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Add a rigid fragment-based protein-ssRNA doking pipeline, performed by the ATTRACT docking engine, as a sampling module of HADDOCK.
Motivation
Introduces a dedicated docking workflow for protein-ssRNA complexes within HADDOCK, eliminating the need for CNS-based sampling;
Could potentially be executed in an anchored manner, when a single fragment is docked using restraints (obtained using experimental data, etc.), and consecutive fragments are docked using restraints towards the previous fragment(s);
Could potentially be expanded to protein-protein and protein-DNA docking (supported by ATTRACT but outside of my current competency).
Description
[attract] module should handle the full docking workflow, consisting of the following steps:
Preparation of the input folder, protein coarse-graining
Sampling, a per-fragment rigid-body energy minimisation, with or without restraints
Scoring with ATTRACT scoring function or with HIPPO
Assembly of RNA fragments into a full-chain docking models
Conversion of a limited number of models back to all-atom representation
Desired feature/enhancement
Add a rigid fragment-based protein-ssRNA doking pipeline, performed by the ATTRACT docking engine, as a sampling module of HADDOCK.
Motivation
Description
[attract] module should handle the full docking workflow, consisting of the following steps:
Additional context
Paper about fragment-based protein-ssRNA doking
Paper about anchored docking
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