Author

Cong Liu

Broad InstituteORCID 0000-0002-1687-2220Unclaimed ORCID profile · follow to get notified of new preprints

Additional preprints under this name without ORCID

Cong Liu3 papers · Okinawa Institute of Science and Technology Graduate University

Biology Disciplines

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Microbiology· 2 Biochemistry· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:experimental assay· 2 Assay:proteomics· 2 Research Focus:cell signaling & trafficking· 1 Assay:cryo-EM· 1 Approach:deep learning· 1 Research Focus:drug response / drug discovery· 1 Research Focus:host-pathogen & immune response· 1

Frequent Co-Authors

Amy E. KeatingiD· 1 shared Austin N. BondiD· 1 shared Biswajit DasiD· 1 shared Chenggong JiiD· 1 shared Daniel LimiD· 1 shared Deborah Tan HungiD· 1 shared Diana K. HuntiD· 1 shared Donald M. CoeniD· 1 shared

Activity by Year

2025-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 12 mutual co-author links

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1 shared paperBiochemistry

Amy E. KeatingORCID

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3 papers

Recent·Most cited

BiochemistrybioRxivPreprintSep 10, 2026

A proteome-wide biochemical screen defines binding determinants of the core autophagy protein LC3B

Jennifer Kosmatka, Cong Liu, Jackson C. Halpin…·Amy E. Keating

The paper screens a proteome-wide peptide library to identify LC3B binding determinants, revealing exceptions to the canonical LIR motif and highlighting sequence features that influence binding affinity and specificity.

3 citations

humanproteomics

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MicrobiologyACS Infectious DiseasesPeer-reviewedMay 13, 2026

Large-Scale Chemical-Genetic Interaction Profiling Identifies a Novel Small-Molecule Inhibitor of Mycobacterium tuberculosis Polyketide Synthase 13

James E. Gomez, Matthew Y. Solomon, Diana K. Hunt…·Deborah Tan Hung

This paper identifies a novel small-molecule inhibitor of Mycobacterium tuberculosis Pks13 through chemical-genetic interaction profiling and validates its mechanism of action.

DOI 10.1021/acsinfecdis.6c00136

humanproteomics

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MicrobiologyCellPeer-reviewedDec 29, 2025

Mechanisms of HSV-1 helicase-primase inhibition and replication fork complex assembly

Zishuo Yu, Pradeep Sathyanarayana, Cong Liu…·Jonathan Abraham

This study determines the structure of HSV-1 helicase-primase inhibited by HPIs and reveals how it interacts with the replication fork complex.

10 citationstop 2%

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