|
95
|
258
|
3u4tA |
Crystal structure of the c-terminal part of the tpr repeat-containing protein q11ti6_cyth3 from cytophaga hutchinsonii. northeast structural genomics consortium target chr11b. |
|
50
|
155
|
3twvA |
Crystal structure of arc4 from human tankyrase 2 in complex with peptide from human numa1 (chimeric peptide) |
|
250
|
950
|
3tjpA |
Crystal structure of pi3k gamma with n6-(3,4-dimethoxyphenyl)-2-morpholino-[4,5'-bipyrimidine]-2',6-diamine |
|
258
|
949
|
3tl5A |
Discovery of gdc-0980: a potent, selective, and orally available class i phosphatidylinositol 3-kinase (pi3k)/mammalian target of rapamycin (mtor) kinase inhibitor for the treatment of cancer |
|
106
|
271
|
3u64A |
The crystal structure of tat-t (tp0956) |
|
51
|
164
|
3twqA |
Crystal structure of arc4 from human tankyrase 2 (apo form) |
|
52
|
160
|
3twuA |
Crystal structure of arc4 from human tankyrase 2 in complex with peptide from human mcl1 |
|
51
|
158
|
3twxA |
Crystal structure of arc4 from human tankyrase 2 in complex with peptide from human fnbp1 (chimeric peptide) |
|
137
|
353
|
3txmA |
Crystal structure of rpn6 from drosophila melanogaster, gd(3+) complex |
|
139
|
353
|
3txnA |
Crystal structure of rpn6 from drosophila melanogaster, native data |
|
47
|
156
|
3twtA |
Crystal structure of arc4 from human tankyrase 2 in complex with peptide from human mcl1 (chimeric peptide) |
|
270
|
949
|
3t8mA |
Rational design of pi3k-alpha inhibitors that exhibit selectivity over the pi3k-beta isoform |
|
48
|
157
|
3twsA |
Crystal structure of arc4 from human tankyrase 2 in complex with peptide from human terf1 (chimeric peptide) |
|
51
|
157
|
3twwA |
Crystal structure of arc4 from human tankyrase 2 in complex with peptide from human lnpep (chimeric peptide) |
|
271
|
714
|
3taxA |
A neutral diphosphate mimic crosslinks the active site of human o-glcnac transferase |
|
48
|
157
|
3twrA |
Crystal structure of arc4 from human tankyrase 2 in complex with peptide from human 3bp2 |
|
137
|
425
|
3tg5A |
Structure of smyd2 in complex with p53 and sah |
|
86
|
321
|
3t9kA |
Crystal structure of acap1 c-portion mutant s554d fused with integrin beta1 peptide |
|
145
|
427
|
3tg4A |
Structure of smyd2 in complex with sam |
|
66
|
195
|
3t5xA |
Pcid2:dss1 structure |
|
51
|
184
|
3t8kA |
The crystal structure of a functionally unknown protein lebu_0176 from leptotrichia buccalis c-1013-b |
|
269
|
1148
|
3shfA |
Crystal structure of the r265s mutant of full-length murine apaf-1 |
|
178
|
615
|
3sy2A |
Crystal structure of the salmonella e3 ubiquitin ligase sopa in complex with the human e2 ubch7 |
|
301
|
1148
|
3sfzA |
Crystal structure of full-length murine apaf-1 |
|
56
|
151
|
3sz7A |
Crystal structure of the sgt2 tpr domain from aspergillus fumigatus |
|
180
|
484
|
3sghA |
Crystal structure of a susd-like protein (bt_3752) from bacteroides thetaiotaomicron vpi-5482 at 1.70 a resolution |
|
165
|
455
|
3snxA |
Crystal structure of a putative susd-like carbohydrate binding protein (bt_1439) from bacteroides thetaiotaomicron vpi-5482 at 1.88 a resolution |
|
64
|
152
|
3si5A |
Kinetochore-bubr1 kinase complex |
|
49
|
162
|
3so8A |
Crystal structure of ankra |
|
166
|
612
|
3sqvA |
Crystal structure of e. coli o157:h7 e3 ubiquitin ligase, nlel, with a human e2, ubch7 |
|
132
|
330
|
3sfyA |
Cryptococcus neoformans protein farnesyltransferase in complex with fpt-ii and ethylenediamine inhibitor 2 |
|
159
|
362
|
3sf4A |
Crystal structure of the complex between the conserved cell polarity proteins inscuteable and lgn |
|
101
|
317
|
3sbtB |
Crystal structure of a aar2-prp8 complex |
|
131
|
330
|
3sfxA |
Cryptococcus neoformans protein farnesyltransferase in complex with fpt-ii and tipifarnib |
|
99
|
318
|
3sbsA |
Crystal structure of aar2 protein |
|
251
|
949
|
3sd5A |
Crystal structure of pi3k gamma with 5-(2,4-dimorpholinopyrimidin-6-yl)-4-(trifluoromethyl)pyridin-2-amine |
|
148
|
428
|
3s7jA |
Structural basis of substrate methylation and inhibition of smyd2 |
|
151
|
429
|
3s7bA |
Structural basis of substrate methylation and inhibition of smyd2 |
|
261
|
945
|
3s2aA |
Crystal structure of pi3k-gamma in complex with a quinoline inhibitor |
|
152
|
429
|
3s7fA |
Structural basis of substrate methylation and inhibition of smyd2 |
|
150
|
429
|
3s7dA |
Structural basis of substrate methylation and inhibition of smyd2 |
|
148
|
425
|
3ru0A |
Cocrystal structure of human smyd3 with inhibitor sinefungin bound |
|
63
|
147
|
3rkvA |
C-terminal domain of protein c56c10.10, a putative peptidylprolyl isomerase, from caenorhabditis elegans |
|
44
|
141
|
3rruA |
X-ray crystal structure of the vhs domain of human tom1-like protein, northeast structural genomics consortium target hr3050e |
|
144
|
332
|
3ro2A |
Structures of the lgn/numa complex |
|
118
|
295
|
3rrmB |
S. cerevisiae dbp5 l327v bound to nup159, gle1 h337r, ip6 and adp |
|
41
|
142
|
3rseG |
Structural and biochemical characterization of two binding sites for nucleation promoting factor wasp-vca on arp2/3 complex |
|
74
|
159
|
3ro3A |
Crystal structure of lgn/minscuteable complex |
|
269
|
949
|
3r7qA |
Structure-based design of thienobenzoxepin inhibitors of pi3- kinase |
|
114
|
293
|
3rrnB |
S. cerevisiae dbp5 l327v bound to gle1 h337r and ip6 |
