|
59
|
164
|
5kgrA |
Spin-labeled t4 lysozyme construct i9v1/v131v1 (30 days) |
|
59
|
161
|
5jwuA |
T4 lysozyme l99a/m102q with 1,2-dihydro-1,2-azaborine bound |
|
143
|
451
|
5jqhA |
Structure of beta2 adrenoceptor bound to carazolol and inactive-state stabilizing nanobody, nb60 |
|
61
|
164
|
5jguA |
Spin-labeled t4 lysozyme construct r119v1 |
|
159
|
514
|
5i0nA |
Pi4k iialpha bound to calcium |
|
59
|
162
|
7lzmA |
Comparison of the crystal structure of bacteriophage t4 lysozyme at low, medium, and high ionic strengths |
|
58
|
162
|
6lzmA |
Comparison of the crystal structure of bacteriophage t4 lysozyme at low, medium, and high ionic strengths |
|
165
|
425
|
6ffiA |
Crystal structure of mglur5 in complex with mmpep at 2.2 a |
|
159
|
425
|
6ffhA |
Crystal structure of mglur5 in complex with fenobam at 2.65 a |
|
52
|
149
|
6et6A |
Crystal structure of muramidase from acinetobacter baumannii ab 5075uw prophage |
|
163
|
429
|
6cm4A |
Structure of the d2 dopamine receptor bound to the atypical antipsychotic drug risperidone |
|
136
|
366
|
6bg5A |
Structure of 1-(benzo[d][1,3]dioxol-5-ylmethyl)-1-(1-propylpiperidin-4-yl)-3-(3-(trifluoromethyl)phenyl)urea bound to dcn1 |
|
134
|
366
|
6bg3A |
Structure of (3s,4s)-1-benzyl-4-(3-(3-(trifluoromethyl)phenyl)ureido)piperidin-3-yl acetate bound to dcn1 |
|
79
|
271
|
5yqrA |
Crystal structure of the ph-like domain of lam6 |
|
165
|
461
|
5zbhA |
The crystal structure of human neuropeptide y y1 receptor with bms-193885 |
|
196
|
558
|
5yqzR |
Structure of the glucagon receptor in complex with a glucagon analogue |
|
164
|
509
|
5zbqA |
The crystal structure of human neuropeptide y y1 receptor with ur-mk299 |
|
65
|
164
|
5xpfA |
High-resolution x-ray structure of the t26h mutant of t4 lysozyme |
|
153
|
454
|
5xszA |
Crystal structure of zebrafish lysophosphatidic acid receptor lpa6 |
|
162
|
549
|
5xezA |
Structure of the full-length glucagon class b g protein-coupled receptor |
|
223
|
875
|
5w0pC |
Crystal structure of rhodopsin bound to visual arrestin determined by x-ray free electron laser |
|
142
|
437
|
5vexA |
Structure of the human glp-1 receptor complex with nnc0640 |
|
176
|
452
|
5wf5A |
Agonist bound human a2a adenosine receptor with d52n mutation at 2.60 a resolution |
|
62
|
164
|
5vnrA |
X-ray strucutre of perdeuterated t4 lysozyme cysteine-free pseudo-wild type at cryogenic temperature |
|
152
|
549
|
5xf1A |
Structure of the full-length glucagon class b g protein-coupled receptor |
|
157
|
424
|
5cgdA |
Structure of the human class c gpcr metabotropic glutamate receptor 5 transmembrane domain in complex with the negative allosteric modulator 3-chloro-5-[6-(5-fluoropyridin-2-yl)pyrimidin-4-yl]benzonitrile - (htl14242) |
|
85
|
346
|
5b2gA |
Crystal structure of human claudin-4 in complex with c-terminal fragment of clostridium perfringens enterotoxin |
|
61
|
196
|
4yx7C |
Complex of spao(spoa1,2) and orgb(apar)::t4lysozyme fusion protein |
|
140
|
442
|
4rwsA |
Crystal structure of cxcr4 and viral chemokine antagonist vmip-ii complex (psi community target) |
|
83
|
315
|
4exmA |
The crystal structure of an engineered phage lysin containing the binding domain of pesticin and the killing domain of t4-lysozyme |
|
156
|
442
|
4ej4A |
Structure of the delta opioid receptor bound to naltrindole |
|
64
|
175
|
4e97A |
T4 lysozyme l99a/m102h with 2-mercaptoethanol bound |
|
63
|
175
|
4ekqA |
T4 lysozyme l99a/m102h with 4-nitrophenol bound |
|
64
|
175
|
4ekpA |
T4 lysozyme l99a/m102h with nitrobenzene bound |
|
64
|
175
|
4eksA |
T4 lysozyme l99a/m102h with isoxazole bound |
|
108
|
330
|
4epiA |
The crystal structure of pesticin-t4 lysozyme hybrid stabilized by engineered disulfide bonds |
|
63
|
175
|
4ekrA |
T4 lysozyme l99a/m102h with 2-cyanophenol bound |
|
159
|
432
|
4dajA |
Structure of the m3 muscarinic acetylcholine receptor |
|
160
|
442
|
4dklA |
Crystal structure of the mu-opioid receptor bound to a morphinan antagonist |
|
161
|
452
|
4djhA |
Structure of the human kappa opioid receptor in complex with jdtic |
|
105
|
322
|
4arjA |
Crystal structure of a pesticin (translocation and receptor binding domain) from y. pestis and t4-lysozyme chimera |
|
165
|
447
|
3vw7A |
Crystal structure of human protease-activated receptor 1 (par1) bound with antagonist vorapaxar at 2.2 angstrom |
|
150
|
462
|
3v2yA |
Crystal structure of a lipid g protein-coupled receptor at 2.80a |
|
151
|
456
|
3v2wA |
Crystal structure of a lipid g protein-coupled receptor at 3.35a |
|
159
|
438
|
3uonA |
Structure of the human m2 muscarinic acetylcholine receptor bound to an antagonist |
|
148
|
475
|
3sn6R |
Crystal structure of the beta2 adrenergic receptor-gs protein complex |
|
58
|
164
|
3sb5A |
Zn-mediated trimer of t4 lysozyme r125c/e128c by synthetic symmetrization |
|
56
|
163
|
3sb9A |
Cu-mediated dimer of t4 lysozyme r76h/r80h by synthetic symmetrization |
|
53
|
162
|
3sbaA |
Zn-mediated hexamer of t4 lysozyme r76h/r80h by synthetic symmetrization |
|
54
|
163
|
3sb7A |
Cu-mediated trimer of t4 lysozyme d61h/k65h/r76h/r80h by synthetic symmetrization |
