Homo sapiens Protein: LYRM4
Summary
InnateDB Protein IDBP-480621.3
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol LYRM4
Protein Name LYR motif containing 4
Synonyms
Species Homo sapiens
Ensembl Protein ENSP00000418787
InnateDB Gene IDBG-235091 (LYRM4)
Protein Structure
UniProt Annotation
Function Required for nuclear and mitochondrial iron-sulfur protein biosynthesis. {ECO:0000269PubMed:17331979, ECO:0000269PubMed:19454487}.
Subcellular Localization Mitochondrion. Nucleus.
Disease Associations Combined oxidative phosphorylation deficiency 19 (COXPD19) [MIM:615595]: A mitochondrial disorder characterized by respiratory distress, hypotonia, and severe lactic acidosis in the newborn period. Other features include gastroesophageal reflux and elevated liver enzymes with normal synthetic function. {ECO:0000269PubMed:23814038}. Note=The disease is caused by mutations affecting the gene represented in this entry.
Tissue Specificity Reduced mRNA levels in Friedreich ataxia patients. {ECO:0000269PubMed:17331979}.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 4 experimentally validated interaction(s) in this database.
Experimentally validated
Total 4 [view]
Protein-Protein 3 [view]
Protein-DNA 1 [view]
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
Biological Process
GO:0044281 small molecule metabolic process
Cellular Component
GO:0005634 nucleus
GO:0005759 mitochondrial matrix
Protein Structure and Domains
PDB ID
InterPro IPR008011 Complex 1 LYR protein
PFAM PF05347
PF13232
PRINTS
PIRSF
SMART
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q9HD34
PhosphoSite PhosphoSite-Q9HD34
TrEMBL
UniProt Splice Variant
Entrez Gene 57128
UniGene Hs.387755
RefSeq NP_065141
HUGO HGNC:21365
OMIM 613311
CCDS CCDS4493
HPRD 12855
IMGT
EMBL AF170070 AF285118 AK291158 AL035653 AL121978 AL162381 BC009552
GenPept AAF25797 AAG01155 AAH09552 BAF83847