differences between the six members of this family has resulted in their classification as Staurosporine either type I or type II PAKs. The type I PAKs are functionally and structurally well-studied, and are directly activated by interaction with Rho-family small GTPases to function in growth factor signaling and regulation of morphogenic processes. In contrast, the type II PAKs bind the Rho-family small GTPases CDC42, RAC1 and RhoV, but are not directly activated by this interaction. Instead, alternate mechanisms of activation and regulation have recently been discovered. The type II PAKs are important for signaling cascades that regulate cell survival, neurite outgrowth and formation of filipodia. PAK6 is expressed in prostate, testis, thyroid, placenta and 36338-96-2 structure neural tissues and is found in both cytoplasmic and nuclear fractions of prostate cells. Androgen receptor is reported to be a downstream target of PAK6, and PAK6 can regulate gene transcription by androgen receptor via a GTPase-independent mechanism possibly related to control of its degradation by the MDM2 E3 ubiquitin ligase. Global deletion of Pak6 in mice results in increased weight and decreased aggression, possibly explained by its role in androgen receptor signaling. In addition, mice with combined deletion of Pak5 and Pak6 show deficits in locomotion, learning and memory not associated with single deletions of either gene, suggesting functional redundancy between the two PAKs. While neuronal substrates specific to PAK6 have not been identified, PACSIN1, an FBAR protein involved in synaptic vesicle recycling, is phosphorylated redundantly by PAK4, PAK5 and PAK6 in vivo PAK6 is overexpressed in prostate cancer, and its targeted inhibition could potentially decrease growth of prostate tumors or sensitize prostate cancer cells to radiotherapy. PAK6 has also been found to acquire somatic mutations in other solid tumors, including mutation of residue Pro52 to leucine in two independent melanomas. Consequently there is i