Tudóstér: Bagossi Péter publikációi

Mótyán, J., Bagossi, P., Benkő, S., Tőzsér, J.: A molecular model of the full-length human NOD-like receptor family CARD domain containing 5 (NLRC5) protein.
BMC Bioinformatics. 14 (1), 1-11, 2013.

Simon-Vecsei, Z., Király, R., Bagossi, P., Tóth, B., Dahlbom, I., Caja, S., Csősz, É., Lindfors, K., Sblattero, D., Nemes, É., Mäki, M., Fésüs, L., Korponay-Szabó, I.: A single conformational transglutaminase 2 epitope contributed by three domains is critical for celiac antibody binding and effects.
PNAS USA 109 (2), 431-436, 2012.

Lajszné Tóth, B., Erdős, M., Székely, A., Ritli, L., Bagossi, P., Sümegi, J., Maródi, L.: Molecular genetic characterization of novel sphingomyelin phosphodiesterase 1 mutations causing Niemann-Pick disease.
JIMD Rep. 3 125-129, 2012.

Ádám, C., Erdei, É., Casado, C., Kovács, L., Gonzalez, A., Majoros, L., Petrényi, K., Bagossi, P., Farkas, I., Molnár, M., Pócsi, I., Ariño, J., Dombrádi, V.: Protein phosphatase CaPpz1 is involved in cation homeostasis, cell wall integrity and virulence of Candida albicans.
Microbiology (Reading, Engl.). 158 (5), 1258-1267, 2012.

Steiber, Z., Silver, D., Tőzsér, J., Bagossi, P., Jakab, A., Berta, A., Csutak, A.: Relationships between estradiol, progesterone, and plasminogen activator inhibitor longitudinally during normal human pregnancy.
Acta Ophthalmol. 90 (S249), T001, 2012.

Mótyán, J., Gyémánt, G., Harangi, J., Bagossi, P.: Computer-aided subsite mapping of alpha-amylases.
Carbohydr. Res. 346 (3), 410-415, 2011.

Austin, B., Tőzsér, J., Bagossi, P., Tropea, J., Waugh, D.: The substrate specificity of Metarhizium anisopliae and Bos taurus carboxypeptidases A: insights into their use as tools for the removal of affinity tags.
Protein Expr. Purif. 77 (1), 53-61, 2011.

Mótyán, J., Fazekas, E., Mori, H., Svensson, B., Bagossi, P., Kandra, L., Gyémánt, G.: Transglycosylation by barley alfa-amylase 1.
J. Mol. Catal. B-Enzym. 72 (3-4), 229-237, 2011.

Korponay-Szabó, I., Fésüs, L., Bagossi, P., Bagossi, P., Csősz, É., Király, R., Simon-Vecsei, Z., Mäki, M.: Diagnosis of gluten-induced autoimmune diseases.
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Bagossi, P., Bander, P., Bozóki, B., Tőzsér, J.: Discovery and significance of new Human T-lymphotropic viruses: HTVL-3 and HTLV-4.
Expert Rev. Anti. Infect. Ther. 7 (10), 1235-1249, 2009.

Boross, P., Bagossi, P., Weber, I., Tőzsér, J.: Drug targets in human T-lymphotropic virus type 1 (HTLV-1) infection.
Inf. Dis. Drug Targets. 9 (2), 159-171, 2009.

Eizert, E., Bander, P., Bagossi, P., Sperka, T., Miklóssy, G., Boross, P., Weber, I., Tőzsér, J.: Amino acid preferences of retroviral proteases for amino-terminal positions in a type 1 cleavage site.
J. Virol. 82 (20), 10111-10117, 2008.

Kókai, E., Bagossi, P., Dombrádi, V.: A protein foszfatáz 1, egy sokoldalú ősi enzim = Protein phosphatase 1, a versatile ancient enzyme.
Biokémia. 32 (2), 22-34, 2008.

Kádas, J., Boross, P., Weber, I., Bagossi, P., Matúz, K., Tőzsér, J.: C-terminal residues of mature human T-lymphotropic virus type 1 protease are critical for dimerization and catalytic activity.
Biochem. J. 416 (3), 357-364, 2008.

Miklóssy, G., Tőzsér, J., Kádas, J., Ishima, R., Louis, J., Bagossi, P.: Novel macromolecular inhibitors of human immunodeficiency virus-l protease.
Protein Eng. Des. Sel. 21 (7), 453-461, 2008.

Kakuk, A., Friedländer, E., Vereb, G., Lisboa, D., Bagossi, P., Tóth, G., Gergely, P., Vereb, G.: Nuclear and nucleolar localization signals and their targeting function in phosphatidylinositol 4-kinase PI4K230.
Exp. Cell Res. 314 (13), 2376-2388, 2008.

Csutak, A., Silver, D., Tőzsér, J., Steiber, Z., Bagossi, P., Hassan, Z., Berta, A.: Plasminogen activator inhibitor in human tears after laser refractive surgery.
J. Cataract. Refract. Surg. 34 (6), 897-901, 2008.

Csősz, É., Bagossi, P., Nagy, Z., Dosztányi, Z., Simon, I., Fésüs, L.: Substrate preference of transglutaminase 2 revealed by logistic regression analysis and intrinsic disorder examination.
J. Mol. Biol. 383 (2), 390-402, 2008.

Sperka, T., Miklóssy, G., Tie, Y., Bagossi, P., Zahuczky, G., Boross, P., Matúz, K., Harrison, R., Weber, I., Tőzsér, J.: Bovine leukemia virus protease: comparison with human T-lymphotropic virus and human immunodeficiency virus protease.
J. Gen. Virol. 88 (7), 2052-2063, 2007.

Varga, A., Bagossi, P., Tőzsér, J., Peitl, B., Szilvássy, Z.: Effect of experimental hypercholesterolaemia on K+ channel alpha-subunit mRNA levels in rabbit hearts.
Eur. J. Pharmacol. 562 (1-2), 130-131, 2007.

Fehér, A., Boross, P., Sperka, T., Miklóssy, G., Kádas, J., Bagossi, P., Oroszlan, S., Weber, I., Tőzsér, J.: Characterization of the murine leukemia virus protease and its comparison with the human immunodeficiency virus type 1 protease.
J. Gen. Virol. 87 (5), 1321-1330, 2006.

Sperka, T., Boross, P., Eizert, E., Tőzsér, J., Bagossi, P.: Effect of mutations on the dimer stability and the pH optimum of the human foamy virus protease.
Protein Eng. Des. Sel. 19 (8), 369-375, 2006.

Boross, P., Tőzsér, J., Bagossi, P.: Improved purification protocol for wild-type and mutant human foamy virus proteases.
Protein Expr. Purif. 46 (2), 343-347, 2006.

Bagossi, P., Sperka, T., Fehér, A., Kádas, J., Zahuczky, G., Miklóssy, G., Boross, P., Tőzsér, J.: Amino Acid Preferences for a Critical Substrate Binding Subsite of Retroviral Proteases in Type 1 Cleavage Sites.
J. Virol. 79 (7), 4213-4218, 2005.

Csősz, É., Bagossi, P., Fésüs, L.: An in silico study of substrate preference for transglutaminase 2.
FEBS J. 272 (Suppl1), 410-410, 2005.

Sperka, T., Pitlik, J., Bagossi, P., Tőzsér, J.: Beta-lactam compounds as apparently uncompetitive inhibitors of HIV-1 protease.
Bioorg. Med. Chem. Lett. 15 (12), 3086-3090, 2005.

Tőzsér, J., Tropea, J., Cherry, S., Bagossi, P., Copeland, T., Wlodawer, A., Waugh, D.: Comparison of the substrate specificity of two potyvirus proteases.
FEBS J. 272 (2), 514-523, 2005.

Bagossi, P., Horváth, G., Vereb, G., Szöllősi, J., Tőzsér, J.: Molecular modeling of nearly full-length ErbB2 receptor.
Biophys. J. 88 (2), 1354-1363, 2005.

Horváth, G., Bagossi, P., Vereb, G., Park, J., Tőzsér, J., Szöllősi, J.: The structure of ErbB2 receptor: an energy transfer and molecular modeling study.
FEBS J. 272 (Suppl1), 221, 2005.

Bagossi, P., Kádas, J., Miklóssy, G., Boross, P., Weber, I., Tőzsér, J.: Development of a microtiter plate fluorescent assay for inhibition studies on the HTLV-1 and HIV-1 proteinases.
J. Virol. Methods. 119 (2), 87-93, 2004.

Kádas, J., Weber, I., Bagossi, P., Miklóssy, G., Boross, P., Oroszlan, S., Tőzsér, J.: Narrow Substrate Specificity and Sensitivity toward Ligand-binding Site Mutations of Human T-cell Leukemia Virus Type 1 Protease.
J. Biol. Chem. 279 (26), 27148-27157, 2004.

Tőzsér, J., Bagossi, P., Zahuczky, G., Specht, S., Majoreva, E., Copeland, T.: Effect of caspase cleavage-site phosphorylation on proteolysis.
Biochem. J. 372 (1), 137-143, 2003.

Zeke, T., Yatzkan, E., Yarden, O., Szirák, K., Fehér, Z., Bagossi, P., Gergely, P., Kókai, E., Szöőr, B., Dombrádi, V.: Expression of protein phosphatase 1 during the asexual development of Neurospora crassa.
Comp. Biochem. Physiol. B, Biochem. Mol. Biol. 134 (1), 161-170, 2003.

Tőzsér, J., Shulenin, S., Kádas, J., Boross, P., Bagossi, P., Copeland, T., Nair, B., Sarngadharan, M., Oroszlan, S.: Human immunodeficiency virus type 1 capsid protein is a substrate of the retroviral proteinase while integrase is resistant toward proteolysis.
Virology. 310 (1), 16-23, 2003.

Fehér, A., Weber, I., Bagossi, P., Boross, P., Mahalingam, B., Louis, J., Copeland, T., Torshin, I., Harrison, R., Tőzsér, J.: Effect of sequence polymorphism and drug resistance on two HIV-1 Gag processing sites.
Eur. J. Biochem. 269 (16), 4114-4120, 2002.

Gáspár, R., Bagossi, P., Bene, L., Matkó, J., Szöllősi, J., Tőzsér, J., Fésüs, L., Waldmann, T., Damjanovich, S.: Clustering of class I HLA oligomers with CD8 and TCR: three-dimensional models based on fluorescence resonance energy transfer and crystallographic data.
J. Immunol. 166 (8), 5078-5086, 2001.

Zahuczky, G., Boross, P., Bagossi, P., Emri, G., Copeland, T., Oroszlan, S., Louis, J., Tőzsér, J.: Cloning of the bovine leukemia virus proteinase in Escherichia coli and comparison of its specificity to that of human T-cell leukemia virus proteinase.
Biochim. Biophys. Acta Prot. Struct. Mol. Enzym. 1478 (1), 1-8, 2000.

Tőzsér, J., Zahuczky, G., Bagossi, P., Louis, J., Copeland, T., Oroszlan, S., Harrison, R., Weber, I.: Comparison of the substrate specificity of the human T-cell leukemia virus and human immunodeficiency virus proteinases.
Eur. J. Biochem. 267 (20), 6287-6295, 2000.

Tőzsér, J., Bagossi, P., Boross, P., Louis, J., Majerova, E., Oroszlan, S., Copeland, T.: Effect of serine and tyrosine phosphorylation on retroviral proteinase substrates.
Eur. J. Biochem. 265 (1), 423-429, 1999.

Boross, P., Bagossi, P., Copeland, T., Oroszlan, S., Louis, J., Tőzsér, J.: Effect of substrate residues on the P2' preference of retroviral proteinases.
Eur. J. Biochem. 264 (3), 921-929, 1999.

Fenyőfalvi, G., Bagossi, P., Copeland, T., Oroszlan, S., Boross, P., Tőzsér, J.: Expression and characterization of human foamy virus proteinase.
FEBS Lett. 462 (3), 397-401, 1999.

Bagossi, P., Zahuczky, G., Tőzsér, J., Weber, I., Harrison, R.: Improved parameters for generating partial charges: correlation with observed dipole moments.
J. Mol. Model. 5 (9), 143-152, 1999.

Bagossi, P., Cheng, Y., Oroszlan, S., Tőzsér, J.: Comparison of the specificity of homo- and heterodimeric linked HIV-1 and HIV-2 proteinase dimers.
Protein Eng. Des. Sel. 11 (6), 439-445, 1998.

Vissi, E., Csordás Tóth, É., Kovács, I., Magyar, Z., Horváth, G., Bagossi, P., Dudits, D., Gergely, P., Dombrádi, V.: Protein phosphatase 1 catalytic subunit isoforms from alfalfa: biochemical characterization and cDNA cloning.
Arch. Biochem. Biophys. 360 (2), 206-214, 1998.

Tőzsér, J., Yin, F., Cheng, Y., Bagossi, P., Weber, I., Harrison, R., Oroszlan, S.: Activity of Tethered Human Immunodeficiency Virus 1 Protease Containing Mutations in the Flap Region of One Subunit.
Eur. J. Biochem. 244 (1), 235-241, 1997.

Tőzsér, J., Bagossi, P., Weber, I., Louis, J., Copeland, T., Oroszlan, S.: Studies on the Symmetry and Sequence Context Dependence of the HIV-1 Proteinase Specificity.
J. Biol. Chem. 272 (27), 16807-16814, 1997.

Bagossi, P., Cheng, Y., Oroszlan, S., Tőzsér, J.: Activity of linked HIV-1 proteinase dimers containing mutations in the active site region.
Protein Eng. Des. Sel. 9 (11), 997-1003, 1996.

Tőzsér, J., Bagossi, P., Weber, I., Copeland, T., Oroszlan, S.: Comparative studies on the substrate specificity of avian myeloblastosis virus proteinase and lentiviral proteinases.
J. Biol. Chem. 271 (12), 6781-6788, 1996.

Pitlik, J., Bagossi, P., Jekő, J., Tőzsér, J.: Synthesis of cephalosporin oligopeptides as potential proteinase inhibitors.
Pharmazie. 51 (10), 700-704, 1996.