TABLE OF CONTENTS
| March 2013 Volume 9, Issue 3 | | | | | Editorial Correspondence Research Highlights News and Views Review Brief Communications Articles Addendum Corrigendum | | | | | | Advertisement | | Nature Reprint Collection on Epigenetics This collection of articles focuses on histone methylation, its links to human disease and the development of chemical modulators of histone methylation states as leads for chromatin-targeted drug discovery. Produced exclusively with support from: | | | | Editorial | Top | | | | Authors on the record p135 doi:10.1038/nchembio.1201 Publication of a paper initiates the process of scientific exchange that requires the ongoing participation of authors. | | Correspondence | Top | | | | Chaetocin is a nonspecific inhibitor of histone lysine methyltransferases pp136 - 137 Fanny L Cherblanc, Kathryn L Chapman, Robert Brown and Matthew J Fuchter doi:10.1038/nchembio.1187
See also: Correspondence by Greiner et al. | | | | Reply to "Chaetocin is a nonspecific inhibitor of histone lysine methyltransferases" p137 Dorothea Greiner, Tiziana Bonaldi, Ragnhild Eskeland, Ernst Roemer and Axel Imhof doi:10.1038/nchembio.1188
See also: Correspondence by Cherblanc et al. | | Research Highlights | Top | | | | Cancer: Priority targets | Synthesis: A radical way of thinking | Photosynthesis: Elusive reductase found | Enzymes: Specificity swap | Antibiotic mechanisms: PAS is doubly poisonous | Pluripotency: Oleate dependency | Neurobiology: A pain paradox | Metabolism: AMPing up life | News and Views | Top | | | | | | Review | Top | | | | | | Brief Communications | Top | | | | A conserved asparagine has a structural role in ubiquitin-conjugating enzymes pp154 - 156 Christopher E Berndsen, Reuven Wiener, Ian W Yu, Alison E Ringel and Cynthia Wolberger doi:10.1038/nchembio.1159
Ubiquitin-conjugating (E2) enzymes contain a conserved asparagine that has been proposed to stabilize an oxyanion intermediate. Structural and biochemical studies of Ubc13 suggest that this residue has a structural role in stabilizing the E2 active site. |
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| | | | | | | | | | Articles | Top | | | | PUMA binding induces partial unfolding within BCL-xL to disrupt p53 binding and promote apoptosis pp163 - 168 Ariele Viacava Follis, Jerry E Chipuk, John C Fisher, Mi-Kyung Yun, Christy R Grace, Amanda Nourse, Katherine Baran, Li Ou, Lie Min, Stephen W White, Douglas R Green and Richard W Kriwacki doi:10.1038/nchembio.1166
π-stacking interactions unique between residues of PUMA and Bcl-xL, which lead to the unfolding of Bcl-xL via an allosteric mechanism, are required to disrupt p53–Bcl-xL interaction and induce apoptosis. This is the first example of regulated protein unfolding for signal transmission.
See also: News and Views by Walensky |
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| | | | | | | | A new structural paradigm in copper resistance in Streptococcus pneumoniae pp177 - 183 Yue Fu, Ho-Ching Tiffany Tsui, Kevin E Bruce, Lok-To Sham, Khadine A Higgins, John P Lisher, Krystyna M Kazmierczak, Michael J Maroney, Charles E Dann III, Malcolm E Winkler and David P Giedroc doi:10.1038/nchembio.1168
Structural analyses reveal that CopA and CupA share a binuclear Cu(I) ion binding motif and that copper is trafficked from a low-affinity site on CupA to a high-affinity site in CopA, making CupA the first membrane-bound copper chaperone important in copper resistance. |
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| | | | Discovery of a chemical probe for the L3MBTL3 methyllysine reader domain pp184 - 191 Lindsey I James, Dalia Barsyte-Lovejoy, Nan Zhong, Liubov Krichevsky, Victoria K Korboukh, J Martin Herold, Christopher J MacNevin, Jacqueline L Norris, Cari A Sagum, Wolfram Tempel, Edyta Marcon, Hongbo Guo, Cen Gao, Xi-Ping Huang, Shili Duan, Andrew Emili, Jack F Greenblatt, Dmitri B Kireev, Jian Jin, William P Janzen, Peter J Brown, Mark T Bedford, Cheryl H Arrowsmith and Stephen V Frye doi:10.1038/nchembio.1157
Methylation of lysine residues regulates chromatin function in part by recruiting readers to these marks. UNC1215, a selective antagonist of the methyllysine reader L3MBTL3 with a polyvalent mode of interaction, reveals BCLAF1 as a methyllysine-dependent interaction partner for L3MBTL3. Chemical compounds |
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| | Addendum | Top | | | | Chemical inhibitor of nonapoptotic cell death with therapeutic potential for ischemic brain injury p192 Alexei Degterev, Zhihong Huang, Michael Boyce, Yaqiao Li, Prakash Jagtap, Noboru Mizushima, Gregory D Cuny, Timothy J Mitchison, Michael A Moskowitz and Junying Yuan doi:10.1038/nchembio0313-192a | | Corrigendum | Top | | | | Conformational stabilization of ubiquitin yields potent and selective inhibitors of USP7 p192 Yingnan Zhang, Lijuan Zhou, Lionel Rouge, Aaron H Phillips, Cynthia Lam, Peter Liu, Wendy Sandoval, Elizabeth Helgason, Jeremy M Murray, Ingrid E Wertz and Jacob E Corn doi:10.1038/nchembio0313-192b | | Top | | | Advertisement | | | | | | | | | | | Natureevents is a fully searchable, multi-disciplinary database designed to maximise exposure for events organisers. The contents of the Natureevents Directory are now live. The digital version is available here. Find the latest scientific conferences, courses, meetings and symposia on natureevents.com. For event advertising opportunities across the Nature Publishing Group portfolio please contact natureevents@nature.com | | | | | | | | |
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1 comment:
UNC1215 is a potent, selective antagonist of L3MBTL3 with cellular activity. UNC1215 has an IC50 of 20 nM and > 100-fold selectivity over 13 HMTs and selected representativ UNC1215
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