'Nature-inspired' drug-protein complexes as inhibitors of Aβ aggregation

Biochemical Society Transactions

Volumn 33, Issue 4, 2005, Pages 543-547

  Bose, M ^a   Gestwicki, J E ^a,b   Devasthali, V ^a   Crabtree, G R ^a   Graef, I A ^a  

^a STANFORD UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF MICHIGAN   (United States)

Author keywords

Aggregation; Amyloid ; Chaperone; FK506 binding protein; Linker; Small molecule ligand

Indexed keywords

AMYLOID BETA PROTEIN; CALCINEURIN; CHAPERONE; CONGO RED; CYCLOSPORIN; FK 506 BINDING PROTEIN; PROTEIN INHIBITOR; RAPAMYCIN; RECOMBINANT PROTEIN; TACROLIMUS;

ALZHEIMER DISEASE; CHEMICAL STRUCTURE; COMPLEX FORMATION; CONFERENCE PAPER; DEGENERATIVE DISEASE; DRUG MECHANISM; DRUG POTENCY; DRUG PROTEIN BINDING; NATURAL SCIENCE; NERVE DEGENERATION; NEUROTOXICITY; NONHUMAN; PRIORITY JOURNAL; PROTEIN AGGREGATION; PROTEIN PROTEIN INTERACTION; REGULATORY MECHANISM;

AGED; ALZHEIMER DISEASE; AMYLOID BETA-PROTEIN; AMYLOID BETA-PROTEIN PRECURSOR; CONGO RED; HUMANS; MULTIPROTEIN COMPLEXES; NERVE DEGENERATION; TACROLIMUS BINDING PROTEINS;

EID: 23844462173     PISSN: 03005127     EISSN: None     Source Type: Journal    
DOI: 10.1042/BST0330543     Document Type: Conference Paper

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