Bcl-2

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Bcl-2
Bcl-2
Structure according to PDB  1G5M

Existing structural data: 1g5m, 2o2f

Properties of human protein
Mass / length primary structure 239 aa; 26.3 kDa
Secondary to quaternary structure Homodimer; Heterodimer
Isoforms Alpha, beta
Identifier
Gene names BCL-2  ; BCL2
External IDs
Occurrence
Parent taxon Euteleostomi
Orthologue
human mouse
Entrez 596 12043
Ensemble ENSG00000171791 ENSMUSG00000057329
UniProt P10415 Q4VBF6
Refseq (mRNA) NM_000633 NM_009741
Refseq (protein) NP_000624 NP_033871
Gene locus Chr 18: 58.94 - 59.14 Mb Chr 1: 108.37 - 108.54 Mb
PubMed search 596 12043

Bcl-2 (abbreviation for B-cell lymphoma 2 ) is a protein and the prototype of the protein family of the same name, which play a role in the regulation of programmed cell death ( apoptosis ). Some members of the family encourage apoptosis while others prevent it. It is believed that at least some of these proteins perform their function by regulating the release of cytochrome c from the mitochondrion by destabilizing or stabilizing the outer mitochondrial membrane. The destabilization of the outer mitochondrial membrane has a proapoptotic effect through the transfer of cytochrome c into the cell cytoplasm, the stabilization of the outer mitochondrial membrane an antiapoptotic effect. In addition, some of these proteins are likely to be involved in activating the procaspases .

Since the correct initiation of apoptosis is very important, a mutation in the genes of these proteins can have serious consequences. This is why this family of proteins is also considered a human proto- oncogene .

Overactivation leads to tissue proliferation and thus to tumors . The protein was first in B cells - Lymphoma isolated (BCL).

Members of the Bcl-2 family.
Bcl-2 family proteins
Anti-apoptotic effect
  • Bcl-2
  • Bcl-xL
Pro-apoptotic effect

Bcl-2 inhibitors such as venetoclax are used in the therapy of B-cell lymphomas .

Individual evidence

  1. Chao, DT & Korsmeyer, SJ (1998): BCL-2 family: regulators of cell death. In: Annu. Rev. Immunol. Vol. 16, pp. 395-419. PMID 9597135