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b Schematic representation of OsBEIIa on the long arm of chromosome 4. Candidate region of the gene related to the sug-h mutant was located within the AL731641 clone.

The T-DNA insertion point in the ctf mutant was located by the plasmid rescue method [6].

The UIM, caspase 3 and kinase dead mutants were expressed in a manner similar to wild type MEKK1, but the PHD mutant was located expressly in large, distinct punctuate structures.

This mutant was located at the plasma membrane and rapidly secreted.

Similarly, the p.E113K mutant was located to the periphery of the cell and colocalized with GFP-h-Ras (Fig.  3D F).

For four of the simulated scenarios, we assumed that the advantageous mutant was located in the middle of the region, and for the other four scenarios, we assumed the advantageous mutants were 220 kb outside the 30 kb region.

The mutation sites of each mutant were located at HlyB, primarily along the transmembrane domain, implying that the corresponding region was important for the improved secretion of the target protein.

Three lines of evidence indicated that the 5.0-kb deletion in the ga1-3 mutant is located at the GA1 locus.

118 among the differentially expressed genes in D4 mutant were located on chromosome 1 (55%), 55 on chromosome 2 (25%), and 42 (20%) on chromosome 3. 60 intergenic regions appeared to be differentially expressed in D4 strain (39 up-regulated and 21 down-regulated, Table S1).

The selected mutant is located at position 18 (shown in boldface type).

Another unexpected structural difference observed in the Trp95Leu mutant is located in the DE loop.