InnateDB Protein
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IDBP-58804.6
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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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MRPS22
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Protein Name
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mitochondrial ribosomal protein S22
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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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ENSP00000310785
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InnateDB Gene
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IDBG-58802 (MRPS22)
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Protein Structure
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Function |
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Subcellular Localization |
Mitochondrion.
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Disease Associations |
Combined oxidative phosphorylation deficiency 5 (COXPD5) [MIM:611719]: A mitochondrial disease resulting in severe metabolic acidosis, edema, hypertrophic cardiomyopathy, tubulopathy, and hypotonia. {ECO:0000269PubMed:17873122}. Note=The disease is caused by mutations affecting the gene represented in this entry.
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Tissue Specificity |
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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 41 experimentally validated interaction(s) in this database.
Experimentally validated |
Total |
41
[view]
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Protein-Protein |
41
[view]
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Protein-DNA |
0
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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 |
Accession |
GO Term |
GO:0003735
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structural constituent of ribosome
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Biological Process |
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Cellular Component |
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PDB ID |
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InterPro |
IPR019374
Ribosomal protein S22, mitochondrial
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PFAM |
PF10245
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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 |
P82650
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PhosphoSite |
PhosphoSite-P82650
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TrEMBL |
Q96Q16
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UniProt Splice Variant |
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Entrez Gene |
56945
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UniGene |
Hs.75724
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RefSeq |
NP_064576
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HUGO |
HGNC:14508
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OMIM |
605810
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CCDS |
CCDS3107
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HPRD |
10430
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IMGT |
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EMBL |
AB061314
AF226045
AF321613
BC009296
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GenPept |
AAF86945
AAH09296
AAK01406
BAB54962
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