Talk:Oxaloacetic acid

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Rated "high" because oxaloacetate redirects here and is highschool/SAT biology content. - tameeria 20:31, 28 April 2007 (UTC)

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Rated "high" because oxaloacetate redirects here and is highschool/SAT biology content. - tameeria 20:31, 28 April 2007 (UTC)

[edit] Merge from Oxaloacetate

In line with normal naming conventions, oxaloacetate has been merged here, and now redirects to this page. At the time of the merge/redirect, the edit history of oxaloacetate was as follows:

  • 14:51, 10 Mar 2005 131.251.0.7
  • 07:24, 10 Mar 2005 RJFJR m (stub to chem-stub)
  • 21:31, 8 Mar 2005 161.97.202.245 (Revert to version by Chris Edgemon [from vandalism])
  • 20:39, 8 Mar 2005 Remuel m (sorted stub)
  • 17:28, 8 Mar 2005 193.63.118.247
  • 17:25, 8 Mar 2005 193.63.119.25
  • 08:30, 28 Oct 2004 Chris Edgemon
  • 10:55, 20 Jul 2004 132.66.16.12
  • 20:15, 18 Jul 2004 132.66.16.12
  • 20:06, 18 Jul 2004 132.66.16.34
  • 04:04, 11 Mar 2004 Moink (wikify, msg:stub)
  • 02:13, 11 Mar 2004 194.81.199.46

For copyright reasons, please do not remove this information. Physchim62 21:21, 24 May 2005 (UTC)

Oxaloacetate is converted into Malate or Phosphoenolpyruvate before it leaves the mitochondria, does that mean it cannot leave in oxaloacetate form?


[edit] Interconversion picture

The picture is misleading because it does not relate to any biological process - at pH7, carboxylic acids are deprotonated - dehydrogenation does not produce free H2, it is coupled to reduction of NAD+ - similarly, NH3 is not released as free ammonia, as shown - etc —Preceding unsigned comment added by 90.242.88.79 (talk) 16:32, 23 September 2007 (UTC)