|
0
|
8
|
4o56B |
Structure of plk1 in complex with peptide |
|
275
|
715
|
5hgvA |
Structure of an o-glcnac transferase point mutant, d554n in complex with peptide |
|
161
|
495
|
4d11A |
Galnac-t2 crystal soaked with udp-5sgalnac, mea2 peptide and manganese (lower resolution dataset) |
|
164
|
495
|
4d0zA |
Galnac-t2 crystal soaked with udp-5sgalnac, mea2 and manganese (higher resolution dataset) |
|
131
|
496
|
4d11C |
Galnac-t2 crystal soaked with udp-5sgalnac, mea2 peptide and manganese (lower resolution dataset) |
|
43
|
173
|
4c1qA |
Crystal structure of the prdm9 set domain in complex with h3k4me2 and adohcy. |
|
5
|
18
|
4b7tB |
Glycogen synthase kinase 3 beta complexed with axin peptide and leucettine l4 |
|
272
|
717
|
4ay5A |
Human o-glcnac transferase (ogt) in complex with udp and glycopeptide |
|
166
|
616
|
4aidA |
Crystal structure of c. crescentus pnpase bound to rnase e recognition peptide |
|
95
|
350
|
4b7tA |
Glycogen synthase kinase 3 beta complexed with axin peptide and leucettine l4 |
|
107
|
349
|
3zrlA |
Identification of 2-(4-pyridyl)thienopyridinones as gsk-3beta inhibitors |
|
103
|
348
|
3zrmA |
Identification of 2-(4-pyridyl)thienopyridinones as gsk-3beta inhibitors |
|
104
|
349
|
3zrkA |
Identification of 2-(4-pyridyl)thienopyridinones as gsk-3beta inhibitors |
|
9
|
23
|
4afjX |
5-aryl-4-carboxamide-1,3-oxazoles: potent and selective gsk-3 inhibitors |
|
107
|
349
|
4afjA |
5-aryl-4-carboxamide-1,3-oxazoles: potent and selective gsk-3 inhibitors |
|
8
|
24
|
3zrkX |
Identification of 2-(4-pyridyl)thienopyridinones as gsk-3beta inhibitors |
|
8
|
23
|
3zrmX |
Identification of 2-(4-pyridyl)thienopyridinones as gsk-3beta inhibitors |
|
168
|
698
|
4aimA |
Crystal structure of c. crescentus pnpase bound to rnase e recognition peptide |
|
0
|
7
|
4aidF |
Crystal structure of c. crescentus pnpase bound to rnase e recognition peptide |
|
8
|
23
|
3zrlX |
Identification of 2-(4-pyridyl)thienopyridinones as gsk-3beta inhibitors |
|
110
|
334
|
3x2vA |
Michaelis-like complex of camp-dependent protein kinase catalytic subunit |
|
2
|
20
|
3x2vS |
Michaelis-like complex of camp-dependent protein kinase catalytic subunit |
|
4
|
17
|
3zdiB |
Glycogen synthase kinase 3 beta complexed with axin peptide and inhibitor 7d |
|
104
|
339
|
3x2uA |
Michaelis-like initial complex of camp-dependent protein kinase catalytic subunit. |
|
116
|
339
|
3x2wA |
Michaelis complex of camp-dependent protein kinase catalytic subunit |
|
2
|
20
|
3x2wS |
Michaelis complex of camp-dependent protein kinase catalytic subunit |
|
2
|
20
|
3x2uS |
Michaelis-like initial complex of camp-dependent protein kinase catalytic subunit. |
|
99
|
349
|
3zdiA |
Glycogen synthase kinase 3 beta complexed with axin peptide and inhibitor 7d |
|
226
|
710
|
3rceA |
Bacterial oligosaccharyltransferase pglb |
|
0
|
8
|
3rceB |
Bacterial oligosaccharyltransferase pglb |
|
60
|
223
|
5x3sA |
Crystal structure of mouse plk1-pbd in complex with phosphopeptide from hef1 (799-809) |
|
0
|
14
|
5hgvB |
Structure of an o-glcnac transferase point mutant, d554n in complex with peptide |
|
88
|
231
|
5cveA |
Crystal structure of human nrmt1 in complex with dimethylated fly h2b peptide and sah |
|
87
|
231
|
5cvdA |
Crystal structure of human nrmt1 in complex with alpha-n-dimethylated human cenp-a peptide |
|
0
|
7
|
5cveD |
Crystal structure of human nrmt1 in complex with dimethylated fly h2b peptide and sah |
|
1
|
13
|
4xbuB |
In vitro crystal structure of pak4 in complex with inka peptide |
|
93
|
293
|
4xbuA |
In vitro crystal structure of pak4 in complex with inka peptide |
|
39
|
153
|
4x5kA |
Human naa50 complex with coenzyme a and an acetylated peptide |
|
51
|
198
|
4pk3A |
Tubulin acetyltransferase complex with bisubstrate analog |
|
50
|
198
|
4pk2A |
Tubulin acetyltransferase complex with bisubstrate analog |
|
106
|
378
|
4nu1A |
Crystal structure of a transition state mimic of the gsk-3/axin complex bound to phosphorylated n-terminal auto-inhibitory ps9 peptide |
|
104
|
360
|
4nm7A |
Crystal structure of gsk-3/axin complex bound to phosphorylated wnt receptor lrp6 e-motif |
|
6
|
19
|
4nm5B |
Crystal structure of gsk-3/axin complex bound to phosphorylated wnt receptor lrp6 c-motif |
|
107
|
379
|
4nm3A |
Crystal structure of gsk-3/axin complex bound to phosphorylated n-terminal auto-inhibitory ps9 peptide |
|
5
|
21
|
4nm0B |
Crystal structure of peptide inhibitor-free gsk-3/axin complex |
|
102
|
359
|
4nm0A |
Crystal structure of peptide inhibitor-free gsk-3/axin complex |
|
73
|
222
|
4o9wA |
Crystal structure of polo-like kinase(plk1)pbd in complex with phospho peptide |
|
76
|
244
|
4o56A |
Structure of plk1 in complex with peptide |
|
108
|
361
|
4nm5A |
Crystal structure of gsk-3/axin complex bound to phosphorylated wnt receptor lrp6 c-motif |
|
5
|
19
|
4nm3B |
Crystal structure of gsk-3/axin complex bound to phosphorylated n-terminal auto-inhibitory ps9 peptide |
