FAPS: A Fast Platform for Protein Structureomics Analysis

Fuente: arXiv
Saved in:
Bibliographic Details
Main Authors: Wilken, Lucas, Paul, Nihjum, Timmerman, Troy, Tolba, Sara A., Arshad, Amara, Wu, Di, Xia, Wenjie, Rasulev, Bakhtiyor, Jansen, Rick, Sun, Dali
Format: Preprint
Published: 2025
Subjects:
Online Access:
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1866911000622530560
author Wilken, Lucas
Paul, Nihjum
Timmerman, Troy
Tolba, Sara A.
Arshad, Amara
Wu, Di
Xia, Wenjie
Rasulev, Bakhtiyor
Jansen, Rick
Sun, Dali
author_facet Wilken, Lucas
Paul, Nihjum
Timmerman, Troy
Tolba, Sara A.
Arshad, Amara
Wu, Di
Xia, Wenjie
Rasulev, Bakhtiyor
Jansen, Rick
Sun, Dali
contents Protein quantification and analysis are well-accepted approaches for biomarker discovery but are limited to identification without structural information. High-throughput omics data (i.e., genomics, transcriptomics, and proteomics) have become pervasive in cancer biology studies and reach well beyond more specialized areas such as metabolomics, epigenomics, pharmacogenomics, and interact-omics. However, large-scale analysis based on the structure of the biomolecules, namely structure-omics, is still underexplored due to a lack of handy tools. In response, we developed the Fast Analysis of Protein Structure (FAPS) database, a platform designed to advance quantitative proteomics to structure-omics analysis, which significantly shortens large-scale structure-omics from weeks to seconds. FAPS can serve as a new protein secondary structure database, providing a centralized and functional database for both simulated and experimentally determined bioinformatics statistics relating to secondary structure. Stored data is generated both through the structure simulation, currently SWISS-MODEL and AlphaFold, performed by high-performance computers, and the pre-existing UniProt database. FAPS provides user-friendly features that create a straightforward and effective way of accessing accurate data on the proportion of secondary structure in different protein chains, providing a fast numerical and visual reference for protein structure calculations and analysis. FAPS is accessible through http://fapsdb.org.
format Preprint
id arxiv_https___arxiv_org_abs_2506_10134
institution arXiv
publishDate 2025
record_format arxiv
spellingShingle FAPS: A Fast Platform for Protein Structureomics Analysis
Wilken, Lucas
Paul, Nihjum
Timmerman, Troy
Tolba, Sara A.
Arshad, Amara
Wu, Di
Xia, Wenjie
Rasulev, Bakhtiyor
Jansen, Rick
Sun, Dali
Quantitative Methods
Protein quantification and analysis are well-accepted approaches for biomarker discovery but are limited to identification without structural information. High-throughput omics data (i.e., genomics, transcriptomics, and proteomics) have become pervasive in cancer biology studies and reach well beyond more specialized areas such as metabolomics, epigenomics, pharmacogenomics, and interact-omics. However, large-scale analysis based on the structure of the biomolecules, namely structure-omics, is still underexplored due to a lack of handy tools. In response, we developed the Fast Analysis of Protein Structure (FAPS) database, a platform designed to advance quantitative proteomics to structure-omics analysis, which significantly shortens large-scale structure-omics from weeks to seconds. FAPS can serve as a new protein secondary structure database, providing a centralized and functional database for both simulated and experimentally determined bioinformatics statistics relating to secondary structure. Stored data is generated both through the structure simulation, currently SWISS-MODEL and AlphaFold, performed by high-performance computers, and the pre-existing UniProt database. FAPS provides user-friendly features that create a straightforward and effective way of accessing accurate data on the proportion of secondary structure in different protein chains, providing a fast numerical and visual reference for protein structure calculations and analysis. FAPS is accessible through http://fapsdb.org.
title FAPS: A Fast Platform for Protein Structureomics Analysis
topic Quantitative Methods
url https://arxiv.org/abs/2506.10134