|
83
|
242
|
8w7hA |
Purine nucleoside phosphorylase in complex with mmv000848 |
|
87
|
307
|
6iuoA |
Crystal structure of fgfr4 kinase domain in complex with a covalent inhibitor |
|
78
|
282
|
7mgjA |
Tnni3k complexed with n-methyl-4-(4-(3-(3-(trifluoromethyl) phenyl) ureido) phenoxy)picolinamide |
|
206
|
539
|
7lovA |
Crystal structure of clostridium difficile toxin b (tcdb) glucosyltransferase in complex with udp and noeuromycin |
|
75
|
283
|
7mgkA |
Tnni3k complexed with 1-(3,5-dichloro-4-((6-(methylamino)pyrimidin-4-yl)oxy)phenyl)-3-(3-(trifluoromethyl)phenyl)urea |
|
111
|
424
|
7lpwB |
Crystal structure of hiv-1 rt in complex with nbd-14189 |
|
142
|
556
|
7lquA |
Crystal structure of hiv-1 rt in complex with nbd-14075 |
|
104
|
424
|
7lpxB |
Crystal structure of hiv-1 rt in complex with nbd-14270 |
|
118
|
359
|
7vbxA |
Crystal structure of human pyruvate dehydrogenase kinase 2 in complex with compound 20 |
|
120
|
361
|
7vbvA |
Crystal structure of human pyruvate dehydrogenase kinase 2 in complex with compound 7 |
|
213
|
625
|
7sesA |
Prmt5/mep50 with compound 29 bound |
|
215
|
625
|
7serA |
Prmt5/mep50 with compound 30 bound |
|
73
|
311
|
7sesB |
Prmt5/mep50 with compound 29 bound |
|
71
|
228
|
7scrA |
Crystal structure of trypanosome brucei hypoxanthine-guanine-xanthine phosphoribzosyltransferase in complex with (4s,7s)-7-hydroxy-4-((guanin-9-yl)methyl)-2,5-dioxaheptan-1,7-diphosphonate |
|
76
|
311
|
7serB |
Prmt5/mep50 with compound 30 bound |
|
141
|
383
|
7rw7A |
Crystal structure of human methionine adenosyltransferase 2a (mat2a) in complex with sam and allosteric inhibitor compound 9 |
|
153
|
556
|
7lpwA |
Crystal structure of hiv-1 rt in complex with nbd-14189 |
|
73
|
303
|
7mx3A |
Crystal structure of human ripk3 complexed with gsk'843 |
|
127
|
384
|
7rwgA |
"crystal structure of human methionine adenosyltransferase 2a (mat2a) in complex with sam and allosteric inhibitor agi-43192 |
|
206
|
625
|
7s1pA |
Prmt5/mep50 crystal structure with sinefungin bound |
|
107
|
424
|
7lquB |
Crystal structure of hiv-1 rt in complex with nbd-14075 |
|
77
|
311
|
7s1rB |
Prmt5/mep50 crystal structure with mta and a phthalazinone inhibitor bound (compound (m)-31) |
|
76
|
311
|
7s1sB |
Prmt5/mep50 crystal structure with mta and mrtx-1719 bound |
|
73
|
306
|
7s1qB |
Prmt5/mep50 crystal structure with mta and a phthalazinone inhibitor bound (compound 9) |
|
69
|
302
|
7s1pB |
Prmt5/mep50 crystal structure with sinefungin bound |
|
129
|
385
|
7rwhA |
Crystal structure of human methionine adenosyltransferase 2a (mat2a) in complex with sam and allosteric inhibitor agi-41998 |
|
212
|
625
|
7s1qA |
Prmt5/mep50 crystal structure with mta and a phthalazinone inhibitor bound (compound 9) |
|
209
|
625
|
7s1sA |
Prmt5/mep50 crystal structure with mta and mrtx-1719 bound |
|
219
|
625
|
7s1rA |
Prmt5/mep50 crystal structure with mta and a phthalazinone inhibitor bound (compound (m)-31) |
|
109
|
326
|
6pf1A |
Crystal structure of the p300 acetyltransferase domain with allosteric inhibitor cpi-090 and coa |
|
101
|
321
|
6pguA |
Crystal structure of the p300 acetyltransferase domain with allosteric inhibitor cpi-076 and coa |
|
71
|
220
|
7msoA |
Crystal structure of polo box domain in complex with cyclic peptide inhibitor |
|
89
|
308
|
7ltxA |
Egfr (t790m/v948r) in complex with quinazolinone allosteric inhibitor |
|
96
|
273
|
7m7vA |
Crystal structure of mtb pks13 thioesterase domain in complex with compound 6 |
|
94
|
301
|
6itjA |
Crystal structure of fgfr1 kinase domain in complex with compound 3 |
|
133
|
381
|
7rw5A |
Crystal structure of human methionine adenosyltransferase 2a (mat2a) in complex with sam and allosteric inhibitor compound 1 |
|
217
|
545
|
7louA |
Crystal structure of clostridium difficile toxin b (tcdb) glucosyltransferase in complex with udp and isofagomine |
|
42
|
154
|
7lqpA |
Rapid development of potent inhibitors of the hiv integrase-ledgf interaction by fragment-linking using off-rate screening |
|
155
|
556
|
7lpxA |
Crystal structure of hiv-1 rt in complex with nbd-14270 |
|
86
|
291
|
8tucA |
Unphosphorylated camkk2 in complex with cc-8977 |
|
128
|
361
|
7vbuA |
Crystal structure of human pyruvate dehydrogenase kinase 2 in complex with compound 5 |
|
115
|
333
|
8g2hA |
Crystal structure of prmt4 with compound yd1113 |
|
85
|
275
|
7kp6A |
Structure of ack1 kinase in complex with a selective inhibitor |
|
99
|
266
|
7tz7B |
Pi3k alpha in complex with an inhibitor |
|
60
|
261
|
7t7mA |
Structure of human glp set-domain (ehmt1) in complex with covalent inhibitor (compound 1) |
|
85
|
273
|
7t0pA |
Jak2 jh2 in complex with jak315 |
|
137
|
403
|
7tevA |
Human ornithine aminotransferase cocrystallized with its inhibitor, (3s,4r)-3-amino-4-(difluoromethyl)cyclopent-1-ene-1-carboxylate |
|
133
|
404
|
7tedA |
Human ornithine aminotransferase cocrystallized with its inhibitor, (s,e)-3-amino-4-(fluoromethylene)cyclopent-1-ene-1-carboxylate |
|
281
|
940
|
7mlkA |
Crystal structure of human pi3ka (p110a subunit) with mmv085400 bound to the active site determined at 2.9 angstroms resolution |
|
91
|
332
|
7n93A |
P70 s6k1 in complex with msc2363318a-1 |
