Thank you this has been VERY VERY helpful and I really appreciate your tutorial. Everything is so clear and I love how you also provided sources on where to find downloads :)
Wonderful tutorial! This will save me a lot of time (8 protein targets and 23 ligands). I was going to be very selective about the ligands, but I don't have to be now.
@Thomas Lemon Hello sir, could you please tell me how did you do that (8 protein target and 23 ligands) at a time. Have you dock one protein with 23 ligand and again another protein with 23 ligand and so on?
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?
Sir it's good to dock all ligands at one time. But how will you interpret the ligand interactions with the receptor. I mean discovery studio can do this ?
I got an error after running the script for docking, but I get the results as log and out files. Is this error message affect the result? "Command line parse error: too many positional options"
Thank you for your informative video, sir! I followed those steps but I got error: "Can't open perl script "Vina_windows.pl": No such file or directory". Can you help me?
Great effort BB!! Keep up the good work... can you please tell me what is your system configuration? like RAM, Processor etc. I am just starting with bioinformatics and your advise will be of much help.
Hello Sir I hope you are doing great I have tried to use the perl script with the new version of Vina (v 1.2.3) but Vina didn't recognize the --log argument in the script. Is there any problem/modification?
This video tutorial is truly helpful for my thesis. I have a question though... Why is the exhaustiveness parameter is not typed out in the configuration file or Vina will carry it out at default ?
Thanks for your excellent video, I have an error could anyone help me?! It Is warning: couldn't find any conformations completely within the search space Warning: check that it is larger enough for all movable atoms, including those in the flexible side chains
Thank you for all the tutorials, sir. I tried to run Autodock Virtual Screening and each time I run the "repair missing atom" it will not complete as in your previous tutorial, it will stop running, the program will hang and I will not be able to proceed. Please, how do I go about it, sir?
if repair missing atom is having issue with u, u can rebuild the model in swissmodel server.. after building the model, u can skip the repair missing atoms step in audotock
Thank you so much for the video. I have a little question about the small peptide as ligands. when I transform it from pdb file into pdbqt file. it was broken (when i visualize them by chimera X or pymol). Do you have any solution for the transformation ?
Thanku sir for very much informative session..i want all binding energy of complex in one notepad file then how can i do this?? Please if you can help because i have huge number of ligands and it is not possible to open one by one file.
Sir I am interested in learning bioinformatics. What basics I should know. I know basic biotechnology and biochemistry but when it come to softwares tools I am confused. What are the programming language I should start with. It will be very helpful if you can make a step by step things to learn for a beginner like me to excel in bioinformatics field.
There is two options, one is software developer, requires advanced programming skills, second one is data analyst, require less programming skills. The choice is totally depends upon what's ur background area.. if ur not familiar with programming my suggestion is go with option 2, its really hard to develop programming skills in short period.
hi the video was very informative, but after running the perl . I got this message. WARNING: The search space volume > 27000 Angstrom^3 (See FAQ) Output will be ligand_out.pdbqt Detected 8 CPUs Reading input ... done. Setting up the scoring function ... done. Analyzing the binding site ... Error: insufficient memory! but there is more than 500 gb available in C drive? any help with this?
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?
Verify if you are not putting the wrong coordinates of the grid box in the config.txt file, in ADT if you've already chose a grid coordinate and tries to edit that grid, the number in the scroll button has to sum with the previous grid coordinate
Sir prepared all files, facing error Phrase error in line all the ligand pdbqt files unexpected multi-MODEL input Use "vina_split" first? getting this error pls solve
Sir , can you please tell me how to do energy minimisation for protein and ligand. Can you post video on result analysis by using pymol software.thank you
Hello I have been having issues with the autodock reading my ligand file. I used the .pdb format, but the program keeps giving me an error message when I input it. Is there a way to fix that?
Sir jese hum docking karte time receptor protein kaa interaction karte hain , us time receptor protein kaa water remove karte hain, or ligand kaa interaction karte hain, but natural condition main recepror protein main water rahega, phir interaction kese hoga..... Sir plz doubt clear kar dijiye .... Usually water active site ko distort krta h interaction ke time, tbhi hum water molecules ko remove karte hain , but jab hum koi medicine/ligand create kar lenge to wo to phir body ke inside receptor protein main water hone se interaction hi nahi hone dega natural condition main..... Plz clear the doubt of my question sir .....
Thank you sir for your guide but after doing it all i am not able to get dlg(data log file) in data folder as you show in "autodock result analysis" video..so please guide us for it.
if u have carefully done the above tutorial.. i am sure u will sure u will get log file at the end.. if u still getting error.. u can post ur error screenshot in our facebook page facebook.com/groups/261045198486665
Sir can we docked two target site for same disease by single ligand? Sir suppose x naam kaa ek ligand h jo A naam ke target site ko inhibit krra ho , phir suppose wahi x naam kaa ligand B naam ke target site ko inhibit krra ho, to sir kya hum ek saath A ligand ko dono target site(A and B) pe ek he saath docking kra skte h..... Multiple target site docking.... Sir plz doubt clear kar dijiye Agar kar sakte hain to kese ? Nahi kar sakte hain to kyu ni kr sakte?
Openbabel 3.1.1 doesn't offer pdbqt format. When Pymol read lots of sdf or mol2, it doesn't work well with error. How can I convert lots of sdf or mol2 into pdbqt?
Hii sir, I am facing this type ofproblem ....pls help me lig_9.pdbqt Configuration file parse error: unknown option centre_x Correct usage: Input: --receptor arg rigid part of the receptor (PDBQT) --flex arg flexible side chains, if any (PDBQT) --ligand arg ligand (PDBQT) Search space (required): --center_x arg X coordinate of the center --center_y arg Y coordinate of the center --center_z arg Z coordinate of the center --size_x arg size in the X dimension (Angstroms) --size_y arg size in the Y dimension (Angstroms) --size_z arg size in the Z dimension (Angstroms) Output (optional): --out arg output models (PDBQT), the default is chosen based on the ligand file name --log arg optionally, write log file Misc (optional): --cpu arg the number of CPUs to use (the default is to try to detect the number of CPUs or, failing that, use 1) --seed arg explicit random seed --exhaustiveness arg (=8) exhaustiveness of the global search (roughly proportional to time): 1+ --num_modes arg (=9) maximum number of binding modes to generate --energy_range arg (=3) maximum energy difference between the best binding mode and the worst one displayed (kcal/mol) Configuration file (optional): --config arg the above options can be put here Information (optional): --help display usage summary --help_advanced display usage summary with advanced options --version display program version
to convert ligand file using open Babel GUI, should we convert one by one or can we upload all ligand in the folder and they will convert all of the ligand automatically?
after giving the command, perl vina_docking.pl it writes perl is not recognised as internal or external command, operable program or batch file. What may be the reason for this.
1. smile to pdbqt (Open Babel or you can use smile converter online tool check > u can upload multiple smile in text format cactus.nci.nih.gov/translate/) 2. pdb to pdqt (Open Babel or Racoon plugin > check this link www.researchgate.net/post/How_can_you_convert_a_large_number_of_pdb_files_to_pdbqt_files) if you any other concerns you can post ur question in our facebook group page facebook.com/groups/261045198486665
1. smile to pdbqt (Open Babel or you can use smile converter online tool check > u can upload multiple smile in text format cactus.nci.nih.gov/translate/) 2. pdb to pdqt (Open Babel or Racoon plugin > check this link www.researchgate.net/post/How_can_you_convert_a_large_number_of_pdb_files_to_pdbqt_files) if you any other concerns you can post ur question in our facebook group page facebook.com/groups/261045198486665
How to rank a list of solutions (i.e 1000 compounds = 1000 log files) from autodock Vina? Do you have some script or method to rank for the best solution (compound) from such a list of log or PDBQT files from Vina? Thank you in advance.
@@jaannawaz2007 dear BB, could you please share the video link for this next video you mentioned to get the results of binding energies in one file because i am using big database and I need all the results in one excel sheet as usually obtained in PyRx tool. I tried to use PyRx tool for my dataset but all time I got some parse error showing that atom are missing in ligand. Vina is working fine but the only issue that I need all the results of binding energy in one single file to analyze easily
Thank you very much sir sir this is very useful for me ...i was searching script for multiple docking using vina since many days but today i found this on your channel this is the best tutorial i have ever seen... Sir actually i want to convert csv file of smiles into pdbqt ...how to do it ? Please if you can help .
Your welcome... Subscribe to our channel to get more interactive contents in Bioinformatics. Regarding your question, you can't convert directly smile format to pdbqt, initially u have to convert into pdb file and from pdb u have to convert into PDBQT. 1. smile to pdbqt (Open Babel or you can use smile converter online tool check > u can upload multiple smile in text format cactus.nci.nih.gov/translate/) 2. pdb to pdqt (Open Babel or Racoon plugin > check this link www.researchgate.net/post/How_can_you_convert_a_large_number_of_pdb_files_to_pdbqt_files) if you any other concerns you can post ur question in our facebook group page facebook.com/groups/261045198486665
Hello sir, I can't complete the docking process it shows "Command line parse error: too many positional options" How to fix this error? Thanks Warm regards Rajesh
Bioinformatics With BB 3 weeks ago Your welcome... Regarding your question, you can't convert directly smile format to pdbqt, initially u have to convert into pdb file and from pdb u have to convert into PDBQT. 1. smile to pdbqt (Open Babel or you can use smile converter online tool check > u can upload multiple smile in text format cactus.nci.nih.gov/translate/) 2. pdb to pdqt (Open Babel or Racoon plugin > check this link www.researchgate.net/post/How_can_you_convert_a_large_number_of_pdb_files_to_pdbqt_files) if you any other concerns you can post ur question in our facebook group page facebook.com/groups/261045198486665
this is the error: sh Vina_windows.pl Vina_windows.pl: line 2: printLigand_file:\t: command not found Vina_windows.pl: line 2: $' ': command not found Vina_windows.pl: line 3: syntax error near unexpected token `;' 'ina_windows.pl: line 3: `$ligfile=;
Thanks sir, i m able to perform the same. I ve a query. What is the meaning and significance of 0,HD1 0,HE2 and +1 in Edit Histidine Hydrogen dialogue box ?
You just saved my undergraduate thesis research. Thank you so much!!
Thank you this has been VERY VERY helpful and I really appreciate your tutorial. Everything is so clear and I love how you also provided sources on where to find downloads :)
Thank you this was very informative and easy to follow. Much appreciated.
Glad it was helpful!
This was SO MUCH helpful!! Thank you for the amazing explanation!
It's an excellent tutorial for virtual screening using autodock vina
Thank you very much. It is an excellent tutorial for virtual screening in Autodock Vina
Wonderful tutorial! This will save me a lot of time (8 protein targets and 23 ligands). I was going to be very selective about the ligands, but I don't have to be now.
@Thomas Lemon Hello sir, could you please tell me how did you do that (8 protein target and 23 ligands) at a time.
Have you dock one protein with 23 ligand and again another protein with 23 ligand and so on?
@@preetimahra8679 I ran a total of 8 scripts, one for each protein.
@@_lemonny Ok, Thank you.
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?
This is another master piece from you sir. Kindly add tutorials about ligand DNA docking using autodock. Thanks regards
Noted
Sir it's good to dock all ligands at one time. But how will you interpret the ligand interactions with the receptor. I mean discovery studio can do this ?
Thank you sir for this wonderful guidance !
ua-cam.com/video/U4Xh_VHs0IE/v-deo.html
hey sir, why don't we just use Pyrx ? is there any difference with accuracy or sth else?
Great job, Thank you so much Professor.
Thank you so much, this is very informative and help me a lot in doing Autodock
I got an error after running the script for docking, but I get the results as log and out files. Is this error message affect the result?
"Command line parse error: too many positional options"
very informative, greeting from brazil
Thank You so much
Thank you for your informative video, sir! I followed those steps but I got error: "Can't open perl script "Vina_windows.pl": No such file or directory". Can you help me?
Is there any special reason for downloading ligands as separate files instead of single *.sdf file.
Multiple Ligand Docking by Autodock Vina through command line in UNIX/LINUX
ua-cam.com/video/U4Xh_VHs0IE/v-deo.html
Thank you! How do I add new atom types in Vina, specifically for Silicon? Is there a parameter file like GPF or DPF that needs to be edited?
Thank you for your work. What software would you recommend to generate 3D conformation of molecules?
winmostar
Now we have instadock which have very easy graphical user interface and very easy to use and runs on autodock vina
Very interesting and informative video kindly can anyone of you can help me. Thanks
Hi, where can I find the citation for the Perl script? Thanks a lot!
Great effort BB!! Keep up the good work... can you please tell me what is your system configuration? like RAM, Processor etc. I am just starting with bioinformatics and your advise will be of much help.
This my System Configuration : Lenovo Legion Y740 9th Gen Intel Core i7 15.6 inch FHD Gaming Laptop (32GB RAM/2TB SSD/NVIDIA RTX 2060 8GB Graphics
Hello Sir
I hope you are doing great
I have tried to use the perl script with the new version of Vina (v 1.2.3) but Vina didn't recognize the --log argument in the script.
Is there any problem/modification?
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.
thank you its was really clair
Can you show us how to dock between DNA and protein, unable to get a secondary structured DNA in PDB format.
Sir aftr entering the ligand file name in the CMD, It is only showing the list of PDBQT files in the ligand.txt file. Vina is not running
thank you for this, is this still the easiest way to use autodock vina for screening a library of ligands?
❤❤❤❤❤
Youre amazing. Thank you so much.
This video tutorial is truly helpful for my thesis. I have a question though... Why is the exhaustiveness parameter is not typed out in the configuration file or Vina will carry it out at default ?
this tutorial is very helpful in my thesis!! i want to add it in citation. which journals can I cite?
do we need to add charges for ligand ? like protein
Thanks for your excellent video, I have an error could anyone help me?!
It Is warning: couldn't find any conformations completely within the search space
Warning: check that it is larger enough for all movable atoms, including those in the flexible side chains
This works.Thankyou .
Is there any way to run this program in google colab???
Thank you for all the tutorials, sir. I tried to run Autodock Virtual Screening and each time I run the "repair missing atom" it will not complete as in your previous tutorial, it will stop running, the program will hang and I will not be able to proceed. Please, how do I go about it, sir?
if repair missing atom is having issue with u, u can rebuild the model in swissmodel server.. after building the model, u can skip the repair missing atoms step in audotock
same thing happens with me
@@jaannawaz2007 could you make video on that, if possible
What is the purpose of the step taken @9:10, changing the histidine hydrogens?
Can you please make a video in which is explained how adding a metal ion ?
sooon
Thank you so much for the video. I have a little question about the small peptide as ligands. when I transform it from pdb file into pdbqt file. it was broken (when i visualize them by chimera X or pymol). Do you have any solution for the transformation ?
Thanks for your lectures Sir
Can you please explain the steps of ( metal complex) docking??
After this step, how to get 2D interactions?
Thanku sir for very much informative session..i want all binding energy of complex in one notepad file then how can i do this?? Please if you can help because i have huge number of ligands and it is not possible to open one by one file.
Please I need an answer to this problem too
@@teuzen7900 he has already given the answer to this problem in his next video please do check
Very informative. Can you guide how to perform autodock vina for large ligands e.g. DNA?
ua-cam.com/video/U4Xh_VHs0IE/v-deo.html
Thankyou!
I am getting an error "IndexError: list index out of range" while choosing the macromolecule. Plz help me with this.
Sir I have downloaded perl in my laptop but still command prompt don't recognize it kindly guide me in this regards
I also have same problem, do ur problem solved?
Is there a script that can help us rank the output files according to the best energies?
In autodock vina the spacing parameter suppose to be at 1 in the gridbox panel
I think you are right, but why no one noticed that in this video?
@@謝承哲-d4rit is in the manual 🤷🤷
1. Will you sahre the script file to run virtual screening?
2. Shed some light on how write the ligands name in ligands.txt file using "command"
check in the description box
Sir I am interested in learning bioinformatics.
What basics I should know.
I know basic biotechnology and biochemistry but when it come to softwares tools I am confused.
What are the programming language I should start with.
It will be very helpful if you can make a step by step things to learn for a beginner like me to excel in bioinformatics field.
There is two options, one is software developer, requires advanced programming skills, second one is data analyst, require less programming skills. The choice is totally depends upon what's ur background area.. if ur not familiar with programming my suggestion is go with option 2, its really hard to develop programming skills in short period.
What is energy range stands for?
I followed all the steps,but it's showing " parse error on line 2 in file " in my ligand pdbqt file? Please help
hi the video was very informative, but after running the perl . I got this message.
WARNING: The search space volume > 27000 Angstrom^3 (See FAQ)
Output will be ligand_out.pdbqt
Detected 8 CPUs
Reading input ... done.
Setting up the scoring function ... done.
Analyzing the binding site ...
Error: insufficient memory! but there is more than 500 gb available in C drive? any help with this?
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?
Verify if you are not putting the wrong coordinates of the grid box in the config.txt file, in ADT if you've already chose a grid coordinate and tries to edit that grid, the number in the scroll button has to sum with the previous grid coordinate
Sir please make a video on DFT studies too pls sir 🙏
Sir prepared all files, facing error
Phrase error in line all the ligand pdbqt files
unexpected multi-MODEL input
Use "vina_split" first?
getting this error
pls solve
Sir , can you please tell me how to do energy minimisation for protein and ligand. Can you post video on result analysis by using pymol software.thank you
Do ligands need not to be minimized or some kind of processing prior VS?
ua-cam.com/video/U4Xh_VHs0IE/v-deo.html
Please give an example with metal docking
hello sir can we converted sdf into pdbqt file and run in autodock vina easy
Sir, what does the other two columns mean in the out_log file?
Hello I have been having issues with the autodock reading my ligand file. I used the .pdb format, but the program keeps giving me an error message when I input it. Is there a way to fix that?
Sir jese hum docking karte time receptor protein kaa interaction karte hain , us time receptor protein kaa water remove karte hain, or ligand kaa interaction karte hain, but natural condition main recepror protein main water rahega, phir interaction kese hoga..... Sir plz doubt clear kar dijiye .... Usually water active site ko distort krta h interaction ke time, tbhi hum water molecules ko remove karte hain , but jab hum koi medicine/ligand create kar lenge to wo to phir body ke inside receptor protein main water hone se interaction hi nahi hone dega natural condition main..... Plz clear the doubt of my question sir .....
ua-cam.com/video/U4Xh_VHs0IE/v-deo.html
Error is coming like could not open "conf_vs.txt" for reading.
Please help me out
I followed all steps but I got error "Configuration file parse error: unknown option num_mod" now what to do pls help
Dear
I would like to know if it would be possible, within the script, it run the vina_split? for poses.... or organize into separate folders?
no i didn't tried to embed split command, but its easy to run split command in a shell after docking.
vina_split --input output.pdqt
Thank you sir for your guide but after doing it all i am not able to get dlg(data log file) in data folder as you show in "autodock result analysis" video..so please guide us for it.
if u have carefully done the above tutorial.. i am sure u will sure u will get log file at the end.. if u still getting error.. u can post ur error screenshot in our facebook page facebook.com/groups/261045198486665
Good day. Please is there any command code to do multiple scoring of different compounds in autodock vina. thanks
Check my next video on VINA
Sir can we docked two target site for same disease by single ligand?
Sir suppose x naam kaa ek ligand h jo A naam ke target site ko inhibit krra ho , phir suppose wahi x naam kaa ligand B naam ke target site ko inhibit krra ho, to sir kya hum ek saath A ligand ko dono target site(A and B) pe ek he saath docking kra skte h..... Multiple target site docking....
Sir plz doubt clear kar dijiye
Agar kar sakte hain to kese ?
Nahi kar sakte hain to kyu ni kr sakte?
It can be done, as we do in blind docking, make grid of both these two pockets, and then perform docking
Openbabel 3.1.1 doesn't offer pdbqt format. When Pymol read lots of sdf or mol2, it doesn't work well with error. How can I convert lots of sdf or mol2 into pdbqt?
ua-cam.com/video/U4Xh_VHs0IE/v-deo.html
check the conversion in this video
Hii sir, I am facing this type ofproblem ....pls help me
lig_9.pdbqt
Configuration file parse error: unknown option centre_x
Correct usage:
Input:
--receptor arg rigid part of the receptor (PDBQT)
--flex arg flexible side chains, if any (PDBQT)
--ligand arg ligand (PDBQT)
Search space (required):
--center_x arg X coordinate of the center
--center_y arg Y coordinate of the center
--center_z arg Z coordinate of the center
--size_x arg size in the X dimension (Angstroms)
--size_y arg size in the Y dimension (Angstroms)
--size_z arg size in the Z dimension (Angstroms)
Output (optional):
--out arg output models (PDBQT), the default is chosen based on
the ligand file name
--log arg optionally, write log file
Misc (optional):
--cpu arg the number of CPUs to use (the default is to try to
detect the number of CPUs or, failing that, use 1)
--seed arg explicit random seed
--exhaustiveness arg (=8) exhaustiveness of the global search (roughly
proportional to time): 1+
--num_modes arg (=9) maximum number of binding modes to generate
--energy_range arg (=3) maximum energy difference between the best binding
mode and the worst one displayed (kcal/mol)
Configuration file (optional):
--config arg the above options can be put here
Information (optional):
--help display usage summary
--help_advanced display usage summary with advanced options
--version display program version
I have perl error when I put perl in command
to convert ligand file using open Babel GUI, should we convert one by one or can we upload all ligand in the folder and they will convert all of the ligand automatically?
ua-cam.com/video/U4Xh_VHs0IE/v-deo.html
I have converted the ligands in open babel in the video in provided link
Thank you for your response
after giving the command, perl vina_docking.pl
it writes perl is not recognised as internal or external command, operable program or batch file. What may be the reason for this.
ua-cam.com/video/U4Xh_VHs0IE/v-deo.html
baba jan how to prepare multiple ligands all at once? thank you!
Can i use this tool for publication? And what's the reference of this tool bcz i have to do mention it in paper.
Refer this book.. www.amazon.com/Bioinformatics-Biomedical-Discoveries-Mathematical-Computational/dp/1498724523
omg, so you need to manually click 100 times to convert sdf to pdbqt one by one??
1. smile to pdbqt (Open Babel or you can use smile converter online tool check > u can upload multiple smile in text format cactus.nci.nih.gov/translate/)
2. pdb to pdqt (Open Babel or Racoon plugin > check this link www.researchgate.net/post/How_can_you_convert_a_large_number_of_pdb_files_to_pdbqt_files)
if you any other concerns you can post ur question in our facebook group page facebook.com/groups/261045198486665
1. smile to pdbqt (Open Babel or you can use smile converter online tool check > u can upload multiple smile in text format cactus.nci.nih.gov/translate/)
2. pdb to pdqt (Open Babel or Racoon plugin > check this link www.researchgate.net/post/How_can_you_convert_a_large_number_of_pdb_files_to_pdbqt_files)
if you any other concerns you can post ur question in our facebook group page facebook.com/groups/261045198486665
How to rank a list of solutions (i.e 1000 compounds = 1000 log files) from autodock Vina? Do you have some script or method to rank for the best solution (compound) from such a list of log or PDBQT files from Vina? Thank you in advance.
iam working on it, next video u will see complete script
U should try vstop.py script
@@jaannawaz2007 dear BB, could you please share the video link for this next video you mentioned to get the results of binding energies in one file because i am using big database and I need all the results in one excel sheet as usually obtained in PyRx tool. I tried to use PyRx tool for my dataset but all time I got some parse error showing that atom are missing in ligand. Vina is working fine but the only issue that I need all the results of binding energy in one single file to analyze easily
Thank you very much sir sir this is very useful for me ...i was searching script for multiple docking using vina since many days but today i found this on your channel this is the best tutorial i have ever seen...
Sir actually i want to convert csv file of smiles into pdbqt ...how to do it ? Please if you can help .
Your welcome... Subscribe to our channel to get more interactive contents in Bioinformatics.
Regarding your question, you can't convert directly smile format to pdbqt, initially u have to convert into pdb file and from pdb u have to convert into PDBQT.
1. smile to pdbqt (Open Babel or you can use smile converter online tool check > u can upload multiple smile in text format cactus.nci.nih.gov/translate/)
2. pdb to pdqt (Open Babel or Racoon plugin > check this link www.researchgate.net/post/How_can_you_convert_a_large_number_of_pdb_files_to_pdbqt_files)
if you any other concerns you can post ur question in our facebook group page facebook.com/groups/261045198486665
Thank you !🙂
C:\>cd "Vina Docking">dir /B > Ligand.txt
Access is denied. Stuck here. Can you help me out..
ua-cam.com/video/U4Xh_VHs0IE/v-deo.html
Sir,
How many nodes do i need for research?
ua-cam.com/video/U4Xh_VHs0IE/v-deo.html
hello sir iam getting a problem with the last step my confg_vs.txt file is not opening it showing an error please help me
ua-cam.com/video/U4Xh_VHs0IE/v-deo.html
Hello sir,
I can't complete the docking process it shows "Command line parse error: too many positional options"
How to fix this error?
Thanks
Warm regards
Rajesh
Good day. I experienced similar error too. I fixed it by renaming my config.txt file to "conf_vs.txt". Try and do same to see if fixed
Try again
post ur query in our facebook page facebook.com/groups/261045198486665
ua-cam.com/video/U4Xh_VHs0IE/v-deo.html
Thanks for this video. Could you tell me how did you convert the 100 files from .sdf to .pdbqt? did you do it one by one or there is a script? thanks
Bioinformatics With BB
3 weeks ago
Your welcome...
Regarding your question, you can't convert directly smile format to pdbqt, initially u have to convert into pdb file and from pdb u have to convert into PDBQT.
1. smile to pdbqt (Open Babel or you can use smile converter online tool check > u can upload multiple smile in text format cactus.nci.nih.gov/translate/)
2. pdb to pdqt (Open Babel or Racoon plugin > check this link www.researchgate.net/post/How_can_you_convert_a_large_number_of_pdb_files_to_pdbqt_files)
if you any other concerns you can post ur question in our facebook group page facebook.com/groups/261045198486665
@@jaannawaz2007 thank you for your help
Very informative.. sir where did you give that pearl script file ? Can you please provide that..
Check in Description Box
Thank you sir
Script file did not work in Linux
could you provide the same for linux
this is the error:
sh Vina_windows.pl
Vina_windows.pl: line 2: printLigand_file:\t: command not found
Vina_windows.pl: line 2: $'
': command not found
Vina_windows.pl: line 3: syntax error near unexpected token `;'
'ina_windows.pl: line 3: `$ligfile=;
Thanks sir. After performing docking of single ligand, i m getting error "insufficient memory". My pc has 6gb ram. What to do now ? Please help
need to work on workstations or u need to increase the specs of ur computers
Thanks sir, i m able to perform the same. I ve a query. What is the meaning and significance of 0,HD1 0,HE2 and +1 in Edit Histidine Hydrogen dialogue box ?
In my protein, 0,HD1 is already been selected. Should I select 0,HE2 (as you did) ?
Sir please reply #Bioinformatics With BB
The problem with Autodock vina is the errors
ua-cam.com/video/U4Xh_VHs0IE/v-deo.html
sir, why the script link is not working??
ua-cam.com/video/U4Xh_VHs0IE/v-deo.html
Very informative, can we get that pearl script file please
Check in Description Box
from where I download script file?
Check in Description Box
Very informative..do I get your mail ID?
ua-cam.com/video/U4Xh_VHs0IE/v-deo.html
8:30
this tutorial is very helpful in my thesis!! i want to add it in citation. which journals can I cite?
Hey,
Have you published any paper related to this ?
If yes then kindly send link