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 L59G 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: | L59G | |
| Domain: | TRANSMEM I | |
| General numbering (KChannelDB): | 161 | |
| Protein: | KCNE1_HUMAN (KCNE) | Swiss-Prot Cross-reference table Family page |
| Other point mutations / same protein | List of mutations in KCNE1_HUMAN | |
| Family alignments |
IsK related channels (minK,MiRP,AMMECR2) Potassium channels 1 TM | |
| Other point mutations / same position |
Position 59 in IsK related channels (minK,MiRP,AMMECR2) family Position 59 in Potassium channels 1 TM family | |
| Reference: | A single transmembrane site in the KCNE-encoded proteins controls the specificity of KvLQT1 channel gating. Melman YF, Krumerman A, McDonald TV J Biol Chem 2002 Jul 12;277(28):25187-94. | Medline |
| Other point mutations / same article | List | |
| Text source | HTML full text | |
| Validation status | Not yet checked |
Relevant sentences:
L59G
cmbi.ru.nl), 17-Aug-2005