InnateDB Protein
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IDBP-480621.3
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Last Modified
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2014-10-13 [Report errors or provide feedback]
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Gene Symbol
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LYRM4
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Protein Name
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LYR motif containing 4
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Synonyms
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Species
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Homo sapiens
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Ensembl Protein
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ENSP00000418787
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InnateDB Gene
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IDBG-235091 (LYRM4)
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Protein Structure
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Function |
Required for nuclear and mitochondrial iron-sulfur protein biosynthesis. {ECO:0000269PubMed:17331979, ECO:0000269PubMed:19454487}.
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Subcellular Localization |
Mitochondrion. Nucleus.
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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.
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Tissue Specificity |
Reduced mRNA levels in Friedreich ataxia patients. {ECO:0000269PubMed:17331979}.
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Comments |
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Number of Interactions
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This gene and/or its encoded proteins are associated with 4 experimentally validated interaction(s) in this database.
Experimentally validated |
Total |
4
[view]
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Protein-Protein |
3
[view]
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Protein-DNA |
1
[view]
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Protein-RNA |
0
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DNA-DNA |
0
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RNA-RNA |
0
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DNA-RNA |
0
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Molecular Function |
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Biological Process |
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Cellular Component |
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PDB ID |
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InterPro |
IPR008011
Complex 1 LYR protein
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PFAM |
PF05347
PF13232
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PRINTS |
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PIRSF |
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SMART |
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TIGRFAMs |
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Modification |
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SwissProt |
Q9HD34
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PhosphoSite |
PhosphoSite-Q9HD34
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TrEMBL |
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UniProt Splice Variant |
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Entrez Gene |
57128
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UniGene |
Hs.387755
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RefSeq |
NP_065141
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HUGO |
HGNC:21365
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OMIM |
613311
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CCDS |
CCDS4493
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HPRD |
12855
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IMGT |
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EMBL |
AF170070
AF285118
AK291158
AL035653
AL121978
AL162381
BC009552
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GenPept |
AAF25797
AAG01155
AAH09552
BAF83847
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