Summary for 8EDK
Entry DOI | 10.2210/pdb8edk/pdb |
Related | 8EDC 8EDI |
Descriptor | Netrin unc-6, alpha-D-mannopyranose-(1-6)-beta-D-mannopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-[alpha-L-fucopyranose-(1-3)][alpha-L-fucopyranose-(1-6)]2-acetamido-2-deoxy-beta-D-glucopyranose, SULFATE ION, ... (6 entities in total) |
Functional Keywords | secreted protein, axon guidance cue, glycoprotein, signaling protein |
Biological source | Caenorhabditis elegans |
Total number of polymer chains | 1 |
Total formula weight | 51263.40 |
Authors | Priest, J.M.,Ozkan, E. (deposition date: 2022-09-04, release date: 2023-01-11, Last modification date: 2024-11-13) |
Primary citation | Priest, J.M.,Nichols, E.L.,Smock, R.G.,Hopkins, J.B.,Mendoza, J.L.,Meijers, R.,Shen, K.,Ozkan, E. Structural insights into the formation of repulsive netrin guidance complexes. Sci Adv, 10:eadj8083-eadj8083, 2024 Cited by PubMed Abstract: Netrins dictate attractive and repulsive responses during axon growth and cell migration, where the presence of the receptor Uncoordinated-5 (UNC-5) on target cells results in repulsion. Here, we showed that UNC-5 is a heparin-binding protein, determined its structure bound to a heparin fragment, and could modulate UNC-5-heparin affinity using a directed evolution platform or structure-based rational design. We demonstrated that UNC-5 and UNC-6/netrin form a large, stable, and rigid complex in the presence of heparin, and heparin and UNC-5 exclude the attractive UNC-40/DCC receptor from binding to UNC-6/netrin to a large extent. with a heparin-binding-deficient UNC-5 fail to establish proper gonad morphology due to abrogated cell migration, which relies on repulsive UNC-5 signaling in response to UNC-6. Combining UNC-5 mutations targeting heparin and UNC-6/netrin contacts results in complete cell migration and axon guidance defects. Our findings establish repulsive netrin responses to be mediated through a glycosaminoglycan-regulated macromolecular complex. PubMed: 38363837DOI: 10.1126/sciadv.adj8083 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.5 Å) |
Structure validation
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