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| Open AccessVisualizing active membrane protein complexes by electron cryotomography
Few tools are available to identify active membrane proteins within their native lipid environment. Here, Gold et al. report on a strategy that can be used for site-specific labelling of membrane proteins via electron cryotomography.
- Vicki A.M. Gold
- , Raffaele Ieva
- & Werner Kühlbrandt
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The palindromic DNA-bound USP/EcR nuclear receptor adopts an asymmetric organization with allosteric domain positioning
Nuclear receptors use DNA- and ligand-binding to regulate gene expression. Here, Maletta et al. report the first structural description of a full inverted repeat-bound nuclear receptor complex, which shows that the protein structure is asymmetric, despite the symmetry of the bound DNA.
- Massimiliano Maletta
- , Igor Orlov
- & Bruno P. Klaholz
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HOP2-MND1 modulates RAD51 binding to nucleotides and DNA
The HOP2-MND1 heterodimer is essential for homologous recombination. Here, Bugreev et al. analyse its mechanism of action in vitroand show that HOP2-MND1 stabilizes an active conformation of Rad51, thus triggering DNA strand exchange.
- Dmitry V. Bugreev
- , Fei Huang
- & Alexander V. Mazin
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X-ray structure of a CDP-alcohol phosphatidyltransferase membrane enzyme and insights into its catalytic mechanism
The CDP-alcohol phosphatidyltransferase family is involved in phospholipid biosynthesis. Here, Nogly et al.report the crystal structure of a bifunctional enzyme from this family, show that magnesium is required for enzymatic activity, and propose a structure-based catalytic mechanism.
- Przemyslaw Nogly
- , Ivan Gushchin
- & Margarida Archer
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Evidence for an electrostatic mechanism of force generation by the bacteriophage T4 DNA packaging motor
Viral DNA packaging motors must generate large forces to package the viral capsid. Here, Migliori et al.provide functional and computational evidence that electrostatic interactions between subdomains of the T4 packaging motor provide the driving force for DNA packaging.
- Amy D. Migliori
- , Nicholas Keller
- & Douglas E. Smith
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Structural basis for catalysis in a CDP-alcohol phosphotransferase
The transfer of a phosphate group from a CDP-linked donor to an acceptor alcohol is catalysed by CDP-alcohol phosphotransferases. Here, Sciara et al. report crystal structures of a CDP-alcohol phosphotransferase, define roles of conserved residues and propose a mechanism of action for this protein family.
- Giuliano Sciara
- , Oliver B. Clarke
- & Filippo Mancia
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Steric hindrance between S4 and S5 of the KCNQ1/KCNE1 channel hampers pore opening
KCNQ1 is a voltage-gated K+channel and gating is modulated by auxiliary subunit KCNE proteins. Here, Nakajo and Kubo identify KCNQ1 phenylalanine residues in the voltage sensor and pore domains that are responsible for the gating modulation by KCNE1.
- Koichi Nakajo
- & Yoshihiro Kubo
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Correlated motions are a fundamental property of β-sheets
Functional changes in protein structures are involved in a large number of biochemical processes. Here, the authors perform a simulation study of known protein structures to show how β-sheets possess the ability to facilitate concerted backbone motions.
- R. Bryn Fenwick
- , Laura Orellana
- & Xavier Salvatella
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Targeting Mycobacterium tuberculosis nucleoid-associated protein HU with structure-based inhibitors
Histone-like HU proteins play roles in chromatin architecture and DNA-dependent processes in bacteria. Here, the authors describe the crystal structure of the DNA-binding domain of HU from Mycobacterium tuberculosis, and show that the pathogen’s growth can be inhibited using HU-targeting small molecules.
- Tuhin Bhowmick
- , Soumitra Ghosh
- & Valakunja Nagaraja
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Visualization of a polytopic membrane protein during SecY-mediated membrane insertion
Membrane protein topogenesis is not fully understood, although the path that proteins take through the ribosome and Sec-complex has been described. Here, Bischoff et al.present the structure of a ribosome-SecY complex containing an intermediate of proteorhodopsin, which provides further insight into this topogenesis.
- Lukas Bischoff
- , Stephan Wickles
- & Roland Beckmann
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Structural analysis of atovaquone-inhibited cytochrome bc1 complex reveals the molecular basis of antimalarial drug action
Atovaquone is an antimalarial drug that inhibits a crucial enzyme, cytochrome bc1complex, within the parasite’s mitochondria. Here the authors report the crystal structure of the enzyme with bound atovaquone, opening the way for rational development of improved antimalarial drugs.
- Dominic Birth
- , Wei-Chun Kao
- & Carola Hunte
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Direct observation of the three regions in α-synuclein that determine its membrane-bound behaviour
α-synuclein is a protein whose aberrant aggregation is associated with Parkinson’s disease. Here, Fusco et al.characterize α-synuclein bound to lipid membranes using a combination of solution and solid-state NMR spectroscopy and provide insights into the molecular processes associated with the aggregation of this protein.
- Giuliana Fusco
- , Alfonso De Simone
- & Gianluigi Veglia
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| Open AccessThe full-length cell–cell fusogen EFF-1 is monomeric and upright on the membrane
Cell–cell fusion in Caenorhabditis elegans is mediated by EFF-1 and AFF-1 proteins. Here, the authors present an electron cryomicroscopy 3D reconstruction of EFF-1 in the membrane, and combine snapshots of membrane fusion in vitrowith a recently reported crystal structure to propose a mechanism for the fusion process.
- Tzviya Zeev-Ben-Mordehai
- , Daven Vasishtan
- & Kay Grünewald
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Article
| Open AccesseIF2B is a decameric guanine nucleotide exchange factor with a γ2ε2 tetrameric core
Eukaryotic Initiation Factor 2 (eIF2) initiates protein synthesis aided by its partner eIF2B, which stimulates guanine nucleotide exchange on eIF2. Here, Gordiyenko et al. show that eIF2B exists as a decamer and propose a model for its subunit arrangement that provides new insight into its function.
- Yuliya Gordiyenko
- , Carla Schmidt
- & Carol V. Robinson
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Structural basis for histone mimicry and hijacking of host proteins by influenza virus protein NS1
The influenza A H3N2 subtype protein NS1 possesses a short sequence resembling the N-terminal tail of histone H3 that is used to hijack host proteins. Here, Qin et al.establish the structural basis for the imperfect NS1 mimicry, which allows the virus to target only a subset of chromatin interactors.
- Su Qin
- , Yanli Liu
- & Jinrong Min
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Structural basis of PcsB-mediated cell separation in Streptococcus pneumoniae
The peptidoglycan hydrolase PcsB is required for cell wall splitting during cell division in Streptococci. Bartual et al.show that PcsB adopts an autoinhibited dimeric structure, and demonstrate the muralytic activity of the uninhibited catalytic domain.
- Sergio G. Bartual
- , Daniel Straume
- & Juan A. Hermoso
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Single-vesicle architecture of synaptobrevin2 in astrocytes
The astrocytic vesicular protein, synaptobrevin2 (Sb2), is implicated in neurotransmitter release, but its vesicular arrangement is poorly understood. Here, Singh et al. use super-resolution fluorescence microscopy to show that the total number of endogenous Sb2 molecules per vesicle is ≤25.
- Priyanka Singh
- , Jernej Jorgačevski
- & Robert Zorec
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| Open AccessThe malaria parasite egress protease SUB1 is a calcium-dependent redox switch subtilisin
In the malarial parasitophorous vacuole, the serine protease SUB1 processes parasite proteins that are required for release from host cells and invasion. Here, the authors report the first crystallographic structure of SUB1 in complex with its cognate prodomain revealing its substrate interactions and providing insight into its regulation.
- Chrislaine Withers-Martinez
- , Malcolm Strath
- & Michael J. Blackman
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Functional and molecular features of the calmodulin-interacting protein IQCG required for haematopoiesis in zebrafish
NUP98–IQCG is a fusion protein found in acute leukaemia that functions as a regulator of transcriptional expression. Here, Chen et al. investigate IQCG-mediated calcium signalling in haematopoiesis, and propose a model where IQCG can store calmodulin, which once released, activates CaM-dependent kinase IV.
- Li-Ting Chen
- , Wen-Xue Liang
- & Sai-Juan Chen
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Mutations in the PQBP1 gene prevent its interaction with the spliceosomal protein U5–15kD
Frameshift mutations in the protein polyglutamine tract-binding protein 1 (PQBP1) are believed to cause X-linked mental retardation. Here, Mizuguchi et al.present the crystal structure of a C-terminal fragment of PQBP1 in complex with the spliceosomal protein U5–15kD, and show details of this interaction that can lead to mechanistic insights into the disease.
- Mineyuki Mizuguchi
- , Takayuki Obita
- & Hitoshi Okazawa
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Protein conformational dynamics dictate the binding affinity for a ligand
The binding affinity of a protein for its ligand is governed by the rates of ligand association and dissociation. Here the authors show that intrinsic conformational dynamics of maltose binding protein dictate the ligand dissociation rate, and hence the affinity of the protein for maltose.
- Moon-Hyeong Seo
- , Jeongbin Park
- & Hak-Sung Kim
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Crystal structure of listeriolysin O reveals molecular details of oligomerization and pore formation
The cytolysin, listeriolysin O (LLO), is expressed by Listeria and forms pores in the phagosomal membrane in response to decreased pH. Here, Yildiz et al. solve the crystal structure of LLO, identify residues that serve as the pH sensor, and determine the mechanism of pore formation in host membranes.
- Stefan Köster
- , Katharina van Pee
- & Özkan Yildiz
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Article
| Open AccessMolecular architecture and the structural basis for anion interaction in prestin and SLC26 transporters
Prestin is an anion transporter-like protein in the mammalian inner ear that amplifies sound-induced vibration by voltage-driven structural rearrangements. Here, Gorbunov et al. show that this electromechanical activity is controlled by the binding of anions to a central cavity within the protein core.
- Dmitry Gorbunov
- , Mattia Sturlese
- & Dominik Oliver
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Structural basis for oligomerization of auxin transcriptional regulators
The transcriptional effects of auxin signalling are mediated by auxin response factors (ARFs) that interact with inhibitory IAA proteins. Nanao et al.present the crystal structure of domain III/IV of ARF5, revealing the structural basis for its interaction with IAAs and its potential to trigger ARF5 oligomerization.
- Max H. Nanao
- , Thomas Vinos-Poyo
- & Renaud Dumas
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An alternate binding site for PPARγ ligands
The nuclear receptor PPARγ regulates insulin sensitivity and is the molecular target of anti-diabetic drugs. Here, Hughes et al. show demonstrate binding of synthetic PPARγ agonists to a previously unknown binding site within PPARγ and show this affects structure and function of the receptor.
- Travis S. Hughes
- , Pankaj Kumar Giri
- & Douglas J. Kojetin
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Article
| Open AccessMolecular insights into the membrane-associated phosphatidylinositol 4-kinase IIα
Type II PI4-kinase dysfunction is associated with diseases including cancer and Alzheimer's disease; however, the development of specific modulators has been hampered by a lack of structural information. Zhou et al. present the crystal structure of PI4KIIα in its ADP-bound form, providing insight into its regulation.
- Qiangjun Zhou
- , Jiangmei Li
- & Chang Chen
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Article
| Open AccessThe structure and substrate specificity of human Cdk12/Cyclin K
Cyclin-dependent kinase 12 (Cdk12) phosphorylates the C-terminal domain (CTD) of RNA polymerase II to regulate transcription. Here, the authors solve the crystal structure of the Cdk12 kinase domain and show that Cdk12 has its highest activity on a CTD substrate that carries a serine 7 phosphorylation.
- Christian A. Bösken
- , Lucas Farnung
- & Matthias Geyer
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60S ribosome biogenesis requires rotation of the 5S ribonucleoprotein particle
Our understanding of ribosome biogenesis is limited by a lack of structural knowledge of assembly intermediates. Here, Leidig et al.report a high-resolution cryo-EM structure of a pre-60S particle that suggests that substantial rearrangements of the 5S RNP are required during ribosome maturation.
- Christoph Leidig
- , Matthias Thoms
- & Roland Beckmann
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Molecular basis for erythromycin-dependent ribosome stalling during translation of the ErmBL leader peptide
In bacteria, the ribosomal stalling during translation of leader peptides is a mechanism of antibiotic resistance that has not been well understood. Here, the structure of a drug-dependent stalled ribosome complex has allowed the authors to propose a detailed mechanism for this translational arrest.
- Stefan Arenz
- , Haripriya Ramu
- & Daniel N. Wilson
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Quantitative live-cell imaging reveals spatio-temporal dynamics and cytoplasmic assembly of the 26S proteasome
The 26S proteasome is assembled in several steps, however the extent to which this assembly occurs before or after transport into the nucleus remains unclear. Pack et al.show that full assembly can occur in the cytoplasm, and that a concatameric form of the fully assembled complex is a substrate for nuclear import.
- Chan-Gi Pack
- , Haruka Yukii
- & Yasushi Saeki
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Activation pathway of Src kinase reveals intermediate states as targets for drug design
Activation of c-src kinase is associated with uncontrolled growth and metastasis of tumour cells. Shukla et al.model conformational changes in c-src during activation, and identify an allosteric site in an intermediate state that may provide a target for small molecule therapeutics.
- Diwakar Shukla
- , Yilin Meng
- & Vijay S. Pande
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Differential affinity of FLIP and procaspase 8 for FADD’s DED binding surfaces regulates DISC assembly
In response to activation of death receptors, a multimeric signalling complex assembles in which FADD binds caspase 8 and FLIP through structurally similar binding surfaces. Majkut et al.show that each surface preferentially binds to one of the two proteins, resulting in the formation of a trimeric intermediate.
- J. Majkut
- , M. Sgobba
- & D. B. Longley
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Structural and functional features of a collagen-binding matrix protein from the mussel byssus
The mussel byssus is a protein-based fibre which possesses structural and mechanical properties ideally suited to surface adhesion. Here, the authors solve the crystal structure of the proximal thread matrix protein 1 and determine its influence on byssus structural characteristics.
- Michael H. Suhre
- , Melanie Gertz
- & Thomas Scheibel
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Radial symmetry in a chimeric glutamate receptor pore
Crystallographic studies have shown that non-NMDA glutamate receptors exhibit fourfold symmetry in the transmembrane domain in the closed state; however, structural data regarding channel opening is lacking. Using chimeric receptors, Wilding et al.provide evidence that this fourfold symmetry is maintained in the open state.
- Timothy J. Wilding
- , Melany N. Lopez
- & James E. Huettner
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Lipidic cubic phase injector facilitates membrane protein serial femtosecond crystallography
Serial femtosecond X-ray crystallography permits the use of very small protein crystals; however, a continuous flow of sample is required. Weierstall et al. design and demonstrate an injector system that can supply microcrystals in the lipidic cubic phase, dramatically reducing the quantities of protein required.
- Uwe Weierstall
- , Daniel James
- & Vadim Cherezov
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An asymmetric heterodomain interface stabilizes a response regulator–DNA complex
Bacterial two-component systems relay extracellular signals to transcriptional networks via response regulators. Narayanan et al.present structures of the response regulator KdpE bound to DNA, and show that asymmetric interactions between the receiver and DNA-binding domains are required to sustain gene expression.
- Anoop Narayanan
- , Shivesh Kumar
- & Dinesh A. Yernool
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A novel allosteric mechanism in the cysteine peptidase cathepsin K discovered by computational methods
Allosteric sites are an increasingly used target for drug design. Here, the authors computationally predict an allosteric site in cathepsin K and subsequently identify a small-molecule allosteric modifier.
- Marko Novinec
- , Matevž Korenč
- & Antonio Baici
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Structural analysis of the transitional state of Arp2/3 complex activation by two actin-bound WCAs
The involvement of one or two nucleation-promoting factors in Arp2/3 complex activation is a matter of debate. Here Boczkowska et al.provide evidence that two nucleation-promoting factors are required, and propose a model of the 11-subunit transitional complex based on distance measurements by FRET.
- Malgorzata Boczkowska
- , Grzegorz Rebowski
- & Roberto Dominguez
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Sequential pH-driven dimerization and stabilization of the N-terminal domain enables rapid spider silk formation
The molecular mechanism by which rapid spider silk assembly occurs in the glands of spiders is challenging to investigate. Here, the authors perform site-directed mutagenesis of the N-terminal domain and propose a three-step mechanism that allows controlled aggregation of spidroins.
- Nina Kronqvist
- , Martins Otikovs
- & Jan Johansson
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Article
| Open AccessX-ray refinement significantly underestimates the level of microscopic heterogeneity in biomolecular crystals
The structural heterogeneity of a biomolecular crystal structure is typically captured using atomic B-factors, determined during structure refinement. Here, the authors use molecular dynamics to show that this strategy is flawed, and that crystallographic B-factors underestimate structural heterogeneity.
- Antonija Kuzmanic
- , Navraj S. Pannu
- & Bojan Zagrovic
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Visualizing autophosphorylation in histidine kinases
The phosphorylation of proteins is a common mechanism for signal transduction. Here, the authors present a structural analysis of a histidine kinase in the process of autophosphorylation, helping to elucidate the catalytic mechanism.
- Patricia Casino
- , Laura Miguel-Romero
- & Alberto Marina
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Structures of an intramembrane vitamin K epoxide reductase homolog reveal control mechanisms for electron transfer
Vitamin K epoxide reductase (VKOR) catalyses the formation of protein disulphide bonds and is the pharmacological target of the anticoagulant drug warfarin. Liu et al. present crystal structures of a bacterial VKOR in two different conformations and reveal how motions of a helix ensure unidirectional electron transfer.
- Shixuan Liu
- , Wei Cheng
- & Weikai Li
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| Open AccessLigand-induced structural changes in the cyclic nucleotide-modulated potassium channel MloK1
The molecular determinants underlying ligand gating of cyclic nucleotide-modulated ion channels remain unclear. Kowal et al.determine the conformational changes underlying cAMP binding to the bacterial channel MloK1, and propose a mechanism for coupling of ligand gating and voltage sensing in eukaryotic HCN channels.
- Julia Kowal
- , Mohamed Chami
- & Henning Stahlberg
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Structure-based discovery of Middle East respiratory syndrome coronavirus fusion inhibitor
MERS-CoV is a novel human coronavirus that has recently caused outbreaks of respiratory illness with high case fatality rate. Here the authors characterize the membrane fusion apparatus of MERS-CoV and develop a peptide that can inhibit virus fusion and replication in vitro.
- Lu Lu
- , Qi Liu
- & Shibo Jiang
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| Open AccessEctopic A-lattice seams destabilize microtubules
Microtubules are tubes in which helical symmetry is broken at a single ‘A-lattice’ seam. Katsuki et al.show that microtubules containing additional A-lattice seams exhibit decreased stability, and propose that such seams may act as trigger points for microtubule catastrophe.
- Miho Katsuki
- , Douglas R. Drummond
- & Robert A. Cross
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Anisotropic energy flow and allosteric ligand binding in albumin
Protein allosteric interactions involve a transfer of structural changes to a remote site. Here, the authors study the relationship between allosteric binding and energy flow, showing how the energy transport mechanism conveys binding energy to remote sites.
- Guifeng Li
- , Donny Magana
- & R. Brian Dyer
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Distinct structural features of TFAM drive mitochondrial DNA packaging versus transcriptional activation
The mitochondrial transcription factor TFAM is a multifunctional DNA-binding protein essential for transcriptional regulation and mitochondrial DNA organization. Here, Ngo et al.present two novel crystal structures that provide additional mechanistic insight into how TFAM performs its diverse functions.
- Huu B. Ngo
- , Geoffrey A. Lovely
- & David C. Chan
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Article
| Open AccessStructural basis for microtubule recognition by the human kinetochore Ska complex
Kinetochores must interact with both polymerizing (straight) and depolymerizing (curved) microtubules to ensure correct mitotic chromosome segregation. Abad et al. reveal how this flexibility is achieved through structural characterization of the interactions between microtubules and the kinetochore protein Ska1.
- Maria Alba Abad
- , Bethan Medina
- & A. Arockia Jeyaprakash
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Structure of the mammalian oligosaccharyl-transferase complex in the native ER protein translocon
Proteins that are translocated across the endoplasmic reticulum (ER) membrane may be subject to glycosylation during transport. Using cryoelectron microscopy of native ER membranes, Pfeffer et al.map the location of oligosaccharyl-transferase within the translocon, providing insight into how these processes are coupled.
- Stefan Pfeffer
- , Johanna Dudek
- & Friedrich Förster