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D K Stammers

Showing results (31-40 of 61) with videos related to

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Bioorganic & Medicinal Chemistry|April 1, 1996
Pyrrolo[2,3-d]pyrimidines and pyrido[2,3-d]pyrimidines as conformationally restricted analogues of the antibacterial agent trimethoprimL F Kuyper, J M Garvey, D P Baccanari, et al.
Journal of Molecular Biology|September 29, 2001
Structural mechanisms of drug resistance for mutations at codons 181 and 188 in HIV-1 reverse transcriptase and the improved resilience of second generation non-nucleoside inhibitorsJ Ren, C Nichols, L Bird, et al.
Biochemistry|October 17, 1998
Crystal structures of HIV-1 reverse transcriptase in complex with carboxanilide derivativesJ Ren, R M Esnouf, A L Hopkins, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 19, 2002
Structure of HIV-2 reverse transcriptase at 2.35-A resolution and the mechanism of resistance to non-nucleoside inhibitorsJ Ren, L E Bird, P P Chamberlain, et al.
Proteins|April 18, 2006
Structural characterization of Salmonella typhimurium YeaZ, an M22 O-sialoglycoprotein endopeptidase homologC E Nichols, C Johnson, M Lockyer, et al.
FEBS Letters|August 19, 1999
2.0 A X-ray structure of the ternary complex of 7,8-dihydro-6-hydroxymethylpterinpyrophosphokinase from Escherichia coli with ATP and a substrate analogueD K Stammers, A Achari, D O Somers, et al.
The Journal of Biological Chemistry|August 5, 1991
Use of the Glu-Glu-Phe C-terminal epitope for rapid purification of the catalytic domain of normal and mutant ras GTPase-activating proteinsR H Skinner, S Bradley, A L Brown, et al.
Journal of Molecular Biology|October 7, 2004
Comparison of ligand-induced conformational changes and domain closure mechanisms, between prokaryotic and eukaryotic dehydroquinate synthasesC E Nichols, J Ren, K Leslie, et al.
Acta Crystallographica. Section F, Structural Biology and Crystallization Communications|November 17, 2007
Structure of the ribosomal interacting GTPase YjeQ from the enterobacterial species Salmonella typhimuriumC E Nichols, C Johnson, H K Lamb, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 15, 1997
Unique features in the structure of the complex between HIV-1 reverse transcriptase and the bis(heteroaryl)piperazine (BHAP) U-90152 explain resistance mutations for this nonnucleoside inhibitorR M Esnouf, J Ren, A L Hopkins, et al.
Pageof 7

Showing results (31-40 of 61) with videos related to

Sort By:
Pageof 7
Bioorganic & Medicinal Chemistry|April 1, 1996
Pyrrolo[2,3-d]pyrimidines and pyrido[2,3-d]pyrimidines as conformationally restricted analogues of the antibacterial agent trimethoprimL F Kuyper, J M Garvey, D P Baccanari, et al.
Journal of Molecular Biology|September 29, 2001
Structural mechanisms of drug resistance for mutations at codons 181 and 188 in HIV-1 reverse transcriptase and the improved resilience of second generation non-nucleoside inhibitorsJ Ren, C Nichols, L Bird, et al.
Biochemistry|October 17, 1998
Crystal structures of HIV-1 reverse transcriptase in complex with carboxanilide derivativesJ Ren, R M Esnouf, A L Hopkins, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 19, 2002
Structure of HIV-2 reverse transcriptase at 2.35-A resolution and the mechanism of resistance to non-nucleoside inhibitorsJ Ren, L E Bird, P P Chamberlain, et al.
Proteins|April 18, 2006
Structural characterization of Salmonella typhimurium YeaZ, an M22 O-sialoglycoprotein endopeptidase homologC E Nichols, C Johnson, M Lockyer, et al.
FEBS Letters|August 19, 1999
2.0 A X-ray structure of the ternary complex of 7,8-dihydro-6-hydroxymethylpterinpyrophosphokinase from Escherichia coli with ATP and a substrate analogueD K Stammers, A Achari, D O Somers, et al.
The Journal of Biological Chemistry|August 5, 1991
Use of the Glu-Glu-Phe C-terminal epitope for rapid purification of the catalytic domain of normal and mutant ras GTPase-activating proteinsR H Skinner, S Bradley, A L Brown, et al.
Journal of Molecular Biology|October 7, 2004
Comparison of ligand-induced conformational changes and domain closure mechanisms, between prokaryotic and eukaryotic dehydroquinate synthasesC E Nichols, J Ren, K Leslie, et al.
Acta Crystallographica. Section F, Structural Biology and Crystallization Communications|November 17, 2007
Structure of the ribosomal interacting GTPase YjeQ from the enterobacterial species Salmonella typhimuriumC E Nichols, C Johnson, H K Lamb, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 15, 1997
Unique features in the structure of the complex between HIV-1 reverse transcriptase and the bis(heteroaryl)piperazine (BHAP) U-90152 explain resistance mutations for this nonnucleoside inhibitorR M Esnouf, J Ren, A L Hopkins, et al.
Pageof 7