-
1
-
-
84889259181
-
-
Available online: (accessed on 14 August 2012)
-
WHO Progress Report 2011: Global HIV/AIDS Response. Available online: http://www.who.int/hiv/pub/progress-report2011/en/index.html (accessed on 14 August 2012).
-
WHO Progress Report 2011: Global HIV/AIDS Response
-
-
-
2
-
-
84855654765
-
Mechanism of HIV antiretroviral drugs progress toward drug resistance
-
Ammaranond, P.; Sanguansittianan, S. Mechanism of HIV antiretroviral drugs progress toward drug resistance. Fundam. Clin. Pharm. 2012, 26, 146-161.
-
(2012)
Fundam. Clin. Pharm.
, vol.26
, pp. 146-161
-
-
Ammaranond, P.1
Sanguansittianan, S.2
-
3
-
-
84858409977
-
The structural biology of HIV-1: Mechanistic and therapeutic insights
-
Engelman, A.; Cherepanov, P. The structural biology of HIV-1: mechanistic and therapeutic insights. Nat. Rev. Micro. 2012, 10, 279-290.
-
(2012)
Nat. Rev. Micro.
, vol.10
, pp. 279-290
-
-
Engelman, A.1
Cherepanov, P.2
-
4
-
-
0026693137
-
Crystal structure at 3.5 Å resolution of HIV-1 reverse transcriptase complexed with an inhibitor
-
Kohlstaedt, L.A.; Wang, J.; Friedman, J.M.; Rice, P.A.; Steitz, T.A. Crystal structure at 3.5 Å resolution of HIV-1 reverse transcriptase complexed with an inhibitor. Science 1992, 256, 1783-1790.
-
(1992)
Science
, vol.256
, pp. 1783-1790
-
-
Kohlstaedt, L.A.1
Wang, J.2
Friedman, J.M.3
Rice, P.A.4
Steitz, T.A.5
-
5
-
-
33645891478
-
HIV-1 reverse transcriptase: A therapeutical target in the spotlight
-
Castro, H.C.; Loureiro, N.I.V.; Pujol-Luz, M.; Souza, A.M.T.; Albuquerque, M.G.; Santos, D.O.; Cabral, L.M.; Frugulhetti, I.C.; Rodrigues, C.R. HIV-1 reverse transcriptase: A therapeutical target in the spotlight. Curr. Med. Chem. 2006, 13, 313-324.
-
(2006)
Curr. Med. Chem.
, vol.13
, pp. 313-324
-
-
Castro, H.C.1
Loureiro, N.I.V.2
Pujol-Luz, M.3
Souza, A.M.T.4
Albuquerque, M.G.5
Santos, D.O.6
Cabral, L.M.7
Frugulhetti, I.C.8
Rodrigues, C.R.9
-
6
-
-
77649232123
-
Therapeutic strategies underpinning the development of novel techniques for the treatment of HIV infection
-
Tan, J.J.; Cong, X.J.; Hu, L.M.; Wang, C.X.; Jia, L.; Liang, X.-J. Therapeutic strategies underpinning the development of novel techniques for the treatment of HIV infection. Drug Discov. Today 2010, 15, 186-197.
-
(2010)
Drug Discov. Today
, vol.15
, pp. 186-197
-
-
Tan, J.J.1
Cong, X.J.2
Hu, L.M.3
Wang, C.X.4
Jia, L.5
Liang, X.-J.6
-
7
-
-
77956900680
-
Looking for an active conformation of the future HIV type-1 non-nucleoside reverse transcriptase inhibitors
-
La Regina, G.; Coluccia, A.; Silvestri, R. Looking for an active conformation of the future HIV type-1 non-nucleoside reverse transcriptase inhibitors. Antivir. Chem. Chemother. 2010, 20, 213-237.
-
(2010)
Antivir. Chem. Chemother.
, vol.20
, pp. 213-237
-
-
La Regina, G.1
Coluccia, A.2
Silvestri, R.3
-
8
-
-
0032786364
-
Expanded-spectrum nonnucleoside reverse transcriptase inhibitors inhibit clinically relevant mutant variants of human immunodeficiency virus type 1
-
Corbett, J.W.; Ko, S.S.; Rodgers, J.D.; Jeffrey, S.; Bacheler, L.T.; Klabe, R.M.; Diamond, S.; Lai, C.M.; Rabel, S.R.; Saye, J.A.; et al. Expanded-spectrum nonnucleoside reverse transcriptase inhibitors inhibit clinically relevant mutant variants of human immunodeficiency virus type 1. Antimicrob. Agents Chemother. 1999, 43, 2893-2897.
-
(1999)
Antimicrob. Agents Chemother.
, vol.43
, pp. 2893-2897
-
-
Corbett, J.W.1
Ko, S.S.2
Rodgers, J.D.3
Jeffrey, S.4
Bacheler, L.T.5
Klabe, R.M.6
Diamond, S.7
Lai, C.M.8
Rabel, S.R.9
Saye, J.A.10
-
9
-
-
0033524008
-
Design of MKC-442 (Emivirine) analogues with improved activity against drug-resistant HIV mutants
-
Hopkins, A.L.; Ren, J.; Tanaka, H.; Baba, M.; Okamato, M.; Stuart, D.I.; Stammers, D.K. Design of MKC-442 (Emivirine) analogues with improved activity against drug-resistant HIV mutants. J. Med. Chem. 1999, 42, 4500-4505.
-
(1999)
J. Med. Chem.
, vol.42
, pp. 4500-4505
-
-
Hopkins, A.L.1
Ren, J.2
Tanaka, H.3
Baba, M.4
Okamato, M.5
Stuart, D.I.6
Stammers, D.K.7
-
10
-
-
0034722975
-
Validation of a model for the complex of HIV-1 reverse transcriptase with sustiva through computation of resistance profiles
-
Rizzo, R.C.; Wang, D.P.; Tirado-Rives, J.; Jorgensen, W.L. Validation of a model for the complex of HIV-1 reverse transcriptase with sustiva through computation of resistance profiles. J. Am. Chem. Soc. 2000, 122, 12898-12900.
-
(2000)
J. Am. Chem. Soc.
, vol.122
, pp. 12898-12900
-
-
Rizzo, R.C.1
Wang, D.P.2
Tirado-Rives, J.3
Jorgensen, W.L.4
-
11
-
-
0037137588
-
Synthesis of novel N-1 (Allyloxymethyl) analogues of 6-benzyl-1- (ethoxymethyl)-5-isopropyluracil (MKC-442, Emivirine) with improved activity against HIV-1 and its mutants
-
El-Brollosy, N.R.; Jørgensen, P.T.; Dahan, B.; Boel, A.M.; Pedersen, E.B.; Nielsen, C. Synthesis of novel N-1 (Allyloxymethyl) analogues of 6-benzyl-1-(ethoxymethyl)-5-isopropyluracil (MKC-442, Emivirine) with improved activity against HIV-1 and its mutants. J. Med. Chem. 2002, 45, 5721-5726.
-
(2002)
J. Med. Chem.
, vol.45
, pp. 5721-5726
-
-
El-Brollosy, N.R.1
Jørgensen, P.T.2
Dahan, B.3
Boel, A.M.4
Pedersen, E.B.5
Nielsen, C.6
-
12
-
-
2342620790
-
Roles of conformational and positional adaptability in structure-based design of TMC125-R165335 (etravirine) and related non-nucleoside reverse transcriptase inhibitors that are highly potent and effective against wild-type and drug-resistant HIV-1 variants
-
Das, K.; Clark, A.D.; Lewi, P.J.; Heeres, J.; de Jonge, M.R.; Koymans, L.M.H.; Vinkers, H.M.; Daeyaert, F.; Ludovici, D.W.; Kukla, M.J.; et al. Roles of conformational and positional adaptability in structure-based design of TMC125-R165335 (etravirine) and related non-nucleoside reverse transcriptase inhibitors that are highly potent and effective against wild-type and drug-resistant HIV-1 variants. J. Med. Chem. 2004, 47, 2550-2560.
-
(2004)
J. Med. Chem.
, vol.47
, pp. 2550-2560
-
-
Das, K.1
Clark, A.D.2
Lewi, P.J.3
Heeres, J.4
De Jonge, M.R.5
Koymans, L.M.H.6
Vinkers, H.M.7
Daeyaert, F.8
Ludovici, D.W.9
Kukla, M.J.10
-
13
-
-
28144445329
-
Crystal structures for HIV-1 reverse transcriptase in complexes with three Pyridinone derivatives: A new class of non-nucleoside inhibitors effective against a broad range of drug-resistant strains
-
Himmel, D.M.; Das, K.; Clark, A.D.; Hughes, S.H.; Benjahad, A.; Oumouch, S.; Guillemont, J.; Coupa, S.; Poncelet, A.; Csoka, I.; et al. Crystal structures for HIV-1 reverse transcriptase in complexes with three Pyridinone derivatives: A new class of non-nucleoside inhibitors effective against a broad range of drug-resistant strains. J. Med. Chem. 2005, 48, 7582-7591.
-
(2005)
J. Med. Chem.
, vol.48
, pp. 7582-7591
-
-
Himmel, D.M.1
Das, K.2
Clark, A.D.3
Hughes, S.H.4
Benjahad, A.5
Oumouch, S.6
Guillemont, J.7
Coupa, S.8
Poncelet, A.9
Csoka, I.10
-
14
-
-
19744364217
-
The molecular basis of resilience to the effect of the Lys103Asn mutation in non-nucleoside HIV-1 reverse transcriptase inhibitors studied by targeted molecular dynamics simulations
-
Rodríguez-Barrios, F.; Balzarini, J.; Gago, F. The molecular basis of resilience to the effect of the Lys103Asn mutation in non-nucleoside HIV-1 reverse transcriptase inhibitors studied by targeted molecular dynamics simulations. J. Am. Chem. Soc. 2005, 127, 7570-7578.
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 7570-7578
-
-
Rodríguez-Barrios, F.1
Balzarini, J.2
Gago, F.3
-
15
-
-
29544447433
-
Computer-Aided design of non-nucleoside inhibitors of HIV-1 reverse transcriptase
-
Jorgensen, W.L.; Ruiz-Caro, J.; Tirado-Rives, J.; Basavapathruni, A.; Anderson, K.S.; Hamilton, A.D. Computer-Aided design of non-nucleoside inhibitors of HIV-1 reverse transcriptase. Bioorg. Med. Chem. Lett. 2006, 16, 663-667.
-
(2006)
Bioorg. Med. Chem. Lett.
, vol.16
, pp. 663-667
-
-
Jorgensen, W.L.1
Ruiz-Caro, J.2
Tirado-Rives, J.3
Basavapathruni, A.4
Anderson, K.S.5
Hamilton, A.D.6
-
16
-
-
33746838109
-
Structural insights into mechanisms of non-nucleoside drug resistance for HIV-1 reverse transcriptases mutated at codons 101 or 138
-
Ren, J.; Nichols, C.E.; Stamp, A.; Chamberlain, P.P.; Ferris, R.; Weaver, K.L.; Short, S.A.; Stammers, D.K. Structural insights into mechanisms of non-nucleoside drug resistance for HIV-1 reverse transcriptases mutated at codons 101 or 138. FEBS J. 2006, 273, 3850-3860.
-
(2006)
FEBS J.
, vol.273
, pp. 3850-3860
-
-
Ren, J.1
Nichols, C.E.2
Stamp, A.3
Chamberlain, P.P.4
Ferris, R.5
Weaver, K.L.6
Short, S.A.7
Stammers, D.K.8
-
17
-
-
34447319100
-
Thiotetrazole alkynylacetanilides as potent and bioavailable non-nucleoside inhibitors of the HIV-1 wild type and K103N/Y181C double mutant reverse transcriptases
-
Gagnon, A.; Amad, M.H.; Bonneau, P.R.; Coulombe, R.; DeRoy, P.L.; Doyon, L.; Duan, J.; Garneau, M.; Guse, I.; Jakalian, A.; et al. Thiotetrazole alkynylacetanilides as potent and bioavailable non-nucleoside inhibitors of the HIV-1 wild type and K103N/Y181C double mutant reverse transcriptases. Bioorg. Med. Chem. Lett. 2007, 17, 4437-4441.
-
(2007)
Bioorg. Med. Chem. Lett.
, vol.17
, pp. 4437-4441
-
-
Gagnon, A.1
Amad, M.H.2
Bonneau, P.R.3
Coulombe, R.4
DeRoy, P.L.5
Doyon, L.6
Duan, J.7
Garneau, M.8
Guse, I.9
Jakalian, A.10
-
18
-
-
0001688950
-
Protective effect of seaweed extracts for chicken embryos infected with influenza B or mumps virus
-
Gerber, P.; Dutcher, J.D.; Adams, E.V.; Sherman, J.H. Protective effect of seaweed extracts for chicken embryos infected with influenza B or mumps virus. Proc. Soc. Exp. Biol. Med. 1958, 99, 590-593.
-
(1958)
Proc. Soc. Exp. Biol. Med.
, vol.99
, pp. 590-593
-
-
Gerber, P.1
Dutcher, J.D.2
Adams, E.V.3
Sherman, J.H.4
-
19
-
-
1542534512
-
Marine natural products for industrial applications
-
Bongiorni, L.; Pietra, F. Marine natural products for industrial applications. Chem. Ind. 1996, 2, 54-58.
-
(1996)
Chem. Ind.
, vol.2
, pp. 54-58
-
-
Bongiorni, L.1
Pietra, F.2
-
20
-
-
33747802067
-
Pharmacological properties of the ubiquitous natural product betulin
-
Alakurtti, S.; Mäkelä, T.; Koskimies, S.; Yli-Kauhaluoma, J. Pharmacological properties of the ubiquitous natural product betulin. Eur. J. Pharm. Sci. 2006, 29, 1-13.
-
(2006)
Eur. J. Pharm. Sci.
, vol.29
, pp. 1-13
-
-
Alakurtti, S.1
Mäkelä, T.2
Koskimies, S.3
Yli-Kauhaluoma, J.4
-
21
-
-
27844474247
-
Drug discovery from medicinal plants
-
Balunas, M.J.; Kinghorn, A.D. Drug discovery from medicinal plants. Life Sci . 2005, 78, 431-441.
-
(2005)
Life Sci.
, vol.78
, pp. 431-441
-
-
Balunas, M.J.1
Kinghorn, A.D.2
-
22
-
-
79958817934
-
What are and where are the bioactive terpenoids metabolites from Dictyotaceae (Phaeophyceae)
-
Paula, J.C.D.; Vallim, M.A.; Teixeira, V.L. What are and where are the bioactive terpenoids metabolites from Dictyotaceae (Phaeophyceae). Rev. Bras. Farmacogn. 2011, 21, 216-228.
-
(2011)
Rev. Bras. Farmacogn.
, vol.21
, pp. 216-228
-
-
Paula, J.C.D.1
Vallim, M.A.2
Teixeira, V.L.3
-
23
-
-
4644262497
-
Antiviral activity of diterpenes isolated from the Brazilian marine alga Dictyota menstrualis against human immunodeficiency virus type 1 (HIV-1)
-
Pereira, H.S.; Leão-Ferreira, L.R.; Moussatché, N.; Teixeira, V.L.; Cavalcanti, D.N.; Costa, L.J.; Diaz, R.; Frugulhetti, I.C.P.P. Antiviral activity of diterpenes isolated from the Brazilian marine alga Dictyota menstrualis against human immunodeficiency virus type 1 (HIV-1). Antivir. Res. 2004, 64, 69-76.
-
(2004)
Antivir. Res.
, vol.64
, pp. 69-76
-
-
Pereira, H.S.1
Leão-Ferreira, L.R.2
Moussatché, N.3
Teixeira, V.L.4
Cavalcanti, D.N.5
Costa, L.J.6
Diaz, R.7
Frugulhetti, I.C.P.P.8
-
24
-
-
3242657912
-
Structure of HIV-1 reverse transcriptase bound to an inhibitor active against mutant reverse transcriptases resistant to other nonnucleoside inhibitors
-
Pata, J.D.; Stirtan, W.G.; Goldstein, S.W.; Steitz, T.A. Structure of HIV-1 reverse transcriptase bound to an inhibitor active against mutant reverse transcriptases resistant to other nonnucleoside inhibitors. Proc. Natl. Acad. Sci. USA 2004, 101, 10548-10553.
-
(2004)
Proc. Natl. Acad. Sci. USA
, vol.101
, pp. 10548-10553
-
-
Pata, J.D.1
Stirtan, W.G.2
Goldstein, S.W.3
Steitz, T.A.4
-
25
-
-
0344152988
-
A dolabellane diterpene from the Brazilian brown alga Dictyota pfaffii
-
Barbosa, J.P.; Teixeira, V.L.; Villaça, R.; Pereira, R.C.; Abrantes, J.L.; Frugulhetti, I.C.P.P. A dolabellane diterpene from the Brazilian brown alga Dictyota pfaffii. Biochem. Syst. Ecol. 2003, 31, 1451-1453.
-
(2003)
Biochem. Syst. Ecol.
, vol.31
, pp. 1451-1453
-
-
Barbosa, J.P.1
Teixeira, V.L.2
Villaça, R.3
Pereira, R.C.4
Abrantes, J.L.5
Frugulhetti, I.C.P.P.6
-
26
-
-
33645531213
-
Inhibition of HIV-1 replication in human primary cells by a dolabellane diterpene isolated from the marine algae Dictyota pfaffii
-
Cirne-Santos, C.C.; Teixeira, V.L.; Castello-Branco, L.R.; Frugulhetti, I.C.P.P.; Bou-Habib, D.C. Inhibition of HIV-1 replication in human primary cells by a dolabellane diterpene isolated from the marine algae Dictyota pfaffii . Planta Medica 2006, 72, 295-299.
-
(2006)
Planta Medica
, vol.72
, pp. 295-299
-
-
Cirne-Santos, C.C.1
Teixeira, V.L.2
Castello-Branco, L.R.3
Frugulhetti, I.C.P.P.4
Bou-Habib, D.C.5
-
27
-
-
84876852661
-
HIV-1 NNRTIs: Structural diversity, pharmacophore similarity, and implications for drug design
-
doi:10.1002/med.20241
-
Zhan, P.; Chen, X.; Li, D.; Fang, Z.; de Clercq, E.; Liu, X. HIV-1 NNRTIs: Structural diversity, pharmacophore similarity, and implications for drug design. Med. Res. Rev. 2011, 33, doi:10.1002/med.20241.
-
(2011)
Med. Res. Rev.
, vol.33
-
-
Zhan, P.1
Chen, X.2
Li, D.3
Fang, Z.4
De Clercq, E.5
Liu, X.6
-
28
-
-
37549017330
-
The dolabellane diterpene Dolabelladienetriol is a typical noncompetitive inhibitor of HIV-1 reverse transcriptase enzyme
-
Cirne-Santos, C.C.; Souza, T.M.L.; Teixeira, V.L.; Fontes, C.F.L.; Rebello, M.A.; Castello-Branco, L.R.R.; Abreu, C.M.; Tanuri, A.; Frugulhetti, I.C.P.P.; Bou-Habib, D.C. The dolabellane diterpene Dolabelladienetriol is a typical noncompetitive inhibitor of HIV-1 reverse transcriptase enzyme. Antivir. Res. 2008, 77, 64-71.
-
(2008)
Antivir. Res.
, vol.77
, pp. 64-71
-
-
Cirne-Santos, C.C.1
Souza, T.M.L.2
Teixeira, V.L.3
Fontes, C.F.L.4
Rebello, M.A.5
Castello-Branco, L.R.R.6
Abreu, C.M.7
Tanuri, A.8
Frugulhetti, I.C.P.P.9
Bou-Habib, D.C.10
-
29
-
-
84889257925
-
-
Available online: (accessed on 14 February 2013)
-
Organic Chemistry Portal-OSIRIS Property Explorer. Available online: http://www. organic-chemistry.org/prog/peo/ (accessed on 14 February 2013).
-
Organic Chemistry Portal-OSIRIS Property Explorer
-
-
-
30
-
-
13244266921
-
Lead- and drug-like compounds: The rule-of-five revolution
-
Lipinski, C.A. Lead- and drug-like compounds: The rule-of-five revolution. Drug Discov. Today Technol. 2004, 1, 337-341.
-
(2004)
Drug Discov. Today Technol.
, vol.1
, pp. 337-341
-
-
Lipinski, C.A.1
-
31
-
-
9744258219
-
Crystallography and the design of anti-AIDS drugs: Conformational flexibility and positional adaptability are important in the design of non-nucleoside HIV-1 reverse transcriptase inhibitors
-
Das, K.; Lewi, P.J.; Hughes, S.H.; Arnold, E. Crystallography and the design of anti-AIDS drugs: Conformational flexibility and positional adaptability are important in the design of non-nucleoside HIV-1 reverse transcriptase inhibitors. Prog. Biophy. Mol. Biol. 2005, 88, 209-231.
-
(2005)
Prog. Biophy. Mol. Biol.
, vol.88
, pp. 209-231
-
-
Das, K.1
Lewi, P.J.2
Hughes, S.H.3
Arnold, E.4
-
32
-
-
47249083852
-
Docking and multivariate methods to explore HIV-1 drug-resistance: A comparative analysis
-
Almerico, A.M.; Tutone, M.; Lauria, A. Docking and multivariate methods to explore HIV-1 drug-resistance: A comparative analysis. J. Comput. Aided Mol. Des. 2008, 22, 287-297.
-
(2008)
J. Comput. Aided Mol. Des.
, vol.22
, pp. 287-297
-
-
Almerico, A.M.1
Tutone, M.2
Lauria, A.3
-
33
-
-
73549115378
-
Non-nucleoside reverse transcriptase inhibitors (NNRTIs), their discovery, development, and use in the treatment of HIV-1 infection: A review of the last 20 years (1989-2009)
-
De Béthune, M.P. Non-nucleoside reverse transcriptase inhibitors (NNRTIs), their discovery, development, and use in the treatment of HIV-1 infection: A review of the last 20 years (1989-2009). Antivir. Res. 2010, 85, 75-90.
-
(2010)
Antivir. Res.
, vol.85
, pp. 75-90
-
-
De Béthune, M.P.1
-
34
-
-
84857687438
-
Ultra-deep sequencing of HIV-1 reverse transcriptase before start of an NNRTI-based regimen in treatment-naive patients
-
Messiaen, P.; Verhofstede, C.; Vandenbroucke, I.; Dinakis, S.; Van Eygen, V.; Thys, K.; Winters, B.; Aerssens, J.; Vogelaers, D.; Stuyver, L.J.; et al. Ultra-deep sequencing of HIV-1 reverse transcriptase before start of an NNRTI-based regimen in treatment-naive patients. Virology 2012, 426, 7-11.
-
(2012)
Virology
, vol.426
, pp. 7-11
-
-
Messiaen, P.1
Verhofstede, C.2
Vandenbroucke, I.3
Dinakis, S.4
Van Eygen, V.5
Thys, K.6
Winters, B.7
Aerssens, J.8
Vogelaers, D.9
Stuyver, L.J.10
-
35
-
-
0035814027
-
Antiviral drug design: Computational analyses of the effects of the L100I mutation for HIV-RT on the binding of NNRTIs
-
Wang, D.P.; Rizzo, R.C.; Tirado-Rives, J.; Jorgensen, W.L. Antiviral drug design: Computational analyses of the effects of the L100I mutation for HIV-RT on the binding of NNRTIs. Bioorg. Med. Chem. Lett. 2001, 11, 2799-2802.
-
(2001)
Bioorg. Med. Chem. Lett.
, vol.11
, pp. 2799-2802
-
-
Wang, D.P.1
Rizzo, R.C.2
Tirado-Rives, J.3
Jorgensen, W.L.4
-
36
-
-
84856711380
-
HIV-1 reverse transcriptase complex with DNA and nevirapine reveals non-nucleoside inhibition mechanism
-
Das, K.; Martinez, S.E.; Bauman, J.D.; Arnold, E. HIV-1 reverse transcriptase complex with DNA and nevirapine reveals non-nucleoside inhibition mechanism. Nat. Struct. Mol. Biol. 2012, 19, 253-259.
-
(2012)
Nat. Struct. Mol. Biol.
, vol.19
, pp. 253-259
-
-
Das, K.1
Martinez, S.E.2
Bauman, J.D.3
Arnold, E.4
-
37
-
-
77953023743
-
The non-nucleoside reverse transcriptase inhibitor efavirenz stimulates replication of human immunodeficiency virus type 1 harboring certain non-nucleoside resistance mutations
-
Wang, J.; Liang, H.; Bacheler, L.; Wu, H.; Deriziotis, K.; Demeter, L.M.; Dykes, C. The non-nucleoside reverse transcriptase inhibitor efavirenz stimulates replication of human immunodeficiency virus type 1 harboring certain non-nucleoside resistance mutations. Virology 2010, 402, 228-237.
-
(2010)
Virology
, vol.402
, pp. 228-237
-
-
Wang, J.1
Liang, H.2
Bacheler, L.3
Wu, H.4
Deriziotis, K.5
Demeter, L.M.6
Dykes, C.7
-
38
-
-
0032573488
-
Structure of a covalently trapped catalytic complex of HIV-1 reverse transcriptase: Implications for drug resistance
-
Huang, H.; Chopra, R.; Verdine, G.L.; Harrison, S.C. Structure of a covalently trapped catalytic complex of HIV-1 reverse transcriptase: implications for drug resistance. Science 1998, 282, 1669-1675.
-
(1998)
Science
, vol.282
, pp. 1669-1675
-
-
Huang, H.1
Chopra, R.2
Verdine, G.L.3
Harrison, S.C.4
-
39
-
-
84889258907
-
-
Available online: (accessed on 25 February 2013)
-
RCSB PDB Protein Data Bank. Available online: http://www.rcsb.org/pdb (accessed on 25 February 2013).
-
RCSB PDB Protein Data Bank
-
-
-
40
-
-
0029075207
-
Structure of HIV-1 RT/TIBO R 86183 complex reveals similarity in the binding of diverse nonnucleoside inhibitors
-
Ding, J.; Das, K.; Moereels, H.; Koymans, L.; Andries, K.; Janssen, P.A.J.; Hughes, S.H.; Arnold, E. Structure of HIV-1 RT/TIBO R 86183 complex reveals similarity in the binding of diverse nonnucleoside inhibitors. Nat. Struct. Mol. Biol. 1995, 2, 407-415.
-
(1995)
Nat. Struct. Mol. Biol.
, vol.2
, pp. 407-415
-
-
Ding, J.1
Das, K.2
Moereels, H.3
Koymans, L.4
Andries, K.5
Janssen, P.A.J.6
Hughes, S.H.7
Arnold, E.8
-
41
-
-
0031473847
-
SWISS-MODEL and the Swiss-PdbViewer: An environment for comparative protein modeling
-
Guex, N.; Peitsch, M.C. SWISS-MODEL and the Swiss-PdbViewer: An environment for comparative protein modeling. Electrophoresis 1997, 18, 2714-2723.
-
(1997)
Electrophoresis
, vol.18
, pp. 2714-2723
-
-
Guex, N.1
Peitsch, M.C.2
-
42
-
-
0000243829
-
Procheck: A program to check the stereochemical quality of protein structures
-
Laskowski, R.A.; MacArthur, M.W.; Moss, D.S.; Thornton, J.M. Procheck: A program to check the stereochemical quality of protein structures. J. Appl. Crystallogr. 1993, 26, 283-291.
-
(1993)
J. Appl. Crystallogr.
, vol.26
, pp. 283-291
-
-
Laskowski, R.A.1
MacArthur, M.W.2
Moss, D.S.3
Thornton, J.M.4
-
43
-
-
33947716119
-
A semiempirical free energy force field with charge-based desolvation
-
Huey, R.; Morris, G.M.; Olson, A.J.; Goodsell, D.S. A semiempirical free energy force field with charge-based desolvation. J. Comput. Chem. 2007, 28, 1145-1152.
-
(2007)
J. Comput. Chem.
, vol.28
, pp. 1145-1152
-
-
Huey, R.1
Morris, G.M.2
Olson, A.J.3
Goodsell, D.S.4
-
44
-
-
11644261806
-
Automated docking using a Lamarckian genetic algorithm and an empirical binding free energy function
-
Morris, G.M.; Goodsell, D.S.; Halliday, R.S.; Huey, R.; Hart, W.E.; Belew, R.K.; Olson, A.J. Automated docking using a Lamarckian genetic algorithm and an empirical binding free energy function. J. Comput. Chem. 1998, 19, 1639-1662.
-
(1998)
J. Comput. Chem.
, vol.19
, pp. 1639-1662
-
-
Morris, G.M.1
Goodsell, D.S.2
Halliday, R.S.3
Huey, R.4
Hart, W.E.5
Belew, R.K.6
Olson, A.J.7
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