|
39
|
129
|
4dc4A |
Lysozyme trimer |
|
83
|
274
|
4dfnA |
Crystal structure of spleen tyrosine kinase complexed with an adamantylpyrazine inhibitor |
|
119
|
424
|
4cyjA |
Chaetomium thermophilum pan2:pan3 complex |
|
134
|
438
|
4d9jA |
Structure of a 16 nm protein cage designed by fusing symmetric oligomeric domains |
|
94
|
388
|
4cswA |
Rhodothermus marinus ycfd-like ribosomal protein l16 arginyl hydroxylase |
|
78
|
203
|
4d5fA |
Tetracycline repressor class h, apo form |
|
110
|
326
|
4dgmA |
Crystal structure of maize ck2 in complex with the inhibitor apigenin |
|
95
|
333
|
4d2pA |
Structure of melk in complex with inhibitors |
|
113
|
316
|
4d9wA |
Thermolysin in complex with ubtln32 |
|
45
|
129
|
4dd2A |
Eval processed hewl, carboplatin aqueous glycerol |
|
105
|
337
|
4dg3E |
Crystal structure of r336a mutant of camp-dependent protein kinase with unphosphorylated turn motif. |
|
94
|
279
|
4dkbA |
Crystal structure of trypanosoma brucei dutpase with dupnp and ca2+ |
|
131
|
340
|
4d09A |
Pde2a catalytic domain in complex with a brain penetrant inhibitor |
|
58
|
197
|
4d7sA |
Structure of the sthk carboxy-terminal region in complex with cgmp |
|
82
|
266
|
4deaA |
Aurora a in complex with yl1-038-18 |
|
44
|
316
|
4dk1A |
Crystal structure of maca-mexa chimeric protein, containing the pseudomonas aeruginosa mexa alpha-hairpin domain. |
|
76
|
280
|
4cv9A |
Mps1 kinase with 3-aminopyridin-2-one inhibitors |
|
45
|
129
|
4ddbA |
Eval processed hewl, cisplatin dmso paratone ph 6.5 |
|
25
|
57
|
4do2A |
Crystal structure of the rop protein mutant d30p/a31g at resolution 1.4 resolution. |
|
139
|
404
|
4d3yA |
The structure of inactive prolegumain from chinese hamster. |
|
74
|
274
|
4dbnA |
Crystal structure of the kinase domain of human b-raf with a [1,3]thiazolo[5,4-b]pyridine derivative |
|
48
|
145
|
4dgaC |
Trimcyp cyclophilin domain from macaca mulatta: hiv-1 ca(o-loop) complex |
|
89
|
342
|
4dinA |
Novel localization and quaternary structure of the pka ri beta holoenzyme |
|
60
|
207
|
4dolA |
Crystal structure of arabidopsis thaliana fatty-acid binding protein at1g53520 (atfap3) |
|
80
|
333
|
4cxaA |
Crystal structure of the human cdk12-cyclin k complex bound to amppnp |
|
96
|
294
|
4dawA |
Crystal structure of pak1 kinase domain with the ruthenium phthalimide complex |
|
33
|
93
|
4dijA |
The central valine concept provides an entry in a new class of non peptide inhibitors of the p53-mdm2 interaction |
|
208
|
583
|
4c3oA |
Structure and function of an oxygen tolerant nife hydrogenase from salmonella |
|
80
|
299
|
4cfxA |
Structure-based design of c8-substituted o6-cyclohexylmethoxyguanine cdk1 and 2 inhibitors. |
|
144
|
448
|
4bmmA |
Crystal structure of trypanosoma cruzi cyp51 bound to the inhibitor (r)-n-(3-(1h-indol-3-yl)-1-oxo-1-(pyridin-4-ylamino)propan-2-yl)-2',3, 5'-trifluoro-(1,1'-biphenyl)-4-carboxamide |
|
81
|
279
|
4c4eA |
Structure-based design of orally bioavailable pyrrolopyridine inhibitors of the mitotic kinase mps1 |
|
97
|
264
|
4ci4A |
Structural basis for gl479 a dual peroxisome proliferator-activated receptor alpha agonist |
|
142
|
408
|
4bofA |
Crystal structure of arginine deiminase from group a streptococcus |
|
159
|
450
|
4c27A |
Crystal structure of trypanosoma cruzi cyp51 bound to the inhibitor (r)-n-(3-(1h-indol-3-yl)-1-oxo-1-(pyridin-4-ylamino)propan-2-yl)-2-fluoro-4-(4-(4-(trifluoromethyl)phenyl)piperazin-1-yl)benzamide |
|
166
|
486
|
4bzcA |
Crystal structure of the tetrameric dgtp-bound wild type samhd1 catalytic core |
|
249
|
945
|
4bfrA |
Discovery and optimization of pyrimidone indoline amide pi3kbeta inhibitors for the treatment of phosphatase and tensin homologue (pten)-deficient cancers |
|
72
|
196
|
4br6A |
Crystal structure of chaetomium thermophilum mnsod |
|
83
|
255
|
4bxjA |
Crystal structure of ampdh3 from pseudomonas aeruginosa |
|
101
|
332
|
4casA |
Serial femtosecond crystallography structure of a photosynthetic reaction center |
|
111
|
327
|
4chxA |
Crystal structure of mltc in complex with disaccharide pentapeptide dhl89 |
|
191
|
548
|
4bjuA |
Genetic and structural validation of aspergillus fumigatus n- acetylphosphoglucosamine mutase as an antifungal target |
|
137
|
442
|
4c1nA |
Corrinoid protein reactivation complex with activator |
|
57
|
150
|
4c44A |
Crystal structure of truncated plant hemoglobin from arabidopsis thaliana |
|
81
|
271
|
4c7tA |
Focal adhesion kinase catalytic domain in complex with a diarylamino- 1,3,5-triazine inhibitor |
|
134
|
458
|
4cckA |
60s ribosomal protein l8 histidine hydroxylase (no66) in complex with mn(ii) and n-oxalylglycine (nog) |
|
230
|
667
|
4babA |
Redesign of a phenylalanine aminomutase into a beta-phenylalanine ammonia lyase |
|
347
|
1039
|
4anjA |
Myosin vi (mdinsert2-gfp fusion) pre-powerstroke state (mg.adp.alf4) |
|
230
|
670
|
4bayA |
Phosphomimetic mutant of lsd1-8a splicing variant in complex with corest |
|
116
|
404
|
4c0jA |
Crystal structure of drosophila miro ef hand and cgtpase domains in the apo state (apo-miros) |
|
134
|
459
|
4ccnA |
60s ribosomal protein l8 histidine hydroxylase (no66 l299c/c300s) in complex with mn(ii), n-oxalylglycine (nog) and 60s ribosomal protein l8 (rpl8 g220c) peptide fragment (complex-2) |
