Motif-weighted Structure Alignment for Classification and Evolutionary Studies of Carbonic Anhydrase

preprint OA: closed CC-BY-4.0
Full text 2,670 characters · extracted from oa-doi-fallback · click to expand
This is a Preprint and has not been peer reviewed. This is version 1 of this Preprint. You must log in to post a comment. There are no comments or no comments have been made public for this article. This is a Preprint and has not been peer reviewed. This is version 1 of this Preprint. Add a Comment You must log in to post a comment. Comments There are no comments or no comments have been made public for this article. Carbonic anhydrases (CAs) attract interest for their critical roles in various physiological processes and potential application in CO2 sequestration to combat global warming. Despite being an important enzyme family, the classification and evolution of CAs remain elusive due to their high sequence diversity and long evolutionary history. In this paper, the in-silico strategy, Motif-weighted Alignment for Structure-based Protein Classification (MASPC) was developed, which uses OmegaFold simulated CA structures combined with weighted structural motif alignment, TM-weighted, to facilitate more precise polymorphic analysis of large enzyme datasets in a robust manner. The MASPC strategy was first validated by 74 ground-truth CA structures extracted from PDB, showing improved performance compared to sequence-based polymorphic analysis (ClustalO-RAxML). Subsequently, MASPC was applied to analyze a representative database, which contains 1603 CAs from 117 model organisms, with focus on α-, β-, and- γ- CA classes, to cover organisms from across life evolution history. The results indicated that α-, β-, and γ-CAs were well grouped in their own classes, with clearer clustering associated with the CA’s organism. The structural differences among the α-, β-, and γ-CAs revealed by MASPC supported the current understanding that CA classes are the results of convergent evolution. The sub-clusters in α- and β-CAs are highly associated with organisms according to their appearance in evolutionary history, demonstrating a close correlation between CA evolution and life evolution. Furthermore, the MASPC method was also applied to identify 27 potential α-CAs from the NCBI database with less than 40% sequence similarity to a template human carbonic anhydrase II (HCA-II) sequence, demonstrating possible applications in enzyme identification studies. https://doi.org/10.32942/X25S7R Bioinformatics, Life Sciences Protein, alignment, evolution, Carbonic Anhydrase, carbon capture Published: 2025-02-24 16:01 Last Updated: 2025-02-24 16:01 CC BY Attribution 4.0 International Conflict of interest statement: None Data and Code Availability Statement: Data and code is available at https://github.com/resplendentHSHI/TMweighted Language: English

Text is read by the "Ask this paper" AI Q&A widget below. Extraction quality varies by source — PMC NXML preserves structure cleanly, OA-HTML may include some navigation residue, and OA-PDF can have broken hyphenation. The publisher copy (via DOI) is the canonical version.

My notes (saved in your browser only)

Ask this paper AI returns verbatim quotes from the full text · source: oa-doi-fallback

Answers must be backed by verbatim quotes from this paper's full text. Hallucinated quotes are dropped automatically; if no verbatim passage answers the question, we say so. How this works

Citation neighborhood (no data yet)

We don't have any in-corpus citations linked to this paper yet. This is a recent paper (2025) — citers typically take a year or two to land, and the OpenAlex reference graph may still be filling in.

Source provenance

europepmc
last seen: 2026-05-20T01:45:00.602351+00:00
unpaywall
last seen: 2026-05-24T02:00:01.246996+00:00
License: CC-BY-4.0