Reviewed,
UniProtKB/Swiss-Prot P98196 (AT11A_HUMAN)
Last modified
October 13, 2009.
Version 82.
History...
Clusters with 100%,
90%,
50% identity |
Documents (5) |
Third-party data |
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Names and origin
| Protein names | Recommended name: Probable phospholipid-transporting ATPase IH EC=3.6.3.1 Alternative name(s): ATPase class VI type 11A ATPase IS | ||||
| Gene names |
| ||||
| Organism | Homo sapiens (Human) [Complete 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 | 1134 AA. |
| Sequence status | Complete. |
| Sequence processing | The displayed sequence is not processed. |
| Protein existence | Evidence at transcript level. |
General annotation (Comments)
| Catalytic activity | ATP + H2O + phospholipid(In) = ADP + phosphate + phospholipid(Out). |
| Subcellular location | |
| Sequence similarities | Belongs to the cation transport ATPase (P-type) family. Type IV subfamily. |
Ontologies
| Keywords | |
|---|---|
| Cellular component | Membrane |
| Coding sequence diversity | Polymorphism |
| Domain | Transmembrane |
| Ligand | ATP-binding Magnesium Metal-binding Nucleotide-binding |
| Molecular function | Hydrolase |
| PTM | Phosphoprotein |
| Technical term | Complete proteome |
| Gene Ontology (GO) | |
| Biological process | ATP biosynthetic process Inferred from electronic annotation. Source: InterPro phospholipid transportInferred from electronic annotation. Source: InterPro |
| Cellular component | integral to membrane Inferred from electronic annotation. Source: UniProtKB-SubCell |
| Molecular function | ATP binding Inferred from electronic annotation. Source: UniProtKB-KW ATPase activity, coupled to transmembrane movement of ions, phosphorylative mechanismInferred from electronic annotation. Source: InterPro magnesium ion bindingInferred from electronic annotation. Source: UniProtKB-KW phospholipid-translocating ATPase activityInferred from electronic annotation. Source: EC |
| Complete GO annotation... | |
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | Feature identifier | ||||
Molecule processing | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Chain | 1 – 1134 | 1134 | Probable phospholipid-transporting ATPase IH | PRO_0000046369 | |||||
Regions | |||||||||
| Topological domain | 1 – 61 | 61 | Cytoplasmic Potential | ||||||
| Transmembrane | 62 – 82 | 21 | Potential | ||||||
| Topological domain | 83 – 88 | 6 | Extracellular Potential | ||||||
| Transmembrane | 89 – 110 | 22 | Potential | ||||||
| Topological domain | 111 – 296 | 186 | Cytoplasmic Potential | ||||||
| Transmembrane | 297 – 318 | 22 | Potential | ||||||
| Topological domain | 319 – 349 | 31 | Extracellular Potential | ||||||
| Transmembrane | 350 – 372 | 23 | Potential | ||||||
| Topological domain | 373 – 881 | 509 | Cytoplasmic Potential | ||||||
| Transmembrane | 882 – 902 | 21 | Potential | ||||||
| Topological domain | 903 – 914 | 12 | Extracellular Potential | ||||||
| Transmembrane | 915 – 934 | 20 | Potential | ||||||
| Topological domain | 935 – 964 | 30 | Cytoplasmic Potential | ||||||
| Transmembrane | 965 – 986 | 22 | Potential | ||||||
| Topological domain | 987 – 1000 | 14 | Extracellular Potential | ||||||
| Transmembrane | 1001 – 1023 | 23 | Potential | ||||||
| Topological domain | 1024 – 1029 | 6 | Cytoplasmic Potential | ||||||
| Transmembrane | 1030 – 1050 | 21 | Potential | ||||||
| Topological domain | 1051 – 1068 | 18 | Extracellular Potential | ||||||
| Transmembrane | 1069 – 1093 | 25 | Potential | ||||||
| Topological domain | 1094 – 1134 | 41 | Cytoplasmic Potential | ||||||
Sites | |||||||||
| Active site | 414 | 1 | 4-aspartylphosphate intermediate By similarity | ||||||
| Metal binding | 825 | 1 | Magnesium By similarity | ||||||
| Metal binding | 829 | 1 | Magnesium By similarity | ||||||
Natural variations | |||||||||
| Natural variant | 317 | 1 | M → L: dbSNP rs368865. | VAR_059138 | |||||
| Natural variant | 317 | 1 | M → V: dbSNP rs368865. Ref.2 | VAR_059139 | |||||
| Natural variant | 1091 | 1 | V → I: dbSNP rs11616795. | VAR_048379 | |||||
Sequences
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References
| « Hide 'large scale' references | |
| [1] | "The DNA sequence and analysis of human chromosome 13." Dunham A., Matthews L.H., Burton J., Ashurst J.L., Howe K.L., Ashcroft K.J., Beare D.M., Burford D.C., Hunt S.E., Griffiths-Jones S., Jones M.C., Keenan S.J., Oliver K., Scott C.E., Ainscough R., Almeida J.P., Ambrose K.D., Andrews D.T. Ross M.T.Nature 428:522-528(2004) [PubMed: 15057823] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA]. |
| [2] | "Prediction of the coding sequences of unidentified human genes. XIV. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro." Kikuno R., Nagase T., Ishikawa K., Hirosawa M., Miyajima N., Tanaka A., Kotani H., Nomura N., Ohara O. DNA Res. 6:197-205(1999) [PubMed: 10470851] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] OF 33-1134, VARIANT VAL-317. Tissue: Brain. |
| [3] | Ohara O., Nagase T., Kikuno R. Submitted (AUG-2005) to the EMBL/GenBank/DDBJ databases Cited for: SEQUENCE REVISION. |
Cross-references
Sequence databases | |
|---|---|
| AL356740, AL139384, AL356752 Genomic DNA. Translation: CAH70242.1. AL139384, AL356740, AL356752 Genomic DNA. Translation: CAI16947.1. AL356752, AL356740, AL139384 Genomic DNA. Translation: CAI16578.1. AB028944 mRNA. Translation: BAA82973.2. | |
| IPI | IPI00255653. |
| RefSeq | NP_056020.2. NP_115565.3. |
| UniGene | Hs.29189 |
3D structure databases | |
| ModBase | Search... |
Protein-protein interaction databases | |
| STRING | P98196. |
Proteomic databases | |
| PRIDE | P98196. |
Genome annotation databases | |
| Ensembl | ENST00000283558; ENSP00000283558; ENSG00000068650; Homo sapiens. [Genome view] ENST00000375630; ENSP00000364781; ENSG00000068650; Homo sapiens. [Genome view] ENST00000375645; ENSP00000364796; ENSG00000068650; Homo sapiens. [Genome view] ENST00000415301; ENSP00000402575; ENSG00000068650; Homo sapiens. [Genome view] ENST00000418678; ENSP00000396374; ENSG00000068650; Homo sapiens. [Genome view] ENST00000419631; ENSP00000410824; ENSG00000068650; Homo sapiens. [Genome view] ENST00000423491; ENSP00000392036; ENSG00000068650; Homo sapiens. [Genome view] ENST00000431624; ENSP00000414418; ENSG00000068650; Homo sapiens. [Genome view] ENST00000432166; ENSP00000392971; ENSG00000068650; Homo sapiens. [Genome view] |
| GeneID | 23250. |
| KEGG | hsa:23250. |
| NMPDR | fig|9606.3.peg.9107. |
| UCSC | uc001vsi.2. human. |
Organism-specific databases | |
| CTD | 23250. |
| GeneCards | GC13P112393. |
| HGNC | HGNC:13552. ATP11A. |
| MIM | 605868. gene. |
| PharmGKB | PA25101. |
| HUGE | Search... |
| GenAtlas | Search... |
Phylogenomic databases | |
| HOVERGEN | P98196. |
Enzyme and pathway databases | |
| BRENDA | 3.6.3.1. 247. |
Gene expression databases | |
| ArrayExpress | P98196. |
| Bgee | P98196. |
| CleanEx | HS_ATP11A. |
| Genevestigator | P98196. |
| GermOnline | ENSG00000068650. Homo sapiens. |
Family and domain databases | |
| InterPro | IPR008250. ATPase_P-typ_ATPase-assoc-reg. IPR001757. ATPase_P-typ_ion-transptr. IPR018303. ATPase_P-typ_P_site. IPR006539. ATPase_P-typ_Plipid-transl. [Graphical view] |
| PANTHER | PTHR11939. ATPase_P. 1 hit. |
| Pfam | PF00122. E1-E2_ATPase. 1 hit. [Graphical view] |
| PRINTS | PR00119. CATATPASE. |
| TIGRFAMs | TIGR01652. ATPase-Plipid. 1 hit. TIGR01494. ATPase_P-type. 3 hits. |
| PROSITE | PS00154. ATPASE_E1_E2. 1 hit. [Graphical view] |
| ProtoNet | Search... |
Other Resources | |
| NextBio | 44946. |
| SOURCE | Search... |
Entry information
| Entry name | AT11A_HUMAN | ||||||||
| Accession | Primary (citable) accession number: P98196 Secondary accession number(s): Q5VXT2 | ||||||||
| Entry history |
| ||||||||
| Entry status | Reviewed (UniProtKB/Swiss-Prot) | ||||||||
| Annotation project | HPI (Human Proteome Initiative) | ||||||||
| 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 13 Human chromosome 13: 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 |
| MIM cross-references Online Mendelian Inheritance in Man (MIM) cross-references in UniProtKB/Swiss-Prot |
| SIMILARITY comments Index of protein domains and families |

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