3BRA
BACE-1 complexed with compound 1
Summary for 3BRA
Entry DOI | 10.2210/pdb3bra/pdb |
Related | 1FKN |
Descriptor | Beta-secretase 1, 4-(2-aminoethyl)phenol (3 entities in total) |
Functional Keywords | alzheimer's disease, aspartic protease, beta-secretase, memapsin 2, fragment screen, alternative splicing, aspartyl protease, glycoprotein, hydrolase, membrane, transmembrane, zymogen |
Biological source | Homo sapiens (human) |
Cellular location | Membrane; Single-pass type I membrane protein: P56817 |
Total number of polymer chains | 1 |
Total formula weight | 45691.19 |
Authors | Kuglstatter, A.,Hennig, M. (deposition date: 2007-12-21, release date: 2008-03-11, Last modification date: 2024-10-30) |
Primary citation | Kuglstatter, A.,Stahl, M.,Peters, J.U.,Huber, W.,Stihle, M.,Schlatter, D.,Benz, J.,Ruf, A.,Roth, D.,Enderle, T.,Hennig, M. Tyramine fragment binding to BACE-1 Bioorg.Med.Chem.Lett., 18:1304-1307, 2008 Cited by PubMed Abstract: Fragment screening revealed that tyramine binds to the active site of the Alzheimer's disease drug target BACE-1. Hit expansion by selection of compounds from the Roche compound library identified tyramine derivatives with improved binding affinities as monitored by surface plasmon resonance. X-ray structures show that the amine of the tyramine fragment hydrogen-bonds to the catalytic water molecule. Structure-guided ligand design led to the synthesis of further low molecular weight compounds that are starting points for chemical leads. PubMed: 18226904DOI: 10.1016/j.bmcl.2008.01.032 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.3 Å) |
Structure validation
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