Author

Eric Z. Pang

University of California, Los AngelesORCID 0000-0002-9035-7016Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Biochemistry· 2

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 2 Research Focus:chromatin & epigenetic regulation· 2 Approach:experimental assay· 2 Research Focus:protein folding & dynamics· 2 Assay:cryo-EM· 1 Organism:human· 1 Approach:microscopy & imaging analysis· 1 Assay:proteomics· 1

Frequent Co-Authors

Bashir A. AliiD· 1 shared Boyu ZhaoiD· 1 shared Brooke M. GardneriD· 1 shared Cameron FlowersiD· 1 shared Chris D. RichardsoniD· 1 shared Connor J. SheedyiD· 1 shared Elizabeth OroudjevaiD· 1 shared James Akira WohlschlegeliD· 1 shared

Activity by Year

2025-2025 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperBiochemistry

Bashir A. AliORCID

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2 papers

Recent·Most cited

Structural basis for L-isoaspartyl-containing protein recognition by the PCMTD1 cullin-RING E3 ubiquitin ligase

Eric Z. Pang, Boyu Zhao, Cameron Flowers, Elizabeth Oroudjeva, Jasmine B. Winter, Vijaya Pandey, Michael R. Sawaya, James Akira Wohlschlegel, Joseph A. Loo, José A. Rodríguez, Steven Gerard Clarke

This paper shows PCMTD1, a cullin-RING ligase, recognizes L-isoaspartyl residues and targets damaged proteins for ubiquitylation and degradation.

Journal of Biological Chemistry · Sep 19, 2025Peer-reviewedBiochemistry

PEX1G843D remains functional in peroxisome biogenesis but is rapidly degraded by the proteasome

Connor J. Sheedy, Soham P. Chowdhury, Bashir A. Ali, Julia Miyamoto, Eric Z. Pang, Julien Bacal, Katherine U. Tavasoli, Chris D. Richardson, Brooke M. Gardner

This study shows that the PEX1G843D mutation impairs PEX1/PEX6 assembly and leads to proteasomal degradation, but overexpression can restore peroxisome function.

Journal of Biological Chemistry · Mar 31, 2025Peer-reviewedBiochemistry