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 S321C 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 S321C in KCNH1_BOVIN

Point mutation:S321C
Domain:Loop 3-4
General numbering (KChannelDB): -
Protein:KCNH1_BOVIN (KCNH1,EA)Swiss-Prot
Cross-reference table
Family page
Protein isoforms2
Other point mutations / same proteinList of mutations in KCNH1_BOVIN
Family alignments eag related KCNH (Kv10-12)
K+ voltage-gated channels (Kv1-12,Kca2-5)
Potassium channels 6 TMs
Other point mutations / same position
Reference:Conformational switch between slow and fast gating modes: allosteric regulation of voltage sensor mobility in the EAG K+ channel.
Schonherr R, Mannuzzu LM, Isacoff EY, Heinemann SH
Neuron 2002 Aug 29;35(5):935-49.
Medline
Other point mutations / same articleList
Text sourceHTML full text
Validation statusNot yet checked

Relevant sentences:

S321C


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