|
45
|
140
|
4e9eA |
Structure of the glycosylase domain of mbd4 |
|
81
|
229
|
4eelA |
Crystal structure of had family hydrolase dr_1622 from deinococcus radiodurans r1 (target efi-501256) with bound citrate and sodium |
|
143
|
393
|
4dnzA |
The crystal structures of cyp199a4 |
|
193
|
531
|
4eg7A |
Trypanosoma brucei methionyl-trna synthetase in complex with inhibitor chem 1331 |
|
146
|
361
|
4dwbA |
Crystal structure of trypanosoma cruzi farnesyl diphosphate synthase in complex with [2-(n-pentylamino)ethane-1,1-diyl]bisphosphonic acid and mg2+ |
|
91
|
257
|
4eosB |
Thr 160 phosphorylated cdk2 wt - human cyclin a3 complex with the inhibitor ro3306 |
|
138
|
359
|
4dzwA |
Crystal structure of trypanosome cruzi farnesyl diphosphate synthase in complex with [2-(cyclohexylamino)ethane-1,1-diyl]bisphosphonic acid and mg2+ |
|
101
|
282
|
4elsA |
Structure of e. coli. 1,4-dihydroxy-2- naphthoyl coenzyme a synthases (menb) in complex with bicarbonate |
|
34
|
91
|
4etoA |
Structure of s100a4 in complex with non-muscle myosin-iia peptide |
|
81
|
276
|
4ebwA |
Structure of focal adhesion kinase catalytic domain in complex with novel allosteric inhibitor |
|
31
|
93
|
4eicA |
Crystal structure of reduced cytochrome c6 from synechococcus sp. pcc 7002 at ultra-high resolution |
|
72
|
276
|
4eheA |
B-raf kinase domain in complex with an aminothienopyrimidine-based inhibitor |
|
80
|
191
|
4dw6A |
Novel n-phenyl-phenoxyacetamide derivatives as potential ethr inhibitors and ethionamide boosters. discovery and optimization using high-throughput synthesis. |
|
185
|
529
|
4eg1A |
Trypanosoma brucei methionyl-trna synthetase in complex with substrate methionine |
|
48
|
146
|
4e91A |
Crystal structure of the n-terminal domain of hiv-1 capsid in complex with inhibitor bd3 |
|
217
|
673
|
4e55A |
Crystal structure of spacer removed cephalosporin acylase mutant |
|
104
|
351
|
4eh6A |
Human p38 map kinase in complex with np-f5 and rl87 |
|
94
|
242
|
4dosA |
Human nuclear receptor liver receptor homologue-1, lrh-1, bound to dlpc and a fragment of tif-2 |
|
63
|
175
|
4ekrA |
T4 lysozyme l99a/m102h with 2-cyanophenol bound |
|
91
|
242
|
4dwxA |
Crystal structure of a family gh-19 chitinase from rye seeds |
|
96
|
257
|
4eorB |
Thr 160 phosphorylated cdk2 wt - human cyclin a3 complex with the inhibitor nu6102 |
|
53
|
219
|
4ekwA |
Crystal structure of the navab voltage-gated sodium channel (wild-type, 3.2 a) |
|
114
|
356
|
4dtfA |
Structure of a vgrg vibrio cholerae toxin acd domain in complex with amp-pnp and mg++ |
|
85
|
300
|
4eonA |
Thr 160 phosphorylated cdk2 h84s, q85m, q131e - human cyclin a3 complex with the inhibitor ro3306 |
|
73
|
276
|
4ehgA |
B-raf kinase domain in complex with an aminopyridimine-based inhibitor |
|
114
|
356
|
4dthA |
Structure of a vgrg vibrio cholerae toxin acd domain in complex with atp and mg++ |
|
100
|
271
|
4em9A |
Human ppar gamma in complex with nonanoic acids |
|
107
|
338
|
4er6A |
Crystal structure of human dot1l in complex with inhibitor sgc0946 |
|
106
|
339
|
4e80A |
Structural basis for the activity of a cytoplasmic rna terminal u-transferase |
|
104
|
350
|
4eh9A |
Human p38 map kinase in complex with np-f11 and rl87 |
|
83
|
273
|
4dtkA |
Novel and selective pan-pim kinase inhibitor |
|
166
|
453
|
4du2A |
Cytochrome p450 bm3h-b7 mri sensor bound to dopamine |
|
143
|
361
|
4e1eA |
Crystal structure of trypanosome cruzi farnesyl diphosphate synthase in complex with [2-(n-hexylamino)ethane-1,1-diyl]bisphosphonic acid and mg2+ |
|
47
|
129
|
4etcA |
Lysozyme, room temperature, 24 kgy dose |
|
47
|
137
|
4dqjA |
Structural investigation of bacteriophage phi6 lysin (in complex with chitotetraose) |
|
64
|
175
|
4eksA |
T4 lysozyme l99a/m102h with isoxazole bound |
|
69
|
219
|
4du6A |
Crystal structure of gtp cyclohydrolase i from yersinia pestis complexed with gtp |
|
78
|
269
|
4enxA |
Crystal structure of pim-1 kinase in complex with inhibitor (2e,5z)-2-(2-chlorophenylimino)-5-(4-hydroxy-3-nitrobenzylidene)thiazolidin-4-one |
|
76
|
276
|
4e26A |
Braf in complex with an organic inhibitor 7898734 |
|
141
|
465
|
4dl1C |
Crystal structure of human myeloperoxidase with covalent thioxanthine analog |
|
171
|
464
|
4ejiA |
Human cytochrome p450 2a13 in complex with two molecules of 4-(methylnitrosamino)-1-(3-puridyl)-1-butanone |
|
110
|
340
|
4ep7A |
Functional implications from the cid1 poly(u) polymerase crystal structure |
|
53
|
144
|
4esaB |
X-ray structure of carbonmonoxy hemoglobin of eleginops maclovinus |
|
91
|
239
|
4dorA |
Human nuclear receptor liver receptor homologue-1, lrh-1, in its apo state bound to a fragment of human shp box1 |
|
154
|
403
|
4ek1A |
Crystal structure of electron-spin labeled cytochrome p450cam |
|
97
|
257
|
4eomB |
Thr 160 phosphorylated cdk2 h84s, q85m, q131e - human cyclin a3 complex with atp |
|
83
|
299
|
4eomA |
Thr 160 phosphorylated cdk2 h84s, q85m, q131e - human cyclin a3 complex with atp |
|
211
|
551
|
4e1gA |
X-ray crystal structure of alpha-linolenic acid bound to the cyclooxygenase channel of cyclooxygenase-2 |
|
92
|
334
|
4ekkA |
Akt1 with amp-pnp |
|
82
|
298
|
4eorA |
Thr 160 phosphorylated cdk2 wt - human cyclin a3 complex with the inhibitor nu6102 |
