|
101
|
286
|
5a9tA |
Imine reductase from amycolatopsis orientalis in complex with (r)- methyltetrahydroisoquinoline |
|
83
|
266
|
5l8jA |
Aurora-a kinase domain in complex with vnar-d01 s93r |
|
64
|
250
|
5c2tB |
Crystal structure of mitochondrial rhodoquinol-fumarate reductase from ascaris suum with rhodoquinone-2 |
|
95
|
291
|
4zjjA |
Pak1 in complex with (s)-n-(tert-butyl)-3-((2-chloro-5-ethyl-8-fluoro-dibenzodiazepin-11-yl)amino)pyrrolidine-1-carboxamide |
|
165
|
439
|
5lyjA |
Tubulin-combretastatin a4 complex |
|
53
|
129
|
5kxzA |
Hen egg white lysozyme at 278k, data set 9 |
|
259
|
662
|
5k3jA |
Crystals structure of acyl-coa oxidase-2 in caenorhabditis elegans bound with fad, ascaroside-coa, and atp |
|
42
|
117
|
5ab8A |
High resolution x-ray structure of the n-terminal truncated form (residues 1-11) of mycobacterium tuberculosis hbn |
|
90
|
241
|
5c4uA |
Identification of a novel allosteric binding site for rorgt inhibitors |
|
92
|
241
|
5c4sA |
Identification of a novel allosteric binding site for rorgt inhibitors |
|
90
|
323
|
5c8mA |
Egfr kinase domain mutant "tmlr" with compound 17 |
|
50
|
129
|
5lioA |
Lysozyme, collected at rotation 360 degree per second |
|
60
|
158
|
4zieA |
Crystal structure of core/latch dimer of bax in complex with bimbh3 |
|
54
|
141
|
5c6eA |
Joint x-ray/neutron structure of equine cyanomet hemoglobin in r state |
|
89
|
291
|
5c03A |
Crystal structure of kinase |
|
47
|
130
|
5lvkA |
Human lysozyme soaked with [h2ind][trans-rucl4(dmso)(hind)] |
|
165
|
427
|
5la6B |
Tubulin-pironetin complex |
|
83
|
286
|
5lvlA |
Human pdk1 kinase domain in complex with compound ps653 bound to the atp-binding site |
|
84
|
287
|
5ackA |
Human pdk1 kinase domain in complex with allosteric compound 7 bound to the pif-pocket |
|
54
|
136
|
5c4yA |
Crystal structure of putative tetr family transcription factor from listeria monocytogenes |
|
339
|
889
|
4zw6A |
X-ray crystal structure of pfa-m1 in complex with hydroxamic acid-based inhibitor 9q |
|
260
|
713
|
5kskA |
Crystal structure of the catalase-peroxidase from b. pseudomallei treated with acetate |
|
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) |
|
29
|
93
|
5lavA |
Novel spiro[3h-indole-3,2 -pyrrolidin]-2(1h)-one inhibitors of the mdm2-p53 interaction: hdm2 (mdm2) in complex with compound 6b |
|
29
|
94
|
5lazA |
Novel spiro[3h-indole-3,2 -pyrrolidin]-2(1h)-one inhibitors of the mdm2-p53 interaction: hdm2 (mdm2) in complex with compound bi-0252 |
|
32
|
104
|
5c0kA |
Fragment-based drug discovery targeting inhibitor of apoptosis proteins: compound 3 |
|
108
|
347
|
5lckA |
A clickable covalent erk 1/2 inhibitor |
|
70
|
277
|
5m55A |
Nek2 bound to arylaminopurine 71 |
|
218
|
581
|
5a4iL |
The mechanism of hydrogen activation by nife-hydrogenases |
|
157
|
440
|
5lp6C |
Crystal structure of tubulin-stathmin-ttl-thiocolchicine complex |
|
49
|
129
|
5lagA |
Room temperature x-ray diffraction of tetragonal hewl with 1m of uridine. second data set (0.62 mgy) |
|
76
|
236
|
5lrrA |
The transcriptional regulator prfa from listeria monocytogenes in complex with glutathione |
|
48
|
129
|
5la8A |
Room temperature x-ray diffraction of tetragonal hewl. third data set (0.93 mgy) |
|
194
|
512
|
5kcmA |
Crystal structure of iron-sulfur cluster containing photolyase phrb mutant i51w |
|
69
|
172
|
4zizB |
Serial femtosecond crystallography of soluble proteins in lipidic cubic phase (c-phycocyanin from t. elongatus) |
|
222
|
532
|
5c05A |
Crystal structure of gamma-terpinene synthase from thymus vulgaris |
|
102
|
289
|
4ytiA |
Discovery of vx-509 (decernotinib): a potent and selective janus kinase (jak) 3 inhibitor for the treatment of autoimmune disease |
|
57
|
162
|
5lzmA |
Comparison of the crystal structure of bacteriophage t4 lysozyme at low, medium, and high ionic strengths |
|
93
|
290
|
4zimA |
Crystal structure of janus kinase 2 in complex with a 9h-carbazole-1-carboxamide inhibitor |
|
201
|
596
|
5aa6A |
Homohexameric structure of the second vanadate-dependent bromoperoxidase (anii) from ascophyllum nodosum |
|
26
|
69
|
5bxzA |
H17 bat influenza ns1 rna binding domain |
|
81
|
289
|
5c01A |
Crystal structure of kinase |
|
28
|
94
|
5lawA |
Novel spiro[3h-indole-3,2 -pyrrolidin]-2(1h)-one inhibitors of the mdm2-p53 interaction: hdm2 (mdm2) in complex with compound 14 |
|
164
|
438
|
5la6A |
Tubulin-pironetin complex |
|
88
|
300
|
5c5oA |
Structure of sars-3cl protease complex with a phenyl-beta-alanyl (s,r)-n-decalin type inhibitor |
|
47
|
129
|
5lafA |
Room temperature x-ray diffraction of tetragonal hewl with 1m of uridine. first data set (0.31 mgy) |
|
95
|
270
|
5lmaA |
Human spleen tyrosine kinase kinase domain in complex with azanaphthyridine inhibitor |
|
141
|
397
|
5l1oA |
X-ray structure of cytochrome p450 pntm with pentalenolactone f |
|
78
|
272
|
5c9cA |
Crystal structure of braf(v600e) in complex with ly3009120 compnd |
