| Type: | Domain | Name: | CYTH-like domain |
| Description: | The entry represents the CYTH domain.The CyaB like adenylyl cyclase and the mammalian thiamine triphosphatases (ThTPases) define a superfamily of catalytic domains called the CYTH (CyaB,thiamine triphosphatase) domain that is present in all three superkingdoms of life. CYTH domains are likely to be domains specialised to bind nucleotidesand other organic phosphates [].The catalytic core of the CYTH domain is predicted to contain an alpha+beta scaffold with 6 conserved beta-strands and 6 conserved alpha-helices. The CYTHdomains contains several nearly universally conserved charged residues that are likely to form the active site. The most prominent of these are an EXEXKmotif associated with strand-1 of the domain, two basic residues in helix-2, a K at the end of strand 3, an E in strand 4, a basic residue in helix-4, a D atthe end of strand 5 and two acidic residues (typically glutamates) in strand 6. The presence of around 6 conserved acidic positions in the majority of theCYTH domains suggests that it coordinates two divalent metal ions. Both CyaB and ThTPase have been shown to require Mg(2+) ions for their nucleotidecyclase and phosphatase activities. The four conserved basic residues in the CYTH domain are most probably involved in the binding of acidic phosphatemoieties of their substrates. The conservation of these two sets of residues in the majority of CYTH domains suggests that most members of this group arelikely to possess an activity dependent on two metal ions, with a preference for nucleotides or related phosphate-moiety -bearing substrates. The proposedbiochemical activity, and the arrangement of predicted strands in the primary structure of the CYTH domain imply that they may adopt a barrel or sandwich-like configuration, with metal ions and the substrates bound in the central cavity []. | Short Name: | CYTH-like_domain |
