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Five appreciably expressed planarian collagen genes encode type IV collagens (col4 1 5), which are basement membrane-specific collagen proteins that form a meshwork instead of long fibrils.
The hrp ('harp') genes encode type III secretory proteins enabling many phytopathogenic bacteria to elicit a hypersensitive response (HR) on non-host or resistant host plants and induce pathogenesis on susceptible hosts.
At least two of the genes predicted to encode type II PI4K (phosphoinositide 4-kinase) in Arabidopsis thaliana (thale cress), namely AtPI4Kgamma4 and AtPI4Kgamma7, encode enzymes with catalytic properties similar to those of members of the PIKK (phosphoinositide kinase-related kinase) family.
These two ncRNAs are antisense to Teg8 (SprA) and SprG, respectively which are predicted to encode type I toxins [40].
IFIH1, or melanoma differentiation associated gene-5 (MDA5), is a pathogen recognition receptor which can, by interacting with RNA virus, initiate antiviral innate immunity and activate genes that encode type I IFNs [34].
They encode type III secretion systems (T3SS) that inject bacterial effector proteins into host cells.
Similar(31)
All three genes appeared to encode type-II transmembrane proteins that are typical of Class I α-1,2-mannosidases.
Attributes assigned to graph nodes encode types of spaces and their sizes.
The attributes assigned to graph nodes encode types of spaces (rooms, corridors, stairs, etc).
Proteins that encode type-1 ZF-CxxC domains include CFP1 and the histone H3 lysine 36 demethylases KDM2A and KDM2B.
MGD2 and MGD3 encode type-B monogalactosyldiacylglycerol (MGDG) synthase and are involved in Pi-starvation induced lipid remodeling for Pi-recycling, a typical response of Pi starvation [ 51].
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