4cts

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Line 1: Line 1:
-
[[Image:4cts.gif|left|200px]]<br /><applet load="4cts" size="350" color="white" frame="true" align="right" spinBox="true"
+
[[Image:4cts.gif|left|200px]]
-
caption="4cts, resolution 2.9&Aring;" />
+
 
-
'''CRYSTAL STRUCTURE ANALYSIS AND MOLECULAR MODEL OF A COMPLEX OF CITRATE SYNTHASE WITH OXALOACETATE AND S-ACETONYL-COENZYME A'''<br />
+
{{Structure
 +
|PDB= 4cts |SIZE=350|CAPTION= <scene name='initialview01'>4cts</scene>, resolution 2.9&Aring;
 +
|SITE=
 +
|LIGAND= <scene name='pdbligand=OAA:OXALOACETATE ION'>OAA</scene>
 +
|ACTIVITY= [http://en.wikipedia.org/wiki/Citrate_(Si)-synthase Citrate (Si)-synthase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.3.3.1 2.3.3.1]
 +
|GENE=
 +
}}
 +
 
 +
'''CRYSTAL STRUCTURE ANALYSIS AND MOLECULAR MODEL OF A COMPLEX OF CITRATE SYNTHASE WITH OXALOACETATE AND S-ACETONYL-COENZYME A'''
 +
 
==Overview==
==Overview==
Line 7: Line 16:
==About this Structure==
==About this Structure==
-
4CTS is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Sus_scrofa Sus scrofa] with <scene name='pdbligand=OAA:'>OAA</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/Citrate_(Si)-synthase Citrate (Si)-synthase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.3.3.1 2.3.3.1] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4CTS OCA].
+
4CTS is a [[Single protein]] structure of sequence from [http://en.wikipedia.org/wiki/Sus_scrofa Sus scrofa]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4CTS OCA].
==Reference==
==Reference==
-
Crystal structure analysis and molecular model of a complex of citrate synthase with oxaloacetate and S-acetonyl-coenzyme A., Wiegand G, Remington S, Deisenhofer J, Huber R, J Mol Biol. 1984 Mar 25;174(1):205-19. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=6716477 6716477]
+
Crystal structure analysis and molecular model of a complex of citrate synthase with oxaloacetate and S-acetonyl-coenzyme A., Wiegand G, Remington S, Deisenhofer J, Huber R, J Mol Biol. 1984 Mar 25;174(1):205-19. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/6716477 6716477]
[[Category: Citrate (Si)-synthase]]
[[Category: Citrate (Si)-synthase]]
[[Category: Single protein]]
[[Category: Single protein]]
Line 20: Line 29:
[[Category: oxo-acid-lyase]]
[[Category: oxo-acid-lyase]]
-
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 19:13:05 2008''
+
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Mar 20 19:09:20 2008''

Revision as of 17:09, 20 March 2008


PDB ID 4cts

Drag the structure with the mouse to rotate
, resolution 2.9Å
Ligands:
Activity: Citrate (Si)-synthase, with EC number 2.3.3.1
Coordinates: save as pdb, mmCIF, xml



CRYSTAL STRUCTURE ANALYSIS AND MOLECULAR MODEL OF A COMPLEX OF CITRATE SYNTHASE WITH OXALOACETATE AND S-ACETONYL-COENZYME A


Overview

The crystal structure of the complex of pig heart citrate synthase and oxaloacetate in the presence of the potent inhibitor S-acetonyl coenzyme A has been determined at a nominal resolution of 2.9 A by Patterson search techniques and refined by restrained crystallographic refinement. The complex crystallizes in the presence of polyvinylpyrrolidone in space group P4(3)2(1)2 with a = 101.5 A and c = 224.6 A, with one dimeric molecule of molecular weight 100,000 in the asymmetric unit. The crystallographic R factor is 0.194 for the 14,332 unique reflections between 6.0 and 2.9 A resolution. The structures of two forms of citrate synthase in the presence and absence of product molecules have been determined recently and shown to differ in the relative arrangement of the large and small domains ("closed" and "open" forms). The third crystal form described here is also closed, but there is substantial rearrangement within the small domain relative to either of the other crystal forms. We conclude that this is a third structural state of the enzyme, and catalytic activity of the enzyme depends on structural changes during the course of the reaction affecting domain conformation also. The three structures are compared, and it is shown that the large domain is considerably more rigid than the small domain. The conformation of the small domain adapts to the ligand. The inhibitor, and the "coenzyme-A-binding segment" of the enzyme are disordered. No electron density is observed for the inhibitor, and only weak density for the coenzyme-A-binding segment. Electron density for oxaloacetate is well defined. It binds in a very similar manner to citrate.

About this Structure

4CTS is a Single protein structure of sequence from Sus scrofa. Full crystallographic information is available from OCA.

Reference

Crystal structure analysis and molecular model of a complex of citrate synthase with oxaloacetate and S-acetonyl-coenzyme A., Wiegand G, Remington S, Deisenhofer J, Huber R, J Mol Biol. 1984 Mar 25;174(1):205-19. PMID:6716477

Page seeded by OCA on Thu Mar 20 19:09:20 2008

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools