Homo sapiens Protein: FMN2
Summary
InnateDB Protein IDBP-107666.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol FMN2
Protein Name formin 2
Synonyms
Species Homo sapiens
Ensembl Protein ENSP00000318884
InnateDB Gene IDBG-107664 (FMN2)
Protein Structure
UniProt Annotation
Function Required for asymmetric spindle positioning, asymmetric oocyte division and polar body extrusion during female germ cell meiosis (By similarity). Actin-binding protein that is involved in actin cytoskeleton assembly and reorganization. Acts as an actin nucleation factor and promotes assembly of actin filaments together with SPIRE1 and SPIRE2. Involved in intracellular vesicle transport along actin fibers, providing a novel link between actin cytoskeleton dynamics and intracellular transport. Plays a role in responses to DNA damage, cellular stress and hypoxia by protecting CDKN1A against degradation, and thereby plays a role in stress- induced cell cycle arrest. Protects cells against apoptosis by protecting CDKN1A against degradation. {ECO:0000250, ECO:0000269PubMed:22330775, ECO:0000269PubMed:23375502}.
Subcellular Localization Cytoplasm, cytoskeleton. Cytoplasm, perinuclear region. Cytoplasm, cytosol. Cell membrane {ECO:0000250}; Peripheral membrane protein {ECO:0000250}; Cytoplasmic side {ECO:0000250}. Cytoplasmic vesicle membrane {ECO:0000250}; Peripheral membrane protein {ECO:0000250}; Cytoplasmic side {ECO:0000250}. Cytoplasm, cell cortex {ECO:0000250}. Nucleus, nucleolus. Note=Recruited to the membranes via its interaction with SPIRE1. Colocalizes with the actin cytoskeleton. Detected at the cleavage furrow during asymmetric oocyte division and polar body extrusion (By similarity). {ECO:0000250}.
Disease Associations
Tissue Specificity Expressed almost exclusively in the developing and mature central nervous system. {ECO:0000269PubMed:10781961}.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
Gene Ontology

Molecular Function
Accession GO Term
GO:0003674 molecular_function
GO:0003779 actin binding
Biological Process
GO:0006974 cellular response to DNA damage stimulus
GO:0007275 multicellular organismal development
GO:0015031 protein transport
GO:0016192 vesicle-mediated transport
GO:0016344 meiotic chromosome movement towards spindle pole
GO:0035556 intracellular signal transduction
GO:0040038 polar body extrusion after meiotic divisions
GO:0042177 negative regulation of protein catabolic process
GO:0043066 negative regulation of apoptotic process
GO:0046907 intracellular transport
GO:0048477 oogenesis
GO:0051017 actin filament bundle assembly
GO:0051295 establishment of meiotic spindle localization
GO:0051758 homologous chromosome movement towards spindle pole involved in homologous chromosome segregation
GO:0070649 formin-nucleated actin cable assembly
GO:0071456 cellular response to hypoxia
Cellular Component
GO:0005575 cellular_component
GO:0005730 nucleolus
GO:0005783 endoplasmic reticulum
GO:0005789 endoplasmic reticulum membrane
GO:0005819 spindle
GO:0005829 cytosol
GO:0005886 plasma membrane
GO:0005902 microvillus
GO:0005938 cell cortex
GO:0015629 actin cytoskeleton
GO:0030659 cytoplasmic vesicle membrane
GO:0048471 perinuclear region of cytoplasm
Protein Structure and Domains
PDB ID
InterPro IPR000591 DEP domain
IPR009408 Formin Homology 1
IPR015425 Formin, FH2 domain
PFAM PF00610
PF06346
PF02181
PRINTS
PIRSF
SMART SM00049
SM00498
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q9NZ56
PhosphoSite PhosphoSite-Q9NZ56
TrEMBL Q96L17
UniProt Splice Variant
Entrez Gene 56776
UniGene Hs.24889
RefSeq NP_064450
HUGO HGNC:14074
OMIM 606373
CCDS CCDS31069
HPRD 10449
IMGT
EMBL AB209153 AF218941 AF218942 AK297716 AL359918 AL513342 AL590490 AL646016 BC014364
GenPept AAF72884 AAF72885 AAH14364 BAD92390 BAG60071 CAQ08405 CAQ10135 CAQ10526 CAQ10976