CYSMA
  
CHUVLMUM




Analysis of p.Asp110Glu variant, CFTR gene, CF Transmembrane conductance Regulator protein (1480 residues)


Data provided and calculated by CYSMA must be considered as predictions.
They are meant for educational purposes only and are provided with NO WARRANTY with respect to their biological reliability.



  • Allele frequency:

    variant D110H gnomAD (123,136 exomes): 1.99e-05
    variant D110Y gnomAD (123,136 exomes): 3.98e-06
    variant D110E gnomAD (123,136 exomes): 1.59e-05


  • Ortholog conservation: Help


    Number of sequences AAPI* AAPIR** Number of divergencies Number of mutant E110 Number of gaps Conservation of D110 Conservation - gap
    50 80.72% 85.17% 1
    show divergencies
    0
    details
    0
    details
    98.00% (49 / 50) 98.00% (49 / 50)


    The wild-type residue D110 is highly conserved among the CFTR orthologs: 98% (49 / 50 CFTR orthologs)
    The variant D110E has never been found among the CFTR orthologs

    *AAPI: Alignment Average Percentage Identity
    **AAPIR: Alignment Average Percentage Identity of the Region (20 residues surrounding position 110). AAPIR appears in green if it is more than 10% compared to AAPI, in red if less than 10%.
    Click here for more details on the alignment.


    CYSMA's visualizing modules for Ortholog conservation:





    ⬇ Download the region alignment (50 residues, Fasta format)
    ⬇ Download the CFTR phylogenic tree



    Display methods


  • Domain conservation: Help

    The domain MSD1 of CF Transmembrane conductance Regulator has been shown to interact with:



    The residue p.Asp110 (MSD1) seems to play a key role in the CFTR function:

    p.Asp110 belongs to the ECL1 (extracellular loop 1) and in involved in the interaction with ECL4.


    The residue p.Asp110 belongs to the domain MSD1.

    69
    422


    MSD1: is the membrane-spanning domain 1, composed of six transmembrane helices (TM1-TM6).
    Four of the six TMs protrude into the cytosol to form the intracellular loops ICL1 (between TM2 and TM3) and ICL2 (between TM4 and TM5). ICL1 contacts NBD1 at the level of the ATP-binding site, while ICL2 binds in a groove located at the surface of NBD2.








    MSD1 of CF Transmembrane conductance Regulator domain alignment including p.Asp110 residue.



    Number of sequences AAPID***
    (from aa 69 to aa 422)
    AAPIR! Number of divergencies Number of mutant Number of gaps Conservation of D110 Conservation - gap
    429 17.13% 11.63% 297
    show divergencies
    24 76 13.05% (56 / 429) 15.86% (56 / 353)



    ***AAPID: Alignment Average Percentage Identity of the Domain (positions are indicated).
    !AAPIR: Alignment Average Percentage Identity of the Region (20 residues surrounding position 110). AAPIR appears in green if it is more than 10% compared to AAPID, in red if less than 10%.

    The wild-type residue D110 belongs to the MSD1 domain and is conserved at 13.05% among the MSD1 homologs (56 / 429 MSD1 homologs)
    The variant D110E has been found among the MSD1 homologs with a notable frequency: 5.59% (24 / 429 MSD1 homologs)

    Divergencies show the amino acids which have been selected in the evolution. Residues present in more than 10% of the sequences are highlighted in blue.
    Please note that CYSMA does not consider splicing alterations.
    Refer to the Help page for more details.



    CYSMA's visualizing modules for MSD1 domain conservation:





    Display methods


  • Refer to the Help page for more details.


  • Secondary structure analysis: Help


    Residue p.Asp110 is predicted to belong to a loop. Probability is 0.966.

    Direct environment is as follow:

    IASYD110PDNK
    HHHCCCCCH


    Display methods











  • 3D analysis: Help


    Models provided and analysed by CYSMA must be considered as predictions, therefore be careful when interpreting the results. All efforts have been made to build structures of quality, however, they are provided with NO WARRANTY as to their accuracy with the real biological molecules studied.

    Wild type and predicted mutant structures have been compared. You will find the results below.


  • Clinical significance:

    The variant D110E has been been described as drug response - reviewed by expert panel - (ClinVar for more details)


  • Patients data: CFTR-France

  • Variant D110E might correspond to:


    Variant details from CFTR-France:
    Name NM_000492.3:c.330C>A
    Protein name NP_000483.3:p.(Asp110Glu)
    Genomic name chr7:g.117171009C>A
    Class disease-causing


    Patients carrying this variant in CFTR-France:
    Total number of patients 1
    CF 1

    (CFTR-France for more details)




  • Additional resources:



  • References


    CYSMA has completed its calculations; Execution time: 11 wallclock secs ( 7.68 usr 0.02 sys + 2.60 cusr 0.06 csys = 10.36 CPU)