|
23
|
57
|
5jlxA |
Antphd with 15bp dna duplex s-monothioated at cytidine-8 |
|
71
|
327
|
3syoA |
Crystal structure of the g protein-gated inward rectifier k+ channel girk2 (kir3.2) in complex with sodium |
|
78
|
327
|
3sypA |
Crystal structure of the g protein-gated inward rectifier k+ channel girk2 (kir3.2) r201a mutant |
|
120
|
354
|
3sxtA |
Crystal structure of the quinol form of methylamine dehydrogenase in complex with the diferrous form of maug |
|
130
|
316
|
3swhA |
Munc13-1, mun domain, c-terminal module |
|
124
|
409
|
3sg5A |
Crystal structure of dimeric gcamp3-d380y, qp(linker 1), lp(linker 2) |
|
144
|
406
|
3ss3A |
Crystal structure of mouse glutaminase c, ligand-free form |
|
142
|
406
|
3ss4A |
Crystal structure of mouse glutaminase c, phosphate-bound form |
|
84
|
290
|
3szpA |
Full-length structure of the vibrio cholerae virulence activator, aphb, a member of the lttr protein family |
|
90
|
296
|
3sykA |
Crystal structure of the aaa+ protein cbbx, selenomethionine structure |
|
87
|
264
|
3sxrA |
Crystal structure of bmx non-receptor tyrosine kinase complex with dasatinib |
|
167
|
546
|
3sraB |
Structure of pseudomonas aerugionsa pvdq covalently acylated with myristic acid from pvdiq |
|
84
|
298
|
3sqqA |
Cdk2 in complex with inhibitor rc-3-96 |
|
138
|
327
|
3sl3A |
Crystal structure of the apo form of the catalytic domain of pde4d2 |
|
74
|
301
|
3snaA |
Crystal structure of sars coronavirus main protease complexed with ac-nsfsq-h (soaking) |
|
44
|
126
|
3sjrA |
Crystal structure of conserved unkown function protein cv_1783 from chromobacterium violaceum atcc 12472 |
|
155
|
480
|
3sn5A |
Crystal structure of human cyp7a1 in complex with cholest-4-en-3-one |
|
115
|
358
|
3smsA |
Human pantothenate kinase 3 in complex with a pantothenate analog |
|
24
|
61
|
3sjaC |
Crystal structure of s. cerevisiae get3 in the open state in complex with get1 cytosolic domain |
|
232
|
567
|
3sksA |
Crystal structure of a putative oligoendopeptidase f from bacillus anthracis str. ames |
|
94
|
332
|
3spgA |
Inward rectifier potassium channel kir2.2 r186a mutant in complex with pip2 |
|
82
|
257
|
3skdA |
Crystal structure of the thermus thermophilus cas3 hd domain in the presence of ni2+ |
|
148
|
475
|
3sn6R |
Crystal structure of the beta2 adrenergic receptor-gs protein complex |
|
96
|
240
|
3smvA |
X-ray crystal structure of l-azetidine-2-carboxylate hydrolase |
|
55
|
164
|
3srcA |
Structure of pseudomonas aeruginosa pvdq bound to ns2028 |
|
116
|
325
|
3shzA |
Crystal structure of the pde5a1 catalytic domain in complex with novel inhibitors |
|
101
|
273
|
3sp6A |
Structural basis for iloprost as a dual pparalpha/delta agonist |
|
37
|
164
|
3sr6A |
Crystal structure of reduced bovine xanthine oxidase in complex with arsenite |
|
21
|
54
|
3sjcC |
Crystal structure of s.cerevisiae get3 in the semi-open state in complex with get1 cytosolic domain |
|
129
|
322
|
3snlA |
Highly potent, selective, and orally active phosphodiestarase 10a inhibitors |
|
104
|
324
|
5iiiA |
Crystal structure of the pre-catalytic ternary complex of dna polymerase lambda with a templating 8-oxo-dg and an incoming datp |
|
136
|
327
|
3sl6A |
Crystal structure of the catalytic domain of pde4d2 with compound 12c |
|
75
|
276
|
3skcA |
Human b-raf kinase in complex with an amide linked pyrazolopyridine inhibitor |
|
35
|
80
|
3sjqC |
Crystal structure of a small conductance potassium channel splice variant complexed with calcium-calmodulin |
|
80
|
269
|
3srvB |
Crystal structure of spleen tyrosine kinase (syk) in complex with a diaminopyrimidine carboxamide inhibitor |
|
133
|
409
|
3sg4A |
Crystal structure of gcamp3-d380y, lp(linker 2) |
|
110
|
267
|
3sngA |
X-ray structure of fully glycosylated bifunctional nuclease tbn1 from solanum lycopersicum (tomato) |
|
76
|
289
|
5itxA |
Crystal structure of human neil1(p2g r242k) bound to duplex dna containing thymine glycol |
|
80
|
193
|
3sfiA |
Ethionamide boosters part 2: combining bioisosteric replacement and structure-based drug design to solve pharmacokinetic issues in a series of potent 1,2,4-oxadiazole ethr inhibitors. |
|
116
|
354
|
3sleA |
Crystal structure of the p107c-maug/pre-methylamine dehydrogenase complex |
|
329
|
783
|
3sdrA |
Structure of a three-domain sesquiterpene synthase: a prospective target for advanced biofuels production |
|
92
|
332
|
3spiA |
Inward rectifier potassium channel kir2.2 in complex with pip2 |
|
82
|
330
|
3spjA |
Apo inward rectifier potassium channel kir2.2 i223l mutant |
|
289
|
908
|
3se6A |
Crystal structure of the human endoplasmic reticulum aminopeptidase 2 |
|
48
|
129
|
3sp3A |
Lysozyme in 20% sucrose |
|
81
|
306
|
3sneA |
Crystal structure of sars coronavirus main protease complexed with ac-estlq-h (soaking) |
|
123
|
322
|
3sniA |
Highly potent, selective, and orally active phosphodiestarase 10a inhibitors |
|
73
|
214
|
3siaA |
Crystal structure of ure3-binding protein, (d127a,n129a) mutant, iodide phased |
|
107
|
324
|
5iijA |
Crystal structure of the pre-catalytic ternary complex of dna polymerase lambda with a templating 8-oxo-dg and an incoming dctp |
|
133
|
328
|
3sl5A |
Crystal structure of the catalytic domain of pde4d2 complexed with compound 10d |
