Target Name: KCNK3
NCBI ID: G3777
Other Name(s): potassium inwardly-rectifying channel, subfamily K, member 3 | PPH4 | KCNK3_HUMAN | TWIK-related acid-sensitive K+ 1 | Potassium channel, subfamily K, member 3 (TASK) | acid-sensitive potassium channel protein TASK-1 | two P domain potassium channel | acid-sensitive potassium channel protein TASK | Two P domain potassium channel | TASK | Kcnk3 channel | TWIK-related acid-sensitive K(+) channel 1 | OAT1 | Two pore potassium channel KT3.1 | TWIK-related acid-sensitive K+ channel | TBAK1 | Acid-sensitive potassium channel protein TASK | cardiac potassium channel | K2p3.1 | Two pore K(+) channel KT3.1 | two pore K(+) channel KT3.1 | two pore potassium channel KT3.1 | Potassium channel subfamily K member 3 | Potassium channel, subfamily K, member 3 (TASK-1) | TASK-1 | potassium channel, two pore domain subfamily K, member 3 | Acid-sensitive potassium channel protein TASK-1 | Potassium two pore domain channel subfamily K member 3 | potassium two pore domain channel subfamily K member 3 | TASK1 | Cardiac potassium channel

KCNK3: A Potassium Channel Subfamily K Member Identified as a Potential Drug Target

Abstract:

KCNK3, a member of the potassium channel subfamily K, has been identified as a potential drug target due to its unique function in neural signaling. Although its primary role is to regulate the rapid depolarization of neural neurons, recent studies have hinted at other potential functions and its involvement in various neurological disorders. In this article, we will explore the biology of KCNK3, its potential drug targets, and the ongoing research in this field.

Introduction:

Potassium channels are critical for maintaining the resting membrane potential of neurons and play a pivotal role in neural signaling. The potassium channel subfamily K, member 3 (KCNK3), is a family of channels that are characterized by the presence of a unique alpha- Helical structure in their extracellular domain. Despite its importance in neurotransmission, little is known about the specific functions of KCNK3 and its potential as a drug target.

History of the Potassium Channel Subfamily K:

The potassium channel subfamily K, also known as the Slow inward current subfamily (IKs), is a family of channels that are characterized by the presence of a unique alpha-helical structure in their extracellular domain. The first member of the subfamily, IK1 , was discovered in 1992, and since then, several additional members have been identified. These channels are involved in various physiological processes, including neurotransmission, muscle contractions, and heart rhythms.

Function and Potential Drug Targets:

KCNK3 is a member of the potassium channel subfamily K, member 3. It is a small, tonic channel that is involved in the rapid depolarization of neural neurons. Its unique alpha-helical structure allows it to regulate the flow of potassium ions into the cell , which is essential for maintaining the resting membrane potential of the neuron.

Recent studies have hinted at the potential functions of KCNK3 beyond its role in neurotransmission. For instance, some researchers have suggested that KCNK3 may be involved in the regulation of muscle contractions and the maintenance of heart rhythms. Additionally, the alpha-helical structure of KCNK3 may be involved in its unique stability, as studies have shown that it is more resistant to depolarization than other members of the potassium channel subfamily K.

Despite its potential functions, little is known about the specific mechanisms of KCNK3's role in neural signaling. Understanding the function of KCNK3 and its potential as a drug target is an important step in the development of new treatments for various neurological disorders.

Conclusion:

In conclusion, KCNK3 is a member of the potassium channel subfamily K, member 3 that has been identified as a potential drug target due to its unique function in neural signaling. The unique alpha-helical structure and its role in the regulation of rapid depolarization of neural neurons make it an attractive target for researchers to explore. Further studies are needed to understand the specific mechanisms of its function and its potential as a drug target.

Protein Name: Potassium Two Pore Domain Channel Subfamily K Member 3

Functions: pH-dependent, voltage-insensitive, background potassium channel protein. Rectification direction results from potassium ion concentration on either side of the membrane. Acts as an outward rectifier when external potassium concentration is low. When external potassium concentration is high, current is inward

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KCNK4 | KCNK5 | KCNK6 | KCNK7 | KCNK9 | KCNMA1 | KCNMB1 | KCNMB2 | KCNMB2-AS1 | KCNMB3 | KCNMB4 | KCNN1 | KCNN2 | KCNN3 | KCNN4 | KCNQ Channels (K(v) 7) | KCNQ1 | KCNQ1DN | KCNQ1OT1 | KCNQ2 | KCNQ3 | KCNQ4 | KCNQ5 | KCNQ5-AS1 | KCNQ5-IT1 | KCNRG | KCNS1 | KCNS2 | KCNS3 | KCNT1 | KCNT2 | KCNU1 | KCNV1 | KCNV2 | KCP | KCTD1 | KCTD10 | KCTD11 | KCTD12 | KCTD13 | KCTD13-DT | KCTD14 | KCTD15 | KCTD16 | KCTD17 | KCTD18 | KCTD19 | KCTD2 | KCTD20 | KCTD21 | KCTD21-AS1 | KCTD3 | KCTD4 | KCTD5 | KCTD5P1 | KCTD6 | KCTD7 | KCTD8 | KCTD9 | KDELR1 | KDELR2 | KDELR3 | KDF1 | KDM1A | KDM1B | KDM2A | KDM2B | KDM3A | KDM3B | KDM4A | KDM4B | KDM4C | KDM4D | KDM4E | KDM5A | KDM5A-GATAD1-EMSY chromatin complex | KDM5B | KDM5C | KDM5D | KDM6A | KDM6B | KDM7A | KDM7A-DT | KDM8 | KDR | KDSR | KEAP1 | Kelch-like protein | KERA | Keratin | KHDC1 | KHDC1L | KHDC1P1 | KHDC3L | KHDC4 | KHDRBS1 | KHDRBS2 | KHDRBS3 | KHK | KHNYN