KEGG   Macaca mulatta (rhesus monkey): 710417
Entry
710417            CDS       T01028                                 
Symbol
PSMA4
Name
(RefSeq) proteasome subunit alpha type-4
  KO
K02728  20S proteasome subunit alpha 3 [EC:3.4.25.1]
Organism
mcc  Macaca mulatta (rhesus monkey)
Pathway
mcc03050  Proteasome
mcc05010  Alzheimer disease
mcc05012  Parkinson disease
mcc05014  Amyotrophic lateral sclerosis
mcc05016  Huntington disease
mcc05017  Spinocerebellar ataxia
mcc05020  Prion disease
mcc05022  Pathways of neurodegeneration - multiple diseases
Brite
KEGG Orthology (KO) [BR:mcc00001]
 09120 Genetic Information Processing
  09123 Folding, sorting and degradation
   03050 Proteasome
    710417 (PSMA4)
 09160 Human Diseases
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    710417 (PSMA4)
   05012 Parkinson disease
    710417 (PSMA4)
   05014 Amyotrophic lateral sclerosis
    710417 (PSMA4)
   05016 Huntington disease
    710417 (PSMA4)
   05017 Spinocerebellar ataxia
    710417 (PSMA4)
   05020 Prion disease
    710417 (PSMA4)
   05022 Pathways of neurodegeneration - multiple diseases
    710417 (PSMA4)
 09180 Brite Hierarchies
  09181 Protein families: metabolism
   01002 Peptidases and inhibitors [BR:mcc01002]
    710417 (PSMA4)
  09182 Protein families: genetic information processing
   03051 Proteasome [BR:mcc03051]
    710417 (PSMA4)
Enzymes [BR:mcc01000]
 3. Hydrolases
  3.4  Acting on peptide bonds (peptidases)
   3.4.25  Threonine endopeptidases
    3.4.25.1  proteasome endopeptidase complex
     710417 (PSMA4)
Peptidases and inhibitors [BR:mcc01002]
 Threonine peptidases
  Family T1: proteasome family
   710417 (PSMA4)
Proteasome [BR:mcc03051]
 Eukaryotic proteasome
  Core particles (20S proteasome)
   alpha type subunits
    710417 (PSMA4)
SSDB
Motif
Pfam: Proteasome Proteasome_A_N TRP_N DsrH
Other DBs
NCBI-GeneID: 710417
NCBI-ProteinID: NP_001244491
Ensembl: ENSMMUG00000010740
UniProt: I0FTI5 A0A1D5QLV9
LinkDB
Position
7:55776048..55784997
AA seq 261 aa
MSRRYDSRTTIFSPEGRLYQVEYAMEAIGHAGTCLGILANDGVLLAAERRNIHKLLDEVF
FSEKIYKLNEDMACSVAGITSDANVLTNELRLIAQRYLLQYQEPIPCEQLVTALCDIKQA
YTQFGGKRPFGVSLLYIGWDKHYGFQLYQSDPSGNYGGWKATCIGNNSAAAVSMLKQDYK
EGEMTLKSALALAIKVLNKTMDVSKLSAEKVEIATLTRENGKTVIRVLKQKEVEQLIKKH
EEEEAKAEREKKEKEQKEKDK
NT seq 786 nt   +upstreamnt  +downstreamnt
atgtctcgaagatatgactccaggaccactatattttctccagaaggtcgcttataccaa
gttgaatatgccatggaagctattggacatgcaggcacctgtttgggaattttagcaaat
gatggtgttttgcttgcagcagagagacgcaacatccacaagcttctcgatgaagtcttt
ttttctgaaaaaatttataaactcaatgaggacatggcttgcagtgtggcaggcataact
tctgatgctaatgttctgactaatgaactaaggctcattgctcaaaggtatttattgcag
tatcaggagccgataccttgtgagcagttggttacagcactatgtgatatcaagcaagca
tatacacaatttggtggaaaacgtccatttggtgtttcattgctgtacattggttgggat
aagcactatggctttcagctctatcagagtgacccaagtggaaattacgggggatggaag
gccacatgcattggaaataatagcgctgcagctgtgtcaatgttgaaacaagactacaaa
gaaggagaaatgaccttgaagtcagcacttgctttagctatcaaagtactaaataagacc
atggatgttagtaaactctccgctgaaaaagtggaaattgcaacactaacaagagagaat
ggaaagacggtaatcagagttctcaaacaaaaagaagtggaacagttgatcaaaaaacat
gaggaagaagaagctaaagctgagcgtgagaagaaagaaaaagaacagaaagaaaaggat
aaatag

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