|
43
|
129
|
5b59A |
Hen egg-white lysozyme modified with a keto-abno. |
|
99
|
292
|
5aepA |
Novel pyrrole carboxamide inhibitors of jak2 as potential treatment of myeloproliferative disorders |
|
90
|
250
|
5aauA |
Optimization of a novel binding motif to to (e)-3-(3,5-difluoro-4-((1r,3r)-2-(2-fluoro-2-methylpropyl)-3-methyl-2,3,4,9-tetrahydro-1h- pyrido(3,4-b)indol-1-yl)phenyl)acrylic acid (azd9496), a potent and orally bioavailable selective estrogen receptor downregulator and antagonist |
|
178
|
456
|
5aexA |
Crystal structure of saccharomyces cerevisiae mep2 |
|
75
|
262
|
5aadA |
Aurora a kinase bound to an imidazopyridine inhibitor (7a) |
|
219
|
581
|
5a4fL |
The mechanism of hydrogen activation by nife-hydrogenases. |
|
349
|
1144
|
4hnvA |
Crystal structure of r54e mutant of s. aureus pyruvate carboxylase |
|
74
|
240
|
5aavB |
Optimization of a novel binding motif to to (e)-3-(3,5-difluoro-4-((1r,3r)-2-(2-fluoro-2-methylpropyl)-3-methyl-2,3,4,9-tetrahydro-1h- pyrido(3,4-b)indol-1-yl)phenyl)acrylic acid (azd9496), a potent and orally bioavailable selective estrogen receptor downregulator and antagonist |
|
197
|
561
|
5aa5C |
Actinobacterial-type nife-hydrogenase from ralstonia eutropha h16 at 2.85 angstrom resolution |
|
90
|
312
|
5abqA |
Crystal structure analysis of fungal versatile peroxidase from pleurotus eryngii. mutant vpi-ss. mutated residues t2k, a49c, a61c, d69s, t70d, s86e, a131k, d146t, q202l, q219k, h232e, q239r, l288r, s301k, a308r,a309k and a314r. |
|
199
|
546
|
5am2A |
Ligand complex structure of soluble epoxide hydrolase |
|
100
|
286
|
5a9rA |
Apo form of imine reductase from amycolatopsis orientalis |
|
67
|
177
|
5afpA |
Neuronal calcium sensor-1 (ncs-1)from rattus norvegicus complex with rhodopsin kinase peptide from homo sapiens |
|
194
|
546
|
5am3A |
Ligand complex structure of soluble epoxide hydrolase |
|
71
|
181
|
5aerA |
Neuronal calcium sensor-1 (ncs-1)from rattus norvegicus complex with d2 dopamine receptor peptide from homo sapiens |
|
101
|
289
|
5a9sA |
Nadph complex of imine reductase from amycolatopsis orientalis |
|
194
|
578
|
5ae2A |
Ether lipid-generating enzyme agps in complex with inhibitor 1e |
|
97
|
309
|
5aa8A |
Structure of c1156y,l1198f mutant human anaplastic lymphoma kinase in complex with pf-06463922 ((10r)-7-amino-12-fluoro-2,10,16-trimethyl- 15-oxo-10,15,16,17-tetrahydro-2h-8,4-(metheno)pyrazolo(4,3-h)(2,5,11) benzoxadiazacyclotetradecine-3-carbonitrile). |
|
89
|
276
|
5autA |
Crystal structure of dapk1 in complex with ans. |
|
27
|
84
|
4zycA |
Discovery of dihydroisoquinolinone derivatives as novel inhibitors of the p53-mdm2 interaction with a distinct binding mode: hdm2 (mdm2) complexed with cpd5 |
|
191
|
575
|
5ae3A |
Ether lipid-generating enzyme agps in complex with antimycin a |
|
99
|
286
|
5a9sB |
Nadph complex of imine reductase from amycolatopsis orientalis |
|
336
|
889
|
4zqtA |
Crystal structure of pfa-m1 with virtual ligand inhibitor |
|
148
|
367
|
5aelA |
T. brucei farnesyl diphosphate synthase complexed with bisphosphonate bph-597 |
|
88
|
276
|
5auuA |
Crystal structure of dapk1 in complex with luteolin. |
|
82
|
270
|
5a6oA |
Crystal structure of the apo form of the unphosphorylated human death associated protein kinase 3 (dapk3) |
|
197
|
578
|
5adzA |
Ether lipid-generating enzyme agps in complex with inhibitor 1a |
|
76
|
206
|
5a9gA |
Manganese superoxide dismutase from sphingobacterium sp. t2 |
|
82
|
239
|
5accA |
A novel oral selective estrogen receptor down-regulator, azd9496, drives tumour growth inhibition in estrogen receptor positive and esr1 mutant models |
|
100
|
309
|
5aa9A |
Structure of l1198f mutant human anaplastic lymphoma kinase in complex with pf-06463922 ((10r)-7-amino-12-fluoro-2,10,16-trimethyl- 15-oxo-10,15,16,17-tetrahydro-2h-8,4-(metheno)pyrazolo(4,3-h)(2,5,11) benzoxadiazacyclotetradecine-3-carbonitrile). |
|
87
|
276
|
5av4A |
Crystal structure of dapk1-genistein complex in the presence of bromide ions. |
|
42
|
152
|
4zyeA |
Crystal structure of sulfolobus solfataricus o6-methylguanine methyltransferase |
|
29
|
83
|
5afgA |
Structure of the stapled peptide bound to mdm2 |
|
85
|
249
|
5aavA |
Optimization of a novel binding motif to to (e)-3-(3,5-difluoro-4-((1r,3r)-2-(2-fluoro-2-methylpropyl)-3-methyl-2,3,4,9-tetrahydro-1h- pyrido(3,4-b)indol-1-yl)phenyl)acrylic acid (azd9496), a potent and orally bioavailable selective estrogen receptor downregulator and antagonist |
|
98
|
309
|
5a9uA |
Structure of c1156y mutant human anaplastic lymphoma kinase in complex with pf-06463922 ((10r)-7-amino-12-fluoro-2,10,16-trimethyl- 15-oxo-10,15,16,17-tetrahydro-2h-8,4-(metheno)pyrazolo(4,3-h)(2,5,11) benzoxadiazacyclotetradecine-3-carbonitrile). |
|
112
|
264
|
5b0kA |
Structure of moen5-sso7d fusion protein in complex with beta-decyl maltoside |
|
71
|
263
|
5aaeA |
Aurora a kinase bound to an imidazopyridine inhibitor (14d) |
|
204
|
547
|
5aibA |
Ligand complex structure of soluble epoxide hydrolase |
|
19
|
83
|
5aurA |
Hydrogenobacter thermophilus cytochrome c552 dimer formed by domain swapping at n-terminal region |
|
192
|
578
|
5ae1A |
Ether lipid-generating enzyme agps in complex with inhibitor zinc69435460 |
|
72
|
262
|
5aagA |
Aurora a kinase bound to an imidazopyridine inhibitor (14b) |
|
222
|
581
|
5a4mL |
Mechanism of hydrogen activation by nife-hydrogenases |
|
98
|
315
|
5aboA |
Crystal structure analysis of fungal versatile peroxidase from pleurotus eryngii. mutant vpi-br. mutated residues t2k, d69s, t70d, s86e, a131k, d146t, q202l, q219k, h232e, q239r, l288r, s301k, a308r, a309k and a314r. |
|
112
|
347
|
5a54A |
Dyrk1a in complex with nitro benzothiazole fragment |
|
47
|
129
|
4zixA |
Structure of hewl using serial femtosecond crystallography of soluble proteins in lipidic cubic phase |
|
314
|
902
|
4homA |
Crystal structure of porcine aminopeptidase-n complexed with substance p |
|
155
|
472
|
5a1rA |
Crystal structure of cytochrome p450 3a4 bound to progesterone |
|
145
|
467
|
5a5jA |
Cytochrome 2c9 p450 inhibitor complex |
|
86
|
302
|
5a46A |
Fgfr1 in complex with dovitinib |
|
44
|
129
|
5a3zA |
Structure of monoclinic lysozyme obtained by multi crystal data collection |
