SANCHEZ OLEA, ROBERTO

SANCHEZ OLEA, ROBERTO

CIENCIAS DE LA VIDA · Nivel 2

Desde 2007 es Professor en Autonomous University of San Luis Potosí

Información*

Nombre ROBERTO SANCHEZ OLEA
Área BIOLOGÍA Y QUÍMICA
Campo CIENCIAS DE LA VIDA
Disciplina BIOLOGÍA CELULAR
Especialidad GTPASAS
CVU 248190
Institución
Dependencia INSTITUTO DE FISICA
Entidad SAN LUIS POTOSI
Nivel 2
Vigencia Inicio: 01/01/2023
Fin: 31/12/2027

* Información del primer trimestre de 2026.
Fuente: SECIHTI.

Publicaciones ORCID

2025
Characterization of the carboxy‐terminal domain of the GPN‐loop GTPase Npa3 reveals an intrinsically disordered region and phosphorylation‐dependent regulation in the absence of BUD27 The FEBS Journal
Proposal of Chemical Inhibitors That Compete with the Binding of RNA Polymerase II Subunits to Essential GTPases GPN Npa3 and Gpn1 ACS Omega
2022
Synthetic negative genome screen of the GPN-loop GTPase NPA3 in Saccharomyces cerevisiae Current Genetics
2019
FRET‐based analysis and molecular modeling of the human GPN-loop GTPases 1 and 3 heterodimer unvelis a dominant-negative protein complex The FEBS Journal
Gpn3 Is Essential for Cell Proliferation of Breast Cancer Cells Independent of Their Malignancy Degree Technology in Cancer Research & Treatment
2017
Gpn3 is polyubiquitinated on lysine 216 and degraded by the proteasome in the cell nucleus in a Gpn1-inhibitable manner FEBS Letters
The Gpn3 Q279* cancer-associated mutant inhibits Gpn1 nuclear export and is deficient in RNA polymerase II nuclear targeting FEBS Letters
Human Gpn1 purified from bacteria binds guanine nucleotides and hydrolyzes GTP as a protein dimer stabilized by its C-terminal tail Protein Expression and Purification
Npa3/ Sc Gpn1 carboxy-terminal tail is dispensable for cell viability and RNA polymerase II nuclear targeting but critical for microtubule stability and function Biochimica et Biophysica Acta (BBA) - Molecular Cell Research
2014
Gpn1 and Gpn3 associate tightly and their protein levels are mutually dependent in mammalian cells FEBS Letters