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Literature summary for 3.4.21.45 extracted from

  • Anastasiou, V.; Mikrou, A.; Papanastasiou, A.; Zarkadis, I.
    The molecular identification of factor H and factor I molecules in rainbow trout provides insights into complement C3 regulation (2011), Fish Shellfish Immunol., 31, 491-499.
    View publication on PubMed

Cloned(Commentary)

Cloned (Comment) Organism
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Oncorhynchus mykiss

Organism

Organism UniProt Comment Textmining
Oncorhynchus mykiss E7BAR3
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Posttranslational Modification

Posttranslational Modification Comment Organism
glycoprotein sequence contains three potential N-glycosylation sites Oncorhynchus mykiss
proteolytic modification CFI mRNA is translated in both a heavy and light chain which is further cleaved at a tetrapeptide processing site Oncorhynchus mykiss

Source Tissue

Source Tissue Comment Organism Textmining
brain low level of mRNA expression Oncorhynchus mykiss
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intestine high level of mRNA expression Oncorhynchus mykiss
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liver high level of mRNA expression Oncorhynchus mykiss
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additional information no expression detected in heart, kidney and spleen Oncorhynchus mykiss
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Subunits

Subunits Comment Organism
More CFI mRNA is translated in both a heavy and light chain which is further cleaved at a tetrapeptide processing site. The light chain of trout CFI comprises the serine protease domain, which contains the catalytic triad, His380-Asp429-Ser525 residues, human CFI numbering, as well as the Asp519 residue located at the bottom of the specificity pocket. All these residues are identical by composition and position in all species tested Oncorhynchus mykiss

Synonyms

Synonyms Comment Organism
CFI
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Oncorhynchus mykiss