|
69
|
308
|
8emeA |
Egfr(t790m/v948r) in complex with znl-0056 |
|
119
|
310
|
7yolA |
Crystal structure of tetra mutant (d67e, a68p, l98i, a301s) of o-acetylserine sulfhydrylase from haemophilus influenzae in complex with high-affinity inhibitory peptide of serine acetyltransferase from haemophilus influenzae at 2.4 a |
|
111
|
303
|
7yoiA |
Crystal structure of i88l single mutant of o-acetylserine sulfhydrylase from haemophilus influenzae in complex with high-affinity inhibitory peptide from serine acetyltransferase of salmonella typhimurium at 2.14 a |
|
111
|
302
|
7yomA |
Crystal structure of tetra mutant (d67e,a68p,l98i,a301s) of o-acetylserine sulfhydrylase from salmonella typhimurium in complex with high-affinity inhibitory peptide from serine acetyltransferase of salmonella typhimurium at 2.8 a |
|
0
|
8
|
7yomB |
Crystal structure of tetra mutant (d67e,a68p,l98i,a301s) of o-acetylserine sulfhydrylase from salmonella typhimurium in complex with high-affinity inhibitory peptide from serine acetyltransferase of salmonella typhimurium at 2.8 a |
|
0
|
8
|
7yoiB |
Crystal structure of i88l single mutant of o-acetylserine sulfhydrylase from haemophilus influenzae in complex with high-affinity inhibitory peptide from serine acetyltransferase of salmonella typhimurium at 2.14 a |
|
1
|
7
|
7yohP |
Crystal structure of i88l single mutant of o-acetylserine sulfhydrylase from haemophilus influenzae in complex with high-affinity inhibitory peptide from serine acetyltransferase of haemophilus influenzae at 2.5 a |
|
103
|
308
|
7yohA |
Crystal structure of i88l single mutant of o-acetylserine sulfhydrylase from haemophilus influenzae in complex with high-affinity inhibitory peptide from serine acetyltransferase of haemophilus influenzae at 2.5 a |
|
110
|
303
|
7yodA |
Crystal structure of a68p single mutant of o-acetylserine sulfhydrylase from haemophilus influenzae in complex with high-affinity inhibitory peptide from serine acetyltransferase of salmonella typhimurium at 2.1 a |
|
76
|
272
|
8dd5A |
Crystal structure of kat6a in complex with inhibitor ctx-648 (pf-9363) |
|
88
|
271
|
8fd9A |
Structure of btk kinase domain with the second-generation inhibitor acalabrutinib |
|
77
|
265
|
8ff0A |
Structure of btk kinase domain with the second-generation inhibitor tirabrutinib |
|
112
|
355
|
8elcA |
Human jnk2 bound to covalent inhibitor yl2056 |
|
135
|
416
|
8etmA |
Human triacylglycerol synthesizing enzyme dgat1 in complex with dgat1in1 inhibitor |
|
295
|
840
|
8fjcA |
Structure of the catalytic domain of streptococcus mutans gtfb complexed to acarbose in tetragonal space group p4322 |
|
144
|
555
|
8ffxA |
Crystal structure of hiv-1 reverse transcriptase in complex with non-nucleoside inhibitor 19980 |
|
111
|
424
|
8ffxB |
Crystal structure of hiv-1 reverse transcriptase in complex with non-nucleoside inhibitor 19980 |
|
84
|
275
|
8fe9A |
Crystal structure of ack1 kinase k161q mutant in complex with the selective inhibitor (r)-9b |
|
111
|
359
|
7ueuA |
Pank3 complex structure with compound pz-4215 |
|
108
|
359
|
7uexA |
Pank3 complex structure with compound pz-4127 |
|
112
|
400
|
8f4uA |
Crystal structure of acetyltransferase eis from m. tuberculosis in complex with azelastine |
|
111
|
359
|
7ueyA |
Pank3 complex structure with compound pz-4128 |
|
112
|
400
|
8f4aA |
Crystal structure of acetyltransferase eis from m. tuberculosis in complex with chlorhexidine |
|
114
|
359
|
7uetA |
Pank3 complex structure with compound pz-4140 |
|
111
|
359
|
7uerA |
Pank3 complex structure with compound pz-4071 |
|
110
|
359
|
7uevA |
Pank3 complex structure with compound pz-4200 |
|
114
|
359
|
7ueqA |
Pank3 complex structure with compound pz-4061 |
|
107
|
359
|
7uesA |
Pank3 complex structure with compound pz-4202 |
|
112
|
351
|
7xc1A |
Crystal structure of erk2 with an allosteric inhibitor 3 |
|
119
|
350
|
8egfA |
Branched chain ketoacid dehydrogenase kinase in complex with inhibitor |
|
112
|
349
|
8egqA |
Branched chain ketoacid dehydrogenase kinase complexes |
|
111
|
350
|
8eguA |
Branched chain ketoacid dehydrogenase kinase complexes |
|
102
|
346
|
7xlpA |
Mek1 bound to ds03090629 |
|
101
|
346
|
7xncA |
Mek1 bound to ds94070624 |
|
81
|
264
|
8e80A |
Structure of lrrk2-chk1 10-pt. mutant complex with heteroaryl-1h-indazole lrrk2 inhibitor 14 |
|
76
|
268
|
8e81A |
Structure of lrrk2-chk1 10-pt. mutant complex with heteroaryl-1h-indazole lrrk2 inhibitor 25 |
|
122
|
377
|
7tunA |
Crystal structure analysis of human ckb complex with a covalent compound |
|
114
|
400
|
8f55A |
Crystal structure of acetyltransferase eis from mycobacterium tuberculosis h37rv in complex with inhibitor sgt1614 |
|
116
|
400
|
8f4tA |
Crystal structure of acetyltransferase eis from m. tuberculosis in complex with proguanil |
|
115
|
400
|
8f57A |
Crystal structure of acetyltransferase eis from m. tuberculosis in complex with inhibitor sgt1615 |
|
112
|
400
|
8f51A |
Crystal structure of acetyltransferase eis from m. tuberculosis in complex with mefloquine |
|
116
|
400
|
8f4wA |
Crystal structure of acetyltransferase eis from m. tuberculosis in complex with venlafaxine |
|
113
|
400
|
8f58A |
Crystal structure of acetyltransferase eis from m. tuberculosis in complex with inhibitor sgt1616 |
|
112
|
400
|
8f4zA |
Crystal structure of acetyltransferase eis from m. tuberculosis in complex with chloroquine |
|
102
|
328
|
7u9iA |
Co-crystal structure of human carm1 in complex with mt556 inhibitor |
|
130
|
386
|
7udqA |
Crystal structure of coq8a-ca157 inhibitor complex in space group p1 |
|
79
|
231
|
7tuxA |
Crystal structure of plasmodium falciparum hypoxanthine-guanine-xanthine phosphoribosyltransferase in complex with [(3s)-4-hydroxy-3-[({2-amino-4-hydroxy-5h-pyrrolo[3,2-d]pyrimidin-7-yl}methyl)amino]butyl]phosphonic acid |
|
79
|
298
|
7xafA |
The crystal structure of trka kinase in complex with 4^6,14-dimethyl-n-(3-(4-methyl-1h-imidazol-1-yl)-5-(trifluoromethyl)phenyl)-10-oxo-5-oxa-11,14-diaza-1(3,6)-imidazo[1,2-b]pyridazina-4(1,3)-benzenacyclo- tetradecaphan-2-yne-45-carboxamide |
|
94
|
325
|
7u99A |
Egfr kinase in complex with a macrocyclic inhibitor |
|
84
|
307
|
7u98A |
Egfr(t790m/v948r) in complex with a macrocyclic inhibitor |
