Kinetic properties and tissular distribution of mammalian phosphomannomutase isozymes - Test2 - elhamkhani - TriplyDB

Kinetic properties and tissular distribution of mammalian phosphomannomutase isozymes

Kinetic properties and tissular distribution of mammalian phosphomannomutase isozymes

http://www.wikidata.org/entity/Q24531435

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The X-ray crystal structures of human alpha-phosphomannomutase 1 reveal the structural basis of congenital disorder of glycosylation type 1a Glycomic Characterization of Induced Pluripotent Stem Cells Derived from a Patient Suffering from Phosphomannomutase 2 Congenital Disorder of Glycosylation (PMM2-CDG)From structure to function: YrbI from Haemophilus influenzae (HI1679) is a phosphatase Mutations in PMM2 that cause congenital disorders of glycosylation, type Ia (CDG-Ia)Conformational response to ligand binding in phosphomannomutase2: insights into inborn glycosylation disorder.Protein inhibitor of activated STAT1 interacts with and up-regulates activities of the pro-proliferative transcription factor Krüppel-like factor 5.Molecular analysis of phosphomannomutase (PMM) genes reveals a unique PMM duplication event in diverse Triticeae species and the main PMM isozymes in bread wheat tissues.A phosphohexomutase from the archaeon Sulfolobus solfataricus is covalently modified by phosphorylation on serine Glycosylation defects and virulence phenotypes of Leishmania mexicana phosphomannomutase and dolicholphosphate-mannose synthase gene deletion mutants.A deeply divergent phosphoglucomutase (PGM) of Giardia lamblia has both PGM and phosphomannomutase activities.Targeted disruption of the mouse phosphomannomutase 2 gene causes early embryonic lethality The normal phenotype of Pmm1-deficient mice suggests that Pmm1 is not essential for normal mouse development.Amino acid determinants of substrate selectivity in the Trypanosoma brucei sphingolipid synthase family.Heterodimerization of Two Pathological Mutants Enhances the Activity of Human Phosphomannomutase2 Towards a therapy for phosphomannomutase 2 deficiency, the defect in CDG-Ia patients.Mammalian phosphomannomutase PMM1 is the brain IMP-sensitive glucose-1,6-bisphosphatase Biochemical phenotype of a common disease-causing mutation and a possible therapeutic approach for the phosphomannomutase 2-associated disorder of glycosylation Phosphoglucomutase is absent in Trypanosoma brucei and redundantly substituted by phosphomannomutase and phospho-N-acetylglucosamine mutase.A mutant of phosphomannomutase1 retains full enzymatic activity, but is not activated by IMP: Possible implications for the disease PMM2-CDG.The α-Phosphoglucomutase ofLactococcus lactisIs Unrelated to the α-d-Phosphohexomutase Superfamily and Is Encoded by the Essential GenepgmH The Analysis of Variants in the General Population Reveals That Is Extremely Tolerant to Missense Mutations and That Diagnosis of PMM2-CDG Can Benefit from the Identification of Modifiers

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P2860

Kinetic properties and tissular distribution of mammalian phosphomannomutase isozymes

http://www.wikidata.org/entity/Q24531435

description

1999 nî lūn-bûn

@nan

1999 թուականի Ապրիլին հրատարակուած գիտական յօդուած

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1999 թվականի ապրիլին հրատարակված գիտական հոդված

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1999年の論文

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1999年論文

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1999年論文

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1999年論文

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1999年論文

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1999年論文

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1999年论文

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name

Kinetic properties and tissular distribution of mammalian phosphomannomutase isozymes

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Kinetic properties and tissular distribution of mammalian phosphomannomutase isozymes

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Kinetic properties and tissular distribution of mammalian phosphomannomutase isozymes

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Kinetic properties and tissular distribution of mammalian phosphomannomutase isozymes

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type

label

Kinetic properties and tissular distribution of mammalian phosphomannomutase isozymes

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Kinetic properties and tissular distribution of mammalian phosphomannomutase isozymes

@en

Kinetic properties and tissular distribution of mammalian phosphomannomutase isozymes

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Kinetic properties and tissular distribution of mammalian phosphomannomutase isozymes

@nl

prefLabel

Kinetic properties and tissular distribution of mammalian phosphomannomutase isozymes

@ast

Kinetic properties and tissular distribution of mammalian phosphomannomutase isozymes

@en

Kinetic properties and tissular distribution of mammalian phosphomannomutase isozymes

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Kinetic properties and tissular distribution of mammalian phosphomannomutase isozymes

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Biochemical Journal

P1476

Kinetic properties and tissular distribution of mammalian phosphomannomutase isozymes

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P2093

Achouri Y

http://www.w3.org/2001/XMLSchema#string

Matthijs G

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Pirard M

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Schollen E

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Van Schaftingen E

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DNA sequencing with chain-terminating inhibitors

Mutations in PMM2, a phosphomannomutase gene on chromosome 16p13, in carbohydrate-deficient glycoprotein type I syndrome (Jaeken syndrome)

Lack of homozygotes for the most frequent disease allele in carbohydrate-deficient glycoprotein syndrome type 1A

Gapped BLAST and PSI-BLAST: a new generation of protein database search programs

Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications

A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding

Use of bacteriophage T7 RNA polymerase to direct selective high-level expression of cloned genes

The yeast SEC53 gene encodes phosphomannomutase.

A family of hexosephosphate mutases in Saccharomyces cerevisiae.

PMM (PMM1), the human homologue of SEC53 or yeast phosphomannomutase, is localized on chromosome 22q13

P304

201-207

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scholarly article

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10.1042/BJ3390201

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P433

1

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P478

339 ( Pt 1)

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Jean-francois Collet

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1999-04-01T00:00:00Z

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10085245

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P932

1220145

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