BMRB Logo
Neural
Disease Protein BMRB entry
Amyotrophic lateral sclerosis Apo-SOD1 15711
apo-SOD1-variant A4V 15712
apo-SOD1-variant D90A 15714
apo-SOD1-variant G85R 15713
Alzheimer's disease Amyloid peptide Abeta(1-40) 5057 6257 17159 17764 17795 17796
Amyloid peptide Abeta(1-42) 5400 17793 17794
Amyloid Precursor Protein APP 4342
Anomalous Copper(II) Binding to Abeta Peptide 17186
Apolipoprotein E 15744
CAPPD* domain of human APP770 6236
Complement repeat56 / Receptor associated protein complex 17055
Kunitz-Type Inhibitor Domain of APP 2024
Calcium-bound Human S100B 5206
Tau protein 17945
Charcot-Marie Tooth Disease Human TrJ disease-related mutant form of PMP22 17455
Mediator Complex Subunit 25(391-543) 17323
Peripheral Myelin Protein 22 17454
Early Onset Neurodegeneration Iowa-mutant B-amyloid fibrils 17774
Friedreich Ataxia Frataxin 4307
Holoprosencephaly Homeobox domain (171-248) 17971
Huntington's Disease N-terminal domain of huntingtin (htt17) 17642 17644
Juvenile Parkinson's Disease Parkin Ubl domain/Endophilin-A1 SH3 domain complex 16813
Machado-Joseph Disease Ataxin-3 16813
Parkinson's Disease A30P alpha-synuclein fibrils 17214 17648
A53T alpha-synuclein fibrils 17649
Alpha-synuclein fibrils 16904 16939 17910
Disordered alpha-synuclein variants 16543 16546 16547 16548
DJ-1 17507
E46K alpha-synuclein fibrils 17654
SH3 domains of BAR protein 16813
Ubiquitin carboxy-terminal hydrolase L1 17260
Ubiquitin like domain in Parkin 5496 5500
Williams syndrome DnaJ domain 11144
WSTF-Phd Zinc Finger 4928
Wilson disease Apo Wilson Copper Binding Domain 4-6 16937
E1064A mutant of Wilson disease protein 16536
Metal Binding Domains 3,4 of Wilson Disease Protein 11041
N-domain of Wilson Disease Protein 16761






Back to Main Page