|
48
|
129
|
4d9zA |
Lysozyme at 318k |
|
89
|
299
|
4d9tA |
Rsk2 c-terminal kinase domain with inhibitor (e)-methyl 3-(4-amino-7-(3-hydroxypropyl)-5-p-tolyl-7h-pyrrolo[2,3-d]pyrimidin-6-yl)-2-cyanoacrylate |
|
101
|
263
|
4cwmA |
High-glycosylation crystal structure of the bifunctional endonuclease (atbfn2) from arabidopsis thaliana |
|
119
|
316
|
4d91A |
Thermolysin in complex with dmso and acetate |
|
252
|
669
|
4c6gA |
Structural investigations into the stereochemistry and activity of a phenylalanine-2,3-aminomutase from taxus chinensis |
|
25
|
101
|
4cvwC |
Structure of the barley limit dextrinase-limit dextrinase inhibitor complex |
|
116
|
285
|
4d3dA |
Structure of imine reductase bcsired from bacillus cereus bag3x2 |
|
9
|
55
|
4dczA |
Crystal structure of a domain from a mycoplasma genitalium terminal organelle protein |
|
33
|
140
|
4dgwB |
Crystal structure of the sf3a splicing factor complex of u2 snrnp |
|
108
|
292
|
4cviA |
Neutron structure of ferric cytochrome c peroxidase - deuterium exchanged at room temperature |
|
56
|
136
|
4d2mA |
Vaccinia virus f1l bound to bim bh3 |
|
75
|
262
|
4dhfA |
Structure of aurora a mutant bound to biogenidec cpd 15 |
|
72
|
279
|
4cv8A |
Mps1 kinase with 3-aminopyridin-2-one inhibitors |
|
94
|
289
|
4d1sA |
Pyrrole-3-carboxamides as potent and selective jak2 inhibitors |
|
96
|
285
|
4d3sA |
Imine reductase from nocardiopsis halophila |
|
36
|
86
|
4d7xA |
Solution structure of the mediator gall11 kix domain of c. glabrata |
|
101
|
334
|
4dglC |
Crystal structure of the ck2 tetrameric holoenzyme |
|
97
|
266
|
4crlB |
Crystal structure of human cdk8-cyclin c in complex with cortistatin a |
|
98
|
293
|
4d0xA |
Pyrrole-3-carboxamides as potent and selective jak2 inhibitors |
|
144
|
405
|
4cppA |
Crystal structures of cytochrome p450-cam complexed with camphane, thiocamphor, and adamantane: factors controlling p450 substrate hydroxylation |
|
64
|
203
|
4dooA |
Crystal structure of arabidopsis thaliana fatty-acid binding protein at3g63170 (atfap1) |
|
113
|
366
|
4cznA |
Crystal structure of the extralong fungal manganese peroxidase from ceriporiopsis subvermispora |
|
130
|
326
|
4d8gA |
Chlamydia trachomatis nrdb with a mn/fe cofactor (procedure 2 - low mn) |
|
168
|
469
|
4d6zA |
Cytochrome p450 3a4 bound to imidazole and an inhibitor |
|
86
|
269
|
4cs2A |
Catalytic domain of pyrrolysyl-trna synthetase mutant y306a, y384f in its apo form |
|
74
|
188
|
4dmbA |
X-ray structure of human hepatitus c virus ns5a-transactivated protein 2 at the resolution 1.9a, northeast structural genomics consortium (nesg) target hr6723 |
|
86
|
246
|
4cxaB |
Crystal structure of the human cdk12-cyclin k complex bound to amppnp |
|
132
|
355
|
4d7rA |
Crystal structure of a chimeric protein with the sec7 domain of rickettsia prowazekii ralf and the capping domain of legionella pneumophila ralf |
|
44
|
129
|
4ddaA |
Eval processed hewl, nag |
|
87
|
294
|
4dehA |
Crystal structure of c-met in complex with triazolopyridinone inhibitor 3 |
|
81
|
286
|
4d87A |
Crystal structure of tyrosinase from bacillus megaterium in complex with sds |
|
137
|
335
|
4dhdA |
Crystal structure of isoprenoid synthase a3msh1 (target efi-501992) from pyrobaculum calidifontis |
|
235
|
717
|
4c51A |
Crystal structure of the catalase-peroxidase (katg) r418l mutant from mycobacterium tuberculosis |
|
113
|
350
|
4dfxE |
Crystal structure of myristoylated k7c catalytic subunit of camp-dependent protein kinase in complex with sp20 and amp-pnp |
|
157
|
426
|
4citA |
Crystal structure of the first bacterial vanadium dependant iodoperoxidase |
|
94
|
333
|
4d2tA |
Structure of melk in complex with inhibitors |
|
79
|
207
|
4d7mA |
Tetr(d) in complex with anhydrotetracycline and magnesium |
|
206
|
652
|
4cdgA |
Crystal structure of the bloom's syndrome helicase blm in complex with nanobody |
|
161
|
469
|
4d75A |
Cytochrome p450 3a4 bound to an inhibitor |
|
128
|
318
|
4ddlA |
Pde10a crystal structure complexed with novel inhibitor |
|
264
|
667
|
4c5rA |
Structural investigations into the stereochemistry and activity of a phenylalanine-2,3-aminomutase from taxus chinensis |
|
106
|
344
|
4dn5A |
Crystal structure of nf-kb-inducing kinase (nik) |
|
74
|
293
|
4d1zA |
Cdk2 in complex with a luciferin derivate |
|
103
|
333
|
4d2wA |
Structure of melk in complex with inhibitors |
|
118
|
374
|
4de8A |
Lytr-cps2a-psr family protein with bound octaprenyl monophosphate lipid |
|
110
|
336
|
4dh1A |
Low temperature x-ray structure of camp dependent protein kinase a catalytic subunit with low mg2+, atp and ip20 |
|
144
|
470
|
4d78A |
Cytochrome p450 3a4 bound to an inhibitor |
|
124
|
307
|
4dffA |
The sar development of dihydroimidazoisoquinoline derivatives as phosphodiesterase 10a inhibitors for the treatment of schizophrenia |
|
106
|
263
|
4cxoA |
Bifunctional endonuclease in complex with ssdna |
|
62
|
152
|
4dc8A |
Crystal structure of myoglobin unexposed to excessive sonicc imaging laser dose. |
