|
3
|
20
|
4gk0C |
Crystal structure of human rev3-rev7-rev1 complex |
|
242
|
880
|
4fvmA |
Crystal structure of yeast dna polymerase alpha |
|
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 |
|
2
|
10
|
4fjoB |
Structure of the rev1 ctd-rev3/7-pol kappa rir complex |
|
18
|
99
|
4flgA |
Hiv-1 protease mutant i47v complexed with reaction intermediate |
|
4
|
30
|
4fjoD |
Structure of the rev1 ctd-rev3/7-pol kappa rir complex |
|
18
|
99
|
4fl8A |
Hiv-1 protease complexed with gem-diol-amine tetrahedral 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 |
|
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 |
|
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 |
|
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 |
|
88
|
366
|
3qsbB |
Structure of e. coli poliiibeta with (z)-5-(1-((4'-fluorobiphenyl-4-yl)methoxyimino)butyl)-2,2-dimethyl-4,6-dioxocyclohexanecarbonitrile |
|
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 |
|
87
|
366
|
3qsbA |
Structure of e. coli poliiibeta with (z)-5-(1-((4'-fluorobiphenyl-4-yl)methoxyimino)butyl)-2,2-dimethyl-4,6-dioxocyclohexanecarbonitrile |
|
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 |
|
79
|
365
|
3q4kA |
Structure of a small peptide ligand bound to e.coli dna sliding clamp |
|
18
|
99
|
3qaaA |
Hiv-1 wild type protease with a substituted bis-tetrahydrofuran inhibitor, grl-044-10a |
|
84
|
366
|
3pweA |
Crystal structure of the e. coli beta clamp mutant r103c, i305c, c260s, c333s at 2.2a resolution |
|
85
|
368
|
3q4lA |
Structure of a small peptide ligand bound to e.coli dna sliding clamp |
|
90
|
366
|
3q4jA |
Structure of a small peptide ligand bound to e.coli dna sliding clamp |
|
19
|
99
|
3pwmA |
Hiv-1 protease mutant l76v with darunavir |
|
17
|
99
|
3pwrA |
Hiv-1 protease mutant l76v complexed with saquinavir |
|
18
|
99
|
3pj6A |
Crystal structures of multidrug-resistant clinical isolate 769 hiv-1 protease variants |
|
13
|
99
|
3phvA |
X-ray analysis of hiv-1 proteinase at 2.7 angstroms resolution confirms structural homology among retroviral enzymes |
|
20
|
99
|
3psuA |
Hiv-1 protease in complex with an isobutyl decorated oligoamine (symmetric binding mode) |
|
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 |
|
16
|
99
|
3oubA |
Mdr769 hiv-1 protease complexed with nc/p1 hepta-peptide |
|
17
|
99
|
3otsA |
Mdr769 hiv-1 protease complexed with ma/ca hepta-peptide |
|
19
|
99
|
3ok9A |
Crystal structure of wild-type hiv-1 protease with new oxatricyclic designed inhibitor grl-0519a |
|
49
|
157
|
3p1gA |
Crystal structure of the xenotropic murine leukemia virus-related virus (xmrv) rnase h domain |
|
16
|
99
|
3otyA |
Mdr769 hiv-1 protease complexed with rt/rh hepta-peptide |
|
17
|
99
|
3ou1A |
Mdr769 hiv-1 protease complexed with rh/in hepta-peptide |
|
16
|
99
|
3oxwA |
Crystal structure of hiv-1 i50v, a71v protease in complex with the protease inhibitor darunavir |
|
17
|
99
|
3oudA |
Mdr769 hiv-1 protease complexed with ca/p2 hepta-peptide |
