|
136
|
325
|
5c28A |
Pde10 complexed with 6-chloro-2-cyclopropyl-5-methyl-pyrimidin-4-amine |
|
126
|
308
|
5c2hA |
Pde10 complexed with 6-chloro-n-[(2,4-dimethylthiazol-5-yl)methyl]-5-methyl-2-[3-(2-quinolyl)propoxy]pyrimidin-4-amine |
|
115
|
350
|
5bvdA |
Tetrahydropyrrolo-diazepenones as inhibitors of erk2 kinase |
|
201
|
729
|
5c18A |
P97-delta709-728 in complex with atp-gamma-s |
|
13
|
65
|
4y7nJ |
The structure insight into 5-carboxycytosine recognition by rna polymerase ii during transcription elongation. |
|
26
|
78
|
5c3iC |
Crystal structure of the quaternary complex of histone h3-h4 heterodimer with chaperone asf1 and the replicative helicase subunit mcm2 |
|
69
|
301
|
5c3nA |
Crystal structure of mers coronavirus main protease in spacegroup c2221 |
|
83
|
284
|
5c5eA |
Structure of kaia dimer in complex with c-terminal kaic peptide at 2.8 a resolution |
|
91
|
308
|
5bvnA |
Fragment-based discovery of potent and selective ddr1/2 inhibitors |
|
51
|
165
|
5c6kA |
Bacteriophage p2 integrase catalytic domain |
|
111
|
348
|
5buiA |
Erk2 complexed with 2-pyridiyl tetrahydroazaindazole |
|
321
|
908
|
5ab2A |
Crystal structure of aminopeptidase erap2 with ligand |
|
127
|
323
|
5c2eA |
Pde10 complexed with6-chloro-n-[(2,4-dimethylthiazol-5-yl)methyl]-5-methyl-2-[2-(2-pyridyl)ethoxy]pyrimidin-4-amine |
|
93
|
365
|
5bv5A |
Structure of cyp119 with t213a and c317h mutations |
|
328
|
910
|
5ab0A |
Crystal structure of aminopeptidase erap2 with ligand |
|
223
|
607
|
5bppA |
Structure of human leukotriene a4 hydrolase in complex with inhibitor 4az |
|
211
|
730
|
5c1bA |
P97-delta709-728 in complex with a ufd1-shp peptide |
|
63
|
153
|
5c6yA |
A sperm whale myoglobin double mutant l29h/f43y mb with a tyr-heme cross-link |
|
180
|
548
|
5bnzA |
Crystal structure of glutamine-trna ligase /glutaminyl-trna synthetase (glnrs) from pseudomonas aeruginosa |
|
93
|
241
|
5c4tA |
Identification of a novel allosteric binding site for rorgt inhibitors |
|
32
|
106
|
5c3kA |
Fragment-based drug discovery targeting inhibitor of apoptosis proteins: compound 4 |
|
67
|
201
|
5c2jA |
Complex structure of the gap domain of mgcracgap and cdc42 |
|
95
|
322
|
5c8kA |
Egfr kinase domain mutant "tmlr" with compound 1 |
|
97
|
344
|
5bx0A |
An automated microscale thermophoresis screening approach for fragment-based lead discovery |
|
83
|
229
|
5bvrA |
Actin binding domain of alpha-actinin from schizosaccharomyces pombe |
|
114
|
381
|
4wc4A |
Trna-processing enzyme complex 2 |
|
27
|
87
|
5c3iB |
Crystal structure of the quaternary complex of histone h3-h4 heterodimer with chaperone asf1 and the replicative helicase subunit mcm2 |
|
93
|
274
|
5c26A |
Crystal structure of syk in complex with compound 1 |
|
97
|
273
|
5c9gA |
Crystal structure of a putative enoyl-coa hydratase/isomerase family protein from hyphomonas neptunium |
|
57
|
146
|
5c6eB |
Joint x-ray/neutron structure of equine cyanomet hemoglobin in r state |
|
109
|
348
|
5bueA |
Erk2 complexed with n-benzylpyridone tetrahydroazaindazole |
|
109
|
350
|
5bujA |
Erk2 complexed with a n-h tetrahydroazaindazole |
|
135
|
325
|
5c1wA |
Pde10 complexed with 4,6-dichloro-2-cyclopropyl-5-methyl-pyrimidine |
|
44
|
129
|
5c6jA |
Crystal structure of gadolinium derivative of hewl solved using free-electron laser radiation |
|
107
|
346
|
5byyA |
Erk5 in complex with small molecule |
|
32
|
106
|
5c7bA |
Fragment-based drug discovery targeting inhibitor of apoptosis proteins: compound 5 |
|
167
|
502
|
4qpxA |
Nv polymerase post-incorporation-like complex |
|
33
|
106
|
5c3hA |
Fragment-based drug discovery targeting inhibitor of apoptosis proteins: compound 1 |
|
133
|
323
|
5c2aA |
Pde10 complexed with 6-chloro-2-cyclopropyl-n-[(2,4-dimethylthiazol-5-yl)methyl]-5-methyl-pyrimidin-4-amine |
|
32
|
107
|
5c83A |
Fragment-based drug discovery targeting inhibitor of apoptosis proteins: compound 21 |
|
33
|
106
|
5c0lA |
Fragment-based drug discovery targeting inhibitor of apoptosis proteins: compound 2 |
|
35
|
106
|
5c7dA |
Fragment-based drug discovery targeting inhibitor of apoptosis proteins: compound 17 |
|
92
|
308
|
5bvoA |
Fragment-based discovery of potent and selective ddr1/2 inhibitors |
|
61
|
151
|
5c3fA |
Crystal structure of mcl-1 bound to bid-mm |
|
107
|
350
|
5bvfA |
Tetrahydropyrrolo-diazepenones as inhibitors of erk2 kinase |
|
25
|
77
|
5bo0A |
Crystal structure of human mcm2 hbd and asf1b chaperoning a histone h3.2-h4 dimer |
|
84
|
273
|
5c1qB |
Serine/threonine-protein kinase pim-1 |
|
99
|
272
|
5bshA |
Crystal structure of medicago truncatula (delta)1-pyrroline-5-carboxylate reductase (mtp5cr) in complex with l-proline |
|
33
|
97
|
5b5eU |
Crystal structure analysis of photosystem ii complex |
|
30
|
108
|
5cpiC |
Nucleosome containing unmethylated sat2r dna |
