5eyp | pdb_00005eyp

TUBULIN-DARPIN COMPLEX

spinqualitylabelsall models 5eyp, resolution 1.90Å Show:Asymmetric Unit Biological Assembly Drag the structure with the mouse to rotate   Export Animated Image   Print3D Structural highlights 5eyp is a 3 chain structure with sequence from [1] and Ovis aries. Full crystallographic information is available from OCA. For a guided tour on the structure components use FirstGlance. Ligands: GDP, GOL, GTP, LOC, MG, SO4 Related: 5eyl Resources: FirstGlance, OCA, PDBe, RCSB, PDBsum, ProSAT Function [D0VWZ0_SHEEP] Tubulin is the major constituent of microtubules. It binds two moles of GTP, one at an exchangeable site on the beta chain and one at a non-exchangeable site on the alpha chain (By similarity).[RuleBase:RU003505][SAAS:SAAS023123_004_019801] [D0VWY9_SHEEP] Tubulin is the major constituent of microtubules. It binds two moles of GTP, one at an exchangeable site on the beta chain and one at a non-exchangeable site on the alpha chain (By similarity).[RuleBase:RU003505] Publication Abstract from PubMed Affinity maturation by random mutagenesis and selection is an established technique to make binding molecules more suitable for applications in biomedical research, diagnostics and therapy. Here we identified an unexpected novel mechanism of affinity increase upon in vitro evolution of a tubulin-specific designed ankyrin repeat protein (DARPin). Structural analysis indicated that in the progenitor DARPin the C-terminal capping repeat (C-cap) undergoes a 25 degrees rotation to avoid a clash with tubulin upon binding. Additionally, the C-cap appears to be involved in electrostatic repulsion with tubulin. Biochemical and structural characterizations demonstrated that the evolved mutants achieved a gain in affinity through destabilization of the C-cap, which relieves the need of a DARPin conformational change upon tubulin binding and removes unfavorable interactions in the complex. Therefore, this specific case of an order-to-disorder transition led to a 100-fold tighter complex with a subnanomolar equilibrium dissociation constant, remarkably associated with a 30% decrease of the binding surface. Destabilizing an interacting motif strengthens the association of a designed ankyrin repeat protein with tubulin.,Ahmad S, Pecqueur L, Dreier B, Hamdane D, Aumont-Nicaise M, Pluckthun A, Knossow M, Gigant B Sci Rep. 2016 Jul 6;6:28922. doi: 10.1038/srep28922. PMID:27380724 From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

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