Entry
Symbol
NUP62, NSP1
Name
nuclear pore complex protein Nup62
Pathway
Disease
H01177 Infantile bilateral striatal necrosis
Brite
KEGG Orthology (KO) [BR:ko00001 ]
09120 Genetic Information Processing
09122 Translation
03013 Nucleocytoplasmic transport
K14306 NUP62, NSP1; nuclear pore complex protein Nup62
09160 Human Diseases
09164 Neurodegenerative disease
05014 Amyotrophic lateral sclerosis
K14306 NUP62, NSP1; nuclear pore complex protein Nup62
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03019 Messenger RNA biogenesis
K14306 NUP62, NSP1; nuclear pore complex protein Nup62
Messenger RNA biogenesis [BR:ko03019 ]
Eukaryotic type
mRNA surveillance and transport factors
Transport factors
Nuclear pore complex
K14306 NUP62, NSP1; nuclear pore complex protein Nup62
BRITE hierarchy
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Genes
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Taxonomy UniProt
Reference
Authors
Carmo-Fonseca M, Kern H, Hurt EC
Title
Human nucleoporin p62 and the essential yeast nuclear pore protein NSP1 show sequence homology and a similar domain organization.
Journal
Eur J Cell Biol 55:17-30 (1991)
Sequence
Reference
Authors
Guan T, Muller S, Klier G, Pante N, Blevitt JM, Haner M, Paschal B, Aebi U, Gerace L
Title
Structural analysis of the p62 complex, an assembly of O-linked glycoproteins that localizes near the central gated channel of the nuclear pore complex.
Journal
Sequence
Reference
Authors
Schlaich NL, Haner M, Lustig A, Aebi U, Hurt EC
Title
In vitro reconstitution of a heterotrimeric nucleoporin complex consisting of recombinant Nsp1p, Nup49p, and Nup57p.
Journal
Sequence
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