KEGG   Puma concolor (puma): 112854009
Entry
112854009         CDS       T08890                                 
Symbol
HAP1
Name
(RefSeq) LOW QUALITY PROTEIN: huntingtin-associated protein 1
  KO
K04647  huntingtin-associated protein 1
Organism
pcoo  Puma concolor (puma)
Pathway
pcoo04727  GABAergic synapse
pcoo05014  Amyotrophic lateral sclerosis
pcoo05016  Huntington disease
pcoo05022  Pathways of neurodegeneration - multiple diseases
Brite
KEGG Orthology (KO) [BR:pcoo00001]
 09150 Organismal Systems
  09156 Nervous system
   04727 GABAergic synapse
    112854009 (HAP1)
 09160 Human Diseases
  09164 Neurodegenerative disease
   05014 Amyotrophic lateral sclerosis
    112854009 (HAP1)
   05016 Huntington disease
    112854009 (HAP1)
   05022 Pathways of neurodegeneration - multiple diseases
    112854009 (HAP1)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   04131 Membrane trafficking [BR:pcoo04131]
    112854009 (HAP1)
Membrane trafficking [BR:pcoo04131]
 Exocytosis
  Calcium ion-dependent exocytosis
   Others
    112854009 (HAP1)
SSDB
Motif
Pfam: HAP1_N bZIP_1
Other DBs
NCBI-GeneID: 112854009
NCBI-ProteinID: XP_025773231
UniProt: A0A6P6HD87
LinkDB
Position
Unknown
AA seq 521 aa
MSPKEPGQGLVGHRFRTRAPVGVTPAPPPTAHSSPEPSAQPAPAPAQALTEGPRMGSRSP
SVSVPAPAGARPTSKAGSPTGTPRASAFAASQRNAQFGPGNSDAQWTRFIFRGPFGPRAT
GLGTEKAAGIWKTPAAYIGQRPGVSGPEHAAFIRELEEALCPDQPPPAGITQEDVKVMLN
LLEKLCTAFPVQLLPPVWESPETGKYSPWMGVPLQRERDLNTAVCIGQSLVRQNSVLMGE
HSKLEAMLGSAREDILHLRYQVSLRDDLLQLYSDSEEEEEEEEEEEPEEEEQQHYHSYGA
PEPTCLREMEVLHDCPQLEALQEQLRLLEEENEQLREEASQLYPLDCVEQVLYVKLYRLC
RSEVQEQDRGLEAEKGLLTAEDFVAEDFVPVEELVPEEELGATEEVASAEEGATEEAELV
SEEAEAWEEVEPELDEATQGNVGTSALEASGLGPSHLNMKRVLQQLANWLDARYSRQLRL
KMLQKGECSHRGLPPASQTSYRSSMKGFAGSQQPAEAPQTA
NT seq 1566 nt   +upstreamnt  +downstreamnt
atgagcccgaaagagcccgggcagggcctcgtggggcaccgcttcagaacccgggctcca
gtgggagtcacccccgcacccccacccacagcccattcctctccagagccctcagcgcag
cctgcacccgcccctgcgcaggcactgacggaaggaccgcgaatgggatccagatcccca
tccgtctcggtacccgcccccgccggagctcgcccgacctccaaggctggatccccgaca
ggaacaccgcgcgcgtccgcattcgcagcctcccagcggaatgcccagtttgggcccggc
aactcggacgcgcagtggactcgcttcatattccgagggccctttggtccccgggccact
ggcctggggactgagaaggcggcgggcatctggaagacgccggctgcctacattggacag
cggcctggggtgtcgggccccgagcacgccgcctttattcgggagctggaggaagcgctg
tgccctgaccaacccccaccagccgggatcacccaagaagatgtcaaagtgatgttaaat
ttgctagagaagctgtgtactgctttccctgtccagcttctcccaccagtctgggagagc
ccagaaacaggaaagtattccccgtggatgggggtccctctgcagagagagcgggaccta
aatactgcagtttgcattggccagtccctggtgagacagaacagtgttctgatgggggag
cacagcaaactggaagccatgctgggctcagccagggaggacattttacacctcagatac
caggtgagcttgagagatgacctccttcagctctactcagactctgaggaggaggaggag
gaagaagaggaggaggagccggaggaggaagagcagcagcactatcattcctatggagcc
cctgagccgacttgtctgcgggagatggaggtcctacatgactgcccgcagctggaagcc
ctgcaggagcagctgaggctgctggaggaggagaacgagcagctgagggaggaggcctct
cagctctacccccttgattgtgtggagcaagttttgtacgtgaagttatacaggctgtgc
cgcagtgaggtgcaagagcaggaccggggcttagaggctgagaaggggttactgacagca
gaggattttgtggcggaagattttgtgcctgtggaggaattggtgcctgaggaggaactg
ggggccacagaagaggtggcgtcagctgaggagggggcaacagaagaggcagagctggtg
tctgaggaggccgaggcctgggaggaggtggagccggagctggatgaggcaacgcagggg
aacgtagggacctcagcgctggaggctagcggcttgggcccctctcacctaaacatgaag
cgtgtcctccagcaactggctaactggctggatgcgcgttatagtcggcagttgaggctg
aagatgctccagaaaggtgagtgctcccacaggggcctccctccggccagccagaccagc
tacagatcatcaatgaaaggctttgctggttcccagcagcctgcagaggccccacagaca
gcctga

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