KEGG   Heterocephalus glaber (naked mole-rat): 101724382
Entry
101724382         CDS       T02812                                 
Symbol
Sept9
Name
(RefSeq) septin 9
  KO
K16938  septin 3/9/12
Organism
hgl  Heterocephalus glaber (naked mole-rat)
Pathway
hgl05100  Bacterial invasion of epithelial cells
Brite
KEGG Orthology (KO) [BR:hgl00001]
 09160 Human Diseases
  09171 Infectious disease: bacterial
   05100 Bacterial invasion of epithelial cells
    101724382 (Sept9)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   03037 Cilium and associated proteins [BR:hgl03037]
    101724382 (Sept9)
   04812 Cytoskeleton proteins [BR:hgl04812]
    101724382 (Sept9)
   04147 Exosome [BR:hgl04147]
    101724382 (Sept9)
Cilium and associated proteins [BR:hgl03037]
 Motile cilia and associated proteins
  Sperm associated proteins
   101724382 (Sept9)
Cytoskeleton proteins [BR:hgl04812]
 Eukaryotic cytoskeleton proteins
  Septins
   Septins
    Group 1
     101724382 (Sept9)
Exosome [BR:hgl04147]
 Exosomal proteins
  Exosomal proteins of haemopoietic cells  (B-cell, T-cell, DC-cell, reticulocyte, and mast cell)
   101724382 (Sept9)
SSDB
Motif
Pfam: Septin MMR_HSR1 RsgA_GTPase Dynamin_N AIG1 GTP_EFTU Roc Ras AAA_16 AAA_22 FtsK_SpoIIIE ABC_tran IIGP NB-ARC AAA_29 G-alpha PduV-EutP VapE-like_dom AAA_7 AAA_24 tRNA_synthFbeta Arf
Other DBs
NCBI-GeneID: 101724382
NCBI-ProteinID: XP_004860849
Position
Un
AA seq 584 aa
MKKSYSGVTRTASGRLRRLGDPTGPALKRSFEVEEVEPPNSTPTRRVQTPLLRTTVASST
QKFQELGVKNSEPSARHVDSLSQRSPKPSLRRVELSGPKVAEPVSRRTELSIDISSKQVE
ASGATGAARFGLKRAEGLGHKTPEPTPRRTEITIVKPQESAHRRMETPASKVPEAPIAPT
ADTAPKRVEIQVPKPADSPACPLPSQPLENSEPAPMSQLHSRLDAKPTLAEALPRNQEAT
EAAPGCVGNMADTPRDAMLKPAPVSRNEKAPADFGYVGIDSILEQMRRKAMKQGFEFNIM
VVGQSGLGKSTLINTLFKSKISRKSVQPTSEERIPKTIEIKSITHDIEEKGVRMKLTVID
TPGFGDHINNENCWQPIMKFINDQYEKYLQEEVNINRKKRIPDTRVHCCLYFIPATGHSL
RPLDIEFMKRLSKVVNIVPVIAKADTLTLEERVYFKQRITADLLSNGIDVYPQKEFDEDA
EDRLVNEKFREMIPFAVVGSDHEYQVNGKRILGRKTKWGTIEVENTTHCEFAYLRDLLIR
THMQNIKDITSSIHFEAYRVKRLNEGNSAMANGVEEKEPEAQEM
NT seq 1755 nt   +upstreamnt  +downstreamnt
atgaagaagtcgtactcaggagtcacacggaccgctagtggccgtctccggaggcttggc
gacccaacgggcccagccttgaagagatctttcgaggttgaggaggttgagccgcccaac
tccaccccgacccggagagtccagactccgctgctccgcaccaccgtggccagctccacc
cagaaattccaggagctgggtgtgaagaactcagagccctcggcccgccatgtagactcc
ttaagccagcgctccccgaaaccctccctgcggagggtcgagctctcggggcccaaggtg
gccgagcctgtgtcaaggcgcacggagctgtccattgacatctcctctaagcaggtggaa
gcctcaggtgccactggggcagcacggtttgggctcaagagggccgaggggttgggccac
aagacgccggagccaacccctcggaggacggagatcaccatcgtcaagccccaggagtca
gcccaccgcaggatggagaccccggcctccaaggttcccgaggcacccattgcccctacc
gccgacacagcccccaagagggttgagatccaggtgcccaagccagctgactcgcctgcc
tgtcccctcccatcccagcccctggagaattctgagcctgccccaatgtcccagctgcac
agcaggctggacgccaagccaaccttggccgaggccctacccaggaaccaggaggccacc
gaggcggctcctggctgtgtgggcaacatggctgacacccccagagacgccatgctcaag
ccggcacccgtgtcacggaatgagaaggcccctgcggactttggctacgtggggatcgac
tccatcctggagcagatgcgcaggaaggccatgaagcagggcttcgagttcaacatcatg
gtggttgggcagagtggcttggggaagtccaccttgatcaacaccctcttcaagtccaaa
atcagccggaagtcggtgcagcccacctcggaagagcgcatccccaagaccatcgagatc
aagtccatcacccacgatatcgaggagaagggcgtccggatgaagctgacagtgatcgac
acgccagggttcggggaccacatcaacaatgagaactgctggcagcccatcatgaagttc
atcaacgaccagtatgagaaatacctgcaggaggaggtgaacatcaaccgcaagaagcgc
atccccgacacgcgcgtgcactgctgtctctacttcatccccgccaccggccactccctt
aggcccctggacatcgagttcatgaagcgcctgagcaaggtggtcaacattgtccctgtc
attgccaaggccgacaccctgacactggaagagagggtctacttcaaacagcggatcact
gcagatctgctgtccaatggcattgacgtgtacccccagaaggagtttgacgaggacgca
gaggaccggctggtgaacgagaagttccgggagatgatcccattcgccgtggtgggcagc
gaccatgagtatcaggtcaacggcaagcggatcctcggcaggaagaccaagtggggcacc
attgaagtcgagaacaccacacactgtgagtttgcctacctgcgggacctcctcatcagg
acgcacatgcagaacatcaaggatatcaccagcagcatccacttcgaggcataccgcgtt
aagcggctcaatgagggcaacagcgccatggccaacggggtcgaggagaaggagcccgaa
gcccaggagatgtag

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