Neogale vison (American mink): 122904734
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Entry
122904734 CDS
T08764
Symbol
PSMC2
Name
(RefSeq) 26S proteasome regulatory subunit 7
KO
K03061
26S proteasome regulatory subunit T1
Organism
nvs
Neogale vison (American mink)
Pathway
nvs03050
Proteasome
nvs05010
Alzheimer disease
nvs05012
Parkinson disease
nvs05014
Amyotrophic lateral sclerosis
nvs05016
Huntington disease
nvs05017
Spinocerebellar ataxia
nvs05020
Prion disease
nvs05022
Pathways of neurodegeneration - multiple diseases
nvs05169
Epstein-Barr virus infection
Brite
KEGG Orthology (KO) [BR:
nvs00001
]
09120 Genetic Information Processing
09123 Folding, sorting and degradation
03050 Proteasome
122904734 (PSMC2)
09160 Human Diseases
09172 Infectious disease: viral
05169 Epstein-Barr virus infection
122904734 (PSMC2)
09164 Neurodegenerative disease
05010 Alzheimer disease
122904734 (PSMC2)
05012 Parkinson disease
122904734 (PSMC2)
05014 Amyotrophic lateral sclerosis
122904734 (PSMC2)
05016 Huntington disease
122904734 (PSMC2)
05017 Spinocerebellar ataxia
122904734 (PSMC2)
05020 Prion disease
122904734 (PSMC2)
05022 Pathways of neurodegeneration - multiple diseases
122904734 (PSMC2)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03051 Proteasome [BR:
nvs03051
]
122904734 (PSMC2)
Proteasome [BR:
nvs03051
]
Eukaryotic proteasome
Regulatory particles
PA700 (19S proteasome)
ATPase subunits
122904734 (PSMC2)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
AAA
PRS7_OB
AAA_lid_3
AAA_22
AAA_2
AAA_5
AAA_16
DUF815
nSTAND3
RuvB_N
AAA_28
AAA_7
AAA_14
Prot_ATP_ID_OB_C
AAA_33
AAA_18
TIP49
Sigma54_activ_2
Mg_chelatase
RNA_helicase
AAA_24
IstB_IS21
Motif
Other DBs
NCBI-GeneID:
122904734
NCBI-ProteinID:
XP_044101794
LinkDB
All DBs
Position
4:complement(145220821..145237698)
Genome browser
AA seq
433 aa
AA seq
DB search
MPDYLGADQRKTKEEEKDDKPIRALDEGDIALLKTYGQSTYSRQIKQVEDDIQQLLKKIN
ELTGIKESDTGLAPPALWDLAADKQTLQSEQPLQVARCTKIINADSEDPKYIINVKQFAK
FVVDLSDQVAPTDIEEGMRVGVDRNKYQIHIPLPPKIDPTVTMMQVEEKPDVTYSDVGGC
KEQIEKLREVVETPLLHPERFVNLGIEPPKGVLLFGPPGTGKTLCARAVANRTDACFIRV
IGSELVQKYVGEGARMVRELFEMARTKKACLIFFDEIDAIGGARFDDGAGGDNEVQRTML
ELINQLDGFDPRGNIKVLMATNRPDTLDPALMRPGRLDRKIEFSLPDLEGRTHIFKIHAR
SMSVERDIRFELLARLCPNSTGAEIRSVCTEAGMFAIRARRKIATEKDFLEAVNKVIKSY
AKFSATPRYMTYN
NT seq
1302 nt
NT seq
+upstream
nt +downstream
nt
atgccggattacctcggtgcggatcagcggaaaaccaaagaggaggagaaggacgacaag
cctatccgagctctggatgagggggatattgccttgctgaaaacttacggtcaaagcact
tattctaggcagataaagcaggttgaagatgacattcaacaacttctcaagaaaattaat
gagctcactggtattaaagagtctgatactggcctggccccaccagcactctgggatttg
gctgcagataagcaaacactgcagagtgaacagcctttgcaggttgcaaggtgtacgaag
ataatcaatgctgactcggaggacccaaagtacattatcaatgtgaagcagtttgccaag
tttgtggtggacctcagtgatcaggtagcaccgaccgacattgaagaagggatgagagtt
ggggtggacagaaataagtatcagattcacattccgctgcctcccaagattgacccaaca
gttaccatgatgcaggtggaagaaaaacctgatgtcacttacagtgatgtgggtggctgt
aaggaacagattgagaaacttagagaagtagttgaaaccccattacttcatcctgaaaga
tttgttaaccttggcatcgagcctcccaagggtgtgctgctctttggtccacctggtaca
ggcaagaccctctgtgctcgggcagttgctaacaggactgatgcttgcttcattcgagtt
attggatctgaacttgtacagaagtacgtcggtgagggggctcgaatggttcgtgagctc
tttgaaatggccagaacgaaaaaagcctgccttatcttctttgatgaaattgatgctatt
ggaggggctcgttttgatgatggtgctggaggagacaacgaagtgcagagaacaatgctg
gaactgatcaatcagctggacggttttgatcctcgaggtaacattaaagtgctgatggcc
actaacagaccagacaccctggatccagcactcatgaggccagggagactggacagaaag
attgaattcagcttacctgatctagagggtcggacccacatttttaagattcatgctcgt
tcaatgagtgttgaaagagatatcagatttgaattgttagcgcgactgtgtccaaatagc
actggtgcggagattagaagtgtctgcacagaagctggcatgtttgccatcagagcacgg
cgaaaaattgctaccgagaaggatttcttggaggctgtaaataaggtcattaagtcttac
gccaaattcagtgctactccccgctatatgacatacaactga
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