Haizhong Zhu

发表

The catalytic inactivation of the N-half of human hexokinase 2 and structural and biochemical characterization of its mitochondrial conformation

Serdal Kirmizialtin, C. Carrasco-López, L. Nedyalkova, 2018, Bioscience reports.

Chromokinesins NOD and KID Use Distinct ATPase Mechanisms and Microtubule Interactions to Perform a Similar Function

Hee-won Park, W. Tempel, J. C. Cochran, 2019, bioRxiv.

Structural basis of small molecule ATPase inhibition of a human mitotic kinesin motor protein

R. Robinson, S. Endow, Hee-won Park, 2017, Scientific Reports.

Studies of a Ring-Cleaving Dioxygenase Illuminate the Role of Cholesterol Metabolism in the Pathogenesis of Mycobacterium tuberculosis

W. Jacobs, N. Strynadka, I. D'Angelo, 2009, PLoS pathogens.

Chromokinesins NOD and KID Use Distinct ATPase Mechanisms and Microtubule Interactions To Perform a Similar Function.

Hee-won Park, W. Tempel, J. C. Cochran, 2019, Biochemistry.

Identification and structure-based drug design of cell-active inhibitors of interleukin 17A at a novel C-terminal site

Justin D Dietrich, A. Petros, P. Richardson, 2022, Scientific Reports.

Turning a Substrate Peptide into a Potent Inhibitor for the Histone Methyltransferase SETD8.

A. Petros, Chaohong Sun, M. Vedadi, 2016, ACS medicinal chemistry letters.

Azaindole-Based Inhibitors of Cdc7 Kinase: Impact of the Pre-DFG Residue, Val 195.

K. Swinger, Eric F. Johnson, N. Soni, 2013, ACS medicinal chemistry letters.

A novel protein–mineral interface

Dominic J. B. Hunter, P. Sadler, M. Guo, 2003, Nature Structural Biology.

The Structural Basis for T-antigen Hydrolysis by Streptococcus pneumoniae

S. Withers, N. Strynadka, W. Wakarchuk, 2008, Journal of Biological Chemistry.

The EED protein-protein interaction inhibitor A-395 inactivates the PRC2 complex.

Jun Guo, Kenneth M Comess, Haizhong Zhu, 2017, Nature chemical biology.

Methylation-state-specific recognition of histones by the MBT repeat protein L3MBTL2

Randy J. Read, Matthieu Schapira, Abdellah Allali-Hassani, 2009, Nucleic acids research.

Structural basis of small molecule ATPase inhibition of a human mitotic kinesin motor protein

R. Robinson, S. Endow, Hee-won Park, 2017, Scientific Reports.

Structural Analysis of a Specialized Type III Secretion System Peptidoglycan-cleaving Enzyme*

B. Finlay, N. Strynadka, L. Worrall, 2015, The Journal of Biological Chemistry.

An intact SAM‐dependent methyltransferase fold is encoded by the human endothelin‐converting enzyme‐2 gene

A. Bochkarev, A. Plotnikov, P. Loppnau, 2009, Proteins.

Crystal Structures of the Tetratricopeptide Repeat Domains of Kinesin Light Chains: Insight into Cargo Recognition Mechanisms

F. Mackenzie, Y. Tong, Hee-won Park, 2012, PloS one.

Assembly of an oxo-zirconium(IV) cluster in a protein cleft.

Dominic J. B. Hunter, P. Sadler, M. Guo, 2004, Angewandte Chemie.

Ferric ion (hydr)oxo clusters in the “Venus flytrap” cleft of FbpA: Mössbauer, calorimetric and mass spectrometric studies

P. Sadler, P. Langridge-Smith, D. Campopiano, 2012, JBIC Journal of Biological Inorganic Chemistry.

Oxo-iron clusters in a bacterial iron-trafficking protein: new roles for a conserved motif.

Dominic J. B. Hunter, P. Sadler, D. Campopiano, 2003, The Biochemical journal.

Site-specific hydrolysis of horse heart cytochrome c and apocytochrome c promoted by palladium(II) complex

Long-gen Zhu, Dexu Zhu, Haizhong Zhu, 1999 .

SAR of amino pyrrolidines as potent and novel protein-protein interaction inhibitors of the PRC2 complex through EED binding.

Hongyu Zhao, Ying Wang, Zhiqin Ji, 2017, Bioorganic & medicinal chemistry letters.

The EED protein-protein interaction inhibitor A-395 inactivates the PRC2 complex.

Mikkel A. Algire, Justin D Dietrich, A. Petros, 2017, Nature chemical biology.

SAR of amino pyrrolidines as potent and novel protein-protein interaction inhibitors of the PRC2 complex through EED binding.

Mikkel A. Algire, Justin D Dietrich, P. Richardson, 2017, Bioorganic & medicinal chemistry letters.