|
53
|
164
|
4bthA |
The leua146trp,pheb24tyr double mutant of the quorum quenching n-acyl homoserine lactone acylase pvdq has an altered substrate specificity towards small acyl chains |
|
82
|
273
|
4bzoA |
Crystal structure of pim1 in complex with a pyrrolo-pyrazinone inhibitor |
|
224
|
1033
|
4bujA |
Crystal structure of the s. cerevisiae ski2-3-8 complex |
|
106
|
385
|
4ci0A |
Electron cryo-microscopy of f420-reducing nife hydrogenase frh |
|
110
|
436
|
4bu2A |
60s ribosomal protein l27a histidine hydroxylase (mina53) in complex with ni(ii) and 2-oxoglutarate (2og) |
|
65
|
226
|
4byyA |
Apo glxr |
|
267
|
736
|
4b3iA |
Crystal structure of mycobacterium tuberculosis fatty acid beta- oxidation complex with coenzymea bound at the hydratase active sites |
|
89
|
287
|
4c61A |
Inhibitors of jak2 kinase domain |
|
87
|
300
|
4cfnA |
Structure-based design of c8-substituted o6-cyclohexylmethoxyguanine cdk1 and 2 inhibitors. |
|
89
|
271
|
4c2vA |
Aurora b kinase in complex with the specific inhibitor barasertib |
|
95
|
310
|
4c57A |
Structure of gak kinase in complex with a nanobody |
|
96
|
309
|
4ccuA |
Structure of the human anaplastic lymphoma kinase in complex with 2-(5-(6-amino-5-((r)-1-(5-fluoro-2-(2h-1,2,3-triazol-2-yl)phenyl)ethoxy) pyridin-3-yl)-4-methylthiazol-2-yl)propan-2-ol |
|
165
|
546
|
4bthB |
The leua146trp,pheb24tyr double mutant of the quorum quenching n-acyl homoserine lactone acylase pvdq has an altered substrate specificity towards small acyl chains |
|
107
|
340
|
4c35A |
Pka-s6k1 chimera with compound 1 (nu1085) bound |
|
96
|
308
|
4cmuA |
Structure of the human anaplastic lymphoma kinase in complex with the inhibitor (10r)-7-amino-12-fluoro-1,3,10,16-tetramethyl-16,17-dihydro- 1h-8,4-(metheno)pyrazolo(4,3-h)(2,5,11)benzoxadiazacyclotetradecin-15(10h)-one |
|
136
|
408
|
4c9oA |
Structure of cyanide and camphor bound d259n mutant of cyp101d1 |
|
71
|
209
|
4cgrA |
Structure of regulator protein sco3201 from streptomyces coelicolor |
|
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 |
|
269
|
945
|
4anxA |
Complexes of pi3kgamma with isoform selective inhibitors. |
|
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. |
|
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 |
|
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 |
|
88
|
280
|
4c4fA |
Structure-based design of orally bioavailable pyrrolopyridine inhibitors of the mitotic kinase mps1 |
|
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 |
|
112
|
338
|
4c37A |
Pka-s6k1 chimera with compound 21a (cct196539) bound |
|
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 |
|
77
|
255
|
4bxeA |
Crystal structure of ampdh3 from pseudomonas aeruginosa in complex with anhydromuramic pentapeptide |
|
75
|
203
|
4c7uA |
Crystal structure of manganese superoxide dismutase from arabidopsis thaliana |
|
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 |
|
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 |
|
120
|
404
|
4c0lA |
Crystal structure of drosophila miro ef hand and cgtpase domains bound to one magnesium ion and mg:gdp (mggdp-miros) |
|
23
|
88
|
4ca3A |
Solution structure of streptomyces virginiae vira acp5b |
|
31
|
118
|
4c79A |
Crystal structure of the smoothened crd, native |
|
35
|
94
|
4cfrA |
Ca-bound s100a4 c3s, c81s, c86s and f45w mutant complexed with non- muscle myosin iia |
|
42
|
148
|
4clnA |
Structure of a recombinant calmodulin from drosophila melanogaster refined at 2.2-angstroms resolution |
|
76
|
217
|
4c4tA |
Structure of beta-phosphoglucomutase in complex with a phosphonate analogue of beta-glucose-1-phosphate and aluminium tetrafluoride |
|
87
|
265
|
4cegA |
Crystal structure of aurora a 122-403 c290a, c393a bound to adp |
|
43
|
153
|
4cicA |
T. potens iscr |
|
151
|
489
|
4cklA |
Structure of 55 kda n-terminal domain of e. coli dna gyrase a subunit with simocyclinone d8 bound |
|
55
|
215
|
4chtB |
Crystal structure of the human topoisomerase iii alpha-rmi1 complex with bound calcium ion |
|
109
|
362
|
4c0aA |
Arf1(delta1-17)in complex with brag2 sec7-ph domain |
