KEGG   Panthera pardus (leopard): 109273597
Entry
109273597         CDS       T06062                                 
Symbol
PSMA4
Name
(RefSeq) proteasome subunit alpha type-4
  KO
K02728  20S proteasome subunit alpha 3 [EC:3.4.25.1]
Organism
ppad  Panthera pardus (leopard)
Pathway
ppad03050  Proteasome
ppad05010  Alzheimer disease
ppad05012  Parkinson disease
ppad05014  Amyotrophic lateral sclerosis
ppad05016  Huntington disease
ppad05017  Spinocerebellar ataxia
ppad05020  Prion disease
ppad05022  Pathways of neurodegeneration - multiple diseases
Brite
KEGG Orthology (KO) [BR:ppad00001]
 09120 Genetic Information Processing
  09123 Folding, sorting and degradation
   03050 Proteasome
    109273597 (PSMA4)
 09160 Human Diseases
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    109273597 (PSMA4)
   05012 Parkinson disease
    109273597 (PSMA4)
   05014 Amyotrophic lateral sclerosis
    109273597 (PSMA4)
   05016 Huntington disease
    109273597 (PSMA4)
   05017 Spinocerebellar ataxia
    109273597 (PSMA4)
   05020 Prion disease
    109273597 (PSMA4)
   05022 Pathways of neurodegeneration - multiple diseases
    109273597 (PSMA4)
 09180 Brite Hierarchies
  09181 Protein families: metabolism
   01002 Peptidases and inhibitors [BR:ppad01002]
    109273597 (PSMA4)
  09182 Protein families: genetic information processing
   03051 Proteasome [BR:ppad03051]
    109273597 (PSMA4)
Enzymes [BR:ppad01000]
 3. Hydrolases
  3.4  Acting on peptide bonds (peptidases)
   3.4.25  Threonine endopeptidases
    3.4.25.1  proteasome endopeptidase complex
     109273597 (PSMA4)
Peptidases and inhibitors [BR:ppad01002]
 Threonine peptidases
  Family T1: proteasome family
   109273597 (PSMA4)
Proteasome [BR:ppad03051]
 Eukaryotic proteasome
  Core particles (20S proteasome)
   alpha type subunits
    109273597 (PSMA4)
SSDB
Motif
Pfam: Proteasome Proteasome_A_N TRP_N
Other DBs
NCBI-GeneID: 109273597
NCBI-ProteinID: XP_019316062
Ensembl: ENSPPRG00000001876
UniProt: A0A9V1G665
LinkDB
Position
Unknown
AA seq 261 aa
MSRRYDSRTTIFSPEGRLYQVEYAMEAIGHAGTCLGILANDGVLLAAERRNIHKLLDEVF
FSEKIYKLNEDMACSVAGITSDANVLTNELRLIAQRYLLQYQEPIPCEQLVTALCDIKQA
YTQFGGKRPFGVSLLYIGWDKHYGFQLYQSDPSGNYGGWKATCIGNNSAAAVSMLKQDYK
EGEMTLKSALALAIKVLNKTMDVSKLSAEKVEIATLTRENGKTVIRVLKQKEVEQLIKNH
EEEEAKAEREKKEKEQKEKEK
NT seq 786 nt   +upstreamnt  +downstreamnt
atgtctcgaagatatgactcccggaccactatattttctccggaaggtcgcttgtaccaa
gttgagtatgccatggaggctattggacatgcaggcacctgcttggggattttagccaac
gatggtgttttgcttgctgcagagagacgcaacatccacaagcttctggatgaagttttt
ttctctgaaaaaatttacaaactaaatgaggacatggcttgcagtgtggcaggcataact
tctgatgctaatgttctgactaatgaactgaggctcattgcacagaggtatttgttacag
tatcaggagccaattccttgtgagcagttggtcacggcactttgtgatatcaaacaagct
tatacacagtttggaggaaaacgtcccttcggcgtgtccctgctttacatcggctgggat
aagcactacggttttcagctctaccagagtgatcccagcgggaattacggaggatggaaa
gccacatgcattggaaataatagtgctgcagctgtgtcaatgttaaaacaagactacaaa
gaaggagaaatgactttgaagtcagcacttgctttagctatcaaagtcctaaataagacc
atggatgtgagtaaactctctgctgaaaaagtggaaatcgccaccctaacaagagagaat
gggaagacggtcatcagagtcctcaaacagaaagaggtggagcagttgatcaaaaaccat
gaagaagaagaagctaaagctgagcgcgagaagaaggaaaaagaacagaaagaaaaggaa
aaatag

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