|
99
|
299
|
4at5A |
Crystal structure of trkb kinase domain in complex with gw2580 |
|
81
|
298
|
4bghA |
Crystal structure of cdk2 in complex with pan-cdk inhibitor |
|
127
|
287
|
4bmuA |
Crystal structure of ribonucleotide reductase di-manganese(ii) nrdf from bacillus cereus |
|
44
|
114
|
4bbdA |
The structure of vaccinia virus n1 r58y mutant |
|
85
|
303
|
4bdjA |
Fragment-based screening identifies a new area for inhibitor binding to checkpoint kinase 2 (chk2) |
|
185
|
628
|
4aysA |
The structure of amylosucrase from d. radiodurans |
|
6
|
46
|
4bl0B |
Crystal structure of yeast bub3-bub1 bound to phospho-spc105 |
|
51
|
129
|
4badA |
Hen egg-white lysozyme structure in complex with the europium tris- hydroxymethyltriazoledipicolinate complex at 1.35 a resolution. |
|
96
|
257
|
4bcpB |
Structure of cdk2 in complex with cyclin a and a 2-amino-4-heteroaryl- pyrimidine inhibitor |
|
36
|
209
|
4bhpA |
A structural model of cap mutant (t127l and s128i) in cgmp-bound state |
|
58
|
209
|
4bh9A |
A structural model of cap mutant (t127l and s128i) in the apo state |
|
152
|
470
|
4azsA |
High resolution (2.2 a) crystal structure of wbdd. |
|
249
|
946
|
4anvA |
Complexes of pi3kgamma with isoform selective inhibitors. |
|
100
|
347
|
4b99A |
Crystal structure of mapk7 (erk5) with inhibitor |
|
40
|
110
|
4aveA |
C.lacteus nerve hb in the deoxy form |
|
37
|
94
|
4bi8A |
Crystal structure of the type vi effector-immunity complex ssp1-rap1a from serratia marcescens |
|
76
|
266
|
4b0gA |
Complex of aurora-a bound to an imidazopyridine-based inhibitor |
|
87
|
253
|
4bcmD |
Structure of cdk2 in complex with cyclin a and a 2-amino-4-heteroaryl- pyrimidine inhibitor |
|
93
|
218
|
4axzA |
Borrelia burgdorferi outer surface lipoprotein bba73 |
|
83
|
235
|
4bizA |
Crystal structure of cpxahdc (orthorhombic form 2) |
|
319
|
862
|
3zhqA |
Crystal structure of the h747a mutant of the suca domain of mycobacterium smegmatis kgd |
|
91
|
252
|
4bciB |
Structure of cdk9 in complex with cyclin t and a 2-amino-4-heteroaryl- pyrimidine inhibitor |
|
102
|
360
|
4at9B |
Crystal structure of the nf90-nf45 dimerisation domain complex with utp |
|
54
|
151
|
4bj5C |
Crystal structure of rif2 in complex with the c-terminal domain of rap1 (rap1-rct) |
|
50
|
129
|
4b4eA |
1.00 a structure of lysozyme crystallized with (r)-2-methyl-2,4- pentanediol |
|
123
|
287
|
4bmrA |
Crystal structure of ribonucleotide reductase apo-nrdf from bacillus cereus (space group p21) |
|
163
|
513
|
4b7gA |
Structure of a bacterial catalase |
|
78
|
291
|
4auaA |
Liganded x-ray crystal structure of cyclin dependent kinase 6 (cdk6) |
|
173
|
459
|
4apaA |
Crystal structure of mycobacterium tuberculosis fumarase (rv1098c) s318a in apo form |
|
125
|
300
|
4bmqA |
Crystal structure of ribonucleotide reductase apo-nrdf from bacillus cereus (space group c2) |
|
95
|
350
|
4b7tA |
Glycogen synthase kinase 3 beta complexed with axin peptide and leucettine l4 |
|
47
|
114
|
4bbbA |
The structure of vaccinia virus n1 q61y mutant |
|
89
|
304
|
4bdeA |
Fragment-based screening identifies a new area for inhibitor binding to checkpoint kinase 2 (chk2) |
|
121
|
346
|
4armA |
Structure of the inactive pesticin t201a mutant |
|
81
|
271
|
4bhnA |
Crystal structures of ask1-inhibitor complexes |
|
277
|
725
|
3zw8A |
Crystal structure of rat peroxisomal multifunctional enzyme type 1 (rpmfe1) in apo form |
|
151
|
450
|
4bjkA |
Cyp51 of trypanosoma brucei bound to (s)-n-(3-(1h-indol-3-yl)-1-oxo-1- (pyridin-4-ylamino)propan-2-yl)-3,3'-difluoro-(1,1'-biphenyl)-4- carboxamide |
|
251
|
791
|
4a2qA |
Structure of duck rig-i tandem cards and helicase domain |
|
43
|
169
|
4bkxA |
The structure of hdac1 in complex with the dimeric elm2-sant domain of mta1 from the nurd complex |
|
147
|
470
|
4ax8A |
Medium resolution structure of the bifunctional kinase- methyltransferase wbdd |
|
33
|
141
|
4bksC |
Von hippel lindau protein:elonginb:elonginc complex, in complex with (2s,4r)-1-ethanoyl-n-[[4-(1,3-oxazol-5-yl)phenyl]methyl]-4-oxidanyl-pyrrolidine-2-carboxamide |
|
105
|
338
|
4b7kA |
Factor inhibiting hif-1 alpha in complex with consensus ankyrin repeat domain-ser peptide (20-mer) |
|
110
|
357
|
4awiA |
Human jnk1alpha kinase with 4-phenyl-7-azaindole ikk2 inhibitor. |
|
40
|
165
|
4bhcA |
Crystal structure of the m. tuberculosis o6-methylguanine methyltransferase r37l variant |
|
141
|
445
|
4azwA |
Crystal structure of monomeric wbdd. |
|
76
|
197
|
4bjaA |
Globin-like protein glb-12 from c.elegans |
|
25
|
106
|
5d8lB |
Human hsf2 dna binding domain in complex with 3-site hse dna at 2.1 angstroms resolution |
|
89
|
252
|
4bcgB |
Structure of cdk9 in complex with cyclin t and a 2-amino-4-heteroaryl- pyrimidine inhibitor |
|
271
|
723
|
3zw9A |
Crystal structure of rat peroxisomal multifunctional enzyme type 1 (rpmfe1) complexed with (2s,3s)-3-hydroxy-2-methylbutanoyl-coa |
|
52
|
160
|
4bd8A |
Bax domain swapped dimer induced by bimbh3 with chaps |
