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The G-patch activators Pfa1 and PINX1 exhibit different modes of interaction with the Prp43 RNA helicase

RNA biology, 2021-04, Vol.18 (4), p.510-522

2021

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The Npa1p complex chaperones the assembly of the earliest eukaryotic large ribosomal subunit precursor

PLoS genetics, 2018-08, Vol.14 (8), p.e1007597-e1007597

2018

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Association of snR190 snoRNA chaperone with early pre-60S particles is regulated by the RNA helicase Dbp7 in yeast

Nature communications, 2021-10, Vol.12 (1), p.6153-6153, Article 6153

2021

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The DEAD-box protein Dbp6 is an ATPase and RNA annealase interacting with the peptidyl transferase center (PTC) of the ribosome

Nucleic acids research, 2023-01, Vol.51 (2), p.744

2023

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Prp43p contains a processive helicase structural architecture with a specific regulatory domain

The EMBO journal, 2010-07, Vol.29 (13), p.2194-2204

2010

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The ATPase and helicase activities of Prp43p are stimulated by the G-patch protein Pfa1p during yeast ribosome biogenesis

The EMBO journal, 2009-12, Vol.28 (24), p.3808-3819

2009

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Functional link between DEAH/RHA helicase Prp43 activation and ATP base binding

Nucleic acids research, 2017-02, Vol.45 (3), p.1539

2017

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The telomerase inhibitor Gno1p/PINX1 activates the helicase Prp43p during ribosome biogenesis

Nucleic acids research, 2014-06, Vol.42 (11), p.7330

2014

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Phylogenetic Diversity of Lhr Proteins and Biochemical Activities of the Thermococcales aLhr2 DNA/RNA Helicase

Biomolecules (Basel, Switzerland), 2021-06, Vol.11 (7), p.950

2021

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Cbf5p, the putative pseudouridine synthase of H/ACA-type snoRNPs, can form a complex with Gar1p and Nop10p in absence of Nhp2p and box H/ACA snoRNAs

RNA (Cambridge), 2004-11, Vol.10 (11), p.1704-1712

2004

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Analysis of the binding of the N-terminal conserved domain of yeast Cbf5p to a box H/ACA snoRNA

RNA (Cambridge), 2006-10, Vol.12 (10), p.1868-1882

2006

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Agonist-induced signaling and trafficking of the μ-opioid receptor: role of serine and threonine residues in the third cytoplasmic loop and C-terminal domain

FEBS letters, 1997-09, Vol.415 (2), p.200-205

1997

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Identification in the μ-opioid receptor of cysteine residues responsible for inactivation of ligand binding by thiol alkylating and reducing agents

FEBS letters, 1997-05, Vol.408 (2), p.135-140

1997

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Implication of the First and Third Extracellular Loops of the μ‐Opioid Receptor in the Formation of the Ligand Binding Site: A Study Using Chimeric μ‐Opioid/Angiotensin Receptors

Journal of neurochemistry, 1998-05, Vol.70 (5), p.2106-2111

1998

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Ionic and energetic changes at competence in the naturally transformable bacterium Streptococcus pneumoniae

Journal of general microbiology, 1989-08, Vol.135 (8), p.2189

1989

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The G-patch activators Pfa1 and PINX1 exhibit different modes of interaction with the Prp43 RNA helicase

The Npa1p complex chaperones the assembly of the earliest eukaryotic large ribosomal subunit precursor

Association of snR190 snoRNA chaperone with early pre-60S particles is regulated by the RNA helicase Dbp7 in yeast

The DEAD-box protein Dbp6 is an ATPase and RNA annealase interacting with the peptidyl transferase center (PTC) of the ribosome

Prp43p contains a processive helicase structural architecture with a specific regulatory domain

The ATPase and helicase activities of Prp43p are stimulated by the G-patch protein Pfa1p during yeast ribosome biogenesis

Functional link between DEAH/RHA helicase Prp43 activation and ATP base binding

The telomerase inhibitor Gno1p/PINX1 activates the helicase Prp43p during ribosome biogenesis

Phylogenetic Diversity of Lhr Proteins and Biochemical Activities of the Thermococcales aLhr2 DNA/RNA Helicase

Cbf5p, the putative pseudouridine synthase of H/ACA-type snoRNPs, can form a complex with Gar1p and Nop10p in absence of Nhp2p and box H/ACA snoRNAs

Analysis of the binding of the N-terminal conserved domain of yeast Cbf5p to a box H/ACA snoRNA

Agonist-induced signaling and trafficking of the μ-opioid receptor: role of serine and threonine residues in the third cytoplasmic loop and C-terminal domain

Identification in the μ-opioid receptor of cysteine residues responsible for inactivation of ligand binding by thiol alkylating and reducing agents

Implication of the First and Third Extracellular Loops of the μ‐Opioid Receptor in the Formation of the Ligand Binding Site: A Study Using Chimeric μ‐Opioid/Angiotensin Receptors

Ionic and energetic changes at competence in the naturally transformable bacterium Streptococcus pneumoniae

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