Thanks for the video! I'd like to know what kinds of mutations prokaryotes can get. Can they get cancerous mutations in their DNA or does something else keep prokaryotes from developing cancer?
Thank you for a really good video but i think the illustration of the ribosome should be fixed. If i'm not mistaken the E site should only occupied the large rRNA subunit. Only the P and A Sites occupied both large and small subunits
Hi, You went pretty deep into the details of this mechanism, and because of that, I want to make some comments... I am wondering based on which data you have ultimately placed IF3 in E-site? Based on the current state of the knowledge in this field it is very contradicting. I would rather recommend only mentioning the IF3 without placing it anywhere in this pathway since it creates a false feeling that it's a solid defined fact. In fact, IF3 could be even bound to the 50S subunit and not cause 70S complex dissociation. www.ncbi.nlm.nih.gov/pmc/articles/PMC6120702/
What about in Eukaryotes. What are the changes? But...... I think there are some mistakes in the initiation part of this vedio. How can the tRNA binds to the ribosome before mRNA comes? The anticodon arm of the tRNA must bind to the codon of the mRNA. right?🤔 Or does it mean that there is nothing wrong with that and it can be done in this way too🤔? It seems to me that the tRNA should come only after the 50S subunit with the mRNA joins with the 30S subunit. Then only the anticodon - codon complementary base pairing will become correct.
A very detailed video. Shine dalgarno sequence is the only missing thing
Best TH-cam channel....for better understanding!! Tq
I wish you could do for eukaryotes as well.
they are extremely informative
Excellent video! My 40 slide lecture made no sense but this short video explained it all. Thanks!
You're welcome!
Same here😂 tq vvvvvmuchh
you're a freaking god
Thank you so much .I wish all lecturers could explain like this
Easiest video to understand translation!
excellent video dear sir, it is very helpful.
excellent videos guys....great job seriously
Really thx, this short video explained full process easily.
Very informative and easy to understand
Thanks a ton!
Thank you so much for this video
This video was very helpful
Thank you sir
I'm in love with your voice
Excellent 👍 thanks 😊
Very helpful . Thank you so much 💗
YOU'RE A LIFE SAVER
Plz make video on eukaryotic translation
this video is very helpful. thank you.
Can you do a video on translating in eukaryotes
Great effort
Keep posting!! ✨
Thnku
I wanna know, e, p,a they are between large and small subunit??
From what I've learned, A and P site are in both large and small subunit and E site are located in large subunit
This video is very helpful 👌
Thanks for the video! I'd like to know what kinds of mutations prokaryotes can get. Can they get cancerous mutations in their DNA or does something else keep prokaryotes from developing cancer?
Please correct me if I am wrong but I think the termination factor should be RF2 and not RF3 .
Can't thank u enough!🙏🙏❤
Thank you for a really good video but i think the illustration of the ribosome should be fixed. If i'm not mistaken the E site should only occupied the large rRNA subunit. Only the P and A Sites occupied both large and small subunits
Just wow!!!
Eukaryotic translation video upload please like this...
great job :)
Perfect
Hello epic Asian~
Where is your vedio on eukaryotes translation
Nice
If2 has gtpase activity not 1
Keşke Türkçe olsaymış
Eukaryotes pls
Teachers can't explain this clearly even after taking weeks 🙄
U have a lot of mistakes in this video
Like what?
What mistakes ?
No mistakes, only missing such as Shine-Dalgarno seq. This helps the ribosome (30s) to recognize the sequence of mRNA upstream.
Hi,
You went pretty deep into the details of this mechanism, and because of that, I want to make some comments...
I am wondering based on which data you have ultimately placed IF3 in E-site? Based on the current state of the knowledge in this field it is very contradicting. I would rather recommend only mentioning the IF3 without placing it anywhere in this pathway since it creates a false feeling that it's a solid defined fact. In fact, IF3 could be even bound to the 50S subunit and not cause 70S complex dissociation.
www.ncbi.nlm.nih.gov/pmc/articles/PMC6120702/
Please make video of eukaryotic translation also.......
What about in Eukaryotes. What are the changes?
But...... I think there are some mistakes in the initiation part of this vedio.
How can the tRNA binds to the ribosome before mRNA comes? The anticodon arm of the tRNA must bind to the codon of the mRNA. right?🤔
Or does it mean that there is nothing wrong with that and it can be done in this way too🤔?
It seems to me that the tRNA should come only after the 50S subunit with the mRNA joins with the 30S subunit. Then only the anticodon - codon complementary base pairing will become correct.
Just mind blowing explanation
Thank you sooooo much for this video this was so easy to understand
Simplest video
Very simply explaned
This needs to be updated, many sources would disagree how your process is set up.
Sound quality plz improve good video 😊🤗
Thanks sir 🙂🙏
nice video 💞💞💞
My exam saviour lecturer👍