-
1
-
-
34147184752
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
-
-
58
-
-
76449098262
-
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
-
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
|