|
264
|
947
|
4hvbA |
Catalytic unit of pi3kg in complex with pi3k/mtor dual inhibitor pf-04979064 |
|
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 |
|
253
|
950
|
4fadA |
Design and synthesis of a novel pyrrolidinyl pyrido pyrimidinone derivative as a potent inhibitor of pi3ka and mtor |
|
265
|
945
|
4f1sA |
Crystal structure of human pi3k-gamma in complex with a pyridyl-triazine-sulfonamide inhibitor |
|
275
|
949
|
4ezkA |
Potent and selective inhibitors of pi3k-delta: obtaining isoform selectivity from the affinity pocket and tryptophan shelf |
|
267
|
949
|
4fa6A |
Design and synthesis of a novel pyrrolidinyl pyrido pyrimidinone derivative as a potent inhibitor of pi3ka and mtor |
|
273
|
951
|
4ezjA |
Potent and selective inhibitors of pi3k-delta: obtaining isoform selectivity from the affinity pocket and tryptophan shelf |
|
93
|
640
|
4pk1A |
Structure of bamb fused to a bama potra domain fragment |
|
186
|
721
|
4ee2A |
Crystal structure of anthrax protective antigen k446m mutant to 1.91-a resolution |
|
20
|
74
|
4fbjB |
Structure of the cif:nedd8 complex - photorhabdus luminescens cycle inhibiting factor in complex with human nedd8 |
|
108
|
386
|
4eutA |
Structure of bx-795 complexed with unphosphorylated human tbk1 kinase-uld domain |
|
22
|
74
|
4f8cB |
Structure of the cif:nedd8 complex - yersinia pseudotuberculosis cycle inhibiting factor in complex with human nedd8 |
|
37
|
124
|
4eoyA |
Plasmodium falciparum atg8 in complex with plasmodium falciparum atg3 peptide |
|
329
|
907
|
4c80A |
Aldehyde oxidoreductase from desulfovibrio gigas (mop), soaked with hydrogen peroxide |
|
256
|
945
|
4dk5A |
Crystal structure of human pi3k-gamma in complex with a pyridyl-triazine inhibitor |
|
98
|
348
|
4ekuA |
Crystal structure of ferm domain of proline-rich tyrosine kinase 2 |
|
19
|
74
|
4eewA |
Crystal structure of the ubl domain of bag6 |
|
52
|
194
|
4dxfA |
Crystal structure of staphylococcal superantigen-like protein 4 |
|
27
|
108
|
4e74A |
Crystal structure of the rho gtpase binding domain of plexin a4a |
|
142
|
650
|
4e3cA |
X-ray crystal structure of human ikk2 in an active conformation |
|
23
|
89
|
4efoA |
Crystal structure of the ubiquitin-like domain of human tbk1 |
|
91
|
311
|
4dxaB |
Co-crystal structure of rap1 in complex with krit1 |
|
331
|
907
|
4c7zA |
Aldehyde oxidoreductase from desulfovibrio gigas (mop), activated with sodium dithionite and sodium sulfide |
|
20
|
103
|
4e71A |
Crystal structure of the rho gtpase binding domain of plexin b2 |
|
12
|
115
|
4dqoC |
Crystal structure of pg16 fab in complex with v1v2 region from hiv-1 strain zm109 |
|
52
|
194
|
4dxgA |
Crystal structure of staphylococcal superantigen-like protein 4 complexed with sialyl lewis x |
|
330
|
907
|
4c7yA |
Aldehyde oxidoreductase from desulfovibrio gigas (mop), soaked with sodium dithionite and sodium sulfide |
|
17
|
79
|
4dwfA |
Crystal structure of a hla-b associated transcript 3 (bat3) from homo sapiens at 1.80 a resolution |
|
14
|
72
|
4dhzE |
The structure of h/ceotub1-ubiquitin aldehyde-ubc13~ub |
|
23
|
82
|
4dbgA |
Crystal structure of hoil-1l-ubl complexed with a hoip-uba derivative |
|
17
|
71
|
4dhjD |
The structure of a ceotub1 ubiquitin aldehyde ubc13~ub complex |
|
20
|
75
|
4dhzB |
The structure of h/ceotub1-ubiquitin aldehyde-ubc13~ub |
|
15
|
76
|
4ddiD |
Crystal structure of human otub1/ubch5b~ub/ub |
|
21
|
81
|
4d2kA |
Crystal structure of drep2 cide domain |
|
18
|
76
|
4ddgD |
Crystal structure of human otub1/ubch5b~ub/ub |
|
21
|
75
|
4dhjB |
The structure of a ceotub1 ubiquitin aldehyde ubc13~ub complex |
|
95
|
330
|
4cyeA |
Crystal structure of avian fak ferm domain fak31-405 at 3.2a |
|
249
|
945
|
4bfrA |
Discovery and optimization of pyrimidone indoline amide pi3kbeta inhibitors for the treatment of phosphatase and tensin homologue (pten)-deficient cancers |
|
34
|
118
|
4co7A |
Crystal structure of human gate-16 |
|
50
|
235
|
4c56C |
X-ray structure of the complex between staphylococcal enterotoxin b, t cell receptor and major histocompatibility complex class ii |
|
90
|
462
|
4c4vA |
Structure of the outer membrane protein insertase bama with one potra domain. |
|
74
|
254
|
4bzaA |
Crystal structure of tama potra domains 1-3 from e. coli |
|
151
|
553
|
4c00A |
Crystal structure of tama from e. coli |
|
277
|
1057
|
4a55A |
Crystal structure of p110alpha in complex with ish2 of p85alpha and the inhibitor pik-108 |
|
269
|
945
|
4anxA |
Complexes of pi3kgamma with isoform selective inhibitors. |
|
27
|
98
|
4chkA |
Crystal structure of the arf5 oligomerization domain |
|
90
|
465
|
4c4vB |
Structure of the outer membrane protein insertase bama with one potra domain. |
|
19
|
76
|
4bvuC |
Structure of shigella effector ospg in complex with host ubch5c- ubiquitin conjugate |
|
27
|
103
|
4bksA |
Von hippel lindau protein:elonginb:elonginc complex, in complex with (2s,4r)-1-ethanoyl-n-[[4-(1,3-oxazol-5-yl)phenyl]methyl]-4-oxidanyl-pyrrolidine-2-carboxamide |
