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3CKR

Crystal structure of BACE-1 in complex with inhibitor

Summary for 3CKR
Entry DOI10.2210/pdb3ckr/pdb
Related3CKP
DescriptorBeta-secretase 1, (4S)-1,4-dibenzyl-N-[(1S,2R)-1-benzyl-3-{[3-(dimethylamino)benzyl]amino}-2-hydroxypropyl]-2-oxoimidazolidine-4-carboxamide (3 entities in total)
Functional Keywordsbeta-secretase, aspartyl protease, alternative splicing, glycoprotein, hydrolase, membrane, transmembrane, zymogen
Biological sourceHomo sapiens (Human)
Cellular locationMembrane; Single-pass type I membrane protein: P56817
Total number of polymer chains3
Total formula weight139587.95
Authors
Min, K. (deposition date: 2008-03-16, release date: 2008-06-03, Last modification date: 2021-11-10)
Primary citationPark, H.,Min, K.,Kwak, H.-S.,Koo, K.D.,Lim, D.,Seo, S.-W.,Choi, J.-U.,Platt, B.,Choi, D.-Y.
Synthesis, SAR, and X-ray structure of human BACE-1 inhibitors with cyclic urea derivatives
Bioorg.Med.Chem.Lett., 18:2900-2904, 2008
Cited by
PubMed: 18434152
DOI: 10.1016/j.bmcl.2008.03.081
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.7 Å)
Structure validation

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