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ChemicalBook--->CAS DataBase List--->143180-74-9

143180-74-9

143180-74-9 Structure

143180-74-9 Structure
IdentificationBack Directory
[Name]

GRANZYME B
[CAS]

143180-74-9
[Synonyms]

GZMB
GRANZYME B
EC 3.4.21.79
GRANZYME B ENZYME
GRANZYME B (HUMAN)
Granzyme B from mouse
Granzyme B from Human, Recombinant
Granzyme B from Mouse, Recombinant
Recombinant Mouse Gzmb Protein, His Tag
GRANZYME B, HUMAN, CELL CULTURE-DERIVED
SensiZyme Granzyme B Activity Assay Kit
[MDL Number]

MFCD01323415
Chemical PropertiesBack Directory
[storage temp. ]

-70°C
[form ]

buffered aqueous solution
Safety DataBack Directory
[Risk Statements ]

42/43
[Safety Statements ]

26-36
[WGK Germany ]

-
Hazard InformationBack Directory
[General Description]

Granzyme B, a 247 amino acid polypeptide, contains a leader sequence, which is cleaved by a signal peptidase and a two amino acid prodomain, which is cleaved by the lysosomal cysteine protease DPPI. The recombinant granzyme B is expressed in Pichia pastoris as the mature form and appears on SDS-PAGE as a triplet (~34, 32, and 30 kDa) due to three different glycosylations.
[Biochem/physiol Actions]

Cytotoxic granules secreted by natural killer (NK) cells and cytotoxic T Lymphocytes cells are part of the mechanism used for protecting the organism from virus infected and tumor cells. Granzyme B, a serine protease, is the most prominent granzyme in a family of 11 found in the cytotoxic granules. The granzymes enter the target cell with the assistance of perforin, a critical molecule of the cytotoxic granules. In the target cell, the granzymes act on specific substrates involved with the cell death via apoptosis.Granzyme B is a neutral serine protease that cleaves aspartic acid residues, inducing cell death by various pathways. It can cleave and activate most of the caspases in vitro and in vivo resulting in a massive amplification of the caspase dependent apoptotic pathway. In addition, granzyme B cleaves directly downstream caspase substrates as PARP DNA-PK2 and DFF45/ICAD leading to cell death. This pathway bypasses inhibition of apoptosis by viral caspase inhibitors found in virus infected cells. It has been shown that granzyme B is capable of inducing cytochrome C release from the mitochondria in a caspase independent way.
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