Version 5.4
Homo sapiens Protein: MRPS16
Summary
InnateDB Protein IDBP-78285.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol MRPS16
Protein Name mitochondrial ribosomal protein S16
Synonyms
Species Homo sapiens
Ensembl Protein ENSP00000362036
InnateDB Gene IDBG-78281 (MRPS16)
Protein Structure
UniProt Annotation
Function
Subcellular Localization Mitochondrion.
Disease Associations Combined oxidative phosphorylation deficiency 2 (COXPD2) [MIM:610498]: A mitochondrial disease resulting in fatal neonatal metabolic acidosis with agenesis of the corpus callosum. {ECO:0000269PubMed:15505824}. 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 25 experimentally validated interaction(s) in this database.
Experimentally validated
Total 25 [view]
Protein-Protein 24 [view]
Protein-DNA 1 [view]
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0003735 structural constituent of ribosome
GO:0005515 protein binding
Biological Process
GO:0006412 translation
Cellular Component
GO:0005622 intracellular
GO:0005739 mitochondrion
GO:0005763 mitochondrial small ribosomal subunit
GO:0005840 ribosome
Protein Structure and Domains
PDB ID
InterPro IPR000307 Ribosomal protein S16
IPR023803 Ribosomal protein S16 domain
PFAM PF00886
PRINTS
PIRSF
SMART
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q9Y3D3
PhosphoSite PhosphoSite-Q9Y3D3
TrEMBL
UniProt Splice Variant
Entrez Gene 51021
UniGene Hs.712101
RefSeq NP_057149
HUGO HGNC:14048
OMIM 609204
CCDS CCDS7323
HPRD 14778
IMGT
EMBL AB049948 AB051351 AF151890 BC021106
GenPept AAD34127 AAH21106 BAB41001 BAB54941

If you use InnateDB for your research, please cite the following publication:

Breuer et al., InnateDB: systems biology of innate immunity and beyond - recent updates and continuing curation. Nucl. Acids Res. (2013) 41 (D1) 

InnateDB is being developed jointly by the Brinkman Laboratory (Simon Fraser University, British Columbia, Canada), the Hancock Laboratory (University of British Columbia, Vancouver, British Columbia) and the Lynn EMBL Australia Group (South Australian Health & Medical Research Institute and Flinders University, Adelaide, Australia).

Funding is currently provided by Allergen and EMBL Australia. Previous funding has been provided by Genome Canada, the Foundation for the National Institutes of Health through the Grand Challenges in Global Health initiative and by Teagasc. InnateDB curated interactions are licensed under the Design Science License. All other data is licensed under the terms of the originating database. Contact: innatedb-mail@sfu.ca