|
|
| Line 1: |
Line 1: |
| {{DISPLAYTITLE:Enamelin}}
| |
| {{Infobox protein
| |
| | name = Enamelin
| |
| | image =
| |
| | caption =
| |
| | width =
| |
| | symbol = ENAM
| |
| | alt_symbols =
| |
| | EntrezGene = 10117
| |
| | HGNCid = 3341
| |
| | OMIM = 606585
| |
| | RefSeq = NM_031889
| |
| | UniProt = Q9NRM1
| |
| | PDB =
| |
| }}
| |
|
| |
| ==Overview==
| |
| '''Enamelin''' is a critical [[protein]] involved in the formation of [[dental enamel]], the hard outer layer of [[teeth]]. It is one of the largest enamel matrix proteins and plays a crucial role in the mineralization process during [[amelogenesis]]. | | '''Enamelin''' is a critical [[protein]] involved in the formation of [[dental enamel]], the hard outer layer of [[teeth]]. It is one of the largest enamel matrix proteins and plays a crucial role in the mineralization process during [[amelogenesis]]. |
|
| |
|
| Line 38: |
Line 21: |
| * [[Ameloblastin]] | | * [[Ameloblastin]] |
| * [[Hydroxyapatite]] | | * [[Hydroxyapatite]] |
|
| |
| ==References==
| |
| * Hu, J. C., & Simmer, J. P. (2007). Developmental biology and genetics of dental enamel. In: "Principles of Bone Biology". Academic Press.
| |
| * Wright, J. T., & Hart, P. S. (2002). The genetics of enamel development. In: "Connective Tissue and Its Heritable Disorders". Wiley-Liss.
| |
|
| |
| ==External Links== | | ==External Links== |
| * [https://www.ncbi.nlm.nih.gov/gene/10117 ENAM gene - NCBI] | | * [https://www.ncbi.nlm.nih.gov/gene/10117 ENAM gene - NCBI] |
| * [https://www.uniprot.org/uniprot/Q9NRM1 Enamelin - UniProt] | | * [https://www.uniprot.org/uniprot/Q9NRM1 Enamelin - UniProt] |
|
| |
| [[Category:Proteins]]
| |
| [[Category:Dental enamel]]
| |
| [[Category:Genetic disorders]]
| |
| [[Category:Developmental biology]]
| |
| {{DISPLAYTITLE:Enamelin}}
| |
| {{Infobox protein
| |
| | name = Enamelin
| |
| | image =
| |
| | caption =
| |
| | width =
| |
| | symbol = ENAM
| |
| | alt_symbols =
| |
| | EntrezGene = 10117
| |
| | HGNCid = 3341
| |
| | OMIM = 606585
| |
| | RefSeq = NM_031889
| |
| | UniProt = Q9NRM1
| |
| | PDB =
| |
| }}
| |
|
| |
| ==Overview==
| |
| '''Enamelin''' is a critical [[protein]] involved in the formation of [[dental enamel]], the hard outer layer of [[teeth]]. It is one of the largest enamel matrix proteins and plays a crucial role in the mineralization process during [[amelogenesis]].
| |
|
| |
| ==Structure==
| |
| Enamelin is a large glycoprotein, initially synthesized as a precursor protein that undergoes extensive post-translational modifications. The protein is rich in [[proline]], [[glutamine]], and [[leucine]] residues, which contribute to its unique structure and function. Enamelin is secreted by [[ameloblasts]] during the secretory stage of enamel formation.
| |
|
| |
| ==Function==
| |
| The primary function of enamelin is to facilitate the growth and organization of [[hydroxyapatite]] crystals, which are the main mineral component of enamel. Enamelin interacts with other enamel matrix proteins, such as [[amelogenin]] and [[ameloblastin]], to regulate crystal nucleation and elongation. It is essential for the proper development of enamel's prismatic structure.
| |
|
| |
| ==Genetics==
| |
| The [[ENAM]] gene, located on [[chromosome 4]] in humans, encodes the enamelin protein. Mutations in the ENAM gene can lead to [[amelogenesis imperfecta]], a genetic condition characterized by defective enamel formation. This condition can result in enamel that is thin, soft, and prone to rapid wear and decay.
| |
|
| |
| ==Pathology==
| |
| Mutations in the ENAM gene are associated with various forms of amelogenesis imperfecta, including hypoplastic and hypomineralized types. These mutations can be inherited in an [[autosomal dominant]] or [[autosomal recessive]] manner, depending on the specific genetic alteration. Clinical manifestations include discolored, pitted, or grooved enamel, and increased susceptibility to dental caries.
| |
|
| |
| ==Research and Clinical Implications==
| |
| Understanding the role of enamelin in enamel formation has significant implications for the development of novel dental treatments and regenerative therapies. Research into enamelin and its interactions with other enamel proteins may lead to advances in biomimetic materials for dental restoration and repair.
| |
|
| |
| ==See Also==
| |
| * [[Amelogenesis imperfecta]]
| |
| * [[Amelogenin]]
| |
| * [[Ameloblastin]]
| |
| * [[Hydroxyapatite]]
| |
|
| |
| ==References==
| |
| * Hu, J. C., & Simmer, J. P. (2007). Developmental biology and genetics of dental enamel. In: "Principles of Bone Biology". Academic Press.
| |
| * Wright, J. T., & Hart, P. S. (2002). The genetics of enamel development. In: "Connective Tissue and Its Heritable Disorders". Wiley-Liss.
| |
|
| |
| ==External Links==
| |
| * [https://www.ncbi.nlm.nih.gov/gene/10117 ENAM gene - NCBI]
| |
| * [https://www.uniprot.org/uniprot/Q9NRM1 Enamelin - UniProt]
| |
|
| |
| [[Category:Proteins]] | | [[Category:Proteins]] |
| [[Category:Dental enamel]] | | [[Category:Dental enamel]] |
| [[Category:Genetic disorders]] | | [[Category:Genetic disorders]] |
| [[Category:Developmental biology]] | | [[Category:Developmental biology]] |
Enamelin is a critical protein involved in the formation of dental enamel, the hard outer layer of teeth. It is one of the largest enamel matrix proteins and plays a crucial role in the mineralization process during amelogenesis.
Structure[edit]
Enamelin is a large glycoprotein, initially synthesized as a precursor protein that undergoes extensive post-translational modifications. The protein is rich in proline, glutamine, and leucine residues, which contribute to its unique structure and function. Enamelin is secreted by ameloblasts during the secretory stage of enamel formation.
Function[edit]
The primary function of enamelin is to facilitate the growth and organization of hydroxyapatite crystals, which are the main mineral component of enamel. Enamelin interacts with other enamel matrix proteins, such as amelogenin and ameloblastin, to regulate crystal nucleation and elongation. It is essential for the proper development of enamel's prismatic structure.
Genetics[edit]
The ENAM gene, located on chromosome 4 in humans, encodes the enamelin protein. Mutations in the ENAM gene can lead to amelogenesis imperfecta, a genetic condition characterized by defective enamel formation. This condition can result in enamel that is thin, soft, and prone to rapid wear and decay.
Pathology[edit]
Mutations in the ENAM gene are associated with various forms of amelogenesis imperfecta, including hypoplastic and hypomineralized types. These mutations can be inherited in an autosomal dominant or autosomal recessive manner, depending on the specific genetic alteration. Clinical manifestations include discolored, pitted, or grooved enamel, and increased susceptibility to dental caries.
Research and Clinical Implications[edit]
Understanding the role of enamelin in enamel formation has significant implications for the development of novel dental treatments and regenerative therapies. Research into enamelin and its interactions with other enamel proteins may lead to advances in biomimetic materials for dental restoration and repair.
See Also[edit]
External Links[edit]
