|
157
|
411
|
3nmzA |
Crystal structure of apc complexed with asef |
|
141
|
334
|
3nmxA |
Crystal structure of apc complexed with asef |
|
41
|
154
|
3nocD |
Designed ankyrin repeat protein (darpin) binders to acrb: plasticity of the interface |
|
221
|
811
|
3mkqA |
Crystal structure of yeast alpha/betaprime-cop subcomplex of the copi vesicular coat |
|
119
|
305
|
3nf1A |
Crystal structure of the tpr domain of kinesin light chain 1 |
|
260
|
950
|
3ml8A |
Discovery of the highly potent pi3k/mtor dual inhibitor pf-04691502 through structure based drug design |
|
255
|
1337
|
3lxuX |
Crystal structure of tripeptidyl peptidase 2 (tpp ii) |
|
158
|
445
|
3myvA |
Crystal structure of a susd superfamily protein (bvu_0732) from bacteroides vulgatus atcc 8482 at 1.80 a resolution |
|
278
|
950
|
3ml9A |
Discovery of the highly potent pi3k/mtor dual inhibitor pf-04691502 through structure based drug design |
|
168
|
468
|
3n71A |
Crystal structure of cardiac specific histone methyltransferase smyd1 |
|
262
|
889
|
3mdjA |
Er aminopeptidase, erap1, bound to the zinc aminopeptidase inhibitor, bestatin |
|
100
|
336
|
3mzlB |
Sec13/sec31 edge element, loop deletion mutant |
|
112
|
291
|
3mkrA |
Crystal structure of yeast alpha/epsilon-cop subcomplex of the copi vesicular coat |
|
107
|
293
|
3mv2B |
Crystal structure of a-cop in complex with e-cop |
|
174
|
472
|
3mx3A |
Crystal structure of a susd homolog (bf0972) from bacteroides fragilis nctc 9343 at 2.00 a resolution |
|
66
|
177
|
3mkqB |
Crystal structure of yeast alpha/betaprime-cop subcomplex of the copi vesicular coat |
|
239
|
947
|
3mjwA |
Pi3 kinase gamma with a benzofuranone inhibitor |
|
258
|
873
|
3lwwA |
Structure of an open and closed conformation of human importin beta bound to the snurportin1 ibb-domain trapped in the same crystallographic asymmetric unit |
|
106
|
293
|
3mv3B |
Crystal structure of a-cop in complex with e-cop |
|
99
|
270
|
3m66A |
Crystal structure of human mitochondrial transcription termination factor 3 |
|
263
|
948
|
3lj3A |
Pi3-kinase-gamma with a pyrrolopyridine-benzofuran inhibitor |
|
134
|
423
|
3mekA |
Crystal structure of human histone-lysine n-methyltransferase smyd3 in complex with s-adenosyl-l-methionine |
|
120
|
476
|
3lvrE |
The crystal structure of asap3 in complex with arf6 in transition state soaked with calcium |
|
35
|
90
|
3ma5A |
Crystal structure of the tetratricopeptide repeat domain protein q2s6c5_salrd from salinibacter ruber. northeast structural genomics consortium target srr115c. |
|
182
|
459
|
3mcxA |
Crystal structure of susd superfamily protein (bt_2365) from bacteroides thetaiotaomicron vpi-5482 at 1.49 a resolution |
|
201
|
590
|
3ls8A |
Crystal structure of human pik3c3 in complex with 3-[4-(4-morpholinyl)thieno[3,2-d]pyrimidin-2-yl]-phenol |
|
126
|
476
|
3lvqE |
The crystal structure of asap3 in complex with arf6 in transition state |
|
102
|
317
|
3mgbA |
Teg 12 ternary structure complexed with pap and the teicoplanin aglycone |
|
122
|
323
|
3ly8A |
Crystal structure of mutant d471e of the periplasmic domain of cadc |
|
119
|
318
|
3lyaA |
Crystal structure of the periplasmic domain of cadc in the presence of k2recl6 |
|
112
|
322
|
3ly9A |
Crystal structure of mutant d471n of the periplasmic domain of cadc |
|
118
|
322
|
3ly7A |
Crystal structure of the periplasmic domain of cadc |
|
260
|
949
|
3l16A |
Discovery of (thienopyrimidin-2-yl)aminopyrimidines as potent, selective, and orally available pan-pi3-kinase and dual pan-pi3-kinase/mtor inhibitors for the treatment of cancer |
|
69
|
185
|
3ltmA |
Structure of a new family of artificial alpha helicoidal repeat proteins (alpha-rep) based on thermostable heat-like repeats |
|
272
|
947
|
3l08A |
Structure of pi3k gamma with a potent inhibitor: gsk2126458 |
|
253
|
949
|
3l13A |
Crystal structures of pan-pi3-kinase and dual pan-pi3-kinase/mtor inhibitors |
|
79
|
191
|
3ltjA |
Structure of a new family of artificial alpha helicoidal repeat proteins (alpha-rep) based on thermostable heat-like repeats |
|
261
|
949
|
3l17A |
Discovery of (thienopyrimidin-2-yl)aminopyrimidines as potent, selective, and orally available pan-pi3-kinase and dual pan-pi3-kinase/mtor inhibitors for the treatment of cancer |
|
81
|
304
|
3ljnA |
Ankyrin repeat protein from leishmania major |
|
271
|
952
|
3l54A |
Structure of pi3k gamma with inhibitor |
|
187
|
480
|
3lewA |
Crystal structure of susd-like carbohydrate binding protein (yp_001298396.1) from bacteroides vulgatus atcc 8482 at 1.70 a resolution |
|
200
|
514
|
3lcaA |
Structure of tom71 complexed with hsp70 ssa1 c terminal tail indicating conformational plasticity |
|
116
|
286
|
3lkuA |
Crystal structure of s. cerevisiae get4 in complex with an n-terminal fragment of get5 |
|
57
|
140
|
3ldzA |
Crystal structure of human stam1 vhs domain in complex with ubiquitin |
|
315
|
866
|
3kedA |
Crystal structure of aminopeptidase n in complex with 2,4-diaminobutyric acid |
|
117
|
321
|
3lpzA |
Crystal structure of c. therm. get4 |
|
145
|
392
|
3l6yA |
Crystal structure of p120 catenin in complex with e-cadherin |
|
115
|
340
|
3l3fX |
Crystal structure of a pfu-pul domain pair of saccharomyces cerevisiae doa1/ufd3 |
|
62
|
203
|
3l82A |
X-ray crystal structure of trf1 and fbx4 complex |
|
167
|
427
|
3l3qA |
Mouse importin alpha-peptm nls peptide complex |
