P26442 (AMFR1_HUMAN) Reviewed, UniProtKB/Swiss-Prot
Last modified
January 25, 2012.
Version 89.
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: Autocrine motility factor receptor, isoform 1 Short name=AMF receptor, isoform 1 | ||
| Gene names |
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| Organism | Homo sapiens (Human) | ||
| Taxonomic identifier | 9606 [NCBI] | ||
| Taxonomic lineage | Eukaryota › Metazoa › Chordata › Craniata › Vertebrata › Euteleostomi › Mammalia › Eutheria › Euarchontoglires › Primates › Haplorrhini › Catarrhini › Hominidae › Homo |
Protein attributes
| Sequence length | 323 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 | Specific receptor for the autocrine motility factor. |
| Subcellular location | |
| Post-translational modification | Phosphorylated in the presence of AMF. O-glycosylated. |
Ontologies
| Keywords | |
|---|---|
| Cellular component | Membrane |
| Coding sequence diversity | Alternative splicing Polymorphism |
| Domain | Signal Transmembrane Transmembrane helix |
| Molecular function | Receptor |
| PTM | Glycoprotein Phosphoprotein |
| Technical term | Complete proteome Reference proteome |
| Gene Ontology (GO) | |
| Biological process | cellular component movement Traceable author statement. Source: ProtInc signal transductionTraceable author statement. Source: ProtInc |
| Cellular component | integral to membrane Non-traceable author statement Ref.1. Source: UniProtKB |
| Molecular function | receptor activity Inferred from physical interaction Ref.1. Source: UniProtKB |
| Complete GO annotation... | |
Alternative products
| This entry describes 2 isoforms produced by alternative splicing. [Align] [Select] | ||||||
| Isoform 1 (identifier: P26442-1) 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: Q9UKV5-1) The sequence of this isoform can be found in the external entry Q9UKV5. Isoforms of the same protein are often annotated in two different entries if their sequences differ significantly. |
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | Feature identifier | ||||
Molecule processing | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Signal peptide | 1 – 17 | 17 | Potential | ||||||
| Chain | 18 – 323 | 306 | Autocrine motility factor receptor, isoform 1 | PRO_0000020700 | |||||
Regions | |||||||||
| Topological domain | 18 – 110 | 93 | Extracellular Potential | ||||||
| Transmembrane | 111 – 137 | 27 | Helical; Potential | ||||||
| Topological domain | 138 – 323 | 186 | Cytoplasmic Potential | ||||||
Amino acid modifications | |||||||||
| Modified residue | 194 | 1 | Phosphoserine Potential | ||||||
| Glycosylation | 24 | 1 | N-linked (GlcNAc...) Potential | ||||||
Natural variations | |||||||||
| Natural variant | 181 | 1 | I → V. Corresponds to variant rs4924 [ dbSNP | Ensembl ]. | VAR_014809 | |||||
Sequences
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References
| [1] | "Purification of human tumor cell autocrine motility factor and molecular cloning of its receptor." Watanabe H., Carmi P., Hogan V., Raz T., Silletti S., Nabi I.R., Raz A. J. Biol. Chem. 266:13442-13448(1991) [PubMed: 1649192] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [MRNA]. |
| [2] | "Identification of an upstream region that controls the transcription of the human autocrine motility factor receptor." Huang B., Xie Y., Raz A. Biochem. Biophys. Res. Commun. 212:727-742(1995) [PubMed: 7626106] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [MRNA]. Tissue: Placenta. |
Cross-references
Sequence databases | |
|---|---|
| EMBL GenBank DDBJ | M63175 mRNA. Translation: AAA36671.1. L35233 mRNA. Translation: AAA79362.1. |
| IPI | IPI00435690. |
| PIR | A39877. |
| UniGene | Hs.295137. |
3D structure databases | |
| ModBase | Search... |
Protein-protein interaction databases | |
| IntAct | P26442. 6 interactions. |
| STRING | P26442. |
Polymorphism databases | |
| DMDM | 113707. |
Proteomic databases | |
| PRIDE | P26442. |
Protocols and materials databases | |
| StructuralBiologyKnowledgebase | Search... |
Genome annotation databases | |
| Ensembl | ENST00000314566; ENSP00000313137; ENSG00000159461. |
Organism-specific databases | |
| GeneCards | GC16M056447. |
| HGNC | HGNC:463. AMFR. |
| HPA | CAB026381. |
| MIM | 603243. gene. |
| neXtProt | NX_P26442. |
| GenAtlas | Search... |
Phylogenomic databases | |
| eggNOG | prNOG16152. |
| GeneTree | ENSGT00530000062938. |
Gene expression databases | |
| ArrayExpress | P26442. |
| Bgee | P26442. |
| CleanEx | HS_AMFR. |
| Genevestigator | P26442. |
| GermOnline | ENSG00000159461. Homo sapiens. |
Family and domain databases | |
| ProtoNet | Search... |
Other | |
| SOURCE | Search... |
Entry information
| Entry name | AMFR1_HUMAN | ||||||||
| Accession | Primary (citable) accession number: P26442 | ||||||||
| 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 16 Human chromosome 16: 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 |

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