NDUFB11

NADH dehydrogenase (ubiquinone) 1 beta subcomplex, 11, 17.3kDa
Identifiers
Symbols	NDUFB11; ESSS; FLJ20494; MGC111182; NP17.3; Np15; P17.3
External IDs	OMIM: 300403 MGI: 1349919 HomoloGene: 10398 GeneCards: NDUFB11 Gene
Gene Ontology Molecular function • NADH dehydrogenase activity • NADH dehydrogenase (ubiquinone) activity • oxidoreductase activity Cellular component • mitochondrion • mitochondrial inner membrane • mitochondrial respiratory chain complex I • membrane • integral to membrane • respiratory chain Biological process • transport • respiratory electron transport chain Sources: Amigo / QuickGO
RNA expression pattern
More reference expression data
Orthologs
Species	Human	Mouse
Entrez	54539	104130
Ensembl	ENSG00000147123	ENSMUSG00000031059
UniProt	Q9NX14	Q4VBC9
RefSeq (mRNA)	NM_001135998.1	NM_019435.4
RefSeq (protein)	NP_001129470.1	NP_062308.2
Location (UCSC)	Chr X: 47 – 47 Mb	Chr X: 20.19 – 20.19 Mb
PubMed search	[1]	[2]

ESSS subunit of NADH:ubiquinone oxidoreductase (complex I)
Identifiers
Symbol	ESSS
Pfam	PF10183
InterPro	IPR019329
Available protein structures: Pfam structures PDB RCSB PDB; PDBe PDBsum structure summary

NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 11, mitochondrial (NADH-ubiquinone oxidoreductase ESSS subunit) is an enzyme that in humans is encoded by the NDUFB11 gene.^[1][2][3]

References

1. ^ Cui Y, Yu L, Gong R, Zhang M, Fan Y, Yue P, Zhao S (Nov 1999). "Cloning and tissue expressional characterization of a full-length cDNA encoding human neuronal protein P17.3". Biochem Genet 37 (5–6): 175–85. doi:10.1023/A:1018734605214. PMID 10544803. 
2. ^ Carroll J, Shannon RJ, Fearnley IM, Walker JE, Hirst J (Dec 2002). "Definition of the nuclear encoded protein composition of bovine heart mitochondrial complex I. Identification of two new subunits". J Biol Chem 277 (52): 50311–7. doi:10.1074/jbc.M209166200. PMID 12381726. 
3. ^ "Entrez Gene: NDUFB11 NADH dehydrogenase (ubiquinone) 1 beta subcomplex, 11, 17.3kDa". http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=54539. 

Further reading

• Petruzzella V, Tessa A, Torraco A, et al. (2007). "The NDUFB11 gene is not a modifier in Leber hereditary optic neuropathy". Biochem. Biophys. Res. Commun. 355 (1): 181–7. doi:10.1016/j.bbrc.2007.01.140. PMID 17292333. 
• Ross MT, Grafham DV, Coffey AJ, et al. (2005). "The DNA sequence of the human X chromosome". Nature 434 (7031): 325–37. doi:10.1038/nature03440. PMC 2665286. PMID 15772651. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=2665286. 
• Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The Status, Quality, and Expansion of the NIH Full-Length cDNA Project: The Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMC 528928. PMID 15489334. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=528928. 
• Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. 36 (1): 40–5. doi:10.1038/ng1285. PMID 14702039. 
• Clark HF, Gurney AL, Abaya E, et al. (2003). "The Secreted Protein Discovery Initiative (SPDI), a Large-Scale Effort to Identify Novel Human Secreted and Transmembrane Proteins: A Bioinformatics Assessment". Genome Res. 13 (10): 2265–70. doi:10.1101/gr.1293003. PMC 403697. PMID 12975309. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=403697. 
• Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=139241.