Switch Laboratory Switch Laboratory

Mapping aggregation-specific interactions in human disease. FoldX plugin for YASARA. The significance of protein misfolding and aggregation on the development of human disease is often underestimated and its consequences poorly understood. Indeed, so far. Only a few dozen aggregation-associated diseases have been identified, mostly neurodegenerative disorders or systemic amyloidoses. Neurodegenerative diseases are associated with a cytotoxic gain-of-function phenotype facilitating the incrimination of pr.

OVERVIEW

The site switchlab.org currently has a traffic classification of zero (the smaller the more traffic). We have crawled twenty pages within the domain switchlab.org and found twenty-seven websites referring to switchlab.org. We were able to precure one contacts and locations for switchlab.org to help you communicate with them. The site switchlab.org has been on the internet for eight hundred weeks, thirty days, sixteen hours, and fourteen minutes.
Pages Parsed
20
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27
Contacts
1
Addresses
1
Online Since
Aug 2009

SWITCHLAB.ORG TRAFFIC

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SWITCHLAB.ORG HISTORY

The site switchlab.org was started on on August 17, 2009. It is now eight hundred weeks, thirty days, sixteen hours, and fourteen minutes young.
REGISTERED
August
2009

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15
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3
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LINKS TO SWITCHLAB.ORG

FoldX plugin for YASARA - FoldX plugin for YASARA

From FoldX plugin for YASARA. Welcome to the homepage of the FoldX plugin for YASARA. FoldX tools menu in YASARA. The FoldX plugin for YASARA is a software package to access and run FoldX commands in YASARA. FoldX is normally run from the command line without graphics. By installing the FoldX plugin for YASARA, you can access the most important FoldX tools at the touch of a button in the 3D graphical YASARA interface. You directly see the result.

Accurate prediction of DnaK-peptide binding via molecular modelling and experimental data Molecular chaperone binding site prediction

Accurate prediction of DnaK-peptide binding via molecular modelling and experimental data. Joost Van Durme, Sebastian Maurer-Stroh, Rodrigo Gallardo, Hannah Wilkinson, Frederic Rousseau and Joost Schymkowitz. VIB Switch Laboratory, Vrije Universiteit Brussel, Brussels, Belgium. Button in the top menu to use the prediction server.

WHAT DOES SWITCHLAB.ORG LOOK LIKE?

Desktop Screenshot of switchlab.org Mobile Screenshot of switchlab.org Tablet Screenshot of switchlab.org

CONTACTS

VIB-Switch Lab

Hannah Wilkinson

Rijvisschetraat 120

Gent, 9052

BE

SWITCHLAB.ORG SERVER

We observed that a lone root page on switchlab.org took five hundred and sixteen milliseconds to download. We could not detect a SSL certificate, so therefore our crawlers consider this site not secure.
Load time
0.516 sec
SSL
NOT SECURE
IP
134.58.50.6

NAME SERVERS

ns1.je-eigen-domein.nl
ns2.je-eigen-domein.nl
ns3.je-eigen-domein.nl
ns4.je-eigen-domein.nl

FAVICON

SERVER SOFTWARE

We detected that this domain is operating the Apache/2.2.14 (Ubuntu) operating system.

SITE TITLE

Switch Laboratory Switch Laboratory

DESCRIPTION

Mapping aggregation-specific interactions in human disease. FoldX plugin for YASARA. The significance of protein misfolding and aggregation on the development of human disease is often underestimated and its consequences poorly understood. Indeed, so far. Only a few dozen aggregation-associated diseases have been identified, mostly neurodegenerative disorders or systemic amyloidoses. Neurodegenerative diseases are associated with a cytotoxic gain-of-function phenotype facilitating the incrimination of pr.

PARSED CONTENT

The site switchlab.org had the following in the homepage, "Mapping aggregation-specific interactions in human disease." I noticed that the webpage stated " The significance of protein misfolding and aggregation on the development of human disease is often underestimated and its consequences poorly understood." They also stated " Only a few dozen aggregation-associated diseases have been identified, mostly neurodegenerative disorders or systemic amyloidoses. Neurodegenerative diseases are associated with a cytotoxic gain-of-function phenotype facilitating the incrimination of pr."

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