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ABSTRACT: Motivation
Membrane proteins are an important class of biological macromolecules involved in many cellular key processes including signalling and transport. They account for one third of genes in the human genome and >50% of current drug targets. Despite their importance, experimental structural data are sparse, resulting in high expectations for computational modelling tools to help fill this gap. However, as many empirical methods have been trained on experimental structural data, which is biased towards soluble globular proteins, their accuracy for transmembrane proteins is often limited.Results
We developed a local model quality estimation method for membrane proteins ('QMEANBrane') by combining statistical potentials trained on membrane protein structures with a per-re
SUBMITTER: Studer G
PROVIDER: S-EPMC4147910 | biostudies-literature | 2014 Sep
REPOSITORIES: biostudies-literature