Year |
Citation |
Score |
2018 |
Kumar S. Highly Efficient Cell Penetrable Probes of Protein Arginine Deiminases (PADs) for Functional Proteomics. Chembiochem : a European Journal of Chemical Biology. PMID 29949677 DOI: 10.1002/Cbic.201800257 |
0.363 |
|
2014 |
Dana D, De S, Rathod P, Davalos AR, Novoa DA, Paroly S, Torres VM, Afzal N, Lankalapalli RS, Rotenberg SA, Chang EJ, Subramaniam G, Kumar S. Development of a highly potent, selective, and cell-active inhibitor of cysteine cathepsin L-A hybrid design approach. Chemical Communications (Cambridge, England). 50: 10875-8. PMID 25089379 DOI: 10.1039/C4Cc04037F |
0.49 |
|
2013 |
Dana D, Davalos AR, De S, Rathod P, Gamage RK, Huestis J, Afzal N, Zavlanov Y, Paroly SS, Rotenberg SA, Subramaniam G, Mark KJ, Chang EJ, Kumar S. Development of cell-active non-peptidyl inhibitors of cysteine cathepsins. Bioorganic & Medicinal Chemistry. 21: 2975-87. PMID 23623677 DOI: 10.1016/J.Bmc.2013.03.062 |
0.469 |
|
2012 |
Dana D, Das TK, Kumar I, Davalos AR, Mark KJ, Ramai D, Chang EJ, Talele TT, Kumar S. Design, synthesis, and evaluation of 2-(arylsulfonyl)oxiranes as cell-permeable covalent inhibitors of protein tyrosine phosphatases. Chemical Biology & Drug Design. 80: 489-99. PMID 22726577 DOI: 10.1111/J.1747-0285.2012.01437.X |
0.448 |
|
2008 |
Liu S, Zhou B, Yang H, He Y, Jiang ZX, Kumar S, Wu L, Zhang ZY. Aryl vinyl sulfonates and sulfones as active site-directed and mechanism-based probes for protein tyrosine phosphatases. Journal of the American Chemical Society. 130: 8251-60. PMID 18528979 DOI: 10.1021/Ja711125P |
0.343 |
|
2008 |
Lee JH, Kumar S, Lawrence DS. Stepwise combinatorial evolution of Akt bisubstrate inhibitors. Chembiochem : a European Journal of Chemical Biology. 9: 507-9. PMID 18224646 DOI: 10.1002/Cbic.200700583 |
0.608 |
|
2007 |
Dai Z, Dulyaninova NG, Kumar S, Bresnick AR, Lawrence DS. Visual snapshots of intracellular kinase activity at the onset of mitosis. Chemistry & Biology. 14: 1254-60. PMID 18022564 DOI: 10.1016/J.Chembiol.2007.10.007 |
0.587 |
|
2007 |
Zhang S, Chen L, Kumar S, Wu L, Lawrence DS, Zhang ZY. An affinity-based fluorescence polarization assay for protein tyrosine phosphatases. Methods (San Diego, Calif.). 42: 261-7. PMID 17532513 DOI: 10.1016/J.Ymeth.2007.02.008 |
0.498 |
|
2007 |
Liang F, Kumar S, Zhang ZY. Proteomic approaches to studying protein tyrosine phosphatases. Molecular Biosystems. 3: 308-16. PMID 17460790 DOI: 10.1039/B700704N |
0.349 |
|
2006 |
Kumar S, Zhou B, Liang F, Yang H, Wang WQ, Zhang ZY. Global analysis of protein tyrosine phosphatase activity with ultra-sensitive fluorescent probes. Journal of Proteome Research. 5: 1898-905. PMID 16889411 DOI: 10.1021/Pr050449X |
0.346 |
|
2005 |
Kumar S, Liang F, Lawrence DS, Zhang ZY. Small molecule approach to studying protein tyrosine phosphatase. Methods (San Diego, Calif.). 35: 9-21. PMID 15588981 DOI: 10.1016/J.Ymeth.2004.07.003 |
0.46 |
|
2004 |
Kumar S, Adediran SA, Nukaga M, Pratt RF. Kinetics of turnover of cefotaxime by the Enterobacter cloacae P99 and GCl beta-lactamases: two free enzyme forms of the P99 beta-lactamase detected by a combination of pre- and post-steady state kinetics. Biochemistry. 43: 2664-72. PMID 14992604 DOI: 10.1021/Bi030212J |
0.467 |
|
2004 |
Nukaga M, Kumar S, Nukaga K, Pratt RF, Knox JR. Hydrolysis of third-generation cephalosporins by class C beta-lactamases. Structures of a transition state analog of cefotoxamine in wild-type and extended spectrum enzymes. The Journal of Biological Chemistry. 279: 9344-52. PMID 14660590 DOI: 10.1074/jbc.M312356200 |
0.487 |
|
2001 |
Kumar S, Pearson AL, Pratt RF. Design, synthesis, and evaluation of alpha-ketoheterocycles as class C beta-lactamase inhibitors. Bioorganic & Medicinal Chemistry. 9: 2035-44. PMID 11504640 DOI: 10.1016/S0968-0896(01)00107-9 |
0.502 |
|
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