General Information of This Target
Target ID
BTDT00138
Target Name
ATP-sensitive inward rectifier potassium channel 11 (KCNJ11)
Target Bioclass
Transporter and channel
Uniprot ID
Q14654
3D Structure
Download
2D Sequence
3D Structure
Source
Predict by Alphafold2
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Alphafold Parameters: msa_mode: mmseqs2_uniref_env model_type: auto num_recycles: auto
Gene Name
KCNJ11
Gene ID
3767
Synonym
IKATP; Inward rectifier K(+) channel Kir6.2; Potassium channel, inwardly rectifying subfamily J member 11
Sequence
MLSRKGIIPEEYVLTRLAEDPAKPRYRARQRRARFVSKKGNCNVAHKNIREQGRFLQDVF
TTLVDLKWPHTLLIFTMSFLCSWLLFAMAWWLIAFAHGDLAPSEGTAEPCVTSIHSFSSA
FLFSIEVQVTIGFGGRMVTEECPLAILILIVQNIVGLMINAIMLGCIFMKTAQAHRRAET
LIFSKHAVIALRHGRLCFMLRVGDLRKSMIISATIHMQVVRKTTSPEGEVVPLHQVDIPM
ENGVGGNSIFLVAPLIIYHVIDANSPLYDLAPSDLHHHQDLEIIVILEGVVETTGITTQA
RTSYLADEILWGQRFVPIVAEEDGRYSVDYSKFGNTVKVPTPLCTARQLDEDHSLLEALT
LASARGPLRKRSVPMAKAKPKFSISPDSLS

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Family
the inward rectifier-type potassium channel family
Function
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. 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.

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Taxonomy ID
9606
TCDB ID
1.A.2.1.17
        Click to Show/Hide the Complete Species Lineage
Kingdom: Metazoa
Phylum: Chordata
Class: Mammalia
Order: Primates
Family: Hominidae
Genus: Homo
Species: Homo sapiens
Toxin Information Related to This Target
                           Toxin Name Activity Data Type Activity Data Reference
 Toxin Info    Kappa-scoloptoxin(15)-Ssd3a Dissociation constant
118 nM
[1]
 Toxin Info    Toxin SSD893 Dissociation constant
123 nM
[1]
 Toxin Info    Omega-scoloptoxin(15)-Ssd3c Dissociation constant
126 nM
[1]
 Toxin Info    Mu-scoloptoxin(15)-Ssm1a Dissociation constant
180 nM
[2]
 Toxin Info    Toxin SSD893 Dissociation constant
260 nM
[1]
 Toxin Info    Omega-scoloptoxin(15)-Ssd3c Dissociation constant
278 nM
[1]
 Toxin Info    Kappa-scoloptoxin(15)-Ssd3a Dissociation constant
283 nM
[1]
 Toxin Info    SsTx-4 (Y16A) IC50
1.8 nM
[3]
 Toxin Info    SsTx-4 (Y49A) IC50
4.1 nM
[3]
 Toxin Info    SsTx-4 IC50
8.2 nM
[3]
 Toxin Info    SsTx-4 (K10A) IC50
9 nM
[3]
 Toxin Info    SsTx-4 (P8A) IC50
9 nM
[3]
 Toxin Info    SsTx-4 (P15A) IC50
9.7 nM
[3]
 Toxin Info    Ssm spooky toxin (K40A,K45A) IC50
10 nM
[3]
 Toxin Info    SsTx-4 (P41A) IC50
10 nM
[3]
 Toxin Info    SsTx-4 (K11A) IC50
10.8 nM
[3]
 Toxin Info    SsTx-4 (F9A) IC50
20.5 nM
[3]
 Toxin Info    SsTx-4 (K40A) IC50
20.5 nM
[3]
 Toxin Info    SsTx-4 (R12A) IC50
25.6 nM
[3]
 Toxin Info    SsTx-4 (K4A) IC50
41 nM
[3]
 Toxin Info    SsTx-4 IC50
42.5 nM
[3]
 Toxin Info    SsTx-4 (K45A) IC50
49.2 nM
[3]
 Toxin Info    SsTx-4 (F43A) IC50
65.6 nM
[3]
 Toxin Info    SsTx-4 (K4A,K40A) IC50
73.8 nM
[3]
 Toxin Info    SsTx-4 (K4A,K45A) IC50
90.2 nM
[3]
 Toxin Info    SsTx-4 (F44A) IC50
131.2 nM
[3]
 Toxin Info    SsTx-4 (K40A,K45A) IC50
155.8 nM
[3]
 Toxin Info    SsTx-4 (F14A) IC50
172.2 nM
[3]
 Toxin Info    SsTx-4 (K4A,K40A,K45A) IC50
319.8 nM
[3]
 Toxin Info    SsTx-4 (K13A) IC50
434.6 nM
[3]
 Toxin Info    SsTx-4 (F43A,F44A) IC50
951.2 nM
[3]
References
Ref 1 A family of orthologous proteins from centipede venoms inhibit the hKir6.2 channel. Sci Rep. 2019 Oct 1;9(1):14088. doi: 10.1038/s41598-019-50688-x.
Ref 2 Centipedes subdue giant prey by blocking KCNQ channels. Proc Natl Acad Sci U S A. 2018 Feb 13;115(7):1646-1651. doi: 10.1073/pnas.1714760115. Epub 2018 Jan 22.
Ref 3 Molecular mechanisms of centipede toxin SsTx-4 inhibition of inwardly rectifying potassium channels. J Biol Chem. 2021 Sep;297(3):101076. doi: 10.1016/j.jbc.2021.101076. Epub 2021 Aug 12.
Ref 4 A novel high-affinity inhibitor against the human ATP-sensitive Kir6.2 channel. J Gen Physiol. 2018 Jul 2;150(7):969-976. doi: 10.1085/jgp.201812017. Epub 2018 May 29.
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