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4p39
From Proteopedia
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== Structural highlights == | == Structural highlights == | ||
<table><tr><td colspan='2'>[[4p39]] is a 4 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=4P39 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4P39 FirstGlance]. <br> | <table><tr><td colspan='2'>[[4p39]] is a 4 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=4P39 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4P39 FirstGlance]. <br> | ||
| - | </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=4p39 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4p39 OCA], [https://pdbe.org/4p39 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4p39 RCSB], [https://www.ebi.ac.uk/pdbsum/4p39 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4p39 ProSAT]</span></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]] 2.401Å</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=4p39 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4p39 OCA], [https://pdbe.org/4p39 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4p39 RCSB], [https://www.ebi.ac.uk/pdbsum/4p39 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4p39 ProSAT]</span></td></tr> | ||
</table> | </table> | ||
== Disease == | == Disease == | ||
Current revision
Crystal structure of the human C5aR antagonist C5a-A8
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