SLX4 Regulatory subunit that interacts with and increases the activity of different structure-specific endonucleases. Has several distinct roles in protecting genome stability by resolving diverse forms of deleterious DNA structures originating from replication and recombination intermediates and from DNA damage. Component of the SLX1-SLX4 structure-specific endonuclease that resolves DNA secondary structures generated during DNA repair and recombination. Has endonuclease activity towards branched DNA substrates, introducing single-strand cuts in duplex DNA close to junctions with ss-DNA. Has a preference for 5'-flap structures, and promotes symmetrical cleavage of static and migrating Holliday junctions (HJs). Resolves HJs by generating two pairs of ligatable, nicked duplex products. Interacts with the structure-specific ERCC4-ERCC1 endonuclease and promotes the cleavage of bubble structures. Interacts with the structure-specific MUS81-EME1 endonuclease and promotes the cleavage of 3'-flap and replication fork-like structures. SLX4 is required for recovery from alkylation-induced DNA damage and is involved in the resolution of DNA double-strand breaks. Belongs to the SLX4 family. 2 alternatively spliced human isoforms have been reported. Note: This description may include information from UniProtKB.
Protein type: DNA repair, damage; Deoxyribonuclease
Chromosomal Location of human Ortholog: 16p13.3
Cellular Component:  cell junction; chromosome, telomeric region; cytosol; nucleoplasm; Slx1-Slx4 complex
Molecular Function:  DNA binding; enzyme activator activity; metal ion binding; protein binding
Biological Process:  DNA double-strand break processing involved in repair via single-strand annealing; DNA repair; DNA replication; double-strand break repair via homologous recombination; negative regulation of telomere maintenance via telomere lengthening; nucleotide-excision repair; positive regulation of t-circle formation; positive regulation of telomere maintenance; resolution of meiotic recombination intermediates; response to intra-S DNA damage checkpoint signaling; t-circle formation; telomeric D-loop disassembly
Disease: Fanconi Anemia, Complementation Group P
Reference #:  Q8IY92 (UniProtKB)
Alt. Names/Synonyms: BTB (POZ) domain containing 12; BTB/POZ domain-containing protein 12; BTBD12; FANCP; KIAA1784; KIAA1987; MUS312; SLX4; SLX4 structure-specific endonuclease subunit; Structure-specific endonuclease subunit SLX4
Gene Symbols: SLX4
Molecular weight: 200,012 Da
Basal Isoelectric point: 5.74  Predict pI for various phosphorylation states
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SLX4

Protein Structure Not Found.


Cross-references to other databases:  AlphaFold  |  STRING  |  cBioPortal  |  Wikipedia  |  Protein Atlas  |  BioGPS  |  Pfam  |  RCSB PDB  |  Phospho.ELM  |  UniProtKB  |  Entrez-Gene  |  GenPept  |  Ensembl Gene  |  InnateDB  |  Ensembl Protein