bioRxiv Science⌕ Search
Home/Archive/bioRxiv

bioRxiv · 10.1101/2021.01.09.426059

MCPdb: The Bacterial Microcompartment Database

Ochoa, J. M.·Bair, K.·Holton, T.·Bobik, T. A.·Yeates, T. O.
View original source ↗Export metadata ↓

Abstract

Bacterial microcompartments are organelle-like structures composed entirely of proteins. They have evolved to carry out several distinct and specialized metabolic functions in a wide variety of bacteria. Their outer shell is constructed from thousands of tessellating protein subunits, encapsulating enzymes that carry out the internal metabolic reactions. The shell proteins are varied, with single, tandem and permuted versions of the PF00936 protein family domain comprising the primary structural component of their polyhedral architecture, which is reminiscent of a viral capsid. While considerable amounts of structural and biophysical data have been generated in the last 15 years, current resources present challenges for understanding the functional and structural properties of microcompartments (MCPs) and their diversity. In order to make the remarkable structural features of bacterial microcompartments accessible to a broad community of scientists and non-specialists, we developed MCPdb: The Bacterial Microcompartment Database (https://mcpdb.mbi.ucla.edu/). MCPdb is a comprehensive resource that categorizes and organizes known microcompartment protein structures and their larger assemblies. To emphazise the critical roles symmetric assembly and architecture play in microcompartment function, each structure in the MCPdb is validated and annotated with respect to: (1) its predicted natural assembly state (2) tertiary structure and topology and (3) the metabolic compartment type from which it derives. The current database includes 134 structures and is available to the public with the anticipation that it will serve as a growing resource for scientists interested in understanding protein-based metabolic organelles in bacteria.

Source connections

Explore related subjects

bioinformaticsPreprint

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Ochoa, J. M., Bair, K., Holton, T., Bobik, T. A., Yeates, T. O.. 2021-01-10. MCPdb: The Bacterial Microcompartment Database. https://doi.org/10.1101/2021.01.09.426059

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

bioRxiv2026

CellChat Hotspot: A Targeted Approach to Cell Cell Communication Analysis With Spatial transcriptomics Validation.

Abstract. In recent years, single cell RNA sequencing (scRNA seq) has enabled the investigation of intercellular communication through Cell Cell Communication (CCC) tools such as CellChat. Despite their potential, these approaches remain challenging to interpret, particularly when global analyses generate complex interaction networks that may include biologically irrelevant signals. To address this limitation, we developed a framework termed CellChat Hotspot, designed to improve the biological interpretability of inferred communication networks. This approach integrates gene set enrichment analysis with a context driven filtering strategy, selecting both genes and cells based on their functional relevance prior to communication inference. Applied to stage II colon cancer data, CellChat Hotspot enabled the identification of condition-specific interaction patterns associated with recurrence. Non recurrent patients showed enrichment of immune related processes, whereas recurrent cases were characterized by pathways associated with invasion and metastasis. Notably, a loss of interaction in the HSPG pathway between CALB1+ and stromal cells was observed in recurrent patients, suggesting a potential disruption of cell matrix adhesion mechanisms. To verify the reliability of this finding, we applied the framework to spatial transcriptomics data, which confirmed the presence of the HSPG2 DAG1 interaction in non-recurrent tumors and its near absence in recurrent ones. Overall, this framework provides a biologically guided strategy for studying intercellular communication in complex systems such as the tumor microenvironment.

bioinformatics↗
bioRxiv2026

SIFT: Syncmer-Informed Selection of Haplotypes for T2T Imputation

Genome patching improves the completeness of fragmented assemblies by filling unresolved gaps with sequences from reference genomes. Pangenome panels provide diverse candidate haplotypes for this task, but identifying suitable references efficiently becomes increasingly challenging as these panels grow. We present SIFT, a compressed indexing method for selecting reference haplotypes for genome patching with ImpuT2T. SIFT combines closed-syncmer parsing, phrase-level indexing, and pseudo-maximal exact match (pseudo-MEM) queries. Closed syncmers provide a context-independent parsing rule with bounded distances between consecutive selected positions, enabling consistent parsing of reference and query sequences. We demonstrate that two closed syncmers determine the distance at which they can occur consecutively in any string, so that equal substrings of two parses represent identical sequences and no gap sequence need be stored. SIFT indexes the reference parse and its reverse using run-length compressed suffix arrays and adapts the Boyer-Moore-Li search procedure to identify pseudo-MEMs between the reference parse and query parse. It then aggregates matching evidence to identify candidate reference haplotypes for downstream patching. This framework connects compressed sequence indexing with haplotype selection and provides a basis for querying large reference panels at the phrase level. SIFT is publicly available under the GNU license at https://github.com/EddieFerro/SIFT.

bioinformatics↗
bioRxiv2026

Assessing the Capacity of Genomic Language Models to Generate Informative Embeddings of Viral Genome Fragments

Genomic language models (gLMs) trained on large volumes of nucleotide sequences are becoming an alternative to classical methods in metagenomic analysis, particularly for studying genomic "dark matter". In this work, we investigate the ability of four gLMs (DNABERT-2, DNABERT-S, ViraLM, and Evo2-7B) to generate taxonomically informative vector representations of short viral genome fragments. We constructed a balanced reference dataset of viruses based on the ICTV Virus Metadata Resource and compared the representations generated by gLMs with conventional k-mer profiles and MinHash sketches using clustering and neighborhood-based metrics (adjusted Rand index (ARI), precision@k, and CROSS precision@k). On the reference dataset, three of the four gLMs outperformed the 4-mer profile in terms of ARI and precision@5 under the same evaluation protocol. The best performance was generally achieved by intermediate model layers. Conventional k-mer profiles consistently outperformed MinHash sketches. We further evaluated the methods on two viral orders (egoviruses and mriyaviruses) absent from the reference dataset, with model layers and k-mer lengths selected exclusively on the reference dataset. DNABERT-S showed the most consistently strong performance across these two orders, ranking first on mriyaviruses and second on egoviruses, while k-mer profiles with Jensen-Shannon distance remained competitive. We also observed the consistency of representations between forward fragments and their reverse complements. Overall, the best-performing gLMs surpassed conventional baselines, although their advantage depended on the dataset and evaluation metric. The consistently strong performance of DNABERT-S suggests a potential benefit of contrastive fine-tuning and indicates that larger models are not necessarily more effective for generating taxonomically informative representations.

bioinformatics↗