KEGG   Neogale vison (American mink): 122913123
Entry
122913123         CDS       T08764                                 
Symbol
KAT5
Name
(RefSeq) histone acetyltransferase KAT5 isoform X1
  KO
K11304  histone acetyltransferase HTATIP [EC:2.3.1.48]
Organism
nvs  Neogale vison (American mink)
Pathway
nvs03082  ATP-dependent chromatin remodeling
nvs05017  Spinocerebellar ataxia
nvs05166  Human T-cell leukemia virus 1 infection
Brite
KEGG Orthology (KO) [BR:nvs00001]
 09120 Genetic Information Processing
  09126 Chromosome
   03082 ATP-dependent chromatin remodeling
    122913123 (KAT5)
 09160 Human Diseases
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    122913123 (KAT5)
  09164 Neurodegenerative disease
   05017 Spinocerebellar ataxia
    122913123 (KAT5)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03000 Transcription factors [BR:nvs03000]
    122913123 (KAT5)
   03036 Chromosome and associated proteins [BR:nvs03036]
    122913123 (KAT5)
Enzymes [BR:nvs01000]
 2. Transferases
  2.3  Acyltransferases
   2.3.1  Transferring groups other than aminoacyl groups
    2.3.1.48  histone acetyltransferase
     122913123 (KAT5)
Transcription factors [BR:nvs03000]
 Eukaryotic type
  Zinc finger
   Cys2HisCys zinc factors
    122913123 (KAT5)
Chromosome and associated proteins [BR:nvs03036]
 Eukaryotic type
  Histone modification proteins
   HATs (histone acetyltransferases)
    122913123 (KAT5)
   HAT complexes
    TIP60 complex
     122913123 (KAT5)
    NuA4 complex
     122913123 (KAT5)
SSDB
Motif
Pfam: MOZ_SAS zf-MYST Tudor-knot Acetyltransf_7 Acetyltransf_1 ROS_MUCR
Other DBs
NCBI-GeneID: 122913123
NCBI-ProteinID: XP_044115624
LinkDB
Position
7:200614440..200621856
AA seq 555 aa
MAEVVSPVPGAGRREPGEVGRTRGPPVADPGAALSPQGEIIEGCRLPVLRRNQDNEDEWP
LAEILSVKDISGRKLFYVHYIDFNKRLDEWVTHERLDLKKIQFPKKEAKTPTKNGLPGSR
PGSPEREVRKTLDLSLQPASAQASGKTLPIPVQITLRFNLPKEREAIPGGEPDQPLSSSS
CLQPNHRSTKRKVEVVSPATPVPSETAPASVFPQNGSARRAVAAQPGRKRKSNCLGTDED
SQDSSDGIPSAPRMTGSLVSDRSHDDIVTRMKNIECIELGRHRLKPWYFSPYPQELTTLP
VLYLCEFCLKYGRSLKCLQRHLTKCDLRHPPGNEIYRKGTISFFEIDGRKNKSYSQNLCL
LAKCFLDHKTLYYDTDPFLFYVMTEYDCKGFHIVGYFSKEKESTEDYNVACILTLPPYQR
RGYGKLLIEFSYELSKVEGKTGTPEKPLSDLGLLSYRSYWSQTILEILMGLKSESGERPQ
ITINEISEITSIKKEDVISTLQYLNLINYYKGQYILTLSEDIVDGHERAMLKRLLRIDSK
CLHFTPKDWSKRGKW
NT seq 1668 nt   +upstreamnt  +downstreamnt
atggcggaggtggtgagtccggtgcccggggcggggcggagggagccaggggaggtgggt
agaacccgaggccccccagtagccgaccctggcgccgcgctgtctccccagggggagata
atcgagggctgccgcctgcccgtgcttcggcggaaccaggacaacgaagatgagtggccc
ctggccgagatcctgagcgtgaaggacatcagtggccgcaagcttttctacgtccattat
atagacttcaacaaacgcctggatgaatgggtgacccacgagcggctggacctaaagaag
attcagttccccaagaaagaggccaagacccccaccaagaacggacttcctgggtctcgc
cccggctctccagagagagaggtgaggaagaccctggacctatctctacagccggcctcc
gcccaggccagcgggaagaccttgccaatcccggtccagatcacactccgcttcaacctg
cccaaggagcgggaggccattcccggtggcgagcctgaccagccgctctcctccagctcc
tgcctgcagcccaaccaccgctcaacgaaacggaaggtggaggtggtttcaccagcaact
ccagtgcccagcgagacagctccagcctcggtttttccccagaatggatcagcccgtagg
gcagtggcagctcagccaggacggaagcgaaaatcaaattgcttgggcactgatgaggac
tcccaggacagctcagatggaataccgtcagcgccacgcatgactggcagcttggtgtcg
gaccggagccacgacgacattgtcacccggatgaagaacatcgagtgcatcgagctgggc
cggcaccgcctgaagccgtggtacttctccccgtacccgcaggagctcaccacgttgccc
gtcctctacctctgcgagttctgcctcaaatacggccgcagcctcaagtgtctgcagcgt
cacttgaccaaatgtgacttgcgacatcctccaggcaacgagatttaccgcaagggcacc
atctctttctttgagattgacggccgtaagaacaagagttattcccagaacctgtgtctc
ttggccaagtgtttcctcgaccacaagacgttgtattatgacacagaccccttcctcttc
tatgtcatgacggagtatgactgcaagggcttccacatcgtgggctacttctccaaggaa
aaggaatccacggaagactacaacgtggcctgcatcctgaccctgcctccctaccagcgc
cggggctatggcaagctgctgatcgagttcagctatgaactctctaaagtggaagggaaa
acggggactcctgagaagcccctttcagaccttggcctcctatcctaccggagctactgg
tcccaaaccattctggagatcctgatggggctgaagtcagagagcggggagaggccacag
atcaccatcaacgagatcagtgaaatcaccagcatcaagaaggaggatgtcatttccact
ctacaatacctcaacctcatcaactactacaagggccagtatatcctcacgctgtcagag
gacatcgtggatggacacgaaagagctatgctcaagaggctccttcggatcgactccaag
tgtctgcacttcactcccaaggactggagcaagaggggaaagtggtga

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