| Theoretical Model:
The protein structure described on this page was determined theoretically, and hence should be interpreted with caution. |
Model Confidence:
Confident (90 > pLDDT > 70)
AlphaFold produces a per-residue confidence score (pLDDT) between 0 and 100. Some regions below 50 pLDDT may be unstructured in isolation.
To the right is an AlphaFold2 3D model of SARS CoV-2 Protein NSP11 (length = 13 amino acids, i.e. SADAQSFLNGFAV color coded by the pLDDT scores. It corresponds to the highest ranked model in terms of the pLDDT confidence scores, i.e., model 5[1].
Morph of the top 5 ranked
AlphaFold2 models of
SARS-CoV-2 Protein NSP11,
rainbow color coded N-C (blue to red)
[1].
Function
Non-structural protein 11 (NSP11) is the 13 amino acid peptide at the C-term of the large SARS-CoV-2 polyprotein ORF1ab (pp1a). It is the cleavage product of pp1a polyprotein by 3CLpro/Mpro protease at the nsp10/11 junction. Its function and whether it is actually expressed is not known.
Structural Highlights
Giri's lab[2] studied NSP11 in solution and by molecular dynamics. Based on CD, they found that NSP11 shows characteristics of an intrinsically disordered protein (IDP). They further studied the its conformational behavior in the presence of negatively charged and neutral liposomes, and found that it remains disordered. However, in SDS micelle, NSP11 adopts an α-helical conformation, suggesting the helical propensity of NSP11, which is very similar to what [AlphaFold[2 predicts. Based on MD simulations NSP11 appears to to have the behavior of an IDP.
See also
Coronavirus_Disease 2019 (COVID-19)
