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Your search keyword '"Kourtis, Savvas"' showing total 12 results
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12 results on '"Kourtis, Savvas"'

4. Interactions between BRD4S, LOXL2, and MED1 drive cell cycle transcription in triple‐negative breast cancer

Author

Pascual‐Reguant, Laura, Serra‐Camprubí, Queralt, Datta, Debayan, Cianferoni, Damiano, Kourtis, Savvas, Gañez‐Zapater, Antoni, Cannatá, Chiara, Espinar, Lorena, Querol, Jessica, García‐López, Laura, Musa‐Afaneh, Sara, Guirola, Maria, Gkanogiannis, Anestis, Miró Canturri, Andrea, Guzman, Marta, Rodríguez, Olga, Herencia‐Ropero, Andrea, Arribas, Joaquin, Serra, Violeta, Serrano, Luis, Tian, Tian V, Peiró, Sandra, and Sdelci, Sara

Published
2023
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5. A metabolic map of the DNA damage response identifies PRDX1 in the control of nuclear ROS scavenging and aspartate availability

Author

Moretton, Amandine, Kourtis, Savvas, Gañez Zapater, Antoni, Calabrò, Chiara, Espinar Calvo, Maria Lorena, Fontaine, Frédéric, Darai, Evangelia, Abad Cortel, Etna, Block, Samuel, Pascual‐Reguant, Laura, Pardo‐Lorente, Natalia, Ghose, Ritobrata, Vander Heiden, Matthew G, Janic, Ana, Müller, André C, Loizou, Joanna I, and Sdelci, Sara

Published
2023
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9. Author Reply to Peer Reviews of Interactions between BRD4S, LOXL2, and MED1 drive cell cycle transcription in triple-negative breast cancer

Author

Pascual-Reguant, Laura, primary, Serra Camprubi, Queralt, additional, Datta, Debayan, additional, Cianferoni, Damiano, additional, Kourtis, Savvas, additional, Gañez Zapater, Antoni, additional, Cannatá, Chiara, additional, Espinar, Lorena, additional, Querol, Jessica, additional, García-López, Laura, additional, Musa-Afaneh, Sara, additional, Guirola, Maria, additional, Gkanogiannis, Anestis, additional, Miro Canturri, Andrea, additional, Guzmán, Marta, additional, Rodríguez, Olga, additional, Herencia-Ropera, Andrea, additional, Arribas, Joaquin, additional, Serra, Violeta, additional, Serrano, Luis, additional, Tian, Tian V, additional, Peiró, Sandra, additional, and Sdelci, Sara, additional

Published
2023
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11. The BRD4S-LOXL2-MED1 interaction at the forefront of cell cycle transcriptional control in triple-negative breast cancer

Author

Pascual-Reguant, Laura, primary, Tian, Tian V., additional, Datta, Deabayan, additional, Cianferoni, Damiano, additional, Kourtis, Savvas, additional, Ganez Zapater, Antoni, additional, Cannata, Chiara, additional, Serra Camprubi, Queralt, additional, Espinar, Lorena, additional, Guirola, Maria, additional, Querol, Jessica, additional, Miro Canturri, Andrea, additional, Arribas, Joaquin, additional, Serrano, Luis, additional, Peiro, Sandra, additional, and Sdelci, Sara, additional

Published
2022
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12. hu.MAP3.0: Atlas of human protein complexes by integration of > 25,000 proteomic experiments.

Author

Fischer SN, Claussen ER, Kourtis S, Sdelci S, Orchard S, Hermjakob H, Kustatscher G, and Drew K

Abstract

Macromolecular protein complexes carry out most functions in the cell including essential functions required for cell survival. Unfortunately, we lack the subunit composition for all human protein complexes. To address this gap we integrated >25,000 mass spectrometry experiments using a machine learning approach to identify > 15,000 human protein complexes. We show our map of protein complexes is highly accurate and more comprehensive than previous maps, placing ~75% of human proteins into their physical contexts. We globally characterize our complexes using protein co-variation data (ProteomeHD.2) and identify co-varying complexes suggesting common functional associations. Our map also generates testable functional hypotheses for 472 uncharacterized proteins which we support using AlphaFold modeling. Additionally, we use AlphaFold modeling to identify 511 mutually exclusive protein pairs in hu.MAP3.0 complexes suggesting complexes serve different functional roles depending on their subunit composition. We identify expression as the primary way cells and organisms relieve the conflict of mutually exclusive subunits. Finally, we import our complexes to EMBL-EBI's Complex Portal (https://www.ebi.ac.uk/complexportal/home) as well as provide complexes through our hu.MAP3.0 web interface (https://humap3.proteincomplexes.org/). We expect our resource to be highly impactful to the broader research community.

Published
2024
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