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Acta Crystallographica. Section F, Structural Biology Communications
|
May 3, 2019
Findable Accessible Interoperable Re-usable (FAIR) diffraction data are coming to protein crystallography
John R Helliwell, Wladek Minor, Manfred S Weiss, et al.
The Journal of Biological Chemistry
|
February 10, 2016
The Structure of the Transcriptional Repressor KstR in Complex with CoA Thioester Cholesterol Metabolites Sheds Light on the Regulation of Cholesterol Catabolism in Mycobacterium tuberculosis
Ngoc Anh Thu Ho, Stephanie S Dawes, Adam M Crowe, et al.
Data in Brief
|
November 24, 2017
Datasets, processing and refinement details for <i>Mtb</i>-AnPRT: inhibitor structures with various space groups
Genevieve L Evans, Daniel P Furkert, Nacim Abermil, et al.
Biochimica Et Biophysica Acta. Proteins and Proteomics
|
August 29, 2017
Anthranilate phosphoribosyltransferase: Binding determinants for 5'-phospho-alpha-d-ribosyl-1'-pyrophosphate (PRPP) and the implications for inhibitor design
Genevieve L Evans, Daniel P Furkert, Nacim Abermil, et al.
Journal of Bacteriology
|
July 20, 2010
Roles of minor pilin subunits Spy0125 and Spy0130 in the serotype M1 Streptococcus pyogenes strain SF370
Wendy D Smith, Jonathan A Pointon, Emily Abbot, et al.
Journal of Molecular Biology
|
February 11, 2005
Crystal Structure of AhpE from Mycobacterium tuberculosis, a 1-Cys peroxiredoxin
Simon Li, Neil A Peterson, Min-Young Kim, et al.
Biochemistry
|
May 22, 2012
Implications of binding mode and active site flexibility for inhibitor potency against the salicylate synthase from Mycobacterium tuberculosis
Gamma Chi, Alexandra Manos-Turvey, Patrick D O'Connor, et al.
Biochemistry
|
January 30, 2007
High-resolution crystal structure of plant carboxylesterase AeCXE1, from Actinidia eriantha, and its complex with a high-affinity inhibitor paraoxon
Nadeesha R Ileperuma, Sean D G Marshall, Christopher J Squire, et al.
Bioorganic & Medicinal Chemistry Letters
|
January 15, 2008
Synthesis and structure-activity relationships of soluble 8-substituted 4-(2-chlorophenyl)-9-hydroxypyrrolo[3,4-c]carbazole-1,3(2H,6H)-diones as inhibitors of the Wee1 and Chk1 checkpoint kinases
Jeff B Smaill, Ho H Lee, Brian D Palmer, et al.
The Journal of Biological Chemistry
|
February 8, 2020
Allosteric regulation of menaquinone (vitamin K<sub>2</sub>) biosynthesis in the human pathogen <i>Mycobacterium tuberculosis</i>
Ghader Bashiri, Laura V Nigon, Ehab N M Jirgis, et al.
Page
of 21
Search research articles
Search
Showing results (181-190 of 202) with videos related to
Sort By:
Page
of 21
Acta Crystallographica. Section F, Structural Biology Communications
|
May 3, 2019
Findable Accessible Interoperable Re-usable (FAIR) diffraction data are coming to protein crystallography
John R Helliwell, Wladek Minor, Manfred S Weiss, et al.
The Journal of Biological Chemistry
|
February 10, 2016
The Structure of the Transcriptional Repressor KstR in Complex with CoA Thioester Cholesterol Metabolites Sheds Light on the Regulation of Cholesterol Catabolism in Mycobacterium tuberculosis
Ngoc Anh Thu Ho, Stephanie S Dawes, Adam M Crowe, et al.
Data in Brief
|
November 24, 2017
Datasets, processing and refinement details for <i>Mtb</i>-AnPRT: inhibitor structures with various space groups
Genevieve L Evans, Daniel P Furkert, Nacim Abermil, et al.
Biochimica Et Biophysica Acta. Proteins and Proteomics
|
August 29, 2017
Anthranilate phosphoribosyltransferase: Binding determinants for 5'-phospho-alpha-d-ribosyl-1'-pyrophosphate (PRPP) and the implications for inhibitor design
Genevieve L Evans, Daniel P Furkert, Nacim Abermil, et al.
Journal of Bacteriology
|
July 20, 2010
Roles of minor pilin subunits Spy0125 and Spy0130 in the serotype M1 Streptococcus pyogenes strain SF370
Wendy D Smith, Jonathan A Pointon, Emily Abbot, et al.
Journal of Molecular Biology
|
February 11, 2005
Crystal Structure of AhpE from Mycobacterium tuberculosis, a 1-Cys peroxiredoxin
Simon Li, Neil A Peterson, Min-Young Kim, et al.
Biochemistry
|
May 22, 2012
Implications of binding mode and active site flexibility for inhibitor potency against the salicylate synthase from Mycobacterium tuberculosis
Gamma Chi, Alexandra Manos-Turvey, Patrick D O'Connor, et al.
Biochemistry
|
January 30, 2007
High-resolution crystal structure of plant carboxylesterase AeCXE1, from Actinidia eriantha, and its complex with a high-affinity inhibitor paraoxon
Nadeesha R Ileperuma, Sean D G Marshall, Christopher J Squire, et al.
Bioorganic & Medicinal Chemistry Letters
|
January 15, 2008
Synthesis and structure-activity relationships of soluble 8-substituted 4-(2-chlorophenyl)-9-hydroxypyrrolo[3,4-c]carbazole-1,3(2H,6H)-diones as inhibitors of the Wee1 and Chk1 checkpoint kinases
Jeff B Smaill, Ho H Lee, Brian D Palmer, et al.
The Journal of Biological Chemistry
|
February 8, 2020
Allosteric regulation of menaquinone (vitamin K<sub>2</sub>) biosynthesis in the human pathogen <i>Mycobacterium tuberculosis</i>
Ghader Bashiri, Laura V Nigon, Ehab N M Jirgis, et al.
Page
of 21