129 related articles for article (PubMed ID: 23499784)
1. Responsive microsecond-lifetime photoluminescent probes for analysis of protein kinases and their inhibitors.
Kasari M; Ligi K; Williams JA; Vaasa A; Enkvist E; Viht K; Pålsson LO; Uri A
Biochim Biophys Acta; 2013 Jul; 1834(7):1330-5. PubMed ID: 23499784
[TBL] [Abstract][Full Text] [Related]
2. Protein-induced long lifetime luminescence of nonmetal probes.
Enkvist E; Vaasa A; Kasari M; Kriisa M; Ivan T; Ligi K; Raidaru G; Uri A
ACS Chem Biol; 2011 Oct; 6(10):1052-62. PubMed ID: 21776959
[TBL] [Abstract][Full Text] [Related]
3. Deoxygenation Increases Photoluminescence Lifetime of Protein-Responsive Organic Probes with Triplet-Singlet Resonant Energy Transfer.
Ligi K; Enkvist E; Uri A
J Phys Chem B; 2016 Jun; 120(22):4945-54. PubMed ID: 27183180
[TBL] [Abstract][Full Text] [Related]
4. Bisubstrate fluorescent probes and biosensors in binding assays for HTS of protein kinase inhibitors.
Uri A; Lust M; Vaasa A; Lavogina D; Viht K; Enkvist E
Biochim Biophys Acta; 2010 Mar; 1804(3):541-6. PubMed ID: 19879386
[TBL] [Abstract][Full Text] [Related]
5. Time-gated luminescence microscopy with responsive nonmetal probes for mapping activity of protein kinases in living cells.
Vaasa A; Ligi K; Mohandessi S; Enkvist E; Uri A; Miller LW
Chem Commun (Camb); 2012 Sep; 48(68):8595-7. PubMed ID: 22822483
[TBL] [Abstract][Full Text] [Related]
6. Structure-based and shape-complemented pharmacophore modeling for the discovery of novel checkpoint kinase 1 inhibitors.
Chen XM; Lu T; Lu S; Li HF; Yuan HL; Ran T; Liu HC; Chen YD
J Mol Model; 2010 Jul; 16(7):1195-204. PubMed ID: 20020310
[TBL] [Abstract][Full Text] [Related]
7. Thiazole- and selenazole-comprising high-affinity inhibitors possess bright microsecond-scale photoluminescence in complex with protein kinase CK2.
Vahter J; Viht K; Uri A; Manoharan GB; Enkvist E
Bioorg Med Chem; 2018 Oct; 26(18):5062-5068. PubMed ID: 30217463
[TBL] [Abstract][Full Text] [Related]
8. High-affinity bisubstrate probe for fluorescence anisotropy binding/displacement assays with protein kinases PKA and ROCK.
Vaasa A; Viil I; Enkvist E; Viht K; Raidaru G; Lavogina D; Uri A
Anal Biochem; 2009 Feb; 385(1):85-93. PubMed ID: 19017524
[TBL] [Abstract][Full Text] [Related]
9. Proteome-wide discovery of unknown ATP-binding proteins and kinase inhibitor target proteins using an ATP probe.
Adachi J; Kishida M; Watanabe S; Hashimoto Y; Fukamizu K; Tomonaga T
J Proteome Res; 2014 Dec; 13(12):5461-70. PubMed ID: 25230287
[TBL] [Abstract][Full Text] [Related]
10. Discovery of strong inhibitory properties of a monoclonal antibody of PKA and use of the antibody and a competitive photoluminescent orthosteric probe for analysis of the protein kinase.
Nonga OE; Lavogina D; Ivan T; Viht K; Enkvist E; Uri A
Biochim Biophys Acta Proteins Proteom; 2020 Aug; 1868(8):140427. PubMed ID: 32283249
[TBL] [Abstract][Full Text] [Related]
11. A subnanomolar fluorescent probe for protein kinase CK2 interaction studies.
Enkvist E; Viht K; Bischoff N; Vahter J; Saaver S; Raidaru G; Issinger OG; Niefind K; Uri A
Org Biomol Chem; 2012 Nov; 10(43):8645-53. PubMed ID: 23032938
[TBL] [Abstract][Full Text] [Related]
12. A fluorescence lifetime based binding assay to characterize kinase inhibitors.
Lebakken CS; Hee Chol Kang ; Vogel KW
J Biomol Screen; 2007 Sep; 12(6):828-41. PubMed ID: 17644772
[TBL] [Abstract][Full Text] [Related]
13. Development of novel molecular probes of the Rio1 atypical protein kinase.
Mielecki M; Krawiec K; Kiburu I; Grzelak K; Zagórski W; Kierdaszuk B; Kowa K; Fokt I; Szymanski S; Swierk P; Szeja W; Priebe W; Lesyng B; LaRonde-LeBlanc N
Biochim Biophys Acta; 2013 Jul; 1834(7):1292-301. PubMed ID: 23523885
[TBL] [Abstract][Full Text] [Related]
14. FRET-based screening assay using small-molecule photoluminescent probes in lysate of cells overexpressing RFP-fused protein kinases.
Manoharan GB; Enkvist E; Kasari M; Viht K; Zenn M; Prinz A; Filhol O; Herberg FW; Uri A
Anal Biochem; 2015 Jul; 481():10-7. PubMed ID: 25866074
[TBL] [Abstract][Full Text] [Related]
15. Alkylation of Staurosporine to Derive a Kinase Probe for Fluorescence Applications.
Disney AJ; Kellam B; Dekker LV
ChemMedChem; 2016 May; 11(9):972-9. PubMed ID: 27008372
[TBL] [Abstract][Full Text] [Related]
16. A high-throughput, nonisotopic, competitive binding assay for kinases using nonselective inhibitor probes (ED-NSIP).
Vainshtein I; Silveria S; Kaul P; Rouhani R; Eglen RM; Wang J
J Biomol Screen; 2002 Dec; 7(6):507-14. PubMed ID: 14599348
[TBL] [Abstract][Full Text] [Related]
17. Targeting protein kinases with selective and semipromiscuous covalent inhibitors.
Miller RM; Taunton J
Methods Enzymol; 2014; 548():93-116. PubMed ID: 25399643
[TBL] [Abstract][Full Text] [Related]
18. Fluorescence labels in kinases: a high-throughput kinase binding assay for the identification of DFG-out binding ligands.
Simard JR; Rauh D
Methods Mol Biol; 2012; 800():95-117. PubMed ID: 21964785
[TBL] [Abstract][Full Text] [Related]
19. Deactivatable Bisubstrate Inhibitors of Protein Kinases.
Sõrmus T; Lavogina D; Enkvist E; Uri A; Viht K
Molecules; 2022 Oct; 27(19):. PubMed ID: 36235226
[TBL] [Abstract][Full Text] [Related]
20. Structure-based rational design of staurosporine-based fluorescent probe with broad-ranging kinase affinity for kinase panel application.
Hirozane Y; Toyofuku M; Yogo T; Tanaka Y; Sameshima T; Miyahisa I; Yoshikawa M
Bioorg Med Chem Lett; 2019 Nov; 29(21):126641. PubMed ID: 31526603
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]