CAMK

<h2 id="types">Types</h2>
<p>There are 2 common types of CAM Kinase proteins: specialized and multi-functional CAM kinases.
</p>
Substrate-specific CAM Kinases
only have one target that they can phosphorylate, such as myosin light chain kinases.<a class="footnote-ref" id="fnref:2" href="#fn:2"><sup>2</sup></a> This group of proteins includes CAMK III. More on <a href="/facts/CAMKIII/m9zRN3n8">CAMKIII</a> can be found following this link.
Multi-functional CAM Kinases
have multiple targets they can phosphorylate and are found in processes including the secretion of neurotransmitters, metabolism of glycogen, and the regulation of various transcription factors.<a class="footnote-ref" id="fnref:3" href="#fn:3"><sup>3</sup></a> CAMK II is the main protein in this subset. More on <a href="/facts/CAMKII/hklT8LuH">CAMKII</a> can be found following this link.
<h2 id="substrate-phosphorylation">Substrate phosphorylation</h2>

<p>Once calcium concentrations in the cell rise, CAM kinases become saturated and bind the maximum of four calcium molecules.<a class="footnote-ref" id="fnref:4" href="#fn:4"><sup>4</sup></a> This calcium saturation activates the kinase and allows it to undergo a conformational change which permits the kinase to bind to its phosphorylation target sites. CAMK removes a phosphate group from ATP, most typically using a Mg2+ ion, and adds it to the CAM protein, rendering it active.<a class="footnote-ref" id="fnref:5" href="#fn:5"><sup>5</sup></a> The CAM Kinase contains a highly concentrated glycine loop where the gamma phosphate from the donor ATP molecule is easily able to bind to the enzyme which then utilizes the metal ion to facilitate a smooth phosphate transfer to the target protein.<a class="footnote-ref" id="fnref:6" href="#fn:6"><sup>6</sup></a> This phosphate transfer then activates the kinase's target and completes the phosphorylation cycle.
</p><p>
Figure 1 shows how the presence of calcium or calmodulin allows for the activation of CAM kinases (CAMK II).</p>
<h2 id="structure">Structure</h2>
<p>All kinases have a common structure of a catalytic core including an ATP binding site along with a larger substrate binding site.<a class="footnote-ref" id="fnref:7" href="#fn:7"><sup>7</sup></a> The catalytic core is typically composed of β-strands with the substrate binding site composed of α-helices.<a class="footnote-ref" id="fnref:8" href="#fn:8"><sup>8</sup></a> Most all CAM kinases includes a variety of domains, including: a catalytic domain, a regulatory domain, an association domain, and a calcium/calmodulin binding domain.<a class="footnote-ref" id="fnref:9" href="#fn:9"><sup>9</sup></a>
</p>
CAMK I
as shown in Figure 2, has a double-lobed structure, consisting of a catalytic, substrate-binding domain and an autoinhibitory domain.<a class="footnote-ref" id="fnref:10" href="#fn:10"><sup>10</sup></a> For the autoinhibitory domain to become functional, it must cause the protein to conform in such a way that this domain completely blocks the substrate domain from taking in new targets. Figure 2 goes into detail showing the structure and domains of CAMK I.
CAMK II
has a variety of different forms, with CAMK 2A being the most common, as shown in Figure 3. CAMK 2A has a ring-like crystalline structure, composed of smaller functional groups. These groups allow for the CaM-dependent phosphorylation of targets, but also allows the structure to autophosphorylate itself and become CaM-independent,<a class="footnote-ref" id="fnref:11" href="#fn:11"><sup>11</sup></a> as seen in Figure 1. This means once the CAMK 2A protein is initially activated by calcium or calmodulin, it can, in turn, further activate itself, so it doesn't become inactive even when it is without calcium or calmodulin. 
<h2 id="family-members">Family members</h2>
<p>Members of the CAMK enzyme class include, but are not limited to:
</p>
<ul><li><a href="/facts/CAMKI/HmYN1JgK">CAMKI</a>
<ul><li>CAMKIα (<a href="/facts/CAMK1/HmYN1JgK">CAMK1</a>)</li>
<li>CAMKIβ (PNCK)</li>
<li><a href="/facts/CAMKI%25CE%25B4/60XIy3Y1">CAMKIδ</a></li>
<li>CAMKIγ (<a href="/facts/CAMK1G_(gene)/C218k0ds">CAMK1G</a>)</li></ul></li>
<li><a href="/facts/CAMKII/hklT8LuH">CAMKII</a>
<ul><li><a href="/facts/CAMKII%25CE%25B1/zAYpLXIU">CAMKIIα</a></li>
<li><a href="/facts/CAMKII%25CE%25B2/M90A06b9">CAMKIIβ</a></li>
<li><a href="/facts/CAMKII%25CE%25B4/stIyJA8c">CAMKIIδ</a></li>
<li><a href="/facts/CAMKII%25CE%25B3/toGhvgzb">CAMKIIγ</a></li></ul></li>
<li><a href="/facts/CAMKIII/m9zRN3n8">CAMKIII</a></li>
<li><a href="/facts/CAMKIV/KLkKPnle">CAMKIV</a></li>
<li>CAMKV CaM kinase like vesicle associated</li>
<li>SCAMK</li>
<li>Ca2+/calmodulin-dependent protein kinase kinase
<ul><li><a href="/facts/CAMKK1/1dSDVMlL">CAMKK1</a></li>
<li><a href="/facts/CAMKK2/RR3QL0uA">CAMKK2</a></li></ul></li></ul>
<h2 id="pseudokinases">Pseudokinases</h2>
<p><a href="/facts/Pseudokinase/CBfkHlRd">Pseudokinases</a> are <a href="/facts/Pseudoenzyme/Vx1xjQJW">pseudoenzymes</a>, proteins that resemble enzymes structurally, but lack catalytic activity.
</p><p>Some of these pseudokinases that are related to the CAMK family include: 
</p>
<ul><li>Tribbles subfamily
<ul><li><a href="/facts/TRIB1/Nc3nyRXf">TRIB1</a></li>
<li><a href="/facts/TRIB2/BzQXSjKD">TRIB2</a></li>
<li><a href="/facts/TRIB3/splqqwQ9">TRIB3</a></li></ul></li></ul>

<h2 id="references">References</h2>

<ol>
<li id="fn:1"><p>Swulius MT, Waxham MN (September 2008). "Ca(2+)/calmodulin-dependent protein kinases". Cellular and Molecular Life Sciences. 65 (17): 2637–57. doi:10.1007/s00018-008-8086-2. PMC 3617042. PMID 18463790. <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3617042" target="_blank">https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3617042</a> <a href="#fnref:1" class="footnote-back-ref">↩</a></p></li>
<li id="fn:2"><p>Swulius MT, Waxham MN (September 2008). "Ca(2+)/calmodulin-dependent protein kinases". Cellular and Molecular Life Sciences. 65 (17): 2637–57. doi:10.1007/s00018-008-8086-2. PMC 3617042. PMID 18463790. <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3617042" target="_blank">https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3617042</a> <a href="#fnref:2" class="footnote-back-ref">↩</a></p></li>
<li id="fn:3"><p>Swulius MT, Waxham MN (September 2008). "Ca(2+)/calmodulin-dependent protein kinases". Cellular and Molecular Life Sciences. 65 (17): 2637–57. doi:10.1007/s00018-008-8086-2. PMC 3617042. PMID 18463790. <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3617042" target="_blank">https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3617042</a> <a href="#fnref:3" class="footnote-back-ref">↩</a></p></li>
<li id="fn:4"><p>Swulius MT, Waxham MN (September 2008). "Ca(2+)/calmodulin-dependent protein kinases". Cellular and Molecular Life Sciences. 65 (17): 2637–57. doi:10.1007/s00018-008-8086-2. PMC 3617042. PMID 18463790. <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3617042" target="_blank">https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3617042</a> <a href="#fnref:4" class="footnote-back-ref">↩</a></p></li>
<li id="fn:5"><p>Adams JA (August 2001). "Kinetic and catalytic mechanisms of protein kinases". Chemical Reviews. 101 (8): 2271–90. doi:10.1021/cr000230w. PMID 11749373. <a href="/wiki/Doi_(identifier)" target="_blank">/wiki/Doi_(identifier)</a> <a href="#fnref:5" class="footnote-back-ref">↩</a></p></li>
<li id="fn:6"><p>Hemmer W, McGlone M, Tsigelny I, Taylor SS (July 1997). "Role of the glycine triad in the ATP-binding site of cAMP-dependent protein kinase". The Journal of Biological Chemistry. 272 (27): 16946–54. doi:10.1074/jbc.272.27.16946. PMID 9202006. S2CID 33795382. <a href="https://doi.org/10.1074%2Fjbc.272.27.16946" target="_blank">https://doi.org/10.1074%2Fjbc.272.27.16946</a> <a href="#fnref:6" class="footnote-back-ref">↩</a></p></li>
<li id="fn:7"><p>Hanks SK (2003). "Genomic analysis of the eukaryotic protein kinase superfamily: a perspective". Genome Biology. 4 (5): 111. doi:10.1186/gb-2003-4-5-111. PMC 156577. PMID 12734000. <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC156577" target="_blank">https://www.ncbi.nlm.nih.gov/pmc/articles/PMC156577</a> <a href="#fnref:7" class="footnote-back-ref">↩</a></p></li>
<li id="fn:8"><p>Taylor SS, Yang J, Wu J, Haste NM, Radzio-Andzelm E, Anand G (March 2004). "PKA: a portrait of protein kinase dynamics". Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics. 1697 (1–2): 259–69. doi:10.1016/j.bbapap.2003.11.029. PMID 15023366. <a href="/wiki/Doi_(identifier)" target="_blank">/wiki/Doi_(identifier)</a> <a href="#fnref:8" class="footnote-back-ref">↩</a></p></li>
<li id="fn:9"><p>Hudmon A, Schulman H (2002-06-01). "Neuronal CA2+/calmodulin-dependent protein kinase II: the role of structure and autoregulation in cellular function". Annual Review of Biochemistry. 71 (1): 473–510. doi:10.1146/annurev.biochem.71.110601.135410. PMID 12045104. <a href="/wiki/Doi_(identifier)" target="_blank">/wiki/Doi_(identifier)</a> <a href="#fnref:9" class="footnote-back-ref">↩</a></p></li>
<li id="fn:10"><p>Swulius MT, Waxham MN (September 2008). "Ca(2+)/calmodulin-dependent protein kinases". Cellular and Molecular Life Sciences. 65 (17): 2637–57. doi:10.1007/s00018-008-8086-2. PMC 3617042. PMID 18463790. <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3617042" target="_blank">https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3617042</a> <a href="#fnref:10" class="footnote-back-ref">↩</a></p></li>
<li id="fn:11"><p>"CAMK2A calcium/calmodulin dependent protein kinase II alpha [Homo sapiens (human)] - Gene - NCBI". www.ncbi.nlm.nih.gov. Retrieved 2020-03-20. <a href="https://www.ncbi.nlm.nih.gov/gene?Db=gene&Cmd=ShowDetailView&TermToSearch=815" target="_blank">https://www.ncbi.nlm.nih.gov/gene?Db=gene&Cmd=ShowDetailView&TermToSearch=815</a> <a href="#fnref:11" class="footnote-back-ref">↩</a></p></li>
</ol>

CAMK open-in-new

CAMK