Hylobates moloch (silvery gibbon): 116473013
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Entry
116473013 CDS
T08803
Name
(RefSeq) proteasome subunit alpha type-4-like
KO
K02728
20S proteasome subunit alpha 3 [EC:
3.4.25.1
]
Organism
hmh
Hylobates moloch (silvery gibbon)
Pathway
hmh03050
Proteasome
hmh05010
Alzheimer disease
hmh05012
Parkinson disease
hmh05014
Amyotrophic lateral sclerosis
hmh05016
Huntington disease
hmh05017
Spinocerebellar ataxia
hmh05020
Prion disease
hmh05022
Pathways of neurodegeneration - multiple diseases
Brite
KEGG Orthology (KO) [BR:
hmh00001
]
09120 Genetic Information Processing
09123 Folding, sorting and degradation
03050 Proteasome
116473013
09160 Human Diseases
09164 Neurodegenerative disease
05010 Alzheimer disease
116473013
05012 Parkinson disease
116473013
05014 Amyotrophic lateral sclerosis
116473013
05016 Huntington disease
116473013
05017 Spinocerebellar ataxia
116473013
05020 Prion disease
116473013
05022 Pathways of neurodegeneration - multiple diseases
116473013
09180 Brite Hierarchies
09181 Protein families: metabolism
01002 Peptidases and inhibitors [BR:
hmh01002
]
116473013
09182 Protein families: genetic information processing
03051 Proteasome [BR:
hmh03051
]
116473013
Enzymes [BR:
hmh01000
]
3. Hydrolases
3.4 Acting on peptide bonds (peptidases)
3.4.25 Threonine endopeptidases
3.4.25.1 proteasome endopeptidase complex
116473013
Peptidases and inhibitors [BR:
hmh01002
]
Threonine peptidases
Family T1: proteasome family
116473013
Proteasome [BR:
hmh03051
]
Eukaryotic proteasome
Core particles (20S proteasome)
alpha type subunits
116473013
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
Proteasome
Proteasome_A_N
TRP_N
Motif
Other DBs
NCBI-GeneID:
116473013
NCBI-ProteinID:
XP_032610190
LinkDB
All DBs
Position
Unknown
AA seq
261 aa
AA seq
DB search
MSRRYDSRTTIFSPEGRLYQVEYAMEAIGHAGTCLGILANDGVLLAAERRNIHKLLDEVF
FSEKIYKLNEDMACSVAGITSDANVLTNELRLIAQRYLLQYQEPIPCEQLVTALCDIKQA
YTQFGGKRPFGVSLLYIGWDKHYGFQLYQSDPSGNYGGWKATCIGNNSAAAVSMLKQDYK
EGEMTLKSALALAIKVLNKTMDVSKLSAEKVEIATLTRKNGKMVIRVLKQKEVEQLIKKH
EEEEAKAEREKKEKEQKEKDK
NT seq
786 nt
NT seq
+upstream
nt +downstream
nt
atgtctcgaagatatgactccaggaccactatattttctccagaaggtcgcttataccaa
gttgaatatgccatggaagctattggacatgcaggcacctgtttgggaattttagcaaat
gatggtgttttgcttgcagcagagagacgcaacatccacaagcttcttgatgaagtcttt
ttttctgaaaaaatttataaactcaatgaggacatggcttgcagtgtggcaggcataact
tctgatgctaatgttctgactaatgaactaaggctcattgctcaaaggtatttattacag
tatcaggagccaataccttgtgagcagctggttacagcactgtgtgatatcaaacaagct
tatacacaatttggaggaaaacgtccctttggtgtttcattgctgtacattggctgggat
aagcactatggctttcagctctatcagagtgaccctagtggaaattacgggggatggaag
gccacatgcattggaaataatagcgctgcagctgtgtcaatgttgaaacaagactacaaa
gaaggagaaatgaccttgaagtcagcacttgctttagctatcaaagtactaaataagacc
atggatgttagtaaactctctgctgaaaaagtggaaattgcaacactaacaagaaagaat
ggaaagatggtaatcagagttctcaaacaaaaagaagtggagcagttgatcaaaaaacac
gaggaagaagaagccaaagctgagcgtgagaagaaggaaaaagaacagaaagaaaaggat
aaatag
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