|
258
|
713
|
5sxrA |
Crystal structure of b. pseudomallei katg with nad bound |
|
256
|
713
|
5syyA |
Crystal structure of the s324g variant of catalase-peroxidase from b. pseudomallei |
|
261
|
713
|
5sw4A |
Crystal structure of native catalase-peroxidase katg at ph8.0 |
|
258
|
713
|
5sx0A |
Crystal structure of an oxoferryl species of catalase-peroxidase katg at ph7.5 |
|
219
|
619
|
5reqB |
Methylmalonyl-coa mutase, y89f mutant, substrate complex |
|
262
|
713
|
5sw5A |
Crystal structure of native catalase-peroxidase katg at ph7.5 |
|
257
|
713
|
5syiA |
Structure of d141a variant of b. pseudomallei katg complexed with inh |
|
96
|
239
|
5syzA |
Human liver receptor homologue-1 (lrh-1) bound to a rjw100 stereoisomer and a fragment of tif-2 |
|
260
|
713
|
5sw6A |
Crystal structure of an oxoferryl species of catalase-peroxidase katg at ph5.6 |
|
259
|
713
|
5sx3A |
Crystal structure of the catalase-peroxidase katg of b. pseudomaallei at ph 4.5 |
|
58
|
146
|
5sw7B |
Structure of the human hemoglobin mutant hb providence (a-gly-c:v1m; b,d:v1m,k82d; ferrous, carbonmonoxy bound) |
|
259
|
713
|
5syhA |
Structure of d141a variant of b. pseudomallei katg |
|
261
|
713
|
5sx7A |
Crystal structure of catalase-peroxidase katg of b. pseudomallei at ph 8.5 |
|
47
|
129
|
5t3fA |
Hen egg-white lysozyme soaked with selenourea for 10 min |
|
259
|
713
|
5sx1A |
Crystal structure of d141e variant of b. pseudomallei katg |
|
260
|
713
|
5sx0B |
Crystal structure of an oxoferryl species of catalase-peroxidase katg at ph7.5 |
|
253
|
713
|
5sxsA |
Crystal structure of catalase-peroxidase katg with isonicotinic acid hydrazide and amp bound |
|
40
|
109
|
5palA |
Crystal structure of the unique parvalbumin component from muscle of the leopard shark (triakis semifasciata). the first x-ray study of an alpha-parvalbumin |
|
107
|
308
|
5pahA |
Human phenylalanine hydroxylase catalytic domain dimer with bound dopamine inhibitor |
|
108
|
363
|
5ceiA |
Crystal structure of cdk8:cyclin c complex with compound 22 |
|
61
|
177
|
5cglA |
Fic protein from neisseria meningitidis (nmfic) mutant e102r in dimeric form |
|
67
|
188
|
5aeqA |
Neuronal calcium sensor (ncs-1)from rattus norvegicus |
|
93
|
282
|
5ceqA |
Dlk in complex with inhibitor 2-((1-cyclopentyl-5-(1-(oxetan-3-yl)piperidin-4-yl)-1h-pyrazol-3-yl)amino)isonicotinonitrile |
|
148
|
437
|
5ca0A |
Crystal structure of t2r-ttl-lexibulin complex |
|
327
|
910
|
5k1vA |
Crystal structure of endoplasmic reticulum aminopeptidase 2 (erap2) in complex with a diaminobenzoic acid derivative ligand. |
|
93
|
281
|
5cenA |
Crystal structure of dlk (kinase domain) |
|
316
|
910
|
5j6sA |
Crystal structure of endoplasmic reticulum aminopeptidase 2 (erap2) in complex with a hydroxamic derivative ligand |
|
80
|
273
|
5kziA |
Crystal structure of human pim-1 kinase in complex with an imidazopyridazine inhibitor. |
|
26
|
92
|
5c5aA |
Crystal structure of hdm2 in complex with nutlin-3a |
|
139
|
385
|
5l90A |
The crystal structure of substrate-free cyp109e1 from bacillus megaterium at 2.55 angstrom resolution |
|
239
|
666
|
5l3dA |
Human lsd1/corest: lsd1 y761h mutation |
|
120
|
348
|
5byzA |
Erk5 in complex with small molecule |
|
255
|
652
|
4z40A |
Active site complex bambc of benzoyl coenzyme a reductase as isolated |
|
133
|
406
|
5lieA |
Crystal structure of mycobacterium tuberculosis cyp126a1 in complex with imidazole |
|
32
|
107
|
5c84A |
Fragment-based drug discovery targeting inhibitor of apoptosis proteins: compound 20 |
|
341
|
889
|
4zx5A |
X-ray crystal structure of pfa-m1 in complex with hydroxamic acid-based inhibitor 10q |
|
44
|
129
|
5c6iA |
Crystal structure of gadolinium derivative of hewl solved using free-electron laser radiation |
|
335
|
889
|
4zw8A |
X-ray crystal structure of pfa-m1 in complex with hydroxamic acid-based inhibitor 9r |
|
34
|
88
|
5m2cA |
Structural tuning of cd81lel (space group p32 1 2) |
|
30
|
95
|
5layA |
Discovery of new natural-product-inspired spiro-oxindole compounds as orally active inhibitors of the mdm2-p53 interaction: hdm2 (mdm2) in complex with compound 6g |
|
101
|
286
|
5a9tA |
Imine reductase from amycolatopsis orientalis in complex with (r)- methyltetrahydroisoquinoline |
|
83
|
266
|
5l8jA |
Aurora-a kinase domain in complex with vnar-d01 s93r |
|
64
|
250
|
5c2tB |
Crystal structure of mitochondrial rhodoquinol-fumarate reductase from ascaris suum with rhodoquinone-2 |
|
95
|
291
|
4zjjA |
Pak1 in complex with (s)-n-(tert-butyl)-3-((2-chloro-5-ethyl-8-fluoro-dibenzodiazepin-11-yl)amino)pyrrolidine-1-carboxamide |
|
165
|
439
|
5lyjA |
Tubulin-combretastatin a4 complex |
|
53
|
129
|
5kxzA |
Hen egg white lysozyme at 278k, data set 9 |
|
259
|
662
|
5k3jA |
Crystals structure of acyl-coa oxidase-2 in caenorhabditis elegans bound with fad, ascaroside-coa, and atp |
|
42
|
117
|
5ab8A |
High resolution x-ray structure of the n-terminal truncated form (residues 1-11) of mycobacterium tuberculosis hbn |
|
90
|
241
|
5c4uA |
Identification of a novel allosteric binding site for rorgt inhibitors |
|
92
|
241
|
5c4sA |
Identification of a novel allosteric binding site for rorgt inhibitors |
