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Ca2+/calmodulin-dependent protein kinase II

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postsynaptic density (PSD). However, if the stimulation does not induce LTP, the translocation is quickly reversible. Binding to the PSD changes CaMKII so that it is less likely to become dephosphorylated. CaMKII transforms from a substrate for Protein Phosphatase 2A (PP2A), which is responsible for dephosphorylating CaMKII, to that of Protein Phosphatase 1. Strack, S. (1997) demonstrated this phenomenon by chemically stimulating hippocampal slices. This experiment illustrates that CaMKII contributes to the enhancement of synaptic strength. Sanhueza et al. found that persistent activation of CaMKII is necessary for the maintenance of LTP. She induced LTP in hippocampal slices and experimentally applied an antagonist (CaMKIINtide) to prevent CaMKII from remaining active. The slices that were applied with CaMKIINtide showed a decrease in Normalized EPSP slope after the drug infusion, meaning that the induced LTP reversed itself. The Normalized EPSP slope remained constant in the control; CaMKII continues to be involved in the LTP maintenance process even after LTP establishment. CaMKII is activated by calcium/calmodulin, but it is maintained by autophosphorylation. CaMKII is activated by the NMDA-receptor-mediated Calcium elevation that occurs during LTP induction. Activation is accompanied by phosphorylation of both the alpha and beta-subunits and Thr286/287.
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occur because there is not enough calcium or calmodulin present to bind to neighboring subunits. As greater amounts of calcium and calmodulin accumulate, autophosphorylation occurs leading to persistent activation of the CaMKII enzyme for a short period of time. However, the Threonine 286 residue eventually becomes dephosphorylated, leading to inactivation of CaMKII.
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In 1998, Giese and colleagues studied knockout mice that have been genetically engineered to prevent CaMKII autophosphorylation. They observed that mice had trouble finding the hidden platform in the Morris water maze task. The Morris water maze task is often used to represent hippocampus-dependent
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Mechanistically, CaMKII phosphorylates AMPA receptors at the P2 serine 831 site. This increases channel conductance of GluA1 subunits of AMPA receptors, which allows AMPA receptors to be more sensitive than normal during LTP. Increased AMPA receptor sensitivity leads to increased synaptic strength.
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of this site will permanently activate the CaMKII enzyme. Once the Threonine 286 residue has been phosphorylated, the inhibitory domain is blocked from the pseudosubstrate site. This effectively blocks autoinhibition, allowing for permanent activation of the CaMKII enzyme. This enables CamKII to be
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CaMK2B has an autophosphorylation site at Thr287. It functions as a targeting or docking module. Reverse transcription-polymerase chain reaction and sequencing analysis identified at least five alternative splicing variants of beta CaMKII (beta, beta6, betae, beta'e, and beta7) in brain and two of
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When alpha-CaMKII is knocked out in mice, LTP is reduced by 50%. This can be explained by the fact that beta-CaMKII is responsible for approximately 65% of CaMKII activity. LTP can be completely blocked if CaMKII is modified so that it cannot remain active. After LTP induction, CaMKII moves to the
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are in a local environment with a voltage potential high enough to displace the positively-charged Mg ion from the channel pore. As a result of the channel being unblocked, Ca ions are able to enter into the postsynaptic neuron through the NMDA receptor channel. This Ca influx activates CaMKII. It
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delivery allows the mice's genetic material to be modified at specific stages of development. It is possible with viral vector delivery to inject a specific gene of choice into a particular region of the brain in an already developed animal. This, in fact, has been done by Tonegawa group in early
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Mayford and colleagues engineered transgenic mice that express CaMKII with a point mutation of Thr-286 to aspartate, which mimics autophosphorylation and increases kinase activity. These mice failed to show LTP response to weak stimuli, and failed to perform hippocampus-dependent spatial learning
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The sensitivity of the CaMKII enzyme to calcium and calmodulin is governed by the variable and self-associative domains. This sensitivity level of CaMKII will also modulate the different states of activation for the enzyme. Initially, the enzyme is activated; however, autophosphorylation does not
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CaMKIIA is one of the major forms of CamKII. It has been found to play a critical role in sustaining activation of CamKII at the postsynaptic density. Studies have found that knockout mice without CaMKIIA demonstrate a low frequency of LTP. Additionally, these mice do not form persistent, stable
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The catalytic domain has several binding sites for ATP and other substrate anchor proteins. It is responsible for the transfer of phosphate from ATP to Ser or Thr residues in substrates. The autoinhibitory domain features a pseudosubstrate site, which binds to the catalytic domain and blocks its
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In addition to increasing the channel conductance of GluA1 subunits, CaMKII has also been shown to aid in the process of AMPA receptor exocytosis. Reserve AMPA receptors are embedded in endosomes within the cell. CaMKII can stimulate the endosomes to move to the outer membrane and activate the
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is the process in which a kinase attaches a phosphate group to itself. When CaMKII autophosphorylates, it becomes persistently active. Phosphorylation of the Threonine 286 site allows for the activation of the catalytic domain. Autophosphorylation is enhanced by the structure of the holoenzyme
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Along with helping to establish LTP, CaMKII has been shown to be crucial in maintaining LTP. Its ability to autophosphorylate is thought to play an important role in this maintenance. Administration of certain CaMKII blockers has been shown not only to block LTP but also to reverse it in a
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LTP can be induced by artificially injecting CaMKII. When CaMKII is infused in postsynaptically in the hippocampal slices and intracellular perfusion or viral expression, there is a two- to threefold increase in the response of the synapse to glutamate and other chemical signals.
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In 2004, Rodrigues and colleagues found that fear conditioning increased phosphorylated CaMKII in lateral amygdala synapses and dendritic spines, indicating that fear conditioning could be responsible for regulating and activating the kinase. They also discovered a drug,
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because it is present in two stacked rings. The close proximity of these adjacent rings increases the probability of phosphorylation of neighboring CaMKII enzymes, furthering autophosphorylation. A mechanism that promotes autophosphorylation features inhibition of the
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learning of fear conditioning. However, after repeated trials, the impaired mice exhibited similar fear memory formation as the control mice. CaMKII may play a role in rapid fear memory, but does not completely prevent fear memory in the long run.
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CaMK2D appears in both neuronal and non-neuronal cell types. It is characterized particularly in many tumor cells, such as a variety of pancreatic, leukemic, breast and other tumor cells. found that CaMK2D is downregulated in human tumor cells.
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embedded AMPA receptors. Exocytosis of endosomes enlarges and increases the number of AMPA receptors in the synapse. The greater number of AMPA receptors increases the sensitivity of the synapse to presynaptic depolarization, and generates LTP.
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Yang, H.-W.; Hu, XD; Zhang, HM; Xin, WJ; Li, MT; Zhang, T; Zhou, LJ; Liu, XG (2003). "Roles of CaMKII, PKA, and PKC in the Induction and Maintenance of LTP of C-Fiber-Evoked Field Potentials in Rat Spinal Dorsal Horn".
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1990s and by Poulsen and colleagues in 2007. Both groups used this method to inject CaMKII into the hippocampus. They found that overexpression of CaMKII resulted in slight enhancement of acquisition of new memories.
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As LTP is thought to underlie the processes of learning and memory, CaMKII is also crucial to memory formation. Behavioral studies involving genetically engineered mice have demonstrated the importance of CaMKII.
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receptors into the membrane and then the PSD of the dendrite. Movement of AMPA receptors increases postsynaptic response to presynaptic depolarization through strengthening the synapses. This produces LTP.
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Bennett, M.K., Erondu, N.E., and Kennedy, M.B. (1983). Purification and characterization of a calmodulin-dependent protein kinase that is highly concentrated in brain. J Biol Chem 258, 12735-12744.
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Poulsen, D.J.; Standing, D.; Bullshields, K.; Spencer, K.; Micevych, P.E.; Babcock, A.M. (2007). "Overexpression of hippocampal Ca/calmodulin-dependent protein kinase II improves spatial memory".
411:(LTP) – the molecular process of strengthening active synapses that is thought to underlie the processes of memory. It is involved in many aspects of this process. LTP is initiated when the 1382:"Hippocampal synaptic plasticity involves competition between Ca/calmodulin-dependent protein kinase II and postsynaptic density 95 for binding to the NR2A subunit of the NMDA receptor" 2415: 2335:"Targeting of a Novel Ca+2/Calmodulin-Dependent Protein Kinase II Is Essential for Extracellular Signal-Regulated Kinase-Mediated Signaling in Differentiated Smooth Muscle Cells" 1973:
Frankland, Paul W.; O'Brien, Cara; Ohno, Masuo; Kirkwood, Alfredo; Silva, Alcino J. (2001). "Alpha-CaMKII-dependent plasticity in the cortex is required for permanent memory".
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However, these results were not entirely conclusive because memory formation deficit could also be associated with sensory motor impairment resulting from genetic alteration.
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The structure of the association domain of CaMKII gamma rendered by pymol from PDB 2ux0 (left) space fill holoenzyme (center) cartoon holoemzyme (right) cartoon monome
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Giese, K. P.; Fedorov, NB; Filipkowski, RK; Silva, AJ (1998). "Autophosphorylation at Thr286 of the  Calcium-Calmodulin Kinase II in LTP and Learning".
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Hudmon, Andy; Schulman, Howard (2002). "Neuronal Ca/Calmodulin-Dependent Protein Kinase II: The Role of Structure and Autoregulation in Cellular Function".
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Collingridge, Graham L.; Benke, Tim A.; Lüthi, Andreas; Isaac, John T. R. (1998). "Modulation of AMPA receptor unitary conductance by synaptic activity".
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Erondu, N.E., and Kennedy, M.B. (1985). Regional distribution of type II Ca2+/calmodulin-dependent protein kinase in rat brain. J Neurosci 5, 3270-3277.
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Davies, SN; Lester, RA; Reymann, KG; Collingridge, GL (1989). "Temporally distinct pre- and post-synaptic mechanisms maintain long-term potentiation".
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Silva, A.; Stevens, C.; Tonegawa, S; Wang, Y (1992). "Deficient hippocampal long-term potentiation in alpha-calcium-calmodulin kinase II mutant mice".
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The other two domains in CaMKII are the variable and self-association domains. Differences in these domains contribute to the various CaMKII isoforms.
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Molecular Neurobiology: Mechanisms Common to Brain, Skin and Immune System. Series: Progress in Clinical and Biological Research. Willey-Liss, Inc
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Anderson, M (2005). "Calmodulin kinase signaling in heart: an intriguing candidate target for therapy of myocardial dysfunction and arrhythmias".
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Irvine, Elaine E.; Von Hertzen, Laura S. J.; Plattner, Florian; Giese, Karl Peter (2006). "αCaMKII autophosphorylation: a fast track to memory".
3786: 2655: 2286:"Identification of alternative splicing variants of the β subunit of human Ca/calmodulin-dependent protein kinase II with different activities" 2237:"Identification of alternative splicing variants of the β subunit of human Ca/calmodulin-dependent protein kinase II with different activities" 3850: 2825: 1865: 1926:"Pavlovian Fear Conditioning Regulates Thr286 Autophosphorylation of Ca/Calmodulin-Dependent Protein Kinase II at Lateral Amygdala Synapses" 881:/calmodulin-dependent protein kinase II—discovery, progress in a quarter of a century, and perspective: implication for learning and memory" 4106: 2640: 821:"A pivotal role for the multifunctional calcium/calmodulin-dependent protein kinase II in T cells: from activation to unresponsiveness" 4163: 3838: 724:
Fährmann, Michael; Kaufhold, Marc-André (2006). "Functional partitioning of epithelial protein kinase CaMKII in signal transduction".
4278: 3095: 3085: 2770: 3777: 2075:"Mice Expressing Activated CaMKII Lack Low Frequency LTP and Do Not Form Stable Place Cells in the CA1 Region of the Hippocampus" 4046: 3718: 3080: 3071: 4434: 1151:"Regulation of brain type II Ca/calmodulin-dependent protein kinase by autophosphorylation: a Ca-triggered molecular switch" 152: 3461: 2958: 2949: 2606: 2552: 4549: 1523:"Bidirectional regulation of protein kinase M zeta in the maintenance of long-term potentiation and long-term depression" 2649: 2385: 1110:
Griffith LC, Lu CS, Sun XX (October 2003). "CaMKII, an enzyme on the move: regulation of temporospatial localization".
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has been shown that there is an increase in CaMKII activity directly in the post synaptic density of dendrites after
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Giese, K. P. (1998). "Autophosphorylation at Thr286 of the  Calcium-Calmodulin Kinase II in LTP and Learning".
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CaMK2G has been shown to be a crucial extracellular signal-regulated kinase in differentiated smooth muscle cells.
4419: 1675:"Pair recordings reveal all-silent synaptic connections and the postsynaptic expression of long-term potentiation" 772:/calmodulin-dependent protein kinase II gamma B impairs positive selection of T cells by modulating TCR signaling" 4535: 4522: 4509: 4496: 4483: 4470: 4457: 3663: 3658: 3653: 3643: 3638: 3633: 3623: 3418: 3193: 2789: 2026:"CaMKII regulates the frequency-response function of hippocampal synapses for the production of both LTD and LTP" 270: 4429: 1333:"Translocation of Autophosphorylated Calcium/Calmodulin-dependent Protein Kinase II to the Postsynaptic Density" 4598: 4383: 4326: 3886: 3877: 3828: 2594: 2439: 2389: 502:
Irvine and colleagues in 2006 showed that preventing autophosphorylation of CaMKII cause mice to have impaired
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The structure of the kinase domain of CaMKII (gamma) rendered by pymol from PDB 2v7O, green sticks = nucleotide
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Researchers speculate these results could be due to lack of stable hippocampal place cells in these animals.
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McGargill, Maureen A.; Sharp, Leslie L.; Bui, Jack D.; Hedrick, Stephen M.; Calbo, Sébastien (July 2005).
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spatial learning. The mice's inability to find the hidden platform implies deficits in spatial learning.
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Lin, Meei Yun; Zal, Tomasz; Ch'en, Irene L.; Gascoigne, Nicholas R. J.; Hedrick, Stephen M. (May 2005).
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Tonegawa S (1994). "Gene targeting: a new approach for the analysis of mammalian memory and learning".
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complex. CaMKII is involved in many signaling cascades and is thought to be an important mediator of
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There is strong evidence that after activation of CaMKII, CaMKII plays a role in the trafficking of
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Rotenberg, Alexander; Mayford, Mark; Hawkins, Robert D; Kandel, Eric R; Muller, Robert U (1996).
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Blitzer, Robert D.; Wong, Tony; Nouranifar, Rabin; Iyengar, Ravi; Landau, Emmanuel M. (1995).
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However, because genetic modifications might cause unintentional developmental changes,
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The structural feature that governs this autoinhibition is the Threonine 286 residue.
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Lisman, J (1994). "The CaM kinase II hypothesis for the storage of synaptic memory".
1168: 702: 417: 412: 2368: 2319: 2270: 2221: 2178: 2108: 2059: 1910: 1759: 1572:"Reversal of synaptic memory by Ca/calmodulin-dependent protein kinase II inhibitor" 1366: 1227: 1061: 854: 805: 315: 68: 4306: 3737: 2562: 2010: 1941: 1806: 1774: 1708: 1656: 1587: 1507: 1276: 539: 115: 1184: 930: 81: 4579: 1306: 1088: 737: 93: 4530: 4465: 4301: 3943: 3575: 3515: 3398: 3318: 3042: 1380:
Gardoni, F; Schrama, LH; Kamal, A; Gispen, WH; Cattabeni, F; Di Luca, M (2001).
837: 820: 515:, that inhibited CaMKII and prevented acquisition of fear conditioning and LTP. 164: 4558: 1894: 788: 760: 352:, an autoinhibitory domain, a variable segment, and a self-association domain. 328: 4031: 2505: 407:
Calcium/ calmodulin dependent protein kinase II is also heavily implicated in
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CaMKII accounts for 1–2% of all proteins in the brain, and has 28 different
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Marganski, W. A.; Gangopadhyay, SS; Je, HD; Gallant, C; Morgan, KG (2005).
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Drug-induced changes in CaMKII function have been implicated in addiction.
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CaMKII gamma holoenzyme in its (A) closed and the (B) open conformations
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Soderling, T (2000). "CaM-kinases: modulators of synaptic plasticity".
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Rodrigues, S. M.; Farb, CR; Bauer, EP; Ledoux, JE; Schafe, GE (2004).
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Mayford, Mark; Wang, Jian; Kandel, Eric R; O'Dell, Thomas J (1995).
340:. The isoforms derive from the alpha, beta, gamma, and delta genes. 1790: 4491: 4133: 4126: 4036: 3933: 3833: 3811: 3806: 3801: 3796: 3791: 3703: 3698: 3693: 3688: 3678: 3648: 3628: 3505: 3500: 3481: 3476: 3466: 3442: 3437: 3432: 3408: 3403: 3393: 3388: 3383: 3373: 3353: 3338: 3333: 3328: 3308: 3303: 3293: 3288: 3283: 3278: 3273: 3263: 3258: 3253: 3248: 3228: 3223: 3218: 3213: 3208: 3203: 3188: 3138: 3133: 3027: 3022: 3017: 3012: 3007: 3002: 2963: 2895: 2890: 2839: 2834: 2760: 2755: 2750: 2716: 2708:
3-methyl-2-oxobutanoate dehydrogenase (acetyl-transferring) kinase
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Calcium/calmodulin dependent protein kinase II association domain
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Crystal structure of calcium/calmodulin-dependent protein kinase
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Biochimica et Biophysica Acta (BBA) - Molecular Cell Research
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them (beta6 and beta7) were first detected in any species.
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Kanaseki, T; Ikeuchi, Y; Sugiura, H; Yamauchi, T (1991).
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The self-association domain (CaMKII AD) is found at the
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Strack, S.; Choi, S; Lovinger, DM; Colbran, RJ (1997).
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active, even in the absence of calcium and calmodulin.
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This article incorporates text from the public domain
4547: 4443: 4407: 4376: 4345: 4294: 4198: 4096: 4079: 4062: 4045: 4016: 3876: 3776: 3717: 3608: 3574: 3514: 3490: 3451: 3417: 3123: 3094: 3070: 3051: 2972: 2948: 2909: 2865: 2848: 2824: 2788: 2769: 2735: 2706: 2639: 2605: 2465: 146: 126: 108: 103: 87: 74: 62: 54: 49: 32: 2284:Wang, P; Wu, YL; Zhou, TH; Sun, Y; Pei, G (2000). 2235:Wang, P; Wu, YL; Zhou, TH; Sun, Y; Pei, G (2000). 1480:Hinds H. L.; Tonegawa, S.; Malinow, R. (1998). 1570:Sanhueza, M; McIntyre, CC; Lisman, JE (2007). 231:, chloride transport in epithelia, positive 4272: 2467:Non-specific serine/threonine protein kinases 2416: 1326: 1324: 1288: 1286: 8: 2386:Calcium-Calmodulin+Dependent+Protein+Kinases 684: 682: 532:that depended on visual or olfactory cues. 4279: 4265: 4257: 4195: 4181: 3571: 3557: 2850:Goodpasture-antigen-binding protein kinase 2462: 2448: 2423: 2409: 2401: 216:and memory. CaMKII is also necessary for 100: 38: 3563:Serine/threonine-specific protein kinases 2737:(isocitrate dehydrogenase (NADP+)) kinase 2454:Serine/threonine-specific protein kinases 2436:Serine/threonine-specific protein kinases 2388:at the U.S. National Library of Medicine 2350: 2301: 2252: 2090: 2041: 1949: 1690: 1595: 1546: 1497: 1413: 1348: 1258: 1043: 1002: 896: 836: 787: 662: 519:Deficit in consolidation of memory traces 4098:Receptor protein serine/threonine kinase 956:10.1146/annurev.biochem.71.110601.135410 885:Biological & Pharmaceutical Bulletin 651:Biological & Pharmaceutical Bulletin 195:serine/threonine-specific protein kinase 4554: 4081:Low-density-lipoprotein receptor kinase 1858:The Neurobiology of Learning and Memory 637: 332:Activation and autoregulation of CaMKII 324:Structure, function, and autoregulation 183:/calmodulin-dependent protein kinase II 348:All of the isoforms of CaMKII have: a 29: 2826:Fas-activated serine/threonine kinase 242:Misregulation of CaMKII is linked to 7: 4107:Bone morphogenetic protein receptors 2641:Dephospho-(reductase kinase) kinase 1673:; Pavlidis, P; Madison, DV (2001). 1032:The Journal of Biological Chemistry 356:ability to phosphorylate proteins. 262:There are two types of CaM kinase: 3096:G-protein coupled receptor kinases 2396:To learn more about the CaMKII ... 2352:10.1161/01.RES.0000182630.29093.0d 1539:10.1523/JNEUROSCI.16-17-05324.1996 1521:Hrabetova, S; Sacktor, TC (1996). 1398:10.1523/JNEUROSCI.21-05-01501.2001 25: 3086:Beta adrenergic receptor kinase-2 2771:(tyrosine 3-monooxygenase) kinase 868:Yamauchi, Takashi (August 2005). 378:Calcium and calmodulin dependence 4557: 3778:Mitogen-activated protein kinase 2151:Journal of Neuroscience Research 1773:Lisman, John; Schulman, Howard; 703:10.1016/j.pharmthera.2004.11.002 565:place cells in the hippocampus. 4164:Anti-Müllerian hormone receptor 4047:(acetyl-CoA carboxylase) kinase 3719:(RNA-polymerase)-subunit kinase 3081:Beta adrenergic receptor kinase 3072:Beta adrenergic receptor kinase 2194:Current Opinion in Neurobiology 1337:Journal of Biological Chemistry 691:Pharmacology & Therapeutics 3787:Extracellular signal-regulated 1942:10.1523/JNEUROSCI.5303-03.2004 1588:10.1523/JNEUROSCI.5049-06.2007 481:Preventing autophosphorylation 1: 3851:P38 mitogen-activated protein 2950:cGMP-dependent protein kinase 2911:cAMP-dependent protein kinase 2607:Pyruvate dehydrogenase kinase 2553:Ataxia telangiectasia mutated 2303:10.1016/S0014-5793(00)01634-3 2254:10.1016/S0014-5793(00)01634-3 2206:10.1016/S0959-4388(00)00090-8 2092:10.1016/S0092-8674(00)81829-2 1692:10.1016/S0896-6273(01)00244-6 1026:Yang, E; Schulman, H (1999). 944:Annual Review of Biochemistry 104:Available protein structures: 2650:AMP-activated protein kinase 2043:10.1016/0092-8674(95)90009-8 1307:10.1126/science.279.5352.870 1260:10.1016/0896-6273(95)90018-7 1212:10.1016/0166-2236(94)90014-0 1169:10.1016/0092-8674(86)90008-5 1089:10.1126/science.279.5352.870 738:10.1016/j.bbamcr.2005.11.012 433:Independent induction of LTP 227:homeostasis and reuptake in 3565:(EC 2.7.11.21-EC 2.7.11.30) 1779:Nature Reviews Neuroscience 1576:The Journal of Neuroscience 1527:The Journal of Neuroscience 1386:The Journal of Neuroscience 983:The Journal of Cell Biology 838:10.4049/jimmunol.174.9.5583 486:Deficit in spatial learning 397:PP1 (protein phosphatase I) 287:, also collectively called 285:Multifunctional CaM kinases 4615: 4569: 3492:Elongation factor 2 kinase 2456:(EC 2.7.11.1-EC 2.7.11.20) 1895:10.1016/j.tins.2006.06.009 1823:Journal of Neurophysiology 789:10.4049/jimmunol.175.2.656 645:Yamauchi, Takashi (2005). 4435:Michaelis–Menten kinetics 4194: 4180: 3887:MAP kinase kinase kinases 3570: 3556: 3419:Myosin light-chain kinase 3125:Ca2+/calmodulin-dependent 2790:Myosin-heavy-chain kinase 2461: 2447: 825:The Journal of Immunology 776:The Journal of Immunology 271:myosin light chain kinase 197:that is regulated by the 99: 37: 4327:Diffusion-limited enzyme 4187:Dual-specificity kinases 2390:Medical Subject Headings 1350:10.1074/jbc.272.21.13467 1045:10.1074/jbc.274.37.26199 498:Deficit in fear memories 3610:Cyclin-dependent kinase 1930:Journal of Neuroscience 1883:Trends in Neurosciences 1856:Rudy, Jerry W. (2004). 1459:10.1126/science.1378648 1200:Trends in Neurosciences 468:time-dependent manner. 442:Mechanistic role in LTP 291:, which play a role in 267:Specialized CaM kinases 995:10.1083/jcb.115.4.1049 409:long-term potentiation 403:Long-term potentiation 333: 320: 312: 169: 4420:Eadie–Hofstee diagram 4353:Allosteric regulation 1835:10.1152/jn.00735.2003 1486:Learning & Memory 331: 318: 310: 167: 4430:Lineweaver–Burk plot 3453:Phosphorylase kinase 2339:Circulation Research 297:transcription factor 273:that phosphorylates 1987:2001Natur.411..309F 1736:1998Natur.393..793B 1633:1989Natur.338..500D 1451:1992Sci...257..201S 1083:(5352): 26199–208. 898:10.1248/bpb.28.1342 664:10.1248/bpb.28.1342 392:Autophosphorylation 387:Autophosphorylation 244:Alzheimer's disease 4389:Enzyme superfamily 4322:Enzyme promiscuity 4064:Tropomyosin kinase 4018:Tau-protein kinase 1499:10.1101/lm.5.4.344 1124:10.1124/mi.3.7.386 463:Maintenance of LTP 334: 321: 313: 170: 4545: 4544: 4254: 4253: 4250: 4249: 4246: 4245: 4176: 4175: 4172: 4171: 3552: 3551: 3548: 3547: 3033:Protein kinase N1 2988:Protein kinase Cζ 2163:10.1002/jnr.21163 1867:978-0-87893-669-4 1038:(37): 26199–208. 472:Behavioral memory 344:Structural domain 277:, causing smooth 248:Angelman syndrome 162: 161: 158: 157: 153:structure summary 16:(Redirected from 4606: 4562: 4561: 4553: 4425:Hanes–Woolf plot 4368:Enzyme activator 4363:Enzyme inhibitor 4337:Enzyme catalysis 4281: 4274: 4267: 4258: 4196: 4182: 3829:C-Jun N-terminal 3572: 3558: 3062:Rhodopsin kinase 3053:Rhodopsin kinase 2983:Protein kinase C 2974:Protein kinase C 2959:Protein kinase G 2920:Protein kinase A 2531:Protein kinase B 2463: 2449: 2425: 2418: 2411: 2402: 2373: 2372: 2354: 2330: 2324: 2323: 2305: 2281: 2275: 2274: 2256: 2232: 2226: 2225: 2189: 2183: 2182: 2146: 2140: 2139: 2119: 2113: 2112: 2094: 2070: 2064: 2063: 2045: 2021: 2015: 2014: 1995:10.1038/35077089 1981:(6835): 309–13. 1970: 1964: 1963: 1953: 1921: 1915: 1914: 1878: 1872: 1871: 1853: 1847: 1846: 1817: 1811: 1810: 1770: 1764: 1763: 1719: 1713: 1712: 1694: 1667: 1661: 1660: 1641:10.1038/338500a0 1616: 1610: 1609: 1599: 1567: 1561: 1560: 1550: 1518: 1512: 1511: 1501: 1477: 1471: 1470: 1434: 1428: 1427: 1417: 1377: 1371: 1370: 1352: 1343:(21): 13467–70. 1328: 1319: 1318: 1290: 1281: 1280: 1262: 1238: 1232: 1231: 1195: 1189: 1188: 1142: 1136: 1135: 1107: 1101: 1100: 1072: 1066: 1065: 1047: 1023: 1017: 1016: 1006: 974: 968: 967: 939: 933: 928: 922: 917: 911: 910: 900: 880: 879: 878: 865: 859: 858: 840: 816: 810: 809: 791: 771: 770: 769: 756: 750: 749: 721: 715: 714: 686: 677: 676: 666: 642: 350:catalytic domain 299:regulation, and 293:neurotransmitter 252:heart arrhythmia 235:selection, and 226: 225: 224: 207: 206: 205: 182: 181: 180: 101: 42: 30: 27:Class of enzymes 21: 4614: 4613: 4609: 4608: 4607: 4605: 4604: 4603: 4599:Protein kinases 4584: 4583: 4582: 4568: 4556: 4548: 4546: 4541: 4453:Oxidoreductases 4439: 4415:Enzyme kinetics 4403: 4399:List of enzymes 4372: 4341: 4312:Catalytic triad 4290: 4285: 4255: 4242: 4190: 4168: 4092: 4075: 4058: 4041: 4012: 3872: 3772: 3743:P70-S6 Kinase 1 3713: 3604: 3566: 3544: 3510: 3486: 3447: 3413: 3119: 3090: 3066: 3047: 2968: 2944: 2905: 2861: 2844: 2820: 2814:Aurora C kinase 2809:Aurora B kinase 2804:Aurora A kinase 2784: 2765: 2731: 2702: 2635: 2601: 2457: 2443: 2429: 2382: 2377: 2376: 2332: 2331: 2327: 2283: 2282: 2278: 2234: 2233: 2229: 2191: 2190: 2186: 2148: 2147: 2143: 2121: 2120: 2116: 2072: 2071: 2067: 2023: 2022: 2018: 1972: 1971: 1967: 1923: 1922: 1918: 1880: 1879: 1875: 1868: 1855: 1854: 1850: 1819: 1818: 1814: 1772: 1771: 1767: 1730:(6687): 793–7. 1721: 1720: 1716: 1669: 1668: 1664: 1627:(6215): 500–3. 1618: 1617: 1613: 1569: 1568: 1564: 1533:(17): 5324–33. 1520: 1519: 1515: 1479: 1478: 1474: 1445:(5067): 201–6. 1436: 1435: 1431: 1379: 1378: 1374: 1330: 1329: 1322: 1301:(5352): 870–3. 1292: 1291: 1284: 1240: 1239: 1235: 1197: 1196: 1192: 1144: 1143: 1139: 1109: 1108: 1104: 1074: 1073: 1069: 1025: 1024: 1020: 976: 975: 971: 941: 940: 936: 929: 925: 918: 914: 877: 875: 874: 873: 871: 867: 866: 862: 818: 817: 813: 768: 766: 765: 764: 762: 758: 757: 753: 723: 722: 718: 688: 687: 680: 644: 643: 639: 634: 622: 597: 589: 580: 571: 562: 557: 555:Different forms 549: 529: 521: 500: 488: 483: 474: 465: 444: 435: 426: 405: 389: 380: 361:Phosphorylation 346: 326: 260: 223: 221: 220: 219: 217: 204: 202: 201: 200: 198: 179: 177: 176: 175: 173: 45: 28: 23: 22: 15: 12: 11: 5: 4612: 4610: 4602: 4601: 4596: 4586: 4585: 4567: 4566: 4543: 4542: 4540: 4539: 4526: 4513: 4500: 4487: 4474: 4461: 4447: 4445: 4441: 4440: 4438: 4437: 4432: 4427: 4422: 4417: 4411: 4409: 4405: 4404: 4402: 4401: 4396: 4391: 4386: 4380: 4378: 4377:Classification 4374: 4373: 4371: 4370: 4365: 4360: 4355: 4349: 4347: 4343: 4342: 4340: 4339: 4334: 4329: 4324: 4319: 4314: 4309: 4304: 4298: 4296: 4292: 4291: 4286: 4284: 4283: 4276: 4269: 4261: 4252: 4251: 4248: 4247: 4244: 4243: 4241: 4240: 4235: 4230: 4225: 4220: 4215: 4210: 4204: 4202: 4192: 4191: 4185: 4178: 4177: 4174: 4173: 4170: 4169: 4167: 4166: 4161: 4156: 4151: 4146: 4141: 4136: 4131: 4130: 4129: 4124: 4119: 4114: 4103: 4101: 4100:(EC 2.7.11.30) 4094: 4093: 4091: 4090: 4086: 4084: 4083:(EC 2.7.11.29) 4077: 4076: 4074: 4073: 4069: 4067: 4066:(EC 2.7.11.28) 4060: 4059: 4057: 4056: 4052: 4050: 4049:(EC 2.7.11.27) 4043: 4042: 4040: 4039: 4034: 4029: 4023: 4021: 4020:(EC 2.7.11.26) 4014: 4013: 4011: 4010: 4005: 4000: 3999: 3998: 3993: 3988: 3983: 3978: 3973: 3968: 3958: 3957: 3956: 3951: 3946: 3941: 3931: 3930: 3929: 3924: 3919: 3914: 3909: 3904: 3899: 3894: 3883: 3881: 3880:(EC 2.7.11.25) 3874: 3873: 3871: 3870: 3869: 3868: 3863: 3858: 3848: 3847: 3846: 3841: 3836: 3826: 3825: 3824: 3819: 3814: 3809: 3804: 3799: 3794: 3783: 3781: 3780:(EC 2.7.11.24) 3774: 3773: 3771: 3770: 3765: 3760: 3755: 3750: 3745: 3740: 3735: 3730: 3724: 3722: 3721:(EC 2.7.11.23) 3715: 3714: 3712: 3711: 3706: 3701: 3696: 3691: 3686: 3681: 3676: 3671: 3666: 3661: 3656: 3651: 3646: 3641: 3636: 3631: 3626: 3621: 3615: 3613: 3612:(EC 2.7.11.22) 3606: 3605: 3603: 3602: 3597: 3592: 3587: 3581: 3579: 3578:(EC 2.7.11.21) 3568: 3567: 3561: 3554: 3553: 3550: 3549: 3546: 3545: 3543: 3542: 3537: 3532: 3527: 3521: 3519: 3518:(EC 2.7.11.21) 3512: 3511: 3509: 3508: 3503: 3497: 3495: 3494:(EC 2.7.11.20) 3488: 3487: 3485: 3484: 3479: 3474: 3469: 3464: 3458: 3456: 3455:(EC 2.7.11.19) 3449: 3448: 3446: 3445: 3440: 3435: 3430: 3424: 3422: 3421:(EC 2.7.11.18) 3415: 3414: 3412: 3411: 3406: 3401: 3396: 3391: 3386: 3381: 3376: 3371: 3366: 3361: 3356: 3351: 3346: 3341: 3336: 3331: 3326: 3321: 3316: 3311: 3306: 3301: 3296: 3291: 3286: 3281: 3276: 3271: 3266: 3261: 3256: 3251: 3246: 3241: 3236: 3231: 3226: 3221: 3216: 3211: 3206: 3201: 3196: 3191: 3186: 3181: 3176: 3171: 3166: 3161: 3156: 3151: 3146: 3141: 3136: 3130: 3128: 3127:(EC 2.7.11.17) 3121: 3120: 3118: 3117: 3112: 3107: 3101: 3099: 3098:(EC 2.7.11.16) 3092: 3091: 3089: 3088: 3083: 3077: 3075: 3074:(EC 2.7.11.15) 3068: 3067: 3065: 3064: 3058: 3056: 3055:(EC 2.7.11.14) 3049: 3048: 3046: 3045: 3040: 3035: 3030: 3025: 3020: 3015: 3010: 3005: 3000: 2995: 2990: 2985: 2979: 2977: 2976:(EC 2.7.11.13) 2970: 2969: 2967: 2966: 2961: 2955: 2953: 2952:(EC 2.7.11.12) 2946: 2945: 2943: 2942: 2937: 2932: 2927: 2922: 2916: 2914: 2913:(EC 2.7.11.11) 2907: 2906: 2904: 2903: 2898: 2893: 2888: 2883: 2878: 2872: 2870: 2869:(EC 2.7.11.10) 2863: 2862: 2860: 2859: 2855: 2853: 2846: 2845: 2843: 2842: 2837: 2831: 2829: 2822: 2821: 2819: 2818: 2817: 2816: 2811: 2806: 2795: 2793: 2786: 2785: 2783: 2782: 2776: 2774: 2767: 2766: 2764: 2763: 2758: 2753: 2748: 2742: 2740: 2733: 2732: 2730: 2729: 2724: 2719: 2713: 2711: 2704: 2703: 2701: 2700: 2699: 2698: 2693: 2688: 2680: 2679: 2678: 2673: 2665: 2664: 2663: 2658: 2646: 2644: 2637: 2636: 2634: 2633: 2628: 2623: 2618: 2612: 2610: 2603: 2602: 2600: 2599: 2598: 2597: 2587: 2586: 2585: 2580: 2575: 2570: 2560: 2555: 2550: 2549: 2548: 2543: 2538: 2528: 2523: 2518: 2513: 2508: 2503: 2498: 2493: 2488: 2483: 2478: 2472: 2470: 2459: 2458: 2452: 2445: 2444: 2430: 2428: 2427: 2420: 2413: 2405: 2399: 2398: 2393: 2381: 2380:External links 2378: 2375: 2374: 2345:(6): 541–549. 2325: 2276: 2227: 2184: 2141: 2114: 2085:(7): 1351–61. 2065: 2036:(6): 891–904. 2016: 1965: 1936:(13): 3281–8. 1916: 1873: 1866: 1848: 1829:(3): 1122–33. 1812: 1791:10.1038/nrn753 1765: 1714: 1685:(3): 691–701. 1671:Montgomery, JM 1662: 1611: 1582:(19): 5190–9. 1562: 1513: 1492:(4): 344–354. 1472: 1429: 1372: 1320: 1282: 1253:(6): 1403–14. 1233: 1206:(10): 406–12. 1190: 1163:(6): 861–870. 1145:Miller, S.G.; 1137: 1118:(7): 386–403. 1102: 1067: 1018: 989:(4): 1049–60. 969: 934: 923: 912: 891:(8): 1342–54. 876: 860: 831:(9): 5583–92. 811: 767: 751: 716: 678: 657:(8): 1342–54. 636: 635: 633: 630: 629: 628: 621: 618: 617: 616: 596: 593: 588: 585: 579: 576: 570: 567: 561: 558: 556: 553: 548: 545: 528: 527:Overexpression 525: 520: 517: 499: 496: 487: 484: 482: 479: 473: 470: 464: 461: 443: 440: 434: 431: 425: 422: 413:NMDA receptors 404: 401: 388: 385: 379: 376: 345: 342: 325: 322: 305: 304: 282: 269:, such as the 259: 256: 229:cardiomyocytes 222: 203: 178: 160: 159: 156: 155: 150: 144: 143: 130: 124: 123: 113: 106: 105: 97: 96: 91: 85: 84: 79: 72: 71: 66: 60: 59: 56: 52: 51: 47: 46: 43: 35: 34: 26: 24: 14: 13: 10: 9: 6: 4: 3: 2: 4611: 4600: 4597: 4595: 4592: 4591: 4589: 4581: 4577: 4573: 4565: 4560: 4555: 4551: 4537: 4533: 4532: 4527: 4524: 4520: 4519: 4514: 4511: 4507: 4506: 4501: 4498: 4494: 4493: 4488: 4485: 4481: 4480: 4475: 4472: 4468: 4467: 4462: 4459: 4455: 4454: 4449: 4448: 4446: 4442: 4436: 4433: 4431: 4428: 4426: 4423: 4421: 4418: 4416: 4413: 4412: 4410: 4406: 4400: 4397: 4395: 4394:Enzyme family 4392: 4390: 4387: 4385: 4382: 4381: 4379: 4375: 4369: 4366: 4364: 4361: 4359: 4358:Cooperativity 4356: 4354: 4351: 4350: 4348: 4344: 4338: 4335: 4333: 4330: 4328: 4325: 4323: 4320: 4318: 4317:Oxyanion hole 4315: 4313: 4310: 4308: 4305: 4303: 4300: 4299: 4297: 4293: 4289: 4282: 4277: 4275: 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3793: 3790: 3789: 3788: 3785: 3784: 3782: 3779: 3775: 3769: 3766: 3764: 3761: 3759: 3756: 3754: 3751: 3749: 3746: 3744: 3741: 3739: 3736: 3734: 3731: 3729: 3726: 3725: 3723: 3720: 3716: 3710: 3707: 3705: 3702: 3700: 3697: 3695: 3692: 3690: 3687: 3685: 3682: 3680: 3677: 3675: 3672: 3670: 3667: 3665: 3662: 3660: 3657: 3655: 3652: 3650: 3647: 3645: 3642: 3640: 3637: 3635: 3632: 3630: 3627: 3625: 3622: 3620: 3617: 3616: 3614: 3611: 3607: 3601: 3598: 3596: 3593: 3591: 3588: 3586: 3583: 3582: 3580: 3577: 3573: 3569: 3564: 3559: 3555: 3541: 3538: 3536: 3533: 3531: 3528: 3526: 3523: 3522: 3520: 3517: 3513: 3507: 3504: 3502: 3499: 3498: 3496: 3493: 3489: 3483: 3480: 3478: 3475: 3473: 3470: 3468: 3465: 3463: 3460: 3459: 3457: 3454: 3450: 3444: 3441: 3439: 3436: 3434: 3431: 3429: 3426: 3425: 3423: 3420: 3416: 3410: 3407: 3405: 3402: 3400: 3397: 3395: 3392: 3390: 3387: 3385: 3382: 3380: 3377: 3375: 3372: 3370: 3367: 3365: 3362: 3360: 3357: 3355: 3352: 3350: 3347: 3345: 3342: 3340: 3337: 3335: 3332: 3330: 3327: 3325: 3322: 3320: 3317: 3315: 3312: 3310: 3307: 3305: 3302: 3300: 3297: 3295: 3292: 3290: 3287: 3285: 3282: 3280: 3277: 3275: 3272: 3270: 3267: 3265: 3262: 3260: 3257: 3255: 3252: 3250: 3247: 3245: 3242: 3240: 3237: 3235: 3232: 3230: 3227: 3225: 3222: 3220: 3217: 3215: 3212: 3210: 3207: 3205: 3202: 3200: 3197: 3195: 3192: 3190: 3187: 3185: 3182: 3180: 3177: 3175: 3172: 3170: 3167: 3165: 3162: 3160: 3157: 3155: 3152: 3150: 3147: 3145: 3142: 3140: 3137: 3135: 3132: 3131: 3129: 3126: 3122: 3116: 3113: 3111: 3108: 3106: 3103: 3102: 3100: 3097: 3093: 3087: 3084: 3082: 3079: 3078: 3076: 3073: 3069: 3063: 3060: 3059: 3057: 3054: 3050: 3044: 3041: 3039: 3036: 3034: 3031: 3029: 3026: 3024: 3021: 3019: 3016: 3014: 3011: 3009: 3006: 3004: 3001: 2999: 2996: 2994: 2991: 2989: 2986: 2984: 2981: 2980: 2978: 2975: 2971: 2965: 2962: 2960: 2957: 2956: 2954: 2951: 2947: 2941: 2938: 2936: 2933: 2931: 2928: 2926: 2923: 2921: 2918: 2917: 2915: 2912: 2908: 2902: 2899: 2897: 2894: 2892: 2889: 2887: 2884: 2882: 2879: 2877: 2874: 2873: 2871: 2868: 2864: 2857: 2856: 2854: 2852:(EC 2.7.11.9) 2851: 2847: 2841: 2838: 2836: 2833: 2832: 2830: 2828:(EC 2.7.11.8) 2827: 2823: 2815: 2812: 2810: 2807: 2805: 2802: 2801: 2800: 2799:Aurora kinase 2797: 2796: 2794: 2792:(EC 2.7.11.7) 2791: 2787: 2781: 2778: 2777: 2775: 2773:(EC 2.7.11.6) 2772: 2768: 2762: 2759: 2757: 2754: 2752: 2749: 2747: 2744: 2743: 2741: 2739:(EC 2.7.11.5) 2738: 2734: 2728: 2725: 2723: 2720: 2718: 2715: 2714: 2712: 2710:(EC 2.7.11.4) 2709: 2705: 2697: 2694: 2692: 2689: 2687: 2684: 2683: 2681: 2677: 2674: 2672: 2669: 2668: 2666: 2662: 2659: 2657: 2654: 2653: 2651: 2648: 2647: 2645: 2643:(EC 2.7.11.3) 2642: 2638: 2632: 2629: 2627: 2624: 2622: 2619: 2617: 2614: 2613: 2611: 2609:(EC 2.7.11.2) 2608: 2604: 2596: 2593: 2592: 2591: 2588: 2584: 2581: 2579: 2576: 2574: 2571: 2569: 2566: 2565: 2564: 2563:EIF-2 kinases 2561: 2559: 2556: 2554: 2551: 2547: 2544: 2542: 2539: 2537: 2534: 2533: 2532: 2529: 2527: 2524: 2522: 2519: 2517: 2514: 2512: 2509: 2507: 2504: 2502: 2499: 2497: 2494: 2492: 2489: 2487: 2484: 2482: 2479: 2477: 2474: 2473: 2471: 2469:(EC 2.7.11.1) 2468: 2464: 2460: 2455: 2450: 2446: 2441: 2437: 2433: 2426: 2421: 2419: 2414: 2412: 2407: 2406: 2403: 2397: 2394: 2391: 2387: 2384: 2383: 2379: 2370: 2366: 2362: 2358: 2353: 2348: 2344: 2340: 2336: 2329: 2326: 2321: 2317: 2313: 2309: 2304: 2299: 2295: 2291: 2287: 2280: 2277: 2272: 2268: 2264: 2260: 2255: 2250: 2247:(2): 107–10. 2246: 2242: 2238: 2231: 2228: 2223: 2219: 2215: 2211: 2207: 2203: 2200:(3): 375–80. 2199: 2195: 2188: 2185: 2180: 2176: 2172: 2168: 2164: 2160: 2156: 2152: 2145: 2142: 2137: 2133: 2129: 2125: 2118: 2115: 2110: 2106: 2102: 2098: 2093: 2088: 2084: 2080: 2076: 2069: 2066: 2061: 2057: 2053: 2049: 2044: 2039: 2035: 2031: 2027: 2020: 2017: 2012: 2008: 2004: 2000: 1996: 1992: 1988: 1984: 1980: 1976: 1969: 1966: 1961: 1957: 1952: 1947: 1943: 1939: 1935: 1931: 1927: 1920: 1917: 1912: 1908: 1904: 1900: 1896: 1892: 1889:(8): 459–65. 1888: 1884: 1877: 1874: 1869: 1863: 1859: 1852: 1849: 1844: 1840: 1836: 1832: 1828: 1824: 1816: 1813: 1808: 1804: 1800: 1796: 1792: 1788: 1785:(3): 175–90. 1784: 1780: 1776: 1775:Cline, Hollis 1769: 1766: 1761: 1757: 1753: 1749: 1745: 1744:10.1038/31709 1741: 1737: 1733: 1729: 1725: 1718: 1715: 1710: 1706: 1702: 1698: 1693: 1688: 1684: 1680: 1676: 1672: 1666: 1663: 1658: 1654: 1650: 1646: 1642: 1638: 1634: 1630: 1626: 1622: 1615: 1612: 1607: 1603: 1598: 1593: 1589: 1585: 1581: 1577: 1573: 1566: 1563: 1558: 1554: 1549: 1544: 1540: 1536: 1532: 1528: 1524: 1517: 1514: 1509: 1505: 1500: 1495: 1491: 1487: 1483: 1476: 1473: 1468: 1464: 1460: 1456: 1452: 1448: 1444: 1440: 1433: 1430: 1425: 1421: 1416: 1411: 1407: 1403: 1399: 1395: 1392:(5): 1501–9. 1391: 1387: 1383: 1376: 1373: 1368: 1364: 1360: 1356: 1351: 1346: 1342: 1338: 1334: 1327: 1325: 1321: 1316: 1312: 1308: 1304: 1300: 1296: 1289: 1287: 1283: 1278: 1274: 1270: 1266: 1261: 1256: 1252: 1248: 1244: 1237: 1234: 1229: 1225: 1221: 1217: 1213: 1209: 1205: 1201: 1194: 1191: 1186: 1182: 1178: 1174: 1170: 1166: 1162: 1158: 1157: 1152: 1148: 1147:Kennedy, M.B. 1141: 1138: 1133: 1129: 1125: 1121: 1117: 1113: 1106: 1103: 1098: 1094: 1090: 1086: 1082: 1078: 1071: 1068: 1063: 1059: 1055: 1051: 1046: 1041: 1037: 1033: 1029: 1022: 1019: 1014: 1010: 1005: 1000: 996: 992: 988: 984: 980: 973: 970: 965: 961: 957: 953: 949: 945: 938: 935: 932: 927: 924: 921: 916: 913: 908: 904: 899: 894: 890: 886: 882: 864: 861: 856: 852: 848: 844: 839: 834: 830: 826: 822: 815: 812: 807: 803: 799: 795: 790: 785: 782:(2): 656–64. 781: 777: 773: 755: 752: 747: 743: 739: 735: 731: 727: 720: 717: 712: 708: 704: 700: 696: 692: 685: 683: 679: 674: 670: 665: 660: 656: 652: 648: 641: 638: 631: 627: 624: 623: 619: 615: 611: 607: 603: 599: 598: 594: 592: 586: 584: 577: 575: 568: 566: 559: 554: 552: 546: 544: 541: 536: 533: 526: 524: 518: 516: 514: 508: 505: 497: 495: 492: 485: 480: 478: 471: 469: 462: 460: 456: 452: 449: 441: 439: 432: 430: 423: 421: 419: 418:LTP induction 414: 410: 402: 400: 398: 393: 386: 384: 377: 375: 373: 368: 365: 362: 357: 353: 351: 343: 341: 339: 330: 323: 317: 309: 302: 298: 294: 290: 289:CaM kinase II 286: 283: 280: 276: 272: 268: 265: 264: 263: 257: 255: 253: 249: 245: 240: 238: 234: 230: 215: 211: 196: 192: 188: 187:CaM kinase II 184: 166: 154: 151: 149: 145: 142: 138: 134: 131: 129: 125: 121: 117: 114: 111: 107: 102: 98: 95: 92: 90: 86: 83: 80: 77: 73: 70: 67: 65: 61: 57: 53: 48: 41: 36: 31: 19: 4531:Translocases 4528: 4515: 4502: 4489: 4476: 4466:Transferases 4463: 4450: 4307:Binding site 3738:P70S6 kinase 3163: 2342: 2338: 2328: 2293: 2290:FEBS Letters 2289: 2279: 2244: 2241:FEBS Letters 2240: 2230: 2197: 2193: 2187: 2157:(4): 735–9. 2154: 2150: 2144: 2127: 2123: 2117: 2082: 2078: 2068: 2033: 2029: 2019: 1978: 1974: 1968: 1933: 1929: 1919: 1886: 1882: 1876: 1857: 1851: 1826: 1822: 1815: 1782: 1778: 1768: 1727: 1723: 1717: 1682: 1678: 1665: 1624: 1620: 1614: 1579: 1575: 1565: 1530: 1526: 1516: 1489: 1485: 1475: 1442: 1438: 1432: 1389: 1385: 1375: 1340: 1336: 1298: 1294: 1250: 1246: 1236: 1203: 1199: 1193: 1160: 1154: 1140: 1115: 1111: 1105: 1080: 1076: 1070: 1035: 1031: 1021: 986: 982: 972: 947: 943: 937: 926: 915: 888: 884: 863: 828: 824: 814: 779: 775: 754: 732:(1): 101–9. 729: 725: 719: 697:(1): 39–55. 694: 690: 654: 650: 640: 590: 581: 572: 563: 550: 540:viral vector 537: 534: 530: 522: 509: 503: 501: 493: 489: 475: 466: 457: 453: 445: 436: 427: 406: 390: 381: 369: 366: 358: 354: 347: 335: 288: 284: 266: 261: 241: 239:activation. 190: 186: 172: 171: 4302:Active site 4189:(EC 2.7.12) 3576:Polo kinase 3516:Polo kinase 2296:(2): 1–11. 1112:Mol. Interv 950:: 473–510. 303:metabolism. 295:secretion, 281:to contract 50:Identifiers 4588:Categories 4505:Isomerases 4479:Hydrolases 4346:Regulation 2867:IκB kinase 2442:2.7.11-12) 1860:. Snauer. 870:"Neuronal 632:References 600:CaMK II — 372:C terminus 237:CD8 T-cell 210:calmodulin 116:structures 4594:EC 2.7.11 4580:IPR013543 4384:EC number 2993:PKC alpha 1406:1874/3794 547:Addiction 94:IPR013543 58:CaMKII_AD 4576:InterPro 4408:Kinetics 4332:Cofactor 4295:Activity 3349:KIAA0999 3244:MAPKAPK5 3239:MAPKAPK3 3234:MAPKAPK2 2369:10316848 2361:16109919 2320:39732332 2312:10858498 2271:39732332 2263:10858498 2222:31122499 2214:10851169 2179:45751857 2171:17171706 2130:: 5–18. 2109:16704390 2060:17934142 2003:11357133 1960:15056707 1911:53151434 1903:16806507 1843:14586032 1799:11994750 1760:47246118 1701:11301028 1606:17494705 1424:11222640 1367:37467211 1228:33109273 1149:(1986). 1132:14993460 1062:16106663 1054:10473573 964:12045104 907:16079472 855:21614214 847:15843557 806:35436952 798:16002660 761:"Active 746:16406114 711:15781121 673:16079472 620:See also 338:isoforms 301:glycogen 214:learning 133:RCSB PDB 89:InterPro 4564:Biology 4518:Ligases 4288:Enzymes 4008:MAP3K14 3986:MAP3K11 3981:MAP3K10 3971:MAP3K13 3966:MAP3K12 3768:RPS6KC1 3763:RPS6KA1 3758:RPS6KA3 3753:RPS6KA2 3748:RPS6KB2 3733:RPS6KA4 3728:RPS6KA5 3379:Kalirin 3344:SNF1LK2 2583:EIF2AK4 2578:EIF2AK3 2432:Kinases 2136:7724650 2101:8980240 2052:7781066 2011:4384100 1983:Bibcode 1951:6730013 1807:5844720 1752:9655394 1732:Bibcode 1709:2441189 1657:4339539 1649:2564640 1629:Bibcode 1597:6672374 1557:8757245 1548:6578881 1508:9166287 1467:1378648 1447:Bibcode 1439:Science 1415:6762931 1359:9153188 1315:9452388 1295:Science 1277:8220445 1269:8845163 1220:7530878 1177:3006921 1097:9452388 1077:Science 1013:1659571 1004:2289961 504:initial 279:muscles 193:) is a 69:PF08332 4550:Portal 4492:Lyases 4238:MAP2K7 4233:MAP2K6 4228:MAP2K5 4223:MAP2K4 4218:MAP2K3 4213:MAP2K2 4208:MAP2K1 4159:ACVRL1 4154:ACVR2B 4149:ACVR2A 4144:ACVR1C 4139:ACVR1B 4122:BMPR1B 4117:BMPR1A 3991:MAP3K7 3976:MAP3K9 3927:MAP3K8 3922:MAP3K7 3917:MAP3K6 3912:MAP3K5 3907:MAP3K4 3902:MAP3K3 3897:MAP3K2 3892:MAP3K1 3866:MAPK14 3861:MAPK13 3856:MAPK11 3844:MAPK10 3822:MAPK15 3817:MAPK12 3709:CDC2L1 3684:CDC2L5 3359:SNF1LK 3184:CAMK2G 3179:CAMK2D 3174:CAMK2B 3169:CAMK2A 3159:CAMK1G 3154:CAMK1D 3149:CAMK1B 3144:CAMK1A 2998:PRKCB1 2935:PRKACA 2930:PRKACB 2925:PRKACG 2901:IKBKAP 2727:BCKDHB 2722:BCKDHA 2696:PRKAG3 2691:PRKAG2 2686:PRKAG1 2676:PRKAB2 2671:PRKAB1 2661:PRKAA2 2656:PRKAA1 2501:STK38L 2392:(MeSH) 2367:  2359:  2318:  2310:  2269:  2261:  2220:  2212:  2177:  2169:  2134:  2107:  2099:  2058:  2050:  2009:  2001:  1975:Nature 1958:  1948:  1909:  1901:  1864:  1841:  1805:  1797:  1758:  1750:  1724:Nature 1707:  1699:  1679:Neuron 1655:  1647:  1621:Nature 1604:  1594:  1555:  1545:  1506:  1465:  1422:  1412:  1365:  1357:  1313:  1275:  1267:  1247:Neuron 1226:  1218:  1185:491812 1183:  1175:  1130:  1095:  1060:  1052:  1011:  1001:  962:  905:  853:  845:  804:  796:  744:  709:  671:  614:CAMK2G 610:CAMK2D 606:CAMK2B 602:CAMK2A 587:CaMK2G 578:CaMK2D 569:CaMK2B 560:CaMK2A 424:In LTP 275:myosin 250:, and 233:T-cell 191:CaMKII 148:PDBsum 122:  112:  82:CL0051 55:Symbol 18:CAMKII 4444:Types 4200:MAP2K 4134:ACVR1 4127:BMPR2 4112:BMPR1 4037:GSK-3 3878:MAP3K 3839:MAPK9 3834:MAPK8 3812:MAPK7 3807:MAPK6 3802:MAPK4 3797:MAPK3 3792:MAPK1 3704:PFTK1 3699:PCTK3 3694:PCTK2 3689:PCTK1 3679:CDK12 3674:CDK10 3649:CDKL5 3629:CDKL2 3506:STK19 3501:EEF2K 3482:PHKG2 3477:PHKG1 3467:PHKA2 3462:PHKA1 3443:MYLK4 3438:MYLK3 3433:MYLK2 3409:DCLK1 3404:Titin 3394:TRIB3 3389:TRIB2 3384:TRIB1 3374:TSSK2 3354:STK40 3339:PSKH1 3334:PRKD3 3329:PRKD2 3309:PHKG2 3304:PHKG1 3294:OBSCN 3289:NUAK2 3284:NUAK1 3279:MKNK2 3274:MKNK1 3264:MARK4 3259:MARK3 3254:MARK2 3249:MARK1 3229:STK11 3224:DAPK3 3219:DAPK2 3214:DAPK1 3209:CHEK2 3204:CHEK1 3189:CAMK4 3164:CAMK2 3139:CAMK1 3134:BRSK2 3028:PRKCQ 3023:PRKCI 3018:PRKCG 3013:PRKCH 3008:PRKCE 3003:PRKCD 2964:PRKG1 2896:IKBKG 2891:IKBKE 2840:STK10 2835:FASTK 2761:IDH3G 2756:IDH3B 2751:IDH3A 2717:BCKDK 2511:ROCK1 2496:STK38 2491:MAST2 2486:MAST1 2481:LATS2 2476:LATS1 2365:S2CID 2316:S2CID 2267:S2CID 2218:S2CID 2175:S2CID 2105:S2CID 2056:S2CID 2007:S2CID 1907:S2CID 1803:S2CID 1756:S2CID 1705:S2CID 1653:S2CID 1504:S2CID 1363:S2CID 1273:S2CID 1224:S2CID 1181:S2CID 1058:S2CID 851:S2CID 802:S2CID 626:Actin 595:Genes 513:KN-62 258:Types 4574:and 4572:Pfam 4536:list 4529:EC7 4523:list 4516:EC6 4510:list 4503:EC5 4497:list 4490:EC4 4484:list 4477:EC3 4471:list 4464:EC2 4458:list 4451:EC1 4027:TPK1 4003:CDC7 3961:MLKs 3954:KSR2 3949:KSR1 3944:BRAF 3939:ARAF 3934:RAFs 3669:CDK9 3664:CDK8 3659:CDK7 3654:CDK6 3644:CDK5 3639:CDK4 3634:CDK3 3624:CDK2 3619:CDK1 3600:PLK4 3595:PLK3 3590:PLK2 3585:PLK1 3540:PLK4 3535:PLK3 3530:PLK2 3525:PLK1 3472:PHKB 3428:MYLK 3399:TRIO 3369:SPEG 3364:SNRK 3324:PKD1 3319:PIM2 3314:PIM1 3299:PASK 3269:MELK 3199:CASK 3194:MLCK 3115:GRK6 3110:GRK5 3105:GRK4 3043:PKN3 3038:PKN2 2940:PRKY 2886:TBK1 2881:IKK2 2876:CHUK 2780:STK4 2746:IDH2 2631:PDK4 2626:PDK3 2621:PDK2 2616:PDK1 2595:WEE1 2590:Wee1 2558:mTOR 2546:AKT3 2541:AKT2 2536:AKT1 2526:SGK3 2521:SGK2 2357:PMID 2308:PMID 2259:PMID 2210:PMID 2167:PMID 2132:PMID 2097:PMID 2079:Cell 2048:PMID 2030:Cell 1999:PMID 1956:PMID 1899:PMID 1862:ISBN 1839:PMID 1795:PMID 1748:PMID 1697:PMID 1645:PMID 1602:PMID 1553:PMID 1463:PMID 1420:PMID 1355:PMID 1311:PMID 1265:PMID 1216:PMID 1173:PMID 1156:Cell 1128:PMID 1093:PMID 1050:PMID 1009:PMID 960:PMID 903:PMID 843:PMID 794:PMID 742:PMID 730:1763 707:PMID 669:PMID 448:AMPA 141:PDBj 137:PDBe 120:ECOD 110:Pfam 78:clan 76:Pfam 64:Pfam 4032:TTK 3996:ZAK 2573:HRI 2568:PKR 2516:SGK 2506:CIT 2347:doi 2298:doi 2294:475 2249:doi 2245:475 2202:doi 2159:doi 2128:390 2087:doi 2038:doi 1991:doi 1979:411 1946:PMC 1938:doi 1891:doi 1831:doi 1787:doi 1740:doi 1728:393 1687:doi 1637:doi 1625:338 1592:PMC 1584:doi 1543:PMC 1535:doi 1494:doi 1455:doi 1443:257 1410:PMC 1402:hdl 1394:doi 1345:doi 1341:272 1303:doi 1299:279 1255:doi 1208:doi 1165:doi 1120:doi 1085:doi 1081:279 1040:doi 1036:274 999:PMC 991:doi 987:115 952:doi 893:doi 833:doi 829:174 784:doi 780:175 734:doi 699:doi 695:106 659:doi 189:or 128:PDB 4590:: 4578:: 2682:γ 2667:β 2652:α 2440:EC 2434:: 2363:. 2355:. 2343:97 2341:. 2337:. 2314:. 2306:. 2292:. 2288:. 2265:. 2257:. 2243:. 2239:. 2216:. 2208:. 2198:10 2196:. 2173:. 2165:. 2155:85 2153:. 2126:. 2103:. 2095:. 2083:87 2081:. 2077:. 2054:. 2046:. 2034:81 2032:. 2028:. 2005:. 1997:. 1989:. 1977:. 1954:. 1944:. 1934:24 1932:. 1928:. 1905:. 1897:. 1887:29 1885:. 1837:. 1827:91 1825:. 1801:. 1793:. 1781:. 1754:. 1746:. 1738:. 1726:. 1703:. 1695:. 1683:29 1681:. 1677:. 1651:. 1643:. 1635:. 1623:. 1600:. 1590:. 1580:27 1578:. 1574:. 1551:. 1541:. 1531:16 1529:. 1525:. 1502:. 1488:. 1484:. 1461:. 1453:. 1441:. 1418:. 1408:. 1400:. 1390:21 1388:. 1384:. 1361:. 1353:. 1339:. 1335:. 1323:^ 1309:. 1297:. 1285:^ 1271:. 1263:. 1251:15 1249:. 1245:. 1222:. 1214:. 1204:17 1202:. 1179:. 1171:. 1161:44 1159:. 1153:. 1126:. 1114:. 1091:. 1079:. 1056:. 1048:. 1034:. 1030:. 1007:. 997:. 985:. 981:. 958:. 948:71 946:. 901:. 889:28 887:. 883:. 872:Ca 849:. 841:. 827:. 823:. 800:. 792:. 778:. 774:. 763:Ca 740:. 728:. 705:. 693:. 681:^ 667:. 655:28 653:. 649:. 612:, 608:, 604:, 254:. 246:, 218:Ca 199:Ca 174:Ca 139:; 135:; 118:/ 4552:: 4538:) 4534:( 4525:) 4521:( 4512:) 4508:( 4499:) 4495:( 4486:) 4482:( 4473:) 4469:( 4460:) 4456:( 4280:e 4273:t 4266:v 4089:- 4072:- 4055:- 2858:- 2438:( 2424:e 2417:t 2410:v 2371:. 2349:: 2322:. 2300:: 2273:. 2251:: 2224:. 2204:: 2181:. 2161:: 2138:. 2111:. 2089:: 2062:. 2040:: 2013:. 1993:: 1985:: 1962:. 1940:: 1913:. 1893:: 1870:. 1845:. 1833:: 1809:. 1789:: 1783:3 1762:. 1742:: 1734:: 1711:. 1689:: 1659:. 1639:: 1631:: 1608:. 1586:: 1559:. 1537:: 1510:. 1496:: 1490:5 1469:. 1457:: 1449:: 1426:. 1404:: 1396:: 1369:. 1347:: 1317:. 1305:: 1279:. 1257:: 1230:. 1210:: 1187:. 1167:: 1134:. 1122:: 1116:3 1099:. 1087:: 1064:. 1042:: 1015:. 993:: 966:. 954:: 909:. 895:: 857:. 835:: 808:. 786:: 748:. 736:: 713:. 701:: 675:. 661:: 208:/ 185:( 20:)

Index

CAMKII

Pfam
PF08332
Pfam
CL0051
InterPro
IPR013543
Pfam
structures
ECOD
PDB
RCSB PDB
PDBe
PDBj
PDBsum
structure summary

serine/threonine-specific protein kinase
calmodulin
learning
cardiomyocytes
T-cell
CD8 T-cell
Alzheimer's disease
Angelman syndrome
heart arrhythmia
myosin light chain kinase
myosin
muscles

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