Equus asinus (ass): 106835533
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Entry
106835533 CDS
T04645
Symbol
PSMC5
Name
(RefSeq) 26S proteasome regulatory subunit 8 isoform X2
KO
K03066
26S proteasome regulatory subunit T6
Organism
eai
Equus asinus (ass)
Pathway
eai03050
Proteasome
eai05010
Alzheimer disease
eai05012
Parkinson disease
eai05014
Amyotrophic lateral sclerosis
eai05016
Huntington disease
eai05017
Spinocerebellar ataxia
eai05020
Prion disease
eai05022
Pathways of neurodegeneration - multiple diseases
eai05169
Epstein-Barr virus infection
Brite
KEGG Orthology (KO) [BR:
eai00001
]
09120 Genetic Information Processing
09123 Folding, sorting and degradation
03050 Proteasome
106835533 (PSMC5)
09160 Human Diseases
09172 Infectious disease: viral
05169 Epstein-Barr virus infection
106835533 (PSMC5)
09164 Neurodegenerative disease
05010 Alzheimer disease
106835533 (PSMC5)
05012 Parkinson disease
106835533 (PSMC5)
05014 Amyotrophic lateral sclerosis
106835533 (PSMC5)
05016 Huntington disease
106835533 (PSMC5)
05017 Spinocerebellar ataxia
106835533 (PSMC5)
05020 Prion disease
106835533 (PSMC5)
05022 Pathways of neurodegeneration - multiple diseases
106835533 (PSMC5)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03051 Proteasome [BR:
eai03051
]
106835533 (PSMC5)
Proteasome [BR:
eai03051
]
Eukaryotic proteasome
Regulatory particles
PA700 (19S proteasome)
ATPase subunits
106835533 (PSMC5)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
AAA
AAA_lid_3
Prot_ATP_ID_OB_C
AAA_2
AAA_5
AAA_16
AAA_22
AAA_lid_PRS2_C
nSTAND3
PRS7_OB
RuvB_N
TIP49
AAA_18
AAA_28
Mg_chelatase
AAA_3
AAA_33
NPHP3_N
AAA_14
Parvo_NS1
ATPase
AAA_17
PhoH
FapA
IstB_IS21
AAA_24
AAA_7
AAA_25
DUF815
DUF7006
Sigma54_activat
bpMoxR
DUF5906
RNA_helicase
ABC_tran
Zeta_toxin
AAA_11
AAA_19
TsaE
HR1
Prominin
Motif
Other DBs
NCBI-GeneID:
106835533
NCBI-ProteinID:
XP_014703452
LinkDB
All DBs
Position
13:49191277..49195606
Genome browser
AA seq
406 aa
AA seq
DB search
MALDGPEQMELEEGKAGSGLRQYYLSKIEELQLIVNDKSQNLRRLQAQRNELNAKVRLLR
EELQLLQEQGSYVGEVVRAMDKKKVLVKVHPEGKFVVDVDKNIDINDVTPNCRVALRNDS
YTLHKILPNKVDPLVSLMMVEKVPDSTYEMIGGLDKQIKEIKEVIELPVKHPELFEALGI
AQPKGVLLYGPPGTGKTLLARAVAHHTDCTFIRVSGSELVQKFIGEGARMVRELFVMARE
HAPSIIFMDEIDSIGSSRLEGGSGGDSEVQRTMLELLNQLDGFEATKNIKVIMATNRIDI
LDSALLRPGRIDRKIEFPPPNEEARLDILKIHSRKMNLTRGINLRKIAELMPGASGAEVK
GVCTEAGMYALRERRVHVTQEDFEMAVAKVMQKDSEKNMSIKKLWK
NT seq
1221 nt
NT seq
+upstream
nt +downstream
nt
atggcgcttgacggaccagaacagatggagctggaagaggggaaggcaggcagtggactc
cgccagtattatctgtccaagattgaagaactccagctgattgtgaatgacaagagccaa
aatctccggaggctgcaggcacagaggaatgagcttaatgcaaaagttcgcttgttgcgg
gaggagctacagctgctgcaggaacagggctcctatgtcggggaagtagtccgggccatg
gataagaagaaagtgttggttaaggtacatcctgagggcaagtttgttgtagacgtggac
aagaacatcgatatcaatgatgtgacacccaattgccgggtggctctaagaaatgacagc
tacactctgcacaagatcctgcccaacaaggtagacccactggtttcactgatgatggtg
gagaaggtaccagattcaacttatgagatgattggcggactagacaagcagatcaaggag
atcaaagaagtgatcgagctgcctgttaagcatcctgagctctttgaagcgctgggcatt
gcgcagcccaagggagtgttgctctatggacccccaggcactgggaagacactgttggcc
cgggctgtggctcatcatacagactgtacctttattcgtgtctctggctctgaattggta
cagaaattcattggggaaggggcaagaatggtgagggagctgtttgtcatggcacgagaa
catgctccatccatcatcttcatggacgaaatcgactccattggctcctcacgactggag
ggaggttctggaggggacagtgaagtgcagcgcacaatgctggagctgctcaaccagctg
gatggctttgaggccaccaagaatatcaaggttattatggctactaataggattgatatc
ctggattcagcgctgcttcgcccagggcgcatcgacagaaaaattgaattcccacccccc
aacgaggaggcccggctggacattttgaagatccattctcggaaaatgaacctgactcgg
gggatcaacctgagaaaaattgctgagctcatgccaggagcatcaggggctgaagtgaag
ggtgtgtgcaccgaagctggcatgtatgccctgcgggaacggcgagtccatgtcacccag
gaggactttgagatggcagtagccaaggtcatgcagaaggatagtgagaaaaacatgtcc
atcaagaagctttggaagtga
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