|
113
|
350
|
5larA |
Crystal structure of p38 alpha mapk14 in complex with vpc00628 |
|
65
|
162
|
4zizA |
Serial femtosecond crystallography of soluble proteins in lipidic cubic phase (c-phycocyanin from t. elongatus) |
|
94
|
254
|
5l7hA |
Mcr in complex with ligand |
|
90
|
274
|
5c27A |
Crystal structure of syk in complex with compound 2 |
|
88
|
325
|
5acbC |
Crystal structure of the human cdk12-cyclink complex |
|
95
|
289
|
4zjiA |
Pak1 in complex with 2-chloro-5-ethyl-8-fluoro-11-(4-methylpiperazin-1-yl)-dibenzodiazepine |
|
88
|
308
|
5bvkA |
Fragment-based discovery of potent and selective ddr1/2 inhibitors |
|
71
|
263
|
5aafA |
Aurora a kinase bound to an imidazopyridine inhibitor (14a) |
|
85
|
263
|
5j87A |
Discovery of n-(3-(5-((3-acrylamido-4-(morpholine-4-carbonyl)phenyl)amino)-1-methyl-6-oxo-1,6-dihydropyridin-3-yl)-2-methylphenyl)-4-(tert-butyl)benzamide (chmfl-btk-01) as a highly selective irreversible btk kinase inhibitor |
|
76
|
287
|
5k0kA |
Crystal structure of the catalytic domain of the proto-oncogene tyrosine-protein kinase mer in complex with inhibitor unc2434 |
|
114
|
350
|
5bveA |
Tetrahydropyrrolo-diazepenones as inhibitors of erk2 kinase |
|
220
|
536
|
5il8A |
Tobacco 5-epi-aristolochene synthase with mopso buffer molecule and ca2+ ions |
|
26
|
124
|
5bqcB |
Crystal structure of norrin in complex with the cysteine-rich domain of frizzled 4 and sucrose octasulfate |
|
25
|
79
|
5kp7B |
Crystal structure of the curacin biosynthetic pathway hmg synthase in complex with holo donor-acp |
|
98
|
312
|
5iuiA |
Crystal structure of anaplastic lyphoma kinase (alk) in complex with 4 |
|
130
|
334
|
5jj6A |
Fic-1 (aa134 - 508) from c. elegans |
|
56
|
129
|
5kxpA |
Hen egg white lysozyme at 278k, data set 2 |
|
54
|
144
|
5jdoF |
T. congolense haptoglobin-haemoglobin receptor in complex with haemoglobin |
|
130
|
349
|
4yxmA |
Structure of thermotoga maritima disa d75n mutant with reaction product c-di-amp |
|
131
|
340
|
5ja0F |
Crystal structure of human fpps with allosterically bound fpp |
|
21
|
62
|
5kaiZ |
Nh3-bound rt xfel structure of photosystem ii 500 ms after the 2nd illumination (2f) at 2.8 a resolution |
|
69
|
272
|
4yxwG |
Bovine heart mitochondrial f1-atpase inhibited by amp-pnp and adp in the presence of thiophosphate. |
|
160
|
428
|
5j2uB |
Tubulin-mmaf complex |
|
88
|
268
|
5k3yA |
Crystal structure of aurorab/incenp in complex with bi 811283 |
|
83
|
193
|
5j3lA |
Structure of transcriptional regulatory repressor protein - ethr from mycobacterium tuberculosis in complex with 1-((2-cyclopentylethyl)sulfonyl)pyrrolidine at 1.66a resolution |
|
151
|
410
|
5jmpA |
Structure of plasmodium falciparum dxr in complex with a beta-substituted fosmidomycin analogue, lc57 and manganese |
|
98
|
260
|
5kyaA |
Brain penetrant liver x receptor (lxr) modulators based on a 2,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole core |
|
219
|
536
|
5ikhA |
Tobacco 5-epi-aristolochene synthase m4 mutant with (-)-premnaspirodiene |
|
58
|
151
|
5jsbA |
Crystal structure of mcl1-inhibitor complex |
|
53
|
129
|
5kxnA |
Hen egg white lysozyme at 100k, data set 4 |
|
214
|
536
|
5ik6A |
Tobacco 5-epi-aristolochene synthase with germacrene a and ppi |
|
165
|
452
|
5jl7A |
Human placental aromatase cytochrome p450 (cyp19a1): androstenedione complex #3 |
|
57
|
129
|
5kxyA |
Hen egg white lysozyme at 278k, data set 8 |
|
129
|
305
|
5ivgA |
Crystal structure of aspergillus terreus aristolochene synthase n299a complexed with farnesyl thiolodiphosphate |
|
135
|
437
|
5jcoA |
Structure and dynamics of single-isoform recombinant neuronal human tubulin |
|
40
|
105
|
5klvF |
Structure of bos taurus cytochrome bc1 with fenamidone inhibited |
|
59
|
144
|
5jggB |
X-ray sequence and high resolution crystal structure of persian sturgeon methemoglobin |
|
136
|
774
|
5k4lA |
Crystal structure of kdm5a in complex with a naphthyridone inhibitor |
|
65
|
186
|
5jfzA |
E. coli ecfict in complex with ecfica mutant e28g |
|
30
|
119
|
5bpbA |
Crystal structure of the cysteine-rich domain of human frizzled 4 - crystal form i |
|
78
|
306
|
5j8iA |
Crystal structure of tl11-113 bound to tak1-tab1 |
|
128
|
324
|
5k32A |
Pde4d crystal structure in complex with small molecule inhibitor |
|
89
|
309
|
5kz0A |
Structure of human anaplastic lymphoma kinase in complex with 2-[(1r)-1-{[2-amino-5-(1,3-dimethyl-1h-pyrazol-4-yl)pyridin-3-yl]oxy}ethyl]-4-fluoro-n,n-dimethylbenzamide |
|
124
|
363
|
5j40A |
The x-ray structure of jcv helicase |
|
84
|
262
|
5jrsA |
Crystal structure of bruton agammaglobulinemia tyrosine kinase complexed with 4-[2-fluoro-3-(4-oxo -3,4-dihydroquinazolin-3-yl)phenyl]-7-(2-hydroxypropan-2-y l)-9h-carbazole-1-carboxamide |
|
21
|
77
|
5kvrA |
X-ray crystal structure of a fragment (1-75) of a transcriptional regulator pdhr from escherichia coli cft073 |
|
217
|
536
|
5ik0A |
Tobacco 5-epi-aristolochene synthase with fpp |
|
193
|
529
|
5j59A |
Trypanosoma brucei methionyl-trna synthetase in complex with inhibitor (chem 1893) |
|
86
|
244
|
5kraA |
Crystal structure of the er-alpha ligand-binding domain (y537s) in complex with ddt and dde |
|
200
|
551
|
5ikrA |
The structure of mefenamic acid bound to human cyclooxygenase-2 |
