Neogale vison (American mink): 122914576
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Entry
122914576 CDS
T08764
Name
(RefSeq) 26S proteasome regulatory subunit 10B-like
KO
K03064
26S proteasome regulatory subunit T4
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
122914576
09160 Human Diseases
09172 Infectious disease: viral
05169 Epstein-Barr virus infection
122914576
09164 Neurodegenerative disease
05010 Alzheimer disease
122914576
05012 Parkinson disease
122914576
05014 Amyotrophic lateral sclerosis
122914576
05016 Huntington disease
122914576
05017 Spinocerebellar ataxia
122914576
05020 Prion disease
122914576
05022 Pathways of neurodegeneration - multiple diseases
122914576
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03051 Proteasome [BR:
nvs03051
]
122914576
Proteasome [BR:
nvs03051
]
Eukaryotic proteasome
Regulatory particles
PA700 (19S proteasome)
ATPase subunits
122914576
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
AAA
Prot_ATP_ID_OB_C
AAA_lid_3
AAA_2
AAA_5
AAA_16
AAA_22
RuvB_N
PRS7_OB
nSTAND3
Prot_ATP_ID_OB_N
AAA_14
DUF815
AAA_7
AAA_11
TIP49
RNA_helicase
AAA_33
AAA_3
AAA_28
NPHP3_N
Csa3_N
bpMoxR
Mg_chelatase
AAA_18
TPR_MLP1_2
DUF5906
TsaE
DUF3829_2nd
AAA_24
AAA_25
NACHT
AAA_lid_PRS2_C
ATPase
AAA_17
Occludin_ELL
Parvo_NS1
IstB_IS21
DUF4140
Med4
Motif
Other DBs
NCBI-GeneID:
122914576
NCBI-ProteinID:
XP_044117145
LinkDB
All DBs
Position
7:complement(202653678..202655174)
Genome browser
AA seq
389 aa
AA seq
DB search
MADPRDKALQDYRKKLLEHKEIDGRLKELREQLKELTKQYEKSENDLKALQSVGQIVGEV
LKQLTEEKFIVKATNGPRYVVGCRRQLDKSKLKPGTRVALDMTTLTIVRYLPREVDPLVY
NMSHEDPGNVSYSEIGGLSEQIRELREVIELPLTNPELLQRVGIIPPKGCLLYGPPGTGK
TLLARAVASQLDCNFLKVVSSSIVDKYIGESARLTREMFNYARDHQPCIIFMDEIDAIGG
RRFSEGTSADREIQRTLMELLNQMDGFDTLHRVKMIMATNRPDTLDPALLRPGRLDRKIH
IDLPNEQARLDILKIHAGPITKHGEIDYEAIVKLSDGFNGADLRNVCTEAGMFAIRADHD
FVVQEDFMKAVRKVADSKKLESKLDYKPV
NT seq
1170 nt
NT seq
+upstream
nt +downstream
nt
atggcggaccctagagataaggcgcttcaggactaccgcaagaagctactggagcacaag
gagatcgacggccgtctcaaggagttaagggaacaattaaaagaacttaccaagcagtat
gaaaaatctgaaaatgatctgaaggccttacaaagtgttgggcagattgtgggtgaagta
cttaagcaactaactgaggaaaaattcattgttaaagctacaaatggaccaagatatgtt
gtgggttgtcgtcgacagcttgacaaaagtaagctgaagccaggaacaagagttgctttg
gatatgactacactaacaatcgtgagatatttgccaagagaggtggatccattggtctac
aacatgtctcatgaggaccctgggaatgtttcttattctgaaattggaggactatcagaa
cagattcgggaattaagagaggtgatagaattgcctcttacaaacccagaattattgcag
cgtgtaggaataatacctccaaaaggctgtttgttatatggaccaccaggcacaggaaaa
acactcttggcacgagctgttgctagccagctggactgcaatttcttaaaggttgtatct
agttctattgtagacaagtacattggtgaaagtgctcgtttgaccagagaaatgtttaat
tatgccagggatcatcaaccatgcattatttttatggatgaaatagatgccattggtggt
cgtcggttttctgagggtacttcagctgatagagagattcagagaactttgatggagtta
ctgaatcaaatggatggatttgatactctacatagagttaaaatgatcatggctacaaac
agaccagatacactggatcctgccttgcttcgtcctggaagattagacagaaaaatacat
attgacttaccaaatgaacaagcaagattagacatattgaaaatccatgcaggtcccatt
acaaagcatggtgaaatagattatgaagcaattgtgaagctttcagatggctttaatgga
gcagacctgagaaatgtttgtactgaagcaggtatgtttgcaattcgtgctgatcatgat
tttgtagtacaggaagacttcatgaaagcagtcagaaaagtggctgattctaagaagcta
gagtctaaattggactacaaacctgtgtga
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