-
2
-
-
78349299437
-
Development of peptide and small-molecule HIV-1 fusion inhibitors that target gp41
-
Cai L, Jiang S. 2010. Development of peptide and small-molecule HIV-1 fusion inhibitors that target gp41. ChemMedChem 5:1813-1824.
-
(2010)
ChemMedChem
, vol.5
, pp. 1813-1824
-
-
Cai, L.1
Jiang, S.2
-
3
-
-
0032433685
-
Evidence that a prominent cavity in the coiled coil of HIV type 1 gp41 is an attractive drug target
-
Chan DC, Chutkowski CT, Kim PS. 1998. Evidence that a prominent cavity in the coiled coil of HIV type 1 gp41 is an attractive drug target. Proc. Natl. Acad. Sci. U. S. A. 95:15613-15617.
-
(1998)
Proc. Natl. Acad. Sci. U. S. A.
, vol.95
, pp. 15613-15617
-
-
Chan, D.C.1
Chutkowski, C.T.2
Kim, P.S.3
-
4
-
-
0030970693
-
Core structure of gp41 from the HIV envelope glycoprotein
-
Chan DC, Fass D, Berger JM, Kim PS. 1997. Core structure of gp41 from the HIV envelope glycoprotein. Cell 89:263-273.
-
(1997)
Cell
, vol.89
, pp. 263-273
-
-
Chan, D.C.1
Fass, D.2
Berger, J.M.3
Kim, P.S.4
-
5
-
-
0032577550
-
HIV entry and its inhibition
-
Chan DC, Kim PS. 1998. HIV entry and its inhibition. Cell 93:681- 684.
-
(1998)
Cell
, vol.93
, pp. 681-684
-
-
Chan, D.C.1
Kim, P.S.2
-
6
-
-
34249935492
-
Human immunodeficiency virus type 1 variants resistant to first- and second-version fusion inhibitors and cytopathic in ex vivo human lymphoid tissue
-
Chinnadurai R, Rajan D, Munch J, Kirchhoff F. 2007. Human immunodeficiency virus type 1 variants resistant to first- and second-version fusion inhibitors and cytopathic in ex vivo human lymphoid tissue. J. Virol. 81:6563- 6572.
-
(2007)
J. Virol.
, vol.81
, pp. 6563-6572
-
-
Chinnadurai, R.1
Rajan, D.2
Munch, J.3
Kirchhoff, F.4
-
7
-
-
34147124231
-
Protein design of a bacterially expressed HIV-1 gp41 fusion inhibitor
-
Deng Y, Zheng Q, Ketas TJ, Moore JP, Lu M. 2007. Protein design of a bacterially expressed HIV-1 gp41 fusion inhibitor. Biochemistry 46: 4360-4369.
-
(2007)
Biochemistry
, vol.46
, pp. 4360-4369
-
-
Deng, Y.1
Zheng, Q.2
Ketas, T.J.3
Moore, J.P.4
Lu, M.5
-
8
-
-
0038671938
-
The hydrophobic pocket contributes to the structural stability of the N-terminal coiled coil of HIV gp41 but is not required for six-helix bundle formation
-
Dwyer JJ, et al. 2003. The hydrophobic pocket contributes to the structural stability of the N-terminal coiled coil of HIV gp41 but is not required for six-helix bundle formation. Biochemistry 42:4945-4953.
-
(2003)
Biochemistry
, vol.42
, pp. 4945-4953
-
-
Dwyer, J.J.1
-
9
-
-
0034924823
-
Mechanisms of viral membrane fusion and its inhibition
-
Eckert DM, Kim PS. 2001. Mechanisms of viral membrane fusion and its inhibition. Annu. Rev. Biochem. 70:777- 810.
-
(2001)
Annu. Rev. Biochem.
, vol.70
, pp. 777-810
-
-
Eckert, D.M.1
Kim, P.S.2
-
10
-
-
45749135859
-
Selection of T1249-resistant human immunodeficiency virus type 1 variants
-
Eggink D, et al. 2008. Selection of T1249-resistant human immunodeficiency virus type 1 variants. J. Virol. 82:6678-6688.
-
(2008)
J. Virol.
, vol.82
, pp. 6678-6688
-
-
Eggink, D.1
-
11
-
-
12144290487
-
Short-term safety and antiretroviral activity of T-1249, a second-generation fusion inhibitor of HIV
-
Eron JJ, et al. 2004. Short-term safety and antiretroviral activity of T-1249, a second-generation fusion inhibitor of HIV. J. Infect. Dis. 189: 1075-1083.
-
(2004)
J. Infect. Dis.
, vol.189
, pp. 1075-1083
-
-
Eron, J.J.1
-
12
-
-
45749112585
-
Identification of a critical motif for the human immunodeficiency virus type 1 (HIV-1) gp41 core structure: implications for designing novel anti-HIV fusion inhibitors
-
He Y, et al. 2008. Identification of a critical motif for the human immunodeficiency virus type 1 (HIV-1) gp41 core structure: implications for designing novel anti-HIV fusion inhibitors. J. Virol. 82:6349-6358.
-
(2008)
J. Virol.
, vol.82
, pp. 6349-6358
-
-
He, Y.1
-
13
-
-
55849137299
-
Potent HIV fusion inhibitors against enfuvirtideresistant HIV-1 strains
-
He Y, et al. 2008. Potent HIV fusion inhibitors against enfuvirtideresistant HIV-1 strains. Proc. Natl. Acad. Sci. U. S. A. 105:16332-16337.
-
(2008)
Proc. Natl. Acad. Sci. U. S. A.
, vol.105
, pp. 16332-16337
-
-
He, Y.1
-
14
-
-
55549105768
-
Conserved salt bridge between the N- and C-terminal heptad repeat regions of the human immunodeficiency virus type 1 gp41 core structure is critical for virus entry and inhibition
-
He Y, et al. 2008. Conserved salt bridge between the N- and C-terminal heptad repeat regions of the human immunodeficiency virus type 1 gp41 core structure is critical for virus entry and inhibition. J. Virol. 82: 11129-11139.
-
(2008)
J. Virol.
, vol.82
, pp. 11129-11139
-
-
He, Y.1
-
15
-
-
34548481743
-
Conserved residue Lys574 in the cavity of HIV-1 gp41 coiled-coil domain is critical for six-helix bundle stability and virus entry
-
He Y, et al. 2007. Conserved residue Lys574 in the cavity of HIV-1 gp41 coiled-coil domain is critical for six-helix bundle stability and virus entry. J. Biol. Chem. 282:25631-25639.
-
(2007)
J. Biol. Chem.
, vol.282
, pp. 25631-25639
-
-
He, Y.1
-
16
-
-
45549093277
-
Design and evaluation of sifuvirtide, a novel HIV-1 fusion inhibitor
-
He Y, et al. 2008. Design and evaluation of sifuvirtide, a novel HIV-1 fusion inhibitor. J. Biol. Chem. 283:11126 -11134.
-
(2008)
J. Biol. Chem.
, vol.283
, pp. 11126-11134
-
-
He, Y.1
-
17
-
-
0032850583
-
Inhibition of human immunodeficiency virus type 1 infectivity by the gp41 core: role of a conserved hydrophobic cavity in membrane fusion
-
Ji H, Shu W, Burling T, Jiang S, Lu M. 1999. Inhibition of human immunodeficiency virus type 1 infectivity by the gp41 core: role of a conserved hydrophobic cavity in membrane fusion. J. Virol. 73:8578-8586.
-
(1999)
J. Virol.
, vol.73
, pp. 8578-8586
-
-
Ji, H.1
Shu, W.2
Burling, T.3
Jiang, S.4
Lu, M.5
-
19
-
-
7244253012
-
N- substituted pyrrole derivatives as novel human immunodeficiency virus type 1 entry inhibitors that interfere with the gp41 six-helix bundle formation and block virus fusion
-
Jiang S, et al. 2004. N-substituted pyrrole derivatives as novel human immunodeficiency virus type 1 entry inhibitors that interfere with the gp41 six-helix bundle formation and block virus fusion. Antimicrob. Agents Chemother. 48:4349-4359.
-
(2004)
Antimicrob. Agents Chemother.
, vol.48
, pp. 4349-4359
-
-
Jiang, S.1
-
20
-
-
20144386372
-
T- 1249 retains potent antiretroviral activity in patients who had experienced virological failure while on an enfuvirtidecontaining treatment regimen
-
Lalezari JP, et al. 2005. T-1249 retains potent antiretroviral activity in patients who had experienced virological failure while on an enfuvirtidecontaining treatment regimen. J. Infect. Dis. 191:1155-1163.
-
(2005)
J. Infect. Dis.
, vol.191
, pp. 1155-1163
-
-
Lalezari, J.P.1
-
21
-
-
58149090406
-
Design, synthesis, and biological evaluation of N-carboxyphenylpyrrole derivatives as potent HIV fusion inhibitors targeting gp41
-
Liu K, et al. 2008. Design, synthesis, and biological evaluation of N-carboxyphenylpyrrole derivatives as potent HIV fusion inhibitors targeting gp41. J. Med. Chem. 51:7843-7854.
-
(2008)
J. Med. Chem.
, vol.51
, pp. 7843-7854
-
-
Liu, K.1
-
22
-
-
34248155890
-
HIV gp41 C-terminal heptad repeat contains multifunctional domains: relation to mechanisms of action of anti-HIV peptides
-
Liu S, et al. 2007. HIV gp41 C-terminal heptad repeat contains multifunctional domains: relation to mechanisms of action of anti-HIV peptides. J. Biol. Chem. 282:9612-9620.
-
(2007)
J. Biol. Chem.
, vol.282
, pp. 9612-9620
-
-
Liu, S.1
-
23
-
-
15744393651
-
Different from the HIV fusion inhibitor C34, the anti-HIV drug Fuzeon (T-20) inhibits HIV-1 entry by targeting multiple sites in gp41 and gp120
-
Liu S, Lu H, Xu Y, Wu S, Jiang S. 2005. Different from the HIV fusion inhibitor C34, the anti-HIV drug Fuzeon (T-20) inhibits HIV-1 entry by targeting multiple sites in gp41 and gp120. J. Biol. Chem. 280: 11259-11273.
-
(2005)
J. Biol. Chem.
, vol.280
, pp. 11259-11273
-
-
Liu, S.1
Lu, H.2
Xu, Y.3
Wu, S.4
Jiang, S.5
-
24
-
-
79952781156
-
In vitro selection and characterization of HIV-1 variants with increased resistance to sifuvirtide, a novel HIV-1 fusion inhibitor
-
Liu Z, et al. 2011. In vitro selection and characterization of HIV-1 variants with increased resistance to sifuvirtide, a novel HIV-1 fusion inhibitor. J. Biol. Chem. 286:3277-3287.
-
(2011)
J. Biol. Chem.
, vol.286
, pp. 3277-3287
-
-
Liu, Z.1
-
25
-
-
0028834461
-
A trimeric structural domain of the HIV-1 transmembrane glycoprotein
-
Lu M, Blacklow SC, Kim PS. 1995. A trimeric structural domain of the HIV-1 transmembrane glycoprotein. Nat. Struct. Biol. 2:1075-1082.
-
(1995)
Nat. Struct. Biol.
, vol.2
, pp. 1075-1082
-
-
Lu, M.1
Blacklow, S.C.2
Kim, P.S.3
-
26
-
-
0031441562
-
A trimeric structural subdomain of the HIV-1 transmembrane glycoprotein
-
Lu M, Kim PS. 1997. A trimeric structural subdomain of the HIV-1 transmembrane glycoprotein. J. Biomol. Struct. Dyn. 15:465- 471.
-
(1997)
J. Biomol. Struct. Dyn.
, vol.15
, pp. 465-471
-
-
Lu, M.1
Kim, P.S.2
-
28
-
-
4344685387
-
Genotype and phenotype patterns of human immunodeficiency virus type 1 resistance to enfuvirtide during long-term treatment
-
Menzo S, et al. 2004. Genotype and phenotype patterns of human immunodeficiency virus type 1 resistance to enfuvirtide during long-term treatment. Antimicrob. Agents Chemother. 48:3253-3259.
-
(2004)
Antimicrob. Agents Chemother.
, vol.48
, pp. 3253-3259
-
-
Menzo, S.1
-
29
-
-
25144489604
-
Impact of human immunodeficiency virus type 1 gp41 amino acid substitutions selected during enfuvirtide treatment on gp41 binding and antiviral potency of enfuvirtide in vitro
-
Mink M, et al. 2005. Impact of human immunodeficiency virus type 1 gp41 amino acid substitutions selected during enfuvirtide treatment on gp41 binding and antiviral potency of enfuvirtide in vitro. J. Virol. 79: 12447-12454.
-
(2005)
J. Virol.
, vol.79
, pp. 12447-12454
-
-
Mink, M.1
-
30
-
-
0141814730
-
The entry of entry inhibitors: a fusion of science and medicine
-
Moore JP, Doms RW. 2003. The entry of entry inhibitors: a fusion of science and medicine. Proc. Natl. Acad. Sci. U. S. A. 100:10598 -10602.
-
(2003)
Proc. Natl. Acad. Sci. U. S. A.
, vol.100
, pp. 10598-10602
-
-
Moore, J.P.1
Doms, R.W.2
-
31
-
-
67749147470
-
Combinations of the first and next generations of human immunodeficiency virus (HIV) fusion inhibitors exhibit a highly potent synergistic effect against enfuvirtide-sensitive and -resistant HIV type 1 strains
-
Pan C, Cai L, Lu H, Qi Z, Jiang S. 2009. Combinations of the first and next generations of human immunodeficiency virus (HIV) fusion inhibitors exhibit a highly potent synergistic effect against enfuvirtide-sensitive and -resistant HIV type 1 strains. J. Virol. 83:7862-7872.
-
(2009)
J. Virol.
, vol.83
, pp. 7862-7872
-
-
Pan, C.1
Cai, L.2
Lu, H.3
Qi, Z.4
Jiang, S.5
-
32
-
-
77449151492
-
HIV-1 gp41 fusion intermediate: a target for HIV therapeutics
-
Pan C, Liu S, Jiang S. 2010. HIV-1 gp41 fusion intermediate: a target for HIV therapeutics. J. Formos. Med. Assoc. 109:94 -105.
-
(2010)
J. Formos. Med. Assoc.
, vol.109
, pp. 94-105
-
-
Pan, C.1
Liu, S.2
Jiang, S.3
-
33
-
-
63149114263
-
Synergistic efficacy of combination of enfuvirtide and sifuvirtide, the first- and next-generation HIV-fusion inhibitors
-
Pan C, Lu H, Qi Z, Jiang S. 2009. Synergistic efficacy of combination of enfuvirtide and sifuvirtide, the first- and next-generation HIV-fusion inhibitors. AIDS 23:639-641.
-
(2009)
AIDS
, vol.23
, pp. 639-641
-
-
Pan, C.1
Lu, H.2
Qi, Z.3
Jiang, S.4
-
34
-
-
57649155175
-
Rationally designed anti-HIV peptides containing multifunctional domains as molecule probes for studying the mechanisms of action of the first and second generation HIV fusion inhibitors
-
Qi Z, et al. 2008. Rationally designed anti-HIV peptides containing multifunctional domains as molecule probes for studying the mechanisms of action of the first and second generation HIV fusion inhibitors. J. Biol. Chem. 283:30376 -30384.
-
(2008)
J. Biol. Chem.
, vol.283
, pp. 30376-30384
-
-
Qi, Z.1
-
35
-
-
33947417638
-
Clinical resistance to enfuvirtide does not affect susceptibility of human immunodeficiency virus type 1 to other classes of entry inhibitors
-
Ray N, et al. 2007. Clinical resistance to enfuvirtide does not affect susceptibility of human immunodeficiency virus type 1 to other classes of entry inhibitors. J. Virol. 81:3240-3250.
-
(2007)
J. Virol.
, vol.81
, pp. 3240-3250
-
-
Ray, N.1
-
36
-
-
63149093637
-
HR-2 mutations in human immunodeficiency virus type 1 gp41 restore fusion kinetics delayed by HR-1 mutations that cause clinical resistance to enfuvirtide
-
Ray N, Blackburn LA, Doms RW. 2009. HR-2 mutations in human immunodeficiency virus type 1 gp41 restore fusion kinetics delayed by HR-1 mutations that cause clinical resistance to enfuvirtide. J. Virol. 83: 2989-2995.
-
(2009)
J. Virol.
, vol.83
, pp. 2989-2995
-
-
Ray, N.1
Blackburn, L.A.2
Doms, R.W.3
-
37
-
-
0031883832
-
Determinants of human immunodeficiency virus type 1 resistance to gp41-derived inhibitory peptides
-
Rimsky LT, Shugars DC, Matthews TJ. 1998. Determinants of human immunodeficiency virus type 1 resistance to gp41-derived inhibitory peptides. J. Virol. 72:986 -993.
-
(1998)
J. Virol.
, vol.72
, pp. 986-993
-
-
Rimsky, L.T.1
Shugars, D.C.2
Matthews, T.J.3
-
38
-
-
77954065271
-
I-TASSER: a unified platform for automated protein structure and function prediction
-
Roy A, Kucukural A, Zhang Y. 2010. I-TASSER: a unified platform for automated protein structure and function prediction. Nat. Protoc. 5:725-738.
-
(2010)
Nat. Protoc.
, vol.5
, pp. 725-738
-
-
Roy, A.1
Kucukural, A.2
Zhang, Y.3
-
39
-
-
0036090585
-
Emergence of resistant human immunodeficiency virus type 1 in patients receiving fusion inhibitor (T-20) monotherapy
-
Wei X, et al. 2002. Emergence of resistant human immunodeficiency virus type 1 in patients receiving fusion inhibitor (T-20) monotherapy. Antimicrob. Agents Chemother. 46:1896-1905.
-
(2002)
Antimicrob. Agents Chemother.
, vol.46
, pp. 1896-1905
-
-
Wei, X.1
-
40
-
-
0030962291
-
Atomic structure of the ectodomain from HIV-1 gp41
-
Weissenhorn W, Dessen A, Harrison SC, Skehel JJ, Wiley DC. 1997. Atomic structure of the ectodomain from HIV-1 gp41. Nature 387: 426-428.
-
(1997)
Nature
, vol.387
, pp. 426-428
-
-
Weissenhorn, W.1
Dessen, A.2
Harrison, S.C.3
Skehel, J.J.4
Wiley, D.C.5
-
41
-
-
36749087580
-
Potent D-peptide inhibitors of HIV-1 entry
-
Welch BD, VanDemark AP, Heroux A, Hill CP, Kay MS. 2007. Potent D-peptide inhibitors of HIV-1 entry. Proc. Natl. Acad. Sci. U. S. A. 104: 16828-16833.
-
(2007)
Proc. Natl. Acad. Sci. U. S. A.
, vol.104
, pp. 16828-16833
-
-
Welch, B.D.1
VanDemark, A.P.2
Heroux, A.3
Hill, C.P.4
Kay, M.S.5
-
42
-
-
0031798443
-
Mutational analysis of residues in the coiledcoil domain of human immunodeficiency virus type 1 transmembrane protein gp41
-
Weng Y, Weiss CD. 1998. Mutational analysis of residues in the coiledcoil domain of human immunodeficiency virus type 1 transmembrane protein gp41. J. Virol. 72:9676 -9682.
-
(1998)
J. Virol.
, vol.72
, pp. 9676-9682
-
-
Weng, Y.1
Weiss, C.D.2
-
43
-
-
0027959493
-
Peptides corresponding to a predictive alpha-helical domain of human immunodeficiency virus type 1 gp41 are potent inhibitors of virus infection
-
Wild CT, Shugars DC, Greenwell TK, McDanal CB, Matthews TJ. 1994. Peptides corresponding to a predictive alpha-helical domain of human immunodeficiency virus type 1 gp41 are potent inhibitors of virus infection. Proc. Natl. Acad. Sci. U. S. A. 91:9770 -9774.
-
(1994)
Proc. Natl. Acad. Sci. U. S. A.
, vol.91
, pp. 9770-9774
-
-
Wild, C.T.1
Shugars, D.C.2
Greenwell, T.K.3
McDanal, C.B.4
Matthews, T.J.5
|