Q8N1S5 (S39AB_HUMAN) Reviewed, UniProtKB/Swiss-Prot
Last modified
April 3, 2013.
Version 71.
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: Zinc transporter ZIP11 Alternative name(s): Solute carrier family 39 member 11 Zrt- and Irt-like protein 11 Short name=ZIP-11 | ||||
| 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 | 342 AA. |
| Sequence status | Complete. |
| Protein existence | Evidence at transcript level |
General annotation (Comments)
| Function | May act as a zinc-influx transporter By similarity. |
| Subcellular location | Membrane; Multi-pass membrane protein Potential. |
| Sequence similarities | Belongs to the ZIP transporter (TC 2.A.5) family. [View classification] |
Ontologies
| Keywords | |
|---|---|
| Biological process | Ion transport Transport Zinc transport |
| Cellular component | Membrane |
| Coding sequence diversity | Alternative splicing Polymorphism |
| Domain | Transmembrane Transmembrane helix |
| Ligand | Zinc |
| Technical term | Complete proteome Reference proteome |
| Gene Ontology (GO) | |
| Biological_process | zinc ion transport Inferred from electronic annotation. Source: UniProtKB-KW |
| Cellular_component | integral to membrane Inferred from electronic annotation. Source: UniProtKB-KW |
| Molecular_function | metal ion transmembrane transporter activity Inferred from electronic annotation. Source: InterPro |
| Complete GO annotation... | |
Alternative products
| This entry describes 2 isoforms produced by alternative splicing. [Align] [Select] | ||||||
| Isoform 1 (identifier: Q8N1S5-1) 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: Q8N1S5-2) The sequence of this isoform differs from the canonical sequence as follows: 144-150: Missing. |
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | Feature identifier | ||||
Molecule processing | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Chain | 1 – 342 | 342 | Zinc transporter ZIP11 | PRO_0000308410 | |||||
Regions | |||||||||
| Transmembrane | 12 – 32 | 21 | Helical; Potential | ||||||
| Transmembrane | 44 – 64 | 21 | Helical; Potential | ||||||
| Transmembrane | 72 – 92 | 21 | Helical; Potential | ||||||
| Transmembrane | 194 – 214 | 21 | Helical; Potential | ||||||
| Transmembrane | 263 – 285 | 23 | Helical; Potential | ||||||
| Transmembrane | 290 – 307 | 18 | Helical; Potential | ||||||
| Transmembrane | 322 – 342 | 21 | Helical; Potential | ||||||
Natural variations | |||||||||
| Alternative sequence | 144 – 150 | 7 | Missing in isoform 2. | VSP_028976 | |||||
| Natural variant | 111 | 1 | T → A. Ref.1 Ref.2 Ref.4 Ref.5 Corresponds to variant rs2466517 [ dbSNP | Ensembl ]. | VAR_036812 | |||||
Experimental info | |||||||||
| Sequence conflict | 113 | 1 | A → T in BAC04504. Ref.2 | ||||||
Sequences
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References
| « Hide 'large scale' references | |
| [1] | "Comparative genomics of the SOX9 region in human and Fugu rubripes: conservation of short regulatory sequence elements within large intergenic regions." Bagheri-Fam S., Ferraz C., Demaille J., Scherer G., Pfeifer D. Genomics 78:73-82(2001) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM 2), VARIANT ALA-111. |
| [2] | "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] (ISOFORMS 1 AND 2), VARIANT ALA-111. Tissue: Kidney and Tongue. |
| [3] | "DNA sequence of human chromosome 17 and analysis of rearrangement in the human lineage." Zody M.C., Garber M., Adams D.J., Sharpe T., Harrow J., Lupski J.R., Nicholson C., Searle S.M., Wilming L., Young S.K., Abouelleil A., Allen N.R., Bi W., Bloom T., Borowsky M.L., Bugalter B.E., Butler J., Chang J.L. Nusbaum C.Nature 440:1045-1049(2006) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA]. |
| [4] | 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 (JUL-2005) to the EMBL/GenBank/DDBJ databases Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA], VARIANT ALA-111. |
| [5] | "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 2), VARIANT ALA-111. Tissue: Blood. |
| + | Additional computationally mapped references. |
Cross-references
Sequence databases | |
|---|---|
| EMBL GenBank DDBJ | AF331643 mRNA. Translation: AAL32175.1. AK095227 mRNA. Translation: BAC04504.1. AK313376 mRNA. Translation: BAG36174.1. AC011120 Genomic DNA. No translation available. AC025198 Genomic DNA. No translation available. AC080037 Genomic DNA. No translation available. AC138336 Genomic DNA. No translation available. CH471099 Genomic DNA. Translation: EAW89107.1. BC035631 mRNA. Translation: AAH35631.1. |
| IPI | IPI00410249. IPI00477112. |
| RefSeq | NP_001153242.1. NM_001159770.1. NP_631916.2. NM_139177.3. |
| UniGene | Hs.221127. |
3D structure databases | |
| ProteinModelPortal | Q8N1S5. |
| ModBase | Search... |
Protein-protein interaction databases | |
| STRING | 9606.ENSP00000255559. |
PTM databases | |
| PhosphoSite | Q8N1S5. |
Polymorphism databases | |
| DMDM | 160177555. |
Proteomic databases | |
| PaxDb | Q8N1S5. |
| PRIDE | Q8N1S5. |
Protocols and materials databases | |
| StructuralBiologyKnowledgebase | Search... |
Genome annotation databases | |
| Ensembl | ENST00000255559; ENSP00000255559; ENSG00000133195. ENST00000542342; ENSP00000445829; ENSG00000133195. |
| GeneID | 201266. |
| KEGG | hsa:201266. |
| UCSC | uc002jja.3. human. uc002jjb.3. human. |
Organism-specific databases | |
| CTD | 201266. |
| GeneCards | GC17M070644. |
| H-InvDB | HIX0014131. |
| HGNC | HGNC:14463. SLC39A11. |
| neXtProt | NX_Q8N1S5. |
| PharmGKB | PA25581. |
| GenAtlas | Search... |
Phylogenomic databases | |
| eggNOG | COG0428. |
| HOGENOM | HOG000232703. |
| HOVERGEN | HBG108448. |
| InParanoid | Q8N1S5. |
| KO | K14717. |
| OMA | KTSWQRS. |
| OrthoDB | EOG44TP8M. |
Gene expression databases | |
| Bgee | Q8N1S5. |
| CleanEx | HS_SLC39A11. |
| Genevestigator | Q8N1S5. |
Family and domain databases | |
| InterPro | IPR003689. ZIP. [Graphical view] |
| Pfam | PF02535. Zip. 1 hit. [Graphical view] |
| ProtoNet | Search... |
Other | |
| ChiTaRS | SLC39A11. human. |
| GenomeRNAi | 201266. |
| NextBio | 90114. |
Entry information
| Entry name | S39AB_HUMAN | ||||||||
| Accession | Primary (citable) accession number: Q8N1S5 Secondary accession number(s): B2R8H7, Q8WZ81 | ||||||||
| 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 17 Human chromosome 17: 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
