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. 1990 Dec;87(23):9333–9337. doi: 10.1073/pnas.87.23.9333

Primary structure of keratinocyte transglutaminase.

M A Phillips 1, B E Stewart 1, Q Qin 1, R Chakravarty 1, E E Floyd 1, A M Jetten 1, R H Rice 1
PMCID: PMC55159  PMID: 1979171

Abstract

The nucleotide and deduced amino acid sequences of the coding regions of human and rat keratinocyte transglutaminases (protein-glutamine: amine gamma-glutamyltransferase; EC 2.3.2.13) have been determined. These yield proteins of approximately 90 kDa that are 92% identical, indicative of the conservation of important structural features. Alignments of amino acid sequences show substantial similarity among the keratinocyte transglutaminase, human clotting factor XIII catalytic subunit, guinea pig liver tissue transglutaminase, and the human erythrocyte band-4.2 protein. The keratinocyte enzyme is most similar to factor XIII, whereas the band-4.2 protein is most similar to the tissue transglutaminase. A salient feature of the keratinocyte transglutaminase is its 105-residue extension beyond the N terminus of the tissue transglutaminase. This extension and the unrelated activation peptide of factor XIII (a 37-residue extension) appear to be added for specialized functions after divergence of the tissue transglutaminase from their common lineage.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

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