Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Andrea Kuchtová"'
Autor:
M. Kathryn Brewer, Maria Machio-Castello, Rosa Viana, Jeremiah L. Wayne, Andrea Kuchtová, Zoe R. Simmons, Sarah Sternbach, Sheng Li, Maria Adelaida García-Gimeno, Jose M. Serratosa, Pascual Sanz, Craig W. Vander Kooi, Matthew S. Gentry
Publikováno v:
iScience, Vol 24, Iss 11, Pp 103276- (2021)
Summary: Lafora disease (LD) is a fatal childhood dementia characterized by progressive myoclonic epilepsy manifesting in the teenage years, rapid neurological decline, and death typically within ten years of onset. Mutations in either EPM2A, encodin
Externí odkaz:
https://doaj.org/article/08a505503d644df58c43dc58bd8a2937
Autor:
Pascual Sanz, Sheng Li, Craig W. Vander Kooi, Jeremiah Wayne, Andrea Kuchtová, Maria Machio-Castello, Zoe R. Simmons, Sarah Sternbach, M. Kathryn Brewer, Matthew S. Gentry, Maria Adelaida Garcia-Gimeno, Rosa Viana, Jose M. Serratosa
Publikováno v:
iScience, Vol 24, Iss 11, Pp 103276-(2021)
Digital.CSIC. Repositorio Institucional del CSIC
instname
iScience
Digital.CSIC. Repositorio Institucional del CSIC
instname
iScience
Summary Lafora disease (LD) is a fatal childhood dementia characterized by progressive myoclonic epilepsy manifesting in the teenage years, rapid neurological decline, and death typically within ten years of onset. Mutations in either EPM2A, encoding
Autor:
Kenyon Weis, Madushi Raththagala, Matthias Thalmann, Savita Sharma, Claudia Mak, David A. Meekins, Craig W. Vander Kooi, Tiffany Henao, Andrea Kuchtová, Tiantian Chen
Publikováno v:
Biochemistry. 60(31)
Glucan phosphatases are members of a functionally diverse family of dual-specificity phosphatase (DSP) enzymes. The plant glucan phosphatase Starch Excess4 (SEX4) binds and dephosphorylates glucans, contributing to processive starch degradation in th
Publikováno v:
Enzymology of Complex Alpha-Glucans
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4c42b6fdd83255438f974798b9719ced
https://doi.org/10.1201/b22412-7
https://doi.org/10.1201/b22412-7
Laforin catalyses glycogen dephosphorylation. Mutations in its gene result in Lafora disease, a fatal progressive myoclonus epilepsy, the hallmark being water-insoluble, hyperphosphorylated carbohydrate inclusions called Lafora bodies. Human laforin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c90318db26fc3496d6b21dabb494165
https://europepmc.org/articles/PMC5829021/
https://europepmc.org/articles/PMC5829021/
Autor:
Andrea Kuchtová, Štefan Janeček
Publikováno v:
Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics. 1854:1260-1268
The CAZy glycoside hydrolase (GH) family GH77 is a monospecific family containing 4-α-glucanotransferases that if from prokaryotes are known as amylomaltases and if from plants including algae are known as disproportionating enzymes (DPE). The famil
Publikováno v:
Biologia. 70:1284-1294
The α-amylase enzyme specificity has been classified in the Carbohydrate-Active enZyme (CAZy) database into the families GH13, GH57, GH119 and eventually also GH126. α-Amylase is a glycoside hydrolase (GH) that catalyses in an endo-fashion the hydr
Autor:
Andrea Kuchtová, Štefan Janeček
Publikováno v:
Microbiology (Reading, England). 162(12)
Among the glycoside hydrolases (GHs) classified within the Carbohydrate-Active enZyme (CAZy) database, the α-amylase family GH13 containing ~30 different enzyme specificities and more than 37 000 sequences represents one of the largest GH families.
Autor:
Andrea Kuchtová, Štefan Janeček
Publikováno v:
FEBS Letters. 586:3360-3366
The glycoside hydrolase family 119 (GH119) contains the α-amylase from Bacillus circulans and five other hypothetical proteins. Until now, nothing has been reported on the catalytic residues and catalytic-domain fold of GH119. Based on a detailed in