1joo: Difference between revisions

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[[Image:1joo.gif|left|200px]]<br /><applet load="1joo" size="350" color="white" frame="true" align="right" spinBox="true"
[[Image:1joo.gif|left|200px]]
caption="1joo" />
 
'''Averaged structure for unligated Staphylococcal nuclease-H124L'''<br />
{{Structure
|PDB= 1joo |SIZE=350|CAPTION= <scene name='initialview01'>1joo</scene>
|SITE=  
|LIGAND=  
|ACTIVITY= [http://en.wikipedia.org/wiki/Micrococcal_nuclease Micrococcal nuclease], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.1.31.1 3.1.31.1]
|GENE=
}}
 
'''Averaged structure for unligated Staphylococcal nuclease-H124L'''
 


==Overview==
==Overview==
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==About this Structure==
==About this Structure==
1JOO is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Staphylococcus_aureus Staphylococcus aureus]. Active as [http://en.wikipedia.org/wiki/Micrococcal_nuclease Micrococcal nuclease], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.1.31.1 3.1.31.1] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1JOO OCA].  
1JOO is a [[Single protein]] structure of sequence from [http://en.wikipedia.org/wiki/Staphylococcus_aureus Staphylococcus aureus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1JOO OCA].  


==Reference==
==Reference==
Solution structures of staphylococcal nuclease from multidimensional, multinuclear NMR: nuclease-H124L and its ternary complex with Ca2+ and thymidine-3',5'-bisphosphate., Wang J, Truckses DM, Abildgaard F, Dzakula Z, Zolnai Z, Markley JL, J Biomol NMR. 1997 Sep;10(2):143-64. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=9369015 9369015]
Solution structures of staphylococcal nuclease from multidimensional, multinuclear NMR: nuclease-H124L and its ternary complex with Ca2+ and thymidine-3',5'-bisphosphate., Wang J, Truckses DM, Abildgaard F, Dzakula Z, Zolnai Z, Markley JL, J Biomol NMR. 1997 Sep;10(2):143-64. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/9369015 9369015]
[[Category: Micrococcal nuclease]]
[[Category: Micrococcal nuclease]]
[[Category: Single protein]]
[[Category: Single protein]]
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[[Category: beta barrel]]
[[Category: beta barrel]]


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Revision as of 13:06, 20 March 2008

File:1joo.gif


PDB ID 1joo

Drag the structure with the mouse to rotate
Activity: Micrococcal nuclease, with EC number 3.1.31.1
Coordinates: save as pdb, mmCIF, xml



Averaged structure for unligated Staphylococcal nuclease-H124L


OverviewOverview

The solution structures of staphylococcal nuclease (nuclease) H124L and its ternary complex, (nuclease-H124L).pdTp.Ca2+, were determined by ab initio dynamic simulated annealing using 1925 NOE, 119 phi, 20 chi 1 and 112 hydrogen bond constraints for the free protein, and 2003 NOE, 118 phi, 20 chi 1 and 114 hydrogen bond constraints for the ternary complex. In both cases, the final structures display only small deviations from idealized covalent geometry. In structured regions, the overall root-mean-square deviations from mean atomic coordinates are 0.46 (+/- 0.05) A and 0.41 (+/- 0.05) A for the backbone heavy atoms of nuclease and its ternary complex, respectively. The backbone conformations of residues in the loop formed by Arg81-Gly86, which is adjacent to the active site, are more precisely defined in the ternary complex than in unligated nuclease. Also, the protein side chains that show NOEs and evidence for hydrogen bonds to pdTp (Arg35, Lys84, Tyr85, Arg87, Tyr113, and Tyr115) are better defined in the ternary complex. As has been observed previously in the X-ray structures of nuclease-WT, the binding of pdTp causes the backbone of Tyr113 to change from an extended to a left-handed alpha-helical conformation. The NMR structures reported here were compared with available X-ray structures: nuclease-H124L [Truckses et al. (1996) Protein Sci., 5, 1907-1916] and the ternary complex of wild-type staphylococcal nuclease [Loll and Lattman (1989) Proteins Struct. Funct. Genet., 5, 183-201]. Overall, the solution structures of nuclease-H124L are consistent with these crystal structures, but small differences were observed between the structures in the solution and crystal environments. These included differences in the conformations of certain side chains, a reduction in the extent of helix 1 in solution, and many fewer hydrogen bonds involving side chains in solution.

About this StructureAbout this Structure

1JOO is a Single protein structure of sequence from Staphylococcus aureus. Full crystallographic information is available from OCA.

ReferenceReference

Solution structures of staphylococcal nuclease from multidimensional, multinuclear NMR: nuclease-H124L and its ternary complex with Ca2+ and thymidine-3',5'-bisphosphate., Wang J, Truckses DM, Abildgaard F, Dzakula Z, Zolnai Z, Markley JL, J Biomol NMR. 1997 Sep;10(2):143-64. PMID:9369015

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