User:Kay Owosela

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(Stoichiometry)
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= Stoichiometry =
= Stoichiometry =
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NHз
+
The stoichiometry of Glutamine Synthetase is as follows:
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(Insert Text Here)
+
Glutamate + NH4+ + ATP --> Glutamine + ADP + Pi + H+
 +
 
 +
In this reaction, Glutamate is used as a major reactant and ATP is used for energy to form Glutamine. It should be noted that along with the enzyme, Me+ which can be either manganese or magnesium is used as a catalyst.
 +
 
 +
This is however, a 2-step reaction. In the first step of this reaction, an intermediate Υ-glutamyl phosphate is formed. The formation of the intermediate is done by phosphoryl transfer an ATP group Y-carboxylate group of glutamate. In the second step of this reaction, NH4+ attacks the activated intermediate to release the phosphate group yielding Glutamine.
 +
 
= Quarternary Structure Polymerization =
= Quarternary Structure Polymerization =

Revision as of 03:24, 8 December 2008

Biol 430 Biology Major Partners: Delo Sarr, Mustapha Hussain

Glutamine synthase

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Contents

Jmol practice

Backbone with ligand

Labeled Ligands in Chain A

Active Site with Amino Acid Residues

Connection between Chain F residue 63 and Chain G residue 319

Stoichiometry

The stoichiometry of Glutamine Synthetase is as follows: Glutamate + NH4+ + ATP --> Glutamine + ADP + Pi + H+

In this reaction, Glutamate is used as a major reactant and ATP is used for energy to form Glutamine. It should be noted that along with the enzyme, Me+ which can be either manganese or magnesium is used as a catalyst.

This is however, a 2-step reaction. In the first step of this reaction, an intermediate Υ-glutamyl phosphate is formed. The formation of the intermediate is done by phosphoryl transfer an ATP group Y-carboxylate group of glutamate. In the second step of this reaction, NH4+ attacks the activated intermediate to release the phosphate group yielding Glutamine.


Quarternary Structure Polymerization

(Insert Text Here)

Active Site

(Insert Text Here)

Glutamine Synthetase Symmetry

Proteopedia Page Contributors and Editors (what is this?)

Kay Owosela, Eran Hodis

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