6YAA
Structure of the (SR) Ca2+-ATPase bound to the inhibitor compound CAD204520 and TNP-ATP
Summary for 6YAA
Entry DOI | 10.2210/pdb6yaa/pdb |
Descriptor | Sarcoplasmic/endoplasmic reticulum calcium ATPase 1, SPIRO(2,4,6-TRINITROBENZENE[1,2A]-2O',3O'-METHYLENE-ADENINE-TRIPHOSPHATE, 4-[2-[(2~{R})-2-[3-propyl-6-(trifluoromethyloxy)-1~{H}-indol-2-yl]piperidin-1-yl]ethyl]morpholine, ... (4 entities in total) |
Functional Keywords | p-type atpase, inhibitory complex, calcium-transporting atpase, hydrolase |
Biological source | Oryctolagus cuniculus (Rabbit) |
Total number of polymer chains | 1 |
Total formula weight | 110799.46 |
Authors | Heit, S.,Marchesini, M.,Gherli, A.,Montanaro, A.,Patrizi, L.,Sorrentino, C.,Pagliaro, L.,Rompietti, C.,Kitara, S.,Olesen, C.E.,Moller, J.V.,Savi, M.,Bocchi, L.,Vilella, R.,Rizzi, F.,Baglione, M.,Rastelli, G.,Loiacona, C.,La Starza, R.,Mecucci, C.,Stegmair, K.,Aversa, F.,Stilli, D.,Lund Winther, A.M.,Sportoletti, P.,Dalby-Brown, W.,Roti, G.,Bublitz, M. (deposition date: 2020-03-11, release date: 2020-05-20, Last modification date: 2024-10-23) |
Primary citation | Marchesini, M.,Gherli, A.,Montanaro, A.,Patrizi, L.,Sorrentino, C.,Pagliaro, L.,Rompietti, C.,Kitara, S.,Heit, S.,Olesen, C.E.,Moller, J.V.,Savi, M.,Bocchi, L.,Vilella, R.,Rizzi, F.,Baglione, M.,Rastelli, G.,Loiacono, C.,La Starza, R.,Mecucci, C.,Stegmaier, K.,Aversa, F.,Stilli, D.,Lund Winther, A.M.,Sportoletti, P.,Bublitz, M.,Dalby-Brown, W.,Roti, G. Blockade of Oncogenic NOTCH1 with the SERCA Inhibitor CAD204520 in T Cell Acute Lymphoblastic Leukemia. Cell Chem Biol, 27:678-, 2020 Cited by PubMed Abstract: The identification of SERCA (sarco/endoplasmic reticulum calcium ATPase) as a target for modulating gain-of-function NOTCH1 mutations in Notch-dependent cancers has spurred the development of this compound class for cancer therapeutics. Despite the innate toxicity challenge associated with SERCA inhibition, we identified CAD204520, a small molecule with better drug-like properties and reduced off-target Ca toxicity compared with the SERCA inhibitor thapsigargin. In this work, we describe the properties and complex structure of CAD204520 and show that CAD204520 preferentially targets mutated over wild-type NOTCH1 proteins in T cell acute lymphoblastic leukemia (T-ALL) and mantle cell lymphoma (MCL). Uniquely among SERCA inhibitors, CAD204520 suppresses NOTCH1-mutated leukemic cells in a T-ALL xenografted model without causing cardiac toxicity. This study supports the development of SERCA inhibitors for Notch-dependent cancers and extends their application to cases with isolated mutations in the PEST degradation domain of NOTCH1, such as MCL or chronic lymphocytic leukemia (CLL). PubMed: 32386594DOI: 10.1016/j.chembiol.2020.04.002 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (3.4 Å) |
Structure validation
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