-
1
-
-
0029804757
-
Differences in the inhibition of human immunodeficiency virus type 1 reverse transcriptase DNA polymerase activity by analogs of nevirapine and [2′,5′-bis-O-(tert-butyldimethylsilyl)-3′-spiro-5″- 4″-amino-1″,2″-oxathiole-2″,2″-dioxide] (TSAO)
-
Arion D, Fletcher RS, Borkow G, Camarasa M-J, Balzarini J, Dmitrienko GI, and Parniak MA (1996) Differences in the inhibition of human immunodeficiency virus type 1 reverse transcriptase DNA polymerase activity by analogs of nevirapine and [2′,5′-bis-O-(tert-butyldimethylsilyl)-3′- spiro-5″-(4″-amino-1″,2″-oxathiole-2″, 2″-dioxide] (TSAO). Mol Pharmacol 50:1057-1064.
-
(1996)
Mol Pharmacol
, vol.50
, pp. 1057-1064
-
-
Arion, D.1
Fletcher, R.S.2
Borkow, G.3
Camarasa, M.-J.4
Balzarini, J.5
Dmitrienko, G.I.6
Parniak, M.A.7
-
2
-
-
0036156328
-
Chimeric human immunodeficiency virus type 1 and feline immunodeficiency virus reverse transcriptases: Role of the subunits in resistance/sensitivity to nonnucleoside reverse transcriptase inhibitors
-
Auwerx J, North TW, Preston BD, Klarmann GJ, De Clercq E, and Balzarini J (2002) Chimeric human immunodeficiency virus type 1 and feline immunodeficiency virus reverse transcriptases: role of the subunits in resistance/sensitivity to nonnucleoside reverse transcriptase inhibitors. Mol Pharmacol 61:400-406.
-
(2002)
Mol Pharmacol
, vol.61
, pp. 400-406
-
-
Auwerx, J.1
North, T.W.2
Preston, B.D.3
Klarmann, G.J.4
De Clercq, E.5
Balzarini, J.6
-
3
-
-
0025992146
-
A leucine zipper-like motif may mediate HIV reverse transcriptase subunit binding
-
Baillon JG, Nashed N, Kumar A, Wilson SH, and Jerina DM (1991) A leucine zipper-like motif may mediate HIV reverse transcriptase subunit binding. New Biol 3:1015-1019.
-
(1991)
New Biol
, vol.3
, pp. 1015-1019
-
-
Baillon, J.G.1
Nashed, N.2
Kumar, A.3
Wilson, S.H.4
Jerina, D.M.5
-
4
-
-
0033169086
-
Suppression of resistance to drugs targeted to human immunodeficiency virus reverse transcriptase by combination therapy
-
Balzarini J (1999) Suppression of resistance to drugs targeted to human immunodeficiency virus reverse transcriptase by combination therapy. Biochem Pharmacol 58:1-27.
-
(1999)
Biochem Pharmacol
, vol.58
, pp. 1-27
-
-
Balzarini, J.1
-
5
-
-
0027202617
-
Human immunodeficiency virus type 1 (HIV-1) strains selected for resistance against the HIV-specific [2′,5′-bis-O-(tert- butyldimethylsilyl)-3′-spiro-5″-(4″-amino-1″, 2″-oxathiole-2″,2″-dioxide)]-β-D-pentofuranosyl (TSAO) nucleoside analogues retain sensitivity to HIV-1-specific nonnucleoside inhibitors
-
Balzarini J, Karlsson A, Vandamme A-M, Pérez-Pérez MJ, Zhang H, Vrang L, Öberg B, Backbro K, Unge T, San-Félix A, et al. (1993) Human immunodeficiency virus type 1 (HIV-1) strains selected for resistance against the HIV-specific [2′,5′-bis-O-(tert- butyldimethylsilyl)-3′-spiro-5″-(4″-amino-1″, 2″-oxathiole-2″,2″-dioxide)]-β-D-pentofuranosyl (TSAO) nucleoside analogues retain sensitivity to HIV-1-specific nonnucleoside inhibitors. Proc Natl Acad Sci USA 90:6952-6956.
-
(1993)
Proc Natl Acad Sci USA
, vol.90
, pp. 6952-6956
-
-
Balzarini, J.1
Karlsson, A.2
Vandamme, A.-M.3
Pérez-Pérez, M.J.4
Zhang, H.5
Vrang, L.6
ÖBerg, B.7
Backbro, K.8
Unge, T.9
San-Félix, A.10
-
6
-
-
0028068907
-
Sensitivity of (138 Gly→Lys) mutated human immunodeficiency virus type 1 (HIV-1) reverse transcriptase (RT) to HIV-1-specific RT inhibitors
-
Balzarini J, Kleim JP, Riess G, Camarasa M-J, De Clercq E, and Karlsson A (1994) Sensitivity of (138 Gly→Lys) mutated human immunodeficiency virus type 1 (HIV-1) reverse transcriptase (RT) to HIV-1-specific RT inhibitors. Biochem Biophys Res Commun 201:1305-1312.
-
(1994)
Biochem Biophys Res Commun
, vol.201
, pp. 1305-1312
-
-
Balzarini, J.1
Kleim, J.P.2
Riess, G.3
Camarasa, M.-J.4
De Clercq, E.5
Karlsson, A.6
-
7
-
-
9544246540
-
Structure/function studies of HIV-11 reverse transcriptase: Dimerization-defective mutant L289K
-
Becerra SP, Kumar A, Lewis MS, Widen SG, Abbotts J, Karawya EM, Hughes SH, Shiloach J, and Wilson SH (1991a) Structure/function studies of HIV-11 reverse transcriptase: dimerization-defective mutant L289K. Biochemistry 30:11708-11719.
-
(1991)
Biochemistry
, vol.30
, pp. 11708-11719
-
-
Becerra, S.P.1
Kumar, A.2
Lewis, M.S.3
Widen, S.G.4
Abbotts, J.5
Karawya, E.M.6
Hughes, S.H.7
Shiloach, J.8
Wilson, S.H.9
-
8
-
-
0026355738
-
Protein-protein interactions of HIV-1 reverse transcriptase: Implications of central and C-terminal regions in subunit binding
-
Becerra SP, Kumar A, Lewis MS, Widen SG, Abbotts J, Karawya EM, Hughes SH, Shiloach J, Wilson SH, and Lewis MS (1991b) Protein-protein interactions of HIV-1 reverse transcriptase: implications of central and C-terminal regions in subunit binding. Biochemistry 30:11707-11719.
-
(1991)
Biochemistry
, vol.30
, pp. 11707-11719
-
-
Becerra, S.P.1
Kumar, A.2
Lewis, M.S.3
Widen, S.G.4
Abbotts, J.5
Karawya, E.M.6
Hughes, S.H.7
Shiloach, J.8
Wilson, S.H.9
Lewis, M.S.10
-
9
-
-
0026530383
-
Quantitative analysis of protein far-UV circular dichroism spectra by neural networks
-
Böhm G, Muhr R, and Jaenicke R (1992) Quantitative analysis of protein far-UV circular dichroism spectra by neural networks. Protein Eng 5:191-195.
-
(1992)
Protein Eng
, vol.5
, pp. 191-195
-
-
Böhm, G.1
Muhr, R.2
Jaenicke, R.3
-
10
-
-
0028024028
-
Subunit specificity of mutations that confer resistance to nonnucleoside inhibitors in human immunodeficiency virus type 1 reverse transcriptase
-
Boyer PL, Ding J, Arnold E, and Hughes SH (1994) Subunit specificity of mutations that confer resistance to nonnucleoside inhibitors in human immunodeficiency virus type 1 reverse transcriptase. Antimicrob Agents Chemother 38:1909-1914.
-
(1994)
Antimicrob Agents Chemother
, vol.38
, pp. 1909-1914
-
-
Boyer, P.L.1
Ding, J.2
Arnold, E.3
Hughes, S.H.4
-
11
-
-
0028899197
-
Comparative anti-HIV evaluation of diverse HIV-1-specific reverse transcriptase inhibitor-resistant virus isolates demonstrates the existence of distinct phenotypic subgroups
-
Buckheit JRW, Fliakas-Bolz V, Decker WD, Roberson JL, Stup TL, Pyle CA, White EL, McMahon JB, Currens MJ, Boyd MR, et al. (1995) Comparative anti-HIV evaluation of diverse HIV-1-specific reverse transcriptase inhibitor-resistant virus isolates demonstrates the existence of distinct phenotypic subgroups. Antiviral Res 26:117-132.
-
(1995)
Antiviral Res
, vol.26
, pp. 117-132
-
-
Buckheit, J.R.W.1
Fliakas-Bolz, V.2
Decker, W.D.3
Roberson, J.L.4
Stup, T.L.5
Pyle, C.A.6
White, E.L.7
McMahon, J.B.8
Currens, M.J.9
Boyd, M.R.10
-
12
-
-
2942525968
-
TSAO compounds: The comprehensive story of a unique family of HIV-1-specific inhibitors of reverse transcriptase
-
Camarasa M-J, San-Félix A, Velázquez S, Pérez-Pérez M-J, Gago F, and Balzarini J (2004) TSAO compounds: the comprehensive story of a unique family of HIV-1-specific inhibitors of reverse transcriptase. Curr Top Med Chem 4:945-963.
-
(2004)
Curr Top Med Chem
, vol.4
, pp. 945-963
-
-
Camarasa, M.-J.1
San-Félix, A.2
Velázquez, S.3
Pérez-Pérez, M.-J.4
Gago, F.5
Balzarini, J.6
-
13
-
-
23244465516
-
High sequence conservation of HIV-1 reverse transcriptase under drug pressure despite a continuous appearance of mutations
-
in press
-
Ceccherini-Silberstein F, Gago F, Santoro M, Gori C, Svicher V, Rodríguez-Barrios F, D'Arrigo R, Ciccozzi M, Bertoli A, d'Arminio Monforte A, et al. (2005) High sequence conservation of HIV-1 reverse transcriptase under drug pressure despite a continuous appearance of mutations. J Virology, in press.
-
(2005)
J Virology
-
-
Ceccherini-Silberstein, F.1
Gago, F.2
Santoro, M.3
Gori, C.4
Svicher, V.5
Rodríguez-Barrios, F.6
D'Arrigo, R.7
Ciccozzi, M.8
Bertoli, A.9
D'Arminio Monforte, A.10
-
14
-
-
0024841242
-
HIV-1 reverse transcriptase/ribonuclease H: High level expression in Escherichia coli from a plasmid constructed using the polymerase chain reaction
-
D'Aquila RT and Summers WC (1989) HIV-1 reverse transcriptase/ ribonuclease H: high level expression in Escherichia coli from a plasmid constructed using the polymerase chain reaction. J Acquir Immune Defic Syndr 2:579-587.
-
(1989)
J Acquir Immune Defic Syndr
, vol.2
, pp. 579-587
-
-
D'Aquila, R.T.1
Summers, W.C.2
-
15
-
-
0003011507
-
Reverse transcriptase inhibitors as anti-HIV drugs
-
(Unger RE, Kreuter J, and Rübsamen-Waigmann H eds) Marcel Dekker, Inc., New York
-
De Clercq E (2000) Reverse transcriptase inhibitors as anti-HIV drugs, in Antivirals against AIDS (Unger RE, Kreuter J, and Rübsamen-Waigmann H eds) pp 107-150, Marcel Dekker, Inc., New York.
-
(2000)
Antivirals Against AIDS
, pp. 107-150
-
-
De Clercq, E.1
-
16
-
-
0036050539
-
Strategies in the design of antiviral drugs
-
De Clercq E (2002) Strategies in the design of antiviral drugs. Nat Rev Drug Discov 1:13-25.
-
(2002)
Nat Rev Drug Discov
, vol.1
, pp. 13-25
-
-
De Clercq, E.1
-
17
-
-
0029075207
-
Structure of HIV-1 RT/TIBO R86183 complex reveals similarity in the binding of diverse nonnucleoside inhibitors
-
Ding J, Das K, Moereels H, Koymans L, Andries K, Janssen PA, Hughes SH, and Arnold E (1995) Structure of HIV-1 RT/TIBO R86183 complex reveals similarity in the binding of diverse nonnucleoside inhibitors. Nat Struct Biol 2:407-415.
-
(1995)
Nat Struct Biol
, vol.2
, pp. 407-415
-
-
Ding, J.1
Das, K.2
Moereels, H.3
Koymans, L.4
Andries, K.5
Janssen, P.A.6
Hughes, S.H.7
Arnold, E.8
-
18
-
-
0028924567
-
Mechanism of inhibition of HIV-1 reverse transcriptase by non-nucleoside inhibitors
-
Esnouf R, Ren J, Ross C, Jones Y, Stammers D, and Stuart D (1995) Mechanism of inhibition of HIV-1 reverse transcriptase by non-nucleoside inhibitors. Nat Struct Biol 2:303-308.
-
(1995)
Nat Struct Biol
, vol.2
, pp. 303-308
-
-
Esnouf, R.1
Ren, J.2
Ross, C.3
Jones, Y.4
Stammers, D.5
Stuart, D.6
-
19
-
-
0027769772
-
Structure/function studies of HIV-1 reverse transcriptase: Dimerization-defective mutant L289K
-
Goel R, Beard WA, Kumar A, Casas-Finet JR, Strub M-P, Stahl SJ, Lewis MS, Bebenek K, Becerra S, Kunkel TA, et al. (1993) Structure/function studies of HIV-1 reverse transcriptase: dimerization-defective mutant L289K. Biochemistry 32: 13012-13018.
-
(1993)
Biochemistry
, vol.32
, pp. 13012-13018
-
-
Goel, R.1
Beard, W.A.2
Kumar, A.3
Casas-Finet, J.R.4
Strub, M.-P.5
Stahl, S.J.6
Lewis, M.S.7
Bebenek, K.8
Becerra, S.9
Kunkel, T.A.10
-
20
-
-
0032574687
-
The p51 subunit of human immunodeficiency virus type 1 reverse transcriptase is essential in loading the p66 subunit on the template primer
-
Harris D, Lee R, Misra HS, Pandey PK, and Pandey VN (1998) The p51 subunit of human immunodeficiency virus type 1 reverse transcriptase is essential in loading the p66 subunit on the template primer. Biochemistry 37:5903-5908.
-
(1998)
Biochemistry
, vol.37
, pp. 5903-5908
-
-
Harris, D.1
Lee, R.2
Misra, H.S.3
Pandey, P.K.4
Pandey, V.N.5
-
21
-
-
0029976422
-
Complexes of HIV-1 reverse transcriptase with inhibitors of the HEPT series reveal conformational changes relevant to the design of potent non-nucleoside inhibitors
-
Hopkins AL, Ren J, Esnouf RM, Willcox BE, Jones EY, Ross C, Miyasaka T, Walker RT, Tanaka H, Stammers DK, et al. (1996) Complexes of HIV-1 reverse transcriptase with inhibitors of the HEPT series reveal conformational changes relevant to the design of potent non-nucleoside inhibitors. J Med Chem 39:1589-1600.
-
(1996)
J Med Chem
, vol.39
, pp. 1589-1600
-
-
Hopkins, A.L.1
Ren, J.2
Esnouf, R.M.3
Willcox, B.E.4
Jones, E.Y.5
Ross, C.6
Miyasaka, T.7
Walker, R.T.8
Tanaka, H.9
Stammers, D.K.10
-
22
-
-
0028099251
-
Resistance of HIV-1 reverse transcriptase against 2′,5′-bis- O-(tert-butyldimethylsilyl)-3′-spiro-5″-(4″-amino-1″, 2″-oxathiole-2″,2″-dioxide) (TSAO) derivatives is determined by the mutation Glu138→Lys on the p51 subunit
-
Jonckheere H, Taymans JM, Balzarini J, Velázquez S, Camarasa M-J, Desmyter J, De Clercq E, and Annë J (1994) Resistance of HIV-1 reverse transcriptase against [2′,5′-bis-O-(tert-butyldimethylsilyl)- 3′-spiro-5″-(4″-amino-1″,2″-oxathiole-2″, 2″-dioxide) (TSAO) derivatives is determined by the mutation Glu138→Lys on the p51 subunit. J Biol Chem 269:25255-25258.
-
(1994)
J Biol Chem
, vol.269
, pp. 25255-25258
-
-
Jonckheere, H.1
Taymans, J.M.2
Balzarini, J.3
Velázquez, S.4
Camarasa, M.-J.5
Desmyter, J.6
De Clercq, E.7
Annë, J.8
-
23
-
-
0026693137
-
Crystal structure of 3.5 Å resolution of HIV-1 reverse transcriptase complexed with an inhibitor
-
Kohlstaedt LA, Wang J, Friedman JM, Rice PA, and Steitz TA (1992) Crystal structure of 3.5 Å resolution of HIV-1 reverse transcriptase complexed with an inhibitor. Science (Wash DC) 256:1783-1790.
-
(1992)
Science (Wash DC)
, vol.256
, pp. 1783-1790
-
-
Kohlstaedt, L.A.1
Wang, J.2
Friedman, J.M.3
Rice, P.A.4
Steitz, T.A.5
-
24
-
-
0035920168
-
Functional characterization of chimeric reverse transcriptases with polypeptide subunits of highly divergent HIV-1 group M and O strains
-
Menéndez-Arias L, Abraha A, Quinones-Mateu ME, Mas A, Camarasa M-J, and Arts EJ (2001) Functional characterization of chimeric reverse transcriptases with polypeptide subunits of highly divergent HIV-1 group M and O strains. J Biol Chem 276:27470-27479.
-
(2001)
J Biol Chem
, vol.276
, pp. 27470-27479
-
-
Menéndez-Arias, L.1
Abraha, A.2
Quinones-Mateu, M.E.3
Mas, A.4
Camarasa, M.-J.5
Arts, E.J.6
-
25
-
-
34248393491
-
Insertion of a small peptide of six amino acids into the β7-β8 loop of the p51 subunit of HIV-1 reverse transcriptase perturbs the heterodimer and affects its activities
-
Pandey PK, Kaushik N, Singh K, Sharma B, Upadhyay AK, Kumar S, Harris D, and Pandey VN (2002) Insertion of a small peptide of six amino acids into the β7-β8 loop of the p51 subunit of HIV-1 reverse transcriptase perturbs the heterodimer and affects its activities. BMC Biochem 3:18-31.
-
(2002)
BMC Biochem
, vol.3
, pp. 18-31
-
-
Pandey, P.K.1
Kaushik, N.2
Singh, K.3
Sharma, B.4
Upadhyay, A.K.5
Kumar, S.6
Harris, D.7
Pandey, V.N.8
-
26
-
-
0035859690
-
The beta7-beta8 loop of the p51 subunit in the heterodimeric (p66/p51) human immunodeficiency virus type 1 reverse transcriptase is essential for the catalytic function of the p66 subunit
-
Pandey PK, Kaushik N, Talele TT, Yadav PN, and Pandey VN (2001) The beta7-beta8 loop of the p51 subunit in the heterodimeric (p66/p51) human immunodeficiency virus type 1 reverse transcriptase is essential for the catalytic function of the p66 subunit. Biochemistry 40:9505-9512.
-
(2001)
Biochemistry
, vol.40
, pp. 9505-9512
-
-
Pandey, P.K.1
Kaushik, N.2
Talele, T.T.3
Yadav, P.N.4
Pandey, V.N.5
-
27
-
-
0032545420
-
Mutational analysis of Tyr-318 within the non-nucleoside reverse transcriptase inhibitor binding pocket of human immunodeficiency virus type 2 reverse transcriptase
-
Pelemans H, Esnouf R, Jonckheere H, De Clercq E, and Balzarini J (1998) Mutational analysis of Tyr-318 within the non-nucleoside reverse transcriptase inhibitor binding pocket of human immunodeficiency virus type 2 reverse transcriptase. J Biol Chem 273:34234-34239.
-
(1998)
J Biol Chem
, vol.273
, pp. 34234-34239
-
-
Pelemans, H.1
Esnouf, R.2
Jonckheere, H.3
De Clercq, E.4
Balzarini, J.5
-
28
-
-
0028947588
-
High resolution structures of HIV-1 RT from four RT-inhibitor complexes
-
Ren J, Esnouf R, Garman E, Somers D, Ross C, Kirby I, Keeling J, Darby G, Jones Y, Stuart D, et al. (1995) High resolution structures of HIV-1 RT from four RT-inhibitor complexes. Nat Struct Biol 2:293-302.
-
(1995)
Nat Struct Biol
, vol.2
, pp. 293-302
-
-
Ren, J.1
Esnouf, R.2
Garman, E.3
Somers, D.4
Ross, C.5
Kirby, I.6
Keeling, J.7
Darby, G.8
Jones, Y.9
Stuart, D.10
-
29
-
-
0034435564
-
Structural basis for the resilience of efavirenz (DMP-266) to drug resistance mutations in HIV-1 reverse transcriptase
-
Ren J, Milton J, Weaver KL, Short SA, Stuart DI, and Stammers DK (2000) Structural basis for the resilience of efavirenz (DMP-266) to drug resistance mutations in HIV-1 reverse transcriptase. Structure Fold Des 8:1089-1094.
-
(2000)
Structure Fold des
, vol.8
, pp. 1089-1094
-
-
Ren, J.1
Milton, J.2
Weaver, K.L.3
Short, S.A.4
Stuart, D.I.5
Stammers, D.K.6
-
30
-
-
0025297454
-
Dimerization of human immunodeficiency virus type 1 reverse transcriptase. A target for chemotherapeutic intervention
-
Restle T, Muller B, and Goody RS (1990) Dimerization of human immunodeficiency virus type 1 reverse transcriptase. A target for chemotherapeutic intervention. J Biol Chem 265:8986-8988.
-
(1990)
J Biol Chem
, vol.265
, pp. 8986-8988
-
-
Restle, T.1
Muller, B.2
Goody, R.S.3
-
31
-
-
0035821586
-
Identification of a putative binding site for TSAO-T derivatives at the p51/p66 interface of HIV-1 reverse transcriptase
-
Rodriguez-Barrios F, Pérez C, San-Félix A, Camarasa M-J, Pelemans H, Balzarini J, and Gago F (2001) Identification of a putative binding site for TSAO-T derivatives at the p51/p66 interface of HIV-1 reverse transcriptase. J Med Chem 44:1853-1865.
-
(2001)
J Med Chem
, vol.44
, pp. 1853-1865
-
-
Rodriguez-Barrios, F.1
Pérez, C.2
San-Félix, A.3
Camarasa, M.-J.4
Pelemans, H.5
Balzarini, J.6
Gago, F.7
-
32
-
-
0034083833
-
Mutations in retroviral genes associated with drug resistance: 2000-2001 update
-
Schinazi RF, Larder BA, and Mellors JW (2001) Mutations in retroviral genes associated with drug resistance: 2000-2001 update. Int Antiviral News 8:65-91.
-
(2001)
Int Antiviral News
, vol.8
, pp. 65-91
-
-
Schinazi, R.F.1
Larder, B.A.2
Mellors, J.W.3
-
33
-
-
0036076157
-
Destabilization of the HIV-1 reverse transcriptase dimer upon interaction with N-acyl hydrazone inhibitors
-
Sluis-Cremer N, Arion D, and Parniak MA (2002) Destabilization of the HIV-1 reverse transcriptase dimer upon interaction with N-acyl hydrazone inhibitors. Mol Pharmacol 62:398-405.
-
(2002)
Mol Pharmacol
, vol.62
, pp. 398-405
-
-
Sluis-Cremer, N.1
Arion, D.2
Parniak, M.A.3
-
34
-
-
0034673154
-
Human immunodeficiency virus type 1 reverse transcriptase dimer destabilization by 1-[spiro[4″-amino-2″,2″-dioxo-1″, 2″-oxathiole-5″,3′-[2′,5′-bis-O-(tert- butyldimethylsilyl)-β-D-ribofuranosyl]]]-3-ethylthymine
-
Sluis-Cremer N, Dmitrienko GI, Balzarini J, Camarasa M-J, and Parniak MA (2000) Human immunodeficiency virus type 1 reverse transcriptase dimer destabilization by 1-[spiro[4″-amino-2″,2″-dioxo-1″, 2″-oxathiole-5″,3′-[2′,5′-bis-O-(tert- butyldimethylsilyl)-β-D-ribofuranosyl]]]-3-ethylthymine. Biochemistry 39:1427-1433.
-
(2000)
Biochemistry
, vol.39
, pp. 1427-1433
-
-
Sluis-Cremer, N.1
Dmitrienko, G.I.2
Balzarini, J.3
Camarasa, M.-J.4
Parniak, M.A.5
-
35
-
-
0037436335
-
Role of residues in the tryptophan repeat motif for HIV-1 reverse transcriptase dimerization
-
Tachedjian G, Aronson H-EG, de los Santos M, Seehra J, McCoy JM, and Goff SP (2003) Role of residues in the tryptophan repeat motif for HIV-1 reverse transcriptase dimerization. J Mol Biol 326:381-396.
-
(2003)
J Mol Biol
, vol.326
, pp. 381-396
-
-
Tachedjian, G.1
Aronson, H.-E.G.2
De Los Santos, M.3
Seehra, J.4
McCoy, J.M.5
Goff, S.P.6
-
36
-
-
0141515727
-
The effect of NNRTIs on HIV reverse transcriptase dimerization
-
Tachedjian G and Goff SP (2003) The effect of NNRTIs on HIV reverse transcriptase dimerization. Curr Opin Investig Drugs 4:966-973.
-
(2003)
Curr Opin Investig Drugs
, vol.4
, pp. 966-973
-
-
Tachedjian, G.1
Goff, S.P.2
-
37
-
-
0035912717
-
Nonnucleoside reverse transcriptase inhibitors are chemical enhancers of dimerization of the HIV type 1 reverse transcriptase
-
Tachedjian G, Orlova M, Sarafianos SG, Arnold E, and Goff SP (2001) Nonnucleoside reverse transcriptase inhibitors are chemical enhancers of dimerization of the HIV type 1 reverse transcriptase. Proc Natl Acad Sci USA 98:7188-7193.
-
(2001)
Proc Natl Acad Sci USA
, vol.98
, pp. 7188-7193
-
-
Tachedjian, G.1
Orlova, M.2
Sarafianos, S.G.3
Arnold, E.4
Goff, S.P.5
-
38
-
-
0028360742
-
Structural basis of asymmetry in the human immunodeficiency virus type 1 reverse transcriptase heterodimer
-
Wang J, Smerdon SJ, Jager J, Kohlstaedt LA, Rice PA, Friedman JM, and Steitz TA (1994) Structural basis of asymmetry in the human immunodeficiency virus type 1 reverse transcriptase heterodimer. Proc Natl Acad Sci USA 91:7242-7246.
-
(1994)
Proc Natl Acad Sci USA
, vol.91
, pp. 7242-7246
-
-
Wang, J.1
Smerdon, S.J.2
Jager, J.3
Kohlstaedt, L.A.4
Rice, P.A.5
Friedman, J.M.6
Steitz, T.A.7
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