A specific small interfering RNA was designed from this cDNA sequence, and interference experiments were performed in MDCK cells. The silencing of the atna cDNA specifically inhibited both the ouabain insensitive Na ATPase activity and the expression of its ? subunit . Structural analysis of ATNA protein The ATNA encoded protein has 811 amino acids with a probable molecularweight of 88,940 Da and an estimated pI of 5.70. As shown in Fig. 5a, the amino acid sequence of the ATNA protein has all P type ATPases structural motifs described for this protein family , including the P type ATPase signature motif DKTGT T, the dehalogenase motif and the phosphatase motif . The amino acid residues considered essential for P type ATPase function seem to be present in ATNA. Sequence alignment through ClustalW and three dimensional topology prediction by CPHmodels 3.0 program allow the homologous residues at the corresponding positions described for AT1A1 PIG and SERCA1 RABIT ATPases, whose crystalline structure was previously elucidated , to be identified in ATNA. The homology comparison is summarized in Table 1.
In fact, all essential residues are identical in ATNA and AT1A1 and differ in only one position from SERCA1 . Although it is reasonable Nutlin-3 molecular weight selleckchem to suppose that homologous residues play similar functions, this requires experimental demonstration. Nevertheless, homology analysis strongly suggests that ATNA CAVPO has the amino acid residues essential for ATP hydrolysis , including the phosphorylatable amino acid and the residues necessary for nucleotide binding , enzyme phosphorylation and enzyme dephosphorylation . Additionally, TMpred and MPEx programs predict at least six transmembrane ? helices that match the P type ATPase core protein, which is considered to be constituted by four characteristic domains: nucleotide binding, kinase, phosphatase, and transmembrane . In this sense, the segments M1, M2, M4, M5, and M6 seem to form the half channels for Na transport. Moreover, ATNA seems to have the essential amino acid residues for cation transport, following a model of alternating access without counter ions.
The relevant residues for this Bleomycin model include Glut 322, Ser 725, Asn 726, Glu 729, Asp 754, and Asp758. The residues Glut 322 and Asp 754, respectively, located in M4 and M6, seem to be involved in Na binding. Thus, Glu 322 would constitute the Na binding site I, while site II should be simultaneously formed by Glu 322 plus Asp 804 . Additional residues such as Ser 725, Asn 726, Glu 729, and Asp758 may also participate in cation coordination. The segment M1 of ATNA has the residue Leu 98, which would function as the cation gatelock for Na occlusion after enzyme phosphorylation and during the E1P E2P transition . Therefore, ATNA could pump one or two Na ions per catalytic cycle.