Neogale vison (American mink): 122894431
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Entry
122894431 CDS
T08764
Symbol
PSMC6
Name
(RefSeq) 26S proteasome regulatory subunit 10B
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
122894431 (PSMC6)
09160 Human Diseases
09172 Infectious disease: viral
05169 Epstein-Barr virus infection
122894431 (PSMC6)
09164 Neurodegenerative disease
05010 Alzheimer disease
122894431 (PSMC6)
05012 Parkinson disease
122894431 (PSMC6)
05014 Amyotrophic lateral sclerosis
122894431 (PSMC6)
05016 Huntington disease
122894431 (PSMC6)
05017 Spinocerebellar ataxia
122894431 (PSMC6)
05020 Prion disease
122894431 (PSMC6)
05022 Pathways of neurodegeneration - multiple diseases
122894431 (PSMC6)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03051 Proteasome [BR:
nvs03051
]
122894431 (PSMC6)
Proteasome [BR:
nvs03051
]
Eukaryotic proteasome
Regulatory particles
PA700 (19S proteasome)
ATPase subunits
122894431 (PSMC6)
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
AAA
Prot_ATP_ID_OB_C
AAA_lid_3
AAA_16
AAA_2
AAA_5
AAA_22
RuvB_N
OB_PRS7
nSTAND3
AAA_14
Prot_ATP_ID_OB_N
DUF815
AAA_7
AAA_11
TIP49
RNA_helicase
AAA_33
AAA_3
NPHP3_N
AAA_18
Phage_scaffold
Mg_chelatase
TPR_MLP1_2
bpMoxR
DUF5906
AAA_lid_PRS2_C
AAA_28
Csa3_N
TsaE
Mua
CLIP1
AAA_24
NACHT
AAA_25
Vpar_1526
CEP131_C
AAA_17
Occludin_ELL
Parvo_NS1
MC5
IstB_IS21
ApoB100_4ins
Med4
Neur
Motif
Other DBs
NCBI-GeneID:
122894431
NCBI-ProteinID:
XP_044088153
LinkDB
All DBs
Position
13:complement(46565291..46587055)
Genome browser
AA seq
389 aa
AA seq
DB search
MADPRDKALQDYRKKLLEHKEIDGRLKELREQLKELTKQYEKSENDLKALQSVGQIVGEV
LKQLTEEKFIVKATNGPRYVVGCRRQLDKSKLKPGTRVALDMTTLTIMRYLPREVDPLVY
NMSHEDPGNVSYSEIGGLSEQIRELREVIELPLTNPELFQRVGIIPPKGCLLYGPPGTGK
TLLARAVASQLDCNFLKVVSSSIVDKYIGESARLIREMFNYARDHQPCIIFMDEIDAIGG
RRFSEGTSADREIQRTLMELLNQMDGFDTLHRVKMIMATNRPDTLDPALLRPGRLDRKIH
IDLPNEQARLDILKIHAGPITKHGEIDYEAIVKLSDGFNGADLRNVCTEAGMFAIRADHD
FVVQEDFMKAVRKVADSKKLESKLDYKPV
NT seq
1170 nt
NT seq
+upstream
nt +downstream
nt
atggcggaccctagagataaggcgcttcaggactaccgcaagaagctactggagcacaag
gagatcgacggccgtctcaaggagttaagggaacaattaaaagaacttaccaagcagtat
gaaaaatctgaaaatgatctgaaggccttacagagtgttgggcagattgtgggtgaagta
cttaagcaactaactgaggaaaaattcattgttaaagctacaaatggaccaagatatgtt
gtgggttgtcgtcgacagcttgacaaaagtaagctgaagccaggaacaagagttgctttg
gatatgactacactaacaatcatgagatatttgccaagagaggtggatccattggtctac
aacatgtctcatgaggaccctgggaatgtttcttattctgaaattggaggactatcagaa
cagattcgggaattaagagaggtgatagaattgcctcttacaaacccagaattattccag
cgtgtaggaataatacctccaaaaggctgtttgttatatggaccaccaggcacaggaaaa
acactcttggcacgagctgttgctagccagctggactgcaatttcttaaaggttgtatct
agttctattgtagacaagtacattggtgaaagtgctcgtttgatcagagaaatgtttaat
tatgccagggatcatcaaccatgcattatttttatggatgaaatagatgccattggtggt
cgtcggttttctgagggtacttcagctgatagagagattcagagaactttgatggagtta
ctgaatcaaatggatggatttgatactctacatagagttaaaatgatcatggctacaaac
agaccagatacactggatcctgccttgcttcgtcctggaagattagacagaaaaatacat
attgacttaccaaatgaacaagcaagattagacatattgaaaatccatgcaggtcccatt
acaaagcatggtgaaatagattatgaagcaattgtgaagctttcagatggctttaatgga
gcagacctgagaaatgtttgtactgaagcaggtatgtttgcaattcgtgctgatcatgat
tttgtagtacaggaagacttcatgaaagcagtcagaaaagtggctgattctaagaagcta
gagtctaaattggactacaaacctgtgtga
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