|
17
|
99
|
3k4vA |
New crystal form of hiv-1 protease/saquinavir structure reveals carbamylation of n-terminal proline |
|
37
|
131
|
3k2pA |
Hiv-1 reverse transcriptase isolated rnaseh domain with the inhibitor beta-thujaplicinol bound at the active site |
|
20
|
99
|
3jvyA |
Hiv-1 protease mutant g86a with darunavir |
|
0
|
9
|
3jtsC |
Gy9-mamu-a*02-hb2m |
|
16
|
99
|
3jw2A |
Hiv-1 protease mutant g86s with darunavir |
|
19
|
99
|
3jvwA |
Hiv-1 protease mutant g86a with symmetric inhibitor dmp323 |
|
134
|
554
|
3is9A |
Crystal structure of the hiv-1 reverse transcriptase (rt) in complex with the alkenyldiarylmethane (adam) non-nucleoside rt inhibitor dimethyl 3,3'-(6-methoxy-6-oxohex-1-ene-1,1-diyl)bis(5-cyano-6-methoxybenzoate). |
|
129
|
555
|
3irxA |
Crystal structure of hiv-1 reverse transcriptase (rt) in complex with the non-nucleoside rt inhibitor (e)-s-methyl 5-(1-(3,7-dimethyl-2-oxo-2,3-dihydrobenzo[d]oxazol-5-yl)-5-(5-methyl-1,3,4-oxadiazol-2-yl)pent-1-enyl)-2-methoxy-3-methylbenzothioate. |
|
141
|
556
|
3isnC |
Crystal structure of hiv-1 rt bound to a 6-vinylpyrimidine inhibitor |
|
103
|
428
|
3is9B |
Crystal structure of the hiv-1 reverse transcriptase (rt) in complex with the alkenyldiarylmethane (adam) non-nucleoside rt inhibitor dimethyl 3,3'-(6-methoxy-6-oxohex-1-ene-1,1-diyl)bis(5-cyano-6-methoxybenzoate). |
|
136
|
556
|
3ithA |
Crystal structure of the hiv-1 reverse transcriptase bound to a 6-vinylpyrimidine inhibitor |
|
109
|
427
|
3isnD |
Crystal structure of hiv-1 rt bound to a 6-vinylpyrimidine inhibitor |
|
102
|
428
|
3irxB |
Crystal structure of hiv-1 reverse transcriptase (rt) in complex with the non-nucleoside rt inhibitor (e)-s-methyl 5-(1-(3,7-dimethyl-2-oxo-2,3-dihydrobenzo[d]oxazol-5-yl)-5-(5-methyl-1,3,4-oxadiazol-2-yl)pent-1-enyl)-2-methoxy-3-methylbenzothioate. |
|
18
|
99
|
3ixoA |
Crystal structure of uncomplexed hiv_1 protease subtype a |
|
98
|
427
|
3ithB |
Crystal structure of the hiv-1 reverse transcriptase bound to a 6-vinylpyrimidine inhibitor |
|
110
|
422
|
3ig1B |
Hiv-1 reverse transcriptase with the inhibitor beta-thujaplicinol bound at the rnase h active site |
|
43
|
203
|
3iawA |
Crystal structure of a chemically synthesized 203 amino acid 'covalent dimer' [gly51;aib51']hiv-1 protease molecule complexed with mvt-101 reduced isostere inhibitor at 1.6 a resolution |
|
16
|
99
|
3i7eA |
Co-crystal structure of hiv-1 protease bound to a mutant resistant inhibitor uic-98038 |
|
17
|
99
|
3i8wA |
Crystal structure of a metallacarborane inhibitor bound to hiv protease |
|
132
|
552
|
3ig1A |
Hiv-1 reverse transcriptase with the inhibitor beta-thujaplicinol bound at the rnase h active site |
|
74
|
427
|
3hvtB |
Structural basis of asymmetry in the human immunodeficiency virus type 1 reverse transcriptase heterodimer |
|
146
|
545
|
3i0rA |
Crystal structure of hiv reverse transcriptase in complex with inhibitor 3 |
|
11
|
99
|
3hvpA |
Conserved folding in retroviral proteases. crystal structure of a synthetic hiv-1 protease |
|
19
|
99
|
3i6oA |
Crystal structure of wild type hiv-1 protease with macrocyclic inhibitor grl-0216a |
|
95
|
555
|
3hvtA |
Structural basis of asymmetry in the human immunodeficiency virus type 1 reverse transcriptase heterodimer |
|
105
|
424
|
3i0sB |
Crystal structure of hiv reverse transcriptase in complex with inhibitor 7 |
|
160
|
558
|
3i0sA |
Crystal structure of hiv reverse transcriptase in complex with inhibitor 7 |
|
102
|
424
|
3i0rB |
Crystal structure of hiv reverse transcriptase in complex with inhibitor 3 |
|
64
|
210
|
3hphA |
Closed tetramer of visna virus integrase (residues 1-219) in complex with ledgf ibd |
|
66
|
209
|
3hpgA |
Visna virus integrase (residues 1-219) in complex with ledgf ibd: examples of open integrase dimer-dimer interfaces |
|
18
|
99
|
3hdkA |
Crystal structure of chemically synthesized [aib51/51']hiv-1 protease |
|
15
|
99
|
3hauA |
Crystal structure of chemically synthesized hiv-1 protease with reduced isostere mvt-101 inhibitor |
|
71
|
219
|
3h47A |
X-ray structure of hexameric hiv-1 ca |
|
43
|
203
|
3hloA |
Crystal structure of chemically synthesized 'covalent dimer' [gly51/d-ala51']hiv-1 protease |
|
18
|
99
|
3h5bA |
Crystal structure of wild type hiv-1 protease with novel p1'-ligand grl-02031 |
|
17
|
99
|
3hboA |
Crystal structure of chemically synthesized [d-ala51/51']hiv-1 protease |
|
77
|
220
|
3h4eA |
X-ray structure of hexameric hiv-1 ca |
|
18
|
99
|
3hawA |
Crystal structure of [l-ala51/51']hiv-1 protease with reduced isostere mvt-101 inhibitor |
|
14
|
99
|
3ggvA |
Hiv protease, pseudo-symmetric inhibitors |
|
18
|
99
|
3gi4A |
Crystal structure of protease inhibitor, kb60 in complex with wild type hiv-1 protease |
|
18
|
99
|
3ggaA |
Hiv protease inhibitors with pseudo-symmetric cores |
|
41
|
203
|
3gi0A |
Crystal structure of a chemically synthesized 203 amino acid 'covalent dimer' [l-ala51,d-ala51'] hiv-1 protease molecule complexed with jg-365 inhibitor |
|
19
|
99
|
3gguA |
Hiv pr drug resistant patient's variant in complex with darunavir |
|
18
|
99
|
3gi6A |
Crystal structure of protease inhibitor, ad78 in complex with wild type hiv-1 protease |
|
18
|
99
|
3gi5A |
Crystal structure of protease inhibitor, kb62 in complex with wild type hiv-1 protease |
|
15
|
99
|
3ggxA |
Hiv protease, pseudo-symmetric inhibitors |
|
40
|
203
|
3fsmA |
Crystal structure of a chemically synthesized 203 amino acid 'covalent dimer' [l-ala51,d-ala51'] hiv-1 protease molecule |
|
16
|
99
|
3fx5A |
Structure of hiv-1 protease in complex with potent inhibitor kni-272 determined by high resolution x-ray crystallography |
|
74
|
204
|
3f9kA |
Two domain fragment of hiv-2 integrase in complex with ledgf ibd |
|
27
|
111
|
3fivA |
Crystal structure of feline immunodeficiency virus protease complexed with a substrate |
