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Amino Acids|July 21, 2016
Origin of problems related to Staudinger reduction in carbopeptoid synthesesBarbara Csordás, Adrienn Nagy, Veronika Harmat, et al.Chemical Science|July 8, 2022
Cryo-EM structure of acylpeptide hydrolase reveals substrate selection by multimerization and a multi-state serine-protease triadAnna J Kiss-Szemán, Pál Stráner, Imre Jákli, et al.The Journal of Biological Chemistry|October 18, 2005
Structural evidence for non-canonical binding of Ca2+ to a canonical EF-hand of a conventional myosinJudit E Debreczeni, László Farkas, Veronika Harmat, et al.Journal of Molecular Biology|September 15, 2004
The structure of MBL-associated serine protease-2 reveals that identical substrate specificities of C1s and MASP-2 are realized through different sets of enzyme-substrate interactionsVeronika Harmat, Péter Gál, József Kardos, et al.Journal of Molecular Biology|June 1, 2005
Extended intermolecular interactions in a serine protease-canonical inhibitor complex account for strong and highly specific inhibitionKrisztián Fodor, Veronika Harmat, Csaba Hetényi, et al.The Journal of Biological Chemistry|April 19, 2012
Monospecific inhibitors show that both mannan-binding lectin-associated serine protease-1 (MASP-1) and -2 Are essential for lectin pathway activation and reveal structural plasticity of MASP-2Dávid Héja, Veronika Harmat, Krisztián Fodor, et al.The Journal of Biological Chemistry|December 15, 2004
The structure of the complex of calmodulin with KAR-2: a novel mode of binding explains the unique pharmacology of the drugIstván Horváth, Veronika Harmat, András Perczel, et al.Journal of Molecular Biology|March 14, 2007
The acylaminoacyl peptidase from Aeropyrum pernix K1 thought to be an exopeptidase displays endopeptidase activityAndrás L Kiss, Balázs Hornung, Krisztina Rádi, et al.Plos One|May 3, 2011
Directed evolution reveals the binding motif preference of the LC8/DYNLL hub protein and predicts large numbers of novel binders in the human proteomePéter Rapali, László Radnai, Dániel Süveges, et al.Journal of Medicinal Chemistry|November 14, 2008
Prolyl oligopeptidase inhibition by N-acyl-pro-pyrrolidine-type moleculesKároly Kánai, Péter Arányi, Zsolt Böcskei, et al.Pageof 5