Journal
NUCLEIC ACIDS RESEARCH
Volume 50, Issue W1, Pages W465-W473Publisher
OXFORD UNIV PRESS
DOI: 10.1093/nar/gkac249
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Funding
- Czech Ministry of Education [INBIO: CZ.02.1.01/0.0/0.0/16 026/0008451, ELIXIR: LM2018131, eINFRA: LM2018140, RECETOX: LM2018121]
- Czech Science Foundation [20-15915Y]
- European Union [857560, 814418]
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The transplantation of loops between structurally related proteins is a method to improve enzyme activity, specificity, and stability. However, there are limited methods for loop-based rational protein design. The unique dynamism and identification of successful excision points are practical challenges. LoopGrafter is a web server that guides users through the loop grafting process, providing step-by-step procedures for loop identification, calculation of geometry, assessment of similarities and dynamics, and selection of loops for transplantation.
The transplantation of loops between structurally related proteins is a compelling method to improve the activity, specificity and stability of enzymes. However, despite the interest of loop regions in protein engineering, the available methods of loop-based rational protein design are scarce. One particular difficulty related to loop engineering is the unique dynamism that enables them to exert allosteric control over the catalytic function of enzymes. Thus, when engaging in a transplantation effort, such dynamics in the context of protein structure need consideration. A second practical challenge is identifying successful excision points for the transplantation or grafting. Here, we present LoopGrafter (https://loschmidt.chemi.muni.cz/loopgrafter/), a web server that specifically guides in the loop grafting process between structurally related proteins. The server provides a step-by-step interactive procedure in which the user can successively identify loops in the two input proteins, calculate their geometries, assess their similarities and dynamics, and select a number of loops to be transplanted. All possible different chimeric proteins derived from any existing recombination point are calculated, and 3D models for each of them are constructed and energetically evaluated. The obtained results can be interactively visualized in a user-friendly graphical interface and downloaded for detailed structural analyses. [GRAPHICS] .
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