|
122
|
389
|
5j3xA |
Structure of c-cbl y371f |
|
116
|
348
|
5a3xA |
Dyrk1a in complex with hydroxy benzothiazole fragment |
|
47
|
129
|
5l3hA |
Re-refinement of 4dd4; cisplatin coordination chemistry determination at hen egg white lysozyme his15 with standard uncertainties |
|
227
|
581
|
5ij5A |
Crystal structure of equine serum albumin in the presence of 50 mm zinc at ph 4.5 |
|
77
|
270
|
5jznA |
Crystal structure of dclk1-kd in complex with nvp-tae684 |
|
86
|
308
|
5bvwA |
Fragment-based discovery of potent and selective ddr1/2 inhibitors |
|
26
|
104
|
5iy51 |
Electron transfer complex of cytochrome c and cytochrome c oxidase at 2.0 angstrom resolution |
|
36
|
153
|
5k39B |
The type ii cohesin dockerin complex from clostridium thermocellum |
|
85
|
245
|
5krfA |
Crystal structure of the er-alpha ligand-binding domain (y537s) in complex with the dynamic way derivative, 1a |
|
9
|
75
|
5iz7D |
Cryo-em structure of thermally stable zika virus strain h/pf/2013 |
|
164
|
452
|
5jkvA |
Human placental aromatase cytochrome p450 (cyp19a1) at 2.75 angstrom with bound polyethylene glycol |
|
53
|
129
|
5kxsA |
Hen egg white lysozyme at 278k, data set 4 |
|
200
|
582
|
5ifoA |
X-ray structure of hsa-myr-kp1019 |
|
53
|
140
|
5jdoE |
T. congolense haptoglobin-haemoglobin receptor in complex with haemoglobin |
|
43
|
137
|
5kaiV |
Nh3-bound rt xfel structure of photosystem ii 500 ms after the 2nd illumination (2f) at 2.8 a resolution |
|
100
|
259
|
5jbwA |
Crystal structure of liuc |
|
110
|
314
|
5kdlA |
Crystal structure of the 4 alanine insertion variant of the gi alpha1 subunit bound to gtpgammas |
|
13
|
42
|
5jemC |
Complex of irf-3 with cbp |
|
116
|
316
|
5a3yA |
Sad structure of thermolysin obtained by multi crystal data collection |
|
338
|
888
|
4zw7A |
X-ray crystal structure of pfa-m1 in complex with hydroxamic acid-based inhibitor 9m |
|
54
|
150
|
5j8eA |
Crystal structure of human hook3's conserved hook domain |
|
167
|
429
|
5jvdB |
Tubulin-tub092 complex |
|
79
|
311
|
5l2qA |
Serine/threonine-protein kinase 40 (stk40) kinase homology domain |
|
96
|
244
|
5iz0A |
Rorgamma in complex with agonist bio592 and coactivator ebi96 |
|
61
|
317
|
4zh4A |
Crystal structure of escherichia coli rna polymerase in complex with cbrp18 |
|
88
|
326
|
5kumA |
Crystal structure of inward rectifier kir2.2 k62w mutant in complex with pip2 |
|
82
|
193
|
5j1uA |
Structure of transcriptional regulatory repressor protein - ethr from mycobacterium tuberculosis in complex with n-(furan-3-ylmethyl)pyrrolidine-1-carboxamide at 1.80a resolution |
|
165
|
452
|
5jkwA |
Human placental aromatase cytochrome p450 (cyp19a1) complexed with testosterone |
|
63
|
241
|
5klvD |
Structure of bos taurus cytochrome bc1 with fenamidone inhibited |
|
48
|
196
|
4yxaC |
Complex of spao(spoa1,2 semet) and orgb(apar)::t4lysozyme fusion protein |
|
196
|
530
|
5j5aA |
Trypanosoma brucei methionyl-trna synthetase in complex with inhibitor (chem 70786556) |
|
65
|
166
|
5kc0A |
Crystal structure of tmribu, hexagonal crystal form |
|
99
|
273
|
5ji0D |
Ppargamma-rxralpha(s427f) heterodimer in complex with src-1, rosiglitazone, and 9-cis-retanoic acid |
|
64
|
195
|
5khhA |
Hcn2 cnbd in complex with inosine-3', 5'-cyclic monophosphate (cimp) |
|
84
|
275
|
5bmmA |
Src in complex with dna-templated macrocyclic inhibitor mc25b |
|
52
|
336
|
4z2yA |
Crystal structure of methyltransferase calo6 |
|
84
|
296
|
5j95A |
Map4k4 in complex with inhibitor |
|
147
|
454
|
5jqvA |
Crystal structure of cytochrome p450 bm3 heme domain t269v/l272w/l322i/a406s (wivs) variant with iron(iii) deuteroporphyrin ix bound |
|
143
|
399
|
5kyoA |
Crystal structure of cyp101j2 |
|
85
|
263
|
5j87A |
Discovery of n-(3-(5-((3-acrylamido-4-(morpholine-4-carbonyl)phenyl)amino)-1-methyl-6-oxo-1,6-dihydropyridin-3-yl)-2-methylphenyl)-4-(tert-butyl)benzamide (chmfl-btk-01) as a highly selective irreversible btk kinase inhibitor |
|
76
|
287
|
5k0kA |
Crystal structure of the catalytic domain of the proto-oncogene tyrosine-protein kinase mer in complex with inhibitor unc2434 |
|
114
|
350
|
5bveA |
Tetrahydropyrrolo-diazepenones as inhibitors of erk2 kinase |
|
220
|
536
|
5il8A |
Tobacco 5-epi-aristolochene synthase with mopso buffer molecule and ca2+ ions |
|
26
|
124
|
5bqcB |
Crystal structure of norrin in complex with the cysteine-rich domain of frizzled 4 and sucrose octasulfate |
|
25
|
79
|
5kp7B |
Crystal structure of the curacin biosynthetic pathway hmg synthase in complex with holo donor-acp |
|
125
|
390
|
5ibgA |
Crystal structure mycobacterium tuberculosis cyp121 in complex with inhibitor fragment 25b |
|
24
|
59
|
5b1nA |
Dhp domain structure of envz from escherichia coli |
|
96
|
270
|
5hbhB |
Cdk8-cycc in complex with 5-{5-chloro-4-[1-(2-methoxy-ethyl)-1,8-diaza-spiro[4.5]dec-8-yl]-pyridin-3-yl}-1-methyl-1,3-dihydro-benzo[c]isothiazole 2,2-dioxide |
|
85
|
291
|
5hezA |
Jak2 kinase (jh1 domain) mutant p1057a in complex with tg101209 |
|
66
|
248
|
4yqpA |
Crystal structure of trmd, a m1g37 trna methyltransferase with sam-competitive compounds |
