-
Hi folks,
Hope this is a right place to ask.
[Alphafold server](https://alphafoldserver.com/) allows user input protein sequence up to 5,000 tokens. My system is a bit larger than this number, 7,207…
-
Thanks for providing the AF3 source!
To test AlphaFold3 using the example 7BBV provided by AlphaFold3 server, I used the following JSON file as input:
```
{
"name": "7BBV",
"modelSeeds": …
-
Related to #20 and the issues mentioned in there, I would suggest to extend ModelCIF to capture all new types of quality estimates introduced with AlphaFold 3 (AF3). I also had a look at RoseTTAFold-A…
-
Apologies if I have missed something (I've been through the paper and the documentation couple of times) but I can't find a description of how the plmblast score is calculated, or how it should be int…
-
### October 2024 >
- [x] short term
- [x] look into gradients again
- [x] publish notebooks (field projection + photonic crystal)
- [x] Update Readme including how to use jax / pyto…
-
Hello there,
I am trying to use NGLViewer in Shiny.
I want to color a specific amino acid in the cartoon representation. However, it seems that NGL is only able to color the selection if I select mo…
-
### What client do you play on?
enUS
### Faction
- [X] Alliance
- [X] Horde
### Content Phase:
- [ ] Generic
- [ ] 1-19
- [ ] 20-29
- [ ] 30-39
- [X] 40-49
- [ ] 50-59
### Curr…
-
```
What steps will reproduce the problem?
1. In Analysis open up Structure --> CING
2. After creating a run, in the Run Settings tab deselect some residues.
3. Submit the Project.
What is the expect…
-
```
What steps will reproduce the problem?
1. In Analysis open up Structure --> CING
2. After creating a run, in the Run Settings tab deselect some residues.
3. Submit the Project.
What is the expect…
-
```
What steps will reproduce the problem?
1. In Analysis open up Structure --> CING
2. After creating a run, in the Run Settings tab deselect some residues.
3. Submit the Project.
What is the expect…