Rectification: CASP here doesn’t stand for CRISPR-Cas tech. In fact its stands for “Critical Assessment of Structure Prediction” which is used for assessing different protein prediction softwares/servers for their ability of correct prediction and then ranked accordingly.
is it necessary we first take gene sequence applied translator to convert it into protein and then apply I-Tasser or we directly apply I-Tasser on protein downloaded from Uniprot
AOA sir how are you? Sir I just want to ask you that after determining the mutations occurring in SARS cov 2 proteins such as in envelope protein, spike protein etc and now what to generate it's 3d structure by homology modelling so how can we do that by I-tasser?
if i use choose file option and my file belongs to .txt file rather than .fasta file then the website will take my file and give the result? or i have to give .fasta file when i use the choose option??
I do not received email regarding password. Now, what I do?
Sir! after translating fasta sequence of gene on expasy and selecting the longest open reading frame what is next step. Can you help me
Great sir , you are par excellence
Thanks a lot
Rectification: CASP here doesn’t stand for CRISPR-Cas tech. In fact its stands for “Critical Assessment of Structure Prediction” which is used for assessing different protein prediction softwares/servers for their ability of correct prediction and then ranked accordingly.
thanks for rectification
is it necessary we first take gene sequence applied translator to convert it into protein and then apply I-Tasser or we directly apply I-Tasser on protein downloaded from Uniprot
yes if have protein sequence then go directly
Salam sir.
Sir normal ka tareeqa to malom ho gya.
Ab ik gene ma mutation hai. Mutation ka protein pa kia asar ha. Wo kese malom karainge?
AOA sir how are you? Sir I just want to ask you that after determining the mutations occurring in SARS cov 2 proteins such as in envelope protein, spike protein etc and now what to generate it's 3d structure by homology modelling so how can we do that by I-tasser?
waslam just put change sequence of each mutation on I-Tasser then confirm it
Can two species of same family contain different amino acid sequence?
yes due to SNP
I don't have a official email id and my personal email isn't accepted by the software. What should I do?
do ask your colleague which have ID then he share you results link
I dont have any official email id. How can i open account here
Institutional ID is required however you can try your personal email here.
if i use choose file option and my file belongs to .txt file rather than .fasta file then the website will take my file and give the result? or i have to give .fasta file when i use the choose option??
use FASTA file
Sir...how can I find the codon sequence and their number....If i have amino acid number 428....sir kindly tell me about this
watch my lecture on EXPASY
Sir email sy registration nhi ho rhi error a rha... Academic email sy registration hogi.. Commercial email sy nhi
academics
please make a lacture on crisper
noted
Personal email sy registration nhi ho rhi
can try