Difference between revisions of "Phosphatase Subfamily egg"

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(Function)
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=== Function ===
 
=== Function ===
In ''C. elegans'', all three members are predicted to be catalytically inactive as the replacements at cysteine and/or arginine at Cx5R motif. Egg-4 and egg-5 functions in controlling the oocyte- to-zygote transition by regulating signaling by the DYRK family kinase MBK-2. Egg-4/egg-5 binds to MBK-2 at the substrate-binding groove of the kinase, and inhibits the ability of the kinase to bind and phosphorylate substrates, thereby inhibiting downstream signaling <cite> Cheng09 , Parry09, Tonks09 </cite>.
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All three ''C. elegans'' members are predicted to be catalytically inactive, due to loss of the cysteine and/or arginine of the Cx5R motif. egg-4 and egg-5 control the oocyte- to-zygote transition by regulating signaling by the DYRK family kinase MBK-2. egg-4/egg-5 binds to MBK-2 at the substrate-binding groove of the kinase, and inhibits the ability of the kinase to bind and phosphorylate substrates, thereby inhibiting downstream signaling <cite> Cheng09 , Parry09, Tonks09 </cite>.
  
 
=== References ===
 
=== References ===

Revision as of 21:12, 7 September 2016

Phosphatase Classification: Fold CC1: Superfamily CC1: Family PTP: Subfamily Egg

Evolution

The eak subfamily is nematode specific. C. elegans has three members: egg-3, egg-4, egg-5.

Domain

The egg subfamily has a single structural domain: the phosphatase domain of CC1 fold.

Function

All three C. elegans members are predicted to be catalytically inactive, due to loss of the cysteine and/or arginine of the Cx5R motif. egg-4 and egg-5 control the oocyte- to-zygote transition by regulating signaling by the DYRK family kinase MBK-2. egg-4/egg-5 binds to MBK-2 at the substrate-binding groove of the kinase, and inhibits the ability of the kinase to bind and phosphorylate substrates, thereby inhibiting downstream signaling [1, 2, 3].

References

Error fetching PMID 19879842:
Error fetching PMID 19879147:
Error fetching PMID 19879835:
  1. Error fetching PMID 19879842: [Cheng09]
  2. Error fetching PMID 19879147: [Parry09]
  3. Error fetching PMID 19879835: [Tonks09]
All Medline abstracts: PubMed | HubMed