Closed jingluodatacurator closed 11 months ago
Hi @jingluodatacurator, please could you email me your highlighted PDF
Uniprot ID looks fine https://www.uniprot.org/uniprotkb?query=Q9UW03 1,439 AA as stated in publication 'BcatrB encodes a 1,439 amino acid protein with homology to ABC transporters of other fungi'
Expt Bc strain used was B05.10 gene replacement mutant = gene deletion
Curation focus is on chemicals mentioned in title/abstract of publication 'Phytoalexin Resveratrol' and 'Fungicide Fenpiclonil'. Other chemicals tested in publication but not annotated at this stage.
Current annotation
Small edits 1) Change Figure 4 to Table 3 2) Add in a comment, relevant copy and pasted text from the publication
@jingluodatacurator, please have a look at these small edits to see if you agree.
Hi @jingluodatacurator, with your new knowledge of how to make pathogen-host interaction (PHI) phenotype annotations, please could you have a go at curating the virulence assays in this publication
From Results section
From Materials and Methods section
Note to self
Next steps for this session 1) needs new PHIPO and PHI-ECO terms _DONE 22_112023 2) Jing to add in PHI phenotypes, AC to check them. 3) AE alteration in archetype is N/A as NTSR 4) Once 1) and 2) have been completed then the session will be ready to approve.
Also added a GO MF annotation
Curation focus is on chemicals mentioned in title/abstract of publication 'Phytoalexin Resveratrol' and 'Fungicide Fenpiclonil'. Other chemicals tested in publication but not annotated at this stage.
Current annotation
Small edits
- Change Figure 4 to Table 3
- Add in a comment, relevant copy and pasted text from the publication
@jingluodatacurator, please have a look at these small edits to see if you agree.
@CuzickA, I agree with your edits thanks.
Hi @jingluodatacurator, with your new knowledge of how to make pathogen-host interaction (PHI) phenotype annotations, please could you have a go at curating the virulence assays in this publication
From Results section
From Materials and Methods section
@CuzickA, I had a go adding PHI phenotype, please check. I have a feeling I have missed something..
Hi @jingluodatacurator, this is a good start on the PHI phenotype
Here is some feedback so you can go back to the session and make some changes 1) We need the wild type control metagenotype as discussed before in recent tickets. This would be wild type B. cinerea atrB on wild type V. vinifera. The AEs can then be updated for 'compared to control' and 'infective ability'. 2) The host strain will not be the same as the pathogen strain (in this case B05.10). If the authors have not mentioned the strain/cultivar of the grapevine then you can use strain 'unknown'. 3) I would annotate with a PHIPO term for 'lesions' as described by the authors in Table 4. 4) The evidence code 'cell growth assay' is only really used for pathogen only expt eg where a pathogen is grown in vitro on an agar plate. I think this needs changing. 5) For the conditions we do not need the 'B5 medium' as this was how the pathogen was prepared. We only want to use one time point per annotation. Choose the time point that the authors describe or which shows the biggest change in phenotype. If different phenotypes are shown at different time points then we can make additional annotations.
Please let me know how you get on and if you have any questions.
Hi @jingluodatacurator, this is a good start on the PHI phenotype
Here is some feedback so you can go back to the session and make some changes
- We need the wild type control metagenotype as discussed before in recent tickets. This would be wild type B. cinerea atrB on wild type V. vinifera. The AEs can then be updated for 'compared to control' and 'infective ability'.
- The host strain will not be the same as the pathogen strain (in this case B05.10). If the authors have not mentioned the strain/cultivar of the grapevine then you can use strain 'unknown'.
- I would annotate with a PHIPO term for 'lesions' as described by the authors in Table 4.
- The evidence code 'cell growth assay' is only really used for pathogen only expt eg where a pathogen is grown in vitro on an agar plate. I think this needs changing.
- For the conditions we do not need the 'B5 medium' as this was how the pathogen was prepared. We only want to use one time point per annotation. Choose the time point that the authors describe or which shows the biggest change in phenotype. If different phenotypes are shown at different time points then we can make additional annotations.
Please let me know how you get on and if you have any questions.
@CuzickA, all points taken and actioned with your help, many thanks.
Session now approved, closing ticket.
Curated by @jingluodatacurator
https://canto.phi-base.org/curs/6a7b64a655a148da
Notes: Uniprot ID: Q9UW03 Strains: SAS56, B05.10 Main expt. for curation: see Results 'Replacement of BcatrB ' section and Materials and Methods 'Construction of the gene-replacement vector' section.