Mannose P Dolichol Utilization Defect Protein 1 (MPDU1)

[Edit]

CDGIF; HBEBP2BPA; Lec35; PQLC5; SL15; Suppressor of Lec15 and Lec35 glycosylation mutation homolog

Mannose P Dolichol Utilization Defect Protein 1 (MPDU1)
MPD synthase (DPM1) catalyzes the synthesis of mannose-P-dolichol (MPD), an essential sugar donor for glycoconjugates and an essential substrate for synthesis of glycosylphosphatidylinositols (GPIs). The Chinese hamster ovary (CHO) Lec15 and Lec35 mutant cells are defective in synthesis and utilization, respectively, of MPD. The SL15 cDNA also suppressed the Lec35 mutation. Sequence analysis indicated that SL15 encodes a transmembrane protein with cytosolic C and N termini. There was no significant sequence similarity between SL15 and the S. cerevisiae MPD synthase, leading the authors to suggest that SL15 plays a distinct role in MPD synthesis. Mao et al. (1998) identified an umbilical cord blood CD34-positive cell cDNA encoding the human homolog of SL15. The predicted human protein contains 247 amino acids.

Organism species: Homo sapiens (Human)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant Mannose P Dolichol Utilization Defect Protein 1 (MPDU1) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to Mannose P Dolichol Utilization Defect Protein 1 (MPDU1) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to Mannose P Dolichol Utilization Defect Protein 1 (MPDU1) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for Mannose P Dolichol Utilization Defect Protein 1 (MPDU1) CLIA Kit Customized Service Offer
n/a ELISA Kit for Mannose P Dolichol Utilization Defect Protein 1 (MPDU1) ELISA Kit Customized Service Offer

Organism species: Mus musculus (Mouse)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant Mannose P Dolichol Utilization Defect Protein 1 (MPDU1) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to Mannose P Dolichol Utilization Defect Protein 1 (MPDU1) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to Mannose P Dolichol Utilization Defect Protein 1 (MPDU1) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for Mannose P Dolichol Utilization Defect Protein 1 (MPDU1) CLIA Kit Customized Service Offer
n/a ELISA Kit for Mannose P Dolichol Utilization Defect Protein 1 (MPDU1) ELISA Kit Customized Service Offer

Organism species: Rattus norvegicus (Rat)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant Mannose P Dolichol Utilization Defect Protein 1 (MPDU1) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to Mannose P Dolichol Utilization Defect Protein 1 (MPDU1) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to Mannose P Dolichol Utilization Defect Protein 1 (MPDU1) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for Mannose P Dolichol Utilization Defect Protein 1 (MPDU1) CLIA Kit Customized Service Offer
n/a ELISA Kit for Mannose P Dolichol Utilization Defect Protein 1 (MPDU1) ELISA Kit Customized Service Offer
  1. "Identification of genes expressed in human CD34(+) hematopoietic stem/progenitor cells by expressed sequence tags and efficient full-length cDNA cloning."Proc. Natl. Acad. Sci. U.S.A. 95:8175-8180(1998) [PubMed] [Europe PMC] [Abstract]
  2. "Complete sequencing and characterization of 21,243 full-length human cDNAs." Nat. Genet. 36:40-45(2004) [PubMed] [Europe PMC] [Abstract]
  3. "DNA sequence of human chromosome 17 and analysis of rearrangement in the human lineage." Nature 440:1045-1049(2006) [PubMed] [Europe PMC] [Abstract]
  4. "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."Genome Res. 14:2121-2127(2004) [PubMed] [Europe PMC] [Abstract]
  5. "Lys-N and trypsin cover complementary parts of the phosphoproteome in a refined SCX-based approach."Anal. Chem. 81:4493-4501(2009) [PubMed] [Europe PMC] [Abstract]
  6. "Initial characterization of the human central proteome."BMC Syst. Biol. 5:17-17(2011) [PubMed] [Europe PMC] [Abstract]
  7. "N-terminal acetylome analyses and functional insights of the N-terminal acetyltransferase NatB."Proc. Natl. Acad. Sci. U.S.A. 109:12449-12454(2012) [PubMed] [Europe PMC] [Abstract]
  8. "A mutation in the human MPDU1 gene causes congenital disorder of glycosylation type If (CDG-If)."J. Clin. Invest. 108:1613-1619(2001) [PubMed] [Europe PMC] [Abstract]
  9. "MPDU1 mutations underlie a novel human congenital disorder of glycosylation, designated type If."J. Clin. Invest. 108:1687-1695(2001) [PubMed] [Europe PMC] [Abstract]
  10. ErratumJ. Clin. Invest. 111:925-925(2001)