1ehw

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[[Image:1ehw.jpg|left|200px]]
[[Image:1ehw.jpg|left|200px]]
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{{Structure
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|PDB= 1ehw |SIZE=350|CAPTION= <scene name='initialview01'>1ehw</scene>, resolution 2.40&Aring;
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The line below this paragraph, containing "STRUCTURE_1ehw", creates the "Structure Box" on the page.
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|SITE=
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|LIGAND= <scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene>
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or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
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|ACTIVITY= <span class='plainlinks'>[http://en.wikipedia.org/wiki/Nucleoside-diphosphate_kinase Nucleoside-diphosphate kinase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.4.6 2.7.4.6] </span>
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{{STRUCTURE_1ehw| PDB=1ehw | SCENE= }}
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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1ehw FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1ehw OCA], [http://www.ebi.ac.uk/pdbsum/1ehw PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1ehw RCSB]</span>
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'''HUMAN NUCLEOSIDE DIPHOSPHATE KINASE 4'''
'''HUMAN NUCLEOSIDE DIPHOSPHATE KINASE 4'''
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[[Category: Milon, L.]]
[[Category: Milon, L.]]
[[Category: Munier, A.]]
[[Category: Munier, A.]]
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[[Category: killer-of-prune]]
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[[Category: Killer-of-prune]]
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[[Category: mitochondrial]]
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[[Category: Mitochondrial]]
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[[Category: nm23]]
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[[Category: Nm23]]
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[[Category: nucleoside diphosphate kinase]]
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[[Category: Nucleoside diphosphate kinase]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Fri May 2 15:07:11 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Mar 30 20:02:50 2008''
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Revision as of 12:07, 2 May 2008

Template:STRUCTURE 1ehw

HUMAN NUCLEOSIDE DIPHOSPHATE KINASE 4


Overview

We demonstrate here the catalytic activity and subcellular localization of the Nm23-H4 protein, product of nm23-H4, a new member of the human nm23/nucleoside diphosphate (NDP) kinase gene family (Milon, L., Rousseau-Merck, M., Munier, A., Erent, M., Lascu, I., Capeau, J., and Lacombe, M. L. (1997) Hum. Genet. 99, 550-557). Nm3-H4 was synthesized in escherichia coli as the full-length protein and as a truncated form missing the N-terminal extension characteristic of mitochondrial targeting. The truncated form possesses NDP kinase activity, whereas the full-length protein is inactive, suggesting that the extension prevents enzyme folding and/or activity. X-ray crystallographic analysis was performed on active truncated Nm23-H4. Like other eukaryotic NDP kinases, it is a hexamer. Nm23-H4 naturally possesses a serine residue at position 129, equivalent to the K-pn mutation of the Drosophila NDP kinase. The x-ray structure shows that the presence of Ser(129) has local structural effects that weaken subunit interactions. Site-directed mutagenesis shows that the serine is responsible for the lability of Nm23-H4 to heat and urea treatment, because the S129P mutant is greatly stabilized. Examination of human embryonic kidney 293 cells transfected with green fluorescent protein fusions by confocal microscopy shows a specific mitochondrial localization of Nm23-H4 that was also demonstrated by Western blot analysis of subcellular fractions of these cells. Import into mitochondria is accompanied by cleavage of the N-terminal extension that results in NDP kinase activity. Submitochondrial fractionation indicates that Nm23-H4 is associated with mitochondrial membranes, possibly to the contact sites between the outer and inner membranes.

About this Structure

1EHW is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.

Reference

The human nm23-H4 gene product is a mitochondrial nucleoside diphosphate kinase., Milon L, Meyer P, Chiadmi M, Munier A, Johansson M, Karlsson A, Lascu I, Capeau J, Janin J, Lacombe ML, J Biol Chem. 2000 May 12;275(19):14264-72. PMID:10799505 Page seeded by OCA on Fri May 2 15:07:11 2008

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