1zin: Difference between revisions

New page: left|200px<br /><applet load="1zin" size="450" color="white" frame="true" align="right" spinBox="true" caption="1zin, resolution 1.6Å" /> '''ADENYLATE KINASE WITH...
 
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[[Image:1zin.gif|left|200px]]<br /><applet load="1zin" size="450" color="white" frame="true" align="right" spinBox="true"  
[[Image:1zin.gif|left|200px]]<br /><applet load="1zin" size="350" color="white" frame="true" align="right" spinBox="true"  
caption="1zin, resolution 1.6&Aring;" />
caption="1zin, resolution 1.6&Aring;" />
'''ADENYLATE KINASE WITH BOUND AP5A'''<br />
'''ADENYLATE KINASE WITH BOUND AP5A'''<br />


==Overview==
==Overview==
Crystal structures of Bacillus stearothermophilus adenylate kinase with, bound Ap5A, Mn2+ Ap5A, and Mg2+ Ap5A have been determined by X-ray, crystallography to resolutions of 1.6 A, 1.85 A, and 1.96 A, respectively., The protein's lid domain is partially open, being both rotated and, translated away from bound Ap5A. The flexibility of the lid domain in the, ternary state and its ability to transfer force directly to the the active, site is discussed in light of our proposed entropic mechanism for, catalytic turnover. The bound Zn2+ atom is demonstrably structural in, nature, with no contacts other than its ligating cysteine residues within, 5 A. The B. stearothermophilus adenylate kinase lid appears to be a, truncated zinc finger domain, lacking the DNA binding finger, which we, have termed a zinc knuckle domain. In the Mg2+ Ap5A and Mn2+ Ap5A, structures, Mg2+ and Mn2+ demonstrate six coordinate octahedral geometry., The interactions of the Mg2+-coordinated water molecules with the protein, and Ap5A phosphate chain demonstrate their involvement in catalyzing, phosphate transfer. The protein selects for beta-y (preferred by Mg2+), rather than alpha-gamma (preferred by Mn2+) metal ion coordination by, forcing the ATP phosphate chain to have an extended conformation.
Crystal structures of Bacillus stearothermophilus adenylate kinase with bound Ap5A, Mn2+ Ap5A, and Mg2+ Ap5A have been determined by X-ray crystallography to resolutions of 1.6 A, 1.85 A, and 1.96 A, respectively. The protein's lid domain is partially open, being both rotated and translated away from bound Ap5A. The flexibility of the lid domain in the ternary state and its ability to transfer force directly to the the active site is discussed in light of our proposed entropic mechanism for catalytic turnover. The bound Zn2+ atom is demonstrably structural in nature, with no contacts other than its ligating cysteine residues within 5 A. The B. stearothermophilus adenylate kinase lid appears to be a truncated zinc finger domain, lacking the DNA binding finger, which we have termed a zinc knuckle domain. In the Mg2+ Ap5A and Mn2+ Ap5A structures, Mg2+ and Mn2+ demonstrate six coordinate octahedral geometry. The interactions of the Mg2+-coordinated water molecules with the protein and Ap5A phosphate chain demonstrate their involvement in catalyzing phosphate transfer. The protein selects for beta-y (preferred by Mg2+) rather than alpha-gamma (preferred by Mn2+) metal ion coordination by forcing the ATP phosphate chain to have an extended conformation.


==About this Structure==
==About this Structure==
1ZIN is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Geobacillus_stearothermophilus Geobacillus stearothermophilus] with ZN and AP5 as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Adenylate_kinase Adenylate kinase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.4.3 2.7.4.3] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1ZIN OCA].  
1ZIN is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Geobacillus_stearothermophilus Geobacillus stearothermophilus] with <scene name='pdbligand=ZN:'>ZN</scene> and <scene name='pdbligand=AP5:'>AP5</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Adenylate_kinase Adenylate kinase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.4.3 2.7.4.3] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1ZIN OCA].  


==Reference==
==Reference==
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[[Category: Geobacillus stearothermophilus]]
[[Category: Geobacillus stearothermophilus]]
[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Berry, M.B.]]
[[Category: Berry, M B.]]
[[Category: Jr., G.N.Phillips.]]
[[Category: Jr., G N.Phillips.]]
[[Category: AP5]]
[[Category: AP5]]
[[Category: ZN]]
[[Category: ZN]]
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[[Category: zinc finger]]
[[Category: zinc finger]]


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