Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Máté Sulyok-Eiler"'
Autor:
Ho-Jin Lee, Shi-Wei Liu, Máté Sulyok-Eiler, Veronika Harmat, Viktor Farkas, Zoltán Bánóczi, Mouna El Khabchi, Hua-Jun Shawn Fan, Kimihiko Hirao, Jong-Won Song
Publikováno v:
Heliyon, Vol 10, Iss 12, Pp e33159- (2024)
The conformational properties of Alanine (Ala) residue have been investigated to understand protein folding and develop force fields. In this work, we examined the neighbor effect on the conformational spaces of Ala residue using model azapeptides, A
Externí odkaz:
https://doaj.org/article/8e15da5995494e1b9144799f408f3421
Autor:
Dániel Horváth, Zsolt Dürvanger, Dóra K. Menyhárd, Máté Sulyok-Eiler, Fruzsina Bencs, Gergő Gyulai, Péter Horváth, Nóra Taricska, András Perczel
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-15 (2023)
Abstract A large group of hormones are stored as amyloid fibrils in acidic secretion vesicles before they are released into the bloodstream and readopt their functional state. Here, we identify an evolutionarily conserved hexapeptide sequence as the
Externí odkaz:
https://doaj.org/article/7faf27c85edf453f974f3266f7d1ff32
Autor:
Kinga Judit Fodor, Dániel Hutai, Tamás Jernei, Angéla Takács, Zsófia Szász, Máté Sulyok-Eiler, Veronika Harmat, Rita Oláh Szabó, Gitta Schlosser, Ferenc Hudecz, László Kőhidai, Antal Csámpai
Publikováno v:
Molecules, Vol 25, Iss 7, p 1599 (2020)
Use of a Pictet-Spengler reaction of tryptamine and l-tryptophan methyl ester and subsequent reduction of the nitro group followed by further cyclocondensation with aryl aldehydes and formyl–substituted carboxylic acids, including ferrocene-based c
Externí odkaz:
https://doaj.org/article/8454f92b0c3a4370822b1582c22c1b2b
Autor:
Dániel Hutai, Ferenc Hudecz, Rita Szabó, Tamás Jernei, Antal Csámpai, Gitta Schlosser, Veronika Harmat, Máté Sulyok-Eiler, Angéla Takács, Zsófia Szász, Kinga Judit Fodor, László Kőhidai
Publikováno v:
Molecules
Volume 25
Issue 7
Molecules, Vol 25, Iss 1599, p 1599 (2020)
Volume 25
Issue 7
Molecules, Vol 25, Iss 1599, p 1599 (2020)
Use of a Pictet-Spengler reaction of tryptamine and l-tryptophan methyl ester and subsequent reduction of the nitro group followed by further cyclocondensation with aryl aldehydes and formyl&ndash
substituted carboxylic acids, including ferrocen
substituted carboxylic acids, including ferrocen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb02b6beb0f95e40340a5def0979a5f6