|
84
|
226
|
4ce6A |
Mutagenesis of a rhodobacteraceae l-haloacid dehalogenase |
|
87
|
267
|
4ch5A |
Structure of pyrrolysyl-trna synthetase in complex with adenylated propionyl lysine |
|
117
|
308
|
4bqoA |
Structural insights into wcbi, a novel polysaccharide biosynthesis enzyme. native protein without disulfide bond between coa and cys14. |
|
31
|
98
|
4co8A |
Structure of the dna binding ets domain of human etv4 |
|
142
|
466
|
4c1mC |
Myeloperoxidase in complex with the revesible inhibitor hx1 |
|
93
|
292
|
4btmA |
Ttbk1 in complex with inhibitor |
|
148
|
450
|
4c0cA |
Crystal structure of trypanosoma cruzi cyp51 bound to the inhibitor (r)-n-(3-(1h-indol-3-yl)-1-oxo-1-(pyridin-4-ylamino)propan-2-yl)-4-(4-(2,4-difluorophenyl)piperazin-1-yl)-2-fluorobenzamide. |
|
119
|
347
|
4c7pA |
Crystal structure of legionella pneumophila ralf f255k mutant |
|
86
|
300
|
4cfwA |
Structure-based design of c8-substituted o6-cyclohexylmethoxyguanine cdk1 and 2 inhibitors. |
|
128
|
539
|
4cidA |
Structural insights into the n-terminus of the ehd2 atpase |
|
82
|
268
|
4bwaA |
Pylrs y306g, y384f, i405r mutant in complex with adenylated norbornene |
|
36
|
123
|
4c9yA |
Structural basis for the microtubule binding of the human kinetochore ska complex |
|
108
|
412
|
4bwkA |
Structure of neurospora crassa pan3 pseudokinase |
|
87
|
297
|
4cfmA |
Structure-based design of c8-substituted o6-cyclohexylmethoxyguanine cdk1 and 2 inhibitors. |
|
13
|
69
|
4c3iJ |
Structure of 14-subunit rna polymerase i at 3.0 a resolution, crystal form c2-100 |
|
87
|
335
|
4ch7A |
Crystal structure of the siroheme decarboxylase nirdl |
|
48
|
129
|
4bs7A |
Hen egg-white lysozyme structure determined at room temperature by in- situ diffraction and sad phasing in chipx |
|
79
|
372
|
4cclA |
X-ray structure of e. coli ycfd |
|
85
|
226
|
4cnqA |
Mutagenesis of a rhodobacteraceae l-haloacid dehalogenase |
|
113
|
430
|
4bugA |
Pilus-presented adhesin, spy0125 (cpa), cys426ala mutant |
|
36
|
92
|
4cayB |
Crystal structure of a human anp32e-h2a.z-h2b complex |
|
98
|
258
|
4cfwB |
Structure-based design of c8-substituted o6-cyclohexylmethoxyguanine cdk1 and 2 inhibitors. |
|
248
|
601
|
4bb9A |
Crystal structure of glucokinase regulatory protein complexed to fructose-1-phosphate |
|
135
|
449
|
4ckaA |
Sterol 14-alpha demethylase (cyp51)from trypanosoma cruzi in complex with (s)-1-(4-fluorophenyl)-2-(1h-imidazol-1-yl)ethyl 4- isopropylphenylcarbamate (lfs) |
|
38
|
95
|
4bx9C |
Human vps33a in complex with a fragment of human vps16 |
|
69
|
291
|
4c0tA |
Candida albicans pkh kinase domain |
|
77
|
264
|
4c3pA |
Structure of dephosphorylated aurora a (122-403) bound to tpx2 and amppcp |
|
269
|
945
|
4anxA |
Complexes of pi3kgamma with isoform selective inhibitors. |
|
128
|
447
|
4by0A |
Crystal structure of trypanosoma cruzi cyp51 bound to the inhibitor (r)-n-(3-(1h-indol-3-yl)-1-oxo-1-(pyridin-4-ylamino)propan-2-yl)-3,3'- difluoro-(1,1'-biphenyl)-4-carboxamide |
|
87
|
302
|
4cfuA |
Structure-based design of c8-substituted o6-cyclohexylmethoxyguanine cdk1 and 2 inhibitors. |
|
32
|
87
|
4cfqA |
Ca-bound truncated (delta13c) and c3s, c81s and c86s mutated s100a4 complexed with non-muscle myosin iia |
|
123
|
436
|
4bxfA |
60s ribosomal protein l27a histidine hydroxylase (mina53 y209c) in complex with mn(ii), 2-oxoglutarate (2og) and 60s ribosomal protein l27a (rpl27a g37c) peptide fragment |
|
114
|
330
|
4c5fA |
Structure of lytic transglycosylase mltc from escherichia coli at 2.3 a resolution. |
|
98
|
250
|
4cj6A |
Crystal structure of the complex of the cellular retinal binding protein mutant r234w with 9-cis-retinal |
|
81
|
272
|
4brxA |
Focal adhesion kinase catalytic domain in complex with a diarylamino- 1,3,5-triazine inhibitor |
|
111
|
293
|
4ccpA |
X-ray structures of recombinant yeast cytochrome c peroxidase and three heme-cleft mutants prepared by site-directed mutagenesis |
|
171
|
462
|
4cdmA |
Crystal structure of m. mazei photolyase soaked with synthetic 8-hdf |
|
152
|
442
|
4bhtA |
Structural determinants of cofactor specificity and domain flexibility in bacterial glutamate dehydrogenases |
|
88
|
280
|
4c4fA |
Structure-based design of orally bioavailable pyrrolopyridine inhibitors of the mitotic kinase mps1 |
|
109
|
308
|
4cc5A |
Fragment-based discovery of 6 azaindazoles as inhibitors of bacterial dna ligase |
|
82
|
267
|
4ch6A |
Structure of pyrrolysyl-trna synthetase in complex with adenylated propargyloxycarbonyl lysine |
|
75
|
255
|
4bxdA |
Crystal structure of ampdh3 from pseudomonas aeruginosa in complex with tetrasaccharide pentapeptide |
|
112
|
338
|
4c37A |
Pka-s6k1 chimera with compound 21a (cct196539) bound |
|
75
|
203
|
4c7uA |
Crystal structure of manganese superoxide dismutase from arabidopsis thaliana |
|
77
|
255
|
4bxeA |
Crystal structure of ampdh3 from pseudomonas aeruginosa in complex with anhydromuramic pentapeptide |
|
138
|
408
|
4c9kA |
Structure of camphor and hydroxycamphor bound wild type cyp101d1 |
|
93
|
308
|
4ccbA |
Structure of the human anaplastic lymphoma kinase in complex with 3-((r)-1-(5-fluoro-2-(2h-1,2,3-triazol-2-yl)phenyl)ethoxy)-5-(5-methyl-1h- pyrazol-4-yl)pyridin-2-amine |
|
277
|
1057
|
4a55A |
Crystal structure of p110alpha in complex with ish2 of p85alpha and the inhibitor pik-108 |
|
74
|
279
|
4c4jA |
Structure-based design of orally bioavailable pyrrolopyridine inhibitors of the mitotic kinase mps1 |
|
23
|
88
|
4ca3A |
Solution structure of streptomyces virginiae vira acp5b |
