User:Tkadm30/Notebook/Cat eye syndrome: Difference between revisions
From OpenWetWare
< User:Tkadm30 | Notebook
(Add reference for CAMK2G/PD pathology relevance) |
No edit summary |
||
Line 1: | Line 1: | ||
=== | __TOC__ | ||
=== Introduction to CES === | |||
* EC 3.5.4.4 [http://brenda-enzymes.org/php/result_flat.php4?ecno=3.5.4.4&Suchword=&organism%5B%5D=Homo+sapiens&show_tm=0 ref] | * EC 3.5.4.4 [http://brenda-enzymes.org/php/result_flat.php4?ecno=3.5.4.4&Suchword=&organism%5B%5D=Homo+sapiens&show_tm=0 ref] | ||
* also named '''Adenosine deaminase CECR1''' | * also named '''Adenosine deaminase CECR1''' | ||
Line 7: | Line 10: | ||
* Litterature review: http://www.omim.org/entry/115470 | * Litterature review: http://www.omim.org/entry/115470 | ||
* related to chromosome 22q11 | * related to chromosome 22q11 | ||
* for PD (Score 8.991) and BPA, see also gene [http://www.uniprot.org/uniprot/Q13555 CAMK2G (KCC2G)] - also known as chromosome 22q10. [1] [2] | * for PD (Score 8.991) and [[BPA|BPA (bis-phenol-A)]], see also gene [http://www.uniprot.org/uniprot/Q13555 CAMK2G (KCC2G)] - also known as chromosome 22q10. [1] [2] | ||
=== Parkinson disease/CES tristable riboswitch device abstraction === | |||
* A Parkinson/CES disease "riboswitch" is a AHL-activated (acyl-homoserine-lactone) xenobiotic compound (recombinase system) modulating Ca2+/Mg2+ specific ions channel to activate RNA polymerase transcription and controlled DNA release of the V. Fischeri specific "LuxR" protein: a functional beta-amyloid ligand (NMDA receptor antagonist) regulated by the CAMK2G | |||
(calmodulin) gene. | |||
=== Glossary === | |||
* ADA | |||
* AHL | |||
* BPA | |||
* CES | |||
* recombinase | |||
* CAMK2G | |||
* Calmodulin | |||
* LuxR | |||
* EnvZ | |||
* PC | |||
* ATP | |||
* LacZ | |||
* PD - Parkinson disease | |||
* cAMP | |||
* riboswitch | |||
* polymerase, | |||
* RNA | |||
* NMDA | |||
* etc... | |||
=== References === | === References === | ||
# http://www.genecards.org/cgi-bin/carddisp.pl?gene=CAMK2G | # http://www.genecards.org/cgi-bin/carddisp.pl?gene=CAMK2G | ||
# http://www.sciencedaily.com/releases/2013/02/130225153122.htm?utm_source=dlvr.it&utm_medium=twitter | # http://www.sciencedaily.com/releases/2013/02/130225153122.htm?utm_source=dlvr.it&utm_medium=twitter |
Revision as of 21:02, 28 February 2013
Introduction to CES
- EC 3.5.4.4 ref
- also named Adenosine deaminase CECR1
- Uniprot accession number Q9NZK5
- reaction type -> deamination
- tissues: brain, liver, thymus...
- Litterature review: http://www.omim.org/entry/115470
- related to chromosome 22q11
- for PD (Score 8.991) and BPA (bis-phenol-A), see also gene CAMK2G (KCC2G) - also known as chromosome 22q10. [1] [2]
Parkinson disease/CES tristable riboswitch device abstraction
- A Parkinson/CES disease "riboswitch" is a AHL-activated (acyl-homoserine-lactone) xenobiotic compound (recombinase system) modulating Ca2+/Mg2+ specific ions channel to activate RNA polymerase transcription and controlled DNA release of the V. Fischeri specific "LuxR" protein: a functional beta-amyloid ligand (NMDA receptor antagonist) regulated by the CAMK2G
(calmodulin) gene.
Glossary
- ADA
- AHL
- BPA
- CES
- recombinase
- CAMK2G
- Calmodulin
- LuxR
- EnvZ
- PC
- ATP
- LacZ
- PD - Parkinson disease
- cAMP
- riboswitch
- polymerase,
- RNA
- NMDA
- etc...