Q99766 (ATP5S_HUMAN) Reviewed, UniProtKB/Swiss-Prot
Last modified
April 3, 2013.
Version 101.
History...
Names·Attributes·General annotation·Ontologies·Alt products·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize order
Names·Attributes·General annotation·Ontologies·Alt products·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize orderNames and origin
| Protein names | Recommended name: ATP synthase subunit s, mitochondrial Alternative name(s): ATP synthase-coupling factor B Short name=FB Mitochondrial ATP synthase regulatory component factor B | ||||
| Gene names |
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| Organism | Homo sapiens (Human) [Reference proteome] | ||||
| Taxonomic identifier | 9606 [NCBI] | ||||
| Taxonomic lineage | Eukaryota › Metazoa › Chordata › Craniata › Vertebrata › Euteleostomi › Mammalia › Eutheria › Euarchontoglires › Primates › Haplorrhini › Catarrhini › Hominidae › Homo![]() |
Protein attributes
| Sequence length | 215 AA. |
| Sequence status | Complete. |
| Sequence processing | The displayed sequence is further processed into a mature form. |
| Protein existence | Evidence at protein level |
General annotation (Comments)
| Function | Involved in regulation of mitochondrial membrane ATP synthase. Necessary for H+ conduction of ATP synthase. Facilitates energy-driven catalysis of ATP synthesis by blocking a proton leak through an alternative proton exit pathway By similarity. |
| Subunit structure | Homotetramer. Associates with ATP synthase By similarity. Ref.2 |
| Subcellular location | Mitochondrion By similarity. Mitochondrion inner membrane By similarity. |
| Sequence similarities | Belongs to the ATP synthase subunit s family. Contains 4 LRR (leucine-rich) repeats. |
| Caution | It is uncertain whether Met-1 or Met-16 is the initiator. |
Ontologies
| Keywords | |
|---|---|
| Biological process | ATP synthesis Hydrogen ion transport Ion transport Transport |
| Cellular component | CF(0) Membrane Mitochondrion Mitochondrion inner membrane |
| Coding sequence diversity | Alternative splicing Polymorphism |
| Domain | Leucine-rich repeat Repeat Transit peptide |
| Ligand | Magnesium Metal-binding |
| Technical term | Complete proteome Direct protein sequencing Reference proteome |
| Gene Ontology (GO) | |
| Biological_process | ATP biosynthetic process Inferred from electronic annotation. Source: UniProtKB-KW |
| Cellular_component | mitochondrial inner membrane Inferred from electronic annotation. Source: UniProtKB-SubCell proton-transporting ATP synthase complex, coupling factor F(o)Inferred from electronic annotation. Source: UniProtKB-KW |
| Molecular_function | hydrogen ion transmembrane transporter activity Non-traceable author statement PubMed 6143319. Source: UniProtKB metal ion bindingInferred from electronic annotation. Source: UniProtKB-KW |
| Complete GO annotation... | |
Alternative products
| This entry describes 3 isoforms produced by alternative splicing. [Align] [Select] | ||||||
| Isoform 1 (identifier: Q99766-1) This isoform has been chosen as the 'canonical' sequence. All positional information in this entry refers to it. This is also the sequence that appears in the downloadable versions of the entry. | ||||||
| Isoform 2 (identifier: Q99766-2) The sequence of this isoform differs from the canonical sequence as follows: 121-136: EGLEHVEKIRLCKCHY → GNYPIVLLIENADDLQ 137-215: Missing. | ||||||
| Isoform 3 (identifier: Q99766-3) The sequence of this isoform differs from the canonical sequence as follows: 122-127: GLEHVE → TSNICC 128-215: Missing. |
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | Feature identifier | ||||
Molecule processing | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Transit peptide | 1 – 40 | 40 | Mitochondrion | ||||||
| Chain | 41 – 215 | 175 | ATP synthase subunit s, mitochondrial | PRO_0000002538 | |||||
Regions | |||||||||
| Repeat | 77 – 102 | 26 | LRR 1 | ||||||
| Repeat | 103 – 131 | 29 | LRR 2 | ||||||
| Repeat | 132 – 156 | 25 | LRR 3 | ||||||
| Repeat | 157 – 188 | 32 | LRR 4 | ||||||
| Region | 1 – 76 | 76 | N-terminal domain | ||||||
Sites | |||||||||
| Metal binding | 74 | 1 | Magnesium; via carbonyl oxygen By similarity | ||||||
| Metal binding | 108 | 1 | Magnesium By similarity | ||||||
Natural variations | |||||||||
| Alternative sequence | 121 – 136 | 16 | EGLEH…CKCHY → GNYPIVLLIENADDLQ in isoform 2. | VSP_040059 | |||||
| Alternative sequence | 122 – 127 | 6 | GLEHVE → TSNICC in isoform 3. | VSP_040060 | |||||
| Alternative sequence | 128 – 215 | 88 | Missing in isoform 3. | VSP_040061 | |||||
| Alternative sequence | 137 – 215 | 79 | Missing in isoform 2. | VSP_040062 | |||||
| Natural variant | 18 | 1 | P → L. Ref.1 Ref.2 Ref.3 Ref.5 Ref.6 Corresponds to variant rs2275592 [ dbSNP | Ensembl ]. | VAR_060296 | |||||
Sequences
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References
| « Hide 'large scale' references | |
| [1] | "Large-scale concatenation cDNA sequencing." Yu W., Andersson B., Worley K.C., Muzny D.M., Ding Y., Liu W., Ricafrente J.Y., Wentland M.A., Lennon G., Gibbs R.A. Genome Res. 7:353-358(1997) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 2), VARIANT LEU-18. Tissue: Brain. |
| [2] | "Factor B and the mitochondrial ATP synthase complex." Belogrudov G.I., Hatefi Y. J. Biol. Chem. 277:6097-6103(2002) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM 1), PARTIAL PROTEIN SEQUENCE, SUBUNIT, VARIANT LEU-18. |
| [3] | "Complete sequencing and characterization of 21,243 full-length human cDNAs." Ota T., Suzuki Y., Nishikawa T., Otsuki T., Sugiyama T., Irie R., Wakamatsu A., Hayashi K., Sato H., Nagai K., Kimura K., Makita H., Sekine M., Obayashi M., Nishi T., Shibahara T., Tanaka T., Ishii S. Sugano S.Nat. Genet. 36:40-45(2004) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 1), VARIANT LEU-18. Tissue: Hippocampus. |
| [4] | "The DNA sequence and analysis of human chromosome 14." Heilig R., Eckenberg R., Petit J.-L., Fonknechten N., Da Silva C., Cattolico L., Levy M., Barbe V., De Berardinis V., Ureta-Vidal A., Pelletier E., Vico V., Anthouard V., Rowen L., Madan A., Qin S., Sun H., Du H. Weissenbach J.Nature 421:601-607(2003) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA]. |
| [5] | Mural R.J., Istrail S., Sutton G.G., Florea L., Halpern A.L., Mobarry C.M., Lippert R., Walenz B., Shatkay H., Dew I., Miller J.R., Flanigan M.J., Edwards N.J., Bolanos R., Fasulo D., Halldorsson B.V., Hannenhalli S., Turner R. Venter J.C.Submitted (SEP-2005) to the EMBL/GenBank/DDBJ databases Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA], VARIANT LEU-18. |
| [6] | "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)." The MGC Project Team Genome Res. 14:2121-2127(2004) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 3), VARIANT LEU-18. Tissue: Uterus. |
| [7] | "Initial characterization of the human central proteome." Burkard T.R., Planyavsky M., Kaupe I., Breitwieser F.P., Buerckstuemmer T., Bennett K.L., Superti-Furga G., Colinge J. BMC Syst. Biol. 5:17-17(2011) [PubMed] [Europe PMC] [Abstract] Cited for: IDENTIFICATION BY MASS SPECTROMETRY [LARGE SCALE ANALYSIS]. |
| + | Additional computationally mapped references. |
Cross-references
Sequence databases | |
|---|---|
| EMBL GenBank DDBJ | U79253 mRNA. Translation: AAB50202.1. AY052377 mRNA. Translation: AAL13058.1. AK290008 mRNA. Translation: BAF82697.1. AL359397 Genomic DNA. No translation available. CH471078 Genomic DNA. Translation: EAW65718.1. CH471078 Genomic DNA. Translation: EAW65722.1. BC011549 mRNA. Translation: AAH11549.1. |
| IPI | IPI00017816. IPI00257300. IPI00455157. |
| RefSeq | NP_001003803.1. NM_001003803.2. NP_001003805.1. NM_001003805.2. NP_056499.2. NM_015684.3. |
| UniGene | Hs.438489. |
3D structure databases | |
| ProteinModelPortal | Q99766. |
| SMR | Q99766. Positions 41-215. |
| ModBase | Search... |
Protein-protein interaction databases | |
| IntAct | Q99766. 1 interaction. |
| STRING | 9606.ENSP00000308334. |
PTM databases | |
| PhosphoSite | Q99766. |
Polymorphism databases | |
| DMDM | 20532387. |
Proteomic databases | |
| PaxDb | Q99766. |
| PRIDE | Q99766. |
Protocols and materials databases | |
| StructuralBiologyKnowledgebase | Search... |
Genome annotation databases | |
| Ensembl | ENST00000245448; ENSP00000245448; ENSG00000125375. ENST00000311459; ENSP00000308334; ENSG00000125375. ENST00000426751; ENSP00000389246; ENSG00000125375. |
| GeneID | 27109. |
| KEGG | hsa:27109. |
| UCSC | uc001wxv.3. human. uc001wxw.2. human. uc001wxx.2. human. |
Organism-specific databases | |
| CTD | 27109. |
| GeneCards | GC14P050782. |
| HGNC | HGNC:18799. ATP5S. |
| HPA | HPA046967. |
| neXtProt | NX_Q99766. |
| GenAtlas | Search... |
Phylogenomic databases | |
| eggNOG | NOG307162. |
| HOGENOM | HOG000230741. |
| HOVERGEN | HBG050615. |
| KO | K07554. |
| OMA | TESCIMY. |
| OrthoDB | EOG4SXNDG. |
Gene expression databases | |
| ArrayExpress | Q99766. |
| Bgee | Q99766. |
| CleanEx | HS_ATP5S. |
| Genevestigator | Q99766. |
| GermOnline | ENSG00000125375. Homo sapiens. |
Family and domain databases | |
| InterPro | IPR026063. ATP_synthase_s. [Graphical view] |
| PANTHER | PTHR13382. PTHR13382. 1 hit. |
| PROSITE | PS51450. LRR. False negative. [Graphical view] |
| ProtoNet | Search... |
Other | |
| ChiTaRS | ATP5S. human. |
| GenomeRNAi | 27109. |
| NextBio | 49778. |
Entry information
| Entry name | ATP5S_HUMAN | ||||||||
| Accession | Primary (citable) accession number: Q99766 Secondary accession number(s): A8K1U3 Q96F77 | ||||||||
| Entry history |
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| Entry status | Reviewed (UniProtKB/Swiss-Prot) | ||||||||
| Annotation program | Chordata Protein Annotation Program | ||||||||
| Disclaimer | Any medical or genetic information present in this entry is provided for research, educational and informational purposes only. It is not in any way intended to be used as a substitute for professional medical advice, diagnosis, treatment or care. | ||||||||
Relevant documents
| Human chromosome 14 Human chromosome 14: entries, gene names and cross-references to MIM |
| Human entries with polymorphisms or disease mutations List of human entries with polymorphisms or disease mutations |
| Human polymorphisms and disease mutations Index of human polymorphisms and disease mutations |
| SIMILARITY comments Index of protein domains and families |

Clusters with
