57
|
163
|
3sbbC |
Disulphide-mediated tetramer of t4 lysozyme r76c/r80c by synthetic symmetrization |
53
|
165
|
3sb8A |
Cu-mediated dimer of t4 lysozyme d61h/k65h by synthetic symmetrization |
56
|
164
|
3sb6A |
Cu-mediated dimer of t4 lysozyme d61h/k65h/r76h/r80h by synthetic symmetrization |
147
|
435
|
3rzeA |
Structure of the human histamine h1 receptor in complex with doxepin |
60
|
166
|
3runA |
New strategy to analyze structures of glycopeptide antibiotic-target complexes |
62
|
164
|
5xpeA |
Neutron structure of the t26h mutant of t4 lysozyme |
166
|
440
|
5x7dA |
Structure of beta2 adrenoceptor bound to carazolol and an intracellular allosteric antagonist |
135
|
441
|
5x33A |
Leukotriene b4 receptor blt1 in complex with biil260 |
154
|
452
|
5wf6A |
Agonist bound human a2a adenosine receptor with s91a mutation at 2.90 a resolution |
223
|
876
|
5w0pA |
Crystal structure of rhodopsin bound to visual arrestin determined by x-ray free electron laser |
55
|
164
|
5vnqA |
Neutron crystallographic strucutre of perdeuterated t4 lysozyme cysteine-free pseudo-wild type at cryogenic temperature |
64
|
162
|
5v7fA |
T4 lysozyme y18ymi |
135
|
364
|
5v86A |
Structure of dcn1 bound to nacm-opt |
61
|
162
|
5v7dA |
T4 lysozyme y18ymbr |
134
|
367
|
5v83A |
Structure of dcn1 bound to nacm-hit |
123
|
423
|
5vbaA |
Structure of espg1 chaperone from the type vii (esx-1) secretion system determined with the assistance of n-terminal t4 lysozyme fusion |
134
|
367
|
5v88A |
Structure of dcn1 bound to nacm-cov |
149
|
437
|
5vewA |
Structure of the human glp-1 receptor complex with pf-06372222 |
61
|
162
|
5v7eA |
T4 lysozyme y18ymcl |
109
|
439
|
5tzyA |
Gpr40 in complex with agopam ap8 and partial agonist mk-8666 |
163
|
445
|
5tzrA |
Gpr40 in complex with partial agonist mk-8666 |
167
|
445
|
5t1aA |
Structure of cc chemokine receptor 2 with orthosteric and allosteric antagonists |
169
|
466
|
5t04A |
Structure of constitutively active neurotensin receptor |
59
|
164
|
5nx0A |
Structure of spin-labelled t4 lysozyme mutant l115c-r119c-r1 at room temperature |
157
|
425
|
5cgcA |
Structure of the human class c gpcr metabotropic glutamate receptor 5 transmembrane domain in complex with the negative allosteric modulator 3-chloro-4-fluoro-5-[6-(1h-pyrazol-1-yl)pyrimidin-4-yl]benzonitrile |
57
|
162
|
5lzmA |
Comparison of the crystal structure of bacteriophage t4 lysozyme at low, medium, and high ionic strengths |
77
|
253
|
5bz6A |
Crystal structure of the n-terminal domain single mutant (s92a) of the human mitochondrial calcium uniporter fused with t4 lysozyme |
62
|
162
|
5kioA |
Pseudo t4 lysozyme mutant - y18phe-i |
48
|
196
|
4yxaC |
Complex of spao(spoa1,2 semet) and orgb(apar)::t4lysozyme fusion protein |
59
|
162
|
5ki8A |
Pseudo t4 lysozyme mutant - y88phe-br |
58
|
162
|
5ki1A |
Pseudo t4 lysozyme mutant - y18f |
60
|
162
|
5ki2A |
Pseudo t4 lysozyme mutant - y18phe-methyl |
62
|
162
|
5ki3A |
Pseudo t4 lysozyme mutant - y18phe-br |
220
|
875
|
4zwjA |
Crystal structure of rhodopsin bound to arrestin by femtosecond x-ray laser |
60
|
164
|
5g27A |
Structure of spin-labelled t4 lysozyme mutant l118c-r1 at room temperature |
161
|
467
|
5glhA |
Human endothelin receptor type-b in complex with et-1 |
77
|
227
|
5ewxA |
Fusion protein of t4 lysozyme and b4 domain of protein a from staphylococcal aureus with chemical cross-linker ey-cbs |
164
|
438
|
5ee7A |
Crystal structure of the human glucagon receptor (gcgr) in complex with the antagonist mk-0893 |
152
|
514
|
5eutA |
Crystal structure of phosphatidyl inositol 4-kinase ii alpha in the apo state |
141
|
421
|
4z9gA |
Crystal structure of human corticotropin-releasing factor receptor 1 (crf1r) in complex with the antagonist cp-376395 in a hexagonal setting with translational non-crystallographic symmetry |
182
|
442
|
5d6lA |
Beta2ar-t4l - cim |
220
|
875
|
5dgyA |
Crystal structure of rhodopsin bound to visual arrestin |
176
|
442
|
5d5bA |
In meso x-ray crystallography structure of the beta2-adrenergic receptor at 100 k |
53
|
165
|
4zpuA |
The structure of dlp12 endolysin exhibits likely active and inactive conformations. |
177
|
442
|
5d5aA |
In meso in situ serial x-ray crystallography structure of the beta2-adrenergic receptor at 100 k |
171
|
444
|
5cxvA |
Structure of the human m1 muscarinic acetylcholine receptor bound to antagonist tiotropium |
155
|
513
|
4yc4A |
Crystal structure of phosphatidyl inositol 4-kinase ii alpha in complex with nucleotide analog |
184
|
524
|
4xeeA |
Structure of active-like neurotensin receptor |
79
|
253
|
4xsjA |
Crystal structure of the n-terminal domain of the human mitochondrial calcium uniporter fused with t4 lysozyme |
190
|
525
|
4xesA |
Structure of active-like neurotensin receptor |