Peromyscus maniculatus bairdii (prairie deer mouse): 102907570
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Entry
102907570 CDS
T11302
Symbol
Psmc2
Name
(RefSeq) 26S proteasome regulatory subunit 7
KO
K03061
26S proteasome regulatory subunit T1
Organism
pmav Peromyscus maniculatus bairdii (prairie deer mouse)
Pathway
pmav03050
Proteasome
pmav05010
Alzheimer disease
pmav05012
Parkinson disease
pmav05014
Amyotrophic lateral sclerosis
pmav05016
Huntington disease
pmav05017
Spinocerebellar ataxia
pmav05020
Prion disease
pmav05022
Pathways of neurodegeneration - multiple diseases
pmav05169
Epstein-Barr virus infection
Brite
KEGG Orthology (KO) [BR:
pmav00001
]
09120 Genetic Information Processing
09123 Folding, sorting and degradation
03050 Proteasome
102907570 (Psmc2)
09160 Human Diseases
09172 Infectious disease: viral
05169 Epstein-Barr virus infection
102907570 (Psmc2)
09164 Neurodegenerative disease
05010 Alzheimer disease
102907570 (Psmc2)
05012 Parkinson disease
102907570 (Psmc2)
05014 Amyotrophic lateral sclerosis
102907570 (Psmc2)
05016 Huntington disease
102907570 (Psmc2)
05017 Spinocerebellar ataxia
102907570 (Psmc2)
05020 Prion disease
102907570 (Psmc2)
05022 Pathways of neurodegeneration - multiple diseases
102907570 (Psmc2)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03051 Proteasome [BR:
pmav03051
]
102907570 (Psmc2)
Proteasome [BR:
pmav03051
]
Eukaryotic proteasome
Regulatory particles
PA700 (19S proteasome)
ATPase subunits
102907570 (Psmc2)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
AAA
OB_PRS7
AAA_lid_3
AAA_22
AAA_2
AAA_5
AAA_16
DUF815
nSTAND3
AAA_14
RuvB_N
AAA_28
AAA_7
Prot_ATP_ID_OB_C
AAA_33
TIP49
AAA_18
RNA_helicase
Mg_chelatase
Sigma54_activ_2
IstB_IS21
AAA_24
Motif
Other DBs
NCBI-GeneID:
102907570
NCBI-ProteinID:
XP_006987871
Ensembl:
ENSPEMG00000022409
LinkDB
All DBs
Position
3:39047540..39066632
Genome browser
AA seq
433 aa
AA seq
DB search
MPDYLGADQRKTKEDEKDDKPIRALDEGDIALLKTYGQSTYSRQIKQVEDDIQQLLKKIN
ELTGIKESDTGLAPPALWDLAADKQTLQSEQPLQVARCTKIINADSEDPKYIINVKQFAK
FVVDLSDQVAPTDIEEGMRVGVDRNKYQIHIPLPPKIDPTVTMMQVEEKPDVTYSDVGGC
KEQIEKLREVVETPLLHPERFVNLGIEPPKGVLLFGPPGTGKTLCARAVANRTDACFIRV
IGSELVQKYVGEGARMVRELFEMARTKKACLIFFDEIDAIGGARFDDGAGGDNEVQRTML
ELINQLDGFDPRGNIKVLMATNRPDTLDPALMRPGRLDRKIEFSLPDLEGRTHIFKIHAR
SMSVERDIRFELLARLCPNSTGAEIRSVCTEAGMFAIRARRKIATEKDFLEAVNKVIKSY
AKFSATPRYMTYN
NT seq
1302 nt
NT seq
+upstream
nt +downstream
nt
atgcctgactacttaggtgcggaccagcggaaaaccaaagaggatgagaaggacgacaag
cccatccgagctctggatgagggggatattgccttactgaaaacttacgggcagagtact
tactccaggcagatcaagcaggttgaggatgacattcaacaacttctcaaaaaaattaat
gaacttactggtatcaaagagtcagacactggcctggcaccaccagccctctgggacctg
gctgcagacaaacaaacacttcagagtgaacagccgctccaggtggcaaggtgtacgaag
ataatcaatgctgattcagaggaccccaaatacatcatcaacgtgaagcagtttgccaag
tttgtggtggatctcagtgatcaggtggcacccactgacattgaagaagggatgagagtt
ggcgtggacagaaataaataccaaattcacattccactacctcctaagattgacccaaca
gttaccatgatgcaggtggaagaaaaacctgacgtcacgtacagtgatgttggtggctgt
aaggaacagattgagaaactgcgcgaggtagttgaaacccctctactccatccagagaga
tttgttaaccttgggattgagcctccgaagggtgtgctgctgttcggtcccccgggcaca
ggcaagacactctgtgctagggcagttgccaacaggactgacgcttgcttcatccgagtt
atcgggtctgagctcgtgcagaaatacgtcggggagggggctcgaatggtccgtgagctt
tttgaaatggcaagaacaaaaaaagcctgccttattttctttgatgaaattgatgccatt
ggaggggctcggtttgatgatggtgctgggggcgacaacgaagtgcagagaacaatgttg
gaactcatcaaccagctggatggttttgatcctcgaggcaacatcaaagtcctgatggcc
actaaccgacctgatactctggatccagcactcatgaggccggggagattggacagaaag
attgagtttagcctacctgatctagagggtcggactcacatctttaagattcacgctcgc
tcgatgagtgttgagagagacattaggtttgagctgctagcccggctgtgtccgaacagc
actggagcggagatcagaagtgtttgcacagaagcgggcatgtttgcaatccgagcacgg
cggaaaattgctacagagaaggatttcttggaagctgtgaataaggtcatcaagtcttac
gccaaattcagcgctactccccgctacatgacatacaattga
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