scholarly article | Q13442814 |
P50 | author | Luis Martinez-Gil | Q38545074 |
Ismael Mingarro | Q38545083 | ||
P2860 | cites work | Signal recognition particle mediates post-translational targeting in eukaryotes | Q24563135 |
The biology of influenza viruses | Q24620598 | ||
Structure and mechanism of the M2 proton channel of influenza A virus | Q24625464 | ||
Influenza virus M2 protein mediates ESCRT-independent membrane scission | Q24634367 | ||
Protein translocation across the endoplasmic reticulum. I. Detection in the microsomal membrane of a receptor for the signal recognition particle | Q24680984 | ||
Different conformations of nascent polypeptides during translocation across the ER membrane | Q24795321 | ||
Membrane Insertion of Marginally Hydrophobic Transmembrane Helices Depends on Sequence Context | Q57208978 | ||
Turns in transmembrane helices: determination of the minimal length of a “helical hairpin” and derivation of a fine-grained turn propensity scale 1 1Edited by F. E. Cohen | Q57209056 | ||
Assembly of Viral Membrane Proteins | Q57971530 | ||
Membrane protein folding and oligomerization: the two-stage model | Q67662788 | ||
A novel antimicrobial peptide from the loach, Misgurnus anguillicaudatus | Q73626443 | ||
Membrane integration of the second transmembrane segment of band 3 requires a closely apposed preceding signal-anchor sequence | Q73992946 | ||
The Sec61p complex mediates the integration of a membrane protein by allowing lipid partitioning of the transmembrane domain | Q74175787 | ||
Transmembrane helix-helix interactions: comparative simulations of the glycophorin a dimer | Q79384860 | ||
Sec61alpha and TRAM are sequentially adjacent to a nascent viral membrane protein during its ER integration | Q79433658 | ||
Specific transmembrane segments are selectively delayed at the ER translocon during opsin biogenesis | Q80628282 | ||
The elusive function of the hepatitis C virus p7 protein | Q27026459 | ||
The NS2 protein of hepatitis C virus is a transmembrane polypeptide | Q27480316 | ||
Backbone Structure of the Amantadine-Blocked Trans-Membrane Domain M2 Proton Channel from Influenza A Virus | Q27644223 | ||
Conformational transition of Sec machinery inferred from bacterial SecYE structures | Q27652527 | ||
Similar Energetic Contributions of Packing in the Core of Membrane and Water-Soluble Proteins | Q27656426 | ||
Structure of the amantadine binding site of influenza M2 proton channels in lipid bilayers | Q27659500 | ||
Structure and mechanism of proton transport through the transmembrane tetrameric M2 protein bundle of the influenza A virus | Q27663887 | ||
Lateral opening of a translocon upon entry of protein suggests the mechanism of insertion into membranes | Q27664605 | ||
Insight into the Mechanism of the Influenza A Proton Channel from a Structure in a Lipid Bilayer | Q27665298 | ||
Unusual architecture of the p7 channel from hepatitis C virus | Q27678504 | ||
Gene mapping of the putative structural region of the hepatitis C virus genome by in vitro processing analysis | Q27860603 | ||
SignalP 4.0: discriminating signal peptides from transmembrane regions | Q29547202 | ||
The p7 protein of hepatitis C virus forms an ion channel that is blocked by the antiviral drug, Amantadine | Q29620670 | ||
Experimentally determined hydrophobicity scale for proteins at membrane interfaces | Q29620679 | ||
Membrane protein folding and stability: physical principles | Q29620789 | ||
Modeling the membrane environment has implications for membrane protein structure and function: influenza A M2 protein. | Q30426896 | ||
Total chemical synthesis of the integral membrane protein influenza A virus M2: role of its C-terminal domain in tetramer assembly. | Q30784429 | ||
Plasma membrane-porating domain in poliovirus 2B protein. A short peptide mimics viroporin activity | Q33304077 | ||
The M2 Ectodomain Is Important for Its Incorporation into Influenza A Virions | Q33782503 | ||
Positive charges of translocating polypeptide chain retrieve an upstream marginal hydrophobic segment from the endoplasmic reticulum lumen to the translocon | Q33907071 | ||
Specific structural alteration of the influenza haemagglutinin by amantadine | Q33922433 | ||
Viroporins. | Q34230206 | ||
Modification of membrane permeability by animal viruses. | Q34314053 | ||
Pore-forming activity of pestivirus p7 in a minimal model system supports genus-specific viroporin function. | Q35031600 | ||
How do helix-helix interactions help determine the folds of membrane proteins? Perspectives from the study of homo-oligomeric helical bundles | Q35089609 | ||
Asn- and Asp-mediated interactions between transmembrane helices during translocon-mediated membrane protein assembly | Q35191191 | ||
Unassisted translocation of large polypeptide domains across phospholipid bilayers | Q36119397 | ||
Integration of a small integral membrane protein, M2, of influenza virus into the endoplasmic reticulum: analysis of the internal signal-anchor domain of a protein with an ectoplasmic NH2 terminus | Q36218495 | ||
Mitochondria as functional targets of proteins coded by human tumor viruses | Q36226733 | ||
Initial structural and dynamic characterization of the M2 protein transmembrane and amphipathic helices in lipid bilayers | Q36631397 | ||
SRP keeps polypeptides translocation-competent by slowing translation to match limiting ER-targeting sites | Q36726739 | ||
The influenza virus M2 protein cytoplasmic tail interacts with the M1 protein and influences virus assembly at the site of virus budding | Q36933890 | ||
A precursor-specific role for Hsp40/Hsc70 during tail-anchored protein integration at the endoplasmic reticulum | Q43125499 | ||
Amiloride derivatives block ion channel activity and enhancement of virus-like particle budding caused by HIV-1 protein Vpu. | Q44015913 | ||
Assembling viral channel forming proteins: Vpu from HIV-1. | Q44993875 | ||
Charge pair interactions in transmembrane helices and turn propensity of the connecting sequence promote helical hairpin insertion. | Q45346838 | ||
Sequential triage of transmembrane segments by Sec61alpha during biogenesis of a native multispanning membrane protein | Q46722763 | ||
Molecular code for transmembrane-helix recognition by the Sec61 translocon | Q46853934 | ||
Structure-based statistical analysis of transmembrane helices | Q47760302 | ||
Signal recognition particle binds to ribosome-bound signal sequences with fluorescence-detected subnanomolar affinity that does not diminish as the nascent chain lengthens | Q52842432 | ||
The protein-conducting channel in the membrane of the endoplasmic reticulum is open laterally toward the lipid bilayer | Q54011077 | ||
Double-spanning plant viral movement protein integration into the endoplasmic reticulum membrane is signal recognition particle-dependent, translocon-mediated, and concerted. | Q54486257 | ||
Free Energy of Amide Hydrogen Bond Formation in Vacuum, in Water, and in Liquid Alkane Solution | Q57207152 | ||
Molecular code for protein insertion in the endoplasmic reticulum membrane is similar for N(in)-C(out) and N(out)-C(in) transmembrane helices | Q36949128 | ||
Influenza A virus lacking M2 protein as a live attenuated vaccine | Q37191791 | ||
Insertion of short transmembrane helices by the Sec61 translocon | Q37261725 | ||
Identification of the functional core of the influenza A virus A/M2 proton-selective ion channel | Q37282382 | ||
The minimalist architectures of viroporins and their therapeutic implications. | Q37619619 | ||
A frequent, GxxxG-mediated, transmembrane association motif is optimized for the formation of interhelical Cα-H hydrogen bonds. | Q37640954 | ||
Protein folding in membranes. | Q37681352 | ||
Influenza virus A M2 protein generates negative Gaussian membrane curvature necessary for budding and scission. | Q37724175 | ||
Inserting membrane proteins: The YidC/Oxa1/Alb3 machinery in bacteria, mitochondria, and chloroplasts | Q37783709 | ||
Membrane protein folding: how important are hydrogen bonds? | Q37809384 | ||
Structural and dynamic mechanisms for the function and inhibition of the M2 proton channel from influenza A virus. | Q37830140 | ||
Membrane protein integration into the endoplasmic reticulum | Q37876968 | ||
Hepatitis C virus and host cell lipids: an intimate connection | Q37877090 | ||
Biogenesis of Mitochondrial Proteins | Q38021397 | ||
Viroporins: structure and biological functions. | Q38023155 | ||
The YidC/Oxa1/Alb3 protein family: common principles and distinct features | Q38056629 | ||
Incorporation of hepatitis C virus E1 and E2 glycoproteins: the keystones on a peculiar virion | Q38195180 | ||
Toward understanding driving forces in membrane protein folding | Q38238311 | ||
Stitching proteins into membranes, not sew simple. | Q38242873 | ||
Antivirals--current trends in fighting influenza. | Q38245448 | ||
Viral M2 ion channel protein: a promising target for anti-influenza drug discovery. | Q38262431 | ||
Membrane pore formation at protein-lipid interfaces | Q38273877 | ||
Hepatitis C virus p7-a viroporin crucial for virus assembly and an emerging target for antiviral therapy | Q38615924 | ||
Membrane integration of poliovirus 2B viroporin. | Q38725275 | ||
Transcending the impenetrable: how proteins come to terms with membranes | Q39641550 | ||
The multifaceted poliovirus 2A protease: regulation of gene expression by picornavirus proteases. | Q39754200 | ||
Cooperation of transmembrane segments during the integration of a double-spanning protein into the ER membrane | Q39790858 | ||
Viroporins from RNA viruses induce caspase-dependent apoptosis | Q40062300 | ||
Membrane leakiness after viral infection and a new approach to the development of antiviral agents | Q40141845 | ||
Subcellular localization and membrane association of SARS-CoV 3a protein. | Q40447673 | ||
Recognition of transmembrane helices by the endoplasmic reticulum translocon. | Q40464906 | ||
The transmembrane domain of influenza A M2 protein forms amantadine-sensitive proton channels in planar lipid bilayers | Q41093991 | ||
The structure of melittin in membranes | Q41158738 | ||
Polar/Ionizable residues in transmembrane segments: effects on helix-helix packing. | Q41872052 | ||
Haemolytic activity of stonustoxin from stonefish (Synanceja horrida) venom: pore formation and the role of cationic amino acid residues | Q42159675 | ||
A dimer is the minimal proton-conducting unit of the influenza a virus M2 channel. | Q42219487 | ||
The surfactant peptide KL4 sequence is inserted with a transmembrane orientation into the endoplasmic reticulum membrane | Q42423801 | ||
P275 | copyright license | Creative Commons Attribution | Q6905323 |
P6216 | copyright status | copyrighted | Q50423863 |
P433 | issue | 7 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | virus | Q808 |
viral protein | Q952587 | ||
viral infectious disease | Q1928978 | ||
membrane protein | Q423042 | ||
protein folding | Q847556 | ||
plasma membrane | Q29548 | ||
influenza virus matrix protein 2 | Q17119463 | ||
viroporin | Q26789532 | ||
P5008 | on focus list of Wikimedia project | ScienceSource | Q55439927 |
P304 | page(s) | 3462-3482 | |
P577 | publication date | 2015-06-26 | |
P13046 | publication type of scholarly work | review article | Q7318358 |
P1433 | published in | Viruses | Q7935305 |
P1476 | title | Viroporins, Examples of the Two-Stage Membrane Protein Folding Model | |
P478 | volume | 7 |
Q92543291 | Biological Function and Application of Picornaviral 2B Protein: A New Target for Antiviral Drug Development |
Q38618537 | Disentangling the Frames, the State of Research on the Alphavirus 6K and TF Proteins. |
Q45330627 | Hydrophobic domains of mouse polyomavirus minor capsid proteins promote membrane association and virus exit from the ER. |
Q40135359 | Ion channel activity of the CSFV p7 viroporin in surrogates of the ER lipid bilayer. |
Q59352342 | Molecular Characterization of the Viroporin Function of Foot-and-Mouth Disease Virus Nonstructural Protein 2B |
Q63547227 | The role of hydrophobic matching on transmembrane helix packing in cells |
Q47149209 | The soluble loop BC region guides, but not dictates, the assembly of the transmembrane cytochrome b6. |
Q103027729 | Viral Bcl2s' transmembrane domain interact with host Bcl2 proteins to control cellular apoptosis |
Search more.