Sir one request : plz suggest some list of good laptops for doing molecular docking project!!!🙏🏻🙏🏻🙏🏻

If you are a long time Linux/*nix user, you may backport latest gromacs from Debian Sid repository and rebuild it from the sources.

the music in the background of the video so annoying , id appracite to you is you make it without music so we can foucs on the explination well

Hi, why did you predict the transmembrane region?what is it's importance?

If you don't have coding experience or a powerful computer, you can use QuandleLabs to use all of the above tools completely online

Autogrid is not running and glg file is also not generated any solution. please help

Dear sir can you please teach me separately in Google meet for downloading the structure of protein protein interaction??

Nice

Excuse, i want to ask if i am not working on gene cloning; rather, I am conducting gene expression experiments. How can I avoid incomplete gene amplification when designing primers?

Can we run in Intel gpu

Good morning sir, I am Manohar Naik your Junior in sku from Kadiri sir , I have a doubt how can I contact you sir I have no number sir

Sir g You are the only one who not work for only to get views but to help someone

great sir thank you, the links in the description are more precious

Sir which software is used to predict the anti-cancer compound ?

3h42 and 3m0c are in complex. did you seprate them before?

why did you use hex when it was non validated

Sir , what if the ligand is not inserted to the protein

After this step, how to get 2D interactions?

I'm getting an error during running autogrid4, it's not running.

From where autogrid4 comes, I'm confused

Great video, Thanks alot and this the best lecture in docking that i have ever seen. but my question: What is the purpose of the step taken @9:10, changing the histidine hydrogens? why not +1? and why you didnt apply force field for the compounds?

Can you please tell me how to run gromacs in could Google colab platform

The best video on KZbin... thank you very much sir

Please share videos on network pharmacology, QASR and DFT for drug discovery

Fucking hindu your video and social media is a bullshit, and your teaching is boring and deficint

You just saved my undergraduate thesis research. Thank you so much!!

Im performing docking on a known active site so i limited the gridbox around the active site only. Some of the conformations i got after docking were outside the grid box. Is that normal?

Thank you so much for this helpful tutorial! I am having an issue if I can ask. When I run the command, the cmd says that access is denied.

Hi, sir , this video is very helpful to understand molecular docking with binding active site. My question is "How to know active binding site of any other protein for good result of molecular docking?????"

Thanks

Exellent ❤

Thank you professor, I want linearized vector it has 7000 basepair. I tried restrictions enzyme, but I can't find valid enzyme.so I want to make primer. Please guide me. I also tried to make primers but I can't fullfil the condition of tm, gc and no of basepair. How can I do.

sir when i want to save the GPF then i get error and shows that you must select macromolecule before writing gpf

This was SO MUCH helpful!! Thank you for the amazing explanation!

this video is a waste of time, dont even bother with it. theres thousands of better options out there

Sir Good evening sir I'm Manohar Naik from Kadiri ,your junior in SKU I have a doubt sir

When I read a paper about andrographolide as a potential inhibitor of SARS-CoV-2 main protease: an in silico approach. The andrographolide compound has a free energy of -3.09 Kcal/mol, but it shows great binding when compared to other compounds having more negative free energy values. I think about pressure, temperature, and pH in the body affecting the inhibitory process

Make a clear cut video of cuda installation with gromacs why you skip that portion?

if its 430000 subcultures are there how to download it in sdf.

please tell me

hlo for link it showing does not exist where i get it

Why is my ligand so far away from the protein??? I know the active site of the protein

why can't I save the final complex in hex docking

Please I have humain gene (hla) how i do primer design

I am getting an error while adding polar hydrogen only. The error is could not find atomic no. For A A. Could you please help me. And ease provide your email id if possible. Thank you

Hello sir , after the splitting command , my compounds doesn’t appear in seperate folder. What should be done now ? Please help me

hi, i have a question, i have nitrogen and carbon genes, then i want to check relation with different mine treatments, but you did not add any values of genes, becuase my results have values of every gene in every treatment

Sir, my laptop has 16 gb RAM and 1 Tb ssd. I've removed hard drive to put ssd. Can install linux and gromacs and run md simulation with these system requirements?

Hello, my input into Open Babel GUI was SDF file of N4-benzoyldeoxycytidine and when I want to convert it into pdbqt file, it says that 0 molecules were converted. Can you help to understand what is wrong? Thank you sir

How to. Docking iodine and bromine compounds