Zobrazeno 1 - 10
of 38
pro vyhledávání: '"Naoyuki Kuwabara"'
Autor:
Axelle Renodon-Corniere, Tsutomu Mikawa, Naoyuki Kuwabara, Kentaro Ito, Dmitri Levitsky, Hiroshi Iwasaki, Masayuki Takahashi
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 7, p 3633 (2024)
Human Rad51 protein (HsRad51)-promoted DNA strand exchange, a crucial step in homologous recombination, is regulated by proteins and calcium ions. Both the activator protein Swi5/Sfr1 and Ca2+ ions stimulate different reaction steps and induce perpen
Externí odkaz:
https://doaj.org/article/d9b8ae8d5e1f4231b8fc79faca7aaa04
Autor:
Naoyuki Kuwabara, Rieko Imae, Hiroshi Manya, Tomohiro Tanaka, Mamoru Mizuno, Hiroki Tsumoto, Motoi Kanagawa, Kazuhiro Kobayashi, Tatsushi Toda, Toshiya Senda, Tamao Endo, Ryuichi Kato
Publikováno v:
Nature Communications, Vol 11, Iss 1, Pp 1-11 (2020)
Fukutin-related protein (FKRP) catalyses the addition of ribitol-phosphate (RboP) to the O-mannosyl glycan of α-dystroglycan and mutations in FKRP cause dystroglycanopathy. Here the authors provide insights into its oligomerization and recognition o
Externí odkaz:
https://doaj.org/article/a2adec609bc8456584e53ec9bdfe4352
Autor:
Keitaro Yamashita, Naoyuki Kuwabara, Takanori Nakane, Tomohiro Murai, Eiichi Mizohata, Michihiro Sugahara, Dongqing Pan, Tetsuya Masuda, Mamoru Suzuki, Tomomi Sato, Atsushi Kodan, Tomohiro Yamaguchi, Eriko Nango, Tomoyuki Tanaka, Kensuke Tono, Yasumasa Joti, Takashi Kameshima, Takaki Hatsui, Makina Yabashi, Hiroshi Manya, Tamao Endo, Ryuichi Kato, Toshiya Senda, Hiroaki Kato, So Iwata, Hideo Ago, Masaki Yamamoto, Fumiaki Yumoto, Toru Nakatsu
Publikováno v:
IUCrJ, Vol 4, Iss 5, Pp 639-647 (2017)
Serial femtosecond crystallography (SFX) using X-ray free-electron lasers (XFELs) holds enormous potential for the structure determination of proteins for which it is difficult to produce large and high-quality crystals. SFX has been applied to vario
Externí odkaz:
https://doaj.org/article/6801e2bc89df4536aa7bf825ab1a4cbf
Publikováno v:
Trends in Glycoscience and Glycotechnology. 32:E195-E200
Publikováno v:
Journal of Biological Chemistry. 295:9076-9086
RNA triphosphatase catalyzes the first step in mRNA cap formation, hydrolysis of the terminal phosphate from the nascent mRNA transcript. The RNA triphosphatase from the protozoan parasite Trypanosoma cruzi, TcCet1, belongs to the family of triphosph
Autor:
Tamao Endo, Hiroki Tsumoto, Motoi Kanagawa, Toshiya Senda, Ryuichi Kato, Naoyuki Kuwabara, Rieko Imae, Hiroshi Manya, Mamoru Mizuno, Tatsushi Toda, Tomohiro Tanaka, Kazuhiro Kobayashi
Publikováno v:
Nature Communications, Vol 11, Iss 1, Pp 1-11 (2020)
Nature Communications
Nature Communications
α-Dystroglycan (α-DG) is a highly-glycosylated surface membrane protein. Defects in the O-mannosyl glycan of α-DG cause dystroglycanopathy, a group of congenital muscular dystrophies. The core M3 O-mannosyl glycan contains tandem ribitol-phosphate
Autor:
Ryuichi Kato, Tomohiro Tanaka, Hiroshi Manya, Tamao Endo, Rieko Imae, Mamoru Mizuno, Naoyuki Kuwabara, Masato Tsuyuguchi
Publikováno v:
Genes to cells 26(7), 485-494 (2021). doi:10.1111/gtc.12853
Genes to Cells
Genes to Cells
Genes to cells 26(7), 485-494 (2021). doi:10.1111/gtc.12853
Defects in the O-mannosyl glycan of ��-dystroglycan (��-DG) are associated with ��-dystroglycanopathy, a group of congenital muscular dystrophies. While ��-DG has many O
Defects in the O-mannosyl glycan of ��-dystroglycan (��-DG) are associated with ��-dystroglycanopathy, a group of congenital muscular dystrophies. While ��-DG has many O
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c4832aa99c08d917a9512815470fca41
https://bib-pubdb1.desy.de/record/472498
https://bib-pubdb1.desy.de/record/472498
Publikováno v:
Methods in molecular biology (Clifton, N.J.). 2132
Protein O-mannose β1,2-N-acetylglucosaminyltransferase 1 (POMGNT1) is one of the gene products responsible for α-dystroglycanopathy, which is a type of congenital muscular dystrophy caused by O-mannosyl glycan defects. The originally identified fun
Publikováno v:
Methods in Molecular Biology ISBN: 9781071604298
Protein O-mannose β1,2-N-acetylglucosaminyltransferase 1 (POMGNT1) is one of the gene products responsible for α-dystroglycanopathy, which is a type of congenital muscular dystrophy caused by O-mannosyl glycan defects. The originally identified fun
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::253efec1bd35cb380b0102f3195fd559
https://doi.org/10.1007/978-1-0716-0430-4_52
https://doi.org/10.1007/978-1-0716-0430-4_52
Publikováno v:
J Biol Chem
RNA triphosphatase catalyzes the first step in mRNA cap formation, hydrolysis of the terminal phosphate from the nascent mRNA transcript. The RNA triphosphatase from the protozoan parasite Trypanosoma cruzi, TcCet1, belongs to the family of triphosph