Difference between revisions of "Phosphtase Subfamily CDC25"
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| − | [[Phosphatase classification|Phosphatase Classification]]: [[ | + | [[Phosphatase classification|Phosphatase Classification]]: [[Phosphatase_Superfamily_CC3|Superfamily CC3 (Rhondanese)]]: [[Phosphatase_Family_CDC25|Family CDC25]]: [[Subfamily_CDC25|Subamily CDC25]] |
CDC25 subfamily has three member genes in human, '''[[Gene_CDC25A|CDC25A]]''', '''[[Gene_CDC25B|CDC25B]]''', '''[[Gene_CDC25C|CDC25C]]'''. They contain a catalytic domain on the C-terminus <cite>fauman98 reynolds99</cite>, and a less-conserved N-terminal regulatory region <cite>forrest01</cite>, which can be phosphorylated and ubiquitinated. CDC25 activates cyclin-dependent kinases ([http://kinase.com/wiki/index.php/Kinase_Family_CDK CDKs]) by dephosphorylating two sites within their ATP binding loop. CDKs regulate key transitions between cell cycle phases, and are key components of the checkpoint pathways involved in DNA damage. Thus, it is not suppressing to find it overexpressed in many human cancers <cite>Boutros07</cite>. | CDC25 subfamily has three member genes in human, '''[[Gene_CDC25A|CDC25A]]''', '''[[Gene_CDC25B|CDC25B]]''', '''[[Gene_CDC25C|CDC25C]]'''. They contain a catalytic domain on the C-terminus <cite>fauman98 reynolds99</cite>, and a less-conserved N-terminal regulatory region <cite>forrest01</cite>, which can be phosphorylated and ubiquitinated. CDC25 activates cyclin-dependent kinases ([http://kinase.com/wiki/index.php/Kinase_Family_CDK CDKs]) by dephosphorylating two sites within their ATP binding loop. CDKs regulate key transitions between cell cycle phases, and are key components of the checkpoint pathways involved in DNA damage. Thus, it is not suppressing to find it overexpressed in many human cancers <cite>Boutros07</cite>. | ||
Revision as of 20:34, 6 December 2014
Phosphatase Classification: Superfamily CC3 (Rhondanese): Family CDC25: Subamily CDC25
CDC25 subfamily has three member genes in human, CDC25A, CDC25B, CDC25C. They contain a catalytic domain on the C-terminus [1, 2], and a less-conserved N-terminal regulatory region [3], which can be phosphorylated and ubiquitinated. CDC25 activates cyclin-dependent kinases (CDKs) by dephosphorylating two sites within their ATP binding loop. CDKs regulate key transitions between cell cycle phases, and are key components of the checkpoint pathways involved in DNA damage. Thus, it is not suppressing to find it overexpressed in many human cancers [4].
CDC25 is found in most animals, but is absent from land plants and green alga Chalmydomonas. In excavates, they are found in Trichomonas, but not Giardia, Leishmania, or Trypanosomes.
References
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