Author Correction: Structural basis for polyglutamate chain initiation and elongation by TTLL family enzymes.

Abstract:

:An amendment to this paper has been published and can be accessed via a link at the top of the paper.

journal_name

Nat Struct Mol Biol

authors

Mahalingan KK,Keith Keenan E,Strickland M,Li Y,Liu Y,Ball HL,Tanner ME,Tjandra N,Roll-Mecak A

doi

10.1038/s41594-020-0498-1

subject

Has Abstract

pub_date

2020-09-01 00:00:00

pages

870

issue

9

eissn

1545-9993

issn

1545-9985

pii

10.1038/s41594-020-0498-1

journal_volume

27

pub_type

已发布勘误
  • ERj1p uses a universal ribosomal adaptor site to coordinate the 80S ribosome at the membrane.

    abstract::Ribosomes translating secretory and membrane proteins are targeted to the endoplasmic reticulum membrane and attach to the protein-conducting channel and ribosome-associated membrane proteins (RAMPs). Recently, a new RAMP, ERj1p, has been identified that recruits BiP to ribosomes and regulates translational activity. ...

    journal_title:Nature structural & molecular biology

    pub_type: 杂志文章

    doi:10.1038/nsmb998

    authors: Blau M,Mullapudi S,Becker T,Dudek J,Zimmermann R,Penczek PA,Beckmann R

    更新日期:2005-11-01 00:00:00

  • Author Correction: Quantifying the dynamics of IRES and cap translation with single-molecule resolution in live cells.

    abstract::An amendment to this paper has been published and can be accessed via a link at the top of the paper. ...

    journal_title:Nature structural & molecular biology

    pub_type: 已发布勘误

    doi:10.1038/s41594-020-00531-z

    authors: Koch A,Aguilera L,Morisaki T,Munsky B,Stasevich TJ

    更新日期:2020-12-01 00:00:00

  • Cabin1 restrains p53 activity on chromatin.

    abstract::The tumor suppressor p53 has been proposed to bind target promoters upon genotoxic stress. However, recent evidence shows that p53 occupies some target promoters without such stress, suggesting that a negative regulator might render p53 transcriptionally inactive on these promoters. Here we show that calcineurin bindi...

    journal_title:Nature structural & molecular biology

    pub_type: 杂志文章

    doi:10.1038/nsmb.1657

    authors: Jang H,Choi SY,Cho EJ,Youn HD

    更新日期:2009-09-01 00:00:00

  • Crystal structure of the tubulin tyrosine carboxypeptidase complex VASH1-SVBP.

    abstract::The cyclic enzymatic removal and ligation of the C-terminal tyrosine of α-tubulin generates heterogeneous microtubules and affects their functions. Here we describe the crystal and solution structure of the tubulin carboxypeptidase complex between vasohibin (VASH1) and small vasohibin-binding protein (SVBP), which fol...

    journal_title:Nature structural & molecular biology

    pub_type: 杂志文章

    doi:10.1038/s41594-019-0254-6

    authors: Adamopoulos A,Landskron L,Heidebrecht T,Tsakou F,Bleijerveld OB,Altelaar M,Nieuwenhuis J,Celie PHN,Brummelkamp TR,Perrakis A

    更新日期:2019-07-01 00:00:00

  • Cation trafficking propels RNA hydrolysis.

    abstract::Catalysis by members of the RNase H superfamily of enzymes is generally believed to require only two Mg2+ ions that are coordinated by active-site carboxylates. By examining the catalytic process of Bacillus halodurans RNase H1 in crystallo, however, we found that the two canonical Mg2+ ions and an additional K+ faile...

    journal_title:Nature structural & molecular biology

    pub_type: 杂志文章

    doi:10.1038/s41594-018-0099-4

    authors: Samara NL,Yang W

    更新日期:2018-08-01 00:00:00

  • Structural basis for the recognition of N-end rule substrates by the UBR box of ubiquitin ligases.

    abstract::The N-end rule pathway is a regulated proteolytic system that targets proteins containing destabilizing N-terminal residues (N-degrons) for ubiquitination and proteasomal degradation in eukaryotes. The N-degrons of type 1 substrates contain an N-terminal basic residue that is recognized by the UBR box domain of the E3...

    journal_title:Nature structural & molecular biology

    pub_type: 杂志文章

    doi:10.1038/nsmb.1907

    authors: Choi WS,Jeong BC,Joo YJ,Lee MR,Kim J,Eck MJ,Song HK

    更新日期:2010-10-01 00:00:00

  • The E3 ligase RNF8 regulates KU80 removal and NHEJ repair.

    abstract::The ubiquitination cascade has a key role in the assembly of repair and signaling proteins at sites of double-strand DNA breaks. The E3 ubiquitin ligase RING finger protein 8 (RNF8) triggers the initial ubiquitination at double-strand DNA breaks, whereas sustained ubiquitination requires the downstream E3 ligase RING ...

    journal_title:Nature structural & molecular biology

    pub_type: 杂志文章

    doi:10.1038/nsmb.2211

    authors: Feng L,Chen J

    更新日期:2012-01-22 00:00:00

  • Tertiary interactions within the ribosomal exit tunnel.

    abstract::Although tertiary folding of whole protein domains is prohibited by the cramped dimensions of the ribosomal tunnel, dynamic tertiary interactions may permit folding of small elementary units within the tunnel. To probe this possibility, we used a beta-hairpin and an alpha-helical hairpin from the cytosolic N terminus ...

    journal_title:Nature structural & molecular biology

    pub_type: 杂志文章

    doi:10.1038/nsmb.1571

    authors: Kosolapov A,Deutsch C

    更新日期:2009-04-01 00:00:00

  • Structures of human DNA polymerases ν and θ expose their end game.

    abstract::Although the two B-family human DNA polymerases, pol δ and pol ε, are responsible for the bulk of nuclear genome replication, at least 14 additional polymerases have roles in nuclear DNA repair and replication. In this issue, newly reported crystal structures of two specialized A-family polymerases, pol δ and pol ε, e...

    journal_title:Nature structural & molecular biology

    pub_type: 评论,杂志文章

    doi:10.1038/nsmb.3006

    authors: Beard WA,Wilson SH

    更新日期:2015-04-01 00:00:00

  • Direct observation of the myosin-Va power stroke and its reversal.

    abstract::Complex forms of cellular motility, including cell division, organelle trafficking or signal amplification in the auditory system, require strong coordination of the myosin motors involved. The most basic mechanism of coordination is via direct mechanical interactions of individual motor heads leading to modification ...

    journal_title:Nature structural & molecular biology

    pub_type: 杂志文章

    doi:10.1038/nsmb.1820

    authors: Sellers JR,Veigel C

    更新日期:2010-05-01 00:00:00

  • Evidence for a group II intron-like catalytic triplex in the spliceosome.

    abstract::To catalyze pre-mRNA splicing, U6 small nuclear RNA positions two metals that interact directly with the scissile phosphates. U6 metal ligands correspond stereospecifically to metal ligands within the catalytic domain V of a group II self-splicing intron. Domain V ligands are organized by base-triple interactions, whi...

    journal_title:Nature structural & molecular biology

    pub_type: 杂志文章

    doi:10.1038/nsmb.2815

    authors: Fica SM,Mefford MA,Piccirilli JA,Staley JP

    更新日期:2014-05-01 00:00:00

  • Crystal structure of a non-neutralizing antibody to the HIV-1 gp41 membrane-proximal external region.

    abstract::The monoclonal antibody 13H11 shares part of its epitope in the HIV-1 gp41 membrane-proximal external region (MPER) with the rare, broadly neutralizing human antibody 2F5. Although 13H11 partially cross-blocked 2F5 binding, 13H11 is non-neutralizing and does not block 2F5 neutralization. We show that unlike 2F5, 13H11...

    journal_title:Nature structural & molecular biology

    pub_type: 杂志文章

    doi:10.1038/nsmb.1944

    authors: Nicely NI,Dennison SM,Spicer L,Scearce RM,Kelsoe G,Ueda Y,Chen H,Liao HX,Alam SM,Haynes BF

    更新日期:2010-12-01 00:00:00

  • Structure of a transcribing RNA polymerase II-DSIF complex reveals a multidentate DNA-RNA clamp.

    abstract::During transcription, RNA polymerase II (Pol II) associates with the conserved elongation factor DSIF. DSIF renders the elongation complex stable and functions during Pol II pausing and RNA processing. We combined cryo-EM and X-ray crystallography to determine the structure of the mammalian Pol II-DSIF elongation comp...

    journal_title:Nature structural & molecular biology

    pub_type: 杂志文章

    doi:10.1038/nsmb.3465

    authors: Bernecky C,Plitzko JM,Cramer P

    更新日期:2017-10-01 00:00:00

  • A metazoan ortholog of SpoT hydrolyzes ppGpp and functions in starvation responses.

    abstract::In nutrient-starved bacteria, RelA and SpoT proteins have key roles in reducing cell growth and overcoming stresses. Here we identify functional SpoT orthologs in metazoa (named Mesh1, encoded by HDDC3 in human and Q9VAM9 in Drosophila melanogaster) and reveal their structures and functions. Like the bacterial enzyme,...

    journal_title:Nature structural & molecular biology

    pub_type: 杂志文章

    doi:10.1038/nsmb.1906

    authors: Sun D,Lee G,Lee JH,Kim HY,Rhee HW,Park SY,Kim KJ,Kim Y,Kim BY,Hong JI,Park C,Choy HE,Kim JH,Jeon YH,Chung J

    更新日期:2010-10-01 00:00:00

  • Structure of an aprataxin-DNA complex with insights into AOA1 neurodegenerative disease.

    abstract::DNA ligases finalize DNA replication and repair through DNA nick-sealing reactions that can abort to generate cytotoxic 5'-adenylation DNA damage. Aprataxin (Aptx) catalyzes direct reversal of 5'-adenylate adducts to protect genome integrity. Here the structure of a Schizosaccharomyces pombe Aptx-DNA-AMP-Zn(2+) comple...

    journal_title:Nature structural & molecular biology

    pub_type: 杂志文章

    doi:10.1038/nsmb.2146

    authors: Tumbale P,Appel CD,Kraehenbuehl R,Robertson PD,Williams JS,Krahn J,Ahel I,Williams RS

    更新日期:2011-10-09 00:00:00

  • Human CWC22 escorts the helicase eIF4AIII to spliceosomes and promotes exon junction complex assembly.

    abstract::The exon-junction complex (EJC) functionally links splicing to subsequent mRNA localization, translation and stability. Sequence-independent binding of the EJC core to RNA is ensured by the DEAD-box helicase eIF4AIII. Here, we identified the splicing factor CWC22 as a new eIF4AIII partner in flies and humans. CWC22 co...

    journal_title:Nature structural & molecular biology

    pub_type: 杂志文章

    doi:10.1038/nsmb.2380

    authors: Barbosa I,Haque N,Fiorini F,Barrandon C,Tomasetto C,Blanchette M,Le Hir H

    更新日期:2012-10-01 00:00:00

  • Chromatin organization marks exon-intron structure.

    abstract::An increasing body of evidence indicates that transcription and splicing are coupled, and it is accepted that chromatin organization regulates transcription. Little is known about the cross-talk between chromatin structure and exon-intron architecture. By analysis of genome-wide nucleosome-positioning data sets from h...

    journal_title:Nature structural & molecular biology

    pub_type: 杂志文章

    doi:10.1038/nsmb.1659

    authors: Schwartz S,Meshorer E,Ast G

    更新日期:2009-09-01 00:00:00

  • Transcription promotes contraction of CAG repeat tracts in human cells.

    abstract::Induced transcription through CAG repeats in human cells increases repeat contraction approximately 15-fold in both confluent and proliferating cells. Repeats are stabilized against contraction by siRNA knockdown of MSH2, MSH3 or XPA, but not by knockdown of MSH6, XPC or FEN1. These results define a pathway for CAG.CT...

    journal_title:Nature structural & molecular biology

    pub_type: 杂志文章

    doi:10.1038/nsmb1042

    authors: Lin Y,Dion V,Wilson JH

    更新日期:2006-02-01 00:00:00

  • SR protein kinases promote splicing of nonconsensus introns.

    abstract::Phosphorylation of the spliceosome is essential for RNA splicing, yet how and to what extent kinase signaling affects splicing have not been defined on a genome-wide basis. Using a chemical genetic approach, we show in Schizosaccharomyces pombe that the SR protein kinase Dsk1 is required for efficient splicing of intr...

    journal_title:Nature structural & molecular biology

    pub_type: 杂志文章

    doi:10.1038/nsmb.3057

    authors: Lipp JJ,Marvin MC,Shokat KM,Guthrie C

    更新日期:2015-08-01 00:00:00

  • Let K-Ras activate its own inhibitor.

    abstract:: ...

    journal_title:Nature structural & molecular biology

    pub_type: 新闻

    doi:10.1038/s41594-018-0066-0

    authors: Statsyuk AV

    更新日期:2018-06-01 00:00:00

  • Computational redesign of protein-protein interaction specificity.

    abstract::We developed a 'computational second-site suppressor' strategy to redesign specificity at a protein-protein interface and applied it to create new specifically interacting DNase-inhibitor protein pairs. We demonstrate that the designed switch in specificity holds in in vitro binding and functional assays. We also show...

    journal_title:Nature structural & molecular biology

    pub_type: 杂志文章

    doi:10.1038/nsmb749

    authors: Kortemme T,Joachimiak LA,Bullock AN,Schuler AD,Stoddard BL,Baker D

    更新日期:2004-04-01 00:00:00

  • Defining the landscape of ATP-competitive inhibitor resistance residues in protein kinases.

    abstract::Kinases are involved in disease development and modulation of their activity can be therapeutically beneficial. Drug-resistant mutant kinases are valuable tools in drug discovery efforts, but the prediction of mutants across the kinome is challenging. Here, we generate deep mutational scanning data to identify mutant ...

    journal_title:Nature structural & molecular biology

    pub_type: 杂志文章

    doi:10.1038/s41594-019-0358-z

    authors: Persky NS,Hernandez D,Do Carmo M,Brenan L,Cohen O,Kitajima S,Nayar U,Walker A,Pantel S,Lee Y,Cordova J,Sathappa M,Zhu C,Hayes TK,Ram P,Pancholi P,Mikkelsen TS,Barbie DA,Yang X,Haq R,Piccioni F,Root DE,Johannes

    更新日期:2020-01-01 00:00:00

  • Publisher Correction: Tauopathies: Protein shapes at the core of chronic traumatic encephalopathy.

    abstract::An amendment to this paper has been published and can be accessed via a link at the top of the paper. ...

    journal_title:Nature structural & molecular biology

    pub_type: 已发布勘误

    doi:10.1038/s41594-019-0251-9

    authors: Fichou Y,Han S

    更新日期:2019-06-01 00:00:00

  • RNA secondary structure in mutually exclusive splicing.

    abstract::Mutually exclusive splicing is a regulated means to generate protein diversity, but the underlying mechanisms are poorly understood. Here comparative genome analysis revealed the built-in intronic elements for controlling mutually exclusive splicing of the 14-3-3ξ pre-mRNA. These elements are clade specific but are ev...

    journal_title:Nature structural & molecular biology

    pub_type: 杂志文章

    doi:10.1038/nsmb.1959

    authors: Yang Y,Zhan L,Zhang W,Sun F,Wang W,Tian N,Bi J,Wang H,Shi D,Jiang Y,Zhang Y,Jin Y

    更新日期:2011-02-01 00:00:00

  • Assembling the mitochondrial outer membrane.

    abstract::The general preprotein translocase of the outer mitochondrial membrane (TOM complex) transports virtually all mitochondrial precursor proteins, but cannot assemble outer-membrane precursors into functional complexes. A recently discovered sorting and assembly machinery (SAM complex) is essential for integration and as...

    journal_title:Nature structural & molecular biology

    pub_type: 杂志文章,评审

    doi:10.1038/nsmb852

    authors: Pfanner N,Wiedemann N,Meisinger C,Lithgow T

    更新日期:2004-11-01 00:00:00

  • A newly discovered function for RNase L in regulating translation termination.

    abstract::The antiviral and antiproliferative effects of interferons are mediated in part by the 2'-5' oligoadenylate-RNase L RNA decay pathway. RNase L is an endoribonuclease that requires 2'-5' oligoadenylates to cleave single-stranded RNA. In this report we present evidence demonstrating a role for RNase L in translation. We...

    journal_title:Nature structural & molecular biology

    pub_type: 杂志文章

    doi:10.1038/nsmb944

    authors: Le Roy F,Salehzada T,Bisbal C,Dougherty JP,Peltz SW

    更新日期:2005-06-01 00:00:00

  • Structural basis for selective activation of ABA receptors.

    abstract::Changing environmental conditions and lessening fresh water supplies have sparked intense interest in understanding and manipulating abscisic acid (ABA) signaling, which controls adaptive responses to drought and other abiotic stressors. We recently discovered a selective ABA agonist, pyrabactin, and used it to discov...

    journal_title:Nature structural & molecular biology

    pub_type: 杂志文章

    doi:10.1038/nsmb.1898

    authors: Peterson FC,Burgie ES,Park SY,Jensen DR,Weiner JJ,Bingman CA,Chang CE,Cutler SR,Phillips GN Jr,Volkman BF

    更新日期:2010-09-01 00:00:00

  • Structural basis for mRNA recognition by elongation factor SelB.

    abstract::In bacteria, incorporation of selenocysteine, the 21(st) amino acid, into proteins requires elongation factor SelB, which has the unusual property of binding to both transfer RNA (tRNA) and mRNA. SelB binds to an mRNA hairpin formed by the selenocysteine insertion sequence (SECIS) with extremely high specificity, the ...

    journal_title:Nature structural & molecular biology

    pub_type: 杂志文章

    doi:10.1038/nsmb890

    authors: Yoshizawa S,Rasubala L,Ose T,Kohda D,Fourmy D,Maenaka K

    更新日期:2005-02-01 00:00:00

  • EJC-independent degradation of nonsense immunoglobulin-mu mRNA depends on 3' UTR length.

    abstract::Inconsistent with prevailing models for nonsense-mediated mRNA decay (NMD) in mammals, the mRNA levels of immunoglobulin-mu (Ig-mu) genes with premature termination codons (PTCs) in the penultimate exon are still reduced by NMD when the intron furthest downstream is deleted. As in yeast, this exon junction complex-ind...

    journal_title:Nature structural & molecular biology

    pub_type: 杂志文章

    doi:10.1038/nsmb1081

    authors: Bühler M,Steiner S,Mohn F,Paillusson A,Mühlemann O

    更新日期:2006-05-01 00:00:00

  • Structure of a kinesin-tubulin complex and implications for kinesin motility.

    abstract::The typical function of kinesins is to transport cargo along microtubules. Binding of ATP to microtubule-attached motile kinesins leads to cargo displacement. To better understand the nature of the conformational changes that lead to the power stroke that moves a kinesin's load along a microtubule, we determined the X...

    journal_title:Nature structural & molecular biology

    pub_type: 杂志文章

    doi:10.1038/nsmb.2624

    authors: Gigant B,Wang W,Dreier B,Jiang Q,Pecqueur L,Plückthun A,Wang C,Knossow M

    更新日期:2013-08-01 00:00:00