-
1
-
-
0036310388
-
Mutation of the catalytic domain of the foamy virus reverse transcriptase leads to loss of processivity and infectivity
-
DOI 10.1128/JVI.76.15.7560-7570.2002
-
Rinke CS, Boyer PL, Sullivan MD, Hughes SH, Linial ML. 2002. Mutation of the catalytic domain of the foamy virus reverse transcriptase leads to loss of processivity and infectivity. J. Virol. 76:7560-7570. http://dx.doi.org/10.1128/ JVI.76.15.7560-7570.2002. (Pubitemid 34760979)
-
(2002)
Journal of Virology
, vol.76
, Issue.15
, pp. 7560-7570
-
-
Rinke, C.S.1
Boyer, P.L.2
Sullivan, M.D.3
Hughes, S.H.4
Linial, M.L.5
-
2
-
-
2642526847
-
Characterization of the polymerase and RNase H activities of human foamy virus reverse transcriptase
-
DOI 10.1128/JVI.78.12.6112-6121.2004
-
Boyer PL, Stenbak CR, Clark PK, Linial ML, Hughes SH. 2004. Characterization of the polymerase and RNase H activities of human foamy virus reverse transcriptase. J. Virol. 78:6112-6121. http://dx.doi.org/10.1128/JVI.78. 12.6112-6121.2004. (Pubitemid 38715909)
-
(2004)
Journal of Virology
, vol.78
, Issue.12
, pp. 6112-6121
-
-
Boyer, P.L.1
Stenbak, C.R.2
Clark, P.K.3
Linial, M.L.4
Hughes, S.H.5
-
3
-
-
77649326990
-
Biophysical and enzymatic properties of the simian and prototype foamy virus reverse transcriptases
-
Hartl MJ, Mayr F, Rethwilm A, Wöhrl BM. 2010. Biophysical and enzymatic properties of the simian and prototype foamy virus reverse transcriptases. Retrovirology 7:5. http://dx.doi.org/10.1186/1742-4690-7-5.
-
(2010)
Retrovirology
, vol.7
, pp. 5
-
-
Hartl, M.J.1
Mayr, F.2
Rethwilm, A.3
Wöhrl, B.M.4
-
4
-
-
46649100031
-
The solution structure of the simian foamy virus protease reveals a monomeric protein
-
Hartl MJ, Wöhrl BM, Rösch P, Schweimer K. 2008. The solution structure of the simian foamy virus protease reveals a monomeric protein. J. Mol. Biol. 381:141-149. http://dx.doi.org/10.1016/j.jmb.2008.05.064.
-
(2008)
J. Mol. Biol.
, vol.381
, pp. 141-149
-
-
Hartl, M.J.1
Wöhrl, B.M.2
Rösch, P.3
Schweimer, K.4
-
5
-
-
79955367748
-
Regulation of foamy virus protease activity by viral RNA: A novel and unique mechanism among retroviruses
-
Hartl MJ, Bodem J, Jochheim F, Rethwilm A, Rösch P, Wöhrl BM. 2011. Regulation of foamy virus protease activity by viral RNA: a novel and unique mechanism among retroviruses. J. Virol. 85:4462-4469. http://dx.doi.org/10.1128/JVI.02211-10.
-
(2011)
J. Virol.
, vol.85
, pp. 4462-4469
-
-
Hartl, M.J.1
Bodem, J.2
Jochheim, F.3
Rethwilm, A.4
Rösch, P.5
Wöhrl, B.M.6
-
6
-
-
0001469617
-
Retroviridae: The retroviruses and their replication
-
Knipe DM, Howley PM (ed), Lippincott Williams & Wilkins, Philadelphia, PA
-
Goff SP. 2007. Retroviridae: The retroviruses and their replication, p 1999-2069. In Knipe DM, Howley PM (ed), Fields virology, 5th ed. Lippincott Williams & Wilkins, Philadelphia, PA.
-
(2007)
Fields Virology, 5th Ed.
, pp. 1999-2069
-
-
Goff, S.P.1
-
7
-
-
84856803486
-
Insights into the structure and activity of prototype foamy virus RNase H
-
Leo B, Hartl MJ, Schweimer K, Mayr F, Wöhrl BM. 2012. Insights into the structure and activity of prototype foamy virus RNase H. Retrovirology 9:14. http://dx.doi.org/10.1186/1742-4690-9-14.
-
(2012)
Retrovirology
, vol.9
, pp. 14
-
-
Leo, B.1
Hartl, M.J.2
Schweimer, K.3
Mayr, F.4
Wöhrl, B.M.5
-
8
-
-
84865838680
-
The solution structure of the prototype foamy virus RNase H domain indicates an important role of the basic loop in substrate binding
-
Leo B, Schweimer K, Rösch P, Hartl MJ, Wöhrl BM. 2012. The solution structure of the prototype foamy virus RNase H domain indicates an important role of the basic loop in substrate binding. Retrovirology 9:73. http://dx.doi.org/10.1186/1742-4690-9-73.
-
(2012)
Retrovirology
, vol.9
, pp. 73
-
-
Leo, B.1
Schweimer, K.2
Rösch, P.3
Hartl, M.J.4
Wöhrl, B.M.5
-
9
-
-
0025718668
-
A recombinant ribonuclease H domain of HIV-1 reverse transcriptase that is enzymatically active
-
Evans DB, Brawn K, Deibel MR, Jr, Tarpley WG, Sharma SK. 1991. A recombinant ribonucleaseHdomain of HIV-1 reverse transcriptase that is enzymatically active. J. Biol. Chem. 266:20583-20585. (Pubitemid 21908502)
-
(1991)
Journal of Biological Chemistry
, vol.266
, Issue.31
, pp. 20583-20585
-
-
Evans, D.B.1
Brawn, K.2
Deibel Jr., M.R.3
Tarpley, W.G.4
Sharma, S.K.5
-
10
-
-
0025975174
-
Reconstitution in vitro of RNase H activity by using purified N-terminal and C-terminal domains of human immunodeficiency virus type 1 reverse transcriptase
-
Hostomsky Z, Hostomska Z, Hudson GO, Moomaw EW, Nodes BR. 1991. Reconstitution in vitro of RNase H activity by using purified N-terminal and C-terminal domains of human immunodeficiency virus type 1 reverse transcriptase. Proc. Natl. Acad. Sci. U. S. A. 88:1148-1152. http://dx.doi.org/10.1073/pnas. 88.4.1148. (Pubitemid 21916182)
-
(1991)
Proceedings of the National Academy of Sciences of the United States of America
, vol.88
, Issue.4
, pp. 1148-1152
-
-
Hostomsky, Z.1
Hostomska, Z.2
Hudson, G.O.3
Moomaw, E.W.4
Nodes, B.R.5
-
11
-
-
0028102093
-
Contributions of DNA polymerase subdomains to the RNase H activity of human immunodeficiency virus type 1 reverse transcriptase
-
Smith JS, Gritsman K, Roth MJ. 1994. Contributions of DNA polymerase subdomains to the RNase H activity of human immunodeficiency virus type 1 reverse transcriptase. J. Virol. 68:5721-5729. (Pubitemid 24258587)
-
(1994)
Journal of Virology
, vol.68
, Issue.9
, pp. 5721-5729
-
-
Smith, J.S.1
Gritsman, K.2
Roth, M.J.3
-
12
-
-
84870824536
-
HIV-1 reverse transcriptase still remains a new drug target: Structure, function, classical inhibitors, and new inhibitors with innovative mechanisms of actions
-
Esposito F, Corona A, Tramontano E. 2012. HIV-1 reverse transcriptase still remains a new drug target: structure, function, classical inhibitors, and new inhibitors with innovative mechanisms of actions. Mol. Biol. Int. 2012:586401. http://dx.doi.org/10.1155/2012/586401.
-
(2012)
Mol. Biol. Int.
, vol.2012
, pp. 586401
-
-
Esposito, F.1
Corona, A.2
Tramontano, E.3
-
13
-
-
33745107517
-
HIV-1 RNase H: Recent progress in an exciting, yet little explored, drug target
-
DOI 10.2174/138955706777435733
-
Tramontano E. 2006. HIV-1 RNase H: recent progress in an exciting, yet little explored, drug target. Mini Rev. Med. Chem. 6:727-737. http://dx.doi.org/10.2174/138955706777435733. (Pubitemid 43881124)
-
(2006)
Mini-Reviews in Medicinal Chemistry
, vol.6
, Issue.6
, pp. 727-737
-
-
Tramontano, E.1
-
14
-
-
77955648999
-
HIV-1 RT-associated RNase H function inhibitors: Recent advances in drug development
-
Tramontano E, Di Santo R. 2010. HIV-1 RT-associated RNase H function inhibitors: recent advances in drug development. Curr. Med. Chem. 17:2837-2853. http://dx.doi.org/10.2174/092986710792065045.
-
(2010)
Curr. Med. Chem.
, vol.17
, pp. 2837-2853
-
-
Tramontano, E.1
Di Santo, R.2
-
15
-
-
84876709287
-
Molecular aspects of the RT/drug interactions. Perspective of dual inhibitors
-
Distinto S, Maccioni E, Meleddu R, Corona A, Alcaro S, Tramontano E. 2013. Molecular aspects of the RT/drug interactions. Perspective of dual inhibitors. Curr. Pharm. Des. 19:1850-1859. http://dx.doi.org/10.2174/ 1381612811319100009.
-
(2013)
Curr. Pharm. Des.
, vol.19
, pp. 1850-1859
-
-
Distinto, S.1
Maccioni, E.2
Meleddu, R.3
Corona, A.4
Alcaro, S.5
Tramontano, E.6
-
16
-
-
84902502321
-
Ribonuclease inhibitors: Structural and molecular biology
-
Le Grice SFJ, GotteM(ed), Springer, London, United Kingdom
-
Rausch JW. 2013. Ribonuclease inhibitors: structural and molecular biology, p 143-172. In Le Grice SFJ, GotteM(ed), Human immnodeficiency virus reverse transcriptase. A bench-to-bedside success. Springer, London, United Kingdom.
-
(2013)
Human Immnodeficiency Virus Reverse Transcriptase. A Bench-to-bedside Success
, pp. 143-172
-
-
Rausch, J.W.1
-
17
-
-
71049185147
-
Structure of HIV-1 reverse transcriptase with the inhibitor beta-thujaplicinol bound at the RNase H active site
-
Himmel DM, Maegley KA, Pauly TA, Bauman JD, Das K, Dharia C, Clark AD, Jr, Ryan K, Hickey MJ, Love RA, Hughes SH, Bergqvist S, Arnold E. 2009. Structure of HIV-1 reverse transcriptase with the inhibitor beta-thujaplicinol bound at the RNase H active site. Structure 17:1625-1635. http://dx.doi.org/10. 1016/j.str.2009.09.016.
-
(2009)
Structure
, vol.17
, pp. 1625-1635
-
-
Himmel, D.M.1
Maegley, K.A.2
Pauly, T.A.3
Bauman, J.D.4
Das, K.5
Dharia, C.6
Clark Jr., A.D.7
Ryan, K.8
Hickey, M.J.9
Love, R.A.10
Hughes, S.H.11
Bergqvist, S.12
Arnold, E.13
-
18
-
-
37249062449
-
HIV-1 reverse transcriptase structure with RNase H inhibitor dihydroxy benzoyl naphthyl hydrazone bound at a novel site
-
Himmel DM, Sarafianos SG, Dharmasena S, Hossain MM, McCoy-Simandle K, Ilina T, Clark AD, Jr, Knight JL, Julias JG, Clark PK, Krogh-Jespersen K, Levy RM, Hughes SH, Parniak MA, Arnold E. 2006. HIV-1 reverse transcriptase structure with RNase H inhibitor dihydroxy benzoyl naphthyl hydrazone bound at a novel site. ACS Chem. Biol. 1:702-712. http://dx.doi.org/10.1021/cb600303y.
-
(2006)
ACS Chem. Biol.
, vol.1
, pp. 702-712
-
-
Himmel, D.M.1
Sarafianos, S.G.2
Dharmasena, S.3
Hossain, M.M.4
McCoy-Simandle, K.5
Ilina, T.6
Clark Jr., A.D.7
Knight, J.L.8
Julias, J.G.9
Clark, P.K.10
Krogh-Jespersen, K.11
Levy, R.M.12
Hughes, S.H.13
Parniak, M.A.14
Arnold, E.15
-
19
-
-
70349638920
-
RNase H active site inhibitors of human immunodeficiency virus type 1 reverse transcriptase: Design, biochemical activity, and structural information
-
Kirschberg TA, Balakrishnan M, Squires NH, Barnes T, Brendza KM, Chen X, Eisenberg EJ, Jin W, Kutty N, Leavitt S, Liclican A, Liu Q, Liu X, Mak J, Perry JK, Wang M, Watkins WJ, Lansdon EB. 2009. RNase H active site inhibitors of human immunodeficiency virus type 1 reverse transcriptase: design, biochemical activity, and structural information. J. Med. Chem. 52:5781-5784. http://dx.doi.org/10.1021/jm900597q.
-
(2009)
J. Med. Chem.
, vol.52
, pp. 5781-5784
-
-
Kirschberg, T.A.1
Balakrishnan, M.2
Squires, N.H.3
Barnes, T.4
Brendza, K.M.5
Chen, X.6
Eisenberg, E.J.7
Jin, W.8
Kutty, N.9
Leavitt, S.10
Liclican, A.11
Liu, Q.12
Liu, X.13
Mak, J.14
Perry, J.K.15
Wang, M.16
Watkins, W.J.17
Lansdon, E.B.18
-
20
-
-
79956334444
-
Structural and binding analysis of pyrimidinol carboxylic acid and N -hydroxy quinazolinedione HIV-1 RNase H inhibitors
-
Lansdon EB, Liu Q, Leavitt SA, Balakrishnan M, Perry JK, Lancaster-Moyer C, Kutty N, Liu X, Squires NH, Watkins WJ, Kirschberg TA. 2011. Structural and binding analysis of pyrimidinol carboxylic acid and N -hydroxy quinazolinedione HIV-1 RNase H inhibitors. Antimicrob. Agents Chemother. 55: 2905-2915. http://dx.doi.org/10.1128/AAC.01594-10.
-
(2011)
Antimicrob. Agents Chemother.
, vol.55
, pp. 2905-2915
-
-
Lansdon, E.B.1
Liu, Q.2
Leavitt, S.A.3
Balakrishnan, M.4
Perry, J.K.5
Lancaster-Moyer, C.6
Kutty, N.7
Liu, X.8
Squires, N.H.9
Watkins, W.J.10
Kirschberg, T.A.11
-
21
-
-
77954521861
-
Structural basis for the inhibition of RNase H activity of HIV-1 reverse transcriptase by RNase H active site-directed inhibitors
-
Su HP, Yan Y, Prasad GS, Smith RF, Daniels CL, Abeywickrema PD, Reid JC, Loughran HM, Kornienko M, Sharma S, Grobler JA, Xu B, Sardana V, Allison TJ, Williams PD, Darke PL, Hazuda DJ, Munshi S. 2010. Structural basis for the inhibition of RNase H activity of HIV-1 reverse transcriptase by RNase H active site-directed inhibitors. J. Virol. 84:7625-7633. http://dx.doi.org/10.1128/JVI. 00353-10.
-
(2010)
J. Virol.
, vol.84
, pp. 7625-7633
-
-
Su, H.P.1
Yan, Y.2
Prasad, G.S.3
Smith, R.F.4
Daniels, C.L.5
Abeywickrema, P.D.6
Reid, J.C.7
Loughran, H.M.8
Kornienko, M.9
Sharma, S.10
Grobler, J.A.11
Xu, B.12
Sardana, V.13
Allison, T.J.14
Williams, P.D.15
Darke, P.L.16
Hazuda, D.J.17
Munshi, S.18
-
22
-
-
0037469137
-
Solution structure of the RNase H domain of the HIV-1 reverse transcriptase in the presence of magnesium
-
DOI 10.1021/bi0204894
-
Pari K, Mueller GA, DeRose EF, Kirby TW, London RE. 2003. Solution structure of the RNaseHdomain of the HIV-1 reverse transcriptase in the presence of magnesium. Biochemistry 42:639-650. http://dx.doi.org/10.1021/bi0204894. (Pubitemid 36133288)
-
(2003)
Biochemistry
, vol.42
, Issue.3
, pp. 639-650
-
-
Pari, K.1
Mueller, G.A.2
DeRose, E.F.3
Kirby, T.W.4
London, R.E.5
-
23
-
-
84867232956
-
Structural basis of the allosteric inhibitor interaction on the HIV-1 reverse transcriptase RNase H domain
-
Christen MT, Menon L, Myshakina NS, Ahn J, Parniak MA, Ishima R. 2012. Structural basis of the allosteric inhibitor interaction on the HIV-1 reverse transcriptase RNase H domain. Chem. Biol. Drug Des. 80:706-716. http://dx.doi.org/10.1111/cbdd.12010.
-
(2012)
Chem. Biol. Drug Des.
, vol.80
, pp. 706-716
-
-
Christen, M.T.1
Menon, L.2
Myshakina, N.S.3
Ahn, J.4
Parniak, M.A.5
Ishima, R.6
-
24
-
-
78650081368
-
Interaction of HIV-1 reverse transcriptase ribonuclease H with an acylhydrazone inhibitor
-
Gong Q, Menon L, Ilina T, Miller LG, Ahn J, Parniak MA, Ishima R. 2011. Interaction of HIV-1 reverse transcriptase ribonuclease H with an acylhydrazone inhibitor. Chem. Biol. Drug Des. 77:39-47. http://dx.doi.org/10.1111/j.1747- 0285.2010.01052.x.
-
(2011)
Chem. Biol. Drug Des.
, vol.77
, pp. 39-47
-
-
Gong, Q.1
Menon, L.2
Ilina, T.3
Miller, L.G.4
Ahn, J.5
Parniak, M.A.6
Ishima, R.7
-
25
-
-
0027931296
-
Construction of an enzymatically active ribonuclease H domain of human immunodeficiency virus type 1 reverse transcriptase
-
Stahl SJ, Kaufman JD, Vikić-Topić S, Crouch RJ, Wingfield PT. 1994. Construction of an enzymatically active ribonucleaseHdomain of human immunodeficiency virus type 1 reverse transcriptase. Protein Eng. 7:1103-1108. http://dx.doi.org/10.1093/protein/7.9.1103. (Pubitemid 24282496)
-
(1994)
Protein Engineering
, vol.7
, Issue.9
, pp. 1103-1108
-
-
Stahl, S.J.1
Kaufman, J.D.2
Vikic-Topic, S.3
Cronch, R.J.4
Wingfield, P.T.5
-
26
-
-
0037474193
-
Inhibition of HIV-1 ribonuclease H by a novel diketo acid, 4-[5-(benzoylamino)thien-2-yl]-2,4-dioxobutanoic acid
-
DOI 10.1074/jbc.C200621200
-
Shaw-Reid CA, Munshi V, Graham P, Wolfe A, Witmer M, Danzeisen R, Olsen DB, Carroll SS, Embrey M, Wai JS, Miller MD, Cole JL, Hazuda DJ. 2003. Inhibition of HIV-1 ribonuclease H by a novel diketo acid, 4-[5-(benzoylamino) thien-2-yl]-2,4-dioxobutanoic acid. J. Biol. Chem. 278:2777-2780. http://dx.doi.org/10.1074/jbc.C200621200. (Pubitemid 36801178)
-
(2003)
Journal of Biological Chemistry
, vol.278
, Issue.5
, pp. 2777-2780
-
-
Shaw-Reid, C.A.1
Munshi, V.2
Graham, P.3
Wolfe, A.4
Witmer, M.5
Danzeisen, R.6
Olsen, D.B.7
Carroll, S.S.8
Embrey, M.9
Wai, J.S.10
Miller, M.D.11
Cole, J.L.12
Hazuda, D.J.13
-
27
-
-
0025908083
-
Crystal structure of the ribonuclease H domain of HIV-1 reverse transcriptase
-
Davies JF, Jr, Hostomska Z, Hostomsky Z, Jordan SR, Matthews DA. 1991. Crystal structure of the ribonuclease H domain of HIV-1 reverse transcriptase Science 252:88 -95. http://dx.doi.org/10.1126/science.1707186.
-
(1991)
Science
, vol.252
, pp. 88-95
-
-
Davies Jr., J.F.1
Hostomska, Z.2
Hostomsky, Z.3
Jordan, S.R.4
Matthews, D.A.5
-
28
-
-
13544276913
-
6-[1-(4-Fluorophenyl)methyl-1H-pyrrol-2-yl)]-2,4-dioxo-5-hexenoic acid ethyl ester a novel diketo acid derivative which selectively inhibits the HIV-1 viral replication in cell culture and the ribonuclease H activity in vitro
-
DOI 10.1016/j.antiviral.2004.11.002
-
Tramontano E, Esposito F, Badas R, Di Santo R, Costi R, La Colla P. 2005. 6-[1-(4-Fluorophenyl)methyl-1H-pyrrol-2-yl)]-2,4-dioxo-5-hexenoic acid ethyl ester a novel diketo acid derivative which selectively inhibits the HIV-1 viral replication in cell culture and the ribonuclease H activity in vitro. Antiviral Res. 65:117-124. http://dx.doi.org/10.1016/j.antiviral.2004.11.002. (Pubitemid 40222288)
-
(2005)
Antiviral Research
, vol.65
, Issue.2
, pp. 117-124
-
-
Tramontano, E.1
Esposito, F.2
Badas, R.3
Di, S.R.4
Costi, R.5
La, C.P.6
-
29
-
-
76149120388
-
AutoDock Vina: Improving the speed and accuracy of docking with a new scoring function, efficient optimization, and multithreading
-
Trott O, Olson AJ. 2010. AutoDock Vina: improving the speed and accuracy of docking with a new scoring function, efficient optimization, and multithreading. J. Comput. Chem. 31:455-461.
-
(2010)
J. Comput. Chem.
, vol.31
, pp. 455-461
-
-
Trott, O.1
Olson, A.J.2
-
30
-
-
84861572493
-
Development of a series of 3-hydroxyquinolin-2(1H)-ones as selective inhibitors of HIV-1 reverse transcriptase associated RNase H activity
-
http://dx.doi.org/10.1016/j.bmcl.2012.04.096
-
Suchaud V, Bailly F, Lion C, Tramontano E, Esposito F, Corona A, Christ F, Debyser Z, Cotelle P. 2012. Development of a series of 3-hydroxyquinolin- 2(1H)-ones as selective inhibitors of HIV-1 reverse transcriptase associated RNase H activity. Bioorg. Med. Chem. Lett. 22:3988-3992. http://dx.doi.org/10. 1016/j.bmcl.2012.04.096.; http://dx.doi.org/10.1016/j.bmcl.2012.04.096.
-
(2012)
Bioorg. Med. Chem. Lett.
, vol.22
, pp. 3988-3992
-
-
Suchaud, V.1
Bailly, F.2
Lion, C.3
Tramontano, E.4
Esposito, F.5
Corona, A.6
Christ, F.7
Debyser, Z.8
Cotelle, P.9
-
31
-
-
79960189034
-
Synthesis, activity, and structural analysis of novel α-hydroxytropolone inhibitors of human immunodeficiency virus reverse transcriptase-associated ribonuclease H
-
Chung S, Himmel DM, Jiang JK, Wojtak K, Bauman JD, Rausch JW, Wilson JA, Beutler JA, Thomas CJ, Arnold E, Le Grice SF. 2011. Synthesis, activity, and structural analysis of novel α-hydroxytropolone inhibitors of human immunodeficiency virus reverse transcriptase-associated ribonuclease H. J. Med. Chem. 54:4462-4473. http://dx.doi.org/10.1021/jm2000757.
-
(2011)
J. Med. Chem.
, vol.54
, pp. 4462-4473
-
-
Chung, S.1
Himmel, D.M.2
Jiang, J.K.3
Wojtak, K.4
Bauman, J.D.5
Rausch, J.W.6
Wilson, J.A.7
Beutler, J.A.8
Thomas, C.J.9
Arnold, E.10
Le Grice, S.F.11
-
32
-
-
77956131587
-
Structure-activity analysis of vinylogous urea inhibitors of human immunodeficiency virus-encoded ribonuclease H
-
Chung S, Wendeler M, Rausch JW, Beilhartz G, Gotte M, O'Keefe BR, Bermingham A, Beutler JA, Liu S, Zhuang X, Le Grice SF. 2010. Structure-activity analysis of vinylogous urea inhibitors of human immunodeficiency virus-encoded ribonuclease H. Antimicrob. Agents Chemother. 54:3913-3921. http://dx.doi.org/ 10.1128/AAC.00434-10.
-
(2010)
Antimicrob. Agents Chemother.
, vol.54
, pp. 3913-3921
-
-
Chung, S.1
Wendeler, M.2
Rausch, J.W.3
Beilhartz, G.4
Gotte, M.5
O'Keefe, B.R.6
Bermingham, A.7
Beutler, J.A.8
Liu, S.9
Zhuang, X.10
Le Grice, S.F.11
-
33
-
-
84858440068
-
Identification of HIV-1 reverse transcriptase dual inhibitors by a combined shape-, 2D-fingerprint- and pharmacophore-based virtual screening approach
-
Distinto S, Esposito F, Kirchmair J, Cardia MC, Gaspari M, Maccioni E, Alcaro S, Markt P, Wolber G, Zinzula L, Tramontano E. 2012. Identification of HIV-1 reverse transcriptase dual inhibitors by a combined shape-, 2D-fingerprint- and pharmacophore-based virtual screening approach. Eur. J. Med. Chem. 50:216-229. http://dx.doi.org/10.1016/j.ejmech.2012.01.056.
-
(2012)
Eur. J. Med. Chem.
, vol.50
, pp. 216-229
-
-
Distinto, S.1
Esposito, F.2
Kirchmair, J.3
Cardia, M.C.4
Gaspari, M.5
Maccioni, E.6
Alcaro, S.7
Markt, P.8
Wolber, G.9
Zinzula, L.10
Tramontano, E.11
-
34
-
-
84883810182
-
Hypericum hircinum L. Components as new single-molecule inhibitors of both HIV-1 reverse transcriptase-associated DNA polymerase and ribonuclease H activities
-
Esposito F, Sanna C, Del Vecchio C, Cannas V, Venditti A, Corona A, Bianco A, Serrilli AM, Guarcini L, Parolin C, Ballero M, Tramontano E. 2013. Hypericum hircinum L. components as new single-molecule inhibitors of both HIV-1 reverse transcriptase-associated DNA polymerase and ribonuclease H activities. Pathog. Dis. 68:116-124. http://dx.doi.org/10.1111/2049-632X.12051.
-
(2013)
Pathog. Dis.
, vol.68
, pp. 116-124
-
-
Esposito, F.1
Sanna, C.2
Del Vecchio, C.3
Cannas, V.4
Venditti, A.5
Corona, A.6
Bianco, A.7
Serrilli, A.M.8
Guarcini, L.9
Parolin, C.10
Ballero, M.11
Tramontano, E.12
-
35
-
-
84868261918
-
New anthraquinone derivatives as inhibitors of the HIV-1 reverse transcriptase-associated ribonucleaseHfunction
-
Esposito F, Corona A, Zinzula L, Kharlamova T, Tramontano E. 2012. New anthraquinone derivatives as inhibitors of the HIV-1 reverse transcriptase-associated ribonucleaseHfunction. Chemotherapy 58:299-307. http://dx.doi.org/10.1159/000343101.
-
(2012)
Chemotherapy
, vol.58
, pp. 299-307
-
-
Esposito, F.1
Corona, A.2
Zinzula, L.3
Kharlamova, T.4
Tramontano, E.5
-
36
-
-
79955072485
-
Alizarine derivatives as new dual inhibitors of the HIV-1 reverse transcriptase-associated DNA polymerase and RNase H activities effective also on the RNase H activity of non-nucleoside resistant reverse transcriptases
-
Esposito F, Kharlamova T, Distinto S, Zinzula L, Cheng YC, Dutschman G, Floris G, Markt P, Corona A, Tramontano E. 2011. Alizarine derivatives as new dual inhibitors of the HIV-1 reverse transcriptase-associated DNA polymerase and RNase H activities effective also on the RNase H activity of non-nucleoside resistant reverse transcriptases. FEBS J. 278:1444-1457. http://dx.doi.org/10. 1111/j.1742-4658.2011.08057.x.
-
(2011)
FEBS J.
, vol.278
, pp. 1444-1457
-
-
Esposito, F.1
Kharlamova, T.2
Distinto, S.3
Zinzula, L.4
Cheng, Y.C.5
Dutschman, G.6
Floris, G.7
Markt, P.8
Corona, A.9
Tramontano, E.10
-
37
-
-
84863025474
-
Mutagenesis of human immunodeficiency virus reverse transcriptase p51 subunit defines residues contributing to vinylogous urea inhibition of ribonuclease H activity
-
Chung S, Miller JT, Johnson BC, Hughes SH, Le Grice SF. 2012. Mutagenesis of human immunodeficiency virus reverse transcriptase p51 subunit defines residues contributing to vinylogous urea inhibition of ribonuclease H activity. J. Biol. Chem. 287:4066-4075. http://dx.doi.org/10.1074/jbc.M111.314781.
-
(2012)
J. Biol. Chem.
, vol.287
, pp. 4066-4075
-
-
Chung, S.1
Miller, J.T.2
Johnson, B.C.3
Hughes, S.H.4
Le Grice, S.F.5
-
38
-
-
43049144549
-
Structural basis for drug resistance mechanisms for non-nucleoside inhibitors of HIV reverse transcriptase
-
Ren J, Stammers DK. 2008. Structural basis for drug resistance mechanisms for non-nucleoside inhibitors of HIV reverse transcriptase. Virus Res. 134:157-170. http://dx.doi.org/10.1016/j.virusres.2007.12.018.
-
(2008)
Virus Res.
, vol.134
, pp. 157-170
-
-
Ren, J.1
Stammers, D.K.2
-
39
-
-
0029869049
-
Human foamy virus replication: A pathway distinct from that of retroviruses and hepadnaviruses
-
Yu SF, Baldwin DN, Gwynn SR, Yendapalli S, Linial ML. 1996. Human foamy virus replication: a pathway distinct from that of retroviruses and hepadnaviruses. Science 271: 1579 -1582. http://dx.doi.org/10.1126/science.271. 5255.1579.
-
(1996)
Science
, vol.271
, pp. 1579-1582
-
-
Yu, S.F.1
Baldwin, D.N.2
Gwynn, S.R.3
Yendapalli, S.4
Linial, M.L.5
-
40
-
-
0032932713
-
Evidence that the human foamy virus genome is DNA
-
Yu SF, Sullivan MD, Linial ML. 1999. Evidence that the human foamy virus genome is DNA. J. Virol. 73:1565-1572. (Pubitemid 29036812)
-
(1999)
Journal of Virology
, vol.73
, Issue.2
, pp. 1565-1572
-
-
Yu, S.F.1
Sullivan, M.D.2
Linial, M.L.3
-
41
-
-
77955552114
-
Molecular biology of foamy viruses
-
Rethwilm A. 2010. Molecular biology of foamy viruses. Med. Microbiol. Immunol. 199:197-207. http://dx.doi.org/10.1007/s00430-010-0158-x.
-
(2010)
Med. Microbiol. Immunol.
, vol.199
, pp. 197-207
-
-
Rethwilm, A.1
|