Novel domain architectures and functional determinants in atypical annexins revealed by phylogenomic analysis.

Abstract:

:The fundamental cellular role and molecular interactions of annexins in vesicle trafficking and membrane remodeling remain to be further clarified in order to better understand and exploit their contributions to health and disease. We focused on distinctive features of atypical annexins from all domains of life using phylogenomic, molecular systematic and experimental approaches, to extend the current paradigm and better account for annexin diversity of structure, function and mechanistic role in membrane homeostasis. The analysis of gene duplications, organization of domain architectures and profile hidden Markov models of subfamily orthologs defined conserved structural features relevant to molecular interactions and functional divergence of seven family clades ANXA-G. Single domain annexins of bacteria, including cyanobacteria, were frequently coupled to enzymatic units conceivably related to membrane metabolism and remodeling. Multiple ANX domains (up to 20) and various distinct functional domains were observed in unique annexins. Canonical type 2 calcium binding ligands were well-preserved in roughly half of all ANX domains, but alternative structural motifs comprised of 'KGD', cysteine or tryptophan residues were prominently conserved in the same strategic interhelical loops. Selective evolutionary constraint, site-specific location and co-occurrence in all kingdoms identify alternative modes of fundamental binding interactions for annexins.

journal_name

Biol Chem

journal_title

Biological chemistry

authors

Fernandez MP,Garcia M,Martin-Almedina S,Morgan RO

doi

10.1515/hsz-2016-0273

subject

Has Abstract

pub_date

2017-06-27 00:00:00

pages

751-763

issue

7

eissn

1431-6730

issn

1437-4315

pii

/j/bchm.just-accepted/hsz-2016-0273/hsz-2016-0273.

journal_volume

398

pub_type

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