1. Gene
  2. KPNB1 - karyopherin subunit beta 1 Gene

KPNB1 - karyopherin subunit beta 1 Gene

Homo sapiens

Also known as IMB1; IPO1; IPOB; Impnb; NTF97

Gene ID: 3837 | Gene type: protein coding

About KPNB1

Cytogenetic location: 17q21.32 Genomic coordinates (GRCh38): 17:47,649,919-47,685,505 (from NCBI)

This gene has 16 transcripts (splice variants), 215 orthologues and 5 paralogues. Ubiquitous expression in testis (RPKM 74.8), appendix (RPKM 47.4) and 25 other tissues.

Summary

Nucleocytoplasmic transport, a signal- and energy-dependent process, takes place through nuclear pore complexes embedded in the nuclear envelope. The import of proteins containing a nuclear localization signal (NLS) requires the NLS import receptor, a heterodimer of importin alpha and beta subunits also known as karyopherins. Importin alpha binds the NLS-containing cargo in the cytoplasm and importin beta docks the complex at the cytoplasmic side of the nuclear pore complex. In the presence of nucleoside triphosphates and the small GTP binding protein Ran, the complex moves into the nuclear pore complex and the importin subunits dissociate. Importin alpha enters the nucleoplasm with its passenger protein and importin beta remains at the pore. Interactions between importin beta and the FG repeats of nucleoporins are essential in translocation through the pore complex. The protein encoded by this gene is a member of the importin beta family. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2013]

KPNB1 Products(2)

mRNA Protein Name
NM_001276453.2 NP_001263382.1 importin subunit beta-1 isoform 2
NM_002265.6 NP_002256.2 importin subunit beta-1 isoform 1
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables enzyme binding IPI
IPI: Inferred from physical interaction
22701565 GOA
enables nuclear import signal receptor activity IDA
IDA: Inferred from direct assay
14645851 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
9405152 GOA
enables protein domain specific binding IPI
IPI: Inferred from physical interaction
11984006 GOA
Biological Process GO Annotation Evidence Reference Source
involved in NLS-bearing protein import into nucleus IDA
IDA: Inferred from direct assay
14645851 GOA
involved in RNA import into nucleus IDA
IDA: Inferred from direct assay
9670026 GOA
involved in astral microtubule organization IMP
IMP: Inferred from mutant phenotype
23783028 GOA
involved in establishment of mitotic spindle localization IMP
IMP: Inferred from mutant phenotype
23783028 GOA
involved in mitotic chromosome movement towards spindle pole IMP
IMP: Inferred from mutant phenotype
23783028 GOA
involved in mitotic metaphase chromosome alignment IMP
IMP: Inferred from mutant phenotype
23783028 GOA
involved in mitotic spindle assembly IMP
IMP: Inferred from mutant phenotype
23783028 GOA
acts upstream of or within protein import into nucleus IDA
IDA: Inferred from direct assay
15964792 GOA
involved in protein import into nucleus IDA
IDA: Inferred from direct assay
7615630 GOA
involved in protein import into nucleus IMP
IMP: Inferred from mutant phenotype
17209048 GOA
involved in ribosomal protein import into nucleus IDA
IDA: Inferred from direct assay
9687515 GOA
Cellular Component GO Annotation Evidence Reference Source
part of NLS-dependent protein nuclear import complex IPI
IPI: Inferred from physical interaction
10353244 GOA
is active in cytoplasm IDA
IDA: Inferred from direct assay
11891849 GOA
located in endoplasmic reticulum tubular network IDA
IDA: Inferred from direct assay
22701565 GOA
located in nuclear envelope IDA
IDA: Inferred from direct assay
22701565 GOA
located in nucleoplasm IDA
IDA: Inferred from direct assay
9670026 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

KPNB1 Protein Structure

IBN_N

IBN_N: Importin-beta N-terminal domain (21 - 100)

HEAT_EZ

HEAT_EZ: HEAT-like repeat (380 - 435)

  • 0
  • 200
  • 400
  • 600
  • 800
  • 876 a.a.
Protein Preferred Names Protein Names

importin subunit beta-1

PTAC97

KPNB1 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
KPNB1 Q14974 P2RY6 Homo sapiens Q15077 30833792
Intra
KPNB1 Q14974 SMNDC1 Homo sapiens O75940 15494309
Cross
KPNB1 Q14974 NSP1 Saccharomyces cerevisiae P14907 12372823
Cross
KPNB1 Q14974 NSP1 Saccharomyces cerevisiae P14907 19680228
Intra
KPNB1 Q14974 KPNA7 Homo sapiens A9QM74 20701745
Intra
KPNB1 Q14974 SLC15A3 Homo sapiens F5H1C8 30833792
Intra
KPNB1 Q14974 CD74 Homo sapiens P04233 30833792
Intra
KPNB1 Q14974 NUP153 Homo sapiens P49790 35044719
Intra
KPNB1 Q14974 NUP153 Homo sapiens P49790 35271311
Intra
KPNB1 Q14974 NUP153 Homo sapiens P49790
FPS
35044719
Intra
KPNB1 Q14974 NUP153 Homo sapiens P49790 26496610
Intra
KPNB1 Q14974 KPNA2 Homo sapiens P52292 17596301
Intra
KPNB1 Q14974 KPNA2 Homo sapiens P52292 35271311
Intra
KPNB1 Q14974 KPNA2 Homo sapiens P52292 9405152
Intra
KPNB1 Q14974 KPNA2 Homo sapiens P52292 26496610
Intra
KPNB1 Q14974 KPNA2 Homo sapiens P52292 20701745
Intra
KPNB1 Q14974 KPNA2 Homo sapiens P52292
SPR
10523667
Intra
KPNB1 Q14974 MAP3K14 Homo sapiens Q99558 30833792
Intra
KPNB1 Q14974 KPNA3 Homo sapiens O00505 35271311
Intra
KPNB1 Q14974 KPNA3 Homo sapiens O00505
SPR
10523667
Intra
KPNB1 Q14974 KPNA3 Homo sapiens O00505 26496610
Intra
KPNB1 Q14974 KPNA1 Homo sapiens P52294 26496610
Intra
KPNB1 Q14974 KPNA1 Homo sapiens P52294
SPR
10523667
Intra
KPNB1 Q14974 KPNA1 Homo sapiens P52294 35271311
Intra
KPNB1 Q14974 KPNA6 Homo sapiens O60684 26496610
Intra
KPNB1 Q14974 KPNA6 Homo sapiens O60684 35271311
Intra
KPNB1 Q14974 KPNA6 Homo sapiens O60684
SPR
10523667
Intra
KPNB1 Q14974 SMN1 Homo sapiens Q16637-3 15494309
Intra
KPNB1 Q14974 SMN1 Homo sapiens Q16637-3 15494309
Intra
KPNB1 Q14974 KPNA4 Homo sapiens O00629 26496610
Intra
KPNB1 Q14974 KPNA4 Homo sapiens O00629 35271311
Intra
KPNB1 Q14974 KPNA4 Homo sapiens O00629 20818336
Intra
KPNB1 Q14974 KPNA4 Homo sapiens O00629
SPR
10523667
Intra
KPNB1 Q14974 UNC93B1 Homo sapiens Q9H1C4 30833792
Intra
KPNB1 Q14974 TNFSF13B Homo sapiens Q9Y275 30833792
Intra
KPNB1 Q14974 ERBB2 Homo sapiens P04626 16314522
Cross
KPNB1 Q14974 L2 Human papillomavirus P03107 15507604
Cross
KPNB1 Q14974 L1 Human papillomavirus P03101 11971900
Cross
KPNB1 Q14974 L1 Human papillomavirus P03101 15507604
Cross
KPNB1 Q14974 Mrtfa Mus musculus Q8K4J6 20818336
Cross
KPNB1 Q14974 rev Human immunodeficiency virus P04620 9405152
Cross
KPNB1 Q14974 rev Human immunodeficiency virus P04620 9405152
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant KPNB1 Proteins

Cat. No. Product Name Accession Purity
HY-P70837 KPNB1 Protein, Human (His) Q14974-1 (M1-A876) ≥95%

Related Diseases

Diseases Alias
Venezuelan Equine Encephalitis

Venezuelan Equine Fever

Venezuelan Equine Encephalomyelitis

Encephalitis Venezuelan Equine

Encephalomyelitis, Venezuelan Equine

Venezuelan Encephalitis

Disorder Due To Venezuelan Equine Encephalitis Virus

Venezuelan Equine Encephalitis Virus Infection

Venezuelan Equine Encephalomyelitis Virus Disease

Influenza

Flu

Influenza With Non-Respiratory Manifestation

Influenza With Other Manifestations

Influenza, Human

Influenza, Susceptibility To

Seasonal Influenza, Virus Identified

Encephalitis

Mumps Encephalitis

Mumps Meningoencephalitis

Herpes Simplex Neuroinvasion

Herpetic Encephalitis

Herpetic Encephalopathy

Herpes Simplex Encephalitis, Myelitis Or Encephalomyelitis

Encephalitis Due To Herpesviridae

Encephalitis Due To Herpesvirus

Herpes Encephalitis

Herpesviral Encephalitis

Herpes Simplex Encephalitis

Hsv - [Herpes Simplex Virus] Encephalitis

Herpes Virus Encephalitis

Simian B Disease

Simian B Disorder

Encephalitis Nec

Idiopathic Encephalitis

Campomelic Dysplasia

Acampomelic Campomelic Dysplasia

Camptomelic Dysplasia

Campomelic Dysplasia With Autosomal Sex Reversal

Cmpd

CMD1

Cmpd1

Cmpd1/Sra1

Acampomelic Campomelic Dysplasia With Autosomal Sex Reversal

Campomelic Dwarfism

Campomelic Syndrome

Dysplasia, Campomelic

Chronic Myeloproliferative Disorder

Familial Dilated Cardiomyopathy

Spinal Muscular Atrophy

Sma

5q Sma

Proximal Sma

Sma-Associated Sma

Spinal Amyotrophies

Spinal Amyotrophy

Spinal Muscle Degeneration

Spinal Muscle Wasting

Muscular Atrophy Spinal

Atrophy, Muscular, Spinal

Hereditary Motor Neuronopathy

Progressive Muscular Atrophy

Sma - [Spinal Muscular Atrophy]

Retinitis Pigmentosa

RP

Rod-Cone Dystrophy

Autosomal Recessive Retinitis Pigmentosa

Non-Syndromic Retinitis Pigmentosa

Pericentral Pigmentary Retinopathy

Pigmentary Retinopathy

Tapetoretinal Degeneration

Rcd

Retinitis Pigmentosa Autosomal Recessive

ARRP

Retinitis Pigmentosa, Autosomal Recessive

Retinitis Pigmentosa 1

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Canis familiaris KPNB1 VGNC VGNC:42506
Bos taurus KPNB1 VGNC VGNC:30707
Mus musculus KPNB1 MGD MGI:107532
Macaca mulatta KPNB1 VGNC VGNC:74203
Felis catus KPNB1 VGNC VGNC:67979
Rattus norvegicus KPNB1 RGD RGD:2909
Others KPNB1 NCBI