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8EDK

Structure of C. elegans UNC-6 LamN and EGF domains

This is a non-PDB format compatible entry.
Summary for 8EDK
Entry DOI10.2210/pdb8edk/pdb
Related8EDC 8EDI
DescriptorNetrin 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 Keywordssecreted protein, axon guidance cue, glycoprotein, signaling protein
Biological sourceCaenorhabditis elegans
Total number of polymer chains1
Total formula weight51263.40
Authors
Priest, J.M.,Ozkan, E. (deposition date: 2022-09-04, release date: 2023-01-11, Last modification date: 2024-11-13)
Primary citationPriest, 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: 38363837
DOI: 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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