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4l1d
From Proteopedia
(Difference between revisions)
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== Structural highlights == | == Structural highlights == | ||
[[4l1d]] is a 3 chain structure with sequence from [http://en.wikipedia.org/wiki/Human Human]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4L1D OCA]. <br> | [[4l1d]] is a 3 chain structure with sequence from [http://en.wikipedia.org/wiki/Human Human]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4L1D OCA]. <br> | ||
| - | <b>Related:</b> [[2x1x|2x1x]], [[1i8l|1i8l]], [[1f97|1f97]]<br> | + | <b>[[Related_structure|Related:]]</b> [[2x1x|2x1x]], [[1i8l|1i8l]], [[1f97|1f97]]<br> |
<b>Activity:</b> <span class='plainlinks'>[http://en.wikipedia.org/wiki/Glucokinase Glucokinase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.1.2 2.7.1.2] </span><br> | <b>Activity:</b> <span class='plainlinks'>[http://en.wikipedia.org/wiki/Glucokinase Glucokinase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.1.2 2.7.1.2] </span><br> | ||
| + | <b>Resources:</b> <span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4l1d FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4l1d OCA], [http://www.rcsb.org/pdb/explore.do?structureId=4l1d RCSB], [http://www.ebi.ac.uk/pdbsum/4l1d PDBsum]</span><br> | ||
== Disease == | == Disease == | ||
[[http://www.uniprot.org/uniprot/SCN3B_HUMAN SCN3B_HUMAN]] Brugada syndrome. The disease is caused by mutations affecting the gene represented in this entry. | [[http://www.uniprot.org/uniprot/SCN3B_HUMAN SCN3B_HUMAN]] Brugada syndrome. The disease is caused by mutations affecting the gene represented in this entry. | ||
Revision as of 10:13, 30 April 2014
Voltage-gated sodium channel beta3 subunit Ig domain
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