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Resolution: standard / high Figure 1.
Alignment of LmxMPK4 from L. mexicana with various MAP kinase amino acid sequences. LmxMPK4, Leishmania mexicana MAP kinase 4 (GenBank accession number AJ293282; [6]); Trypanosoma brucei MAP kinase, TbMAPK2 (GeneDB accession number Tb10.70.2070; [10]); Trypanosoma cruzi MAP kinase (GeneDB accession number Tc00.1047053511299.70); Chlamydomonas reinhardtii MAP kinase (GenBank accession number BAB18271); Dictyostelium discoideum ERK1 (GenBank accession number U11077; [13]); Homo sapiens ERK2 (GenBank accession number CAA77753; [14]). Roman numerals I to XI indicate kinase subdomains. The kinase domain is located
between the two inverted triangles (▼). Arrows (↓) mark the potential regulatory phosphorylation
sites in the TXY motif at Thr190 and Tyr192, filled circles (●) indicate conserved
amino acid residues it is not clear what you mean by conserved aa residues, and open
circles (○) depict the residues of the phosphate anchor ribbon for ATP binding. The
asterisks (*) show the residues of the P+1 specificity pocket. The open triangle (Δ)
marks the invariant lysine residue (K59), which is essential for the phosphate transfer
reaction. The CD-domain is shaded in light grey. Dashes indicate gaps introduced to
optimize the alignment; dots represent identical residues. The carboxy-terminal peptide
used to generate antibodies is underlined. (50), the terminal 50 amino acid residues
of the Dictyostelium kinase have been omitted. Numbering corresponds to LmxMPK4.
Wang et al. Kinetoplastid Biology and Disease 2005 4:6 doi:10.1186/1475-9292-4-6 |