2010년 12월 27일 월요일

ClustalXeed, Software download Sites

ClustalXeed: a GUI-based grid computation version for high performance and terabyte size multiple sequence alignment


ClustalXeed: a GUI-based grid computation version for high performance and terabyte size multiple sequence alignment
Taeho Kim, Hyun Joo



The Software Download Site :

http://www.mediafire.com/?thypv8h3dxzc9q1      clustalXeed-1.0.tar.gz (linux version)

http://www.mediafire.com/?7nr42a443ugwmf6   ClustalXeed-Manual-1a.pdf (including installation)


or download both files in a zip format:

http://www.mediafire.com/?4j1af1va86pc66y     
clustalXeed-1.0.tar.gz (linux version) + ClustalXeed-Manual-1a.pdf (including installation)


** The software runs on a Linux OS. For more information, send a mail to : phyjoo@inje.ac.kr

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2010년 9월 28일 화요일

ClustalXeed - Cloud Computing


       Web source: http://portal.eqentia.com/cloudcomputing/source/13027-BioMed-Central

Timeline of Clustal* Series -Cute and Compressed View

The history of Clustal Series...
[web source: http://www.dipity.com/timeline/Clustalw]

Accurate and Fast MSA tool may accelerate the discovery of mitochondrial DNA mutations

Does strong hypertrophic condition induce fast mitochondrial
DNA mutation of rabbit heart?




Homo- and heteroplasmic mitochondrial DNA (mtDNA) mutations were observed and identified in an isoproterenol-induced rabbit model of cardiac hypertrophy. Genes encoding proteins essential for catalyzing mitochondrial electron transfer and for generating the proton motive force, such as NADH dehydrogenases (ND2, ND3, ND4, and ND6), cytochrome b, and ATPase 8, showed increased susceptibility for mutation. Specifically, five mutations caused amino acid changes and were located in Complex I and Complex V gene clusters. To our knowledge, this is the first demonstration of a relationship between cardiac hypertrophy induced by a strong sympathetic load and rapid mtDNA mutations.

Ref: T. Kim et al. Mitochondrion 8 (2008) 279.283

Application of in silico sequence homology searching


A putative prokaryotic inward rectifier K+ (Kir) channel
was discovered by in silico sequence homology and membrane topology analyses with respect to the number of transmembrane domains (TMs) and the presence of K+ selectivity filter and/or ATP binding sites..


New Kir6.2 Channel Discovered
Ref: The Journal of Microbiology (2010) Vol. 48, No. 3, pp. 325-330

2010년 9월 27일 월요일

Are you suffer from huge Phylogenetic Tree Drawing?


ClustalXeed provides a scalable vector graphics option for big tree drawing...