2l7m
From Proteopedia
(Difference between revisions)
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== Structural highlights == | == Structural highlights == | ||
[[2l7m]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2L7M OCA]. <br> | [[2l7m]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2L7M OCA]. <br> | ||
| - | <b>Related:</b> [[2l7f|2l7f]]<br> | + | <b>[[Related_structure|Related:]]</b> [[2l7f|2l7f]]<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=2l7m FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2l7m OCA], [http://www.rcsb.org/pdb/explore.do?structureId=2l7m RCSB], [http://www.ebi.ac.uk/pdbsum/2l7m PDBsum]</span><br> | ||
== Disease == | == Disease == | ||
[[http://www.uniprot.org/uniprot/PITX2_HUMAN PITX2_HUMAN]] Peters anomaly;Axenfeld anomaly;Rieger anomaly;Ring dermoid of cornea;Axenfeld-Rieger syndrome. The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry. | [[http://www.uniprot.org/uniprot/PITX2_HUMAN PITX2_HUMAN]] Peters anomaly;Axenfeld anomaly;Rieger anomaly;Ring dermoid of cornea;Axenfeld-Rieger syndrome. The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry. | ||
Revision as of 10:23, 30 April 2014
Solution Structure of the Pitx2 Homeodomain R24H mutant
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