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CD ComputaBio Unveils Protein Structure Modeling Service for Drug Development
CD ComputaBio Unveils Protein Structure Modeling Service for Drug Development
CD ComputaBio recently announced the launch of protein structure modeling service to help researchers understand the structural properties of target proteins, analyze their structure-function relationships, and can be used for drug screening, the discovery of potential therapeutic drugs for a certain disease, or the study of the interaction mode between targets and drugs.

CD ComputaBio, a reliable computational biology service provider located in New York, is always hammering away at research and trials in order to provide customers with access to the latest software, technologies, and expertise at a competitive price and fast turnaround time. The company recently announced the launch of protein structure modeling service to help researchers understand the structural properties of target proteins, analyze their structure-function relationships, and can be used for drug screening, the discovery of potential therapeutic drugs for a certain disease, or the study of the interaction mode between targets and drugs.

 

In recent years, the rapid development of structural biology has provided a structural basis for studying and understanding the biological functions of proteins. In general, the three-dimensional structure of proteins is mainly determined by experimental methods, such as X-ray crystallography or NMR spectroscopy (nuclear magnetic resonance spectroscopy). In fact, technical difficulties make the determination of protein three-dimensional structure quite slow, and for many reasons, the three-dimensional structure of some proteins is still elusive. With the help of computer simulation technology, scientists have developed a series of prediction methods.

 

“CD ComputaBio uses computational modeling to predict the three-dimensional structure of proteins. We have extensive experience in modeling various proteins. The resulting structural models are all quality-validated and can be used for a variety of purposes, such as annotating genes with unknown functions and structure-based drug design. Structural modeling programs also work seamlessly with downstream computational modeling protocols, including docking and molecular dynamics simulations,” said the Product Manager of CD ComputaBio.

 

The protein structure modeling service range available at CD ComputaBio covers:

1. Homology Detection and Structure Comparison Service

2. Antibody Modeling Service

3. Fold Recognition Service

4. Fusion Protein Modeling Service

5. Homology Modeling Service

6. Membrane Protein Modeling Service

 

These services use internationally leading and excellent protein modeling software. CD ComputaBio has an excellent molecular simulation and drug design team, and its technicians have rich research experience in large pharmaceutical companies and high-quality project execution capabilities, and can provide customers with high-quality protein structure modeling services. Its team of experts can provide accurate modeling for the system of your choice, so you don't have to worry about technical issues.

 

“The services provided by CD ComputaBio are based on cutting-edge computational platforms and technology in this field with accuracy and sensitivity. We can provide a fast turnaround, clear and concise written reports, and custom service to help customers resolve their technical challenges,” the product manager further added.

 

 

About CD ComputaBio

With years of experience, CD ComputaBio can provide customers with professional computational biology services. Utilizing rich experience and powerful technology in computational science, the company can provide customers with many computational biology analysis services such as molecular dynamics simulation, drug design, virtual screening, quantum chemical calculations, etc.

 

Media Contact

Company Name: CD ComputaBio

Contact Person: Vivian Smith

Phone: 1-631-371-4691

Country: United States

Website: https://www.computabio.com