4pwy: Difference between revisions

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-'''Unreleased structure'''
+{{STRUCTURE_4pwy|  PDB=4pwy  |  SCENE=  }}
+===Crystal structure of a Calmodulin-lysine N-methyltransferase fragment===
-The entry 4pwy is ON HOLD
+==Disease==
+[[http://www.uniprot.org/uniprot/CMKMT_HUMAN CMKMT_HUMAN]] Atypical hypotonia - cystinuria syndrome;2p21 microdeletion syndrome without cystinuria;2p21 microdeletion syndrome.
-Authors: Tempel, W., Hong, B.S., Walker, J.R., Li, Y., Bountra, C., Arrowsmith, C.H., Edwards, A.M., Brown, P.J., Structural Genomics Consortium (SGC)
+==Function==
+[[http://www.uniprot.org/uniprot/CMKMT_HUMAN CMKMT_HUMAN]] Catalyzes the trimethylation of 'Lys-116' in calmodulin.<ref>PMID:20975703</ref>
-Description: Crystal structure of a Calmodulin-lysine N-methyltransferase fragment
+==About this Structure==
+[[4pwy]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4PWY OCA].
+==Reference==
+<references group="xtra"/><references/>
+[[Category: Calmodulin-lysine N-methyltransferase]]
+[[Category: Arrowsmith, C H.]]
+[[Category: Bountra, C.]]
+[[Category: Brown, P J.]]
+[[Category: Edwards, A M.]]
+[[Category: Hong, B S.]]
+[[Category: Li, Y.]]
+[[Category: SGC, Structural Genomics Consortium.]]
+[[Category: Tempel, W.]]
+[[Category: Walker, J R.]]
+[[Category: Methyl transferase]]
+[[Category: Sgc]]
+[[Category: Structural genomic]]
+[[Category: Structural genomics consortium]]
+[[Category: Transferase]]

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