KChannelDB: Extraction of mutation data from the literature

logo    2005, KChannelDB.


This data was extracted from Medline abstracts and full texts (when available) in an automated manner.

The table below describes the selected point mutation and provides links to other documents. The sentence(s) where the point mutation F656C was found are listed after the table.

The mutated residues are also indicated in the family sequence alignments and hyperlinked to the corresponding mutation pages.


Point mutation F656C in KCNH2_HUMAN

Point mutation:F656C
Domain:TRANSMEM VI
General numbering (KChannelDB): 658
Protein:KCNH2_HUMAN (KCNH2,ERG, ERG1, HERG, HERG)Swiss-Prot
Cross-reference table
Family page
Protein isoforms4
Other point mutations / same protein / same positionPoint mutations at position 656 in KCNH2_HUMAN
Other point mutations / same proteinList of mutations in KCNH2_HUMAN
Family alignments eag related KCNH (Kv10-12)
K+ voltage-gated channels (Kv1-12,Kca2-5)
Potassium channels 6 TMs
Other point mutations / same position Position 656 in eag related KCNH (Kv10-12) family
Position 644 in K+ voltage-gated channels (Kv1-12,Kca2-5) family
Position 404 in Potassium channels 6 TMs family
Reference:Blockade of HERG cardiac K+ current by antifungal drug miconazole.
Kikuchi K, Nagatomo T, Abe H, Kawakami K, Duff HJ, Makielski JC, January CT, Nakashima Y
Br J Pharmacol 2004 Dec 13;.
Medline
Other point mutations / same articleList
Text sourceabstract
Validation statusNot yet checked

Relevant sentences:

F656C


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F.Horn (kchanneldbcmbi.ru.nl), 17-Aug-2005