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Recombinant Human Phosphoglucomutase-1 (PGM1)

This Human PGM1 recombinant protein was produced in E. coli, where the gene sequence encoding Human PGM1 (1-562aa) was expressed with the N-terminal 6xHis-SUMO tag. The purity of this PGM1 protein was greater than 90% by SDS-PAGE.PGM1 is an enzyme with the primary function of catalyzing the interconversion of glucose-6-phosphate (G6P) and glucose-1-phosphate (G1P) in the sugar metabolism pathway. Specifically, it converts G6P to G1P or G1P to G6P. This enzymatic activity is crucial for cellular energy metabolism and the synthesis and breakdown of sugars. PGM1 is involved in multiple sugar metabolism pathways, including sugar isomerization, sugar alcohol phosphorylation, and glycogen synthesis and breakdown. These pathways are essential for maintaining cellular energy balance and survival.The PGM1 gene is located in the human genome, and mutations or genetic variations can lead to a rare inherited metabolic disorder known as PGM1 deficiency disease (PGM1-CDG). This is a glycoprotein glycosylation disorder, and patients typically exhibit multisystem symptoms, including growth retardation, neurological issues, and immune system problems.

ACP03962

This Human PGM1 recombinant protein was produced in E. coli, where the gene sequence encoding Human PGM1 (1-562aa) was expressed with the N-terminal 6xHis-SUMO tag. The purity of this PGM1 protein was greater than 90% by SDS-PAGE.PGM1 is an enzyme with the primary function of catalyzing the interconversion of glucose-6-phosphate (G6P) and glucose-1-phosphate (G1P) in the sugar metabolism pathway. Specifically, it converts G6P to G1P or G1P to G6P. This enzymatic activity is crucial for cellular energy metabolism and the synthesis and breakdown of sugars. PGM1 is involved in multiple sugar metabolism pathways, including sugar isomerization, sugar alcohol phosphorylation, and glycogen synthesis and breakdown. These pathways are essential for maintaining cellular energy balance and survival.The PGM1 gene is located in the human genome, and mutations or genetic variations can lead to a rare inherited metabolic disorder known as PGM1 deficiency disease (PGM1-CDG). This is a glycoprotein glycosylation disorder, and patients typically exhibit multisystem symptoms, including growth retardation, neurological issues, and immune system problems.

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Specifications


Cat.No ACP03962 Target NamePGM1
Target SynonymsCDG1T; Glucose phosphomutase 1; GSD14; OTTHUMP00000010519; OTTHUMP00000010520; PGM 1; PGM1; PGM1_HUMAN; Phosphoglucomutase 1; Phosphoglucomutase-1; Phosphoglucomutase1FormLiquid or Lyophilized powder
Expression SystemE.coliExpression Range1-562aa
Mol Weight77.4kDaProtein LengthFull length
PurityGreater than 90% as determined by SDS-PAGE.Storage Buffer5%-50% glycerol. Lyophilized powder form: the buffer before lyophilization is Tris/PBS-based buffer, 6% Trehalose, Liquid form: default storage buffer is Tris/PBS-based buffer, pH 8.0.

Immunogen Information


Target SpeciesHumanUniprot IDP36871
Background Information
  • Uniprot Id

    P36871

  • Target Species

    Human

  • Target Name

    PGM1

  • Target Full Name

    Phosphoglucomutase-1

  • Target Function

    This enzyme participates in both the breakdown and synthesis of glucose.

  • Target Involvement

    Congenital disorder of glycosylation 1T (CDG1T)

  • Target Subcellular Location

    [Isoform 1]: Cytoplasm.

  • Target Protein Families

    Phosphohexose mutase family

  • Target Research Area

    Metabolism

  • Target Synonyms

    CDG1T; Glucose phosphomutase 1; GSD14; OTTHUMP00000010519; OTTHUMP00000010520; PGM 1; PGM1; PGM1_HUMAN; Phosphoglucomutase 1; Phosphoglucomutase-1; Phosphoglucomutase1

  • Target Background

    The protein encoded by this gene is an isozyme of phosphoglucomutase (PGM) and belongs to the phosphohexose mutase family. There are several PGM isozymes, which are encoded by different genes and catalyze the transfer of phosphate between the 1 and 6 positions of glucose. In most cell types, this PGM isozyme is predominant, representing about 90% of total PGM activity. In red cells, PGM2 is a major isozyme. This gene is highly polymorphic. Mutations in this gene cause glycogen storage disease type 14. Alternativley spliced transcript variants encoding different isoforms have been identified in this gene.

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