|
79
|
193
|
5ipaA |
Structure of transcriptional regulatory repressor protein - ethr from mycobacterium tuberculosis in complex with (e)-3-(furan-3-yl)-1-(pyrrolidin-1-yl)prop-2-en-1-one at 1.78a resolution |
|
145
|
406
|
5ik1A |
Open state of p450cam after soaking in camphor |
|
211
|
536
|
5ikaA |
Tobacco 5-epi-aristolochene synthase with ppi |
|
97
|
292
|
5ih6A |
Human casein kinase 1 isoform delta (kinase domain) in complex with epiblastin a derivative |
|
80
|
193
|
5iozA |
Structure of transcriptional regulatory repressor protein - ethr from mycobacterium tuberculosis in complex with n-(cyclopentylmethyl)cyclopentanecarboxamide at 2.02a resolution |
|
82
|
193
|
5ip6A |
Structure of transcriptional regulatory repressor protein - ethr from mycobacterium tuberculosis in complex with n-((tetrahydrofuran-3-yl)methyl)pyrrolidine-1-carboxamide at 1.93a resolution |
|
99
|
312
|
5iuhA |
Crystal structure of the anaplastic lymphoma kinase (alk) in complex with 5d |
|
203
|
551
|
5iktA |
The structure of tolfenamic acid bound to human cyclooxygenase-2 |
|
224
|
581
|
5ijeA |
Crystal structure of equine serum albumin in the presence of 30 mm zinc at ph 7.4 |
|
219
|
536
|
5ik9A |
Tobacco 5-epi-aristolochene with farnesyl monophosphate |
|
85
|
193
|
5ioyA |
Structure of transcriptional regulatory repressor protein - ethr from mycobacterium tuberculosis in complex with n-(cyclopentylmethyl)pyrrolidine-1-carboxamide at 1.77a resolution |
|
200
|
551
|
5ikvA |
The structure of flufenamic acid bound to human cyclooxygenase-2 |
|
101
|
312
|
5iugA |
Crystal structure of anaplastic lymphoma kinase (alk) in complex with 5a |
|
199
|
580
|
5ijfA |
Crystal structure of human serum albumin in the presence of 0.5 mm zinc at ph 9.0 |
|
81
|
289
|
5itqA |
Crystal structure of human neil1, free protein |
|
192
|
551
|
5ikqA |
The structure of meclofenamic acid bound to human cyclooxygenase-2 |
|
156
|
464
|
5iutA |
Structure of p450 2b4 f202w mutant |
|
166
|
438
|
5itzA |
Crystal structure of the sac domain of cpap in a complex with tubulin and darpin |
|
78
|
271
|
5itaA |
Crystal structure of braf kinase domain bound to az-vem |
|
172
|
430
|
5itzB |
Crystal structure of the sac domain of cpap in a complex with tubulin and darpin |
|
85
|
317
|
5iu2A |
Discovery of imidazoquinolines as a novel class of potent, selective and in vivo efficacious cot kinase inhibitors |
|
29
|
85
|
5it3A |
Swirm domain of human lsd1 |
|
78
|
273
|
5ipjA |
Crystal structure of human pim-1 kinase in complex with a quinazolinone-pyrrolopyrrolone inhibitor. |
|
231
|
580
|
5iihA |
Crystal structure of equine serum albumin in the presence of 2.5 mm zinc at ph 7.4 |
|
227
|
581
|
5iiuA |
Crystal structure of equine serum albumin in the presence of 10 mm zinc at ph 6.9 |
|
61
|
151
|
5if4A |
Discovery of potent myeloid cell leukemia-1 (mcl-1) inhibitors using structure-based design |
|
242
|
580
|
5id9A |
Crystal structure of equine serum albumin in complex with phosphorodithioate derivative of myristoyl cyclic phosphatidic acid (cpa) |
|
47
|
129
|
5ii3A |
The x-ray structure of the adduct formed in the reaction between hen egg white lysozyme and compound 3, a platin(ii) compound containing a o, s bidentate ligand |
|
210
|
536
|
5ilkA |
Tobacco 5-epi-aristolochene synthase with partial density from mopso or bis-tris buffer molecule in the active site |
|
127
|
306
|
5imiA |
Crystal structure of s303a aspergillus terreus aristolochene synthase complexed with (1s,8s,9ar)-1,9a-dimethyl-8-(prop-1-en-2-yl)decahydroquinolizin-5-ium |
|
141
|
437
|
5ij9A |
Cryo em density of microtubule assembled from human tubb3-d417h mutant |
|
91
|
300
|
5ig1A |
Crystal structure of s. rosetta camkii kinase domain |
|
140
|
426
|
5ij9B |
Cryo em density of microtubule assembled from human tubb3-d417h mutant |
|
55
|
151
|
5iezA |
Discovery of potent myeloid cell leukemia-1 (mcl-1) inhibitors using structure-based design |
|
94
|
257
|
5if1B |
Crystal structure apo cdk2/cyclin a |
|
233
|
582
|
5id7A |
Crystal structure of human serum albumin in complex with phosphorodithioate derivative of myristoyl cyclic phosphatidic acid (cpa) |
|
93
|
293
|
5ih5A |
Human casein kinase 1 isoform delta (kinase domain) in complex with epiblastin a |
|
84
|
292
|
5imxA |
Anaplastic lymphoma kinase (alk) catalytic domain complexed with novel inhibitor 3-sulfonylpyrazol-4-amino pyrimidine |
|
228
|
581
|
5iixA |
Crystal structure of equine serum albumin in the presence of 15 mm zinc at ph 6.5 |
|
82
|
298
|
5ieyA |
Crystal structure of a cdk inhibitor bound to cdk2 |
|
132
|
370
|
5ihxA |
Crystal structure of a c-terminally truncated aspergillus nidulans mitochondrial tyrosyl-trna synthetase |
|
81
|
274
|
5iisA |
Design, synthesis and structure activity relationship of potent pan-pim kinase inhibitors derived from the pyridyl-amide scaffold |
|
96
|
293
|
5ih4A |
Human casein kinase 1 isoform delta apo (kinase domain) |
|
84
|
298
|
5if1A |
Crystal structure apo cdk2/cyclin a |
|
143
|
426
|
5ij0B |
Cryo em density of microtubule assembled from human tubb3 |
|
82
|
296
|
5imeA |
Crystal structure of p21-activated kinase 1 (pak1) in complex with compound 9 |
|
50
|
129
|
5ihgA |
The x-ray structure of the adduct formed in the reaction between hen egg white lysozyme a compound i, a platin(ii) compound containing a o, s bidentate ligand |
|
147
|
437
|
5ij0A |
Cryo em density of microtubule assembled from human tubb3 |
|
61
|
246
|
5imjA |
Crystal structure of a z-ring associated protein from escherichia coli |
|
79
|
298
|
5ievA |
Crystal structure of bay 1000394 (roniciclib) bound to cdk2 |
