| Entry |
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| Name |
(RefSeq) tubulin beta-8 chain-like isoform X1
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| KO |
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| Organism |
hmh Hylobates moloch (silvery gibbon)
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| Pathway |
| hmh05022 | Pathways of neurodegeneration - multiple diseases |
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| Brite |
KEGG Orthology (KO) [BR:hmh00001]
09140 Cellular Processes
09141 Transport and catabolism
04145 Phagosome
116464579
09144 Cellular community - eukaryotes
04540 Gap junction
116464579
09142 Cell motility
04814 Motor proteins
116464579
09160 Human Diseases
09171 Infectious disease: bacterial
05132 Salmonella infection
116464579
09164 Neurodegenerative disease
05010 Alzheimer disease
116464579
05012 Parkinson disease
116464579
05014 Amyotrophic lateral sclerosis
116464579
05016 Huntington disease
116464579
05020 Prion disease
116464579
05022 Pathways of neurodegeneration - multiple diseases
116464579
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03036 Chromosome and associated proteins [BR:hmh03036]
116464579
09183 Protein families: signaling and cellular processes
04812 Cytoskeleton proteins [BR:hmh04812]
116464579
04147 Exosome [BR:hmh04147]
116464579
Chromosome and associated proteins [BR:hmh03036]
Eukaryotic type
Centrosome formation proteins
Microtubules and associated factors
Other tubulins
116464579
Cytoskeleton proteins [BR:hmh04812]
Eukaryotic cytoskeleton proteins
Microtubules
Tubulins
116464579
Exosome [BR:hmh04147]
Exosomal proteins
Exosomal proteins of other body fluids (saliva and urine)
116464579
Exosomal proteins of colorectal cancer cells
116464579
Exosomal proteins of bladder cancer cells
116464579
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| SSDB |
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| Motif |
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| Other DBs |
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| LinkDB |
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| Position |
Unknown
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| AA seq |
443 aa
MREIVLTQTGQCGNQIGTKFWEVISDEHAIDSAGTYHGDSHLQLERINVYYEASGGRYVP
RAVLVDLETGTMDYVRSGPFGQIFRPDNFIFGELGAGNNWAKGYYTEGVELMESVKEVVR
KEAESCDCLQGFQLTHSLGGGIESGMGTLLINKIWEEYPDRMINTFSILPSPKVSDTVVE
PYNAILSVHGLIENADETFCIGNEALYDICSRTLELPASTCDDLNHLVSVTICGVTMCLR
FPGQLNADLRKLAINMVLFPRLHFFMPGFAPLTSRGSQQYWVLTVAELTQQMFDAKNMMV
ACEPCHGRYLMAGAIFMGCMPMREVDEQMLNIQNKNSSYFADWLFNNVKTAICDIPPQGL
KMSATFIGNNTAIQELFKSVSEQFTAMFRHKAFLHRYTGEGMDETEFAEAESNTNDLVSE
YQQHQDAKAKEEEFEEYAEEEVA |
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| NT seq |
1332 nt +upstreamnt +downstreamnt
atgagggagattgtgctcacgcagaccgggcaatgcgggaaccagattggcaccaagttc
tgggaggtgatctctgatgagcatgccatagactccgctggcacctaccacggggacagc
cacctgcagctggagcgcatcaatgtgtactacgaggccagcggtggcaggtacgtgccc
cgcgctgtgctcgtggatctggagacgggcaccatggactatgtgcgctcggggcccttc
gggcagatcttcaggccagacaacttcatcttcggtgagcttggggccggaaacaactgg
gccaagggatactatacagaaggcgtggagctgatggagtcagtgaaggaagttgtcaga
aaggaggctgagagctgtgactgcctgcagggtttccagctgacccactccctgggtggg
gggattgagtctgggatgggtacccttctcattaataagatctgggaggagtatccagac
agaatgataaacacatttagtattctgccctcgcccaaggtgtcagacaccgtggtagag
ccctataatgccatcctttcagtccacgggctcatagaaaatgcggatgagaccttttgc
ataggtaatgaagcgctatatgacatatgttccaggactctagaactgcctgcatccacc
tgtgatgacctgaaccacctggtgtctgttaccatctgtggggtcaccatgtgcctgcgc
ttcccaggccagctgaatgctgacctgcggaagctggccataaacatggtcctgtttccc
cggctgcatttcttcatgcctggctttgccccactgactagccggggcagccagcagtac
tgggtcttgaccgtggctgagcttactcagcagatgtttgatgctaagaacatgatggtt
gcctgtgagccctgtcatggccgctacctaatggcgggtgccattttcatgggttgcatg
cccatgagggaggtggatgaacaaatgttgaacattcaaaataagaacagcagctacttt
gctgactggctcttcaacaacgtaaaaacagccatctgtgacatcccaccccaggggcta
aaaatgtcagccaccttcattgggaataatacagccatccaggaactcttcaagagtgtc
tcagagcagtttacagcaatgttcaggcacaaggccttcctccaccggtacacgggcgag
ggaatggatgagactgaattcgctgaggctgagagcaacacaaacgacctggtgtctgaa
tatcagcaacatcaggatgccaaggccaaggaggaggagtttgaggagtatgctgaggag
gaggtggcctag |
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