Protein Bioinformatics Research Group

Publications

1. Bakos, É, Bujdosó-Székely, V, Patik, I, Király, L, Langó, T, Kozák, E, Cserepes, MT, Tóvári, J and Özvegy-Laczka, C (2025) Cancer-type OATP1B3-V1 is a functional plasma membrane transporter mediating increased uptake of chemotherapeutics in vitro and in vivo. Eur J Pharm Sci 209: 107046.
2. Fichó, E, Pancsa, R, Magyar, C, Kalman, ZE, Schád, É, Németh, BZ, Simon, I, Dobson, L and Tusnády, GE (2025) MFIB 2.0: a major update of the database of protein complexes formed by mutual folding of the constituting protein chains. Nucleic Acids Res 53: D487-D494.
3. Dobson, L, Tusnády, GE and Tompa, P (2025) Regularly updated benchmark sets for statistically correct evaluations of AlphaFold applications. Brief Bioinform 26: .
4. Tusnády, GE and Gerdán, C (2025) TmDet 4.0: determining membrane orientation of transmembrane proteins from 3D structure. Nucleic Acids Res : .
5. Langó, T, Kuffa, KR and Tusnády, GE (2025) Optimized Biotinylated Peptide Detection Method for Characterizing the Cell Surface Proteome. Methods Mol Biol 2908: 13-31.
6. Bajtai, E, Kiss, C, Bakos, É, Langó, T, Lovrics, A, Schád, É, Tisza, V, Hegedűs, K, Fürjes, P, Szabó, Z, Tusnády, GE, Szakács, G, Tantos, Á, Spisák, S, Tóvári, J and Füredi, A (2025) Therapy-induced senescence is a transient drug resistance mechanism in breast cancer. Mol Cancer 24: 128.
7. Garami, K, Péczka, N, Petri, L, Imre, T, Langó, T, Szabó, Z, Orgován, Z, Szabó, PT, Keserü, GM and Ábrányi-Balogh, P (2025) Target Agnostic Photoaffinity Labelling by Sulfonylhydrazones. Angew Chem Int Ed Engl 64: e202408701.
8. Németh, BZ, Kiss, B, Sahin-Tóth, M, Magyar, C and Pál, G (2025) The High-Affinity Chymotrypsin Inhibitor Eglin C Poorly Inhibits Human Chymotrypsin-Like Protease: Gln192 and Lys218 Are Key Determinants. Proteins 93: 543-554.
9. Köller, Z, Németh, BZ, Kiss, B, Nagy, ZA, Schlosser, G, Magyar, C, Demcsák, A, Sahin-Tóth, M and Pál, G (2025) To be, or not to be cleaved: Directed evolution of a canonical serine protease inhibitor against active and inactive protease pair identifies binding loop residue critical for prevention of proteolytic cleavage. Protein Sci 34: e70146.
10. Füredi, A, Tóth, S, Hegedüs, K, Szabó, PT, Gaál, A, Barta, G, Naszályi, LN, Kiss, K, Bölcskei, K, Szeltner, Z, Bajtai, E, Gombos, B, Kiss, D, Cserepes, MT, Kiss, A, Pokreisz, P, Kenner, L, Högler, S, Magyar, C, Cowles, JD, Csiszar, Á, Tóvári, J, Szüts, D, Helyes, Z, Varga, Z, Mező, G and Szakács, G (2025) Safe delivery of a highly toxic anthracycline derivative through liposomal nanoformulation achieves complete cancer regression. Mol Cancer 24: 269.

News

2020-06-02 - Paper published
2019-03-08 - PhD degree
2019-02-07 - Paper published
2018-11-14 - Scientific Students' Association third prize
2018-10-30 - Paper published