1zm8

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[[Image:1zm8.gif|left|200px]]
[[Image:1zm8.gif|left|200px]]
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{{Structure
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|PDB= 1zm8 |SIZE=350|CAPTION= <scene name='initialview01'>1zm8</scene>, resolution 1.90&Aring;
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The line below this paragraph, containing "STRUCTURE_1zm8", creates the "Structure Box" on the page.
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|SITE=
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|LIGAND= <scene name='pdbligand=MN:MANGANESE+(II)+ION'>MN</scene>, <scene name='pdbligand=NA:SODIUM+ION'>NA</scene>, <scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene>
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|GENE= nucA ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=1167 Anabaena sp.])
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{{STRUCTURE_1zm8| PDB=1zm8 | SCENE= }}
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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1zm8 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1zm8 OCA], [http://www.ebi.ac.uk/pdbsum/1zm8 PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1zm8 RCSB]</span>
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'''Apo Crystal structure of Nuclease A from Anabaena sp.'''
'''Apo Crystal structure of Nuclease A from Anabaena sp.'''
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[[Category: Pedersen, L C.]]
[[Category: Pedersen, L C.]]
[[Category: Pingoud, A.]]
[[Category: Pingoud, A.]]
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[[Category: metal dependent]]
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[[Category: Metal dependent]]
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[[Category: nuca]]
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[[Category: Nuca]]
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[[Category: nuclease]]
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[[Category: Nuclease]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sat May 3 17:47:58 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Mar 31 01:38:36 2008''
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Revision as of 14:47, 3 May 2008

Template:STRUCTURE 1zm8

Apo Crystal structure of Nuclease A from Anabaena sp.


Overview

Nuclease A (NucA) is a nonspecific endonuclease from Anabaena sp. capable of degrading single- and double-stranded DNA and RNA in the presence of divalent metal ions. We have determined the structure of the delta(2-24),D121A mutant of NucA in the presence of Zn2+ and Mn2+ (PDB code 1ZM8). The mutations were introduced to remove the N-terminal signal peptide and to reduce the activity of the nonspecific nuclease, thereby reducing its toxicity to the Escherichia coli expression system. NucA contains a betabeta alpha metal finger motif and a hydrated Mn2+ ion at the active site. Unexpectedly, NucA was found to contain additional metal binding sites approximately 26 A apart from the catalytic metal binding site. A structural comparison between NucA and the closest analog for which structural data exist, the Serratia nuclease, indicates several interesting differences. First, NucA is a monomer rather than a dimer. Second, there is an unexpected structural homology between the N-terminal segments despite a poorly conserved sequence, which in Serratia includes a cysteine bridge thought to play a regulatory role. In addition, although a sequence alignment had suggested that NucA lacks a proposed catalytic residue corresponding to Arg57 in Serratia, the structure determined here indicates that Arg93 in NucA is positioned to fulfill this role. Based on comparison with DNA-bound nuclease structures of the betabeta alpha metal finger nuclease family and available mutational data on NucA, we propose that His124 acts as a catalytic base, and Arg93 participates in the catalysis possibly through stabilization of the transition state.

About this Structure

1ZM8 is a Single protein structure of sequence from Anabaena sp.. Full crystallographic information is available from OCA.

Reference

Structural insights into the mechanism of nuclease A, a betabeta alpha metal nuclease from Anabaena., Ghosh M, Meiss G, Pingoud A, London RE, Pedersen LC, J Biol Chem. 2005 Jul 29;280(30):27990-7. Epub 2005 May 15. PMID:15897201 Page seeded by OCA on Sat May 3 17:47:58 2008

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