# Dealing with dimers

**URL:** <https://ask.bioexcel.eu/t/dealing-with-dimers/42>\
**Category:** HADDOCK\
**Created:** [April 6, 2016, 10:12am UTC](https://ask.bioexcel.eu/t/dealing-with-dimers/42 "2016-04-06T10:12:03Z")\
**Posts on this page:** 1\
**Showing post:** 14

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**Author:** ![amjjbonvin](https://dub1.discourse-cdn.com/flex013/user_avatar/ask.bioexcel.eu/amjjbonvin/32/23_2.png) [@amjjbonvin](https://ask.bioexcel.eu/u/amjjbonvin)\
**Post date:** [April 11, 2016, 11:44am UTC](https://ask.bioexcel.eu/t/dealing-with-dimers/42/14 "2016-04-11T11:44:48Z")

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Looking at your data, the active residues you give for your dimer to not form a contiguous surface on the protein and to satisfy them the complex is distorted… The question is: how confident are you in your data?

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