|
50
|
129
|
4b4jA |
1.25 a structure of lysozyme crystallized with (rs)-2-methyl-2,4- pentanediol |
|
57
|
152
|
4bpjA |
Mcl-1 bound to alpha beta puma bh3 peptide 3 |
|
89
|
252
|
4bcfB |
Structure of cdk9 in complex with cyclin t and a 2-amino-4-heteroaryl- pyrimidine inhibitor |
|
82
|
322
|
4bciA |
Structure of cdk9 in complex with cyclin t and a 2-amino-4-heteroaryl- pyrimidine inhibitor |
|
70
|
246
|
4bj4A |
Structure of pseudomonas aeruginosa amidase ampdh2 |
|
132
|
467
|
4asuD |
F1-atpase in which all three catalytic sites contain bound nucleotide, with magnesium ion released in the empty site |
|
52
|
202
|
4b7wA |
Ligand binding domain human hepatocyte nuclear factor 4alpha: apo form |
|
202
|
646
|
4b6eA |
Discovery of an allosteric mechanism for the regulation of hcv ns3 protein function |
|
53
|
157
|
4bd7A |
Bax domain swapped dimer induced by octylmaltoside |
|
108
|
345
|
4arqB |
Structure of the pesticin s89c, s285c double mutant |
|
106
|
331
|
4bkyA |
Crystal structure of unphosphorylated maternal embryonic leucine zipper kinase (melk) in complex with pyrrolopyrazole inhibitor |
|
49
|
129
|
4b4iA |
1.20 a structure of lysozyme crystallized with (s)-2-methyl-2,4- pentanediol |
|
89
|
252
|
4bchB |
Structure of cdk9 in complex with cyclin t and a 2-amino-4-heteroaryl- pyrimidine inhibitor |
|
95
|
299
|
4aszA |
Crystal structure of apo trkb kinase domain |
|
148
|
470
|
4azvA |
Co-crystal structure of wbdd and kinase inhibitor gw435821x. |
|
98
|
258
|
4bcoB |
Structure of cdk2 in complex with cyclin a and a 2-amino-4-heteroaryl- pyrimidine inhibitor |
|
77
|
299
|
4bduA |
Bax bh3-in-groove dimer (gfp) |
|
68
|
243
|
4au7A |
The structure of the suv4-20h2 ternary complex with histone h4 |
|
74
|
389
|
4aybC |
Rnap at 3.2ang |
|
86
|
252
|
4bcjB |
Structure of cdk9 in complex with cyclin t and a 2-amino-4-heteroaryl- pyrimidine inhibitor |
|
166
|
616
|
4aidA |
Crystal structure of c. crescentus pnpase bound to rnase e recognition peptide |
|
186
|
578
|
4bbyA |
Mammalian alkyldihydroxyacetonephosphate synthase: wild-type |
|
81
|
252
|
4bptA |
Structural and thermodynamic insight into phenylalanine hydroxylase from the human pathogen legionella pneumophila |
|
98
|
354
|
4b48A |
Bacterial translation initiation factor if2 (1-363), complex with gtp |
|
84
|
271
|
4bicA |
Crystal structures of ask1-inhibitor complexes |
|
28
|
93
|
4avpA |
Crystal structure of the dna-binding domain of human etv1. |
|
104
|
318
|
4bllA |
Crystal structure of fungal versatile peroxidase i from pleurotus ostreatus - crystal form ii |
|
23
|
86
|
4bpfA |
High resolution crystal structure of bacillus subtilis dltc s36a |
|
125
|
356
|
4bg4B |
Crystal structure of litopenaeus vannamei arginine kinase in a ternary analog complex with arginine, adp-mg and no3 |
|
139
|
416
|
4aw2A |
Crystal structure of cdc42 binding protein kinase alpha (mrck alpha) |
|
78
|
293
|
4bc6A |
Crystal structure of human serine threonine kinase-10 bound to novel bosutinib isoform 1, previously thought to be bosutinib |
|
97
|
299
|
4at3A |
Crystal structure of trkb kinase domain in complex with cpd5n |
|
102
|
329
|
4blzA |
Crystal structure of fungal versatile peroxidase i from pleurotus ostreatus - crystal form vi |
|
139
|
397
|
4b7sA |
Pikc d50n mutant bound to the 10-dml analog with the 3-(n,n- dimethylamino)propanoate anchoring group |
|
85
|
321
|
4bcfA |
Structure of cdk9 in complex with cyclin t and a 2-amino-4-heteroaryl- pyrimidine inhibitor |
|
130
|
356
|
4bg4A |
Crystal structure of litopenaeus vannamei arginine kinase in a ternary analog complex with arginine, adp-mg and no3 |
|
80
|
207
|
4b3aA |
Tetracycline repressor class d mutant h100a in complex with tetracycline |
|
111
|
337
|
4bm3A |
Crystal structure of manganese peroxidase 4 from pleurotus ostreatus - crystal form iii |
|
23
|
66
|
5dm6V |
Crystal structure of the 50s ribosomal subunit from deinococcus radiodurans |
|
118
|
369
|
4at7B |
Crystal structure of the nf90-nf45 dimerisation domain complex |
|
226
|
598
|
4avzA |
Tailspike protein mutant e372q of e. coli bacteriophage hk620 |
|
123
|
290
|
4bmpA |
Crystal structure of bacillus cereus ribonucleotide reductase di- iron nrdf in complex with nrdi (2.1 a resolution) |
|
83
|
321
|
4bcjA |
Structure of cdk9 in complex with cyclin t and a 2-amino-4-heteroaryl- pyrimidine inhibitor |
|
91
|
296
|
4bggA |
Crystal structure of the acvr1 kinase in complex with ldn-213844 |
|
26
|
79
|
5e5aB |
Crystal structure of the chromatin-tethering domain of human cytomegalovirus ie1 protein bound to the nucleosome core particle |
|
139
|
380
|
4arfA |
Crystal structure of the peptidase domain of collagenase h from clostridium histolyticum in complex with the peptidic inhibitor isoamylphosphonyl-gly-pro-ala at 1.77 angstrom resolution. |
|
104
|
329
|
4blyA |
Crystal structure of fungal versatile peroxidase i from pleurotus ostreatus - crystal form v |
|
55
|
149
|
4b4yA |
Crystal structure of the neuroglobin from the photosymbiotic marine acoel symsagittifera roscoffensis |
|
211
|
645
|
4b76A |
Discovery of an allosteric mechanism for the regulation of hcv ns3 protein function |
|
282
|
947
|
3zw3A |
Fragment based discovery of a novel and selective pi3 kinase inhibitor |
