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 G628C 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: | G628C | |
| Domain: | Loop 5-6 | |
| General numbering (KChannelDB): | - | |
| Protein: | KCNH2_HUMAN (KCNH2,ERG, ERG1, HERG, HERG) | Swiss-Prot Cross-reference table Family page |
| Protein isoforms | 4 | |
| Other point mutations / same protein / same position | Point mutations at position 628 in KCNH2_HUMAN | |
| Other point mutations / same protein | List 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 628 in eag related KCNH (Kv10-12) family Position 616 in K+ voltage-gated channels (Kv1-12,Kca2-5) family Position 376 in Potassium channels 6 TMs family | |
| Reference: | Trapping of a methanesulfonanilide by closure of the HERG potassium channel activation gate. Mitcheson JS, Chen J, Sanguinetti MC J Gen Physiol 2000 Mar;115(3):229-40. | Medline |
| Other point mutations / same article | List | |
| Text source | HTML full text | |
| Validation status | Not yet checked |
Relevant sentences:
G628C
cmbi.ru.nl), 17-Aug-2005