Neogale vison (American mink): 122906450
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Entry
122906450 CDS
T08764
Symbol
PSMD11
Name
(RefSeq) 26S proteasome non-ATPase regulatory subunit 11
KO
K03036
26S proteasome regulatory subunit N6
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
122906450 (PSMD11)
09160 Human Diseases
09172 Infectious disease: viral
05169 Epstein-Barr virus infection
122906450 (PSMD11)
09164 Neurodegenerative disease
05010 Alzheimer disease
122906450 (PSMD11)
05012 Parkinson disease
122906450 (PSMD11)
05014 Amyotrophic lateral sclerosis
122906450 (PSMD11)
05016 Huntington disease
122906450 (PSMD11)
05017 Spinocerebellar ataxia
122906450 (PSMD11)
05020 Prion disease
122906450 (PSMD11)
05022 Pathways of neurodegeneration - multiple diseases
122906450 (PSMD11)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03051 Proteasome [BR:
nvs03051
]
122906450 (PSMD11)
Proteasome [BR:
nvs03051
]
Eukaryotic proteasome
Regulatory particles
PA700 (19S proteasome)
non-ATPase subunits
122906450 (PSMD11)
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
RPN6_N
PCI
RPN6_C_helix
TPR_12
TPR_ESP1
DDRGK
DUF2153
TPR_3
DUF8517
YPL108W_C
Motif
Other DBs
NCBI-GeneID:
122906450
NCBI-ProteinID:
XP_044104330
UniProt:
A0A8C7BNS2
LinkDB
All DBs
Position
5:30963642..30992482
Genome browser
AA seq
422 aa
AA seq
DB search
MAAAAVVEFQRAQSLLSTDREASIDILHSIVKRDIQENDEEAVQVKEQSILELGSLLAKT
GQAAELGGLLKYVRPFLNSISKAKAARLVRSLLDLFLDMEAATGQEVELCLECIEWAKSE
KRTFLRQALEARLVSLYFDTKRYQEALHLGSQLLRELKKMDDKALLVEVQLLESKTYHAL
SNLPKARAALTSARTTANAIYCPPKLQATLDMQSGIIHAAEEKDWKTAYSYFYEAFEGYD
SIDSPKAITSLKYMLLCKIMLNTPEDVQALVSGKLALRYAGRQTEALKCVAQASKNRSLA
DFEKALTDYRAELRDDPIISTHLAKLYDNLLEQNLIRVIEPFSRVQIEHISSLIKLSKAD
VERKLSQMILDKKFHGILDQGEGVLIIFDEPPVDKTYEAALETIQNMSKVVDSLYNKAKK
LT
NT seq
1269 nt
NT seq
+upstream
nt +downstream
nt
atggcggcggcggcggtggtggagttccagagagcccagtctctactcagcaccgaccgg
gaggcctccatcgacattctccactccatcgtgaagcgtgacattcaagagaatgatgag
gaggcagtgcaggtcaaagagcagagtatcctggaactggggtctctcttggcaaagact
ggacaagctgccgagcttggaggactcctgaagtatgtgcgacccttcttgaattccatc
agcaaggctaaggcagctcgcctggtccgatctcttcttgatctgtttcttgatatggaa
gcagctacagggcaggaggtcgagttgtgtttagagtgcatcgaatgggccaaatcagag
aaacgaactttcttacgccaagctttggaggcaagactggtgtctttgtactttgatacc
aagaggtaccaggaagcattgcatttgggttctcagctgctgcgggagttgaaaaagatg
gatgacaaagcccttttggtggaagtacagcttttagaaagcaaaacataccatgccctg
agcaacctgccgaaagcccgagctgccttaacttctgctcgaactacagcaaatgctatc
tactgcccccctaaattgcaggccaccttggatatgcagtcaggtattatccatgcagca
gaagagaaggattggaaaactgcatactcctatttctatgaggcatttgagggttatgat
tccatcgatagcccaaaggccatcacatctctgaagtacatgttgctgtgcaaaatcatg
ctcaacaccccagaagatgtccaggctttggtgagcgggaagcttgcacttcggtatgcg
gggaggcagacagaagcattaaaatgtgtggctcaggctagcaagaacagatcactggca
gattttgaaaaggccctgacagattatcgggcagagctccgggatgacccaatcatcagt
acacacttggccaagttgtatgataacttactggaacagaatctgatccgagtcattgag
cctttttcccgagttcagattgaacacatatctagcctcatcaaactctccaaggccgac
gtggaaaggaaattgtcacagatgattcttgacaagaaatttcatgggatcttggaccag
ggggagggtgtcttgattattttcgatgaacccccagtagataaaacttatgaagctgct
ctggaaacaattcagaacatgagtaaagtagtggattccctctacaacaaagccaagaag
ctgacatag
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