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Results 1 - 10 of 641 > >>
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EC Number BRENDA No. Title Journal Volume Pages Year Organism PubMed ID
Display the word mapDisplay the reaction diagram Show all sequences 2.7.10.2760655 Bivalent inhibitors of c-Src tyrosine kinase that bind a regulatory domain Bioconjug. Chem. 27 1745-1749 2016 Homo sapiens 27266260
Display the word mapDisplay the reaction diagram Show all sequences 2.7.10.2761673 Development of potent inhibitors of receptor tyrosine kinases by ligand-based drug design and target-biased phenotypic screening J. Med. Chem. 61 2104-2110 2018 Homo sapiens 29466002
Display the word mapDisplay the reaction diagram Show all sequences 2.7.10.2762207 Directed evolution of a highly specific FN3 monobody to the SH3 domain of human Lyn tyrosine kinase PLoS ONE 11 e0145872 2016 Homo sapiens 26731115
Display the word mapDisplay the reaction diagram Show all sequences 2.7.10.2760677 Discovery and rational design of 2-aminopyrimidine-based derivatives targeting Janus kinase 2 (JAK2) and FMS-like tyrosine kinase 3 (FLT3) Bioorg. Chem. 104 104361 2020 Homo sapiens 33142418
Display the word mapDisplay the reaction diagram Show all sequences 2.7.10.2761906 Phosphoproteomics analysis identifies novel candidate substrates of the nonreceptor tyrosine kinase, Src-related kinase lacking C-terminal regulatory tyrosine and N-terminal myristoylation sites (SRMS) Mol. Cell. Proteomics 17 925-947 2018 Homo sapiens 29496907
Display the word mapDisplay the reaction diagram Show all sequences 2.7.10.2762522 Role and mechanism of nonreceptor tyrosine kinase Tec in endotoxin/lipopolysaccharide-induced interleukin-8 production in human alveolar epithelial cells A549 Zhonghua Shao Shang Za Zhi 35 580-586 2019 Homo sapiens 31474037
Display the word mapDisplay the reaction diagram Show all sequences 2.7.10.2762208 Src family tyrosine kinase signaling regulates FilGAP through association with RBM10 PLoS ONE 11 e0146593 2016 Homo sapiens 26751795
Display the word mapDisplay the reaction diagram Show all sequences 2.7.10.2761668 Structure-based design and synthesis of 3-amino-1,5-dihydro-4H-pyrazolopyridin-4-one derivatives as tyrosine kinase 2 inhibitors J. Med. Chem. 59 733-749 2016 Homo sapiens 26701356
Display the word mapDisplay the reaction diagram Show all sequences 2.7.10.2760693 Structure-based discovery of novel 4,5,6-trisubstituted pyrimidines as potent covalent Brutons tyrosine kinase inhibitors Bioorg. Med. Chem. Lett. 26 3052-3059 2016 Homo sapiens 27210433
Display the word mapDisplay the reaction diagram Show all sequences 2.7.10.2761527 The N-terminal domain of the non-receptor tyrosine kinase ABL confers protein instability and suppresses tumorigenesis J. Biol. Chem. 295 9069-9075 2020 Homo sapiens 32439806
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