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3BRA

BACE-1 complexed with compound 1

Summary for 3BRA
Entry DOI10.2210/pdb3bra/pdb
Related1FKN
DescriptorBeta-secretase 1, 4-(2-aminoethyl)phenol (3 entities in total)
Functional Keywordsalzheimer's disease, aspartic protease, beta-secretase, memapsin 2, fragment screen, alternative splicing, aspartyl protease, glycoprotein, hydrolase, membrane, transmembrane, zymogen
Biological sourceHomo sapiens (human)
Cellular locationMembrane; Single-pass type I membrane protein: P56817
Total number of polymer chains1
Total formula weight45691.19
Authors
Kuglstatter, A.,Hennig, M. (deposition date: 2007-12-21, release date: 2008-03-11, Last modification date: 2024-10-30)
Primary citationKuglstatter, 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: 18226904
DOI: 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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