|
120
|
440
|
4eb6A |
Tubulin-vinblastine: stathmin-like complex |
|
25
|
82
|
4eieA |
Crystal structure of cytochrome c6c from synechococcus sp. pcc 7002 |
|
216
|
535
|
4di5A |
Co-crystal structure of wt 5-epi-aristolochene synthase from nicotiana tobaccum with geraniline |
|
148
|
493
|
4ej3A |
Crystal structure of a crispr associated protein from thermus thermophilus hb8 |
|
116
|
284
|
4e9uA |
Crystal structure of dehydrosqualene synthase (crtm) from s. aureus complexed with a thiocyanate inhibitor |
|
111
|
348
|
4ehvA |
Human p38 map kinase in complex with np-f10 and rl87 |
|
64
|
175
|
4ekpA |
T4 lysozyme l99a/m102h with nitrobenzene bound |
|
89
|
327
|
4ekgA |
Crystal structure of dot1l in complex with epz003696 |
|
91
|
257
|
4eonB |
Thr 160 phosphorylated cdk2 h84s, q85m, q131e - human cyclin a3 complex with the inhibitor ro3306 |
|
64
|
204
|
4e4eA |
Crystal structure of the y34f mutant of saccharomyces cerevisiae manganese superoxide dismutase |
|
37
|
97
|
4e9mA |
Nod1 card domain with three disulfide-clinched, domain-swapped dimers in the asymmetric unit |
|
235
|
801
|
4dvyP |
Crystal structure of the helicobacter pylori caga oncoprotein |
|
114
|
356
|
4dtlA |
Structure of a vgrg vibrio cholerae toxin acd domain in complex with atp and mn++ |
|
284
|
785
|
4dbqA |
Myosin vi d179y (md-insert2-cam, delta-insert1) post-rigor state |
|
128
|
290
|
4dr0A |
Crystal structure of bacillus subtilis dimanganese(ii) nrdf |
|
88
|
298
|
4el9A |
Structure of n-terminal kinase domain of rsk2 with afzelin |
|
175
|
455
|
4dueA |
Cytochrome p450 bm3h-2g9c6 mri sensor bound to serotonin |
|
25
|
74
|
4e45B |
Crystal structure of the hmhf1/hmhf2 histone-fold tetramer in complex with fanconi anemia associated helicase hfancm |
|
48
|
129
|
4etaA |
Lysozyme, room temperature, 400 kgy dose |
|
57
|
205
|
4etvA |
Crystal structure of mouse ryanodine receptor 2 (2699-2904) |
|
38
|
98
|
4drbA |
The crystal structure of fancm bound mhf complex |
|
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 |
|
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+ |
|
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 |
|
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 |
|
96
|
257
|
4eorB |
Thr 160 phosphorylated cdk2 wt - human cyclin a3 complex with the inhibitor nu6102 |
|
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 |
|
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 |
|
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++ |
|
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 |
|
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 |
|
47
|
129
|
4etcA |
Lysozyme, room temperature, 24 kgy dose |
|
104
|
350
|
4eh9A |
Human p38 map kinase in complex with np-f11 and rl87 |
