|
88
|
323
|
5j9yA |
Egfr-t790m in complex with pyrazolopyrimidine inhibitor 1b |
|
73
|
306
|
5jk3A |
Crystal structure of tl11-128 bound to tak1-tab1 |
|
18
|
60
|
5ju5A |
Crystal structure of the human tankyrase 1 (tnks) sam domain (d1055r), crystal form 1 |
|
107
|
348
|
5k5xA |
Crystal structure of human pdgfra |
|
53
|
140
|
5kerA |
Deer mouse recombinant hemoglobin from high altitude species |
|
124
|
443
|
5ji3E |
Hsluv complex |
|
116
|
316
|
5js3E |
Thermolysin in complex with jc114. |
|
98
|
347
|
5k5nA |
Crystal structure of gsk-3beta complexed with pf-04802367, a highly selective brain-penetrant kinase inhibitor |
|
91
|
289
|
5kbqA |
Pak1 in complex with bis-anilino pyrimidine inhibitor |
|
142
|
426
|
5jcoC |
Structure and dynamics of single-isoform recombinant neuronal human tubulin |
|
20
|
63
|
5jtiA |
Crystal structure of the human tankyrase 1 (tnks) sam domain (d1055r), crystal form 2 |
|
89
|
268
|
5k1xA |
Catalytic domain of polyspecific pyrrolysyl-trna synthetase mutant y306a/n346a/c348a/y384f in complex with amppnp |
|
91
|
246
|
5kctA |
Crystal structure of the er-alpha ligand-binding domain (y537s) in complex with an n-ethyl, 4-chlorobenzyl obhs-n derivative |
|
35
|
96
|
5j9pC |
Kcsa in vitro |
|
51
|
145
|
5jdoD |
T. congolense haptoglobin-haemoglobin receptor in complex with haemoglobin |
|
70
|
272
|
5j8fA |
Human mof k274p crystal structure |
|
26
|
78
|
5ja4A |
Crystal structure of human tonsl and mcm2 hbds binding to a histone h3-h4 tetramer |
|
25
|
78
|
5j8yA |
Crystal structure of the scm-sam and sfmbt-sam heterodimer |
|
53
|
141
|
5jdoC |
T. congolense haptoglobin-haemoglobin receptor in complex with haemoglobin |
|
199
|
530
|
5j58A |
Trypanosoma brucei methionyl-trna synthetase in complex with inhibitor (chem 1856) |
|
23
|
69
|
5j8yC |
Crystal structure of the scm-sam and sfmbt-sam heterodimer |
|
75
|
273
|
5j8cA |
Human mof c316s, e350q crystal structure |
|
46
|
123
|
5iz2A |
Crystal structure of the n. clavipes spidroin ntd at ph 6.5 |
|
126
|
363
|
5j4yA |
The crystal structure of n-(4-(2-(thiazolo[5,4-c]pyridin-2-yl)phenoxy)phenyl)acetamide bound to jcv helicase |
|
42
|
144
|
5iy5D |
Electron transfer complex of cytochrome c and cytochrome c oxidase at 2.0 angstrom resolution |
|
84
|
219
|
5ixkA |
Rorgamma in complex with inverse agonist bio399. |
|
47
|
129
|
5j7cA |
A picomolar affinity fn3 domain in complex with hen egg-white lysozyme |
|
93
|
309
|
5j7hA |
Crystal structure of anaplastic lymphoma kinase (alk) bound by brigatinib |
|
164
|
437
|
5iyzA |
Tubulin-mmae complex |
|
46
|
129
|
5ilfA |
The x-ray structure of the adduct formed in the reaction between hen egg white lysozyme and compound 4, a platin(ii) compound containing a o, s bidentate ligand |
|
21
|
66
|
5j6xA |
Crystal structure of the apo-zalpha of zebrafish pkz |
|
125
|
363
|
5j4vA |
The crystal structure of inhibitor bound to jcv helicase |
|
99
|
219
|
5iztA |
Crystal structure of a c-terminal proteolytic fragment of an outer surface protein from borrelia burgdorferi |
|
79
|
303
|
5j5tA |
Glk co-crystal structure with aminopyrrolopyrimidine inhibitor |
|
217
|
536
|
5iliA |
Tobacco 5-epi-aristolochene synthase with capso buffer molecule and mg2+ ions |
|
218
|
536
|
5il3A |
Tobacco 5-epi-aristolochene synthase with mopso buffer molecule and mg2+ ions |
|
107
|
292
|
5j6dA |
Discovery of acyl guanidine tryptophan hydroxylase-1 inhibitors |
|
78
|
276
|
5j5sA |
Src kinase in complex with a sulfonamide inhibitor |
|
218
|
536
|
5iljA |
Tobacco 5-epi-aristolochene synthase with bis-tris buffer molecule |
|
177
|
430
|
5iyzB |
Tubulin-mmae complex |
|
64
|
226
|
5iy5B |
Electron transfer complex of cytochrome c and cytochrome c oxidase at 2.0 angstrom resolution |
|
100
|
338
|
5izfA |
Complex of pka with the bisubstrate protein kinase inhibitor arc-1408 |
|
114
|
259
|
5iy5C |
Electron transfer complex of cytochrome c and cytochrome c oxidase at 2.0 angstrom resolution |
|
83
|
309
|
5j79A |
The identification and pharmacological characterization of 6-(tert-butylsulfonyl)-n-(5-fluoro-1h-indazol-3-yl)quinolin-4-amine (gsk583), a highly potent and selective inhibitor of rip2 kinase, compound 3 complex |
|
169
|
464
|
5iuzA |
Structure of p450 2b4 f202w mutant (cymal-5) |
|
126
|
363
|
5j47A |
The x-ray structure of inhibitor bound to jcv helicase |
|
149
|
461
|
5ik2D |
Caldalaklibacillus thermarum f1-atpase (epsilon mutant) |
|
14
|
65
|
5ip9J |
Structure of rna polymerase ii-tfiif complex |
|
14
|
65
|
5ip7J |
Structure of rna polymerase ii-tfg1 peptide complex |
|
79
|
193
|
5ipaA |
Structure of transcriptional regulatory repressor protein - ethr from mycobacterium tuberculosis in complex with (e)-3-(furan-3-yl)-1-(pyrrolidin-1-yl)prop-2-en-1-one at 1.78a resolution |
