FNBP1
Sign in to saveAlso known as FBP17, formin binding protein 1
Formin-binding protein 1 is a protein that in humans is encoded by the FNBP1 gene.
Gene data
FNBP1- Name
- formin binding protein 1
- Type
- protein-coding
- Position
- 129,887,179–130,043,243 (−)
- Aliases
- FBP17
- Ensembl
- ENSG00000187239
- RefSeq RNA
- NM_001363755.1, NM_001411018.1, NM_001438006.1, NM_001438159.1, NM_001438160.1
- RefSeq protein
- NP_001350684.1, NP_001397947.1, NP_001424935.1, NP_001425088.1, NP_001425089.1
The protein encoded by this gene is a member of the formin-binding-protein family. The protein contains an N-terminal Fer/Cdc42-interacting protein 4 (CIP4) homology (FCH) domain followed by a coiled-coil domain, a proline-rich motif, a second coiled-coil domain, a Rho family protein-binding domain (RBD), and a C-terminal SH3 domain. This protein binds sorting nexin 2 (SNX2), tankyrase (TNKS), and dynamin; an interaction between this protein and formin has not been demonstrated yet in human. [provided by RefSeq, Jul 2008].
Gene Ontology
Biological process
Molecular function
Pathways
via MyGene.info
Gene · Ensembl
formin binding protein 1
- Symbol
- FNBP1
- Biotype
- Protein coding
- Organism
- Homo sapiens
- Location
- 9:129,887,179-130,043,243
- Strand
- Reverse (−)
- Assembly
- GRCh38
via Ensembl · EMBL-EBI
Wikidata facts
- Instance of
- gene
- Image
- Protein FNBP1 PDB 2efl.png
Show 8 more facts
- HomoloGene ID
- 100983
- found in taxon
- Homo sapiens
- exact match
- identifiers.org/ncbigene/23048
- genomic end
- 132805473
- genomic start
- 132649466
- chromosome
- human chromosome 9
- cytogenetic location
- 9q34.11
- expressed in
- sural nerve
Sources (3)
via Wikidata · CC0
~1 min read
Encyclopedic overview
4 sectionsContents
- Function
- Interactions
- References
- Further reading
Formin-binding protein 1 is a protein that in humans is encoded by the FNBP1 gene.
== Function ==
Excerpted from Wikipedia’s “FNBP1” article, available under the CC BY-SA 4.0 licence.