Protein detail
CXB1
Gap junction beta-1 protein (Connexin-32) (Cx32) (GAP junction 28 kDa liver protein)
Protein symbol CXB1 | UniProt ID | EVMP score 0.38 |
Frequency | Transmembrane count 4 | Protein classification Disease related genesHuman disease related genesPotential drug targetsPredicted membrane proteinsTransporters |
Basic Information
Protein Names
Gap junction beta-1 protein (Connexin-32) (Cx32) (GAP junction 28 kDa liver protein)
Protein Class
Disease related genesHuman disease related genesPotential drug targetsPredicted membrane proteinsTransporters
Protein Function
- Human disease related genes:Nervous system diseases:Neurodegenerative diseases
- Disease related genes
- Transporters:Transporter channels and pores
- Potential drug targets
Transmembrane
23..45; Helical; 76..95; Helical; 131..153; Helical; 192..214; Helical
Transmembrane Count
4
Ensembl
Entrez Gene Symbol
Gene Synonym
CMTXCMTX1CX32
Gene Description
Gap junction protein beta 1
Chromosome
X
Position
71212811-71225516
EVMP Score
0.38
Fluorescence & Localization
Tissue Specificchoroid plexusCell SpecificAdrenal cortex cellsSingle-Nuclei Brain SpecificBergmann gliaBlood Cell Specificintermediate monocyteBlood Lineage Specificmonocytes
Function & Pathway
Protein Function
- Human disease related genes:Nervous system diseases:Neurodegenerative diseases
- Disease related genes
- Transporters:Transporter channels and pores
- Potential drug targets
Cellular Component
Molecular Function
Biological Process
Reactome
Mediation Categories
Fusion and delivery mediation
Relations & Evidence
Enzyme-Mediated Modification
18 records.
| Substrate Gene Symbol | Enzyme Gene Symbol | Enzyme UniProt ID | Residue Type | Residue Offset | Modification | Database | References |
|---|---|---|---|---|---|---|---|
| GJB1 | PRKACA | P17612 | S | 233 | phosphorylation | phosphoELM_MIMPPhosphoSite_MIMPMIMPHPRD_MIMPSIGNORProtMapperHPRDKEASIGNOR_ProtMapper | ProtMapper:8390988HPRD:8390988KEA:8390988SIGNOR:8390988 |
| GJB1 | PRKCA | P17252 | S | 229 | phosphorylation | phosphoELM_MIMPPhosphoSite_MIMPMIMPHPRD_MIMPSIGNORProtMapperHPRDKEASIGNOR_ProtMapper | ProtMapper:8390988HPRD:8390988KEA:8390988SIGNOR:8390988 |
| GJB1 | PRKCA | P17252 | S | 233 | phosphorylation | phosphoELM_MIMPPhosphoSite_MIMPMIMPHPRD_MIMPSIGNORProtMapperHPRDKEASIGNOR_ProtMapper | ProtMapper:8390988HPRD:8390988KEA:8390988SIGNOR:8390988 |
| GJB1 | EPHA1 | P21709 | Y | 243 | phosphorylation | PhosphoSite | |
| GJB1 | MST1R | Q04912 | Y | 243 | phosphorylation | PhosphoSite | |
| GJB1 | EPHB1 | P54762 | Y | 243 | phosphorylation | PhosphoSite | |
| GJB1 | PRKCB | P05771 | S | 229 | phosphorylation | phosphoELM_MIMPPhosphoSite_MIMPMIMPHPRD_MIMPKEA | KEA:17570479 |
| GJB1 | PRKCB | P05771 | S | 233 | phosphorylation | MIMPHPRD_MIMPphosphoELM_MIMPPhosphoSite_MIMP | |
| GJB1 | PRKCG | P05129 | S | 229 | phosphorylation | MIMPHPRD_MIMPphosphoELM_MIMPPhosphoSite_MIMP | |
| GJB1 | PRKCG | P05129 | S | 233 | phosphorylation | MIMPHPRD_MIMPphosphoELM_MIMPPhosphoSite_MIMP |
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Ligand-Receptor Signaling
26 records.
| Category | Parent | Database | Transmitter | Receiver | Secreted | Plasma Membrane (Transmembrane) | Plasma Membrane (Peripheral) |
|---|---|---|---|---|---|---|---|
| extracellular | extracellular | OmniPath | No | No | No | No | No |
| intracellular | intracellular | LOCATE | No | No | No | No | No |
| intracellular | intracellular | GO_Intercell | No | No | No | No | No |
| intracellular | intracellular | OmniPath | No | No | No | No | No |
| cell_surface_ligand | cell_surface_ligand | Baccin2019 | Yes | No | No | No | No |
| cell_surface_ligand | cell_surface_ligand | OmniPath | Yes | No | No | No | No |
| gap_junction | gap_junction | GO_Intercell | Yes | Yes | No | No | No |
| gap_junction | gap_junction | Ramilowski_location | Yes | Yes | No | No | No |
| gap_junction | gap_junction | UniProt_location | Yes | Yes | No | No | No |
| gap_junction | gap_junction | Almen2009 | Yes | Yes | No | No | No |
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Regulatory Interaction Network
3 records.
| Source Protein Symbol | Source UniProt ID | Target Protein Symbol | Target UniProt ID | Is Directed | Is Stimulation | Is Inhibition | Database | References |
|---|---|---|---|---|---|---|---|---|
| KAPCA | P17612 | CXB1 | P08034 | Yes | No | No | phosphoELM_MIMPPhosphoSite_MIMPMIMPHPRD_MIMPiPTMnetPhosphoPointSIGNORProtMapperHPRDPhosphoSite_KEAKEAHPRD_KEASIGNOR_ProtMapperHPRD-phos | HPRD:8390988HPRD-phos:8390988ProtMapper:8390988KEA:8390988SIGNOR:8390988 |
| KPCA | P17252 | CXB1 | P08034 | Yes | Yes | No | phosphoELM_MIMPPhosphoSite_MIMPMIMPHPRD_MIMPiPTMnetPhosphoPointSIGNORProtMapperHPRDPhosphoSite_KEAKEAHPRD_KEASIGNOR_ProtMapperHPRD-phos | HPRD:8390988HPRD-phos:8390988ProtMapper:8390988KEA:8390988SIGNOR:8390988 |
| RON | Q04912 | CXB1 | P08034 | Yes | No | No | PhosphoSitePhosphoSite_ProtMapperProtMapper | PhosphoSite:30401746 |
Protein Complex Composition
Isolation & Detection Technology
1 record.
| EV Isolation Method | Detection Method | Number of References | References |
|---|---|---|---|
| Differential UltracentrifugationDensity Gradient CentrifugationUltrafiltration / Tangential Flow FiltrationSize Exclusion Chromatography | Mass spectrometry | 14 | 3228482532341357332044243561146232944193346239184074865828986585309501853194160638321535395581342914823930944935 |
Sequence, Structure & Domains
Sequences
Length
283
Mass
32,025
Sequence
MNWTGLYTLLSGVNRHSTAIGRVWLSVIFIFRIMVLVVAAESVWGDEKSSFICNTLQPGCNSVCYDQFFPISHVRLWSLQLILVSTPALLVAMHVAHQQHIEKKMLRLEGHGDPLHLEEVKRHKVHISGTLWWTYVISVVFRLLFEAVFMYVFYLLYPGYAMVRLVKCDVYPCPNTVDCFVSRPTEKTVFTVFMLAASGICIILNVAEVVYLIIRACARRAQRRSNPPSRKGSGFGHRLSPEYKQNEINKLLSEQDGSLKDILRRSPGTGAGLAEKSDRCSAC
3D Structural Models
Turn
41..43; 45..50
Helix
3..11; 19..40; 60..68; 73..102; 130..156; 184..216
Beta Strand
52..54; 159..161; 164..168; 173..175; 177..180
3D Structure
Electron microscopy (10); NMR spectroscopy (1)
Domain & Motif Annotations
Protein Families
- Connexin family
- Beta-type (group I) subfamily
Sequence Similarities
Belongs to the connexin family. Beta-type (group I) subfamily.
Clinical Relevance
Disease Involvement
Charcot-Marie-Tooth diseaseDejerine-Sottas syndromeDisease variantNeurodegenerationNeuropathy
Antibody