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Literature summary for 2.7.11.26 extracted from

  • Koehler, C.; Dinekov, M.; Goetz, J.
    Active glycogen synthase kinase-3 and tau pathology-related tyrosine phosphorylation in pR5 human tau transgenic mice (2013), Neurobiol. Aging, 34, 1369-1379.
    View publication on PubMed

Protein Variants

Protein Variants Comment Organism
additional information generation of several mutant mice, overview. Analysis of pathomechanisms in tauopathies using pR5 mice that express the P301L tau mutation found in familial forms of frontotemporal dementia, overview Mus musculus

Metals/Ions

Metals/Ions Comment Organism Structure
Mg2+ required Mus musculus

Natural Substrates/ Products (Substrates)

Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
ATP + [tau-protein] Mus musculus
-
ADP + O-phospho-[tau-protein]
-
?
ATP + [tau-protein] Mus musculus C57BL/6
-
ADP + O-phospho-[tau-protein]
-
?

Organism

Organism UniProt Comment Textmining
Mus musculus Q2NL51
-
-
Mus musculus Q9WV60
-
-
Mus musculus C57BL/6 Q2NL51
-
-
Mus musculus C57BL/6 Q9WV60
-
-

Source Tissue

Source Tissue Comment Organism Textmining
neuron GSK3 exists in neurons as 3 isoforms (GSK3alpha, beta, and beta2) that are encoded by 2 separate genes, immunohistochemic study of isozyme localization in neurons, detailed overview Mus musculus
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
ATP + [tau-protein]
-
Mus musculus ADP + O-phospho-[tau-protein]
-
?
ATP + [tau-protein]
-
Mus musculus C57BL/6 ADP + O-phospho-[tau-protein]
-
?

Synonyms

Synonyms Comment Organism
glycogen synthase kinase-3
-
Mus musculus
GSK3alpha
-
Mus musculus
GSK3beta
-
Mus musculus

Cofactor

Cofactor Comment Organism Structure
ATP
-
Mus musculus

General Information

General Information Comment Organism
malfunction functional status of glycogen synthase kinase-3 and correlated appearance of distinct tau phospho-epitopes: neurons displaying increases in activation of phosphorylation of glycogen synthase kinase-3alpha/beta at tyrosine 279/216 also show an intense rather than moderate AT8 (phospho-Ser202/Thr205 tau) immunoreactivity, and immunoreactivity for AT100 (phospho-Ser212/Thr214 tau) and phosphorylated Ser422, phospho-epitopes associated with fibrillar tau pathology. These neurons are rare in 8.5-month-old, but numerous in 18.5- and 28-month-old pR5 mice. Tau- rather than an amyloid-beta peptide-induced pathology is associated with increased neuronal tyrosine phosphorylation. Tyrosine phosphorylation only increases in neurons with fibrillar tau pathology Mus musculus