|
150
|
555
|
8iakB |
Cryo-em structure of the yeast spt-orm2 (orm2-s3a-n71a) complex |
|
20
|
71
|
8iakC |
Cryo-em structure of the yeast spt-orm2 (orm2-s3a-n71a) complex |
|
21
|
72
|
8iamC |
Cryo-em structure of the yeast spt-orm2 (orm2-s3d) complex |
|
142
|
495
|
8iajA |
Cryo-em structure of the yeast spt-orm2 (orm2-s3a) complex |
|
145
|
495
|
8iamA |
Cryo-em structure of the yeast spt-orm2 (orm2-s3d) complex |
|
49
|
182
|
8iajD |
Cryo-em structure of the yeast spt-orm2 (orm2-s3a) complex |
|
143
|
555
|
8iajB |
Cryo-em structure of the yeast spt-orm2 (orm2-s3a) complex |
|
64
|
277
|
8jf3A |
C-src in complex with compound 9 |
|
70
|
305
|
8u1fA |
Fgfr2 kinase domain bound to irreversible inhibitor cmpd 10 |
|
82
|
286
|
8udvA |
The x-ray co-crystal structure of human fgfr3 v555m and compound 17 |
|
84
|
288
|
8udtA |
The x-ray co-crystal structure of human fgfr3 and kin-3248 |
|
87
|
288
|
8uduA |
The x-ray co-crystal structure of human fgfr3 and compound 17 |
|
88
|
335
|
8u37A |
Crystal structure of the catalytic domain of human pkc alpha (d463n, v568i, s657e) in complex with nvp-cjl037 at 2.48-a resolution |
|
88
|
335
|
8uakA |
Crystal structure of the catalytic domain of human pkc alpha (d463n, v568i, s657e) in complex with darovasertib (nvp-lxs196) at 2.82-a resolution |
|
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 |
|
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 |
|
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 |
|
120
|
361
|
7vbvA |
Crystal structure of human pyruvate dehydrogenase kinase 2 in complex with compound 7 |
|
118
|
359
|
7vbxA |
Crystal structure of human pyruvate dehydrogenase kinase 2 in complex with compound 20 |
|
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 |
|
73
|
303
|
7mx3A |
Crystal structure of human ripk3 complexed with gsk'843 |
|
76
|
311
|
7serB |
Prmt5/mep50 with compound 30 bound |
|
153
|
556
|
7lpwA |
Crystal structure of hiv-1 rt in complex with nbd-14189 |
|
141
|
383
|
7rw7A |
Crystal structure of human methionine adenosyltransferase 2a (mat2a) in complex with sam and allosteric inhibitor compound 9 |
|
107
|
424
|
7lquB |
Crystal structure of hiv-1 rt in complex with nbd-14075 |
|
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 |
|
77
|
311
|
7s1rB |
Prmt5/mep50 crystal structure with mta and a phthalazinone inhibitor bound (compound (m)-31) |
|
129
|
385
|
7rwhA |
Crystal structure of human methionine adenosyltransferase 2a (mat2a) in complex with sam and allosteric inhibitor agi-41998 |
|
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 |
|
76
|
311
|
7s1sB |
Prmt5/mep50 crystal structure with mta and mrtx-1719 bound |
|
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 |
