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Search Count: 29

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8F1C image
Voltage-Gated Potassium Channel Kv3.1 With Novel Positive Modulator (9M)-9-{5-Chloro-6-[(3,3-Dimethyl-2,3-Dihydro-1-Benzofuran-4-Yl)Oxy]-4-Methylpyridin-3-Yl}-2-Methyl-7,9-Dihydro-8H-Purin-8-One (Compound 4)

8F1D image
Voltage-Gated Potassium Channel Kv3.1 Apo

7L1U image
Orexin Receptor 2 (Ox2R) In Complex With G Protein And Natural Peptide-Agonist Orexin B (Oxb)

7L1V image
Orexin Receptor 2 (Ox2R) In Complex With G Protein And Small-Molecule Agonist Compound 1

6X3L image
Sortilin-Progranulin Interaction With Compound 2

6X48 image
Sortilin-Progranulin Interaction With Compound 17

6X4H image
Sortilin-Progranulin Interaction With Compound 24

6CYB image
Pde2 In Complex With Compound 7

6CYC image
Pde2 In Complex With Compound 5

6CYD image
Pde2 In Complex With Compound 7

6B96 image
Crystal Structure Of Pde2 In Complex With Compound 16
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:1.88 Å Release Date: 2017-11-22
Classification: HYDROLASE
Ligands: ZN, MG, CZV, EDO

6B97 image
Crystal Structure Of Pde2 In Complex With Complex 9
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:1.76 Å Release Date: 2017-11-22
Classification: HYDROLASE
Ligands: ZN, MG, CZY, EDO

6B98 image
Pde2 In Complex With Compound 1
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:1.97 Å Release Date: 2017-11-22
Classification: HYDROLASE
Ligands: ZN, MG, D07

5HJP image
Identification Of Lxrbeta Selective Agonists For The Treatment Of Alzheimer'S Disease

5HJS image
Identification Of Lxrbeta Selective Agonists For The Treatment Of Alzheimer'S Disease

4ZPE image
Bace1 In Complex With 4-(Cyclohexylamino)-1-(3-Fluorophenyl)-8-(3-Isopropoxybenzyl)-1,3,8-Triazaspiro[4.5]Dec-3-En-2-One

4ZPF image
Bace1 In Complex With 8-(3-((1-Aminopropan-2-Yl)Oxy)Benzyl)-4-(Cyclohexylamino)-1-(3-Fluorophenyl)-1,3,8-Triazaspiro[4.5]Dec-3-En-2-One

4ZPG image
Bace1 In Complex With 8-Benzyl-4-(Cyclohexylamino)-1-(3-Fluorophenyl)-7-Methyl-1,3,8-Triazaspiro[4.5]Dec-3-En-2-One

4PMM image
The Structure Of Trka Kinase Bound To The Inhibitor N-(3-Cyclopropyl-1-Phenyl-1H-Pyrazol-5-Yl)-2-{4-[3-Methoxy-4-(4-Methyl-1H-Imidazol-1-Yl)Phenyl]-1H-1,2,3-Triazol-1-Yl}Acetamide

4PMP image
The Structure Of Trka Kinase Bound To The Inhibitor 1-Cyclopropyl-1-[3-(1,3-Thiazol-2-Yl)Benzyl]-3-[4-(Trifluoromethoxy)Phenyl]Urea
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