|
215
|
632
|
3rc8A |
Human mitochondrial helicase suv3 in complex with short rna fragment |
|
36
|
91
|
4lupA |
Crystal structure of the complex formed by region of e. coli sigmae bound to its -10 element non template strand |
|
28
|
96
|
2mapA |
Solution structure of the complex formed by the region 2 of e. coli sigmae and its cognate -10 promoter element non template strand tgtcaaa. |
|
108
|
280
|
2vlaA |
Crystal structure of restriction endonuclease bpuji recognition domain in complex with cognate dna |
|
108
|
280
|
5hnfA |
Crystal structure of pyrene- and phenanthrene-modified dna in complex with the bpuj1 endonuclease binding domain |
|
94
|
278
|
5hltA |
Crystal structure of pyrene- and phenanthrene-modified dna in complex with the bpuj1 endonuclease binding domain |
|
107
|
279
|
5hnhA |
Crystal structure of pyrene- and phenanthrene-modified dna in complex with the bpuj1 endonuclease binding domain |
|
60
|
185
|
4cxfA |
Structure of cnrh in complex with the cytosolic domain of cnry |
|
157
|
410
|
5jmwA |
Structure of plasmodium falciparum dxr in complex with a beta-substituted fosmidomycin analogue, lc50 and manganese |
|
153
|
410
|
5jbiA |
Structure of plasmodium falciparum dxr in complex with a beta-substituted fosmidomycin analogue, lc52 and manganese |
|
154
|
410
|
5jazA |
Structure of plasmodium falciparum dxr in complex with a beta-substituted fosmidomycin analogue, lc51 and manganese |
|
154
|
410
|
5jo0A |
Structure of plasmodium falciparum dxr in complex with a beta-substituted fosmidomycin analogue, lc56 and manganese |
|
153
|
410
|
5jc1A |
Structure of plasmodium falciparum dxr in complex with a beta-substituted fosmidomycin analogue, lc55 and manganese |
|
157
|
410
|
5jnlA |
Structure of plasmodium falciparum dxr in complex with a beta-substituted fosmidomycin analogue, lc54 and manganese |
|
320
|
867
|
4xmtA |
Crystal structure of met260ala mutant of e. coli aminopeptidase n in complex with l-2,3-diaminopropionic acid |
|
223
|
607
|
5bppA |
Structure of human leukotriene a4 hydrolase in complex with inhibitor 4az |
|
342
|
889
|
4zx4A |
X-ray crystal structure of pfa-m1 in complex with hydroxamic acid-based inhibitor 10o |
|
336
|
889
|
4zw5A |
X-ray crystal structure of pfa-m1 in complex with hydroxamic acid-based inhibitor 9f |
|
333
|
889
|
4zw3A |
X-ray crystal structure of pfa-m1 in complex with hydroxamic acid-based inhibitor 9b |
|
339
|
888
|
4zx6A |
X-ray crystal structure of pfa-m1 in complex with hydroxamic acid-based inhibitor 10s |
|
224
|
608
|
5aenA |
Structure of human leukotriene a4 hydrolase in complex with inhibitor dimethyl(2- (4-phenoxyphenoxy)ethyl)amine |
|
337
|
889
|
4zx3A |
X-ray crystal structure of pfa-m1 in complex with hydroxamic acid-based inhibitor 10b |
|
336
|
889
|
4zqtA |
Crystal structure of pfa-m1 with virtual ligand inhibitor |
|
324
|
866
|
4xndA |
Crystal structure of e. coli aminopeptidase n in complex with l-beta homotryptophan |
|
129
|
397
|
4zn6A |
X-ray crystal structure of 1-deoxy-d-xylulose 5-phosphate reductoisomerase (ispc) from acinetobacter baumannii |
|
304
|
864
|
4pvbA |
Crystal structure of aminopeptidase n in complex with the phosphonic acid analogue of leucine (d-(s)-leup) |
|
219
|
607
|
4dprA |
Structure of human leukotriene a4 hydrolase in complex with inhibitor captopril |
|
146
|
392
|
4ar9A |
Crystal structure of the peptidase domain of collagenase t from clostridium tetani at 1.69 angstrom resolution. |
|
185
|
628
|
4aysA |
The structure of amylosucrase from d. radiodurans |
|
139
|
391
|
4ar8A |
Crystal structure of the peptidase domain of collagenase t from clostridium tetani complexed with the peptidic inhibitor isoamyl- phosphonyl-gly-pro-ala at 2.05 angstrom resolution. |
|
139
|
380
|
4arfA |
Crystal structure of the peptidase domain of collagenase h from clostridium histolyticum in complex with the peptidic inhibitor isoamylphosphonyl-gly-pro-ala at 1.77 angstrom resolution. |
|
43
|
169
|
4bkxA |
The structure of hdac1 in complex with the dimeric elm2-sant domain of mta1 from the nurd complex |
|
134
|
379
|
4aicA |
X-ray structure of 1-deoxy-d-xylulose 5-phosphate reductoisomerase, dxr, rv2870c, from mycobacterium tuberculosis, in complex with fosmidomycin, manganese and nadph |
|
133
|
378
|
4a03A |
Crystal structure of mycobacterium tuberculosis dxr in complex with the antibiotic fr900098 and cofactor nadph |
|
138
|
381
|
4ar1A |
Crystal structure of the peptidase domain of collagenase h from clostridium histolyticum at 2.01 angstrom resolution. |
|
125
|
378
|
3zhyA |
Structure of mycobacterium tuberculosis dxr in complex with a di- substituted fosmidomycin analogue |
|
147
|
410
|
3wqsB |
Crystal structure of pfdxr complexed with inhibitor-126 |
|
120
|
376
|
3zi0A |
Structure of mycobacterium tuberculosis dxr in complex with a fosmidomycin analogue |
|
156
|
410
|
3wqrA |
Crystal structure of pfdxr complexed with inhibitor-12 |
|
153
|
410
|
3wqqA |
Crystal structure of pfdxr complexed with inhibitor-3 |
|
118
|
379
|
3zhzA |
Structure of mycobacterium tuberculosis dxr in complex with a fosmidomycin analogue |
|
126
|
379
|
3zhxA |
Structure of mycobacterium tuberculosis dxr in complex with a fosmidomycin analogue |
|
121
|
374
|
3vvlA |
Crystal structure of l-serine-o-acetyltransferase found in d-cycloserine biosynthetic pathway |
|
116
|
374
|
3vvmA |
Crystal structure of g52a-p55g mutant of l-serine-o-acetyltransferase found in d-cycloserine biosynthetic pathway |
|
219
|
608
|
3u9wA |
Structure of human leukotriene a4 hydrolase in complex with inhibitor sc57461a |
|
252
|
632
|
3ueqA |
Crystal structure of amylosucrase from neisseria polysaccharea in complex with turanose |
|
241
|
651
|
3ucqA |
Crystal structure of amylosucrase from deinococcus geothermalis |
|
245
|
651
|
3uerA |
Crystal structure of amylosucrase from deinococcus geothermalis in complex with turanose |
|
335
|
889
|
3t8vA |
A bestatin-based chemical biology strategy reveals distinct roles for malaria m1- and m17-family aminopeptidases |
|
45
|
126
|
3t0yA |
Structure of the phyr anti-anti-sigma domain bound to the anti-sigma factor, nepr |
