|
19
|
99
|
4jecA |
Joint neutron and x-ray structure of per-deuterated hiv-1 protease in complex with clinical inhibitor amprenavir |
|
112
|
424
|
4i2qB |
Crystal structure of k103n/y181c mutant of hiv-1 reverse transcriptase in complex with rilpivirine (tmc278) analogue |
|
165
|
556
|
4ifyA |
Hiv-1 reverse transcriptase with bound fragment at the knuckles site |
|
15
|
99
|
4hvpA |
Structure of complex of synthetic hiv-1 protease with a substrate-based inhibitor at 2.3 angstroms resolution |
|
20
|
99
|
4hegA |
Crystal structure of hiv-1 protease mutants r8q complexed with inhibitor grl-0519 |
|
103
|
428
|
4h4oB |
Crystal structure of hiv-1 reverse transcriptase (rt) in complex with (e)-3-(3-(2-(2-(2,4-dioxo-3,4-dihydropyrimidin-1(2h)-yl)ethoxy)- 4-fluorophenoxy)-5-fluorophenyl)acrylonitrile (jlj506), a non-nucleoside inhibitor |
|
19
|
99
|
4hlaA |
Crystal structure of wild type hiv-1 protease in complex with darunavir |
|
102
|
428
|
4h4mB |
Crystal structure of hiv-1 reverse transcriptase in complex with (e)-3-(3-chloro-5-(4-chloro-2-(2-(2,4-dioxo-3,4- dihydropyrimidin-1(2h)-yl)ethoxy)phenoxy)phenyl)acrylonitrile (jlj494), a non-nucleoside inhibitor |
|
20
|
99
|
4he9A |
Crystal structure of hiv-1 protease mutants i54m complexed with inhibitor grl-0519 |
|
141
|
549
|
4h4oA |
Crystal structure of hiv-1 reverse transcriptase (rt) in complex with (e)-3-(3-(2-(2-(2,4-dioxo-3,4-dihydropyrimidin-1(2h)-yl)ethoxy)- 4-fluorophenoxy)-5-fluorophenyl)acrylonitrile (jlj506), a non-nucleoside inhibitor |
|
19
|
99
|
4hdfA |
Crystal structure of hiv-1 protease mutants v82a complexed with inhibitor grl-0519 |
|
135
|
548
|
4h4mA |
Crystal structure of hiv-1 reverse transcriptase in complex with (e)-3-(3-chloro-5-(4-chloro-2-(2-(2,4-dioxo-3,4- dihydropyrimidin-1(2h)-yl)ethoxy)phenoxy)phenyl)acrylonitrile (jlj494), a non-nucleoside inhibitor |
|
19
|
99
|
4hdpA |
Crystal structure of hiv-1 protease mutants i50v complexed with inhibitor grl-0519 |
|
18
|
99
|
4hdbA |
Crystal structure of hiv-1 protease mutants d30n complexed with inhibitor grl-0519 |
|
44
|
155
|
4gvmA |
Hiv-1 integrase catalytic core domain a128t mutant complexed with allosteric inhibitor |
|
49
|
155
|
4gw6A |
Hiv-1 integrase catalytic core domain complexed with allosteric inhibitor |
|
16
|
99
|
4gb2A |
Hiv-1 protease (mutant q7k l33i l63i) in complex with a bicyclic pyrrolidine inhibitor |
|
157
|
556
|
4g1qA |
Crystal structure of hiv-1 reverse transcriptase (rt) in complex with rilpivirine (tmc278, edurant), a non-nucleoside rt-inhibiting drug |
|
117
|
424
|
4g1qB |
Crystal structure of hiv-1 reverse transcriptase (rt) in complex with rilpivirine (tmc278, edurant), a non-nucleoside rt-inhibiting drug |
|
69
|
218
|
4fw2A |
Crystal structure of rsv three-domain integrase with disordered n-terminal domain |
|
71
|
218
|
4fw1A |
Crystal structure of two-domain rsv integrase covalently linked with dna |
|
18
|
99
|
4flgA |
Hiv-1 protease mutant i47v complexed with reaction intermediate |
|
19
|
99
|
3r4bA |
Crystal structure of wild-type hiv-1 protease in complex with tmc310911 |
|
19
|
99
|
4fm6A |
Hiv-1 protease mutant v32i complexed with reaction intermediate |
|
20
|
99
|
4fe6A |
Crystal structure of hiv-1 protease in complex with an enamino-oxindole inhibitor |
|
18
|
99
|
4fl8A |
Hiv-1 protease complexed with gem-diol-amine tetrahedral intermediate |
|
43
|
148
|
3qioA |
Crystal structure of hiv-1 rnase h with engineered e. coli loop and n-hydroxy quinazolinedione inhibitor |
|
18
|
99
|
3qrmA |
Hiv-1 protease (mutant q7k l33i l63i) in complex with a three-armed pyrrolidine-based inhibitor |
|
16
|
99
|
3qpjA |
Hiv-1 protease (mutant q7k l33i l63i) in complex with a three-armed pyrrolidine-based inhibitor |
|
19
|
99
|
3qihA |
Hiv-1 protease (mutant q7k l33i l63i) in complex with a novel inhibitor |
|
115
|
425
|
3qipB |
Structure of hiv-1 reverse transcriptase in complex with an rnase h inhibitor and nevirapine |
|
17
|
99
|
3qroA |
Hiv-1 protease (mutant q7k l33i l63i) in complex with a three-armed pyrrolidine-based inhibitor |
|
19
|
99
|
3qp0A |
Hiv-1 protease (mutant q7k l33i l63i) in complex with a novel inhibitor |
|
43
|
148
|
3qinA |
Crystal structure of hiv-1 rnase h p15 with engineered e. coli loop and pyrimidinol carboxylic acid inhibitor |
|
139
|
553
|
3qo9A |
Crystal structure of hiv-1 reverse transcriptase (rt) in complex with tsao-t, a non-nucleoside rt inhibitor (nnrti) |
|
101
|
423
|
3qlhB |
Hiv-1 reverse transcriptase in complex with manicol at the rnase h active site and tmc278 (rilpivirine) at the nnrti binding pocket |
|
144
|
555
|
3qlhA |
Hiv-1 reverse transcriptase in complex with manicol at the rnase h active site and tmc278 (rilpivirine) at the nnrti binding pocket |
|
105
|
424
|
3qo9B |
Crystal structure of hiv-1 reverse transcriptase (rt) in complex with tsao-t, a non-nucleoside rt inhibitor (nnrti) |
|
164
|
556
|
3qipA |
Structure of hiv-1 reverse transcriptase in complex with an rnase h inhibitor and nevirapine |
|
18
|
99
|
3qrsA |
Hiv-1 protease (mutant q7k l33i l63i) in complex with a three-armed pyrrolidine-based inhibitor |
|
18
|
99
|
3qn8A |
Hiv-1 protease (mutant q7k l33i l63i) in complex with a novel inhibitor |
|
16
|
99
|
3qbfA |
Hiv-1 protease (mutant q7k l33i l63i) in complex with a three-armed pyrrolidine-based inhibitor |
|
18
|
99
|
3qaaA |
Hiv-1 wild type protease with a substituted bis-tetrahydrofuran inhibitor, grl-044-10a |
|
17
|
99
|
3pwrA |
Hiv-1 protease mutant l76v complexed with saquinavir |
|
19
|
99
|
3pwmA |
Hiv-1 protease mutant l76v with darunavir |
|
18
|
99
|
3pj6A |
Crystal structures of multidrug-resistant clinical isolate 769 hiv-1 protease variants |
|
20
|
99
|
3psuA |
Hiv-1 protease in complex with an isobutyl decorated oligoamine (symmetric binding mode) |
|
13
|
99
|
3phvA |
X-ray analysis of hiv-1 proteinase at 2.7 angstroms resolution confirms structural homology among retroviral enzymes |
|
16
|
99
|
3oucA |
Mdr769 hiv-1 protease complexed with p2/nc hepta-peptide |
|
16
|
99
|
3oq7A |
Crystal structures of multidrug-resistant clinical isolate 769 hiv-1 protease variants |
