2bd0: Difference between revisions

From Proteopedia
Jump to navigationJump to search
OCA (talk | contribs)
No edit summary
OCA (talk | contribs)
No edit summary
Line 1: Line 1:
[[Image:2bd0.gif|left|200px]]
{{Seed}}
[[Image:2bd0.png|left|200px]]


<!--
<!--
Line 9: Line 10:
{{STRUCTURE_2bd0|  PDB=2bd0  |  SCENE=  }}  
{{STRUCTURE_2bd0|  PDB=2bd0  |  SCENE=  }}  


'''Chlorobium tepidum Sepiapterin Reductase complexed with NADP and Sepiapterin'''
===Chlorobium tepidum Sepiapterin Reductase complexed with NADP and Sepiapterin===




==Overview==
<!--  
Sepiapterin reductase (SR) is involved in the last step of tetrahydrobiopterin (BH(4)) biosynthesis by reducing the di-keto group of 6-pyruvoyl tetrahydropterin. Chlorobium tepidum SR (cSR) generates a distinct BH(4) product, L-threo-BH(4) (6R-(1'S,2'S)-5,6,7,8-BH(4)), whereas animal enzymes produce L-erythro-BH(4) (6R-(1'R,2'S)-5,6,7,8-BH(4)) although it has high amino acid sequence similarities to the other animal enzymes. To elucidate the structural basis for the different reaction stereospecificities, we have determined the three-dimensional structures of cSR alone and complexed with NADP and sepiapterin at 2.1 and 1.7 A resolution, respectively. The overall folding of the cSR, the binding site for the cofactor NADP(H), and the positions of active site residues were quite similar to the mouse and the human SR. However, significant differences were found in the substrate binding region of the cSR. In comparison to the mouse SR complex, the sepiapterin in the cSR is rotated about 180 degrees around the active site and bound between two aromatic side chains of Trp-196 and Phe-99 so that its pterin ring is shifted to the opposite side, but its side chain position is not changed. The swiveled sepiapterin binding results in the conversion of the side chain configuration, exposing the opposite face for hydride transfer from NADPH. The different sepiapterin binding mode within the conserved catalytic architecture presents a novel strategy of switching the reaction stereospecificities in the same protein fold.
The line below this paragraph, {{ABSTRACT_PUBMED_16308317}}, adds the Publication Abstract to the page
(as it appears on PubMed at http://www.pubmed.gov), where 16308317 is the PubMed ID number.
-->
{{ABSTRACT_PUBMED_16308317}}


==About this Structure==
==About this Structure==
Line 30: Line 34:
[[Category: Chlorobium tepidum]]
[[Category: Chlorobium tepidum]]
[[Category: Sepiapterin reductase]]
[[Category: Sepiapterin reductase]]
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sat May  3 20:07:41 2008''
 
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Jul 27 20:26:39 2008''