Homo sapiens Protein: MATR3
Summary
InnateDB Protein IDBP-483661.4
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol MATR3
Protein Name matrin 3
Synonyms ALS21; MPD2; VCPDM;
Species Homo sapiens
Ensembl Protein ENSP00000423587
InnateDB Gene IDBG-47535 (MATR3)
Protein Structure
UniProt Annotation
Function May play a role in transcription or may interact with other nuclear matrix proteins to form the internal fibrogranular network. In association with the SFPQ-NONO heteromer may play a role in nuclear retention of defective RNAs. {ECO:0000269PubMed:11525732}.
Subcellular Localization Nucleus matrix.
Disease Associations Amyotrophic lateral sclerosis 21 (ALS21) [MIM:606070]: A neurodegenerative disorder affecting upper and lower motor neurons, resulting in muscle weakness and respiratory failure. Some patients may develop myopathic features or dementia. {ECO:0000269PubMed:19344878, ECO:0000269PubMed:24686783}. Note=The disease is caused by mutations affecting the gene represented in this entry.
Tissue Specificity
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 80 experimentally validated interaction(s) in this database.
They are also associated with 7 interaction(s) predicted by orthology.
Experimentally validated
Total 80 [view]
Protein-Protein 80 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 7 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0000166 nucleotide binding
GO:0003676 nucleic acid binding
GO:0005198 structural molecule activity
GO:0005515 protein binding
GO:0008270 zinc ion binding
GO:0044822 poly(A) RNA binding
Biological Process
Cellular Component
GO:0005634 nucleus
GO:0005637 nuclear inner membrane
GO:0016020 membrane
GO:0016363 nuclear matrix
Protein Structure and Domains
PDB ID
InterPro IPR000504 RNA recognition motif domain
IPR000690 Zinc finger, C2H2-type matrin
IPR003604 Zinc finger, U1-type
PFAM PF00076
PRINTS
PIRSF
SMART SM00360
SM00451
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt P43243
PhosphoSite PhosphoSite-P43243
TrEMBL Q9H4N1
UniProt Splice Variant
Entrez Gene 9782
UniGene Hs.602545
RefSeq NP_001181885
HUGO HGNC:6912
OMIM 164015
CCDS CCDS54908
HPRD 05270
IMGT
EMBL AB018266 AC011404 AF117236 AK001388 AK316420 AY007157 BC015031 CH471062 M63483
GenPept AAF17217 AAG02007 AAH15031 BAA34443 BAG50899 BAH14791 EAW62114 EAW62115 EAW62116 EAW62117