|
120
|
339
|
3zh9B |
Bacillus subtilis dna clamp loader delta protein (yqen) |
|
49
|
153
|
3wngA |
Cyclic hexapeptide pkidnp in complex with hiv-1 integrase |
|
48
|
153
|
3wnhA |
Cyclic hexapeptide pkzdnv in complex with hiv-1 integrase |
|
47
|
154
|
3wneA |
Cyclic hexapeptide pkidng in complex with hiv-1 integrase |
|
1
|
21
|
3vu7Z |
Crystal structure of rev1-rev7-rev3 ternary complex |
|
18
|
99
|
3vf5A |
Crystal structure of hiv-1 protease mutant i47v with novel p1'-ligands grl-02031 |
|
18
|
99
|
3vf7A |
Crystal structure of hiv-1 protease mutant l76v with novel p1'-ligands grl-02031 |
|
48
|
165
|
3v1rA |
Crystal structures of the reverse transcriptase-associated ribonuclease h domain of xmrv with inhibitor beta-thujaplicinol |
|
17
|
99
|
3vfbA |
Crystal structure of hiv-1 protease mutant n88d with novel p1'-ligands grl-02031 |
|
47
|
157
|
3v1qA |
Crystal structures of the reverse transcriptase-associated ribonuclease h domain of xenotropic murine leukemia-virus related virus |
|
56
|
325
|
3v7lA |
Apo structure of rat dna polymerase beta k72e variant |
|
18
|
99
|
3vfaA |
Crystal structure of hiv-1 protease mutant v82a with novel p1'-ligands grl-02031 |
|
53
|
165
|
3v1oA |
Crystal structures of the reverse transcriptase-associated ribonuclease h domain of xenotropic murine leukemia-virus related virus |
|
94
|
325
|
3uxnA |
Crystal structure of rat dna polymerase beta, wild type apoenzyme |
|
15
|
99
|
3upjA |
Human immunodeficiency virus type 2 protease mutant with lys 57 replaced by leu (k57l) complex with u096333 [4-hydroxy-3-[1-(phenyl)propyl]-7-methoxycoumarin] |
|
16
|
99
|
3uf3A |
Crystal structure of multidrug resistant hiv-1 protease clinical isolate pr20 |
|
19
|
99
|
3ufnA |
Crystal structure of multidrug resistant hiv-1 protease clinical isolate pr20 in complex with saquinavir |
|
16
|
99
|
3uhlA |
Crystal structure of multidrug resistant hiv-1 protease clinical isolate pr20 in complex with p2-nc substrate analog |
|
95
|
325
|
3uxoA |
Crystal structure of rat dna polymerase beta mutator i260q apoenzyme |
|
16
|
99
|
3ucbA |
Crystal structure of multidrug resistant hiv-1 protease clinical isolate pr20 in complex with darunavir |
|
17
|
99
|
3u7sA |
Hiv pr drug resistant patient's variant in complex with darunavir |
|
18
|
99
|
3ttpA |
Structure of multiresistant hiv-1 protease in complex with darunavir |
|
100
|
367
|
5froA |
Crystal structure of the prototype foamy virus (pfv) intasome in complex with magnesium and the insti xz446 (compound 4f) |
|
204
|
1151
|
5c52A |
Probing the structural and molecular basis of nucleotide selectivity by human mitochondrial dna polymerase gamma |
|
70
|
240
|
5cp2A |
Human dna polymerase lambda l431a mutant- apoenzyme and complex with 6 paired dna |
|
17
|
99
|
3tofA |
Hiv-1 protease - epoxydic inhibitor complex (ph 6 - orthorombic crystal form p212121) |
|
19
|
103
|
3tkgA |
Crystal structure of hiv model protease precursor/saquinavir complex |
|
74
|
244
|
4xq8A |
Human dna polymerase lambda- mgdatp binary complex and complex with 6 paired dna |
|
73
|
246
|
5cr0A |
Human dna polymerase lambda l431a mutant- mgdctp binary and complex with 6 paired dna |
|
18
|
99
|
3togA |
Hiv-1 protease - epoxydic inhibitor complex (ph 9 - monoclinic crystal form p21) |
|
16
|
99
|
3tkwA |
Crystal structure of hiv protease model precursor/darunavir complex |
|
17
|
99
|
3tlhA |
Structural studies of hiv and fiv proteases complexed withan efficient inhibitor of fiv pr |
|
18
|
99
|
3tohA |
Hiv-1 protease - epoxydic inhibitor complex (ph 9 - orthorombic crystal form p212121) |
|
18
|
99
|
3tl9A |
Crystal structure of hiv protease model precursor/saquinavir complex |
|
110
|
326
|
4z6eA |
Structure of human dna polymerase beta 279na mutant complexed with g in the template base paired with incoming non-hydrolyzable ttp and manganese |
|
101
|
329
|
4ymnA |
Structure of human dna polymerase beta complexed with n7bg in the template base paired with incoming non-hydrolyzable ctp |
|
110
|
326
|
4z6cA |
Structure of human dna polymerase beta 279na mutant complexed with g in the template base paired with incoming non-hydrolyzable ctp |
|
147
|
435
|
5kg1A |
Human dna polymerase eta-dna ternary complex: reaction first with 1 mm mn2+ for 1800s then with 5 mm mn2+ for 60s at 30 degree |
|
106
|
424
|
3tamB |
Crystal structure of hiv-1 reverse transcriptase (k103n mutant) in complex with inhibitor m06 |
|
147
|
435
|
5kfyA |
Human dna polymerase eta-dna ternary complex: reaction first with 1 mm mn2+ for 1800s then with 5 mm mn2+ for 60s at 4 degree |
|
103
|
324
|
4xa5A |
Crystal structure of the pre-catalytic ternary complex of dna polymerase lambda with a templating a and an incoming 8-oxo-dgtp |
|
147
|
435
|
5kg6A |
Human dna polymerase eta-dna ternary complex: reaction first with 1 mm mn2+ for 1800s then with 10 mm ca2+ for 60s |
|
147
|
435
|
5kfzA |
Human dna polymerase eta-dna ternary complex: reaction first with 1 mm mn2+ for 1800s then with 5 mm mn2+ for 60s at 14 degree |
|
17
|
99
|
3th9A |
Crystal structure of hiv-1 protease mutant q7k v32i l63i with a cyclic sulfonamide inhibitor |
|
147
|
435
|
5kg4A |
Human dna polymerase eta-dna ternary complex: reaction first with 1 mm mn2+ for 1800s then with 10 mm mg2+ for 60s |
|
160
|
557
|
3tamA |
Crystal structure of hiv-1 reverse transcriptase (k103n mutant) in complex with inhibitor m06 |
|
147
|
435
|
5kg3A |
Human dna polymerase eta-dna ternary complex: reaction first with 1 mm mn2+ for 1800s then with 10 mm mn2+ for 60s |
|
152
|
435
|
5kfuA |
Human dna polymerase eta r61a-dna ternary complex: reaction with 1 mm mg2+ for 80s |
|
146
|
435
|
5kfxA |
Human dna polymerase eta r61a-dna ternary complex: reaction with 1 mm mg2+ for 300s |
|
80
|
226
|
3tirA |
Pseudo-atomic model of the rous sarcoma virus capsid hexamer |
