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Wade M. Borcherds, Ph.D. - Publications

Affiliations: 
2013 Cell Biology, Microbiology, Molecular Biology University of South Florida, Tampa, FL, United States 
Area:
General Biology, General Biophysics
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28 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2022 Fenton M, Borcherds W, Chen L, Anbanandam A, Levy R, Chen J, Daughdrill G. Two short linear motifs in the MDMX acidic domain bind overlapping sites on MDMX and p53. Journal of Molecular Biology. 167844. PMID 36181774 DOI: 10.1016/j.jmb.2022.167844  0.746
2022 González-Foutel NS, Glavina J, Borcherds WM, Safranchik M, Barrera-Vilarmau S, Sagar A, Estaña A, Barozet A, Garrone NA, Fernandez-Ballester G, Blanes-Mira C, Sánchez IE, de Prat-Gay G, Cortés J, Bernadó P, et al. Conformational buffering underlies functional selection in intrinsically disordered protein regions. Nature Structural & Molecular Biology. 29: 781-790. PMID 35948766 DOI: 10.1038/s41594-022-00811-w  0.709
2020 Sang P, Shi Y, Lu J, Chen L, Yang L, Borcherds W, Abdulkadir S, Li Q, Daughdrill G, Chen J, Cai J. Correction to α-Helix-Mimicking Sulfono-γ-AApeptide Inhibitors for p53-MDM2/MDMX Protein-Protein Interactions. Journal of Medicinal Chemistry. PMID 32822169 DOI: 10.1021/Acs.Jmedchem.0C01284  0.687
2020 Sang P, Shi Y, Lu J, Chen L, Yang L, Borcherds W, Abdulkadir S, Li Q, Daughdrill GW, Chen J, Cai J. α-Helix-Mimicking Sulfono-γ-AApeptide Inhibitors for p53-MDM2/MDMX Protein-Protein Interactions. Journal of Medicinal Chemistry. PMID 31971801 DOI: 10.1021/Acs.Jmedchem.9B00993  0.715
2020 Fenton MJ, Borcherds WM, Daughdrill GW, Chen L, Chen J. MDMX Acidic Domain Requires the WF Motif for the Initiation of the Secondary Interaction with the P53DBD Biophysical Journal. 118: 38a-39a. DOI: 10.1016/J.Bpj.2019.11.391  0.657
2020 Levy R, Borcherds WM, He F, Daughdrill GW, Chen J. Protein Disorder Regulates the DNA Binding Specificity of p53 Biophysical Journal. 118: 215a. DOI: 10.1016/J.Bpj.2019.11.1279  0.744
2020 Gregory-Lott E, Borcherds WM, He F, Zhou M, Daughdrill GW. Conformational Flexibility of p53 Transactivation Domain Controls DNA Binding Specificity and Promoter Selectivity Biophysical Journal. 118: 213a. DOI: 10.1016/J.Bpj.2019.11.1271  0.714
2019 He F, Borcherds W, Song T, Wei X, Das M, Chen L, Daughdrill GW, Chen J. Interaction between p53 N terminus and core domain regulates specific and nonspecific DNA binding. Proceedings of the National Academy of Sciences of the United States of America. PMID 30988205 DOI: 10.1073/Pnas.1903077116  0.73
2019 Sowemimo OT, Knox-Brown P, Borcherds W, Rindfleisch T, Thalhammer A, Daughdrill GW. Conserved Glycines Control Disorder and Function in the Cold-Regulated Protein, COR15A. Biomolecules. 9. PMID 30832369 DOI: 10.3390/biom9030084  0.666
2019 Levy R, Gregory E, Borcherds W, Daughdrill G. p53 Phosphomimetics Preserve Transient Secondary Structure but Reduce Binding to Mdm2 and MdmX. Biomolecules. 9. PMID 30832340 DOI: 10.3390/biom9030083  0.754
2019 Sowemimo O, Borcherds W, Knox-Brown P, Rindfleisch T, Thalhammer A, Daughdrill G. Evolution of Transient Helicity and Disorder in Late Embryogenesis Abundant Protein COR15A Biophysical Journal. 116: 473a. DOI: 10.1016/J.Bpj.2018.11.2553  0.692
2018 Borcherds WM, Daughdrill GW. Using NMR Chemical Shifts to Determine Residue-Specific Secondary Structure Populations for Intrinsically Disordered Proteins. Methods in Enzymology. 611: 101-136. PMID 30471686 DOI: 10.1016/Bs.Mie.2018.09.011  0.751
2018 Poosapati A, Gregory E, Borcherds WM, Chemes LB, Daughdrill GW. Uncoupling the folding and binding of an intrinsically disordered protein. Journal of Molecular Biology. PMID 29890118 DOI: 10.1016/J.Jmb.2018.05.045  0.718
2017 Borcherds W, Becker A, Chen L, Chen J, Chemes LB, Daughdrill GW. Optimal Affinity Enhancement by a Conserved Flexible Linker Controls p53 Mimicry in MdmX. Biophysical Journal. PMID 28487147 DOI: 10.1016/J.Bpj.2017.04.017  0.742
2017 Crabtree MD, Borcherds W, Poosapati A, Shammas SL, Daughdrill GW, Clarke J. Conserved helix-flanking prolines modulate IDP:target affinity by altering the lifetime of the bound complex. Biochemistry. PMID 28425697 DOI: 10.1021/Acs.Biochem.7B00179  0.739
2016 Wei X, Wu S, Song T, Chen L, Gao M, Borcherds W, Daughdrill GW, Chen J. Secondary interaction between MDMX and p53 core domain inhibits p53 DNA binding. Proceedings of the National Academy of Sciences of the United States of America. PMID 27114532 DOI: 10.1073/Pnas.1603838113  0.737
2015 Ytreberg FM, Borcherds W, Wu H, Daughdrill GW. Using chemical shifts to generate structural ensembles for intrinsically disordered proteins with converged distributions of secondary structure. Intrinsically Disordered Proteins. 3: e984565. PMID 28232883 DOI: 10.1016/J.Bpj.2014.11.1256  0.733
2015 Chen L, Borcherds W, Wu S, Becker A, Schonbrunn E, Daughdrill GW, Chen J. Autoinhibition of MDMX by intramolecular p53 mimicry. Proceedings of the National Academy of Sciences of the United States of America. 112: 4624-9. PMID 25825738 DOI: 10.1073/Pnas.1420833112  0.725
2015 Ytreberg FM, Borcherds W, Wu H, Daughdrill GW. Using Chemical Shifts to Generate Structural Ensembles for Intrinsically Disordered Proteins with Converged Distributions of Secondary Structure Biophysical Journal. 108: 227a-228a. DOI: 10.1016/J.BPJ.2014.11.1256  0.348
2014 Borcherds W, Theillet FX, Katzer A, Finzel A, Mishall KM, Powell AT, Wu H, Manieri W, Dieterich C, Selenko P, Loewer A, Daughdrill GW. Disorder and residual helicity alter p53-Mdm2 binding affinity and signaling in cells. Nature Chemical Biology. 10: 1000-2. PMID 25362358 DOI: 10.1038/nchembio.1668  0.743
2013 Borcherds W, Kashtanov S, Wu H, Daughdrill GW. Structural divergence is more extensive than sequence divergence for a family of intrinsically disordered proteins. Proteins. 81: 1686-98. PMID 23606624 DOI: 10.1002/Prot.24303  0.766
2013 Borcherds WM, Kashtanov S, Daughdrill GW. Structural Divergence Exceeds Sequence Divergence for a Family of Intrinsically Disordered Proteins Biophysical Journal. 104: 54a. DOI: 10.1016/J.Bpj.2012.11.339  0.767
2013 Ytreberg FM, Kashtanov S, Borcherds W, Wu H, Daughdrill GW. De Novo Generation of Bound Structures for an Intrinsically Disordered Protein using Only Alpha Carbon Chemical Shifts Biophysical Journal. 104: 191a. DOI: 10.1016/J.Bpj.2012.11.1075  0.724
2012 Kashtanov S, Borcherds W, Wu H, Daughdrill GW, Ytreberg FM. Using chemical shifts to assess transient secondary structure and generate ensemble structures of intrinsically disordered proteins. Methods in Molecular Biology (Clifton, N.J.). 895: 139-52. PMID 22760318 DOI: 10.1007/978-1-61779-927-3_11  0.675
2012 Borcherds WM, Daughdrill GW, Mishall K, Wu H. Crossing the Entropic Barrier to Coupled Folding and Binding Biophysical Journal. 102: 62a-63a. DOI: 10.1016/J.Bpj.2011.11.372  0.742
2011 Daughdrill GW, Borcherds WM, Wu H. Disorder predictors also predict backbone dynamics for a family of disordered proteins. Plos One. 6: e29207. PMID 22195023 DOI: 10.1371/Journal.Pone.0029207  0.679
2011 Pine AT, Mishall KM, Borcherds WM, Wu H, Daughdrill GW. Structural Basis for the Dynamic Behavior of a Family of Disordered Proteins Biophysical Journal. 100: 59a-60a. DOI: 10.1016/J.Bpj.2010.12.522  0.771
2011 Borcherds WM, Wu H, Pine AT, Mishall KM, Daughdrill GW. Evolution of Structure and Dynamics for a Family of Disordered Proteins Biophysical Journal. 100: 519a. DOI: 10.1016/J.Bpj.2010.12.3036  0.738
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