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Boross Péter

Boross Péter

Boross Péter
Name: Boross Péter
Profession: biochemist, chemist

Publication list

Uploaded publications:
36
Publications in DEA:
36
OA:
6
Date range:
1996-2012
2012
  1. Tie, Y., Wang, Y., Boross, P., Chiu, T., Ghosh, A., Tőzsér, J., Louis, J., Harrison, R., Weber, I.: Critical differences in HIV-1 and HIV-2 protease specificity for clinical inhibitors.
    Protein Sci. 21 (3), 339-350, 2012.
    Journal metrics:
    Q1 Biochemistry
    D1 Medicine (miscellaneous)
    Q2 Molecular Biology
2009
  1. 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.
    Journal metrics:
    Q1 Medicine (miscellaneous)
    Q1 Microbiology (medical)
    Q2 Molecular Medicine
    Q1 Pharmacology
2008
  1. 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.
    Journal metrics:
    D1 Immunology
    D1 Insect Science
    D1 Microbiology
    D1 Virology
  2. 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.
    Journal metrics:
    D1 Biochemistry
    Q1 Cell Biology
    Q1 Molecular Biology
2007
  1. Amano, M., Koh, Y., Das, D., Li, J., Leschenko, S., Wang, Y., Boross, P., Weber, I., Ghosh, A., Mitsuya, H.: A novel bis-tetrahydrofuranylurethane-containing nonpeptidic protease inhibitor (PI), GRL-98065, is potent against multiple-PI-resistant human immunodeficiency virus in vitro.
    Antimicrob. Agents Chemother. 51 (6), 2143-2155, 2007.
    Journal metrics:
    D1 Infectious Diseases
    D1 Pharmacology
    D1 Pharmacology (medical)
  2. Tie, Y., Kovalevsky, A., Boross, P., Wang, Y., Ghosh, A., Tőzsér, J., Harrison, R., Weber, I.: Atomic resolution crystal structures of HIV-1 protease and mutants V82A and I84V with saquinavir.
    Proteins. 67 (1), 232-242, 2007.
    Journal metrics:
    Q1 Biochemistry
    Q1 Molecular Biology
    Q2 Structural Biology
  3. 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.
    Journal metrics:
    Q1 Virology
  4. Olivares, I., Mulky, A., Boross, P., Tőzsér, J., Kappes, J., López-Galindez, C., Menéndez-Arias, L.: HIV-1 protease dimer interface mutations that compensate for viral reverse transcriptase instability in infectious virions.
    J. Mol. Biol. 372 (2), 369-381, 2007.
    Journal metrics:
    Q1 Molecular Biology
    Q1 Structural Biology
  5. Wang, Y., Tie, Y., Boross, P., Tőzsér, J., Ghosh, A., Harrison, R., Weber, I.: Potent new antiviral compound shows similar inhibition and structural interactions with drug resistant mutants and wild type HIV-1 protease.
    J. Med. Chem. 50 (18), 4509-4515, 2007.
    Journal metrics:
    D1 Drug Discovery
    Q1 Molecular Medicine
2006
  1. 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.
    Journal metrics:
    Q2 Biochemistry
    Q1 Bioengineering
    Q1 Biotechnology
    Q2 Molecular Biology
  2. 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.
    Journal metrics:
    Q2 Biotechnology
  3. Liu, F., Kovalevsky, A., Louis, J., Wang, Y., Harrison, R., Weber, I., Boross, P.: Mechanism of drug resistance revealed by the crystal structure of the unliganded HIV-1 protease with F53L mutation.
    J. Mol. Biol. 358 (5), 1191-1199, 2006.
    Journal metrics:
    Q1 Molecular Biology
    Q1 Structural Biology
  4. Fang, B., Boross, P., Tőzsér, J., Weber, I.: Structural and kinetic analysis of caspase-3 reveals role for s5 binding site in substrate recognition.
    J. Mol. Biol. 360 (3), 654-666, 2006.
    Journal metrics:
    Q1 Molecular Biology
    Q1 Structural Biology
  5. Kovalevsky, A., Tie, Y., Liu, F., Boross, P., Wang, Y., Leschenko, S., Ghosh, A., Harrison, R., Weber, I.: Susceptibility of Potent Antiviral Inhibitor to Highly Drug Resistant Mutations D30N, I50V and L90M of HIV-1 Protease.
    J. Med. Chem. 49 (4), 1379-1387, 2006.
    Journal metrics:
    D1 Drug Discovery
    Q1 Molecular Medicine
2005
  1. 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.
    Journal metrics:
    D1 Immunology
    D1 Insect Science
    D1 Microbiology
    D1 Virology
  2. Liu, F., Boross, P., Tőzsér, J., Louis, J., Harrison, R., Weber, I.: Analysis of HIV-1 protease mutants to understand mechanisms of resistance.
    FEBS J. 272 (Suppl1), 12, 2005.
  3. Liu, F., Boross, P., Wang, Y., Tőzsér, J., Louis, J., Harrison, R., Weber, I.: Kinetic, Stability, and Structural Changes in High-resolution Crystal Structures of HIV-1 Protease with Drug-resistant Mutations L24I, I50V, and G73S.
    J. Mol. Biol. 354 (4), 789-800, 2005.
    Journal metrics:
    D1 Molecular Biology
    Q1 Structural Biology
  4. Tie, Y., Boross, P., Wang, Y., Gaddis, L., Liu, F., Chen, X., Tőzsér, J., Harrison, R., Weber, I.: Molecular basis for substrate recognition and drug resistance from 1.1 to 1.6 A angstroms resolution crystal structures of HIV-1 protease mutants with substrate analogs.
    FEBS J. 272 (20), 5265-5277, 2005.
    Journal metrics:
    Q1 Biochemistry
    Q2 Cell Biology
    Q2 Molecular Biology
  5. Vana, M., Chen, A., Boross, P., Weber, I., Colman, D., Barklis, E., Leis, J.: Mutations affecting cleavage at the p10-capsid protease cleavage site block Rous sarcoma virus replication.
    Retrovirology. 2 (1), 58, 2005.
    Journal metrics:
    Q1 Infectious Diseases
    Q1 Virology
2004
  1. Mahalingam, B., Wang, Y., Boross, P., Tőzsér, J., Louis, J., Harrison, R., Weber, I.: Crystal structures of HIV protease V82A and L90M mutants reveal changes in the indinavir-binding site.
    Eur. J. Biochem. 271 (8), 1516-1524, 2004.
  2. Fehér, A., Boross, P., Sperka, T., Oroszlan, S., Tőzsér, J.: Expression of the murine leukemia virus protease in fusion with maltose-binding protein in Escherichia coli.
    Protein Expr. Purif. 35 (1), 62-68, 2004.
    Journal metrics:
    Q2 Biotechnology
  3. 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.
    Journal metrics:
    D1 Biochemistry
    D1 Cell Biology
    D1 Molecular Biology
Show all
updated: 2024-07-21, 02:21

SCImago quartiles of
scientific journal articles

Number of scientific articles: 35
Q1/D1 11 (31.4%)
Q1 23 (65.7%)
Q2 3 (8.6%)
N/A 9 (25.7%)
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SCImago subject areas and categories

Biochemistry, Genetics and Molecular Biology (18)
Molecular Biology (12)
Biochemistry (9)
Structural Biology (7)
Cell Biology (4)
Biotechnology (3)
Molecular Medicine (3)
Biophysics (2)
Genetics (1)
Immunology and Microbiology (7)
Virology (7)
Immunology (2)
Microbiology (2)
Medicine (4)
Infectious Diseases (2)
Medicine (miscellaneous) (2)
Microbiology (medical) (1)
Pharmacology (medical) (1)
Pharmacology, Toxicology and Pharmaceutics (4)
Drug Discovery (2)
Pharmacology (2)
Agricultural and Biological Sciences (2)
Insect Science (2)
Chemical Engineering (1)
Bioengineering (1)

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Other co-authors

Show more
Kovalevsky, Andrey Yu
Mahalingam, Bhuvaneshwari
Fischer, Christopher C.
López-Galindez, Cecilio
Menéndez-Arias, Luis
Sarngadharan, Mangalasseril G.