Ulaganathan V - Search Results

1

Structural basis for inhibition of Eg5 by dihydropyrimidines: stereoselectivity of antimitotic inhibitors enastron, dimethylenastron and fluorastrol.

Kaan HY, Ulaganathan V, Rath O, Prokopcová H, Dallinger D, Kappe CO, Kozielski F. Kaan HY, et al. Among authors: ulaganathan v. J Med Chem. 2010 Aug 12;53(15):5676-83. doi: 10.1021/jm100421n. J Med Chem. 2010. PMID: 20597485

2

An allosteric transition trapped in an intermediate state of a new kinesin-inhibitor complex.

Kaan HY, Ulaganathan V, Hackney DD, Kozielski F. Kaan HY, et al. Among authors: ulaganathan v. Biochem J. 2009 Dec 14;425(1):55-60. doi: 10.1042/BJ20091207. Biochem J. 2009. PMID: 19793049

3

Structure-activity relationship and multidrug resistance study of new S-trityl-L-cysteine derivatives as inhibitors of Eg5.

Kaan HY, Weiss J, Menger D, Ulaganathan V, Tkocz K, Laggner C, Popowycz F, Joseph B, Kozielski F. Kaan HY, et al. Among authors: ulaganathan v. J Med Chem. 2011 Mar 24;54(6):1576-86. doi: 10.1021/jm100991m. Epub 2011 Feb 23. J Med Chem. 2011. PMID: 21344920

4

Structure-activity relationships and molecular docking of novel dihydropyrimidine-based mitotic Eg5 inhibitors.

Prokopcová H, Dallinger D, Uray G, Kaan HY, Ulaganathan V, Kozielski F, Laggner C, Kappe CO. Prokopcová H, et al. Among authors: ulaganathan v. ChemMedChem. 2010 Oct 4;5(10):1760-9. doi: 10.1002/cmdc.201000252. ChemMedChem. 2010. PMID: 20737530

5

Structural insights into a unique inhibitor binding pocket in kinesin spindle protein.

Ulaganathan V, Talapatra SK, Rath O, Pannifer A, Hackney DD, Kozielski F. Ulaganathan V, et al. J Am Chem Soc. 2013 Feb 13;135(6):2263-72. doi: 10.1021/ja310377d. Epub 2013 Feb 4. J Am Chem Soc. 2013. PMID: 23305346

6

The crystal structure and biochemical characterization of Kif15: a bifunctional molecular motor involved in bipolar spindle formation and neuronal development.

Klejnot M, Falnikar A, Ulaganathan V, Cross RA, Baas PW, Kozielski F. Klejnot M, et al. Among authors: ulaganathan v. Acta Crystallogr D Biol Crystallogr. 2014 Jan;70(Pt 1):123-33. doi: 10.1107/S1399004713028721. Epub 2013 Dec 24. Acta Crystallogr D Biol Crystallogr. 2014. PMID: 24419385 Free PMC article.

7

Identification of novel scaffolds to inhibit human mitotic kinesin Eg5 targeting the second allosteric binding site using in silico methods.

Makala H, Ulaganathan V. Makala H, et al. Among authors: ulaganathan v. J Recept Signal Transduct Res. 2018 Feb;38(1):12-19. doi: 10.1080/10799893.2017.1387922. Epub 2017 Oct 17. J Recept Signal Transduct Res. 2018. PMID: 29041840

8

Tackling drug resistance with efflux pump inhibitors: from bacteria to cancerous cells.

Lowrence RC, Subramaniapillai SG, Ulaganathan V, Nagarajan S. Lowrence RC, et al. Among authors: ulaganathan v. Crit Rev Microbiol. 2019 May;45(3):334-353. doi: 10.1080/1040841X.2019.1607248. Epub 2019 Jun 28. Crit Rev Microbiol. 2019. PMID: 31248314 Review.

9

Coarse grained modelling highlights the binding differences in the two different allosteric sites of the Human Kinesin EG5 and its implications in inhibitor design.

Alexandar SP, Yennamalli RM, Ulaganathan V. Alexandar SP, et al. Among authors: ulaganathan v. Comput Biol Chem. 2022 Aug;99:107708. doi: 10.1016/j.compbiolchem.2022.107708. Epub 2022 Jun 9. Comput Biol Chem. 2022. PMID: 35717732

10

Structure of Staphylococcus aureus1,4-dihydroxy-2-naphthoyl-CoA synthase (MenB) in complex with acetoacetyl-CoA.

Ulaganathan V, Agacan MF, Buetow L, Tulloch LB, Hunter WN. Ulaganathan V, et al. Acta Crystallogr Sect F Struct Biol Cryst Commun. 2007 Nov 1;63(Pt 11):908-13. doi: 10.1107/S1744309107047720. Epub 2007 Oct 20. Acta Crystallogr Sect F Struct Biol Cryst Commun. 2007. PMID: 18007038 Free PMC article.

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