UniProt ID | KCJ11_HUMAN | |
---|---|---|
UniProt AC | Q14654 | |
Protein Name | ATP-sensitive inward rectifier potassium channel 11 | |
Gene Name | KCNJ11 | |
Organism | Homo sapiens (Human). | |
Sequence Length | 390 | |
Subcellular Localization |
Membrane Multi-pass membrane protein. |
|
Protein Description | This receptor is controlled by G proteins. Inward rectifier potassium channels are characterized by a greater tendency to allow potassium to flow into the cell rather than out of it. Their voltage dependence is regulated by the concentration of extracellular potassium; as external potassium is raised, the voltage range of the channel opening shifts to more positive voltages. The inward rectification is mainly due to the blockage of outward current by internal magnesium. Can be blocked by extracellular barium (By similarity). Subunit of ATP-sensitive potassium channels (KATP). Can form cardiac and smooth muscle-type KATP channels with ABCC9. KCNJ11 forms the channel pore while ABCC9 is required for activation and regulation.. | |
Protein Sequence | MLSRKGIIPEEYVLTRLAEDPAEPRYRARQRRARFVSKKGNCNVAHKNIREQGRFLQDVFTTLVDLKWPHTLLIFTMSFLCSWLLFAMAWWLIAFAHGDLAPSEGTAEPCVTSIHSFSSAFLFSIEVQVTIGFGGRMVTEECPLAILILIVQNIVGLMINAIMLGCIFMKTAQAHRRAETLIFSKHAVIALRHGRLCFMLRVGDLRKSMIISATIHMQVVRKTTSPEGEVVPLHQVDIPMENGVGGNSIFLVAPLIIYHVIDANSPLYDLAPSDLHHHQDLEIIVILEGVVETTGITTQARTSYLADEILWGQRFVPIVAEEDGRYSVDYSKFGNTIKVPTPLCTARQLDEDHSLLEALTLASARGPLRKRSVPMAKAKPKFSISPDSLS | |
Overview of Protein Modification Sites with Functional and Structural Information | ||
* ASA = Accessible Surface Area
Locations | Modification | Substrate Peptides & Secondary Structure |
ASA (%) | Reference | Orthologous Protein Cluster |
---|---|---|---|---|---|
26 | Phosphorylation | EDPAEPRYRARQRRA CCCCCHHHHHHHHHH | 18083107 | ||
93 | Phosphorylation | FAMAWWLIAFAHGDL HHHHHHHHHHHHCCC | - | ||
137 | Phosphorylation | TIGFGGRMVTEECPL EEECCCEECCCCCCH | - | ||
180 | Phosphorylation | QAHRRAETLIFSKHA HHHHHHHHHHCCCHH | - | ||
184 | Phosphorylation | RAETLIFSKHAVIAL HHHHHHCCCHHHHHH | 24719451 | ||
208 | Phosphorylation | RVGDLRKSMIISATI EECCHHHHHEEEEEE | - | ||
224 | Phosphorylation | MQVVRKTTSPEGEVV EEEEECCCCCCCCEE | - | ||
285 | Phosphorylation | HQDLEIIVILEGVVE CCCCEEEEEEECEEC | - | ||
298 | Phosphorylation | VETTGITTQARTSYL ECCCCCCCCCCHHHH | 18280666 | ||
332 | Ubiquitination | RYSVDYSKFGNTIKV CEEEEHHHCCCEEEC | 21890473 | ||
332 | Ubiquitination | RYSVDYSKFGNTIKV CEEEEHHHCCCEEEC | 21890473 | ||
332 | Ubiquitination | RYSVDYSKFGNTIKV CEEEEHHHCCCEEEC | 21890473 | ||
341 | Phosphorylation | GNTIKVPTPLCTARQ CCEEECCCCCCCCHH | 18280666 | ||
372 | Phosphorylation | RGPLRKRSVPMAKAK CCCCHHCCCCCCCCC | 24719451 | ||
385 | Phosphorylation | AKPKFSISPDSLS-- CCCCCCCCCCCCC-- | 7502040 | ||
388 | Phosphorylation | KFSISPDSLS----- CCCCCCCCCC----- | 28348404 |
Modified Location | Modified Residue | Modification | Type of Upstream Proteins | Gene Name of Upstream Proteins | UniProt AC of Upstream Proteins | Sources |
---|---|---|---|---|---|---|
180 | T | Phosphorylation | Kinase | CAMK2A | Q9UQM7 | PSP |
224 | T | Phosphorylation | Kinase | CAMK2A | Q9UQM7 | PSP |
224 | T | Phosphorylation | Kinase | CAMK2D | Q13557 | PSP |
341 | T | Phosphorylation | Kinase | MAPK1 | P28482 | Uniprot |
372 | S | Phosphorylation | Kinase | PKA-FAMILY | - | GPS |
385 | S | Phosphorylation | Kinase | MAPK1 | P28482 | Uniprot |
Modified Location | Modified Residue | Modification | Function | Reference | ||
---|---|---|---|---|---|---|
Oops, there are no descriptions of PTM sites of KCJ11_HUMAN !! |
* Distance = the distance between SAP position and PTM sites.
Modified Location | Modification | Variant Position (Distance <= 10) |
Residue Change | SAP | Related Disease | Reference |
---|---|---|---|---|---|---|
Oops, there are no SNP-PTM records of KCJ11_HUMAN !! |
Interacting Protein | Gene Name | Interaction Type | PPI Reference | Domain-Domain Interactions |
---|---|---|---|---|
KCNJ8_HUMAN | KCNJ8 | physical | 11136227 | |
1433B_HUMAN | YWHAB | physical | 23772394 | |
MINY2_HUMAN | FAM63B | physical | 26186194 | |
MINY2_HUMAN | FAM63B | physical | 28514442 |
Kegg Disease | |
---|---|
OMIM Disease | |
601820 | Familial hyperinsulinemic hypoglycemia 2 (HHF2) |
606176 | Diabetes mellitus, permanent neonatal (PNDM) |
610582 | Transient neonatal diabetes mellitus 3 (TNDM3) |
Note=Defects in KCNJ11 may contribute to non-insulin-dependent diabetes mellitus (NIDDM), also known as diabetes mellitus type 2. | |
616329 | |
Kegg Drug | |
DrugBank | |
DB01119 | Diazoxide |
DB00222 | Glimepiride |
DB01016 | Glyburide |
DB00308 | Ibutilide |
DB00922 | Levosimendan |
DB01154 | Thiamylal |
DB00661 | Verapamil |
DB01392 | Yohimbine |
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