Kammlott U - Search Results

1

In vivo activation of the p53 pathway by small-molecule antagonists of MDM2.

Vassilev LT, Vu BT, Graves B, Carvajal D, Podlaski F, Filipovic Z, Kong N, Kammlott U, Lukacs C, Klein C, Fotouhi N, Liu EA. Vassilev LT, et al. Among authors: kammlott u. Science. 2004 Feb 6;303(5659):844-8. doi: 10.1126/science.1092472. Epub 2004 Jan 2. Science. 2004. PMID: 14704432

2

3,5,6-Trisubstituted naphthostyrils as CDK2 inhibitors.

Liu JJ, Dermatakis A, Lukacs C, Konzelmann F, Chen Y, Kammlott U, Depinto W, Yang H, Yin X, Chen Y, Schutt A, Simcox ME, Luk KC. Liu JJ, et al. Among authors: kammlott u. Bioorg Med Chem Lett. 2003 Aug 4;13(15):2465-8. doi: 10.1016/s0960-894x(03)00488-8. Bioorg Med Chem Lett. 2003. PMID: 12852944

3

Deconstruction of a nutlin: dissecting the binding determinants of a potent protein-protein interaction inhibitor.

Fry DC, Wartchow C, Graves B, Janson C, Lukacs C, Kammlott U, Belunis C, Palme S, Klein C, Vu B. Fry DC, et al. Among authors: kammlott u. ACS Med Chem Lett. 2013 May 24;4(7):660-5. doi: 10.1021/ml400062c. eCollection 2013 Jul 11. ACS Med Chem Lett. 2013. PMID: 24900726 Free PMC article.

4

X-ray structure of a novel matrix metalloproteinase inhibitor complexed to stromelysin.

Dunten P, Kammlott U, Crowther R, Levin W, Foley LH, Wang P, Palermo R. Dunten P, et al. Among authors: kammlott u. Protein Sci. 2001 May;10(5):923-6. doi: 10.1110/ps.48401. Protein Sci. 2001. PMID: 11316871 Free PMC article.

5

Crystal structure of human cytosolic phosphoenolpyruvate carboxykinase reveals a new GTP-binding site.

Dunten P, Belunis C, Crowther R, Hollfelder K, Kammlott U, Levin W, Michel H, Ramsey GB, Swain A, Weber D, Wertheimer SJ. Dunten P, et al. Among authors: kammlott u. J Mol Biol. 2002 Feb 15;316(2):257-64. doi: 10.1006/jmbi.2001.5364. J Mol Biol. 2002. PMID: 11851336

6

Peptide and peptide mimetic inhibitors of antigen presentation by HLA-DR class II MHC molecules. Design, structure-activity relationships, and X-ray crystal structures.

Bolin DR, Swain AL, Sarabu R, Berthel SJ, Gillespie P, Huby NJ, Makofske R, Orzechowski L, Perrotta A, Toth K, Cooper JP, Jiang N, Falcioni F, Campbell R, Cox D, Gaizband D, Belunis CJ, Vidovic D, Ito K, Crowther R, Kammlott U, Zhang X, Palermo R, Weber D, Guenot J, Nagy Z, Olson GL. Bolin DR, et al. Among authors: kammlott u. J Med Chem. 2000 Jun 1;43(11):2135-48. doi: 10.1021/jm000034h. J Med Chem. 2000. PMID: 10841792

7

A new series of potent oxindole inhibitors of CDK2.

Luk KC, Simcox ME, Schutt A, Rowan K, Thompson T, Chen Y, Kammlott U, DePinto W, Dunten P, Dermatakis A. Luk KC, et al. Among authors: kammlott u. Bioorg Med Chem Lett. 2004 Feb 23;14(4):913-7. doi: 10.1016/j.bmcl.2003.12.009. Bioorg Med Chem Lett. 2004. PMID: 15012993

8

Protein farnesyltransferase: structure and implications for substrate binding.

Dunten P, Kammlott U, Crowther R, Weber D, Palermo R, Birktoft J. Dunten P, et al. Among authors: kammlott u. Biochemistry. 1998 Jun 2;37(22):7907-12. doi: 10.1021/bi980531o. Biochemistry. 1998. PMID: 9609683

9

Protein farnesyltransferase: structure and implications for substrate binding.

Dunten P, Kammlott U, Crowther R, Weber D, Palermo R, Birktoft J. Dunten P, et al. Among authors: kammlott u. Biochemistry. 1998 Sep 15;37(37):13042. doi: 10.1021/bi9850470. Biochemistry. 1998. PMID: 9737895 No abstract available.

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