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Pharmaceutical companies are today facing a real crisis where a lack of new drug launches is failing to compensate for those that are nearing the end of their patented life time. The vast majority of drugs work by strongly binding to a specific protein and altering its normal function. The need for very specific and strong binding of a drug to its protein target is the reason for the difficulty in designing drugs. To address this, the industry spends $2bn p.a. on high throughput screening, where thousands of experiments are carried out at once to try and pick out promising leads for drugs. Our offering represents a generational leap in virtual screening methods.
Structural data on the interaction of small molecules and molecular fragments (including co-solvents, cofactors, inhibitors, peptides and any other suitable molecules) with the target protein is collated.
We are looking to complete the three step process of our screening method by writing a volume matching algo...
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