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Entry ID Original Release date Data summary Entry Title Citation Title Authors
50802 2022-12-16 Chemical Shifts: 1 set
Backbone 1H, 13C, and 15N Chemical Shift Assignment for Brd3-BD1 bound to inhibitor PCC Physachenolide C is a Potent, Selective BET Inhibitor Download bibtex for citation iamge A Gunatilaka, Andrew J Ambrose, Christopher J Zerio, Donna D Zhang, Duc T Ngo, Eli Chapman, E Wijeratne, Jared Sivinski, Luis Villa-Celis, Michael W Clarkson, Nancy C Horton, Niloofar Ghadirian, Raimund Fromme, Ya-Ming M Xu
50801 2022-12-16 Chemical Shifts: 1 set
Backbone 1H, 13C, and 15N Chemical Shift Assignment for Brd3-BD1 Physachenolide C is a Potent, Selective BET Inhibitor Download bibtex for citation iamge A Gunatilaka, Andrew J Ambrose, Christopher J Zerio, Donna D Zhang, Duc T Ngo, Eli Chapman, E Wijeratne, Jared Sivinski, Luis Villa-Celis, Michael W Clarkson, Nancy C Horton, Niloofar Ghadirian, Raimund Fromme, Ya-Ming M Xu
27945 2019-11-08 Chemical Shifts: 1 set
Backbone 1H, 13C, and 15N Chemical Shift Assignments for Free Cellular Retinoic Acid Binding Protein 2 Retinoic Acid Binding Leads to CRABP2 Rigidification and Dimerization Download bibtex for citation iamge Anderson S Pinheiro, Anwar Iqbal, Carolina Lixa, Fabio Almeida, Michael W Clarkson, Thomas M Moon, Wolfgang Peti
27946 2019-11-08 Chemical Shifts: 1 set
Backbone 1H, 13C, and 15N Chemical Shift Assignments for RA-bound Cellular Retinoic Acid Binding Protein 2 Retinoic Acid Binding Leads to CRABP2 Rigidification and Dimerization Download bibtex for citation iamge Anderson S Pinheiro, Anwar Iqbal, Carolina Lixa, Fabio Almeida, Michael W Clarkson, Thomas M Moon, Wolfgang Peti
7259 2007-11-21 Chemical Shifts: 1 set
The solution structure of the BRCT domain from human polymerase reveals homology with the TdT BRCT domain Solution Structure of Polymerase mu's BRCT Domain Reveals an Element Essential for Its Role in Nonhomologous End Joining. Download bibtex for citation iamge A L Lee, A Tripathy, C J Galban, D A Ramsden, E F DeRose, G A Mueller, J M Havener, M W Clarkson, R E London, S A Gilmore