Panthera pardus (leopard): 109268118
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Entry
109268118 CDS
T06062
Symbol
PSMC2
Name
(RefSeq) 26S protease regulatory subunit 7
KO
K03061
26S proteasome regulatory subunit T1
Organism
ppad
Panthera pardus (leopard)
Pathway
ppad03050
Proteasome
ppad05010
Alzheimer disease
ppad05012
Parkinson disease
ppad05014
Amyotrophic lateral sclerosis
ppad05016
Huntington disease
ppad05017
Spinocerebellar ataxia
ppad05020
Prion disease
ppad05022
Pathways of neurodegeneration - multiple diseases
ppad05169
Epstein-Barr virus infection
Brite
KEGG Orthology (KO) [BR:
ppad00001
]
09120 Genetic Information Processing
09123 Folding, sorting and degradation
03050 Proteasome
109268118 (PSMC2)
09160 Human Diseases
09172 Infectious disease: viral
05169 Epstein-Barr virus infection
109268118 (PSMC2)
09164 Neurodegenerative disease
05010 Alzheimer disease
109268118 (PSMC2)
05012 Parkinson disease
109268118 (PSMC2)
05014 Amyotrophic lateral sclerosis
109268118 (PSMC2)
05016 Huntington disease
109268118 (PSMC2)
05017 Spinocerebellar ataxia
109268118 (PSMC2)
05020 Prion disease
109268118 (PSMC2)
05022 Pathways of neurodegeneration - multiple diseases
109268118 (PSMC2)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03051 Proteasome [BR:
ppad03051
]
109268118 (PSMC2)
Proteasome [BR:
ppad03051
]
Eukaryotic proteasome
Regulatory particles
PA700 (19S proteasome)
ATPase subunits
109268118 (PSMC2)
BRITE hierarchy
SSDB
Ortholog
Paralog
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:
109268118
NCBI-ProteinID:
XP_019306795
Ensembl:
ENSPPRG00000013608
UniProt:
A0A9V1FPS7
LinkDB
All DBs
Position
Unknown
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
atgccggattacctcggtgccgatcagcggaaaaccaaagaggatgagaaggacgacaag
cccatccgagctctggatgagggggatattgccttgctgaaaacttacggtcagagcact
tactctaggcagataaagcaggttgaagatgacattcaacaacttctcaagaagatcaat
gagcttactggtatcaaagaatctgatactggcctggccccaccagcactctgggatttg
gctgcagataagcaaacactgcagagtgaacagcctttgcaggttgcgaggtgtacaaag
atcatcaatgctgattcggaggacccaaagtacattatcaacgtgaagcagtttgccaag
tttgtggtggaccttagtgatcaggtggcacctactgacattgaagaagggatgagagtt
ggtgtggacagaaataagtatcaaattcacattccgctgcctcccaagattgacccaaca
gttaccatgatgcaggtggaggaaaaacctgatgtcacatacagtgacgtgggtggctgt
aaagaacagattgagaaacttcgagaagtagttgaaaccccattacttcatccggagagg
tttgttaaccttggcattgagcctcccaagggtgtgctgctctttggcccaccgggtaca
ggcaagacactctgtgctcgggcagttgctaacaggacagatgcttgcttcattcgagtt
attggatctgaacttgtacagaagtacgttggtgagggggctcgaatggttcgggagctc
tttgaaatggccagaacaaaaaaagcctgccttatcttctttgatgaaattgatgctatt
ggaggggctcgttttgatgatggtgctggaggagacaacgaagtgcagagaacgatgctg
gaactgatcaatcaactggacggttttgatcctcgaggtaacattaaagtgctgatggcc
actaacagacctgacactttggatccagcactgatgaggccagggagattggacagaaag
attgaatttagcttacctgatctagagggtcggactcatatttttaagatccacgctcgc
tcaatgagcgtggaaagagatatcagatttgaactgttagcacgactgtgtccaaatagc
actggtgctgagattagaagtgtatgcacagaagctggtatgtttgctatcagagcacgg
cgaaaaattgctactgagaaggatttcctggaggctgtaaataaggtcattaagtcttat
gccaaattcagtgctactccccgctatatgacatacaactga
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