Skip Header

Contribute Send feedback
Read comments (?) or add your own

P26442 (AMFR1_HUMAN) Reviewed, UniProtKB/Swiss-Prot

Last modified January 25, 2012. Version 89. Feed History...

Clusters with 100%, 90%, 50% identity | Documents (4) | Third-party data text xml rdf/xml gff fasta
to top of pageNames·Attributes·General annotation·Ontologies·Alt products·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize order

Names and origin

Protein namesRecommended name:
Autocrine motility factor receptor, isoform 1

Short name=AMF receptor, isoform 1
Gene names
Name:AMFR
OrganismHomo sapiens (Human)
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length323 AA.
Sequence statusComplete.
Sequence processingThe displayed sequence is further processed into a mature form.
Protein existenceEvidence at protein level

General annotation (Comments)

Function

Specific receptor for the autocrine motility factor.

Subcellular location

Membrane; Single-pass type I membrane protein.

Post-translational modification

Phosphorylated in the presence of AMF.

O-glycosylated.

Ontologies

Keywords
   Cellular componentMembrane
   Coding sequence diversityAlternative splicing
Polymorphism
   DomainSignal
Transmembrane
Transmembrane helix
   Molecular functionReceptor
   PTMGlycoprotein
Phosphoprotein
   Technical termComplete proteome
Reference proteome
Gene Ontology (GO)
   Biological processcellular component movement

Traceable author statement. Source: ProtInc

signal transduction

Traceable author statement. Source: ProtInc

   Cellular componentintegral to membrane

Non-traceable author statement Ref.1. Source: UniProtKB

   Molecular functionreceptor 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 keyPosition(s)LengthDescriptionGraphical viewFeature identifier

Molecule processing

Signal peptide1 – 1717 Potential
Chain18 – 323306Autocrine motility factor receptor, isoform 1
PRO_0000020700

Regions

Topological domain18 – 11093Extracellular Potential
Transmembrane111 – 13727Helical; Potential
Topological domain138 – 323186Cytoplasmic Potential

Amino acid modifications

Modified residue1941Phosphoserine Potential
Glycosylation241N-linked (GlcNAc...) Potential

Natural variations

Natural variant1811I → V.
Corresponds to variant rs4924 [ dbSNP | Ensembl ].
VAR_014809

Sequences

Sequence LengthMass (Da)Tools
Isoform 1 [UniParc].

Last modified August 1, 1992. Version 1.
Checksum: 0A7AF4DCF90A8700

FASTA32334,325
        10         20         30         40         50         60 
MRDSACWSQR KDELLQQARK RFLNKSSEDD AASESFLPSE GASSDPVTLR RRMLAAARNG 

        70         80         90        100        110        120 
GFRSSRPPSA PLPSSAASCA LCPTDWRRPV PILPLHGKAG LTALPLYKAC GLIVFGQLIN 

       130        140        150        160        170        180 
LILLCNTFYV TFLFPLETLQ ILTVGMISSG VDWTAWGGGR SGGSEPVACL QQAASTPASC 

       190        200        210        220        230        240 
IRPTNAGVLS TTPSGKSVGE AHSVSPPPRR GVTSVIKLLS LLWKHVDCAR ARPTGSCTPE 

       250        260        270        280        290        300 
QQGILEKELL VRYLEQRRGK SRAIGCDEVT PFCPTTSGTD FPSLQSKAGL ISVNSGAPAS 

       310        320 
HECAPWVPSP LSISLSRLDL GSG 

« Hide

Isoform 2 [UniParc].

See Q9UKV5.

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.
IPIIPI00435690.
PIRA39877.
UniGeneHs.295137.

3D structure databases

ModBaseSearch...

Protein-protein interaction databases

IntActP26442. 6 interactions.
STRINGP26442.

Polymorphism databases

DMDM113707.

Proteomic databases

PRIDEP26442.

Protocols and materials databases

StructuralBiologyKnowledgebaseSearch...

Genome annotation databases

EnsemblENST00000314566; ENSP00000313137; ENSG00000159461.

Organism-specific databases

GeneCardsGC16M056447.
HGNCHGNC:463. AMFR.
HPACAB026381.
MIM603243. gene.
neXtProtNX_P26442.
GenAtlasSearch...

Phylogenomic databases

eggNOGprNOG16152.
GeneTreeENSGT00530000062938.

Gene expression databases

ArrayExpressP26442.
BgeeP26442.
CleanExHS_AMFR.
GenevestigatorP26442.
GermOnlineENSG00000159461. Homo sapiens.

Family and domain databases

ProtoNetSearch...

Other

SOURCESearch...

Entry information

Entry nameAMFR1_HUMAN
AccessionPrimary (citable) accession number: P26442
Entry history
Integrated into UniProtKB/Swiss-Prot: August 1, 1992
Last sequence update: August 1, 1992
Last modified: January 25, 2012
This is version 89 of the entry and version 1 of the sequence. [Complete history]
Entry statusReviewed (UniProtKB/Swiss-Prot)
Annotation programChordata Protein Annotation Program
DisclaimerAny 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