|
93
|
294
|
4yo4A |
Crystal structure of dapk1 catalytic domain in complex with the hinge binding fragment phthalazine |
|
61
|
182
|
4yxcA |
Complex of flim(spoa)::flin fusion protein and flih(apar)::t4lysozyme fusion protein |
|
49
|
140
|
4yifA |
Crystal structure of rv0880 |
|
126
|
322
|
4ys7A |
Co-crystal structure of 2-[2-(5,8-dimethyl[1,2,4]triazolo[1,5-a]pyrazin-2-yl)ethyl]-3-methyl-3h-imidazo[4,5-f]quinoline (compound 39) with pde10a |
|
50
|
129
|
4z41A |
X-ray structure of the adduct formed in the reaction between lysozyme and a platinum(ii) compound with a s,o bidentate ligand (9a=chloro-(1-(3'-hydroxy)-3-(methylthio)-3-thioxo-prop-1-en-1-olate-o,s)-(dimethylsulfoxide-s)-platinum(ii)) |
|
167
|
548
|
4wkuB |
N-alkylboronic acid inhibitors reveal determinants of ligand specificity in the quorum-quenching and siderophore biosynthetic enzyme pvdq |
|
108
|
341
|
4z1vA |
Structure of factor inhibiting hif (fih) in complex with fe, no, and nog |
|
24
|
71
|
4z2mH |
Crystal structure of human spt16 mid-aid/h3-h4 tetramer fact histone complex |
|
116
|
349
|
4yu2A |
Crystal structure of dyrk1a with harmine-derivatized annh-75 inhibitor |
|
90
|
214
|
4ymvC |
Crystal structure of an amino acid abc transporter with atps |
|
123
|
515
|
4yfxF |
Escherichia coli rna polymerase in complex with myxopyronin b |
|
68
|
250
|
4ysxB |
Crystal structure of mitochondrial rhodoquinol-fumarate reductase from ascaris suum with the specific inhibitor nn23 |
|
72
|
248
|
4yqaA |
Crystal structure of trmd, a m1g37 trna methyltransferase with sam-competitive compounds |
|
97
|
333
|
4umpA |
Structure of melk in complex with inhibitors |
|
264
|
947
|
4hvbA |
Catalytic unit of pi3kg in complex with pi3k/mtor dual inhibitor pf-04979064 |
|
134
|
396
|
4umzA |
Pikc d50n mutant in complex with the engineered substrate mimic bearing a 2-dimethylaminomethylbenzoate group |
|
311
|
982
|
4f7zA |
Conformational dynamics of exchange protein directly activated by camp |
|
107
|
331
|
4umuA |
Structure of melk in complex with inhibitors |
|
189
|
637
|
4r0mA |
Structure of mcyg a-pcp complexed with phenylalanyl-adenylate |
|
59
|
169
|
4upgA |
X-ray structure of calcium-free human sorcin |
|
203
|
771
|
4qj5B |
Structure of a fragment of human phospholipase c-beta3 delta472-581, bound to ip3 and in complex with galphaq |
|
178
|
428
|
4wbnB |
Crystal structure of tubulin-stathmin-ttl complex solved by native-sad phasing |
|
8
|
70
|
3jamZ |
Cryoem structure of 40s-eif1a-eif1 complex from yeast |
|
98
|
328
|
4umrA |
Structure of melk in complex with inhibitors |
|
281
|
905
|
4f5cA |
Crystal structure of the spike receptor binding domain of a porcine respiratory coronavirus in complex with the pig aminopeptidase n ectodomain |
|
279
|
951
|
4ezlA |
Potent and selective inhibitors of pi3k-delta: obtaining isoform selectivity from the affinity pocket and tryptophan shelf |
|
68
|
270
|
4tq0A |
Crystal structure of human atg5-atg16n69 |
|
163
|
439
|
4wbnA |
Crystal structure of tubulin-stathmin-ttl complex solved by native-sad phasing |
|
23
|
145
|
3jamS |
Cryoem structure of 40s-eif1a-eif1 complex from yeast |
|
275
|
949
|
4ezkA |
Potent and selective inhibitors of pi3k-delta: obtaining isoform selectivity from the affinity pocket and tryptophan shelf |
|
96
|
265
|
4rx5A |
Bruton's tyrosine kinase (btk) with pyridazinone compound 23 |
|
75
|
233
|
4wqbA |
Thiosulfate dehydrogenase (tsda) from allochromatium vinosum - bisulfite soak |
|
88
|
300
|
4tl0A |
Crystal structure of death-associated protein kinase 1 with a crucial phosphomimicking mutation |
|
304
|
864
|
4pvbA |
Crystal structure of aminopeptidase n in complex with the phosphonic acid analogue of leucine (d-(s)-leup) |
|
219
|
772
|
4qj4B |
Structure of a fragment of human phospholipase c-beta3 delta472-569, bound to ip3 and in complex with galphaq |
|
209
|
544
|
4ud6Q |
Structure of methylviologen-treated anaerobically purified d. fructosovorans nife-hydrogenase |
|
273
|
951
|
4ezjA |
Potent and selective inhibitors of pi3k-delta: obtaining isoform selectivity from the affinity pocket and tryptophan shelf |
|
176
|
480
|
4urxS |
The crystal structure of h-ras and sos in complex with ligands |
|
253
|
950
|
4fadA |
Design and synthesis of a novel pyrrolidinyl pyrido pyrimidinone derivative as a potent inhibitor of pi3ka and mtor |
|
194
|
675
|
4r71A |
Structure of the qbeta holoenzyme complex in the p1211 crystal form |
|
41
|
150
|
3jamN |
Cryoem structure of 40s-eif1a-eif1 complex from yeast |
|
169
|
486
|
4tnzA |
Structure basis of cellular dntp regulation, samhd1-gtp-datp-dttp complex |
|
70
|
318
|
4un0C |
Crystal structure of the human cdk12-cyclink complex |
|
265
|
945
|
4f1sA |
Crystal structure of human pi3k-gamma in complex with a pyridyl-triazine-sulfonamide inhibitor |
|
267
|
949
|
4fa6A |
Design and synthesis of a novel pyrrolidinyl pyrido pyrimidinone derivative as a potent inhibitor of pi3ka and mtor |
|
17
|
70
|
5gaeJ |
Rnc in complex with a translocating secyeg |
|
94
|
268
|
4f7nB |
Crystal structure of human cdk8/cycc in complex with compound 11 (1-[3-tert-butyl-1-(4-methylphenyl)-1h-pyrazol-5-yl]-3-(5-hydroxypentyl)urea) |
|
57
|
205
|
4ettA |
Crystal structure of rabbit ryanodine receptor 1 mutant e2764k |
|
45
|
110
|
4f6gA |
Aquomet structure of his100trp cerebratulus lacteus mini-hemoglobin |
|
117
|
354
|
4fa9A |
Crystal structure of wt maug in complex with pre-methylamine dehydrogenase aged 30 days |
