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The Y78A mutant presented a significant difference when compared to others, p ≤ 0.05. Figure 3: Structural and mutational analysis of ScASNase1.

The inflorescence stems of the double mutant presented a prostrate phenotype with dynamic modulus properties greatly reduced relative to that of the wild type (WT) line due to severe reductions in macromolecular lignin content.

Though both mutations affected mitochondrial ISC enzymes activities and mitochondria ultrastructure, the hFXNI154F mutant presented a more severe phenotype with affected cytosolic and nuclear ISC enzyme activities, mitochondrial iron accumulation and an increased sensitivity to oxidative stress.

The H. pylori SsrASTOP mutant presented a multifaceted phenotype including (i) increased susceptibility to sub-lethal doses of chloramphenicol, (ii) hypersensitivity to amoxicillin, and (iii) deficient natural transformation capacity.

Additionally, the Δ oppD mutant presented a reduced ability to adhere to and infect macrophages compared to the wild-type, although both strains exhibit the same potential to colonize spleens and cause injury and death to infected mice.

Functional analysis, comparing Dmd mdx/Large myd mice with the more severely affected parental lineage Large myd and the milder Dmd mdx strain, showed that, overall, the double mutant presented a worse performance in the test bar for the front legs (Fig. 4).

DNA binding experiments (data not reported here) showed that only the R146K mutant presented an in vitro DNA binding property in the presence of attI1 but not in the presence of the attC element.

Thus, since the ci2 rat mutant presents a wide range of behavioural and neurochemical lateralization anomalies, in addition to representing a model of Usher syndrome type 1, it may prove useful to understand the mechanisms underlying abnormal rotational behaviour and its relevance as a model of disturbances in cerebral asymmetry and their consequences.

However, the PHD mutant presents a strikingly different localization than wild type MEKK1.

To our knowledge, this is the first report of a metazoan mutant presenting a mutation in the consensus sequence of any SOCS-box protein, allowing for the first assessment of the in vivo function of the cullin box.

An A. thaliana mutant presenting a T-DNA insertion in the Fd-GOGAT1 (GLS1, gene; At5g04140) gene was used in the present study.