1xuu: Difference between revisions
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New page: left|200px<br /><applet load="1xuu" size="450" color="white" frame="true" align="right" spinBox="true" caption="1xuu, resolution 1.9Å" /> '''Crystal structure of ... |
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[[Image:1xuu.jpg|left|200px]]<br /><applet load="1xuu" size=" | [[Image:1xuu.jpg|left|200px]]<br /><applet load="1xuu" size="350" color="white" frame="true" align="right" spinBox="true" | ||
caption="1xuu, resolution 1.9Å" /> | caption="1xuu, resolution 1.9Å" /> | ||
'''Crystal structure of sialic acid synthase (NeuB) in complex with Mn2+ and Malate from Neisseria meningitidis'''<br /> | '''Crystal structure of sialic acid synthase (NeuB) in complex with Mn2+ and Malate from Neisseria meningitidis'''<br /> | ||
==Overview== | ==Overview== | ||
In Neisseria meningitidis and related bacterial pathogens, sialic acids | In Neisseria meningitidis and related bacterial pathogens, sialic acids play critical roles in mammalian cell immunity evasion and are synthesized by a conserved enzymatic pathway that includes sialic acid synthase (NeuB, SiaC, or SynC). NeuB catalyzes the condensation of phosphoenolpyruvate (PEP) and N-acetylmannosamine, directly forming N-acetylneuraminic acid (or sialic acid). In this paper we report the development of a coupled assay to monitor NeuB reaction kinetics and an 18O-labeling study that demonstrates the synthase operates via a C-O bond cleavage mechanism. We also report the first structure of a sialic acid synthase, that of NeuB, revealing a unique domain-swapped homodimer architecture consisting of a (beta/alpha)8 barrel (TIM barrel)-type fold at the N-terminal end and a domain with high sequence identity and structural similarity to the ice binding type III antifreeze proteins at the C-terminal end of the enzyme. We have determined the structures of NeuB in the malate-bound form and with bound PEP and the substrate analog N-acetylmannosaminitol to 1.9 and 2.2 A resolution, respectively. Typical of other TIM barrel proteins, the active site of NeuB is located in a cavity at the C-terminal end of the barrel; however, the positioning of the swapped antifreeze-like domain from the adjacent monomer provides key residues for hydrogen bonding with substrates in the active site of NeuB, a structural feature that leads to distinct modes of substrate binding from other PEP-utilizing enzymes that lack an analogous antifreeze-like domain. Our observation of a direct interaction between a highly ordered manganese and the N-acetylmannosaminitol in the NeuB active site also suggests an essential role for the ion as an electrophilic catalyst that activates the N-acetylmannosamine carbonyl to the addition of PEP. | ||
==About this Structure== | ==About this Structure== | ||
1XUU is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Neisseria_meningitidis Neisseria meningitidis] with MN and MLT as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http:// | 1XUU is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Neisseria_meningitidis Neisseria meningitidis] with <scene name='pdbligand=MN:'>MN</scene> and <scene name='pdbligand=MLT:'>MLT</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1XUU OCA]. | ||
==Reference== | ==Reference== | ||
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[[Category: Gilbert, M.]] | [[Category: Gilbert, M.]] | ||
[[Category: Gunawan, J.]] | [[Category: Gunawan, J.]] | ||
[[Category: Lovering, A | [[Category: Lovering, A L.]] | ||
[[Category: Simard, D.]] | [[Category: Simard, D.]] | ||
[[Category: Strynadka, N | [[Category: Strynadka, N C.]] | ||
[[Category: Tanner, M | [[Category: Tanner, M E.]] | ||
[[Category: Wakarchuk, W | [[Category: Wakarchuk, W W.]] | ||
[[Category: MLT]] | [[Category: MLT]] | ||
[[Category: MN]] | [[Category: MN]] | ||
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[[Category: tim barrel]] | [[Category: tim barrel]] | ||
''Page seeded by [http:// | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 15:58:52 2008'' | ||