDG and PMM2 (phosphomannomutase 2)-deficiency CDG, and 23 first- and
5                                              Phosphomannomutase-2 (PMM2) deficiency represents the mo
6 cid/base residue Asp(21) suggests that alpha-phosphomannomutase (alpha-PMM) uses a different method o
7 ich includes the sarcoplasmic Ca(2+)-ATPase, phosphomannomutase, and phosphoserine phosphatase.
8                                              Phosphomannomutase deficiency (PMM2 congenital disorder
9  of glycosylation (CDG) are mutations in the phosphomannomutase gene PMM2, which affect protein N-lin
10 esis of the O-antigen) and ManBcoreproteins (phosphomannomutase involved in the biosynthesis of a man
11           It is caused by mutations in alpha-phosphomannomutase (of which there are two isozymes, alp
12 was used to identify potential inhibitors of phosphomannomutase/ phosphoglucomutase, and one compound
13                                        alpha-Phosphomannomutase/phosphoglucomutase (alphaPMM/PGM) fro
14  the Le2152 gene, which encodes an AlgC-type phosphomannomutase/phosphoglucomutase (PMM).
15                                   The enzyme phosphomannomutase/phosphoglucomutase (PMM/PGM) from Pse
16                                   The enzyme phosphomannomutase/phosphoglucomutase (PMM/PGM) from Pse
17                                   The enzyme phosphomannomutase/phosphoglucomutase (PMM/PGM) from the
18                                              Phosphomannomutase/phosphoglucomutase (PMM/PGM) is a ubi
19 onas aeruginosa, the dual-specificity enzyme phosphomannomutase/phosphoglucomutase catalyzes the tran
20  The phosphorylated form of 52 kDa bacterial phosphomannomutase/phosphoglucomutase is less accessible
21                                              Phosphomannomutase/phosphoglucomutase occupies a central
22 osphate, catalyzed by Pseudomonas aeruginosa phosphomannomutase/phosphoglucomutase, has been studied
23 B. melitensis 16M by removing genes encoding phosphomannomutase/phosphomannoisomerase (delta manBA) a
24 rasite GPI anchor biosynthesis, the putative phosphomannomutase (PMM) (EC 5.4.2.8), HAD5.
25 key enzymes: phosphomannose isomerase (PMI), phosphomannomutase (PMM) and GDP-mannose pyrophosphoryla
26 spectrometry (ACESI-MS) to assay the enzymes phosphomannomutase (PMM) and phosphomannose isomerase (P
27                                              Phosphomannomutase (PMM) deficiency causes congenital di
28 ts from mutations in pmm2, which encodes the phosphomannomutase (Pmm) that converts mannose-6-phospha
29                                  The enzymes phosphomannomutase (PMM), phospho-N-acetylglucosamine mu
30 transposon interruption in the gene encoding phosphomannomutase (pmm), suggesting that this activity
31 ose-6-phosphate to mannose-1-phosphate, by a phosphomannomutase (PMM), to produce GDP-mannose, the pr
32 Ia), results from a deficiency of the enzyme phosphomannomutase (PMM).
33 s of the ure1 operon, virB2, or pmm encoding phosphomannomutase were constructed and compared to the