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```
But a general approach for complex superposition? Without alignments given:
first do all-against-all superposition within one complex to get symmetry
classes
then to the same for the other co…
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We did a lot of curation on NMDA receptors subunits at Fraunhofer with @cthoyt and we want to contribute them here.
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I've finally had a chance to start looking through kinase:inhibitor complexes that @steven-albanese deposited [here](https://github.com/choderalab/mcce-charges/tree/master/pdbs).
The criteria I am us…
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For Reactome complexes that are controllers of enzymatic reactions, these should be aligned with GO-CAM to specify gene product IDs and not PRO IDs. To do this, we will need to handle two different ca…
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Il y a une erreur dans la donnée : la donnée `caption` renvoie le contenu de la transcription. C'est une erreur d'accessibilité, il faut ajouter un champ "Légende" qui servira de `caption` au tableau.…
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```
java.lang.ClassCastException: java.lang.String cannot be cast to java.lang.Integer
at org.intermine.webservice.server.complexes.ExportService.getComplex(ExportService.java:192)
at org.int…
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Seems like that there are several complexes with the same name (9-1-1, see https://mecu.dallago.us/protein?protein=O60921&experiment=5 or search for `9-9-1` in the complex search page). This doesn't s…
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**Describe the bug**
some metals (and metalloids) do not accept dative bonds.
When attempting to construct them, None is returned instead of an RDMol instance.
This is not a SMILES parsing problem…
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currently in AmiGO
filter results says
"total gene products" 274
at the top of the filters and the results. This is no longer correct now that complexes are included as "annotation objects"
…
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Currently, the implementation of TOGL ignores the following features:
- handling higher-order information properly
- expanding simplicial complexes
- making use of the dimension of features