메뉴 건너뛰기




Volumn 13, Issue 10, 2017, Pages 1115-1122

Crystal structures of trimeric HIV envelope with entry inhibitors BMS-378806 and BMS-626529

Author keywords

[No Author keywords available]

Indexed keywords

4 BENZOYL 1 [(4 METHOXY 1H PYRROLO[2,3 B]PYRIDIN 3 YL)OXOACETYL] 2 METHYLPIPERAZINE; GLYCOPROTEIN GP 120; SOLVENT; TEMSAVIR; BMS-378806; BMS-626529; GLYCOPROTEIN GP 41; MOLECULAR LIBRARY; PIPERAZINE DERIVATIVE; TRIAZOLE DERIVATIVE;

EID: 85030974417     PISSN: 15524450     EISSN: 15524469     Source Type: Journal    
DOI: 10.1038/nchembio.2460     Document Type: Article
Times cited : (109)

References (60)
  • 1
    • 34147184752 scopus 로고    scopus 로고
    • Continued improvement in survival among HIV-infected individuals with newer forms of highly active antiretroviral therapy
    • Lima, V.D. et al. Continued improvement in survival among HIV-infected individuals with newer forms of highly active antiretroviral therapy. AIDS 21, 685-692 (2007).
    • (2007) AIDS , vol.21 , pp. 685-692
    • Lima, V.D.1
  • 2
    • 84961896758 scopus 로고    scopus 로고
    • Narrowing the gap in life expectancy between HIV-infected and HIV-uninfected individuals with access to care
    • Marcus, J.L. et al. Narrowing the gap in life expectancy between HIV-infected and HIV-uninfected individuals with access to care. J. Acquir. Immune Defic. Syndr. 73, 39-46 (2016).
    • (2016) J. Acquir. Immune Defic. Syndr. , vol.73 , pp. 39-46
    • Marcus, J.L.1
  • 3
    • 0033372529 scopus 로고    scopus 로고
    • Combination antiretroviral therapy and recent declines in AIDS incidence and mortality
    • Vittinghoff, E. et al. Combination antiretroviral therapy and recent declines in AIDS incidence and mortality. J. Infect. Dis. 179, 717-720 (1999).
    • (1999) J. Infect. Dis. , vol.179 , pp. 717-720
    • Vittinghoff, E.1
  • 4
    • 84936846696 scopus 로고    scopus 로고
    • Crystal structure, conformational fixation and entry-related interactions of mature ligand-free HIV-1 env
    • Kwon, Y.D. et al. Crystal structure, conformational fixation and entry-related interactions of mature ligand-free HIV-1 Env. Nat. Struct. Mol. Biol. 22, 522-531 (2015).
    • (2015) Nat. Struct. Mol. Biol. , vol.22 , pp. 522-531
    • Kwon, Y.D.1
  • 5
    • 0032546844 scopus 로고    scopus 로고
    • The HIV-1 envelope glycoproteins: Fusogens, antigens, and immunogens
    • Wyatt, R. & Sodroski, J. The HIV-1 envelope glycoproteins: fusogens, antigens, and immunogens. Science 280, 1884-1888 (1998).
    • (1998) Science , vol.280 , pp. 1884-1888
    • Wyatt, R.1    Sodroski, J.2
  • 6
    • 84909606387 scopus 로고    scopus 로고
    • Conformational dynamics of single HIV-1 envelope trimers on the surface of native virions
    • Munro, J.B. et al. Conformational dynamics of single HIV-1 envelope trimers on the surface of native virions. Science 346, 759-763 (2014).
    • (2014) Science , vol.346 , pp. 759-763
    • Munro, J.B.1
  • 7
    • 0027692502 scopus 로고
    • A synthetic peptide from HIV-1 gp41 is a potent inhibitor of virus-mediated cell-cell fusion
    • Wild, C., Greenwell, T. & Matthews, T. A synthetic peptide from HIV-1 gp41 is a potent inhibitor of virus-mediated cell-cell fusion. AIDS Res. Hum. Retroviruses 9, 1051-1053 (1993).
    • (1993) AIDS Res. Hum. Retroviruses , vol.9 , pp. 1051-1053
    • Wild, C.1    Greenwell, T.2    Matthews, T.3
  • 8
    • 20544456150 scopus 로고    scopus 로고
    • Enfuvirtide: A review of its use in the management of HIV infection
    • Oldfield, V., Keating, G.M. & Plosker, G. Enfuvirtide: a review of its use in the management of HIV infection. Drugs 65, 1139-1160 (2005).
    • (2005) Drugs , vol.65 , pp. 1139-1160
    • Oldfield, V.1    Keating, G.M.2    Plosker, G.3
  • 9
    • 27644510382 scopus 로고    scopus 로고
    • Maraviroc (UK-427,857), a potent, orally bioavailable, and selective small-molecule inhibitor of chemokine receptor CCR5 with broad-spectrum anti-human immunodeficiency virus type 1 activity
    • Dorr, P. et al. Maraviroc (UK-427,857), a potent, orally bioavailable, and selective small-molecule inhibitor of chemokine receptor CCR5 with broad-spectrum anti-human immunodeficiency virus type 1 activity. Antimicrob. Agents Chemother. 49, 4721-4732 (2005).
    • (2005) Antimicrob. Agents Chemother , vol.49 , pp. 4721-4732
    • Dorr, P.1
  • 10
    • 77954920017 scopus 로고    scopus 로고
    • Rational design of envelope identifies broadly neutralizing human monoclonal antibodies to HIV-1
    • Wu, X. et al. Rational design of envelope identifies broadly neutralizing human monoclonal antibodies to HIV-1. Science 329, 856-861 (2010).
    • (2010) Science , vol.329 , pp. 856-861
    • Wu, X.1
  • 11
    • 84866493348 scopus 로고    scopus 로고
    • Broad and potent neutralization of HIV-1 by a gp41-specific human antibody
    • Huang, J. et al. Broad and potent neutralization of HIV-1 by a gp41-specific human antibody. Nature 491, 406-412 (2012).
    • (2012) Nature , vol.491 , pp. 406-412
    • Huang, J.1
  • 12
    • 0028235930 scopus 로고
    • Cross-neutralizing activity against divergent human immunodeficiency virus type 1 isolates induced by the gp41 sequence ELDKWAS
    • Muster, T. et al. Cross-neutralizing activity against divergent human immunodeficiency virus type 1 isolates induced by the gp41 sequence ELDKWAS. J. Virol. 68, 4031-4034 (1994).
    • (1994) J. Virol. , vol.68 , pp. 4031-4034
    • Muster, T.1
  • 13
    • 84999836139 scopus 로고    scopus 로고
    • Identification of a CD4-binding-site antibody to HIV that evolved near-pan neutralization breadth
    • Huang, J. et al. Identification of a CD4-binding-site antibody to HIV that evolved near-pan neutralization breadth. Immunity 45, 1108-1121 (2016).
    • (2016) Immunity , vol.45 , pp. 1108-1121
    • Huang, J.1
  • 14
    • 0032543307 scopus 로고    scopus 로고
    • Structure of an HIV gp120 envelope glycoprotein in complex with the CD4 receptor and a neutralizing human antibody
    • Kwong, P.D. et al. Structure of an HIV gp120 envelope glycoprotein in complex with the CD4 receptor and a neutralizing human antibody. Nature 393, 648-659 (1998).
    • (1998) Nature , vol.393 , pp. 648-659
    • Kwong, P.D.1
  • 15
    • 23844440296 scopus 로고    scopus 로고
    • Identification of N-phenyl-N′-(2,2,6,6-tetramethyl-piperidin-4-yl)-oxalamides as a new class of HIV-1 entry inhibitors that prevent gp120 binding to CD4
    • Zhao, Q. et al. Identification of N-phenyl-N′-(2,2,6,6-tetramethyl-piperidin-4-yl)-oxalamides as a new class of HIV-1 entry inhibitors that prevent gp120 binding to CD4. Virology 339, 213-225 (2005).
    • (2005) Virology , vol.339 , pp. 213-225
    • Zhao, Q.1
  • 16
    • 84861048825 scopus 로고    scopus 로고
    • Structure-based design, synthesis, and characterization of dual hotspot small-molecule HIV-1 entry inhibitors
    • LaLonde, J.M. et al. Structure-based design, synthesis, and characterization of dual hotspot small-molecule HIV-1 entry inhibitors. J. Med. Chem. 55, 4382-4396 (2012).
    • (2012) J. Med. Chem. , vol.55 , pp. 4382-4396
    • LaLonde, J.M.1
  • 17
    • 55249083812 scopus 로고    scopus 로고
    • Small-molecule CD4 mimics interact with a highly conserved pocket on HIV-1 gp120
    • Madani, N. et al. Small-molecule CD4 mimics interact with a highly conserved pocket on HIV-1 gp120. Structure 16, 1689-1701 (2008).
    • (2008) Structure , vol.16 , pp. 1689-1701
    • Madani, N.1
  • 18
    • 21044438453 scopus 로고    scopus 로고
    • Scorpion-toxin mimics of CD4 in complex with human immunodeficiency virus gp120 crystal structures, molecular mimicry, and neutralization breadth
    • Huang, C.C. et al. Scorpion-toxin mimics of CD4 in complex with human immunodeficiency virus gp120 crystal structures, molecular mimicry, and neutralization breadth. Structure 13, 755-768 (2005).
    • (2005) Structure , vol.13 , pp. 755-768
    • Huang, C.C.1
  • 19
    • 0141680855 scopus 로고    scopus 로고
    • Discovery of 4-benzoyl-1-[(4-methoxy-1H-pyrrolo[2,3-b]pyridin-3-yl)oxoacetyl]-2- (R)-methylpiperazine (BMS-378806): A novel HIV-1 attachment inhibitor that interferes with CD4-gp120 interactions
    • Wang, T. et al. Discovery of 4-benzoyl-1-[(4-methoxy-1H-pyrrolo[2,3-b]pyridin-3-yl)oxoacetyl]-2- (R)-methylpiperazine (BMS-378806): a novel HIV-1 attachment inhibitor that interferes with CD4-gp120 interactions. J. Med. Chem. 46, 4236-4239 (2003).
    • (2003) J. Med. Chem. , vol.46 , pp. 4236-4239
    • Wang, T.1
  • 20
    • 0141856289 scopus 로고    scopus 로고
    • Biochemical and genetic characterizations of a novel human immunodeficiency virus type 1 inhibitor that blocks gp120-CD4 interactions
    • Guo, Q. et al. Biochemical and genetic characterizations of a novel human immunodeficiency virus type 1 inhibitor that blocks gp120-CD4 interactions. J. Virol. 77, 10528-10536 (2003).
    • (2003) J. Virol. , vol.77 , pp. 10528-10536
    • Guo, Q.1
  • 21
    • 33645766774 scopus 로고    scopus 로고
    • Envelope conformational changes induced by human immunodeficiency virus type 1 attachment inhibitors prevent CD4 binding and downstream entry events
    • Ho, H.T. et al. Envelope conformational changes induced by human immunodeficiency virus type 1 attachment inhibitors prevent CD4 binding and downstream entry events. J. Virol. 80, 4017-4025 (2006).
    • (2006) J. Virol. , vol.80 , pp. 4017-4025
    • Ho, H.T.1
  • 22
    • 0141703204 scopus 로고    scopus 로고
    • A small molecule HIV-1 inhibitor that targets the HIV-1 envelope and inhibits CD4 receptor binding
    • Lin, P.F. et al. A small molecule HIV-1 inhibitor that targets the HIV-1 envelope and inhibits CD4 receptor binding. Proc. Natl. Acad. Sci. USA 100, 11013-11018 (2003).
    • (2003) Proc. Natl. Acad. Sci. USA , vol.100 , pp. 11013-11018
    • Lin, P.F.1
  • 23
    • 72249103816 scopus 로고    scopus 로고
    • Inhibitors of human immunodeficiency virus type 1 (HIV-1) attachment. 5. An evolution from indole to azaindoles leading to the discovery of 1-(4-benzoylpiperazin-1-yl)-2-(4,7-dimethoxy-1H-pyrrolo[2,3-c]pyridin-3-yl)ethane-1,2-dione (BMS-488043), a drug candidate that demonstrates antiviral activity in HIV-1-infected subjects
    • Wang, T. et al. Inhibitors of human immunodeficiency virus type 1 (HIV-1) attachment. 5. An evolution from indole to azaindoles leading to the discovery of 1-(4-benzoylpiperazin-1-yl)-2-(4,7-dimethoxy-1H-pyrrolo[2,3-c]pyridin-3-yl)ethane-1,2-dione (BMS-488043), a drug candidate that demonstrates antiviral activity in HIV-1-infected subjects. J. Med. Chem. 52, 7778-7787 (2009).
    • (2009) J. Med. Chem. , vol.52 , pp. 7778-7787
    • Wang, T.1
  • 24
    • 33747622811 scopus 로고    scopus 로고
    • Small-molecule HIV-1 gp120 inhibitors to prevent HIV-1 entry: An emerging opportunity for drug development
    • Kadow, J., Wang, H.G. & Lin, P.F. Small-molecule HIV-1 gp120 inhibitors to prevent HIV-1 entry: an emerging opportunity for drug development. Curr. Opin. Investig. Drugs 7, 721-726 (2006).
    • (2006) Curr. Opin. Investig. Drugs , vol.7 , pp. 721-726
    • Kadow, J.1    Wang, H.G.2    Lin, P.F.3
  • 25
    • 84862569941 scopus 로고    scopus 로고
    • In vitro antiviral characteristics of HIV-1 attachment inhibitor BMS-626529, the active component of the prodrug BMS-663068
    • Nowicka-Sans, B. et al. In vitro antiviral characteristics of HIV-1 attachment inhibitor BMS-626529, the active component of the prodrug BMS-663068. Antimicrob. Agents Chemother. 56, 3498-3507 (2012).
    • (2012) Antimicrob. Agents Chemother , vol.56 , pp. 3498-3507
    • Nowicka-Sans, B.1
  • 26
    • 84877927926 scopus 로고    scopus 로고
    • Compartmental absorption modeling and site of absorption studies to determine feasibility of an extended-release formulation of an HIV-1 attachment inhibitor phosphate ester prodrug
    • Brown, J. et al. Compartmental absorption modeling and site of absorption studies to determine feasibility of an extended-release formulation of an HIV-1 attachment inhibitor phosphate ester prodrug. J. Pharm. Sci. 102, 1742-1751 (2013).
    • (2013) J. Pharm. Sci. , vol.102 , pp. 1742-1751
    • Brown, J.1
  • 27
    • 84947033432 scopus 로고    scopus 로고
    • Safety and efficacy of the HIV-1 attachment inhibitor prodrug BMS-663068 in treatment-experienced individuals: 24 week results of AI438011, a phase 2b, randomised controlled trial
    • Lalezari, J.P. et al. Safety and efficacy of the HIV-1 attachment inhibitor prodrug BMS-663068 in treatment-experienced individuals: 24 week results of AI438011, a phase 2b, randomised controlled trial. Lancet HIV 2, e427-e437 (2015).
    • (2015) Lancet HIV , vol.2 , pp. e427-e437
    • Lalezari, J.P.1
  • 28
    • 84866124136 scopus 로고    scopus 로고
    • Pharmacodynamics, safety, and pharmacokinetics of BMS-663068, an oral HIV-1 attachment inhibitor in HIV-1-infected subjects
    • Nettles, R.E. et al. Pharmacodynamics, safety, and pharmacokinetics of BMS-663068, an oral HIV-1 attachment inhibitor in HIV-1-infected subjects. J. Infect. Dis. 206, 1002-1011 (2012).
    • (2012) J. Infect. Dis. , vol.206 , pp. 1002-1011
    • Nettles, R.E.1
  • 29
    • 84883462497 scopus 로고    scopus 로고
    • Prediction of virological response and assessment of resistance emergence to the HIV-1 attachment inhibitor BMS-626529 during 8-day monotherapy with its prodrug BMS-663068
    • Ray, N. et al. Prediction of virological response and assessment of resistance emergence to the HIV-1 attachment inhibitor BMS-626529 during 8-day monotherapy with its prodrug BMS-663068. J. Acquir. Immune Defic. Syndr. 64, 7-15 (2013).
    • (2013) J. Acquir. Immune Defic. Syndr. , vol.64 , pp. 7-15
    • Ray, N.1
  • 30
    • 84894062192 scopus 로고    scopus 로고
    • Genotypic correlates of susceptibility to HIV-1 attachment inhibitor BMS-626529, the active agent of the prodrug BMS-663068
    • Zhou, N. et al. Genotypic correlates of susceptibility to HIV-1 attachment inhibitor BMS-626529, the active agent of the prodrug BMS-663068. J. Antimicrob. Chemother. 69, 573-581 (2014).
    • (2014) J. Antimicrob. Chemother , vol.69 , pp. 573-581
    • Zhou, N.1
  • 31
    • 84909640954 scopus 로고    scopus 로고
    • Structure and immune recognition of trimeric pre-fusion HIV-1 env
    • Pancera, M. et al. Structure and immune recognition of trimeric pre-fusion HIV-1 Env. Nature 514, 455-461 (2014).
    • (2014) Nature , vol.514 , pp. 455-461
    • Pancera, M.1
  • 32
    • 84884678235 scopus 로고    scopus 로고
    • A next-generation cleaved, soluble HIV-1 env trimer, BG505 SOSIP.664 gp140, expresses multiple epitopes for broadly neutralizing but not non-neutralizing antibodies
    • Sanders, R.W. et al. A next-generation cleaved, soluble HIV-1 Env trimer, BG505 SOSIP.664 gp140, expresses multiple epitopes for broadly neutralizing but not non-neutralizing antibodies. PLoS Pathog. 9, e1003618 (2013).
    • (2013) PLoS Pathog. , vol.9 , pp. e1003618
    • Sanders, R.W.1
  • 33
    • 11144358392 scopus 로고    scopus 로고
    • Small-molecule inhibitors of HIV-1 entry block receptor-induced conformational changes in the viral envelope glycoproteins
    • Si, Z. et al. Small-molecule inhibitors of HIV-1 entry block receptor-induced conformational changes in the viral envelope glycoproteins. Proc. Natl. Acad. Sci. USA 101, 5036-5041 (2004).
    • (2004) Proc. Natl. Acad. Sci. USA , vol.101 , pp. 5036-5041
    • Si, Z.1
  • 34
    • 80053132436 scopus 로고    scopus 로고
    • Broad neutralization coverage of HIV by multiple highly potent antibodies
    • Walker, L.M. et al. Broad neutralization coverage of HIV by multiple highly potent antibodies. Nature 477, 466-470 (2011).
    • (2011) Nature , vol.477 , pp. 466-470
    • Walker, L.M.1
  • 35
    • 84921607768 scopus 로고    scopus 로고
    • Broad and potent HIV-1 neutralization by a human antibody that binds the gp41-gp120 interface
    • Huang, J. et al. Broad and potent HIV-1 neutralization by a human antibody that binds the gp41-gp120 interface. Nature 515, 138-142 (2014).
    • (2014) Nature , vol.515 , pp. 138-142
    • Huang, J.1
  • 36
    • 33744459472 scopus 로고    scopus 로고
    • Toward the structural genomics of complexes: Crystal structure of a PE/PPE protein complex from mycobacterium tuberculosis
    • Strong, M. et al. Toward the structural genomics of complexes: crystal structure of a PE/PPE protein complex from Mycobacterium tuberculosis. Proc. Natl. Acad. Sci. USA 103, 8060-8065 (2006).
    • (2006) Proc. Natl. Acad. Sci. USA , vol.103 , pp. 8060-8065
    • Strong, M.1
  • 37
    • 1842562351 scopus 로고    scopus 로고
    • Localized changes in the gp120 envelope glycoprotein confer resistance to human immunodeficiency virus entry inhibitors BMS-806 and #155
    • Madani, N. et al. Localized changes in the gp120 envelope glycoprotein confer resistance to human immunodeficiency virus entry inhibitors BMS-806 and #155. J. Virol. 78, 3742-3752 (2004).
    • (2004) J. Virol. , vol.78 , pp. 3742-3752
    • Madani, N.1
  • 38
    • 78751688945 scopus 로고    scopus 로고
    • In vivo patterns of resistance to the HIV attachment inhibitor BMS-488043
    • Zhou, N. et al. In vivo patterns of resistance to the HIV attachment inhibitor BMS-488043. Antimicrob. Agents Chemother. 55, 729-737 (2011).
    • (2011) Antimicrob. Agents Chemother , vol.55 , pp. 729-737
    • Zhou, N.1
  • 39
    • 84864386257 scopus 로고    scopus 로고
    • HIV gp120 H375 is unique to HIV-1 subtype CRF01-AE and confers strong resistance to the entry inhibitor BMS-599793, a candidate microbicide drug
    • Schader, S.M. et al. HIV gp120 H375 is unique to HIV-1 subtype CRF01-AE and confers strong resistance to the entry inhibitor BMS-599793, a candidate microbicide drug. Antimicrob. Agents Chemother. 56, 4257-4267 (2012).
    • (2012) Antimicrob. Agents Chemother , vol.56 , pp. 4257-4267
    • Schader, S.M.1
  • 40
    • 84922062993 scopus 로고    scopus 로고
    • A broad HIV-1 inhibitor blocks envelope glycoprotein transitions critical for entry
    • Herschhorn, A. et al. A broad HIV-1 inhibitor blocks envelope glycoprotein transitions critical for entry. Nat. Chem. Biol. 10, 845-852 (2014).
    • (2014) Nat. Chem. Biol. , vol.10 , pp. 845-852
    • Herschhorn, A.1
  • 41
    • 84994422976 scopus 로고    scopus 로고
    • Release of gp120 restraints leads to an entry-competent intermediate state of the HIV-1 envelope glycoproteins
    • Herschhorn, A. et al. Release of gp120 restraints leads to an entry-competent intermediate state of the HIV-1 envelope glycoproteins. MBio 7, e01598-16 (2016).
    • (2016) MBio , vol.7 , pp. e01598-e01616
    • Herschhorn, A.1
  • 42
    • 75749133275 scopus 로고    scopus 로고
    • Structure of HIV-1 gp120 with gp41-interactive region reveals layered envelope architecture and basis of conformational mobility
    • Pancera, M. et al. Structure of HIV-1 gp120 with gp41-interactive region reveals layered envelope architecture and basis of conformational mobility. Proc. Natl. Acad. Sci. USA 107, 1166-1171 (2010).
    • (2010) Proc. Natl. Acad. Sci. USA , vol.107 , pp. 1166-1171
    • Pancera, M.1
  • 43
    • 84929354492 scopus 로고    scopus 로고
    • Homology models of the HIV-1 attachment inhibitor BMS-626529 bound to gp120 suggest a unique mechanism of action
    • Langley, D.R. et al. Homology models of the HIV-1 attachment inhibitor BMS-626529 bound to gp120 suggest a unique mechanism of action. Proteins 83, 331-350 (2015).
    • (2015) Proteins , vol.83 , pp. 331-350
    • Langley, D.R.1
  • 44
    • 33745116948 scopus 로고    scopus 로고
    • Prediction of the binding mode between BMS-378806 and HIV-1 gp120 by docking and molecular dynamics simulation
    • Kong, R., Tan, J.J., Ma, X.H., Chen, W.Z. & Wang, C.X. Prediction of the binding mode between BMS-378806 and HIV-1 gp120 by docking and molecular dynamics simulation. Biochim. Biophys. Acta 1764, 766-772 (2006).
    • (2006) Biochim. Biophys. Acta , vol.1764 , pp. 766-772
    • Kong, R.1    Tan, J.J.2    Ma, X.H.3    Chen, W.Z.4    Wang, C.X.5
  • 45
    • 67650395305 scopus 로고    scopus 로고
    • Docking and 3D-QSAR studies of BMS-806 analogs as HIV-1 gp120 entry inhibitors
    • Teixeira, C., Serradji, N., Maurel, F. & Barbault, F. Docking and 3D-QSAR studies of BMS-806 analogs as HIV-1 gp120 entry inhibitors. Eur. J. Med. Chem. 44, 3524-3532 (2009).
    • (2009) Eur. J. Med. Chem. , vol.44 , pp. 3524-3532
    • Teixeira, C.1    Serradji, N.2    Maurel, F.3    Barbault, F.4
  • 46
    • 84877103976 scopus 로고    scopus 로고
    • The investigations on HIV-1 gp120 bound with BMS-488043 by using docking and molecular dynamics simulations
    • Li, L., Chen, H., Zhao, R.N. & Han, J.G. The investigations on HIV-1 gp120 bound with BMS-488043 by using docking and molecular dynamics simulations. J. Mol. Model. 19, 905-917 (2013).
    • (2013) J. Mol. Model. , vol.19 , pp. 905-917
    • Li, L.1    Chen, H.2    Zhao, R.N.3    Han, J.G.4
  • 47
    • 85013157801 scopus 로고    scopus 로고
    • Quaternary contact in the initial interaction of CD4 with the HIV-1 envelope trimer
    • Liu, Q. et al. Quaternary contact in the initial interaction of CD4 with the HIV-1 envelope trimer. Nat. Struct. Mol. Biol. 24, 370-378 (2017).
    • (2017) Nat. Struct. Mol. Biol. , vol.24 , pp. 370-378
    • Liu, Q.1
  • 48
    • 84904127504 scopus 로고    scopus 로고
    • CD4-induced activation in a soluble HIV-1 env trimer
    • Guttman, M. et al. CD4-induced activation in a soluble HIV-1 Env trimer. Structure 22, 974-984 (2014).
    • (2014) Structure , vol.22 , pp. 974-984
    • Guttman, M.1
  • 49
    • 79955744829 scopus 로고    scopus 로고
    • Understanding the binding mode and function of BMS-488043 against HIV-1 viral entry
    • Da, L.T., Quan, J.M. & Wu, Y.D. Understanding the binding mode and function of BMS-488043 against HIV-1 viral entry. Proteins 79, 1810-1819 (2011).
    • (2011) Proteins , vol.79 , pp. 1810-1819
    • Da, L.T.1    Quan, J.M.2    Wu, Y.D.3
  • 50
    • 84867071637 scopus 로고    scopus 로고
    • Spontaneous rearrangement of the β20/β21 strands in simulations of unliganded HIV-1 glycoprotein, gp120
    • Shrivastava, I.H., Wendel, K. & LaLonde, J.M. Spontaneous rearrangement of the β20/β21 strands in simulations of unliganded HIV-1 glycoprotein, gp120. Biochemistry 51, 7783-7793 (2012).
    • (2012) Biochemistry , vol.51 , pp. 7783-7793
    • Shrivastava, I.H.1    Wendel, K.2    LaLonde, J.M.3
  • 51
    • 23244434512 scopus 로고    scopus 로고
    • Human immunodeficiency virus type 1 env clones from acute and early subtype B infections for standardized assessments of vaccine-elicited neutralizing antibodies
    • Li, M. et al. Human immunodeficiency virus type 1 env clones from acute and early subtype B infections for standardized assessments of vaccine-elicited neutralizing antibodies. J. Virol. 79, 10108-10125 (2005).
    • (2005) J. Virol. , vol.79 , pp. 10108-10125
    • Li, M.1
  • 52
    • 73949127978 scopus 로고    scopus 로고
    • Tiered categorization of a diverse panel of HIV-1 env pseudoviruses for assessment of neutralizing antibodies
    • Seaman, M.S. et al. Tiered categorization of a diverse panel of HIV-1 Env pseudoviruses for assessment of neutralizing antibodies. J. Virol. 84, 1439-1452 (2010).
    • (2010) J. Virol. , vol.84 , pp. 1439-1452
    • Seaman, M.S.1
  • 53
    • 0031059866 scopus 로고    scopus 로고
    • Processing of X-ray diffraction data collected in oscillation mode
    • Otwinowski, Z. & Minor, W. Processing of X-ray diffraction data collected in oscillation mode. Methods Enzymol. 276, 307-326 (1997).
    • (1997) Methods Enzymol. , vol.276 , pp. 307-326
    • Otwinowski, Z.1    Minor, W.2
  • 54
    • 0035066836 scopus 로고    scopus 로고
    • Global indicators of X-ray data quality
    • Weiss, M.S. Global indicators of X-ray data quality. J. Appl. Crystallogr. 34, 130-135 (2001).
    • (2001) J. Appl. Crystallogr , vol.34 , pp. 130-135
    • Weiss, M.S.1
  • 55
    • 84861425552 scopus 로고    scopus 로고
    • Linking crystallographic model and data quality
    • Karplus, P.A. & Diederichs, K. Linking crystallographic model and data quality. Science 336, 1030-1033 (2012).
    • (2012) Science , vol.336 , pp. 1030-1033
    • Karplus, P.A.1    Diederichs, K.2
  • 56
    • 0028103275 scopus 로고
    • The CCP4 suite: Programs for protein crystallography
    • Collaborative Computational Project
    • Collaborative Computational Project, Number 4. The CCP4 suite: programs for protein crystallography. Acta Crystallogr. D Biol. Crystallogr. 50, 760-763 (1994).
    • (1994) Acta Crystallogr. D Biol. Crystallogr , vol.50 , Issue.4 , pp. 760-763
  • 57
  • 58
    • 76449098262 scopus 로고    scopus 로고
    • PHENIX: A comprehensive python-based system for macromolecular structure solution
    • Adams, P.D. et al. PHENIX: a comprehensive Python-based system for macromolecular structure solution. Acta Crystallogr. D Biol. Crystallogr. 66, 213-221 (2010).
    • (2010) Acta Crystallogr. D Biol. Crystallogr , vol.66 , pp. 213-221
    • Adams, P.D.1
  • 59
    • 3242886389 scopus 로고    scopus 로고
    • MOLPROBITY: Structure validation and all-atom contact analysis for nucleic acids and their complexes
    • Davis, I.W., Murray, L.W., Richardson, J.S. & Richardson, D.C. MOLPROBITY: structure validation and all-atom contact analysis for nucleic acids and their complexes. Nucleic Acids Res. 32, W615-W619 (2004).
    • (2004) Nucleic Acids Res. , vol.32 , pp. W615-W619
    • Davis, I.W.1    Murray, L.W.2    Richardson, J.S.3    Richardson, D.C.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.