1pjs
From Proteopedia
(New page: 200px<br /><applet load="1pjs" size="450" color="white" frame="true" align="right" spinBox="true" caption="1pjs, resolution 2.40Å" /> '''The co-crystal struc...) |
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| - | [[Image:1pjs.gif|left|200px]]<br /><applet load="1pjs" size=" | + | [[Image:1pjs.gif|left|200px]]<br /><applet load="1pjs" size="350" color="white" frame="true" align="right" spinBox="true" |
caption="1pjs, resolution 2.40Å" /> | caption="1pjs, resolution 2.40Å" /> | ||
'''The co-crystal structure of CysG, the multifunctional methyltransferase/dehydrogenase/ferrochelatase for siroheme synthesis, in complex with it NAD cofactor'''<br /> | '''The co-crystal structure of CysG, the multifunctional methyltransferase/dehydrogenase/ferrochelatase for siroheme synthesis, in complex with it NAD cofactor'''<br /> | ||
==Overview== | ==Overview== | ||
| - | Sulfur metabolism depends on the iron-containing porphinoid siroheme. In | + | Sulfur metabolism depends on the iron-containing porphinoid siroheme. In Salmonella enterica, the S-adenosyl-L-methionine (SAM)-dependent bismethyltransferase, dehydrogenase and ferrochelatase, CysG, synthesizes siroheme from uroporphyrinogen III (uro'gen III). The reactions mediated by CysG encompass two branchpoint intermediates in tetrapyrrole biosynthesis, diverting flux first from protoporphyrin IX biosynthesis and then from cobalamin (vitamin B(12)) biosynthesis. We determined the first structure of this multifunctional siroheme synthase by X-ray crystallography. CysG is a homodimeric gene fusion product containing two structurally independent modules: a bismethyltransferase and a dual-function dehydrogenase-chelatase. The methyltransferase active site is a deep groove with a hydrophobic patch surrounded by hydrogen bond donors. This asymmetric arrangement of amino acids may be important in directing substrate binding. Notably, our structure shows that CysG is a phosphoprotein. From mutational analysis of the post-translationally modified serine, we suggest a conserved role for phosphorylation in inhibiting dehydrogenase activity and modulating metabolic flux between siroheme and cobalamin pathways. |
==About this Structure== | ==About this Structure== | ||
| - | 1PJS is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Salmonella_typhimurium Salmonella typhimurium] with PO4, SAH, NAD and PGE as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http:// | + | 1PJS is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Salmonella_typhimurium Salmonella typhimurium] with <scene name='pdbligand=PO4:'>PO4</scene>, <scene name='pdbligand=SAH:'>SAH</scene>, <scene name='pdbligand=NAD:'>NAD</scene> and <scene name='pdbligand=PGE:'>PGE</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1PJS OCA]. |
==Reference== | ==Reference== | ||
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[[Category: Salmonella typhimurium]] | [[Category: Salmonella typhimurium]] | ||
[[Category: Single protein]] | [[Category: Single protein]] | ||
| - | [[Category: Daniels, D | + | [[Category: Daniels, D S.]] |
| - | [[Category: Getzoff, E | + | [[Category: Getzoff, E D.]] |
| - | [[Category: Leech, H | + | [[Category: Leech, H K.]] |
| - | [[Category: Stroupe, M | + | [[Category: Stroupe, M E.]] |
| - | [[Category: Warren, M | + | [[Category: Warren, M J.]] |
[[Category: NAD]] | [[Category: NAD]] | ||
[[Category: PGE]] | [[Category: PGE]] | ||
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[[Category: sam]] | [[Category: sam]] | ||
| - | ''Page seeded by [http:// | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 14:29:31 2008'' |
Revision as of 12:29, 21 February 2008
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The co-crystal structure of CysG, the multifunctional methyltransferase/dehydrogenase/ferrochelatase for siroheme synthesis, in complex with it NAD cofactor
Overview
Sulfur metabolism depends on the iron-containing porphinoid siroheme. In Salmonella enterica, the S-adenosyl-L-methionine (SAM)-dependent bismethyltransferase, dehydrogenase and ferrochelatase, CysG, synthesizes siroheme from uroporphyrinogen III (uro'gen III). The reactions mediated by CysG encompass two branchpoint intermediates in tetrapyrrole biosynthesis, diverting flux first from protoporphyrin IX biosynthesis and then from cobalamin (vitamin B(12)) biosynthesis. We determined the first structure of this multifunctional siroheme synthase by X-ray crystallography. CysG is a homodimeric gene fusion product containing two structurally independent modules: a bismethyltransferase and a dual-function dehydrogenase-chelatase. The methyltransferase active site is a deep groove with a hydrophobic patch surrounded by hydrogen bond donors. This asymmetric arrangement of amino acids may be important in directing substrate binding. Notably, our structure shows that CysG is a phosphoprotein. From mutational analysis of the post-translationally modified serine, we suggest a conserved role for phosphorylation in inhibiting dehydrogenase activity and modulating metabolic flux between siroheme and cobalamin pathways.
About this Structure
1PJS is a Single protein structure of sequence from Salmonella typhimurium with , , and as ligands. Full crystallographic information is available from OCA.
Reference
CysG structure reveals tetrapyrrole-binding features and novel regulation of siroheme biosynthesis., Stroupe ME, Leech HK, Daniels DS, Warren MJ, Getzoff ED, Nat Struct Biol. 2003 Dec;10(12):1064-73. Epub 2003 Nov 2. PMID:14595395
Page seeded by OCA on Thu Feb 21 14:29:31 2008
Categories: Salmonella typhimurium | Single protein | Daniels, D S. | Getzoff, E D. | Leech, H K. | Stroupe, M E. | Warren, M J. | NAD | PGE | PO4 | SAH | Nad | Nucleotide binding motif | Phosphoserine | Rossman fold | Sah | Sam
