|
160
|
556
|
4ig0A |
Hiv-1 reverse transcriptase with bound fragment at the 507 site |
|
28
|
85
|
4ipyA |
Hiv capsid c-terminal domain |
|
119
|
424
|
4ifvB |
Detecting allosteric sites of hiv-1 reverse transcriptase by x-ray crystallographic fragment screening |
|
144
|
556
|
4i2qA |
Crystal structure of k103n/y181c mutant of hiv-1 reverse transcriptase in complex with rilpivirine (tmc278) analogue |
|
41
|
105
|
4jmuA |
Crystal structure of hiv matrix residues 1-111 in complex with inhibitor |
|
17
|
99
|
4j54A |
Crystal structure of multidrug resistant hiv-1 protease clinical isolate pr20 with the potent antiviral inhibitor grl-0519a |
|
125
|
424
|
4ig3B |
Hiv-1 reverse transcriptase with bound fragment near knuckles site |
|
155
|
554
|
4i2pA |
Crystal structure of hiv-1 reverse transcriptase in complex with rilpivirine (tmc278) based analogue |
|
18
|
99
|
4i8wA |
Crystal structure of wild type hiv-1 protease in complex with non-peptidic inhibitor, grl007 |
|
15
|
99
|
4j55A |
Crystal structure of multidrug resistant hiv-1 protease clinical isolate pr20 with the potent antiviral inhibitor grl-02031 |
|
150
|
556
|
4iclA |
Hiv-1 reverse transcriptase with bound fragment at the incoming dntp binding site |
|
153
|
552
|
4i7fA |
Hiv-1 reverse transcriptase in complex with a phosphonate analog of nevirapine |
|
109
|
425
|
4i7fB |
Hiv-1 reverse transcriptase in complex with a phosphonate analog of nevirapine |
|
114
|
424
|
4i2pB |
Crystal structure of hiv-1 reverse transcriptase in complex with rilpivirine (tmc278) based analogue |
|
114
|
424
|
4iclB |
Hiv-1 reverse transcriptase with bound fragment at the incoming dntp binding site |
|
116
|
424
|
4ig0B |
Hiv-1 reverse transcriptase with bound fragment at the 507 site |
|
49
|
154
|
4id1A |
Hiv-1 integrase catalytic core domain complexed with allosteric inhibitor |
|
167
|
556
|
4ig3A |
Hiv-1 reverse transcriptase with bound fragment near knuckles site |
|
164
|
556
|
4id5A |
Hiv-1 reverse transcriptase with bound fragment at the rnase h primer grip site |
|
116
|
424
|
4ifyB |
Hiv-1 reverse transcriptase with bound fragment at the knuckles site |
|
122
|
424
|
4id5B |
Hiv-1 reverse transcriptase with bound fragment at the rnase h primer grip site |
|
20
|
99
|
4i8zA |
Crystal structure of wild type hiv-1 protease in complex with non-peptidic inhibitor, grl008 |
|
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 |
|
114
|
424
|
4idkB |
Hiv-1 reverse transcriptase with bound fragment at the 428 site |
|
45
|
154
|
4jlhA |
Hiv-1 integrase catalytic core domain a128t mutant complexed with allosteric inhibitor |
|
161
|
556
|
4idkA |
Hiv-1 reverse transcriptase with bound fragment at the 428 site |
|
167
|
556
|
4ifvA |
Detecting allosteric sites of hiv-1 reverse transcriptase by x-ray crystallographic fragment screening |
|
16
|
99
|
4j5jA |
Crystal structure of multidrug resistant hiv-1 protease clinical isolate pr20 in complex with amprenavir |
|
19
|
99
|
4jecA |
Joint neutron and x-ray structure of per-deuterated hiv-1 protease in complex with clinical inhibitor amprenavir |
|
15
|
99
|
4hvpA |
Structure of complex of synthetic hiv-1 protease with a substrate-based inhibitor at 2.3 angstroms resolution |
|
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 |
|
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 |
|
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 |
|
49
|
155
|
4gw6A |
Hiv-1 integrase catalytic core domain complexed with allosteric inhibitor |
|
110
|
312
|
4gx9A |
Crystal structure of a dna polymerase iii alpha-epsilon chimera |
|
44
|
155
|
4gvmA |
Hiv-1 integrase catalytic core domain a128t mutant complexed with allosteric inhibitor |
|
115
|
313
|
4gx8A |
Crystal structure of a dna polymerase iii alpha-epsilon chimera |
|
16
|
99
|
4gb2A |
Hiv-1 protease (mutant q7k l33i l63i) in complex with a bicyclic pyrrolidine inhibitor |
|
1
|
8
|
4gk5G |
Crystal structure of human rev3-rev7-rev1-polkappa complex |
|
44
|
162
|
4gigA |
Crystal structure of t69a mutant of trapped dnae intein precursor |
|
3
|
20
|
4gk0C |
Crystal structure of human rev3-rev7-rev1 complex |
|
242
|
880
|
4fvmA |
Crystal structure of yeast dna polymerase alpha |
