4l1h

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Current revision (10:13, 30 October 2024) (edit) (undo)
 
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== Structural highlights ==
== Structural highlights ==
<table><tr><td colspan='2'>[[4l1h]] is a 1 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=4L1H OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4L1H FirstGlance]. <br>
<table><tr><td colspan='2'>[[4l1h]] is a 1 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=4L1H OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4L1H FirstGlance]. <br>
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</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=4l1h FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4l1h OCA], [https://pdbe.org/4l1h PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4l1h RCSB], [https://www.ebi.ac.uk/pdbsum/4l1h PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4l1h ProSAT]</span></td></tr>
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.68&#8491;</td></tr>
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=4l1h FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4l1h OCA], [https://pdbe.org/4l1h PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4l1h RCSB], [https://www.ebi.ac.uk/pdbsum/4l1h PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4l1h ProSAT]</span></td></tr>
</table>
</table>
== Function ==
== Function ==

Current revision

Bence-Jones immunoglobulin REI variable portion with seven point mutations

PDB ID 4l1h

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