Neural Diseases

Disease Protein BMRB entry
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
Beta-amyloid 15775 18052 18127 18128 18131 18175 19009
Beta-amyloid modulated by congo red 26516
Beta-amyloid modulated by lacmoid 26508
Beta-amyloid precursor transmembrane domain 18080 18648 18649
Calcium-bound human S100B 5206
CAPPD* domain of human APP770 6236
Complement repeat 56 / Receptor associated protein complex 17055
Kunitz-Type inhibitor domain of APP 2024
Tau protein 17945
Amyotrophic lateral sclerosis Angiogenin 18197
apo-SOD1 15711
apo-SOD1-variant A4V 15712
apo-SOD1-variant D90A 15714
apo-SOD1-variant G85R 15713
Cu(I), Zn(II) superoxide dismutase 18509
SOD1 monomer 26570
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
Creutzfeldt-Jakob disease Human prion protein with E219K polymorphism 18426
Human prion protein V210I mutant 18550
Early Onset Neurodegeneration Iowa-mutant B-amyloid fibrils 17774
Epilepsy Human membrane protein TMEM14A 18219 18222
Friedreich Ataxia Frataxin 4342
Holoprosencephaly Homeobox domain (171-248) 17971
Huntington's Disease N-terminal domain of huntingtin (htt17) 17642 17644
Juvenile Parkinson's Disease IBR Domain 15074
Parkin RING 2 18642
Parkin Ubl domain/Endophilin-A1 SH3 domain complex 16813
Machado-Joseph Disease Ataxin-3 17333
Multiple sclerosis Myelin basic protein with DPC micelles 18520
Myelin basic protein 6100 6857 15131 20062
Parkinson's Disease A30P alpha-synuclein fibrils 17214 17648
A53T alpha-synuclein fibrils 17649
Alpha-synuclein fibril mutation A53T and E46K 18207 18208 18232 18243
Alpha-synuclein fibrils 16904 16939 17910
Disordered alpha-synuclein variants 16543 16546 16547 16548
DJ-1 17507
E46K alpha-synuclein fibrils 17654
N-terminal domain of human cerebral dopamine neurotrophic factor 18269
SH3 domains of BAR protein 16813
Ubiquitin carboxy-terminal hydrolase L1 17260
Ubiquitin like domain in Parkin 5496 5500
Vestibular Neuronitis Brain acid soluble protein 1 18417
Williams syndrome DnaJ domain 11144
WSTF-Phd Zinc finger 4928
Rett Syndrome Zinc finger protein Kaiso 18462
PTP1B 25375
Spinal Muscular Atrophy R3H domain of human Smubp-2 18391
Tudor domain of human SMN protein 18005 18006 18007 18008
Spinocerebellar Ataxia 28 AFG3-like protein 2 18156
Wilson disease Apo Wilson Copper Binding Domain 4-6 16937
ATX1 Antioxidant Protein 1 Homolog 18299
E1064A mutant of Wilson Disease Protein 16536
Human copper transporter 1 18408 18409 18410
Metal Binding Domains 3,4 of Wilson disease protein 11041
N-domain of Wilson disease protein 16761
Wolff-Parkinson-White syndrome AMP-activated protein kinase alpha 2 catalytic subunit 18497

Associated Human Genes

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