3 Ontology Annotations
| GO Term | Gene Name |
|---|---|
| GO:0005267 | IPR005410 |
| GO:0071805 | IPR005410 |
| GO:0016021 | IPR005410 |
| Type: | Family | Name: | Two pore domain potassium channel, THIK |
| Description: | Potassium channels are the most diverse group of the ion channel family [, ]. They are important in shaping the action potential, and in neuronal excitability and plasticity []. The potassium channel family iscomposed of several functionally distinct isoforms, which can be broadly separated into 2 groups []: the practically non-inactivating 'delayed' group and the rapidly inactivating 'transient' group.These are all highly similar proteins, with only small amino acid changes causing the diversity of the voltage-dependent gating mechanism,channel conductance and toxin binding properties. Each type of K+channel is activated by different signals and conditions depending on their type of regulation: some open in response to depolarisation of the plasma membrane; others in response to hyperpolarisation or an increase in intracellular calcium concentration; some can be regulated by binding of a transmitter, together with intracellular kinases; while others are regulated by GTP-binding proteins or other second messengers []. In eukaryotic cells, K+channels are involved in neural signalling and generation of the cardiac rhythm, act as effectors in signal transduction pathways involving G protein-coupled receptors (GPCRs) and may have a role in target cell lysis by cytotoxic T-lymphocytes []. In prokaryotic cells, they play a role in themaintenance of ionic homeostasis [].All K+channels discovered so far possess a core of alpha subunits, each comprising either one or two copies of a highly conserved pore loop domain (P-domain). The P-domain contains the sequence (T/SxxTxGxG), which hasbeen termed the K+selectivity sequence. In families that contain one P-domain, four subunits assemble to form a selective pathway for K+across the membrane. However, it remains unclear how the 2 P-domain subunits assemble to form a selective pore. The functional diversity of these families can arise through homo- or hetero-associations of alpha subunits or association with auxiliary cytoplasmic beta subunits. K+channel subunits containing one pore domain can be assigned into one of two superfamilies: those that possess six transmembrane (TM) domains and those that possess only two TM domains. The six TM domain superfamily can be further subdivided into conserved gene families: the voltage-gated (Kv) channels; the KCNQ channels (originally known as KvLQT channels); the EAG-like K+channels; and three types of calcium (Ca)-activated K+channels (BK, IK and SK) []. The 2TM domain family comprises inward-rectifying K+channels. In addition, there are K+channel alpha-subunits that possess two P-domains. These are usually highly regulated K+selective leak channels.The THIK (Tandem pore-domain Halothane Inhibited K+ channel) family contains two members: THIK-1 and THIK-2. Both proteins were first isolated from rat and have subsequently been found in human. THIK-1 is expressed ubiquitously and is activated by arachidonic acid and inhibited by the volatile anaesthetic halothane. The second member, THIK-2, shares 58% amino acid identity with THIK-1, but is not functionally expressed. THIK-2 is strongly expressed in several tissues, and is particularly abundant in the brain []. | Short Name: | 2pore_dom_K_chnl_THIK |
| GO Term | Gene Name |
|---|---|
| GO:0005267 | IPR005410 |
| GO:0071805 | IPR005410 |
| GO:0016021 | IPR005410 |
