1YIG

Crystal Structure of the Human EB1 C-terminal Dimerization Domain

Summary for 1YIG

• Entry DOI: 10.2210/pdb1yig/pdb
• Related: 1YIB
• Descriptor: Microtubule-associated protein RP/EB family member 1 (2 entities in total)
• Functional Keywords: coiled coil; four helix bundle, structural protein
• Biological source: Homo sapiens (human)
• Cellular location: Cytoplasm, cytoskeleton: Q15691
• Total number of polymer chains: 2
• Total formula weight: 17232.54

Authors

Slep, K.C.,Rogers, S.L.,Elliott, S.L.,Ohkura, H.,Kolodziej, P.A.,Vale, R.D. (deposition date: 2005-01-11, release date: 2005-03-08, Last modification date: 2024-11-13)

Primary citation

Slep, K.C.,Rogers, S.L.,Elliott, S.L.,Ohkura, H.,Kolodziej, P.A.,Vale, R.D.
Structural determinants for EB1-mediated recruitment of APC and spectraplakins to the microtubule plus end
J.Cell Biol., 168:587-598, 2005

PubMed Abstract: EB1 is a member of a conserved protein family that localizes to growing microtubule plus ends. EB1 proteins also recruit cell polarity and signaling molecules to microtubule tips. However, the mechanism by which EB1 recognizes cargo is unknown. Here, we have defined a repeat sequence in adenomatous polyposis coli (APC) that binds to EB1's COOH-terminal domain and identified a similar sequence in members of the microtubule actin cross-linking factor (MACF) family of spectraplakins. We show that MACFs directly bind EB1 and exhibit EB1-dependent plus end tracking in vivo. To understand how EB1 recognizes APC and MACFs, we solved the crystal structure of the EB1 COOH-terminal domain. The structure reveals a novel homodimeric fold comprised of a coiled coil and four-helix bundle motif. Mutational analysis reveals that the cargo binding site for MACFs maps to a cluster of conserved residues at the junction between the coiled coil and four-helix bundle. These results provide a structural understanding of how EB1 binds two regulators of microtubule-based cell polarity.

PubMed: 15699215
DOI: 10.1083/jcb.200410114

Experimental method

X-RAY DIFFRACTION (2 Å)