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| <StructureSection load='6onb' size='340' side='right'caption='[[6onb]], [[Resolution|resolution]] 1.70Å' scene=''> | | <StructureSection load='6onb' size='340' side='right'caption='[[6onb]], [[Resolution|resolution]] 1.70Å' scene=''> |
| == Structural highlights == | | == Structural highlights == |
- | <table><tr><td colspan='2'>[[6onb]] is a 4 chain structure with sequence from [http://en.wikipedia.org/wiki/Caeel Caeel]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6ONB OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6ONB FirstGlance]. <br> | + | <table><tr><td colspan='2'>[[6onb]] is a 4 chain structure with sequence from [https://en.wikipedia.org/wiki/Caenorhabditis_elegans Caenorhabditis elegans]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6ONB OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6ONB FirstGlance]. <br> |
- | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=NAG:N-ACETYL-D-GLUCOSAMINE'>NAG</scene>, <scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene></td></tr> | + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.696Å</td></tr> |
- | <tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">zig-8, Y39E4B.8 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=6239 CAEEL]), rig-5, C36F7.4, CELE_C36F7.4 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=6239 CAEEL])</td></tr> | + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=NAG:N-ACETYL-D-GLUCOSAMINE'>NAG</scene>, <scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene></td></tr> |
- | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6onb FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6onb OCA], [http://pdbe.org/6onb PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6onb RCSB], [http://www.ebi.ac.uk/pdbsum/6onb PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6onb ProSAT]</span></td></tr> | + | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=6onb FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6onb OCA], [https://pdbe.org/6onb PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6onb RCSB], [https://www.ebi.ac.uk/pdbsum/6onb PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6onb ProSAT]</span></td></tr> |
| </table> | | </table> |
| == Function == | | == Function == |
- | [[http://www.uniprot.org/uniprot/ZIG8_CAEEL ZIG8_CAEEL]] Together with zig-5, required postembryonically to maintain the position of ASI and ASH head neuron cell bodies and ventral nerve cord axons of PVQ, PVP and HSN neurons by preventing their displacement that could occur during body growth and movement. May act by reducing L1CAM-like protein sax-7 (long isoform) adhesion.<ref>PMID:22829780</ref> | + | [https://www.uniprot.org/uniprot/ZIG8_CAEEL ZIG8_CAEEL] Together with zig-5, required postembryonically to maintain the position of ASI and ASH head neuron cell bodies and ventral nerve cord axons of PVQ, PVP and HSN neurons by preventing their displacement that could occur during body growth and movement. May act by reducing L1CAM-like protein sax-7 (long isoform) adhesion.<ref>PMID:22829780</ref> |
| <div style="background-color:#fffaf0;"> | | <div style="background-color:#fffaf0;"> |
| == Publication Abstract from PubMed == | | == Publication Abstract from PubMed == |
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| __TOC__ | | __TOC__ |
| </StructureSection> | | </StructureSection> |
- | [[Category: Caeel]] | + | [[Category: Caenorhabditis elegans]] |
| [[Category: Large Structures]] | | [[Category: Large Structures]] |
- | [[Category: Cheng, S]] | + | [[Category: Cheng S]] |
- | [[Category: Kurleto, J D]] | + | [[Category: Kurleto JD]] |
- | [[Category: Ozkan, E]] | + | [[Category: Ozkan E]] |
- | [[Category: Cell adhesion]]
| + | |
- | [[Category: Cell surface receptor]]
| + | |
- | [[Category: Heterodimer]]
| + | |
- | [[Category: Immunoglobulin superfamily]]
| + | |
- | [[Category: Nervous system]]
| + | |
| Structural highlights
Function
ZIG8_CAEEL Together with zig-5, required postembryonically to maintain the position of ASI and ASH head neuron cell bodies and ventral nerve cord axons of PVQ, PVP and HSN neurons by preventing their displacement that could occur during body growth and movement. May act by reducing L1CAM-like protein sax-7 (long isoform) adhesion.[1]
Publication Abstract from PubMed
The evolution of complex nervous systems was accompanied by the expansion of numerous protein families, including cell-adhesion molecules, surface receptors, and their ligands. These proteins mediate axonal guidance, synapse targeting, and other neuronal wiring-related functions. Recently, 32 interacting cell surface proteins belonging to two newly defined families of the Ig superfamily (IgSF) in fruit flies were discovered to label different subsets of neurons in the brain and ventral nerve cord. They have been shown to be involved in synaptic targeting and morphogenesis, retrograde signaling, and neuronal survival. Here, we show that these proteins, Dprs and DIPs, are members of a widely distributed family of two- and three-Ig domain molecules with neuronal wiring functions, which we refer to as Wirins. Beginning from a single ancestral Wirin gene in the last common ancestor of Bilateria, numerous gene duplications produced the heterophilic Dprs and DIPs in protostomes, along with two other subfamilies that diversified independently across protostome phyla. In deuterostomes, the ancestral Wirin evolved into the IgLON subfamily of neuronal receptors. We show that IgLONs interact with each other and that their complexes can be broken by mutations designed using homology models based on Dpr and DIP structures. The nematode orthologs ZIG-8 and RIG-5 also form heterophilic and homophilic complexes, and crystal structures reveal numerous apparently ancestral features shared with Dpr-DIP complexes. The evolutionary, biochemical, and structural relationships we demonstrate here provide insights into neural development and the rise of the metazoan nervous system.
Family of neural wiring receptors in bilaterians defined by phylogenetic, biochemical, and structural evidence.,Cheng S, Park Y, Kurleto JD, Jeon M, Zinn K, Thornton JW, Ozkan E Proc Natl Acad Sci U S A. 2019 May 14;116(20):9837-9842. doi:, 10.1073/pnas.1818631116. Epub 2019 May 1. PMID:31043568[2]
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.
References
- ↑ Benard CY, Blanchette C, Recio J, Hobert O. The secreted immunoglobulin domain proteins ZIG-5 and ZIG-8 cooperate with L1CAM/SAX-7 to maintain nervous system integrity. PLoS Genet. 2012;8(7):e1002819. doi: 10.1371/journal.pgen.1002819. Epub 2012 Jul , 19. PMID:22829780 doi:http://dx.doi.org/10.1371/journal.pgen.1002819
- ↑ Cheng S, Park Y, Kurleto JD, Jeon M, Zinn K, Thornton JW, Ozkan E. Family of neural wiring receptors in bilaterians defined by phylogenetic, biochemical, and structural evidence. Proc Natl Acad Sci U S A. 2019 May 14;116(20):9837-9842. doi:, 10.1073/pnas.1818631116. Epub 2019 May 1. PMID:31043568 doi:http://dx.doi.org/10.1073/pnas.1818631116
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