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 | |
| Domain: | Loop 3-4 | |
| General numbering (KChannelDB): | - | |
| Protein: | KCNH1_BOVIN (KCNH1,EA) | Swiss-Prot Cross-reference table Family page |
| Protein isoforms | 2 | |
| Other point mutations / same protein | List 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 article | List | |
| Text source | HTML full text | |
| Validation status | Not yet checked |
Relevant sentences:
S321C
cmbi.ru.nl), 17-Aug-2005