| P50 | author | José A Carrodeguas | Q57036044 |
| | Julian Pardo | Q59221412 |
| P2093 | author name string | Alfredo Lagunas-Martínez | |
| | Angélica Ospina | |
| P2860 | cites work | Molecular characterization of mitochondrial apoptosis-inducing factor | Q22001452 |
| | Identification of a novel PSD-95/Dlg/ZO-1 (PDZ)-like protein interacting with the C terminus of presenilin-1 | Q22010752 |
| | Bcl-x(L) sequesters its C-terminal membrane anchor in soluble, cytosolic homodimers | Q24292693 |
| | Induction of apoptotic program in cell-free extracts: requirement for dATP and cytochrome c | Q24309066 |
| | Cleavage of BID by caspase 8 mediates the mitochondrial damage in the Fas pathway of apoptosis | Q24310597 |
| | A short Nur77-derived peptide converts Bcl-2 from a protector to a killer | Q24319007 |
| | A transmembrane helix dimer: structure and implications | Q27735013 |
| | Smac, a mitochondrial protein that promotes cytochrome c-dependent caspase activation by eliminating IAP inhibition | Q28115131 |
| | Identification of DIABLO, a mammalian protein that promotes apoptosis by binding to and antagonizing IAP proteins | Q28117928 |
| | A conserved GXXXG motif in APH-1 is critical for assembly and activity of the gamma-secretase complex | Q28185671 |
| | Two isoforms of PSAP/MTCH1 share two proapoptotic domains and multiple internal signals for import into the mitochondrial outer membrane | Q28239032 |
| | Exposure of any of two proapoptotic domains of presenilin 1-associated protein/mitochondrial carrier homolog 1 on the surface of mitochondria is sufficient for induction of apoptosis in a Bax/Bak-independent manner | Q28274421 |
| | Characterization of the signal that directs Bcl-x(L), but not Bcl-2, to the mitochondrial outer membrane | Q28580739 |
| | MTCH2/MIMP is a major facilitator of tBID recruitment to mitochondria | Q28594262 |
| | Self-association of transmembrane domain 2 (TM2), but not TM1, in carnitine palmitoyltransferase 1A: role of GXXXG(A) motifs | Q28771361 |
| | The Bcl2 family: regulators of the cellular life-or-death switch | Q29614982 |
| | Mitochondrial control of cell death | Q29617739 |
| | The Fas death factor | Q29620461 |
| | Apoptogenic interactions of plasmalemmal type-1 VDAC and Aβ peptides via GxxxG motifs induce Alzheimer's disease - a basic model of apoptosis? | Q30155609 |
| | The GxxxG motif: a framework for transmembrane helix-helix association | Q30839523 |
| | GxxxG motifs within the amyloid precursor protein transmembrane sequence are critical for the etiology of Abeta42. | Q33276402 |
| | Bcl-XL inhibits membrane permeabilization by competing with Bax. | Q33343021 |
| | Statistical characterization of the GxxxG glycine repeats in the flagellar biosynthesis protein FliH and its Type III secretion homologue YscL | Q33431015 |
| | Bax forms multispanning monomers that oligomerize to permeabilize membranes during apoptosis | Q33854131 |
| | Characterization of the GXXXG motif in the first transmembrane segment of Japanese encephalitis virus precursor membrane (prM) protein | Q33934111 |
| | The mitochondrial permeability transition pore | Q34034610 |
| | Sequence specificity in the dimerization of transmembrane alpha-helices | Q34279030 |
| | Mutational analysis of the role of GXXXG motif in the function of human organic anion transporter 1 (hOAT1). | Q34580122 |
| | Conserved GXXXG- and S/T-like motifs in the transmembrane domains of NS4B protein are required for hepatitis C virus replication | Q35077451 |
| | The BCL-2 family reunion | Q35568029 |
| | The N-terminal domain of Bcl-xL reversibly binds membranes in a pH-dependent manner. | Q35574660 |
| | Folding of helical membrane proteins: the role of polar, GxxxG-like and proline motifs | Q35863914 |
| | The C-terminal transmembrane domain of Bcl-xL mediates changes in mitochondrial morphology | Q36259561 |
| | Embedded together: the life and death consequences of interaction of the Bcl-2 family with membranes | Q36799170 |
| | Bcl-xL forms two distinct homodimers at non-ionic detergents: implications in the dimerization of Bcl-2 family proteins | Q38296400 |
| | The dimerization motif of the glycophorin A transmembrane segment in membranes: importance of glycine residues | Q38338136 |
| | Amino-terminal hydrophobic region of Helicobacter pylori vacuolating cytotoxin (VacA) mediates transmembrane protein dimerization. | Q39518483 |
| | Control of Bax homodimerization by its carboxyl terminus. | Q40122436 |
| | Mutational analysis of ABCG2: role of the GXXXG motif | Q40534113 |
| | During apoptosis bcl-2 changes membrane topology at both the endoplasmic reticulum and mitochondria | Q40554731 |
| | Bcl-xL regulates apoptosis by heterodimerization-dependent and -independent mechanisms | Q40976477 |
| | Neurotransmitter release - four years of SNARE complexes | Q41541527 |
| | Dimerisation of the Rhodobacter sphaeroides RC-LH1 photosynthetic complex is not facilitated by a GxxxG motif in the PufX polypeptide | Q42963873 |
| | The single transmembrane domains of ErbB receptors self-associate in cell membranes | Q43821697 |
| | Essential role of a GXXXG motif for membrane channel formation by Helicobacter pylori vacuolating toxin | Q44299992 |
| | The GxxxG motif of the transmembrane domain of subunit e is involved in the dimerization/oligomerization of the yeast ATP synthase complex in the mitochondrial membrane | Q44402671 |
| | Transport-deficient Pit2 phosphate transporters still modify cell surface oligomers structure in response to inorganic phosphate | Q44926872 |
| | Membrane promotes tBID interaction with BCL(XL). | Q45815145 |
| | Two GxxxG-like motifs facilitate promiscuous interactions of the human ErbB transmembrane domains | Q46053700 |
| | The yeast F(1)F(0)-ATP synthase: analysis of the molecular organization of subunit g and the importance of a conserved GXXXG motif | Q46484164 |
| | Mutational analysis of putative helix-helix interacting GxxxG-motifs and tryptophan residues in the two-peptide bacteriocin lactococcin G. | Q46648531 |
| | Generation of monoclonal antibody recognized by the GXXXG motif (glycine zipper) of prion protein. | Q51803094 |
| | Statistical analysis of amino acid patterns in transmembrane helices: the GxxxG motif occurs frequently and in association with beta-branched residues at neighboring positions. | Q52081092 |
| | BCL-XL dimerization by three-dimensional domain swapping. | Q53964467 |
| | A dimerization motif for transmembrane α–helices | Q54246480 |
| | Heat-Induced Dimerization of BCL-xLthrough α-Helix Swapping† | Q57266759 |
| | A conserved membrane-spanning amino acid motif drives homomeric and supports heteromeric assembly of presynaptic SNARE proteins | Q73675955 |
| | Pro-apoptotic cleavage products of Bcl-xL form cytochrome c-conducting pores in pure lipid membranes | Q74001282 |
| | Sequence-specific Dimerization of the Transmembrane Domain of the “BH3-only” Protein BNIP3 in Membranes and Detergent | Q79130136 |
| | A trimerizing GxxxG motif is uniquely inserted in the severe acute respiratory syndrome (SARS) coronavirus spike protein transmembrane domain | Q80280648 |
| | Structure assembly of Bcl-x(L) through alpha5-alpha5 and alpha6-alpha6 interhelix interactions in lipid membranes | Q84569267 |
| P433 | issue | 19 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | transmembrane protein | Q424204 |
| | identical protein binding | Q14762994 |
| | BCL2 like 1 | Q21173156 |
| P1104 | number of pages | 8 | |
| P304 | page(s) | 2935-2942 | |
| P577 | publication date | 2011-08-16 | |
| P1433 | published in | FEBS Letters | Q1388051 |
| P1476 | title | Protein oligomerization mediated by the transmembrane carboxyl terminal domain of Bcl-XL | |
| P478 | volume | 585 | |