Evidence map›Paper›PMID 40875922›Full record

ArticleJournal of chemical theory and computation2025

Identification of Protein Cryptic Sites via Conformational Dynamics Capturing and Water-Based Pocket Characterization in Molecular Dynamics Simulations.

Tianming Qu, Steven L Austin, Lianqing Zheng, James Zhang, Wei Yang

Abstract read
In one paragraph

Article in Journal of chemical theory and computation, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Tianming QuDepartment of Chemistry and Biochemistry, Florida State University, 95 Chieftan Way Room 118, Tallahassee, Florida 32306, United States.ORCID 0009-0009-1618-1727
Steven L AustinInstitute of Molecular Biophysics, Florida State University, 91 Chieftan Way 101 KLB, Tallahassee, Florida 32306, United States.
Lianqing ZhengInstitute of Molecular Biophysics, Florida State University, 91 Chieftan Way 101 KLB, Tallahassee, Florida 32306, United States.
James ZhangInstitute of Molecular Biophysics, Florida State University, 91 Chieftan Way 101 KLB, Tallahassee, Florida 32306, United States.ORCID 0009-0002-7743-7748
Wei YangDepartment of Chemistry and Biochemistry, Florida State University, 95 Chieftan Way Room 118, Tallahassee, Florida 32306, United States.ORCID 0000-0002-4520-3253

Funding

New Generation of General AMBER Force Field for Biomedical ResearchR01GM147673 · NIGMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI WANG, JUNMEI, YANG, WEI · 2022 to 2025
$1.5M
Free Energy Sampling of Long-Timescale Biomolecular DynamicsR01GM124621 · NIGMS · FLORIDA STATE UNIVERSITY · PI YANG, WEI · 2020 to 2023
$1.4M
NIGMS NIH HHS R01 GM124621NIGMS NIH HHS R01 GM147673
6 · The paper itself

Abstract

Employing molecular dynamics (MD) simulation to study the formation of novel protein cryptic sites has attracted increasing interest in the field of drug discovery. One specific challenge in this area is finding a viable method to accurately identify and characterize cryptic site transitions from MD simulation results while minimizing the need for extensive human input. Since the formation of cryptic sites often involves significant conformational changes in the protein structure, a method capable of capturing and describing these dynamic pocket transitions with precision is essential. In this paper, we present a new procedure, Conformational Dynamics Capturing and Water-Based Characterization (CDC-WBC). This procedure dynamically identifies the cryptic site region by tracking protein conformational changes observed during molecular dynamics (MD) simulations. The procedure also incorporates water density information to enhance the characterization of cryptic sites across frames. We evaluate the CDC-WBC procedure by applying it to characterize the opening process of the two well-studied cryptic sites in TEM1 β-lactamase. The results demonstrate that the CDC-WBC method accurately captures the open-closed transitions of the two cryptic sites. For comparison, three commonly used protein cavity detection methods in cryptic sites studies, POVME2, Epock, and MDpocket, are applied to identify the "CBT" cryptic site in TEM1 β-lactamase. The results show that the CDC-WBC method outperforms these methods in characterizing the transitions of the "CBT" cryptic site. Additionally, using a benchmark set of 84 protein systems (93 cryptic pockets) from the CryptoSite data set, CDC-WBC consistently shows better performance in distinguishing between the open and closed states of cryptic sites, further highlighting its capability for precise characterization of dynamic cryptic site transitions. The detailed implementation of the CDC-WBC procedure and demo data sets are uploaded to GitHub: https://github.com/TianmingQu/CDC-WBC.git.

Indexed as

beta-LactamasesMolecular Dynamics SimulationWaterProtein Conformationbeta-Lactamasesbeta-lactamase TEM-1Water

Identifiers

PMID40875922
PMCPMC12435771

What Socratic holds

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.