7uqc
From Proteopedia
(Difference between revisions)
| (One intermediate revision not shown.) | |||
| Line 1: | Line 1: | ||
| - | '''Unreleased structure''' | ||
| - | + | ==phospho-GlialCAM peptide AA370-389 with Fab MS39p2w174== | |
| - | + | <StructureSection load='7uqc' size='340' side='right'caption='[[7uqc]], [[Resolution|resolution]] 2.65Å' scene=''> | |
| - | + | == Structural highlights == | |
| - | + | <table><tr><td colspan='2'>[[7uqc]] is a 10 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=7UQC OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7UQC FirstGlance]. <br> | |
| - | + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.65Å</td></tr> | |
| - | [[Category: | + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=CL:CHLORIDE+ION'>CL</scene>, <scene name='pdbligand=SEP:PHOSPHOSERINE'>SEP</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'>[https://proteopedia.org/fgij/fg.htm?mol=7uqc FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7uqc OCA], [https://pdbe.org/7uqc PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7uqc RCSB], [https://www.ebi.ac.uk/pdbsum/7uqc PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7uqc ProSAT]</span></td></tr> | ||
| + | </table> | ||
| + | == Disease == | ||
| + | [https://www.uniprot.org/uniprot/HECAM_HUMAN HECAM_HUMAN] Macrocephaly-intellectual disability-autism syndrome;Megalencephalic leukoencephalopathy with subcortical cysts. The disease is caused by variants affecting the gene represented in this entry. The disease is caused by variants affecting the gene represented in this entry. | ||
| + | == Function == | ||
| + | [https://www.uniprot.org/uniprot/HECAM_HUMAN HECAM_HUMAN] Involved in regulating cell motility and cell-matrix interactions. May inhibit cell growth through suppression of cell proliferation.<ref>PMID:15885354</ref> <ref>PMID:15917256</ref> | ||
| + | == References == | ||
| + | <references/> | ||
| + | __TOC__ | ||
| + | </StructureSection> | ||
| + | [[Category: Homo sapiens]] | ||
| + | [[Category: Large Structures]] | ||
| + | [[Category: Fernandez D]] | ||
| + | [[Category: Lanz TV]] | ||
| + | [[Category: Robinson WH]] | ||
Current revision
phospho-GlialCAM peptide AA370-389 with Fab MS39p2w174
| |||||||||||
