Anchoring of Coagulation factor VIIa to the membrane through its GLA domain
Vitamin K-dependent carboxylation/gamma-carboxyglutamic (GLA) domain is a protein domain that contains post-translational modifications of many glutamate residues by vitamin K-dependent carboxylation to form γ-carboxyglutamate (Gla). Proteins with this domain are known informally as Gla proteins. The Gla residues are responsible for the high-affinity binding of calcium ions.
The GLA domain binds calcium ions by chelating them between two carboxylic acid residues. These residues are part of a region that starts at the N-terminal extremity of the mature form of Gla proteins, and that ends with a conserved aromatic residue. This results in a conserved Gla-x(3)-Gla-x-Cys motif that is found in the middle of the domain, and which seems to be important for substrate recognition by the carboxylase.
The 3D structures of several Gla domains have been solved. Calcium ions induce conformational changes in the Gla domain and are necessary for the Gla domain to fold properly. A common structural feature of functional Gla domains is the clustering of N-terminal hydrophobic residues into a hydrophobic patch that mediates interaction with the cell surface membrane.
At present, the following human Gla-containing proteins (Gla proteins) have been characterized to the level of primary structure: the blood coagulation factors II (prothrombin), VII, IX, and X, the anticoagulant proteins C and S, and the factor X-targeting protein Z. The bone Gla protein osteocalcin, the calcification-inhibiting matrix Gla protein (MGP), the cell growth regulating "growth arrest specific gene 6" protein GAS6, periostin (a factor necessary for migration and adhesion of epithelial cells), two transmembrane Gla proteins (TMGPs), and two proline-rich Gla-proteins (PRGPs), the function of which at present are unknown.
In all cases in which their function was known, the presence of the Gla residues in these proteins turned out to be essential for functional activity.
Human proteins containing this domain
Only major, known functions are listed in this list; knowledge about these is not complete.
- Thrombin (F2) (a.k.a. coagulation factor II; also its precursor prothrombin) – involved in coagulation
- Factor VII (F7) – involved in coagulation
- Factor IX (F9) – involved in coagulation
- Factor X (F10) – involved in coagulation
- Protein C (PROC) – roles in regulating anticoagulation, inflammation, cell death, and maintaining the permeability of blood vessel walls
- Protein S (PROS1) – involved in coagulation
- Protein Z (PROZ) – involved in coagulation
- Osteocalcin (BGLAP) – involved in bone mineralization
- Matrix gla protein (MGP) – inhibitor of calcification of soft tissue and plays a role in bone organization
- GAS6 – thought to be involved in the stimulation of cell proliferation
- Transthyretin (TTR) previously known as prealbumin – carries thryroxine (T4) in blood and into cerebral spinal fluid
- Inter-alpha-trypsin inhibitor heavy chain H2 (ITIH2) – pays a role in pancreas islets and many other cells
- Periostin – a factor necessary for cell migration (embryonic development, and immune responses) and adhesion of epithelial cells, over-expressed in some cancers
- Proline rich gla 1 (PRRG1)
- Proline rich gla 2 (PRRG2)
- Proline rich gla 3 (PRRG3)
- Proline rich gla 4 (PRRG4)
- Friedman PA, Przysiecki CT (1987). "Vitamin K-dependent carboxylation". Int. J. Biochem. 19 (1): 1–7. doi:10.1016/0020-711X(87)90116-9. PMID 3106112.
- Vermeer C (1990). "Gamma-carboxyglutamate-containing proteins and the vitamin K-dependent carboxylase". Biochem. J. 266 (3): 625–636. PMC 1131186. PMID 2183788.
- Price PA, Fraser JD, Metz-Virca G (1987). "Molecular cloning of matrix Gla protein: implications for substrate recognition by the vitamin K-dependent gamma-carboxylase". Proc. Natl. Acad. Sci. U.S.A. 84 (23): 8335–8339. doi:10.1073/pnas.84.23.8335. PMC 299537. PMID 3317405.
- Freedman SJ, Furie BC, Furie B, Baleja JD (1995). "Structure of the metal-free gamma-carboxyglutamic acid-rich membrane binding region of factor IX by two-dimensional NMR spectroscopy". J. Biol. Chem. 270 (14): 7980–7987. doi:10.1074/jbc.270.14.7980. PMID 7713897.
- Freedman SJ, Furie BC, Furie B, Baleja JD, Blostein MD, Jacobs M (1996). "Identification of the phospholipid binding site in the vitamin K-dependent blood coagulation protein factor IX". J. Biol. Chem. 271 (27): 16227–16236. doi:10.1074/jbc.271.27.16227. PMID 8663165.
- Suttie, J.W. (1993-03-01). "Synthesis of vitamin K-dependent proteins". The FASEB Journal. The Federation of American Societies for Experimental Biology. Retrieved 2014-11-17.
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