Q8IY50 (S35F3_HUMAN) Reviewed, UniProtKB/Swiss-Prot
Last modified
May 29, 2013.
Version 62.
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: Solute carrier family 35 member F3 | ||
| Gene names |
| ||
| 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 | 421 AA. |
| Sequence status | Complete. |
| Protein existence | Evidence at transcript level |
General annotation (Comments)
| Function | Putative solute transporter Potential. |
| Subcellular location | Membrane; Multi-pass membrane protein Potential. |
| Sequence similarities | Belongs to the SLC35F solute transporter family. |
Ontologies
| Keywords | |
|---|---|
| Biological process | Transport |
| Cellular component | Membrane |
| Coding sequence diversity | Alternative splicing Polymorphism |
| Domain | Transmembrane Transmembrane helix |
| Technical term | Complete proteome Reference proteome |
| Gene Ontology (GO) | |
| Biological_process | transport Inferred from electronic annotation. Source: UniProtKB-KW |
| Cellular_component | integral to membrane Inferred from electronic annotation. Source: UniProtKB-KW |
| Complete GO annotation... | |
Alternative products
| This entry describes 2 isoforms produced by alternative splicing. [Align] [Select] | ||||||
| Isoform 1 (identifier: Q8IY50-1) 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: Q8IY50-2) The sequence of this isoform differs from the canonical sequence as follows: 1-26: MKKHSARVAPLSACNSPVLTLTKVEG → MGIREFPSGA...YQPWAASCKR | ||||||
| Note: No experimental confirmation available. |
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | Feature identifier | ||||
Molecule processing | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Chain | 1 – 421 | 421 | Solute carrier family 35 member F3 | PRO_0000307879 | |||||
Regions | |||||||||
| Transmembrane | 66 – 86 | 21 | Helical; Potential | ||||||
| Transmembrane | 98 – 118 | 21 | Helical; Potential | ||||||
| Transmembrane | 149 – 169 | 21 | Helical; Potential | ||||||
| Transmembrane | 179 – 199 | 21 | Helical; Potential | ||||||
| Transmembrane | 208 – 228 | 21 | Helical; Potential | ||||||
| Transmembrane | 232 – 252 | 21 | Helical; Potential | ||||||
| Transmembrane | 266 – 286 | 21 | Helical; Potential | ||||||
| Transmembrane | 305 – 325 | 21 | Helical; Potential | ||||||
| Transmembrane | 326 – 346 | 21 | Helical; Potential | ||||||
| Transmembrane | 352 – 372 | 21 | Helical; Potential | ||||||
Natural variations | |||||||||
| Alternative sequence | 1 – 26 | 26 | MKKHS…TKVEG → MGIREFPSGAPRGKSIAVGM RRSPDVSPRRLSDISPQLRQ LKYLVVDEAIKEDLKWSRSV EDLTSGPVGLTSIEERILRI TGYYGYQPWAASCKR in isoform 2. | VSP_028850 | |||||
| Natural variant | 231 | 1 | S → C. Ref.4 Corresponds to variant rs17853780 [ dbSNP | Ensembl ]. | VAR_036700 | |||||
Sequences
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References
Cross-references
Sequence databases | |
|---|---|
| EMBL GenBank DDBJ | AK095031 mRNA. Translation: BAC04479.1. AL713868, AL122008 Genomic DNA. Translation: CAI14569.1. AL122008, AL713868 Genomic DNA. Translation: CAI22849.1. AL122008 Genomic DNA. Translation: CAI22850.1. CH471098 Genomic DNA. Translation: EAW69991.1. BC037878 mRNA. Translation: AAH37878.1. |
| IPI | IPI00167687. IPI00395585. |
| RefSeq | NP_775779.1. NM_173508.2. |
| UniGene | Hs.158748. |
3D structure databases | |
| ProteinModelPortal | Q8IY50. |
| ModBase | Search... |
Protein-protein interaction databases | |
| MINT | MINT-4724984. |
| STRING | 9606.ENSP00000355577. |
Protein family/group databases | |
| TCDB | 2.A.7.24.8. drug/metabolite transporter (DMT) superfamily. |
PTM databases | |
| PhosphoSite | Q8IY50. |
Polymorphism databases | |
| DMDM | 160177558. |
Proteomic databases | |
| PaxDb | Q8IY50. |
| PRIDE | Q8IY50. |
Protocols and materials databases | |
| StructuralBiologyKnowledgebase | Search... |
Genome annotation databases | |
| Ensembl | ENST00000366617; ENSP00000355576; ENSG00000183780. ENST00000366618; ENSP00000355577; ENSG00000183780. |
| GeneID | 148641. |
| KEGG | hsa:148641. |
| UCSC | uc001hvy.1. human. uc001hwa.1. human. |
Organism-specific databases | |
| CTD | 148641. |
| GeneCards | GC01P234040. |
| HGNC | HGNC:23616. SLC35F3. |
| HPA | HPA051327. |
| neXtProt | NX_Q8IY50. |
| PharmGKB | PA134938022. |
| GenAtlas | Search... |
Phylogenomic databases | |
| eggNOG | NOG264574. |
| HOGENOM | HOG000060188. |
| HOVERGEN | HBG108446. |
| KO | K15288. |
| OMA | VGHVCKS. |
Gene expression databases | |
| Bgee | Q8IY50. |
| CleanEx | HS_SLC35F3. |
| Genevestigator | Q8IY50. |
Family and domain databases | |
| InterPro | IPR000620. DMT. IPR026505. Solute_c_fam_35_mem_F3/F4. [Graphical view] |
| PANTHER | PTHR19346. PTHR19346. 1 hit. |
| Pfam | PF00892. EamA. 1 hit. [Graphical view] |
| ProtoNet | Search... |
Other | |
| ChiTaRS | SLC35F3. human. |
| GenomeRNAi | 148641. |
| NextBio | 85960. |
Entry information
| Entry name | S35F3_HUMAN | ||||||||
| Accession | Primary (citable) accession number: Q8IY50 Secondary accession number(s): Q5TDD6, Q8N9C9 | ||||||||
| Entry history |
| ||||||||
| 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 1 Human chromosome 1: 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
