-
1
-
-
0035663379
-
Infection with HIV-2
-
Bock P.J., and Markovitz D.M. Infection with HIV-2. AIDS 15 (2001) S35-S45
-
(2001)
AIDS
, vol.15
-
-
Bock, P.J.1
Markovitz, D.M.2
-
2
-
-
27244461500
-
Epidemiology and natural history of HIV-2
-
Kanki P.J., and De Cock K.M. Epidemiology and natural history of HIV-2. AIDS 8 (1994) S85-S93
-
(1994)
AIDS
, vol.8
-
-
Kanki, P.J.1
De Cock, K.M.2
-
3
-
-
34748817979
-
HIV-1 and HIV-2 prevalence and associated risk factors among postnatal women in Harare, Zimbabwe
-
& the ZVITAMBO Study Group
-
Humphrey J.H., Nathoo K.J., Hargrove J.W., Iliff P.J., Mutasa K.E., Moulton L.H., et al., & the ZVITAMBO Study Group. HIV-1 and HIV-2 prevalence and associated risk factors among postnatal women in Harare, Zimbabwe. Epidemiol. Infect. 135 (2007) 933-942
-
(2007)
Epidemiol. Infect.
, vol.135
, pp. 933-942
-
-
Humphrey, J.H.1
Nathoo, K.J.2
Hargrove, J.W.3
Iliff, P.J.4
Mutasa, K.E.5
Moulton, L.H.6
-
4
-
-
16744369116
-
Human immunodeficiency virus type 2 (HIV-2) in Portugal: clinical spectrum, circulating subtypes, virus isolation, and plasma viral load
-
Soriano V., Gomes P., Heneine W., Holgiun A., Doruana M., Antunes R., et al. Human immunodeficiency virus type 2 (HIV-2) in Portugal: clinical spectrum, circulating subtypes, virus isolation, and plasma viral load. J. Med. Virol. 61 (2000) 111-116
-
(2000)
J. Med. Virol.
, vol.61
, pp. 111-116
-
-
Soriano, V.1
Gomes, P.2
Heneine, W.3
Holgiun, A.4
Doruana, M.5
Antunes, R.6
-
5
-
-
37349047404
-
Prevalence of HIV-2 and HIV-1 group O infections among new HIV diagnoses in France: 2003-2006
-
Barin F., Cazein F., Lot F., Pillonel J., Brunet S., Thierry D., et al. Prevalence of HIV-2 and HIV-1 group O infections among new HIV diagnoses in France: 2003-2006. AIDS 21 (2007) 2351-2353
-
(2007)
AIDS
, vol.21
, pp. 2351-2353
-
-
Barin, F.1
Cazein, F.2
Lot, F.3
Pillonel, J.4
Brunet, S.5
Thierry, D.6
-
6
-
-
0028102110
-
Reduced rate of disease development after HIV-2 infection as compared to HIV-1
-
Marlink R., Kanki P.J., Thior I., Travers K., Eisen G., Siby T., et al. Reduced rate of disease development after HIV-2 infection as compared to HIV-1. Science 265 (1994) 1587-1590
-
(1994)
Science
, vol.265
, pp. 1587-1590
-
-
Marlink, R.1
Kanki, P.J.2
Thior, I.3
Travers, K.4
Eisen, G.5
Siby, T.6
-
7
-
-
0242608112
-
Factors associated with clinical progression in HIV-2 infected patients: the French ANRS Cohort
-
French HIV-2 Cohort Study Group
-
Matheron S., Pueyo S., Damond F., Simon F., Leprêtre A., Campa P., et al., French HIV-2 Cohort Study Group. Factors associated with clinical progression in HIV-2 infected patients: the French ANRS Cohort. AIDS 17 (2003) 2593-2601
-
(2003)
AIDS
, vol.17
, pp. 2593-2601
-
-
Matheron, S.1
Pueyo, S.2
Damond, F.3
Simon, F.4
Leprêtre, A.5
Campa, P.6
-
8
-
-
21644472626
-
The replicative fitness of primary human immunodeficiency virus type 1 (HIV-1) group M, HIV-1 group O, and HIV-2 isolates
-
Ariën K.K., Abraha A., Quiñones-Mateu M.E., Kestens L., Vanham G., and Arts E.J. The replicative fitness of primary human immunodeficiency virus type 1 (HIV-1) group M, HIV-1 group O, and HIV-2 isolates. J. Virol. 79 (2005) 8979-8990
-
(2005)
J. Virol.
, vol.79
, pp. 8979-8990
-
-
Ariën, K.K.1
Abraha, A.2
Quiñones-Mateu, M.E.3
Kestens, L.4
Vanham, G.5
Arts, E.J.6
-
9
-
-
0034628636
-
Genetic analysis of HIV type 2 in monotypic and dual HIV infections
-
Sarr A.D., Sankale J.L., Gueye-Ndiaye A., Essex M., Mboup S., and Kanki P.J. Genetic analysis of HIV type 2 in monotypic and dual HIV infections. AIDS Res. Hum. Retroviruses 16 (2000) 295-298
-
(2000)
AIDS Res. Hum. Retroviruses
, vol.16
, pp. 295-298
-
-
Sarr, A.D.1
Sankale, J.L.2
Gueye-Ndiaye, A.3
Essex, M.4
Mboup, S.5
Kanki, P.J.6
-
10
-
-
0034943095
-
Antiretroviral therapy for HIV-2 infected patients
-
Smith N.A., Shaw T., Berry N., Vella C., Okorafor L., Taylor D., et al. Antiretroviral therapy for HIV-2 infected patients. J. Infect. 42 (2001) 126-133
-
(2001)
J. Infect.
, vol.42
, pp. 126-133
-
-
Smith, N.A.1
Shaw, T.2
Berry, N.3
Vella, C.4
Okorafor, L.5
Taylor, D.6
-
11
-
-
0033999842
-
Emergence of drug resistant mutations in human immunodeficiency virus type 2-infected subjects undergoing antiretroviral therapy
-
Rodes B., Holgiun A., Soriano V., Dourana M., Mansinho K., Antunes F., and Gonzalez-Lahoz J. Emergence of drug resistant mutations in human immunodeficiency virus type 2-infected subjects undergoing antiretroviral therapy. J. Clin. Microbiol. 38 (2000) 1370-1374
-
(2000)
J. Clin. Microbiol.
, vol.38
, pp. 1370-1374
-
-
Rodes, B.1
Holgiun, A.2
Soriano, V.3
Dourana, M.4
Mansinho, K.5
Antunes, F.6
Gonzalez-Lahoz, J.7
-
12
-
-
0035958773
-
Overview of the effectiveness of triple combination therapy in antiretroviral-naïve HIV-1 infected adults
-
Barlett J.A., DeMasi R., Quinn J., Moxham C., and Rousseau F. Overview of the effectiveness of triple combination therapy in antiretroviral-naïve HIV-1 infected adults. AIDS 15 (2001) 1369-1377
-
(2001)
AIDS
, vol.15
, pp. 1369-1377
-
-
Barlett, J.A.1
DeMasi, R.2
Quinn, J.3
Moxham, C.4
Rousseau, F.5
-
13
-
-
0031804609
-
Inhibitors of HIV-1 protease: a major success in structure-assisted drug design
-
Wlodawer A., and Vondrasek J. Inhibitors of HIV-1 protease: a major success in structure-assisted drug design. Annu. Rev. Biophys. Biomol. Struct. 27 (1998) 249-284
-
(1998)
Annu. Rev. Biophys. Biomol. Struct.
, vol.27
, pp. 249-284
-
-
Wlodawer, A.1
Vondrasek, J.2
-
14
-
-
46649109609
-
Structures of HIV protease guide inhibitor design to overcome drug resistance
-
Caldwell G.W., Atta-ur-Rahman M.R., Player, and Choudhary M.I. (Eds), Bentham Science Publishers, International (UAE, USA, The Netherlands, Pakistan)
-
Weber I.T., Kovalevsky A.Y., and Harrison R.W. Structures of HIV protease guide inhibitor design to overcome drug resistance. In: Caldwell G.W., Atta-ur-Rahman M.R., Player, and Choudhary M.I. (Eds). Frontiers in Drug Design and Discovery vol. 3 (2007), Bentham Science Publishers, International (UAE, USA, The Netherlands, Pakistan) 45-62
-
(2007)
Frontiers in Drug Design and Discovery
, vol.3
, pp. 45-62
-
-
Weber, I.T.1
Kovalevsky, A.Y.2
Harrison, R.W.3
-
15
-
-
19944429697
-
Polymorphism of the human immunodeficiency virus type 2 (HIV-2) protease gene and selection of drug resistant mutations in HIV-2-infected patients treated with protease inhibitors
-
Damond F., Brun-Vezinet F., Matheron S., Peytavin G., Campa P., Pueyo S., et al. Polymorphism of the human immunodeficiency virus type 2 (HIV-2) protease gene and selection of drug resistant mutations in HIV-2-infected patients treated with protease inhibitors. J. Clin. Microbiol. 43 (2005) 484-487
-
(2005)
J. Clin. Microbiol.
, vol.43
, pp. 484-487
-
-
Damond, F.1
Brun-Vezinet, F.2
Matheron, S.3
Peytavin, G.4
Campa, P.5
Pueyo, S.6
-
16
-
-
33645121140
-
Susceptibility of protease inhibitors in HIV-2 primary isolates from patients failing antiretroviral therapy
-
Rodes B., Sheldon J., Toro C., Jimenez V., Alvarez M.A., and Soriano V. Susceptibility of protease inhibitors in HIV-2 primary isolates from patients failing antiretroviral therapy. J. Antimicrob. Chemother. 57 (2006) 709-713
-
(2006)
J. Antimicrob. Chemother.
, vol.57
, pp. 709-713
-
-
Rodes, B.1
Sheldon, J.2
Toro, C.3
Jimenez, V.4
Alvarez, M.A.5
Soriano, V.6
-
17
-
-
33846648687
-
Natural polymorphisms in the human immunodeficiency virus type 2 protease can accelerate time to development of resistance to protease inhibitors
-
Ntemgwa M., Brenner B.G., Oliveira M., Moisi D., and Wainberg M.A. Natural polymorphisms in the human immunodeficiency virus type 2 protease can accelerate time to development of resistance to protease inhibitors. Antimicrob. Agents Chemother. 51 (2007) 604-610
-
(2007)
Antimicrob. Agents Chemother.
, vol.51
, pp. 604-610
-
-
Ntemgwa, M.1
Brenner, B.G.2
Oliveira, M.3
Moisi, D.4
Wainberg, M.A.5
-
18
-
-
37549038589
-
HIV-1 protease inhibitors: effects on HIV-2 replication and resistance
-
Menéndez-Arias L., and Tözsér J. HIV-1 protease inhibitors: effects on HIV-2 replication and resistance. Trends Pharmacol. Sci. 29 (2008) 42-49
-
(2008)
Trends Pharmacol. Sci.
, vol.29
, pp. 42-49
-
-
Menéndez-Arias, L.1
Tözsér, J.2
-
19
-
-
0025989978
-
Comparative analysis of the sequences and structures of HIV-1 and HIV-2 proteases
-
Gustchina A., and Weber I.T. Comparative analysis of the sequences and structures of HIV-1 and HIV-2 proteases. Proteins 10 (1991) 325-339
-
(1991)
Proteins
, vol.10
, pp. 325-339
-
-
Gustchina, A.1
Weber, I.T.2
-
20
-
-
0027943157
-
Crystal structure at 1.9-Å resolution of human immunodeficiency virus (HIV) II protease complexed with L-735,524, an orally bioavailable inhibitor of the HIV protease
-
Chen Z., Li Y., Chen E., Hall D.L., Darke P.L., Culberson C., et al. Crystal structure at 1.9-Å resolution of human immunodeficiency virus (HIV) II protease complexed with L-735,524, an orally bioavailable inhibitor of the HIV protease. J. Biol. Chem. 269 (1994) 26344-26348
-
(1994)
J. Biol. Chem.
, vol.269
, pp. 26344-26348
-
-
Chen, Z.1
Li, Y.2
Chen, E.3
Hall, D.L.4
Darke, P.L.5
Culberson, C.6
-
21
-
-
12144290826
-
HIV-2 protease sequences of subtypes A and B harbor multiple mutations associated with protease inhibitor resistance in HIV-1
-
Pieniazek D., Rayfield M., Hu D.J., Nkengasong J.N., Soriano V., Heneine W., et al. HIV-2 protease sequences of subtypes A and B harbor multiple mutations associated with protease inhibitor resistance in HIV-1. AIDS 18 (2004) 495-502
-
(2004)
AIDS
, vol.18
, pp. 495-502
-
-
Pieniazek, D.1
Rayfield, M.2
Hu, D.J.3
Nkengasong, J.N.4
Soriano, V.5
Heneine, W.6
-
22
-
-
0027321544
-
Crystal structure of human immunodeficiency virus (HIV) type 2 protease in complex with a reduced amide inhibitor and comparison with HIV-1 protease structures
-
Tong L., Pav S., Pargellis C., Do F., Lamarre D., and Anderson P.C. Crystal structure of human immunodeficiency virus (HIV) type 2 protease in complex with a reduced amide inhibitor and comparison with HIV-1 protease structures. Proc. Natl Acad. Sci. USA 90 (1993) 8387-8391
-
(1993)
Proc. Natl Acad. Sci. USA
, vol.90
, pp. 8387-8391
-
-
Tong, L.1
Pav, S.2
Pargellis, C.3
Do, F.4
Lamarre, D.5
Anderson, P.C.6
-
23
-
-
0027370067
-
The crystallographic structure of the protease from human immunodeficiency virus type 2 with two synthetic peptidic transition state analog inhibitors
-
Mulichak A.M., Hui J.O., Tomasselli A.G., Heinrikson R.L., Curry K.A., Tomich C.-S., et al. The crystallographic structure of the protease from human immunodeficiency virus type 2 with two synthetic peptidic transition state analog inhibitors. J. Biol. Chem. 268 (1993) 13103-13109
-
(1993)
J. Biol. Chem.
, vol.268
, pp. 13103-13109
-
-
Mulichak, A.M.1
Hui, J.O.2
Tomasselli, A.G.3
Heinrikson, R.L.4
Curry, K.A.5
Tomich, C.-S.6
-
24
-
-
0029643790
-
Crystal structures of HIV-2 protease in complex with inhibitors containing the hydroxyethylamine dipeptide isostere
-
Tong L., Pav S., Mui S., Lamarre D., Yoakim C., Beaulieu P., and Anderson P.C. Crystal structures of HIV-2 protease in complex with inhibitors containing the hydroxyethylamine dipeptide isostere. Structure 3 (1995) 33-40
-
(1995)
Structure
, vol.3
, pp. 33-40
-
-
Tong, L.1
Pav, S.2
Mui, S.3
Lamarre, D.4
Yoakim, C.5
Beaulieu, P.6
Anderson, P.C.7
-
25
-
-
54249094386
-
Comparative analysis of the X-ray structures of HIV-1 and HIV-2 proteases in complex with CGP 53820, a novel pseudosymmetric inhibitor
-
Priestle J.P., Fässler A., Rösel J., Tintelnot-Blomley M., Strop P., and Grütter M.G. Comparative analysis of the X-ray structures of HIV-1 and HIV-2 proteases in complex with CGP 53820, a novel pseudosymmetric inhibitor. Structure 15 (2006) 381-389
-
(2006)
Structure
, vol.15
, pp. 381-389
-
-
Priestle, J.P.1
Fässler, A.2
Rösel, J.3
Tintelnot-Blomley, M.4
Strop, P.5
Grütter, M.G.6
-
26
-
-
38949203748
-
Design of HIV protease inhibitors targeting protein backbone: an effective strategy for combating drug resistance
-
Ghosh A.K., Chapsal B.D., Weber I.T., and Mitsua H. Design of HIV protease inhibitors targeting protein backbone: an effective strategy for combating drug resistance. Acc. Chem. Res. 41 (2008) 78-86
-
(2008)
Acc. Chem. Res.
, vol.41
, pp. 78-86
-
-
Ghosh, A.K.1
Chapsal, B.D.2
Weber, I.T.3
Mitsua, H.4
-
27
-
-
10744226241
-
Novel bis-tetrahydrofuranylurethane-containing nonpeptidic protease inhibitor (PI) TMC-114 (UIC-94017) with potent activity against multi-PI-resistant human immunodeficiency virus in vitro
-
Koh Y., Nakata H., Maeda K., Ogata H., Bilcer G., Devasamudram T., et al. Novel bis-tetrahydrofuranylurethane-containing nonpeptidic protease inhibitor (PI) TMC-114 (UIC-94017) with potent activity against multi-PI-resistant human immunodeficiency virus in vitro. Antimicrob. Agents Chemother. 47 (2003) 3123-3129
-
(2003)
Antimicrob. Agents Chemother.
, vol.47
, pp. 3123-3129
-
-
Koh, Y.1
Nakata, H.2
Maeda, K.3
Ogata, H.4
Bilcer, G.5
Devasamudram, T.6
-
28
-
-
19544386471
-
TMC114, a novel human immunodeficiency virus type 1 protease inhibitor active against protease inhibitor-resistant viruses, including a broad range of clinical isolates
-
De Meyer S., Azijin H., Surleraux D., Jochmans D., Tahri A., Pauwels R., et al. TMC114, a novel human immunodeficiency virus type 1 protease inhibitor active against protease inhibitor-resistant viruses, including a broad range of clinical isolates. Antimicrob. Agents Chemother. 49 (2005) 2314-2321
-
(2005)
Antimicrob. Agents Chemother.
, vol.49
, pp. 2314-2321
-
-
De Meyer, S.1
Azijin, H.2
Surleraux, D.3
Jochmans, D.4
Tahri, A.5
Pauwels, R.6
-
29
-
-
34047207229
-
Efficacy and safety of darunavir-ritonavir at week 48 in treatment-experienced patients with HIV-1 infection in POWER 1 and 2: a pooled subgroup analysis of data from two randomised trials
-
POWER 1 and 2 Study Groups
-
Clotet B., Bellos N., Molina J.M., Cooper D., Goffard J.C., Lazzarin A., et al., POWER 1 and 2 Study Groups. Efficacy and safety of darunavir-ritonavir at week 48 in treatment-experienced patients with HIV-1 infection in POWER 1 and 2: a pooled subgroup analysis of data from two randomised trials. Lancet 369 (2007) 1169-1178
-
(2007)
Lancet
, vol.369
, pp. 1169-1178
-
-
Clotet, B.1
Bellos, N.2
Molina, J.M.3
Cooper, D.4
Goffard, J.C.5
Lazzarin, A.6
-
30
-
-
11144354478
-
High resolution crystal structures of HIV-1 protease with a potent non-peptide inhibitor (UIC-94017) active against multi-drug-resistant clinical strains
-
Tie Y., Boross P., Wang Y.-F., Gaddis L., Hussain A.K., Leshchenko S., et al. High resolution crystal structures of HIV-1 protease with a potent non-peptide inhibitor (UIC-94017) active against multi-drug-resistant clinical strains. J. Mol. Biol. 338 (2004) 341-352
-
(2004)
J. Mol. Biol.
, vol.338
, pp. 341-352
-
-
Tie, Y.1
Boross, P.2
Wang, Y.-F.3
Gaddis, L.4
Hussain, A.K.5
Leshchenko, S.6
-
31
-
-
6344231715
-
Structural and thermodynamic basis for the binding of TMC-114, a next-generation human immunodeficiency virus type 1 protease inhibitor
-
King N.M., Prabu-Jeyabalan M., Nalivaika E.A., Wigerinck P., de Bethune M.-P., and Schiffer C.A. Structural and thermodynamic basis for the binding of TMC-114, a next-generation human immunodeficiency virus type 1 protease inhibitor. J. Virol. 78 (2004) 12012-12021
-
(2004)
J. Virol.
, vol.78
, pp. 12012-12021
-
-
King, N.M.1
Prabu-Jeyabalan, M.2
Nalivaika, E.A.3
Wigerinck, P.4
de Bethune, M.-P.5
Schiffer, C.A.6
-
32
-
-
33144466093
-
Effectiveness of nonpeptidic clinical inhibitor TMC114 to highly drug resistant mutations D30N, I50V, and L90M of HIV-1 protease
-
Kovalevsky A.Y., Tie Y., Liu F., Boross P., Wang Y.-F., Leshchenko S., et al. Effectiveness of nonpeptidic clinical inhibitor TMC114 to highly drug resistant mutations D30N, I50V, and L90M of HIV-1 protease. J. Med. Chem. 49 (2006) 1379-1387
-
(2006)
J. Med. Chem.
, vol.49
, pp. 1379-1387
-
-
Kovalevsky, A.Y.1
Tie, Y.2
Liu, F.3
Boross, P.4
Wang, Y.-F.5
Leshchenko, S.6
-
33
-
-
33748955158
-
Ultra-high resolution crystal structure of HIV-1 protease mutant reveals two binding sites for clinical inhibitor TMC114
-
Kovalevsky A.Y., Liu F., Leshchenko S., Ghosh A.K., Louis J.M., Harrison R.W., and Weber I.T. Ultra-high resolution crystal structure of HIV-1 protease mutant reveals two binding sites for clinical inhibitor TMC114. J. Mol. Biol. 363 (2006) 161-173
-
(2006)
J. Mol. Biol.
, vol.363
, pp. 161-173
-
-
Kovalevsky, A.Y.1
Liu, F.2
Leshchenko, S.3
Ghosh, A.K.4
Louis, J.M.5
Harrison, R.W.6
Weber, I.T.7
-
34
-
-
34250169806
-
A novel bis-tetrahydrofuranylurethane-containing nonpeptidic protease inhibitor (PI), GRL-98065, is potent against multiple-PI-resistant human immunodeficiency virus in vitro
-
Amano M., Koh Y., Das D., Li J., Leshchenko S., Wang Y.-F., et al. A novel bis-tetrahydrofuranylurethane-containing nonpeptidic protease inhibitor (PI), GRL-98065, is potent against multiple-PI-resistant human immunodeficiency virus in vitro. Antimicrob. Agents Chemother. 51 (2007) 2143-2155
-
(2007)
Antimicrob. Agents Chemother.
, vol.51
, pp. 2143-2155
-
-
Amano, M.1
Koh, Y.2
Das, D.3
Li, J.4
Leshchenko, S.5
Wang, Y.-F.6
-
35
-
-
40449087448
-
Inhibition of HIV-2 protease by HIV-1 protease inhibitors in clinical use
-
Brower E.T., Bacha U.M., Kawasaki Y., and Freire E. Inhibition of HIV-2 protease by HIV-1 protease inhibitors in clinical use. Chem. Biol. Drug Des. 71 (2008) 298-305
-
(2008)
Chem. Biol. Drug Des.
, vol.71
, pp. 298-305
-
-
Brower, E.T.1
Bacha, U.M.2
Kawasaki, Y.3
Freire, E.4
-
36
-
-
33747479539
-
Structure-based design of novel HIV-1 protease inhibitors to combat drug resistance
-
Ghosh A.K., Sridhar P.M., Leshchenko S., Hussain A.K., Li J., Kovalevsky A.Y., et al. Structure-based design of novel HIV-1 protease inhibitors to combat drug resistance. J. Med. Chem. 49 (2006) 5252-5261
-
(2006)
J. Med. Chem.
, vol.49
, pp. 5252-5261
-
-
Ghosh, A.K.1
Sridhar, P.M.2
Leshchenko, S.3
Hussain, A.K.4
Li, J.5
Kovalevsky, A.Y.6
-
37
-
-
34548513265
-
Potent antiviral compound shows similar inhibition and structural interactions with drug resistant mutants and wild type HIV-1 protease
-
Wang Y.-F., Tie Y., Boross P.I., Tozser J., Ghosh A.K., Harrison R.W., and Weber I.T. Potent antiviral compound shows similar inhibition and structural interactions with drug resistant mutants and wild type HIV-1 protease. J. Med. Chem. 50 (2007) 4509-4515
-
(2007)
J. Med. Chem.
, vol.50
, pp. 4509-4515
-
-
Wang, Y.-F.1
Tie, Y.2
Boross, P.I.3
Tozser, J.4
Ghosh, A.K.5
Harrison, R.W.6
Weber, I.T.7
-
39
-
-
0003505803
-
-
Wiley-VCH, New York, NY
-
Nishio M., Hirota M., and Umezawa Y. The C-H/π Interaction. Evidence, Nature, and Consequences (1998), Wiley-VCH, New York, NY
-
(1998)
The C-H/π Interaction. Evidence, Nature, and Consequences
-
-
Nishio, M.1
Hirota, M.2
Umezawa, Y.3
-
40
-
-
0025787584
-
Zinc inhibition of renin and the protease from human immunodeficiency virus type 1
-
Zhang Z.Y., Reardon I.M., Hui J.O., O'Connell K.L., Poorman R.A., Tomasselli A.G., and Heinrikson R.L. Zinc inhibition of renin and the protease from human immunodeficiency virus type 1. Biochemistry 30 (1991) 8717-8721
-
(1991)
Biochemistry
, vol.30
, pp. 8717-8721
-
-
Zhang, Z.Y.1
Reardon, I.M.2
Hui, J.O.3
O'Connell, K.L.4
Poorman, R.A.5
Tomasselli, A.G.6
Heinrikson, R.L.7
-
41
-
-
34447133502
-
Mutational and structural studies aimed at characterizing the monomer of HIV-1 protease and its precursor
-
Ishima R., Torchia D.A., and Louis J.M. Mutational and structural studies aimed at characterizing the monomer of HIV-1 protease and its precursor. J. Biol. Chem. 8 (2007) 17190-17199
-
(2007)
J. Biol. Chem.
, vol.8
, pp. 17190-17199
-
-
Ishima, R.1
Torchia, D.A.2
Louis, J.M.3
-
42
-
-
0031059866
-
Processing of X-ray diffraction data in oscillation mode
-
Otwinowski Z., and Minor W. Processing of X-ray diffraction data in oscillation mode. Methods Enzymol. 276 (1997) 307-326
-
(1997)
Methods Enzymol.
, vol.276
, pp. 307-326
-
-
Otwinowski, Z.1
Minor, W.2
-
43
-
-
0028103275
-
The CCP4 suite: programs for protein crystallography
-
Collaborative Computational Project, Number 4
-
Collaborative Computational Project, Number 4. The CCP4 suite: programs for protein crystallography. Acta Crystallogr., Sect D: Biol. Crystallogr. 50 (1994) 760-763
-
(1994)
Acta Crystallogr., Sect D: Biol. Crystallogr.
, vol.50
, pp. 760-763
-
-
-
44
-
-
0037779018
-
Graphical user interface to the CCP4 program suite
-
Potterton E., Briggs P., Turkenburg M., and Dodson E.A. Graphical user interface to the CCP4 program suite. Acta Crystallogr., Sect D: Biol. Crystallogr. 59 (2003) 1131-1137
-
(2003)
Acta Crystallogr., Sect D: Biol. Crystallogr.
, vol.59
, pp. 1131-1137
-
-
Potterton, E.1
Briggs, P.2
Turkenburg, M.3
Dodson, E.A.4
-
46
-
-
84889120137
-
Improved methods for building protein models in electron density maps and the location of errors in these models
-
Jones T.A., Zou J.Y., Cowan S.W., and Kjeldgaard M. Improved methods for building protein models in electron density maps and the location of errors in these models. Acta Crystallogr., Sect A: Found. Crystallogr. 47 (1991) 110-119
-
(1991)
Acta Crystallogr., Sect A: Found. Crystallogr.
, vol.47
, pp. 110-119
-
-
Jones, T.A.1
Zou, J.Y.2
Cowan, S.W.3
Kjeldgaard, M.4
-
48
-
-
0033119938
-
Further additions to MolScript version 1.4, including reading and contouring of electron-density maps
-
Esnouf R.M. Further additions to MolScript version 1.4, including reading and contouring of electron-density maps. Acta Crystallogr., Sect D: Biol. Crystallogr. 55 (1999) 938-940
-
(1999)
Acta Crystallogr., Sect D: Biol. Crystallogr.
, vol.55
, pp. 938-940
-
-
Esnouf, R.M.1
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