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Caspase-activated DNase

DFFB
Protein DFFB PDB 1ibx.png
Available structures
PDB Ortholog search: PDBe RCSB
Identifiers
Aliases DFFB, DNA fragmentation factor, 40kDa, beta polypeptide (caspase-activated DNase), CAD, CPAN, DFF-40, DFF2, DFF40, DNA fragmentation factor subunit beta
External IDs MGI: 1196287 HomoloGene: 3241 GeneCards: DFFB
RNA expression pattern
PBB GE DFFB 206752 s at fs.png
More reference expression data
Orthologs
Species Human Mouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_007859

RefSeq (protein)

NP_001269598
NP_001307061
NP_001307065
NP_004393

NP_031885.3
NP_031885

Location (UCSC) Chr 1: 3.86 – 3.89 Mb Chr 4: 153.96 – 153.98 Mb
PubMed search
DNA fragmentation factor 40 kDa
PDB 1v0d EBI.jpg
crystal structure of caspase-activated dnase (cad)
Identifiers
Symbol DFF40
Pfam PF09230
InterPro IPR015311
SCOP 1v0d
SUPERFAMILY 1v0d

1IBX

NM_001320136

NM_007859

NP_001269598
NP_001307061
NP_001307065
NP_004393

NP_031885.3
NP_031885

Caspase-Activated DNase (CAD) or DNA fragmentation factor subunit beta is a protein that in humans is encoded by the DFFB gene. It breaks up the DNA during apoptosis and promotes cell differentiation. It is usually an inactive monomer inhibited by ICAD. This is cleaved before dimerization.

Apoptosis is a cell death process that removes toxic and/or useless cells during mammalian development. The apoptotic process is accompanied by shrinkage and fragmentation of the cells and nuclei and degradation of the chromosomal DNA into nucleosomal units. DNA fragmentation factor (DFF) is a heterodimeric protein of 40-kD (DFFB) and 45-kD (DFFA) subunits. DFFA is the substrate for caspase-3 and triggers DNA fragmentation during apoptosis. DFF becomes activated when DFFA is cleaved by caspase-3. The cleaved fragments of DFFA dissociate from DFFB, the active component of DFF. DFFB has been found to trigger both DNA fragmentation and chromatin condensation during apoptosis. Multiple alternatively spliced transcript variants encoding distinct isoforms have been found for this gene, but the biological validity of some variants has not been determined.


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