Hippoglossus hippoglossus (Atlantic halibut): 117766980
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Entry
117766980 CDS
T07778
Name
(RefSeq) neuronal-specific septin-3-like isoform X1
KO
K16938
septin 3/9/12
Organism
hhip
Hippoglossus hippoglossus (Atlantic halibut)
Pathway
hhip05100
Bacterial invasion of epithelial cells
Brite
KEGG Orthology (KO) [BR:
hhip00001
]
09160 Human Diseases
09171 Infectious disease: bacterial
05100 Bacterial invasion of epithelial cells
117766980
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
03037 Cilium and associated proteins [BR:
hhip03037
]
117766980
04812 Cytoskeleton proteins [BR:
hhip04812
]
117766980
04147 Exosome [BR:
hhip04147
]
117766980
Cilium and associated proteins [BR:
hhip03037
]
Motile cilia and associated proteins
Sperm associated proteins
117766980
Cytoskeleton proteins [BR:
hhip04812
]
Eukaryotic cytoskeleton proteins
Septins
Septins
Group 1
117766980
Exosome [BR:
hhip04147
]
Exosomal proteins
Exosomal proteins of haemopoietic cells (B-cell, T-cell, DC-cell, reticulocyte, and mast cell)
117766980
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Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Septin
MMR_HSR1
RsgA_GTPase
AIG1
GTP_EFTU
Roc
Dynamin_N
AAA_16
Ras
NB-ARC
AAA_22
ABC_tran
URGCP_GTPase
AAA_29
IIGP
FtsK_SpoIIIE
G-alpha
P-loop_TraG
Sigma54_activat
AAA_7
AAA_14
Motif
Other DBs
NCBI-GeneID:
117766980
NCBI-ProteinID:
XP_034450347
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All DBs
Position
8:16028192..16115186
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AA seq
639 aa
AA seq
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MKKGLYPVRSASARARRTDREGSGITSPSESTALKRSFEVEEADSSTHPSPLSRRTTNPL
RSSTTSTSSQRSYDLSSRNSDYSSTRSSPSESSNPRSPNTSMRRIELSGGRNPDTASSRR
TEISIEVSSKQIDNSPSAGIARFGLKRPEVSLGSRSTPLDSSSNSISTSTNRRAELAMTR
SSEPPAPPRRMDAQLSSAPVSRIPDPPQRKAETPSPILSPADGVSRKPEMPVFRQPDGLV
PGSAMENNNNHPPPAPSAPLPSLAEPRVERVRSPITETPTSRPTDRPEVISSYSGMTMSE
AVMPDAVVSPPMGGLYGEKVGGPVVDFSYVGIDAILEQMRRKAMKQGFELNIMVVGQSGL
GKSTLMNTLFKSKVSRKSVLATAQEKIPKTIEIKSISHDIEEKGVRMKLTVIDTPGFGDQ
INNENCWQPIMKFINDQYEAYLQEEININRKKRIPDSRVHCCIYFIPPTGHCLRPLDVEF
MRRLSKVVNIVPVIAKADTLTLEERDFFKKKIREELRANGIDVYPQKEFDEDAEDRMINE
KIREMIPFAVVGSDQEYQVNGRRLLGRKTKWGTIEVENIAHCEFAYLRDLLIRTHMQNIK
DITSSIHYEMYRVRRLNENNSVAAHANGIPEHHHAAHEM
NT seq
1920 nt
NT seq
+upstream
nt +downstream
nt
atgaagaaaggtttatatccagtgagatccgccagcgctcgagcaagaagaacagacaga
gagggatctggcatcaccagtcccagtgagtccactgcactgaaacggtcgtttgaggtg
gaggaggcggattcatccacacacccctcgcccctgtctcgtcggaccactaaccctctc
cgctcatcaaccacctccacatccagccagcggagctacgacctgagctcccgcaactct
gactactcctccaccagatcttccccctccgagtcctccaatccacgttccccaaatacc
agcatgaggcgcattgagttatcagggggtcgtaaccccgacacagcctcttcccgccgc
acagaaatctccatcgaggtctcctccaagcaaattgacaactcgcccagcgccggcatc
gcccgctttggcctcaaacgacctgaggtaagcctgggcagtcggagcacccctctcgac
agctcctccaactccatctccacttccacaaacaggcgtgcagagctcgccatgacacgg
tccagtgaaccccccgcccctccgaggaggatggatgcccagctgtcctctgccccagtc
tctaggatccctgaccccccccagagaaaagcagagaccccgtcccccatcctcagccca
gctgatggagtctcccggaagccagagatgcctgtcttcagacagccggatggtttagtg
ccaggcagcgcaatggagaacaacaacaaccacccgcctcctgccccaagcgctcccctg
ccttccctggcagagccccgggtggagagggtgcggtcgcccatcacagagacacccacg
tcccgaccaacagacaggccagaggtgatatccagctacagtggcatgaccatgtctgag
gcggtgatgcccgatgctgtggtgtccccaccgatgggcggcctgtacggggagaaggtc
ggtggccctgtggtggacttcagttacgttgggatcgacgccattctggaacagatgagg
aggaaggccatgaagcagggttttgagctcaacattatggttgtgggacagagtggcctg
ggaaagtctactctgatgaacacgctgttcaagtctaaagtcagccgtaagtcggtgctg
gctactgcccaggagaagatccccaaaacaatcgaaattaagtccatcagtcacgacatt
gaggagaagggagtgagaatgaagttgacggtcattgacactccaggcttcggcgaccag
atcaacaatgagaactgctggcagcctatcatgaagttcattaacgaccagtatgaggca
tacctgcaggaggagatcaacatcaacaggaagaaaaggatcccagactccagagttcac
tgctgcatatacttcatccccccgaccggacactgtctgcggcctctggatgtagaattc
atgagacgtctcagtaaagtggtcaacattgtcccagtcattgccaaggcagatacactc
accctggaggagagggacttcttcaaaaagaagatcagggaagagctacgagccaacggg
attgacgtgtaccctcagaaggaatttgacgaggatgcagaggacagaatgattaacgag
aagatcagggagatgatcccatttgctgtggtgggcagtgaccaggagtaccaggtcaat
ggcaggaggctgctggggaggaagaccaagtggggaaccattgaagttgagaacatagcc
cactgtgagtttgcctatttaagggatctcctcatcaggacccatatgcagaacattaag
gacatcaccagcagcatccactatgaaatgtaccgcgtgaggcgcctcaatgagaacaac
tccgtggcggctcacgccaacggtatcccagagcatcatcacgccgcccatgagatgtag
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