Heterocephalus glaber (naked mole-rat): 101701639 Help Entry 101701639         CDS       T02812                                  Symbol Psma4 Name (RefSeq) proteasome subunit alpha 4   KO K02728   20S proteasome subunit alpha 3 [EC:3.4.25.1] Organism hgl  Heterocephalus glaber (naked mole-rat) Pathway hgl03050   Proteasome hgl05010   Alzheimer disease hgl05012   Parkinson disease hgl05014   Amyotrophic lateral sclerosis hgl05016   Huntington disease hgl05017   Spinocerebellar ataxia hgl05020   Prion disease hgl05022   Pathways of neurodegeneration - multiple diseases Brite KEGG Orthology (KO) [BR:hgl00001]  09120 Genetic Information Processing   09123 Folding, sorting and degradation    03050 Proteasome     101701639 (Psma4)  09160 Human Diseases   09164 Neurodegenerative disease    05010 Alzheimer disease     101701639 (Psma4)    05012 Parkinson disease     101701639 (Psma4)    05014 Amyotrophic lateral sclerosis     101701639 (Psma4)    05016 Huntington disease     101701639 (Psma4)    05017 Spinocerebellar ataxia     101701639 (Psma4)    05020 Prion disease     101701639 (Psma4)    05022 Pathways of neurodegeneration - multiple diseases     101701639 (Psma4)  09180 Brite Hierarchies   09181 Protein families: metabolism    01002 Peptidases and inhibitors [BR:hgl01002]     101701639 (Psma4)   09182 Protein families: genetic information processing    03051 Proteasome [BR:hgl03051]     101701639 (Psma4) Enzymes [BR:hgl01000]  3. Hydrolases   3.4  Acting on peptide bonds (peptidases)    3.4.25  Threonine endopeptidases     3.4.25.1  proteasome endopeptidase complex      101701639 (Psma4) Peptidases and inhibitors [BR:hgl01002]  Threonine peptidases   Family T1: proteasome family    101701639 (Psma4) Proteasome [BR:hgl03051]  Eukaryotic proteasome   Core particles (20S proteasome)    alpha type subunits     101701639 (Psma4) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  Proteasome Proteasome_A_N TRP_N Motif Other DBs NCBI-GeneID:  101701639 NCBI-ProteinID:  XP_004872150 UniProt:  A0A0P6JGW8 LinkDB All DBs Position Un AA seq 261 aa AA seqDB search MSRRYDSRTTIFSPEGRLYQVEYAMEAIGHAGTCLGILANDGVLLAAERRNIHKLLDEVF FSEKIYKLNEDMACSVAGITSDANVLTNELRLIAQRYLLQYQEPIPCEQLVTALCDIKQA YTQFGGKRPFGVSLLYIGWDKHYGFQLYQSDPSGNYGGWKATCIGNNSAAAVSMLKQDYK EGEMTLKSALALAIKVLNKTMDVSKLSAEKVEIATLTRENGKTVIRVLKQKEVEQLIKKH EEEEAKAEREKKEKEQKEKDK NT seq 786 nt NT seq  +upstreamnt  +downstreamnt atgtctcgaagatatgactccaggaccactatattttctccagaaggtcgcttataccaa gttgaatatgccatggaagccattggacatgcaggcacctgtttgggaattttagcaaac gatggtgttttgcttgcagcagagagacgcaacattcacaagcttcttgatgaagtcttt ttctctgaaaaaatttataaactcaatgaggacatggcttgcagcgtggcaggtataact tctgatgctaatgttctgactaatgaactgaggctcattgcacaaaggtatttattacaa tatcaggagccaattccatgtgagcagttggttacagcactgtgtgatatcaaacaggcc tatacacaatttggaggaaagcgtccctttggtgtctcgttgctgtacattggctgggat aagcactatggctttcagctctatcagagtgaccccagtggaaattatgggggctggaaa gccacatgcattggaaataacagtgctgcagctgtgtcaatgttgaaacaggactacaaa gaaggagaaatgactctgaagtcggcgcttgctttagctatcaaagtgctgaacaagacc atggacgttagtaagctgtctgctgagaaagtggaaatcgccacattaaccagagagaat gggaagacggtgataagagttctcaagcaaaaggaagtggaacagttgatcaagaaacat gaggaagaagaagctaaagctgagcgtgagaagaaagaaaaagaacagaaagaaaaagat aaatag

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