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All posts created by debbie

| posted 10 Apr, 2023 12:15
The current position is to call membrane proteins found by DeepTMHMM.
https://dtu.biolib.com/DeepTMHMM
See the powerpoint at this forum post for current details.
https://seaphages.org/forums/topic/5438/

debbie
Posted in: AnnotationMembrane proteins
| posted 07 Apr, 2023 16:42
Kathleen,
I would careful to apply minor tail proteins to small proteins, especially when they are situated in a non-canonical place. Too often, the motifs of capsid proteins and tail proteins can look very similar - too similar to know what it is!
debbie
Posted in: Cluster A Annotation Tipsminor tail proteins
| posted 06 Apr, 2023 17:27
Alison,
Hi. The hit to tail tube protein is what we call "major tail protein". Its place in EC is in the typical position in a genome.
As for what should be called a tail tube protein is something that needs further investigation.
debbie
Edited 06 Apr, 2023 17:30
Posted in: Cluster EC Annotation TipsMajor tail protein
| posted 03 Apr, 2023 12:54
Hi Ellen,
If you hit a single stranded DNA binding protein downstream of a RecE, it is likely that you have its companion protein, RecT-like DNA pairing protein and I would call it.
To learn more about RecE and RecT, reading this paper may help.
https://pubmed.ncbi.nlm.nih.gov/18923412/
Posted in: AnnotationSSB protein or RecT-like pairing protein
| posted 30 Mar, 2023 17:54
Hi all,
It is apparent that RefSeq (GenBank records that start out NC_XXx) are not updating with any changes sent to NCBI. Use with caution.
debbie
Posted in: Bioinformatic Tools and AnalysesRefSeq Warning
| posted 30 Mar, 2023 17:52
Hi all,
I just checked Wizard, and genes 16 (capsid maturation protease), 19 (major capsid hexamer protein) and 20 (Hypotheticall Protein) are all correct at phagesDB, Phamerator and in the Genbank file KU998234. They are disparate in the RefSeq file (NC_030913) at GenBank, BUT we have no control over their updates.
Avoid RefSeq files as much as possible, because we cannot update them.
Since Phamerator and phagesDB are informed by the same data set, they will always be the same unless you catch them in their updates. As for forums and such, since most folks ask questions when their genome is in draft form, lease ignore the number and refer to a gene by its stop.

Currently as we are curate files (for functional calls) that information goes to GenBank first, then those changes are recognized and phamerated. that output is then picked up web Phamerator, phagesdb, starterator and their outputs are then posted. The timing for each program is automated and set differently for each one, but as updates post, the rest is then processed and posted pretty quickly.

debbie
Posted in: Cluster DC Annotation Tipscapsid maturation proteases
| posted 30 Mar, 2023 16:18
Hi Beth,
Before trying anything else, have your students close the program (maybe even restart their computer) and then try again.
debbie
Posted in: DNA MasterDNA Master errors
| posted 29 Mar, 2023 12:54
I am willing to call this a head-to-tail stopper because the first hit is to gp20 of L5. while we have not updated the label of that gene, when you HHpred it, it is a good hit to the 5A21_G project, which is the gene that we are assigning the function had-to-tail stopper.
debbie
Posted in: Annotationhead-to-tail stopper
| posted 29 Mar, 2023 12:44
I would call this the helicase loader. I am not sure of the answer to your questions, but it is in the neighborhood.
debbie
Posted in: Request a new function on the SEA-PHAGES official listphage helicase loader protein
| posted 24 Mar, 2023 21:28
Hi Adam,
My answer is I don't know.
This cluster of genomes is not like the others. It is a podo and I am not sure it fits the canonical features of podos.
In order to answer this question, a review of podovirus structures is warranted. What are the canonical featured of them? So a deep dive into the literature is warranted here.
Next, the cryoEM data is pouring in to the PDB, so what we have access to now vs when this cluster first appeared has grown.
Next, in the literature you can find good reviews about podos and myos tails(and learn that the tail structures of siphos is a bit more elusive). We'll need to apply that to this.
Next, your are cherry-picking one gene is a very non-canonical place in the genome. Structural genes frequently hit heads and tails and until we can clearly determine what we have going on here, I recommend that we prudently wait on jumping the gun.
Finally, the same terminology doesn't always cross from sipho, myo and podo. So some thought will be required.
Keep us posted as you do your investigations.
debbie
Posted in: AnnotationKikiko_42