KEGG   Puma concolor (puma): 112854962
Entry
112854962         CDS       T08890                                 
Symbol
PSMA4
Name
(RefSeq) proteasome subunit alpha type-4
  KO
K02728  20S proteasome subunit alpha 3 [EC:3.4.25.1]
Organism
pcoo  Puma concolor (puma)
Pathway
pcoo03050  Proteasome
pcoo05010  Alzheimer disease
pcoo05012  Parkinson disease
pcoo05014  Amyotrophic lateral sclerosis
pcoo05016  Huntington disease
pcoo05017  Spinocerebellar ataxia
pcoo05020  Prion disease
pcoo05022  Pathways of neurodegeneration - multiple diseases
Brite
KEGG Orthology (KO) [BR:pcoo00001]
 09120 Genetic Information Processing
  09123 Folding, sorting and degradation
   03050 Proteasome
    112854962 (PSMA4)
 09160 Human Diseases
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    112854962 (PSMA4)
   05012 Parkinson disease
    112854962 (PSMA4)
   05014 Amyotrophic lateral sclerosis
    112854962 (PSMA4)
   05016 Huntington disease
    112854962 (PSMA4)
   05017 Spinocerebellar ataxia
    112854962 (PSMA4)
   05020 Prion disease
    112854962 (PSMA4)
   05022 Pathways of neurodegeneration - multiple diseases
    112854962 (PSMA4)
 09180 Brite Hierarchies
  09181 Protein families: metabolism
   01002 Peptidases and inhibitors [BR:pcoo01002]
    112854962 (PSMA4)
  09182 Protein families: genetic information processing
   03051 Proteasome [BR:pcoo03051]
    112854962 (PSMA4)
Enzymes [BR:pcoo01000]
 3. Hydrolases
  3.4  Acting on peptide bonds (peptidases)
   3.4.25  Threonine endopeptidases
    3.4.25.1  proteasome endopeptidase complex
     112854962 (PSMA4)
Peptidases and inhibitors [BR:pcoo01002]
 Threonine peptidases
  Family T1: proteasome family
   112854962 (PSMA4)
Proteasome [BR:pcoo03051]
 Eukaryotic proteasome
  Core particles (20S proteasome)
   alpha type subunits
    112854962 (PSMA4)
SSDB
Motif
Pfam: Proteasome Proteasome_A_N TRP_N
Other DBs
NCBI-GeneID: 112854962
NCBI-ProteinID: XP_025774266
UniProt: A0A6P6HG11
LinkDB
Position
Unknown
AA seq 261 aa
MSRRYDSRTTIFSPEGRLYQVEYAMEAIGHAGTCLGILANDGVLLAAERRNIHKLLDEVF
FSEKIYKLNEDMACSVAGITSDANVLTNELRLIAQRYLLQYQEPIPCEQLVTALCDIKQA
YTQFGGKRPFGVSLLYIGWDKHYGFQLYQSDPSGNYGGWKATCIGNNSAAAVSMLKQDYK
EGEMTLKSALALAIKVLNKTMDVSKLSAEKVEIATLTRENGKTVIRVLKQKEVEQLIKNH
EEEEAKAEREKKEKEQKEKEK
NT seq 786 nt   +upstreamnt  +downstreamnt
atgtctcgaagatatgactcccgaaccactatattttctccagaaggtcgcttgtaccaa
gttgagtatgccatggaggctattggacatgcaggcacctgcttggggattttagccaac
gatggtgttttgcttgctgcagagagacgcaacatccacaagcttctggatgaagttttt
ttctctgaaaaaatttacaaactgaatgaggacatggcttgcagtgtggcaggcataact
tctgatgctaatgttctgactaatgaactgaggctcattgcacagaggtatttgttacag
tatcaggagccaattccttgtgagcagttggtcacggcactttgtgatatcaaacaagct
tatacacagtttggaggaaaacgtcccttcggcgtgtccctgctttacatcggctgggat
aagcactacggttttcagctctaccagagtgaccccagcgggaattacggaggatggaaa
gccacatgcattggaaataatagtgctgcagctgtgtcaatgttaaaacaagactacaaa
gaaggagaaatgactttgaagtcagcacttgctttagctatcaaagtcctaaataagacc
atggatgtgagtaaactctctgctgaaaaagtggaaatcgccaccctaacaagagagaac
gggaagacggtcatcagagtcctcaaacagaaagaggtggagcagttgatcaaaaaccat
gaagaagaagaggctaaagctgagcgcgagaagaaagaaaaagaacagaaagaaaaggaa
aaatag

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