2.4.1.131: GDP-Man:Man3GlcNAc2-PP-dolichol alpha-1,2-mannosyltransferase

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For detailed information about GDP-Man:Man3GlcNAc2-PP-dolichol alpha-1,2-mannosyltransferase, go to the full flat file.

Reaction

2 GDP-alpha-D-mannose +

Synonyms

Alg11, Alg2 mannosyltransferase, At2G40190, galactomannan deficiency protein 3, GDP-Man:Man3GlcNAc2-PP-dolichol-alpha1,2-mannosyltransferase, GDP-mannose-oligosaccharide-lipid mannosyltransferase, gmd3, guanosine diphosphomannose-oligosaccharide-lipid mannosyltransferase, hALG11, LEW3, mannosyltransferase, guanosine diphosphomannose-oligosaccharide-lipid, oligosaccharide-lipid mannosyltransferase

ECTree

     2 Transferases

         2.4 Glycosyltransferases

             2.4.1 Hexosyltransferases

                2.4.1.131 GDP-Man:Man3GlcNAc2-PP-dolichol alpha-1,2-mannosyltransferase

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Results	in table
2	Activating Compound
3418	AA Sequence
1	CAS Registry Number
7	Cloned(Commentary)
16	Disease/ Diagnostics
5	General Information
17	Inhibitors
4	KM Value [mM]
13	Localization
4	Metals/Ions
4	Molecular Weight [Da]
8	Natural Substrates/ Products (Substrates)
16	Organism
6	Pathway
6	PDB ID
5	pH Optimum
1	Posttranslational Modification
27	Protein Variants
4	Purification (Commentary)
1	Reaction
1	Reaction Type
15	Reference
13	Source Tissue
2	Specific Activity [micromol/min/mg]
3	Storage Stability
27	Substrates and Products (Substrate)
2	Subunits
18	Synonyms
1	Systematic Name
6	Temperature Optimum [°C]

Disease

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Disease on EC 2.4.1.131 - GDP-Man:Man3GlcNAc2-PP-dolichol alpha-1,2-mannosyltransferase

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DISEASE

TITLE OF PUBLICATION

LINK TO PUBMED

Congenital Disorders of Glycosylation

A severe human metabolic disease caused by deficiency of the endoplasmatic mannosyltransferase hALG11 leads to congenital disorder of glycosylation-Ip.

20080937

Congenital, Hereditary, and Neonatal Diseases and Abnormalities

A severe human metabolic disease caused by deficiency of the endoplasmatic mannosyltransferase hALG11 leads to congenital disorder of glycosylation-Ip.

20080937

Intellectual Disability

Improved diagnostics lead to identification of three new patients with congenital disorder of glycosylation-Ip.

22213132

Lipoma

Gene expression and single nucleotide polymorphism array analyses of spindle cell lipomas and conventional lipomas with 13q14 deletion.

21563233

Liver Neoplasms

Prognostic gene biomarker identification in liver cancer by data mining.

34150040

Metabolic Diseases

A severe human metabolic disease caused by deficiency of the endoplasmatic mannosyltransferase hALG11 leads to congenital disorder of glycosylation-Ip.

20080937

Seizures

Improved diagnostics lead to identification of three new patients with congenital disorder of glycosylation-Ip.

22213132

Strabismus

Improved diagnostics lead to identification of three new patients with congenital disorder of glycosylation-Ip.

22213132

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