{{Short description|Protein family}} {{cs1 config|name-list-style=vanc|display-authors=6}} {{Infobox gene}} {{Infobox protein | name = Collybistin | AltNames = | image = | width = | caption = | Symbol = ARHGEF9 | AltSymbols = | IUPHAR_id = | ATC_prefix = | ATC_suffix = | ATC_supplemental = | CAS_number = | CAS_supplemental = | DrugBank = | EntrezGene = 23229 | HGNCid = | OMIM = | PDB = | RefSeq = NP_056000 | UniProt = O43307 | ECnumber = | Chromosome = X | Arm = q | Band = 11.1 | LocusSupplementaryData = | Wikidata = }} thumb|Collybistin Opening and Closing Structure '''Collybistin''' is a brain specific<ref name="Kins_2000" /> protein identified as a regulator of the localization of gephyrin, a primary scaffolding protein.<ref>{{cite journal | vauthors = Soykan T, Schneeberger D, Tria G, Buechner C, Bader N, Svergun D, Tessmer I, Poulopoulos A, Papadopoulos T, Varoqueaux F, Schindelin H, Brose N | date = September 2014 | title = A conformational switch in collybistin determines the differentiation of inhibitory postsynapses | journal = The EMBO Journal | volume = 33 | issue = 18 | pages = 2113–2133 | doi = 10.15252/embj.201488143 | pmc = 4195776 | pmid = 25082542 }}</ref> In humans, it is encoded by the ''ARHGEF9'' gene.<ref name="pmid10559246">{{cite journal | vauthors = Reid T, Bathoorn A, Ahmadian MR, Collard JG | date = December 1999 | title = Identification and characterization of hPEM-2, a guanine nucleotide exchange factor specific for Cdc42 | journal = The Journal of Biological Chemistry | volume = 274 | issue = 47 | pages = 33587–33593 | doi = 10.1074/jbc.274.47.33587 | doi-access = free | pmid = 10559246 }}</ref><ref name="pmid9455477">{{cite journal | vauthors = Ishikawa K, Nagase T, Nakajima D, Seki N, Ohira M, Miyajima N, Tanaka A, Kotani H, Nomura N, Ohara O | date = February 1998 | title = Prediction of the coding sequences of unidentified human genes. VIII. 78 new cDNA clones from brain which code for large proteins in vitro | journal = DNA Research | volume = 4 | issue = 5 | pages = 307–313 | doi = 10.1093/dnares/4.5.307 | doi-access = free | pmid = 9455477 }}</ref><ref name="entrez">{{cite web | title = Entrez Gene: ARHGEF9 Cdc42 guanine nucleotide exchange factor (GEF) 9| url = https://www.ncbi.nlm.nih.gov/gene?Db=gene&Cmd=ShowDetailView&TermToSearch=23229}}</ref> Collybistin induces the formation of submembrane gephyrin aggregates that accumulate glycine and GABA receptors. In 2000 it was identified as a gephyrin binding partner, and an important determinant of inhibitory postsynaptic membrane formation and plasticity.<ref name="Kins_2000">{{cite journal | vauthors = Kins S, Betz H, Kirsch J | title = Collybistin, a newly identified brain-specific GEF, induces submembrane clustering of gephyrin | journal = Nature Neuroscience | volume = 3 | issue = 1 | pages = 22–29 | date = January 2000 | pmid = 10607391 | doi = 10.1038/71096 }}</ref> Gephyrin and collybistin are recruited to developing postsynaptic membranes of inhibitory synapses by the trans-synaptic adhesion molecule neuroligin-2,<ref>{{cite journal | vauthors = Poulopoulos A, Aramuni G, Meyer G, Soykan T, Hoon M, Papadopoulos T, Zhang M, Paarmann I, Fuchs C, Harvey K, Jedlicka P, Schwarzacher SW, Betz H, Harvey RJ, Brose N, Zhang W, Varoqueaux F | title = Neuroligin 2 drives postsynaptic assembly at perisomatic inhibitory synapses through gephyrin and collybistin | journal = Neuron | volume = 63 | issue = 5 | pages = 628–642 | date = September 2009 | pmid = 19755106 | doi = 10.1016/j.neuron.2009.08.023 | doi-access = free }}</ref> where they provide the scaffold for the clustering of inhibitory postsynaptic receptors to form a functioning inhibitory synapse. thumb|Collybistin guiding Gephrin to the Glycine Receptor
== Structure == The gene ARHGEF9 (aka ARHDH) codes for Collybistin. ARHGEF9 can be found in various regions of the brain, such as the cerbral cortex, hippocampus and cerebellum, but only in locations where neurological synapse fire.There are three domains in the structure of collybistin;<ref name=":02">{{cite journal | vauthors = Ludolphs M, Schneeberger D, Soykan T, Schäfer J, Papadopoulos T, Brose N, Schindelin H, Steinem C | title = Specificity of Collybistin-Phosphoinositide Interactions: IMPACT OF THE INDIVIDUAL PROTEIN DOMAINS | journal = The Journal of Biological Chemistry | volume = 291 | issue = 1 | pages = 244–254 | date = January 2016 | pmid = 26546675 | doi = 10.1074/jbc.M115.673400 | doi-access = free | pmc = 4697159 }}</ref> the src-homology 3 (SH3) domain, the dbl-homology (DH) domain, and the pleckstrin homology (PH) domain. The SH3 domain, located at the N-terminus, binds to the regulatory sequences and prevents the protein from staying active.<ref>{{cite journal | vauthors = Harvey K, Duguid IC, Alldred MJ, Beatty SE, Ward H, Keep NH, Lingenfelter SE, Pearce BR, Lundgren J, Owen MJ, Smart TG, Lüscher B, Rees MI, Harvey RJ | title = The GDP-GTP exchange factor collybistin: an essential determinant of neuronal gephyrin clustering | journal = The Journal of Neuroscience | volume = 24 | issue = 25 | pages = 5816–5826 | date = June 2004 | pmid = 15215304 | doi = 10.1523/JNEUROSCI.1184-04.2004 | pmc = 6729214 }}</ref> SH3 acts as the regulator within the collybistin structure since most activity depends on the interactions with other proteins at the SH3 domain. Similarly, Without the PH domain, the protein is rendered useless as it cannot complete the plasma membrane targeting and clustering of gephrin.<ref name=":02" /> The DH domain is responsible for interacting and binding with GTPases.<ref>{{cite journal | vauthors = Xiang S, Kim EY, Connelly JJ, Nassar N, Kirsch J, Winking J, Schwarz G, Schindelin H | title = The crystal structure of Cdc42 in complex with collybistin II, a gephyrin-interacting guanine nucleotide exchange factor | journal = Journal of Molecular Biology | volume = 359 | issue = 1 | pages = 35–46 | date = May 2006 | pmid = 16616186 | doi = 10.1016/j.jmb.2006.03.019 }}</ref> The DH domain regulates binding with gephrin.
Collybistin is categorized as a modular protein structure.<ref name=":2">{{cite journal | vauthors = Soykan T, Schneeberger D, Tria G, Buechner C, Bader N, Svergun D, Tessmer I, Poulopoulos A, Papadopoulos T, Varoqueaux F, Schindelin H, Brose N | title = A conformational switch in collybistin determines the differentiation of inhibitory postsynapses | journal = The EMBO Journal | volume = 33 | issue = 18 | pages = 2113–2133 | date = September 2014 | pmid = 25082542 | doi = 10.15252/embj.201488143 | pmc = 4195776 }}</ref><ref>{{cite journal | vauthors = Del Sol A, Araúzo-Bravo MJ, Amoros D, Nussinov R | date = 2007-05-25 | title = Modular architecture of protein structures and allosteric communications: potential implications for signaling proteins and regulatory linkages | journal = Genome Biology | volume = 8 | issue = 5 | page = R92 | doi = 10.1186/gb-2007-8-5-r92 | doi-access = free | pmc = 1929157 | pmid = 17531094 }}</ref> The protein has the ability of rearranging its conformation to be more efficient in its activity, or folding certain domains to inhibit protein activity.
== Function == Collybistin is responsible for the gephyrin-dependent clustering of GABA receptors in the brain. ARHGEF9 functions to organize synapes and inhibit them when necessary. Additionally, ARHGEF9 is responsible guanine nucleotide exchange factors (GEFs).<ref name=":0">{{cite journal | vauthors = Imam N, Choudhury S, Hemmen K, Heinze KG, Schindelin H | date = December 2022 | title = Deciphering the conformational dynamics of gephyrin-mediated collybistin activation | journal = Biophysical Reports | volume = 2 | issue = 4 | article-number = 100079 | doi = 10.1016/j.bpr.2022.100079 | pmc = 9680708 | pmid = 36425671 }}</ref> Through immunohistochemistry<ref>{{cite journal | vauthors = Ibaraki K, Mizuno M, Aoki H, Niwa A, Iwamoto I, Hara A, Tabata H, Ito H, Nagata KI | title = Biochemical and Morphological Characterization of a Guanine Nucleotide Exchange Factor ARHGEF9 in Mouse Tissues | journal = Acta Histochemica Et Cytochemica | volume = 51 | issue = 3 | pages = 119–128 | date = June 2018 | pmid = 30083020 | doi = 10.1267/ahc.18009 | pmc = 6066644 }}</ref> it was discovered that the production of collybistin changes throughout developmental stages of organisms. Any mutations within this gene may cause various negative symptoms within the organism. The organism may experience things such as intellectual disabilities, anxiety,<ref>{{cite journal | vauthors = Saiepour L, Fuchs C, Patrizi A, Sassoè-Pognetto M, Harvey RJ, Harvey K | title = Complex role of collybistin and gephyrin in GABAA receptor clustering | journal = The Journal of Biological Chemistry | volume = 285 | issue = 38 | pages = 29623–29631 | date = September 2010 | pmid = 20622020 | doi = 10.1074/jbc.M110.121368 | doi-access = free | pmc = 2937993 }}</ref> hyperekplexia,<ref>{{cite journal | vauthors = Wang JY, Zhou P, Wang J, Tang B, Su T, Liu XR, Li BM, Meng H, Shi YW, Yi YH, He N, Liao WP | date = January 2018 | title = ARHGEF9 mutations in epileptic encephalopathy/intellectual disability: toward understanding the mechanism underlying phenotypic variation | journal = Neurogenetics | volume = 19 | issue = 1 | pages = 9–16 | doi = 10.1007/s10048-017-0528-2 | pmid = 29130122 }}</ref> etc. In a study done in 2011,<ref>{{cite journal | vauthors = Shimojima K, Sugawara M, Shichiji M, Mukaida S, Takayama R, Imai K, Yamamoto T | date = August 2011 | title = Loss-of-function mutation of collybistin is responsible for X-linked mental retardation associated with epilepsy | journal = Journal of Human Genetics | volume = 56 | issue = 8 | pages = 561–565 | doi = 10.1038/jhg.2011.58 | pmid = 21633362 }}</ref> there was a direct link found between a nonsynonymous deletion in the ARHGEF9 gene and mental disability, along with physical disability. Similarly, it has been reported that missense mutations within the gene have also caused mental and physical disabilities to the organism with the mutated gene.
== Clinical significance == Pentylenetetrazol (PTZ)<ref>{{cite web | vauthors = Ra Park H | date = April 4, 2026 | title = Lilii bulbus Exerts Anti-Seizure Effects by Modulating GABAergic Synapse Organization in the Pentylenetetrazol Kindling Model | url = https://www.mdpi.com/2072-6643/18/7/1159 | access-date = April 19, 2026 }}</ref> induced seizures severely damage a wide range of synapes in the brain, including collybistin. However, when collybistin is overexpressed in the brain, it has the ability to prevent PTZ- induced seizures and protects the neurotransmitter pathways in the brain. If collybistin is not overexpressed and falls victim to PTZ, then gephrin is not clustered and synapes are not stabilized. Additionally, the inhibitory receptors become weakened, which may cause the seizure to become stronger and life-threatening.
Similarly, a missense mutation of the gene, referred to as a R290H gene variant,<ref>{{cite journal | vauthors = Papadopoulos T, Schemm R, Grubmüller H, Brose N | title = Lipid binding defects and perturbed synaptogenic activity of a Collybistin R290H mutant that causes epilepsy and intellectual disability | journal = The Journal of Biological Chemistry | volume = 290 | issue = 13 | pages = 8256–8270 | date = March 2015 | pmid = 25678704 | doi = 10.1074/jbc.M114.633024 | doi-access = free | pmc = 4375481 }}</ref> was recently discovered as a cause of epilepsy in human patients. This mutation alters the communication within the protein, specifically the folding of the DH and PH domains. Improper folding may lead to degradation or for the cell to be targeted by the ubiquitin proteasome pathway<ref>{{cite journal | vauthors = de Groot C, Floriou-Servou A, Tsai YC, Früh S, Kohler M, Parkin G, Schwerdel C, Bosshard G, Kaila K, Fritschy JM, Tyagarajan SK | date = October 2017 | title = RhoGEF9 splice isoforms influence neuronal maturation and synapse formation downstream of α2 GABAA receptors | journal = PLoS Genetics | volume = 13 | issue = 10 | article-number = e1007073 | doi = 10.1371/journal.pgen.1007073 | doi-access = free | pmc = 5673238 | pmid = 29069083 }}</ref> for termination. This mutation causes the protein to become weaker and prevents it from binding to other proteins, such as gephyrin, and inhibits plasma membrane connection. Similar to the PTZ-induced seizures, the R290H gene variant weakens the inhibitory receptors and prevents the development of the synapse. Due to activity of regulatory inhibition being reduced, the neurons become overactive, which leads to epilespy and other mental disabilities.
== Role in mortality == Without collybistin, there is a lack of proper regulator positioning,<ref name=":4">{{cite journal | vauthors = Sigel E, Steinmann ME | title = Structure, function, and modulation of GABA(A) receptors | journal = The Journal of Biological Chemistry | volume = 287 | issue = 48 | pages = 40224–40231 | date = November 2012 | pmid = 23038269 | doi = 10.1074/jbc.R112.386664 | doi-access = free | pmc = 3504738 | language = English | bibcode = 2012JBiCh.28740224S }}</ref> synapse organization, and inhibition signalling. Additionally, collybistin is responsible for synaptic scaffolding and cytoskeleton organization.<ref>{{cite journal | vauthors = Hines RM, Maric HM, Hines DJ, Modgil A, Panzanelli P, Nakamura Y, Nathanson AJ, Cross A, Deeb T, Brandon NJ, Davies P, Fritschy JM, Schindelin H, Moss SJ | date = August 2018 | title = Developmental seizures and mortality result from reducing GABA<sub>A</sub> receptor α2-subunit interaction with collybistin | journal = Nature Communications | volume = 9 | issue = 1 | page = 3130 | doi = 10.1038/s41467-018-05481-1 | pmc = 6081406 | pmid = 30087324 }}</ref> With specific binding to the a2 subunit, collybistin is crucial for the proper function of sites that tell nuerons when to fire. In a 2018 study, a mutated collybistin protein lead to an increase in mortality rates in mice within the first 20 days after birth. The mice that faced early mortality had a disconnection in the neuropathways and receptors between collybistin and GABA<sub>A</sub> receptors. The signalling from the GABA receptors became weaker and decayed at a more rapid rate. The animals suffer from spontaneous seizures that increased in strength each time. As seizure strength increased, there was a larger disruption in brain function and breathing. The seizures were identified as the ultimate cause of death, while a decline in the proper function of collybistin was found to be the proximate cause of death.
== Isoforms == There are currently 3 known isoforms of Collybistin. Each isoform is similar in that they contain a RhoGEF binding (DH) domain, and a pleckstrin homology (PH) domain.<ref>{{cite journal | vauthors = Miller MB, Yan Y, Eipper BA, Mains RE | title = Neuronal Rho GEFs in synaptic physiology and behavior | journal = The Neuroscientist | volume = 19 | issue = 3 | pages = 255–273 | date = June 2013 | pmid = 23401188 | pmc = 3927235 | doi = 10.1177/1073858413475486 }}</ref> Where they differ is at the N-terminus in both sequence and whether or not a Src-homology (SH3) domain will be present. The SH3 group, which is responsible for the inhibition of protein activity, is connected to the N-Terminus of Collybistin.<ref>{{cite journal | vauthors = Imam N, Choudhury S, Hemmen K, Heinze KG, Schindelin H | date = December 2022 | title = Deciphering the conformational dynamics of gephyrin-mediated collybistin activation | journal = Biophysical Reports | volume = 2 | issue = 4 | article-number = 100079 | doi = 10.1016/j.bpr.2022.100079 | pmc = 9680708 | pmid = 36425671 }}</ref> However, the isoform connected to the SH3- part of this terminus are constantly active and continuously signal to other proteins.<ref>{{cite journal | vauthors = Chiou TT, Bonhomme B, Jin H, Miralles CP, Xiao H, Fu Z, Harvey RJ, Harvey K, Vicini S, De Blas AL | title = Differential regulation of the postsynaptic clustering of γ-aminobutyric acid type A (GABAA) receptors by collybistin isoforms | journal = The Journal of Biological Chemistry | volume = 286 | issue = 25 | pages = 22456–22468 | date = June 2011 | pmid = 21540179 | doi = 10.1074/jbc.M111.236190 | doi-access = free | pmc = 3121391 }}</ref> This region is able to cluster gephrin without being instructed to do so by neurotransmitters or other proteins. The next isoform to discuss for Collybistin is connected to the SH3+ end of the N-Terminus. This isoform will remain folded until it is required for clustering. Similarly, the last isoform also remains folded until neuroligin-2 or neuroligin-4 bind to the protein.<ref>{{cite journal | vauthors = Soykan T, Schneeberger D, Tria G, Buechner C, Bader N, Svergun D, Tessmer I, Poulopoulos A, Papadopoulos T, Varoqueaux F, Schindelin H, Brose N | title = A conformational switch in collybistin determines the differentiation of inhibitory postsynapses | journal = The EMBO Journal | volume = 33 | issue = 18 | pages = 2113–2133 | date = September 2014 | pmid = 25082542 | doi = 10.15252/embj.201488143 | pmc = 4195776 }}</ref> They also differ in the C-terminus sequence. The isoforms are referred to as CB1, CB2, and CB3. These three forms have been identified in rats, while only CB3 has been identified in humans and is referred to as hPEM2.<ref>{{cite journal | vauthors = Fritschy JM, Panzanelli P, Tyagarajan SK | title = Molecular and functional heterogeneity of GABAergic synapses | journal = Cellular and Molecular Life Sciences | volume = 69 | issue = 15 | pages = 2485–2499 | date = August 2012 | pmid = 22314501 | doi = 10.1007/s00018-012-0926-4 | pmc = 11115047 | url = https://www.zora.uzh.ch/id/eprint/74586/1/Fritschy_review_psd_clsm_rev_2012.pdf }}</ref>
== Splice variants == Splice variants are the same proteins structurally, but they contain different mRNA sequences produced by alternative splicing. Splice variants of collybistin retain the DH and PH domains, however they dffer in the SH3 groups of the N-terminal and the C-terminal domain.<ref>https://journals.biologists.com/jcs/article/124/16/2786/31903/Collybistin-splice-variants-differentially?guestAccessKey=</ref> SH3- variants are able to induce translocation to submembrane locations due to them being enzymatically active. The splice variant most commonly found in the central nervous system is SH3+. This splice variant is autoinhibited. The SH3+ and the SH3- variants both increase the production of gephyrin clustering. SH3+ does so by producing non-synaptic clusters that do not have fractions. Whereas, the SH3- variant focuses on the gephyrin clusters at postsynaptic sites. Additionally the SH3- variant is able to form ternary complexes, but SH3+ is unable to. Although these variants are able to increase the levels of gephyrin clustering, they also directly impact GABAergic synapse formation. Additionally, these any muattions related to these variants result in cognitive impairments.
== Resistance == The absence of collybistin is commonly noticed in the brain, especially not in the cerbral cortex, hippocampus, or cerebellum, however resistance to collybistin does occur.<ref>{{cite journal | vauthors = Patrizi A, Viltono L, Frola E, Harvey K, Harvey RJ, Sassoè-Pognetto M | date = January 2012 | title = Selective localization of collybistin at a subset of inhibitory synapses in brain circuits | journal = The Journal of Comparative Neurology | volume = 520 | issue = 1 | pages = 130–141 | doi = 10.1002/cne.22702 | pmid = 21681748 | hdl = 2318/91801 | hdl-access = free }}</ref> Parts of the brain remain completely normal in the absence of collybistin. There are several reasons why parts of the brain are resistant to this protein, such as, the presence of other proteins like SynArfGEF, different scaffolding processes, or even different synapes organization. Many times collybsitin is not needed for maintenance in every part of the brain. Inhibitory synapses that are resistant to collybistin are still able to maintain gephyrin clustering and GABA receptor anchoring, many times through the use of a different protein. Resistance is dependent one the synaptic site. Glycinergic synapes are able to function like normal with the deletion of collybistin, meaning that the protein is not essential in this area of brains synaptic system. Through the study of resistance to collybistin, it was found that there are backup mechanisms in the brain to attampt to alleviate the possible damage that a delteion of collybistin could cause.
== Related proteins == Gephyrin: Originally discovered in 1982,<ref>{{cite journal | vauthors = Choii G, Ko J | date = April 2015 | title = Gephyrin: a central GABAergic synapse organizer | journal = Experimental & Molecular Medicine | volume = 47 | issue = 4 | page = e158 | doi = 10.1038/emm.2015.5 | doi-access = free | pmid = 25882190 }}</ref> this scaffolding protein is required for the clustering of glycine and γ-aminobutyric receptors. Similarly to collybistin, this protein is necessary for brain function and has three domains; the G domain, C domain, and the E domain. The C domain is responsible for binding to other proteins and posttranslational modifications. The G and E domain are responsible for clustering gephyrin into large structures. Gephyrin is located near inhibitory synapses under the cell membrane, especially close to where glycine and GABA signalling occurs. This protein adds structure and ensures proper function of the brain inhibitory system.
Neuroglin-2 (NL2): This protein also inhibits synaptic activity.<ref>https://repositoriobibliotecas.uv.cl/serveruv/api/core/bitstreams/50b13040-79b9-46ee-9bc7-bbe282ea158f/content</ref><ref>{{Cite web |title=NLGN2 neuroligin 2 [Homo sapiens (human)] - Gene - NCBI|url=https://www.ncbi.nlm.nih.gov/gene/57555|access-date=2026-04-27|website=www.ncbi.nlm.nih.gov}}</ref><ref>{{cite web | title = UniProt | website = UniProt | url = https://www.uniprot.org/uniprotkb/Q8NFZ4/entry | access-date = 2026-04-27 }}</ref> As a postsynaptic adhesion protein,<ref>{{cite journal | vauthors = Heshmati M, Aleyasin H, Menard C, Christoffel DJ, Flanigan ME, Pfau ML, Hodes GE, Lepack AE, Bicks LK, Takahashi A, Chandra R, Turecki G, Lobo MK, Maze I, Golden SA, Russo SJ | title = Cell-type-specific role for nucleus accumbens neuroligin-2 in depression and stress susceptibility | journal = Proceedings of the National Academy of Sciences of the United States of America | volume = 115 | issue = 5 | pages = 1111–1116 | date = January 2018 | pmid = 29339486 | doi = 10.1073/pnas.1719014115 | doi-access = free | pmc = 5798379 | bibcode = 2018PNAS..115.1111H }}</ref> NL2 is bound to neurexin in the postsynaptic membrane. The binding of these two proteins craetes a connection between the postsynaptic membrane and the presynaptic membrane. This allows for neurotransmitters to align with the receptors. Additionally NL2 activates collybistin activity in the SH3+ isoform and directs the process of scaffolding formation.
Cdc42: This protein is a [https://www.sciencedirect.com/topics/biochemistry-genetics-and-molecular-biology/lysosomal-trafficking-regulator trafficking regulator]<ref>{{cite journal | vauthors = Cerione RA | title = Cdc42: new roads to travel | journal = Trends in Cell Biology | volume = 14 | issue = 3 | pages = 127–132 | date = March 2004 | pmid = 15003621 | doi = 10.1016/j.tcb.2004.01.008 | language = English }}</ref> a part of the Rho family of GTPases.<ref name=":3">{{cite journal | vauthors = Neudauer CL, Joberty G, Tatsis N, Macara IG | title = Distinct cellular effects and interactions of the Rho-family GTPase TC10 | journal = Current Biology | volume = 8 | issue = 21 | pages = 1151–1160 | date = October 1998 | pmid = 9799731 | doi = 10.1016/S0960-9822(07)00486-1 | language = English | bibcode = 1998CBio....8.1151N }}</ref> Cdc42 onitors the protein activity in the membrane and assists in directing proteins to the correct areas; this is done through blocking certain pathways so proteins do not end up in an area they are not needed. This protein is also essential in the proper function of NL2. In activated forms, are directly associated with the COPI complex and activates signally pathways. Cdc42 then helps to align gephyrin in the membrane for collybistin to bind. If Cdc42 stays active or stays inactive, then its trafficking network no longer works.
TC10: This protein, a part of the Rho family of GTPases,<ref name=":3" /> regulates signalling pathways and cytoskeleton remodeling. TC10 adds strcture to the cell and assists in controlling the behavior of the cell. Additionally, TC10 switched between active and inactive states to control molecular processing. In its active state, TC10 has long and strong membrane extensions with low GTPase activity. This protein is located near the nucleus of the cell.
GABA<sub>A</sub> Receptor: The GABA<sub>A</sub> receptor is one of the primary inhibitory receptors in the brain.<ref>{{cite journal | vauthors = Sigel E, Steinmann ME | title = Structure, function, and modulation of GABA(A) receptors | journal = The Journal of Biological Chemistry | volume = 287 | issue = 48 | pages = 40224–40231 | date = November 2012 | pmid = 23038269 | doi = 10.1074/jbc.R112.386664 | doi-access = free | pmc = 3504738 | language = English | bibcode = 2012JBiCh.28740224S }}</ref> These receptors are Ligand-gated ion channels that open during binding of neurotransmitters. There are five subunit proteins of the GABA receptors and those five subunits each have subunits of their own. There are both synaptic and extrasynaptic GABA receptors. Synaptic receptors are located in postsynaptic sites and cause fast inhibition that lasts a short amount of time. Extrasynaptic receptors are located outside of the synapses and cause shlower and long lasting inhibition. Collybistin helps to keep the receptors position at the synapses and anchors them.
Profilin: This protein binds to gephyrin and helps to maintain the structure of the cell membrane to allow for clustering.<ref>{{cite journal | vauthors = Witke W | title = The role of profilin complexes in cell motility and other cellular processes | journal = Trends in Cell Biology | volume = 14 | issue = 8 | pages = 461–469 | date = August 2004 | pmid = 15308213 | doi = 10.1016/j.tcb.2004.07.003 | language = English }}</ref> This protein is an actin regulator that is typically found in eukaryotes.<ref>{{cite journal | vauthors = Giesemann T, Schwarz G, Nawrotzki R, Berhörster K, Rothkegel M, Schlüter K, Schrader N, Schindelin H, Mendel RR, Kirsch J, Jockusch BM | date = September 2003 | title = Complex formation between the postsynaptic scaffolding protein gephyrin, profilin, and Mena: a possible link to the microfilament system | journal = The Journal of Neuroscience | volume = 23 | issue = 23 | pages = 8330–8339 | doi = 10.1523/JNEUROSCI.23-23-08330.2003 | pmc = 6740687 | pmid = 12967995 }}</ref> Profilin I can be found in most mammilian cells, whereas Profilin IIa is found in the neurological cells in mammals. Profilin helps wil regulation and organization of actin filaments. Additionally, once Profilin is directly bound to gephyrin, it assists in building large clustered structures.
== Interactions == ARHGEF9 has been shown to interact with GPHN<ref name="pmid10607391">{{cite journal | vauthors = Kins S, Betz H, Kirsch J | year = 2000 | title = Collybistin, a newly identified brain-specific GEF, induces submembrane clustering of gephyrin | journal = Nature Neuroscience | volume = 3 | issue = 1 | pages = 22–29 | doi = 10.1038/71096 | pmid = 10607391 | s2cid = 24878249 }}</ref> and SMURF1.<ref name=pmid18208356>{{cite journal | vauthors = Yamaguchi K, Ohara O, Ando A, Nagase T | date = April 2008 | title = Smurf1 directly targets hPEM-2, a GEF for Cdc42, via a novel combination of protein interaction modules in the ubiquitin-proteasome pathway | journal = Biological Chemistry | volume = 389 | issue = 4 | pages = 405–413 | doi = 10.1515/BC.2008.036 | pmid = 18208356 | s2cid = 27505034 }}</ref>
== References == {{Reflist}}
== Further reading == {{refbegin | 2}} * {{cite journal | vauthors = Suzuki Y, Yamashita R, Shirota M, Sakakibara Y, Chiba J, Mizushima-Sugano J, Nakai K, Sugano S | year = 2004 | title = Sequence Comparison of Human and Mouse Genes Reveals a Homologous Block Structure in the Promoter Regions | journal = Genome Research | volume = 14 | issue = 9 | pages = 1711–1718 | doi = 10.1101/gr.2435604 | pmc = 515316 | pmid = 15342556 }} * {{cite journal | vauthors = Harvey K, Duguid IC, Alldred MJ, Beatty SE, Ward H, Keep NH, Lingenfelter SE, Pearce BR, Lundgren J, Owen MJ, Smart TG, Lüscher B, Rees MI, Harvey RJ | year = 2004 | title = The GDP-GTP exchange factor collybistin: an essential determinant of neuronal gephyrin clustering | journal = The Journal of Neuroscience | volume = 24 | issue = 25 | pages = 5816–5826 | doi = 10.1523/JNEUROSCI.1184-04.2004 | doi-access = free | pmc = 6729214 | pmid = 15215304 }} * {{cite journal | vauthors = Grosskreutz Y, Hermann A, Kins S, Fuhrmann JC, Betz H, Kneussel M | year = 2002 | title = Identification of a gephyrin-binding motif in the GDP/GTP exchange factor collybistin | journal = Biological Chemistry | volume = 382 | issue = 10 | pages = 1455–1462 | doi = 10.1515/BC.2001.179 | pmid = 11727829 | s2cid = 2415901 }} * {{cite journal | vauthors = Kins S, Betz H, Kirsch J | year = 2000 | title = Collybistin, a newly identified brain-specific GEF, induces submembrane clustering of gephyrin | journal = Nature Neuroscience | volume = 3 | issue = 1 | pages = 22–29 | doi = 10.1038/71096 | pmid = 10607391 | s2cid = 24878249 }} {{refend}}
== External links == * {{UCSC gene info|ARHGEF9}}
{{PDB Gallery|geneid=23229}}
Category:GTP-binding protein regulators