1kb0

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
(New page: 200px<br /><applet load="1kb0" size="450" color="white" frame="true" align="right" spinBox="true" caption="1kb0, resolution 1.44&Aring;" /> '''Crystal Structure of...)
Line 1: Line 1:
-
[[Image:1kb0.jpg|left|200px]]<br /><applet load="1kb0" size="450" color="white" frame="true" align="right" spinBox="true"
+
[[Image:1kb0.jpg|left|200px]]<br /><applet load="1kb0" size="350" color="white" frame="true" align="right" spinBox="true"
caption="1kb0, resolution 1.44&Aring;" />
caption="1kb0, resolution 1.44&Aring;" />
'''Crystal Structure of Quinohemoprotein Alcohol Dehydrogenase from Comamonas testosteroni'''<br />
'''Crystal Structure of Quinohemoprotein Alcohol Dehydrogenase from Comamonas testosteroni'''<br />
==Overview==
==Overview==
-
Quinoprotein alcohol dehydrogenases are redox enzymes that participate in, distinctive catabolic pathways that enable bacteria to grow on various, alcohols as the sole source of carbon and energy. The x-ray structure of, the quinohemoprotein alcohol dehydrogenase from Comamonas testosteroni has, been determined at 1.44 A resolution. It comprises two domains. The, N-terminal domain has a beta-propeller fold and binds one pyrroloquinoline, quinone cofactor and one calcium ion in the active site. A, tetrahydrofuran-2-carboxylic acid molecule is present in the, substrate-binding cleft. The position of this oxidation product provides, valuable information on the amino acid residues involved in the reaction, mechanism and their function. The C-terminal domain is an alpha-helical, type I cytochrome c with His(608) and Met(647) as heme-iron ligands. This, is the first reported structure of an electron transfer system between a, quinoprotein alcohol dehydrogenase and cytochrome c. The shortest distance, between pyrroloquinoline quinone and heme c is 12.9 A, one of the longest, physiological edge-to-edge distances yet determined between two redox, centers. A highly unusual disulfide bond between two adjacent cysteines, bridges the redox centers. It appears essential for electron transfer. A, water channel delineates a possible pathway for proton transfer from the, active site to the solvent.
+
Quinoprotein alcohol dehydrogenases are redox enzymes that participate in distinctive catabolic pathways that enable bacteria to grow on various alcohols as the sole source of carbon and energy. The x-ray structure of the quinohemoprotein alcohol dehydrogenase from Comamonas testosteroni has been determined at 1.44 A resolution. It comprises two domains. The N-terminal domain has a beta-propeller fold and binds one pyrroloquinoline quinone cofactor and one calcium ion in the active site. A tetrahydrofuran-2-carboxylic acid molecule is present in the substrate-binding cleft. The position of this oxidation product provides valuable information on the amino acid residues involved in the reaction mechanism and their function. The C-terminal domain is an alpha-helical type I cytochrome c with His(608) and Met(647) as heme-iron ligands. This is the first reported structure of an electron transfer system between a quinoprotein alcohol dehydrogenase and cytochrome c. The shortest distance between pyrroloquinoline quinone and heme c is 12.9 A, one of the longest physiological edge-to-edge distances yet determined between two redox centers. A highly unusual disulfide bond between two adjacent cysteines bridges the redox centers. It appears essential for electron transfer. A water channel delineates a possible pathway for proton transfer from the active site to the solvent.
==About this Structure==
==About this Structure==
-
1KB0 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Comamonas_testosteroni Comamonas testosteroni] with CA, HEC, TFB, PQQ and GOL as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1KB0 OCA].
+
1KB0 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Comamonas_testosteroni Comamonas testosteroni] with <scene name='pdbligand=CA:'>CA</scene>, <scene name='pdbligand=HEC:'>HEC</scene>, <scene name='pdbligand=TFB:'>TFB</scene>, <scene name='pdbligand=PQQ:'>PQQ</scene> and <scene name='pdbligand=GOL:'>GOL</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1KB0 OCA].
==Reference==
==Reference==
Line 14: Line 14:
[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Oubrie, A.]]
[[Category: Oubrie, A.]]
-
[[Category: Rozeboom, H.J.]]
+
[[Category: Rozeboom, H J.]]
[[Category: CA]]
[[Category: CA]]
[[Category: GOL]]
[[Category: GOL]]
Line 24: Line 24:
[[Category: oxidoreductase]]
[[Category: oxidoreductase]]
-
''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Tue Nov 20 19:00:59 2007''
+
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 13:32:07 2008''

Revision as of 11:32, 21 February 2008


1kb0, resolution 1.44Å

Drag the structure with the mouse to rotate

Crystal Structure of Quinohemoprotein Alcohol Dehydrogenase from Comamonas testosteroni

Overview

Quinoprotein alcohol dehydrogenases are redox enzymes that participate in distinctive catabolic pathways that enable bacteria to grow on various alcohols as the sole source of carbon and energy. The x-ray structure of the quinohemoprotein alcohol dehydrogenase from Comamonas testosteroni has been determined at 1.44 A resolution. It comprises two domains. The N-terminal domain has a beta-propeller fold and binds one pyrroloquinoline quinone cofactor and one calcium ion in the active site. A tetrahydrofuran-2-carboxylic acid molecule is present in the substrate-binding cleft. The position of this oxidation product provides valuable information on the amino acid residues involved in the reaction mechanism and their function. The C-terminal domain is an alpha-helical type I cytochrome c with His(608) and Met(647) as heme-iron ligands. This is the first reported structure of an electron transfer system between a quinoprotein alcohol dehydrogenase and cytochrome c. The shortest distance between pyrroloquinoline quinone and heme c is 12.9 A, one of the longest physiological edge-to-edge distances yet determined between two redox centers. A highly unusual disulfide bond between two adjacent cysteines bridges the redox centers. It appears essential for electron transfer. A water channel delineates a possible pathway for proton transfer from the active site to the solvent.

About this Structure

1KB0 is a Single protein structure of sequence from Comamonas testosteroni with , , , and as ligands. Full crystallographic information is available from OCA.

Reference

Crystal structure of quinohemoprotein alcohol dehydrogenase from Comamonas testosteroni: structural basis for substrate oxidation and electron transfer., Oubrie A, Rozeboom HJ, Kalk KH, Huizinga EG, Dijkstra BW, J Biol Chem. 2002 Feb 1;277(5):3727-32. Epub 2001 Nov 19. PMID:11714714

Page seeded by OCA on Thu Feb 21 13:32:07 2008

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools