-
1
-
-
0027318776
-
Crystal structure of human immunodeficiency virus type 1 reverse transcriptase complexed with double-stranded DNA at 3.0 A resolution shows bent DNA
-
Jacobo-Molina A, Ding J, Nanni RG, et al. Crystal structure of human immunodeficiency virus type 1 reverse transcriptase complexed with double-stranded DNA at 3.0 A resolution shows bent DNA. Proc Natl Acad Sci USA 1993; 90: 6320-6324.
-
(1993)
Proc Natl Acad Sci USA
, vol.90
, pp. 6320-6324
-
-
Jacobo-Molina, A.1
Ding, J.2
Nanni, R.G.3
-
2
-
-
0028924567
-
Mechanism of inhibition of HIV-1 reverse transcriptase by non-nucleoside inhibitors
-
Esnouf R, Ren J, Ross C, Jones Y, Stammers D, Stuart D. Mechanism of inhibition of HIV-1 reverse transcriptase by non-nucleoside inhibitors. Nat Struct Biol 1995; 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
-
3
-
-
0028925773
-
Mechanism of inhibition of HIV-1 reverse transcriptase by nonnucleoside inhibitors
-
Spence RA, Kati WM, Anderson KS, Johnson KA. Mechanism of inhibition of HIV-1 reverse transcriptase by nonnucleoside inhibitors. Science 1995; 267: 988-993.
-
(1995)
Science
, vol.267
, pp. 988-993
-
-
Spence, R.A.1
Kati, W.M.2
Anderson, K.S.3
Johnson, K.A.4
-
4
-
-
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-butyldimethylsily1)-beta-D-ribofuranosyl]]]-3- ethylthymine
-
Sluis-Cremer N, Dmitrienko GI, Balzarini J, Camarasa MJ, Parniak MA. 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-butyldimethylsily1)-beta-D-ribofuranosyl]]]-3- ethylthymine. Biochemistry 2000; 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
-
5
-
-
0036076157
-
Destabilization of the HIV-1 reverse transcriptase dimer upon interaction with N-acyl hydrazone inhibitors
-
Sluis-Cremer N, Arion D, Parniak MA. Destabilization of the HIV-1 reverse transcriptase dimer upon interaction with N-acyl hydrazone inhibitors. Mol Pharmacol 2002; 62: 398-405.
-
(2002)
Mol Pharmacol
, vol.62
, pp. 398-405
-
-
Sluis-Cremer, N.1
Arion, D.2
Parniak, M.A.3
-
6
-
-
33646501535
-
Dimerization of human immunodeficiency virus type 1 reverse transcriptase as an antiviral target
-
Srivastava S, Sluis-Crenter N, Tachedjian G. Dimerization of human immunodeficiency virus type 1 reverse transcriptase as an antiviral target. Curr Pharm Des 2006; 12: 1879-1894.
-
(2006)
Curr Pharm Des
, vol.12
, pp. 1879-1894
-
-
Srivastava, S.1
Sluis-Crenter, N.2
Tachedjian, G.3
-
7
-
-
0028308202
-
Inhibition of human immunodeficiency virus type 1 reverse transcriptase dimerization using synthetic peptides derived from the connection domain
-
Divita G, Restle T, Goody RS, Chermann JC, Baillon JG. Inhibition of human immunodeficiency virus type 1 reverse transcriptase dimerization using synthetic peptides derived from the connection domain. J Biol Chem 1994; 269: 13080-13083.
-
(1994)
J Biol Chem
, vol.269
, pp. 13080-13083
-
-
Divita, G.1
Restle, T.2
Goody, R.S.3
Chermann, J.C.4
Baillon, J.G.5
-
8
-
-
34248393491
-
Insertion of a small peptide of six amino acids into the beta7-beta8 loop the p51 subunit of HIV-1 reverse transcriptase perturbs heterodimer and affects its activities
-
Pandey PK, Kaushik N, Singh K, et al. Insertion of a small peptide of six amino acids into the beta7-beta8 loop the p51 subunit of HIV-1 reverse transcriptase perturbs heterodimer and affects its activities. BMC Biochem 2002; 3: 18.
-
(2002)
BMC Biochem
, vol.3
, pp. 18
-
-
Pandey, P.K.1
Kaushik, N.2
Singh, K.3
-
9
-
-
0037436335
-
Role of residues in the tryptophan repeat motif for HIV-1 reverse, transcriptase dimerization
-
Tachedjian G, Aronson HE, de los Santos M, Seehra J, McCoy JM, Goff SP. Role of residues in the tryptophan repeat motif for HIV-1 reverse, transcriptase dimerization. J Mol Biol 2003; 326: 381-396.
-
(2003)
J Mol Biol
, vol.326
, pp. 381-396
-
-
Tachedjian, G.1
Aronson, H.E.2
de los3
Santos, M.4
Seehra, J.5
McCoy, J.M.6
Goff, S.P.7
-
10
-
-
19544363941
-
Relationship between enzyme activity and dimeric structure of recombinant HIV-1 reverse transcriptase
-
Tachedjian G, Radzio J, Sluis-Cremer N. Relationship between enzyme activity and dimeric structure of recombinant HIV-1 reverse transcriptase. Proteins 2005; 60: 5-13.
-
(2005)
Proteins
, vol.60
, pp. 5-13
-
-
Tachedjian, G.1
Radzio, J.2
Sluis-Cremer, N.3
-
11
-
-
22444443468
-
The amino acid Asn136 in HIV-1 reverse trariscriptase (RT) maintains efficient association of both RT subunits and enables the rational design of novel RT inhibitors
-
Balzarini J, Auwerx J, Rodriguez-Barrios F, et al. The amino acid Asn136 in HIV-1 reverse trariscriptase (RT) maintains efficient association of both RT subunits and enables the rational design of novel RT inhibitors. Mol Pharmacol 2005; 68: 49-60.
-
(2005)
Mol Pharmacol
, vol.68
, pp. 49-60
-
-
Balzarini, J.1
Auwerx, J.2
Rodriguez-Barrios, F.3
-
12
-
-
20244372866
-
The N 137 and P 140 amino acids in the p51 and the P95 amino acid in the p66 subunit of human immunodeficiency virus type 1 (HIV-1) reverse transcriptase are instrumental to maintain catalytic activity and to design new classes of anti-HIV-1 drugs
-
Auwerx J, Van Nieuwenhove J, Rodriguez-Barrios F, et al. The N 137 and P 140 amino acids in the p51 and the P95 amino acid in the p66 subunit of human immunodeficiency virus type 1 (HIV-1) reverse transcriptase are instrumental to maintain catalytic activity and to design new classes of anti-HIV-1 drugs. FEBS Lett 2005; 579: 2294-2300.
-
(2005)
FEBS Lett
, vol.579
, pp. 2294-2300
-
-
Auwerx, J.1
Van Nieuwenhove, J.2
Rodriguez-Barrios, F.3
-
13
-
-
33746948397
-
Structure-activity relationships of [2′,5′-bis-O-(tert-butyldimethylsilyl)-beta-D-ribofuranosyl] - 3′-spiro-5′ ′-(4′ ′-amino-1′, ′,2′ ′-oxathiole-2′ ′,2′ ′-dioxide)thymine derivatives as inhibitors of HIV-1 reverse transcriptase dimerization
-
Sluis-Cremer N, Harnamouch N, San Felix A, Velazquez S, Balzarini J, Camarasa MJ. Structure-activity relationships of [2′,5′-bis-O-(tert-butyldimethylsilyl)-beta-D-ribofuranosyl]- 3′-spiro-5′ ′-(4′ ′-amino-1′, ′,2′ ′-oxathiole-2′ ′,2′ ′-dioxide)thymine derivatives as inhibitors of HIV-1 reverse transcriptase dimerization. J Med Chem 2006; 49: 4834-4841.
-
(2006)
J Med Chem
, vol.49
, pp. 4834-4841
-
-
Sluis-Cremer, N.1
Harnamouch, N.2
San Felix, A.3
Velazquez, S.4
Balzarini, J.5
Camarasa, M.J.6
-
14
-
-
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_Goff SP. Nonnucleoside reverse transcriptase inhibitors are chemical enhancers of dimerization of the HIV type 1 reverse transcriptase. Proc Natl Acad Sci USA 2001; 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
-
15
-
-
11844282799
-
Efavirenz enhances the proteolytic processing of an HIV-1 pol polyprotein precursor and reverse transcriptase homodimer formation
-
Tachedjian G, Moore KL, Goff SP, Sluis-Cremer N. Efavirenz enhances the proteolytic processing of an HIV-1 pol polyprotein precursor and reverse transcriptase homodimer formation. FEBS Lett 2005; 579: 379-384.
-
(2005)
FEBS Lett
, vol.579
, pp. 379-384
-
-
Tachedjian, G.1
Moore, K.L.2
Goff, S.P.3
Sluis-Cremer, N.4
-
16
-
-
33644683832
-
Effects of efavirenz binding on the subunit equilibria of HIV-1 reverse transcriptase
-
Venezia CF, Howard KJ, Ignatov ME, Holladay LA, Barkley MD. Effects of efavirenz binding on the subunit equilibria of HIV-1 reverse transcriptase. Biochemistry 2006; 45: 2779-2789.
-
(2006)
Biochemistry
, vol.45
, pp. 2779-2789
-
-
Venezia, C.F.1
Howard, K.J.2
Ignatov, M.E.3
Holladay, L.A.4
Barkley, M.D.5
-
17
-
-
34547578940
-
Probing nonnucleoside inhibitor-induced active-site distortion in HIV-1 reverse transcriptase by transient kinetic analyses
-
Xia Q, Radzio J, Anderson KS, Sluis-Cremer N. Probing nonnucleoside inhibitor-induced active-site distortion in HIV-1 reverse transcriptase by transient kinetic analyses. Protein Sci 2007; 16: 1728-1737.
-
(2007)
Protein Sci
, vol.16
, pp. 1728-1737
-
-
Xia, Q.1
Radzio, J.2
Anderson, K.S.3
Sluis-Cremer, N.4
-
18
-
-
0022495870
-
Production of acquired immunodeficiency syndrome-associated retrovirus in human and nonhuman cells transfected with an infectious molecular clone
-
Adachi A, Gendelman HE, Koenig S, et al. Production of acquired immunodeficiency syndrome-associated retrovirus in human and nonhuman cells transfected with an infectious molecular clone. J Virol 1986; 59: 284-291.
-
(1986)
J Virol
, vol.59
, pp. 284-291
-
-
Adachi, A.1
Gendelman, H.E.2
Koenig, S.3
-
19
-
-
0034612275
-
Analysis of mutations and suppressors affecting interactions between the subunits of the HIV type 1 reverse transcriptase
-
Tachedjian G, Aronson HE, Goff SP. Analysis of mutations and suppressors affecting interactions between the subunits of the HIV type 1 reverse transcriptase. Proc Nat Acad Sci USA 2000; 97: 6334-6339.
-
(2000)
Proc Nat Acad Sci USA
, vol.97
, pp. 6334-6339
-
-
Tachedjian, G.1
Aronson, H.E.2
Goff, S.P.3
-
20
-
-
34249033110
-
Characterization of novel non-nucleoside reverse transcriptase (RT) inhibitor resistance mutations at residues 132 and 135 in the 51 kDa subunit of HIV-1 RT
-
Nissley DV, Radzio J, Ambrose Z, et al. Characterization of novel non-nucleoside reverse transcriptase (RT) inhibitor resistance mutations at residues 132 and 135 in the 51 kDa subunit of HIV-1 RT. Biochem J 2007; 404:151-157.
-
(2007)
Biochem J
, vol.404
, pp. 151-157
-
-
Nissley, D.V.1
Radzio, J.2
Ambrose, Z.3
-
21
-
-
0033118205
-
Mixed reconstitution of mutated subunits of HIV-1 reverse transcriptase coexpressed in Escherichia coli - two tags tie it up
-
Maier G, Dietrich U, Panhans B, et al. Mixed reconstitution of mutated subunits of HIV-1 reverse transcriptase coexpressed in Escherichia coli - two tags tie it up. Eur J Biochem 1999; 261: 10-18.
-
(1999)
Eur J Biochem
, vol.261
, pp. 10-18
-
-
Maier, G.1
Dietrich, U.2
Panhans, B.3
-
22
-
-
0033840455
-
Human immunodeficiency virus type I mutations selected in patients failing efavirenz combination therapy
-
Bacheler LT, Anton ED, Kudish P, et al. Human immunodeficiency virus type I mutations selected in patients failing efavirenz combination therapy. Antimicrob, Agents Chemother 2000; 44: 2475-2484.
-
(2000)
Antimicrob, Agents Chemother
, vol.44
, pp. 2475-2484
-
-
Bacheler, L.T.1
Anton, E.D.2
Kudish, P.3
-
23
-
-
0031805095
-
S-1153 inhibits replication of known drug-resistant strains of human immunodeficiency virus type 1
-
Fujiwara T, Sato A, el-Farrash M, et al. S-1153 inhibits replication of known drug-resistant strains of human immunodeficiency virus type 1. Antimicrob Agents Chemother 1998; 42: 1340-1345.
-
(1998)
Antimicrob Agents Chemother
, vol.42
, pp. 1340-1345
-
-
Fujiwara, T.1
Sato, A.2
el-Farrash, M.3
-
24
-
-
0037223722
-
Amino acid substitutions at Position 190 of human immunodeficiency virus type 1 reverse transcriptase increase susceptibility to delavirdine and impair virus replication
-
Huang W, Gamamik A, Limoli K, Petropoulos CJ, Whitcomb JM. Amino acid substitutions at Position 190 of human immunodeficiency virus type 1 reverse transcriptase increase susceptibility to delavirdine and impair virus replication. J Virol 2003; 77: 1512-1523.
-
(2003)
J Virol
, vol.77
, pp. 1512-1523
-
-
Huang, W.1
Gamamik, A.2
Limoli, K.3
Petropoulos, C.J.4
Whitcomb, J.M.5
-
25
-
-
0028347888
-
Mutational analysis of residue 190 of human immunodeficiency virus type 1 reverse transcriptase
-
Kleim JP, Bender R, Kirsch R, Meichsner C, Paessens A, Riess G. Mutational analysis of residue 190 of human immunodeficiency virus type 1 reverse transcriptase. Virology 1994; 200: 696-701.
-
(1994)
Virology
, vol.200
, pp. 696-701
-
-
Kleim, J.P.1
Bender, R.2
Kirsch, R.3
Meichsner, C.4
Paessens, A.5
Riess, G.6
-
26
-
-
0030879805
-
Characteristics of the Pro225His mutation in human immunodeficiency virus type 1 (HIV-1) reverse transcriptase that appears under selective pressure of dose-escalating quinoxaline treatment of HIV-1
-
Pelemans H, Esnouf R, Dunkler A, et al. Characteristics of the Pro225His mutation in human immunodeficiency virus type 1 (HIV-1) reverse transcriptase that appears under selective pressure of dose-escalating quinoxaline treatment of HIV-1. J Virol 1997; 71: 8195-8203.
-
(1997)
J Virol
, vol.71
, pp. 8195-8203
-
-
Pelemans, H.1
Esnouf, R.2
Dunkler, A.3
-
27
-
-
0035984019
-
A mutation in the 3′ region of the human immunodeficiency virus type 1 reverse transcriptase (Y318F) associated with normucleoside reverse transcriptase inhibitor resistance
-
Harrigan PR, Salim M, Stammers DK, et al. A mutation in the 3′ region of the human immunodeficiency virus type 1 reverse transcriptase (Y318F) associated with normucleoside reverse transcriptase inhibitor resistance. J Virol 2002; 76: 6836-6840.
-
(2002)
J Virol
, vol.76
, pp. 6836-6840
-
-
Harrigan, P.R.1
Salim, M.2
Stammers, D.K.3
-
28
-
-
41749111903
-
Efavirenz accelerates HIV-1 reverse transcriptase ribonuclease H cleavage leading to diminished zidovudine excision
-
in press
-
Radzio J, Sluis-Cremer N. Efavirenz accelerates HIV-1 reverse transcriptase ribonuclease H cleavage leading to diminished zidovudine excision. Mol Pharmacol 2007; in press.
-
(2007)
Mol Pharmacol
-
-
Radzio, J.1
Sluis-Cremer, N.2
-
29
-
-
0030859022
-
Kinetic analysis of four HIV-1 reverse transcriptase enzymes mutated in the primer grip region of p66. Implications for DNA synthesis and dimerization
-
Wohrl BM, Krebs R, Thrall SH, Le Grice SF, Scheidig AJ, Goody RS, Kinetic analysis of four HIV-1 reverse transcriptase enzymes mutated in the primer grip region of p66. Implications for DNA synthesis and dimerization. J Biol Chem 1997; 272: 17581-17587.
-
(1997)
J Biol Chem
, vol.272
, pp. 17581-17587
-
-
Wohrl, B.M.1
Krebs, R.2
Thrall, S.H.3
Le Grice, S.F.4
Scheidig, A.J.5
Goody, R.S.6
-
30
-
-
24044513654
-
The role of Thr139 in the human immunodeficiency virus type 1 reverse transcriptase sensitivity to (+)-calanolide A
-
Auwerx J, Rodriguez-Barrios F, Ceccherini-Silberstein F, et al. The role of Thr139 in the human immunodeficiency virus type 1 reverse transcriptase sensitivity to (+)-calanolide A. Mol Pharmacol 2005; 68: 652-659.
-
(2005)
Mol Pharmacol
, vol.68
, pp. 652-659
-
-
Auwerx, J.1
Rodriguez-Barrios, F.2
Ceccherini-Silberstein, F.3
-
31
-
-
0031940767
-
A mutation at position 190 of human immunodeficiency virus type 1 reverse transcriptase interacts with mutations at positions 74 and 75 via the template primer
-
Boyer PL, Gao HQ, Hughes SH. A mutation at position 190 of human immunodeficiency virus type 1 reverse transcriptase interacts with mutations at positions 74 and 75 via the template primer. Antimicrob Agents Chemother 1998, 42: 447-452.
-
(1998)
Antimicrob Agents Chemother
, vol.42
, pp. 447-452
-
-
Boyer, P.L.1
Gao, H.Q.2
Hughes, S.H.3
-
32
-
-
33646237789
-
The HIV-1 reverse transcriptase mutants G190S and G190A, which confer resistance to non-nucleoside reverse transcriptase inhibitors, demonstrate reductions in RNase H activity and DNA synthesis from tRNA(Lys, 3) that correlate with reductions in replication efficiency
-
Wang J, Dykes C, Domaoal RA, Koval CE, Bambara RA, Demeter LM. The HIV-1 reverse transcriptase mutants G190S and G190A, which confer resistance to non-nucleoside reverse transcriptase inhibitors, demonstrate reductions in RNase H activity and DNA synthesis from tRNA(Lys, 3) that correlate with reductions in replication efficiency. Virology 2006; 348: 462-474.
-
(2006)
Virology
, vol.348
, pp. 462-474
-
-
Wang, J.1
Dykes, C.2
Domaoal, R.A.3
Koval, C.E.4
Bambara, R.A.5
Demeter, L.M.6
-
33
-
-
0029745634
-
A drug resistance mutation in the inhibitor binding pocket of human immunodeficiency virus type 1 reverse transcriptase impairs DNA synthesis and RNA degradation
-
Fan N, Rank KB, Slade DE, et al. A drug resistance mutation in the inhibitor binding pocket of human immunodeficiency virus type 1 reverse transcriptase impairs DNA synthesis and RNA degradation. Biochemistry 1996; 35: 9737-9745.
-
(1996)
Biochemistry
, vol.35
, pp. 9737-9745
-
-
Fan, N.1
Rank, K.B.2
Slade, D.E.3
-
34
-
-
0342908170
-
Molecular modeling of HIV-1 reverse transcriptase drug-resistant mutant strains: Implications for the mechanism of polymerase action
-
Kroeger Smith MB, Michejda CJ, Hughes SH, et al. Molecular modeling of HIV-1 reverse transcriptase drug-resistant mutant strains: implications for the mechanism of polymerase action. Protein Eng 1997;10: 1379-1383.
-
(1997)
Protein Eng
, vol.10
, pp. 1379-1383
-
-
Kroeger Smith, M.B.1
Michejda, C.J.2
Hughes, S.H.3
-
35
-
-
0030596068
-
Crystal structures of 8-Cl and 9-Cl TIBO complexed with wild-type HIV-1 RT and 8-Cl TIBO complexed with the Tyr181 Cys HIV-1 RT drug-resistant mutant
-
Das K, Ding J, Hsiou Y, et al. Crystal structures of 8-Cl and 9-Cl TIBO complexed with wild-type HIV-1 RT and 8-Cl TIBO complexed with the Tyr181 Cys HIV-1 RT drug-resistant mutant. J Mol Biol 1996; 264: 1085-1100.
-
(1996)
J Mol Biol
, vol.264
, pp. 1085-1100
-
-
Das, K.1
Ding, J.2
Hsiou, Y.3
-
36
-
-
0030966369
-
Mutations within the primer grip region of HIV-1 reverse transcriptase result in loss of RNase H function
-
Palaniappan C, Wisniewski M, Jacques PS, Le Grice SF, Fay PJ, Bambara RA. Mutations within the primer grip region of HIV-1 reverse transcriptase result in loss of RNase H function. J Biol Chem 1997; 272: 11157-11164.
-
(1997)
J Biol Chem
, vol.272
, pp. 11157-11164
-
-
Palaniappan, C.1
Wisniewski, M.2
Jacques, P.S.3
Le Grice, S.F.4
Fay, P.J.5
Bambara, R.A.6
-
37
-
-
0028926938
-
Nevirapine alters the cleavage specificity of ribonuclease H of human immunodeficiency virus 1 reverse transcriptase
-
Palaniappan C, Fay PJ, Bambara RA. Nevirapine alters the cleavage specificity of ribonuclease H of human immunodeficiency virus 1 reverse transcriptase. J Biol Chem 1995; 270: 4861-4869.
-
(1995)
J Biol Chem
, vol.270
, pp. 4861-4869
-
-
Palaniappan, C.1
Fay, P.J.2
Bambara, R.A.3
-
38
-
-
33751538895
-
Substrate-dependent inhibition or stimulation of HIV RNase H activity by non-nucleoside reverse transcriptase inhibitors (NNRTIs)
-
Hang JQ, Li Y, Yang Y, Cammack N, Mirzadegan T, Klumpp K. Substrate-dependent inhibition or stimulation of HIV RNase H activity by non-nucleoside reverse transcriptase inhibitors (NNRTIs). Biochem Biophys Res Commun 2007; 352: 341-350.
-
(2007)
Biochem Biophys Res Commun
, vol.352
, pp. 341-350
-
-
Hang, J.Q.1
Li, Y.2
Yang, Y.3
Cammack, N.4
Mirzadegan, T.5
Klumpp, K.6
-
39
-
-
0032993043
-
The P236L delavirdine-resistant human immunodeficiency virus type 1 mutant is replication defective and demonstrates alterations in both RNA 5′-end- and DNA 3′-end-directed RNase H activities
-
Gerondelis P, Archer RH, Palaniappan C, et al. The P236L delavirdine-resistant human immunodeficiency virus type 1 mutant is replication defective and demonstrates alterations in both RNA 5′-end- and DNA 3′-end-directed RNase H activities. J Virol 1999; 73: 5803-5813.
-
(1999)
J Virol
, vol.73
, pp. 5803-5813
-
-
Gerondelis, P.1
Archer, R.H.2
Palaniappan, C.3
-
40
-
-
0033863784
-
Mutants of human immunodeficiency virus type 1 (HIV-1) reverse transcriptase resistant to nonnucleoside reverse transcriptase inhibitors demonstrate altered rates of RNase H cleavage that correlate with HIV-1 replication fitness in cell culture
-
Archer RH, Dykes C, Gerondelis P, et al. Mutants of human immunodeficiency virus type 1 (HIV-1) reverse transcriptase resistant to nonnucleoside reverse transcriptase inhibitors demonstrate altered rates of RNase H cleavage that correlate with HIV-1 replication fitness in cell culture. J Virol 2000; 74: 8390-8401.
-
(2000)
J Virol
, vol.74
, pp. 8390-8401
-
-
Archer, R.H.1
Dykes, C.2
Gerondelis, P.3
-
41
-
-
0032478535
-
Effects of mutations in the polymerase domain on the polymerase, RNase H and strand transfer activities of human immunodeficiency virus type 1 reverse transcriptase
-
Gao HQ, Boyer PL, Arnold E, Hughes SH. Effects of mutations in the polymerase domain on the polymerase, RNase H and strand transfer activities of human immunodeficiency virus type 1 reverse transcriptase. J Mol Biol 1998; 277: 559-572
-
(1998)
J Mol Biol
, vol.277
, pp. 559-572
-
-
Gao, H.Q.1
Boyer, P.L.2
Arnold, E.3
Hughes, S.H.4
-
42
-
-
13444257639
-
Dissecting the effects of DNA polymerase and ribonuclease H inhibitor combinations on HIV-1 reverse-transcriptase activities
-
Shaw-Reid CA, Feuston B, Munshi V, et al. Dissecting the effects of DNA polymerase and ribonuclease H inhibitor combinations on HIV-1 reverse-transcriptase activities. Biochemistry 2005; 44: 1595-1606.
-
(2005)
Biochemistry
, vol.44
, pp. 1595-1606
-
-
Shaw-Reid, C.A.1
Feuston, B.2
Munshi, V.3
-
43
-
-
0036782103
-
Inhibitor binding alters the directions of domain motions in HIV-1 reverse transcriptase
-
Temiz NA, Bahar I. Inhibitor binding alters the directions of domain motions in HIV-1 reverse transcriptase. Proteins 2002; 49: 61-70.
-
(2002)
Proteins
, vol.49
, pp. 61-70
-
-
Temiz, N.A.1
Bahar, I.2
-
44
-
-
4544265135
-
Conformational changes in HIV-1 reverse transcriptase induced by nonnucleoside reverse transcriptase inhibitor binding
-
Sluis-Cremer N, Temiz NA, Bahar I. Conformational changes in HIV-1 reverse transcriptase induced by nonnucleoside reverse transcriptase inhibitor binding. Curr HIV Res 2004; 2: 323-332.
-
(2004)
Curr HIV Res
, vol.2
, pp. 323-332
-
-
Sluis-Cremer, N.1
Temiz, N.A.2
Bahar, I.3
-
45
-
-
0037764052
-
Steered molecular dynamics simulation on the binding of NNRTI to HIV-1 RT
-
Shen L, Shen J, Luo X, et al. Steered molecular dynamics simulation on the binding of NNRTI to HIV-1 RT. Biophys J 3003; 84: 3547-3563.
-
Biophys J
, vol.3003
, Issue.84
, pp. 3547-3563
-
-
Shen, L.1
Shen, J.2
Luo, X.3
-
46
-
-
33751433927
-
Potent nonnucleoside reverse transcriptase inhibitors target HIV-1 Gag-Pol
-
Figueiredo A, Moore KL, Mak J, Sluis-Cremer N, de Bethune MP, Tachedjian G. Potent nonnucleoside reverse transcriptase inhibitors target HIV-1 Gag-Pol. PLoS Pathog 2006; 2: e119.
-
(2006)
PLoS Pathog
, vol.2
-
-
Figueiredo, A.1
Moore, K.L.2
Mak, J.3
Sluis-Cremer, N.4
de Bethune, M.P.5
Tachedjian, G.6
|