4pwy: Difference between revisions
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{{STRUCTURE_4pwy| PDB=4pwy | SCENE= }} | |||
===Crystal structure of a Calmodulin-lysine N-methyltransferase fragment=== | |||
==Disease== | |||
[[http://www.uniprot.org/uniprot/CMKMT_HUMAN CMKMT_HUMAN]] Atypical hypotonia - cystinuria syndrome;2p21 microdeletion syndrome without cystinuria;2p21 microdeletion syndrome. | |||
==Function== | |||
[[http://www.uniprot.org/uniprot/CMKMT_HUMAN CMKMT_HUMAN]] Catalyzes the trimethylation of 'Lys-116' in calmodulin.<ref>PMID:20975703</ref> | |||
==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]] | |||
Revision as of 10:12, 16 April 2014
Crystal structure of a Calmodulin-lysine N-methyltransferase fragment
Disease
[CMKMT_HUMAN] Atypical hypotonia - cystinuria syndrome;2p21 microdeletion syndrome without cystinuria;2p21 microdeletion syndrome.
Function
[CMKMT_HUMAN] Catalyzes the trimethylation of 'Lys-116' in calmodulin.[1]
About this Structure
4pwy is a 1 chain structure. Full crystallographic information is available from OCA.
Reference
- ↑ Magnani R, Dirk LM, Trievel RC, Houtz RL. Calmodulin methyltransferase is an evolutionarily conserved enzyme that trimethylates Lys-115 in calmodulin. Nat Commun. 2010 Jul 27;1:43. doi: 10.1038/ncomms1044. PMID:20975703 doi:https://dx.doi.org/10.1038/ncomms1044