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IID00992
UniprotQ8IVP5
ProteinFUN14 domain-containing protein 1
GeneFUNDC1
OrganismHomo sapiens
Sequence LLPS PhaSepDB
PhaSePro
LLPSDB
DrLLPS
Network xml rdf
Structure
Experiment
  :order   disorder   conflict   PDB cluster   ProS   Pfam Domain   SEG
155
 order/disorder by at least rule
     disorder by at least rule
     order by at least rule
 order/disorder by majority rule
Seq 10-26 Hetero dimer : IID00346Complex
 Evidence NMR 2n9x B Reference
       Region 2n9x B 10-26 order
       Region 2n9x B 10-10 high_rmsd
       Region 2n9x B 26-26 high_rmsd
Seq 16-23 Hetero dimer : IID00346Complex
 Evidence X-RAY 5gmv D Reference
       Region 5gmv D 16-23 order
 Evidence X-RAY 5gmv C Reference
       Region 5gmv C 16-23 order
SeqProS predicted 10-18 This region is predicted to be disordered by NeProc and AlphaFold (pLDDT < 68.5). Hetero dimer : IID00346Complex
       Region 2n9x B 10-26 order
SeqProS predicted 10-18 This region is predicted to be disordered by NeProc and AlphaFold (pLDDT < 68.5). Hetero dimer : IID00346Complex
       Region 5gmv C 16-23 order
       Region 5gmv D 16-23 order
Seqphosphorylation
    13-13 Phosphoserine; by CK2
    17-17 Phosphoserine; by ULK1
    18-18 Phosphotyrosine; by SRC
 
Prediction
NeProc
Disorder 1-18,67-72
Order 19-66,73-155
ProS 15-18,67-72
AlphaFold
Disorder 1-31,33-50,90-97
Order 32-32,51-89,98-155
SEG 144-153
Function
Function in SwissProt
Integral mitochondrial outer-membrane protein that mediates the formation of mitochondria-associated endoplasmic reticulum membranes (MAMs) (PubMed:33972548). In turn, mediates angiogenesis and neoangiogenesis through interference with intracellular Ca(2+) communication and regulation of the vascular endothelial growth factor receptor KDR/VEGFR2 expression at both mRNA and protein levels (PubMed:33972548). Acts also as an activator of hypoxia-induced mitophagy, an important mechanism for mitochondrial quality and homeostasis, by interacting with and recruiting LC3 protein family to mitochondria (PubMed:22267086, PubMed:24671035, PubMed:24746696, PubMed:27653272). Mechanistically, recruits DRP1 at ER-mitochondria contact sites leading to DRP1 oligomerization and GTPase activity to facilitate mitochondrial fission during hypoxia (PubMed:27145933, PubMed:33978709). Additionally, plays a role in hepatic ferroptosis by interacting directly with glutathione peroxidase/GPX4 to facilitate its recruitment into mitochondria through TOM/TIM complex where it is degraded by mitophagy (PubMed:36828120).
Biological Process
Diagram with PDB data
FUNDC1/MAP1LC3BLC3B-FUNDC1 complex