86
|
303
|
8xloA |
Fgfr1 kinase domain with a dual-warhead covalent inhibitor cxf-007 |
89
|
299
|
8xlqA |
Fgfr4 kinase domain with a dual-warhead covalent inhibitor cxf-007 |
100
|
337
|
8jotA |
Crystal structure of csf-1r kinase domain with sulfatinib |
94
|
306
|
8jmzA |
Fgfr1 kinase domain with sulfatinib |
78
|
274
|
8sv9A |
Crystal structure of ulk1 kinase domain with inhibitor mr-2088 |
169
|
462
|
8gktA |
Human mitochondrial serine hydroxymethyltransferase (shmt2) in complex with plp, glycine and agf320 inhibitor |
158
|
462
|
8gksA |
Human mitochondrial serine hydroxymethyltransferase (shmt2) in complex with plp, glycine and agf291 inhibitor |
170
|
462
|
8gkyA |
Human mitochondrial serine hydroxymethyltransferase (shmt2) y105f in complex with plp, glycine and agf359 inhibitor |
153
|
462
|
8gkuA |
Human mitochondrial serine hydroxymethyltransferase (shmt2) in complex with plp, glycine and agf355 inhibitor |
162
|
462
|
8gkzA |
Human mitochondrial serine hydroxymethyltransferase (shmt2) y105f in complex with plp, glycine and agf362 inhibitor |
164
|
462
|
8gkwA |
Human mitochondrial serine hydroxymethyltransferase (shmt2) in complex with plp, glycine and agf359 inhibitor |
108
|
328
|
8g2iA |
Crystal structure of prmt4 with compound yd1290 |
21
|
72
|
8iajC |
Cryo-em structure of the yeast spt-orm2 (orm2-s3a) complex |
41
|
149
|
8iakD |
Cryo-em structure of the yeast spt-orm2 (orm2-s3a-n71a) complex |
41
|
149
|
8iamD |
Cryo-em structure of the yeast spt-orm2 (orm2-s3d) complex |
142
|
555
|
8iamB |
Cryo-em structure of the yeast spt-orm2 (orm2-s3d) complex |
146
|
495
|
8iakA |
Cryo-em structure of the yeast spt-orm2 (orm2-s3a-n71a) complex |
80
|
297
|
8uv0A |
Discovery of (4-pyrazolyl)-2-aminopyrimidines as potent and selective inhibitors of cyclin-dependent kinase 2 |
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 |
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 |
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 |
141
|
383
|
7rw7A |
Crystal structure of human methionine adenosyltransferase 2a (mat2a) in complex with sam and allosteric inhibitor compound 9 |
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 |