4m49: Difference between revisions

Proteopedia Page Contributors and Editors (what is this?)Proteopedia Page Contributors and Editors (what is this?)

@@ Line 1: / Line 1: @@
-'''Unreleased structure'''
+{{STRUCTURE_4m49|  PDB=4m49  |  SCENE=  }}
+===Lactate Dehydrogenase A in complex with a substituted pyrazine inhibitor compound 18===
-The entry 4m49 is ON HOLD
+==Disease==
+[[http://www.uniprot.org/uniprot/LDHA_HUMAN LDHA_HUMAN]] Defects in LDHA are the cause of glycogen storage disease type 11 (GSD11) [MIM:[http://omim.org/entry/612933 612933]]. A metabolic disorder that results in exertional myoglobinuria, pain, cramps and easy fatigue.<ref>PMID:2334430</ref>
-Authors: Eigenbrot, C., Ultsch, M.
+==About this Structure==
+[[4m49]] is a 4 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4M49 OCA].
-Description: Lactate Dehydrogenase A in complex with a substituted pyrazine inhibitor compound 18
+==Reference==
+<references group="xtra"/><references/>
+[[Category: Homo sapiens]]
+[[Category: L-lactate dehydrogenase]]
+[[Category: Eigenbrot, C.]]
+[[Category: Ultsch, M.]]
+[[Category: Dehydrogenase/reductase]]
+[[Category: Nicotinamide adenine dinucleotide nadh]]
+[[Category: Oxidoreductase-oxidoreductase inhibitor complex]]