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S

S. Terzyan

State University System of Florida

H指数:26

被引数:2,743

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Design and evaluation of novel analogs of 2-amino-4-boronobutanoic acid (ABBA) as inhibitors of human gamma-glutamyl transpeptidase

设计和评估新型2-氨基-4-硼代丁酸 (ABBA) 类似物作为人 γ-谷氨酰转肽酶的抑制剂

BIOORGANIC & MEDICINAL CHEMISTRY

IF3

2022-11-013

OAAI

SARS-CoV-2 main protease inhibitory efficacy of natural peptidic α-hydroxy amides for therapeutic applications of COVID-19

IF4.2

2021-05-140

OA

Crystal structures of glutathione- and inhibitor-bound human GGT1: critical interactions within the cysteinylglycine binding site

JOURNAL OF BIOLOGICAL CHEMISTRY

IF3.9

2021-01-0110

OAAI

Discovery and Development of a Novel mPGES-1/5-LOX Dual Inhibitor LFA-9 for Prevention and Treatment of Chronic Inflammatory Diseases

inflammation research

IF4.1

2020-12-018

OA

Structural basis of resistance of mutant RET protein-tyrosine kinase to its inhibitors nintedanib and vandetanib

突变型RET蛋白酪氨酸激酶对其抑制剂nintedanib和vandetanib抗性的结构基础

JOURNAL OF BIOLOGICAL CHEMISTRY

IF3.9

2019-07-0144

OAAI

Glycan Bound to the Selectin Low Affinity State Engages Glu-88 to Stabilize the High Affinity State under Force

JOURNAL OF BIOLOGICAL CHEMISTRY

IF3.9

2017-02-0135

OAAI

Depleting cysteine: A novel approach to tumor therapy

CANCER RESEARCH

IF16.6

2015-08-011

PRE

Human γ-Glutamyl Transpeptidase 1 STRUCTURES OF THE FREE ENZYME, INHIBITOR-BOUND TETRAHEDRAL TRANSITION STATES, AND GLUTAMATE-BOUND ENZYME REVEAL NOVEL MOVEMENT WITHIN THE ACTIVE SITE DURING CATALYSIS

JOURNAL OF BIOLOGICAL CHEMISTRY

IF3.9

2015-07-0155

OAAI

Sensitizing tumors to pro-oxidant therapy by inhibiting gamma-glutamyl transpeptidase

CANCER RESEARCH

IF16.6

2014-10-011

PRE

Inhibition of human γ-glutamyl transpeptidase: development of more potent, physiologically relevant, uncompetitive inhibitors

抑制人类 γ-谷氨酰转肽酶: 开发更有效，生理相关，无竞争性的抑制剂

BIOCHEMICAL JOURNAL

IF4.3

2013-02-2833

OAAI

Structure-Based Design of Highly Selective β-Secretase Inhibitors: Synthesis, Biological Evaluation, and Protein-Ligand X-ray Crystal Structure

JOURNAL OF MEDICINAL CHEMISTRY

IF6.8

2012-09-0634

OA

Putative sequences on Ro60 three-dimensional structure accessible for 4-hydroxy-2-nonenal (HNE) modification compared to in vitro HNE modification of Ro60 sequences

MOLECULAR IMMUNOLOGY

IF3

2012-04-013

OAAI

Inhibition of anthrax lethal factor: lability of hydroxamate as a chelating group

APPLIED MICROBIOLOGY AND BIOTECHNOLOGY

IF4.3

2012-01-2510

OAAI

Structure of the APPL1 BAR-PH domain and characterization of its interaction with Rab5

IF8.3

2007-06-21128

OAAI

Comparison of cytochromes b5 from insects and vertebrates

PROTEINS-STRUCTURE FUNCTION AND BIOINFORMATICS

IF2.8

2007-02-1321

PREAI

Crystal structure of a glycosylated Fab from an IgM cryoglobulin with properties of a natural proteolytic antibody

BIOCHEMICAL JOURNAL

IF4.3

2006-04-1149

OAAI

Structural basis of Rab5-Rabaptin5 interaction in endocytosis

NATURE STRUCTURAL & MOLECULAR BIOLOGY

IF10.1

2004-09-19118

PREAI

Characterization of Lys-698 to Met substitution in human plasminogen catalytic domain

PROTEINS-STRUCTURE FUNCTION AND BIOINFORMATICS

IF2.8

2004-05-2010

PREAI

L-arginine nitrates

JOURNAL OF MOLECULAR STRUCTURE

IF4.7

2004-01-0145

PREAI

Crystal structure of GGA2 VHS domain and its implication in plasticity in the ligand binding pocket

IF3

2003-02-0828

PREAI