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searching for Inner mitochondrial membrane 141 found (271 total)

alternate case: inner mitochondrial membrane

PDSS1 (594 words) [view diff] exact match in snippet view article find links to article

biosynthesis. The protein may be peripherally associated with the inner mitochondrial membrane, though no transit peptide has been definitively identified to

and cytosol by transporting citrate through the impermeable inner mitochondrial membrane in exchange for malate from the cytosol. The citrate transported

Inner mitochondrial membrane peptidase subunit 2 (IMMP2L) is an enzyme that in humans is encoded by the IMMP2L gene on chromosome 7. This protein catalyzes

Tim50 is a subunit of the Tim23 translocase complex in the inner mitochondrial membrane. Mutations in TIMM50 can lead to epilepsy, severe intellectual

complex (CETF) is a flavoprotein located on the matrix face of the inner mitochondrial membrane and functions as a specific electron acceptor for primary dehydrogenases

membrane and the return transfer of protons from the outer to the inner mitochondrial membrane. They also reduce the mitochondrial membrane potential in mammalian

M, Maarse AC (Dec 1996). "The preprotein translocase of the inner mitochondrial membrane: evolutionary conservation of targeting and assembly of Tim17"

reaction becomes: RCOO− + CoASH + ATP → RCO-SCoA+ AMP + 2Pi The inner mitochondrial membrane is impermeable to fatty acids and a specialized carnitine carrier

membrane and the return transfer of protons from the outer to the inner mitochondrial membrane. They also reduce the mitochondrial membrane potential in mammalian

that in humans is encoded by the IMMT gene.) IMMT encodes an inner mitochondrial membrane (IMM) protein in the nucleus. It is posttranslational transported

mitochondrial fusion. In addition to the mitofusins, OPA1 regulates inner mitochondrial membrane fusion, and DRP1 is responsible for mitochondrial fission. Mitofusin-2

membrane and the return transfer of protons from the outer to the inner mitochondrial membrane. They also reduce the mitochondrial membrane potential in mammalian

TIMM8A translocase of inner mitochondrial membrane 8 homolog A (yeast)". "Entrez Gene: TIMM8A translocase of inner mitochondrial membrane 8A". Zong NC, Li

localized to two subcellular domains, the matrix side of the inner mitochondrial membrane where it is thought to be involved in the synthesis of phosphatidylglycerol

via the carnitine-acylcarnitine translocase. Once inside the inner mitochondrial membrane, the same Carnitine O-palmitoyltransferase family is then responsible

National Library of Medicine. "Entrez Gene: TIMM22 translocase of inner mitochondrial membrane 22 homolog (yeast)". Gerhard DS, Wagner L, Feingold EA, et al

(May 2006). "Mutation of DNAJC19, a human homologue of yeast inner mitochondrial membrane co-chaperones, causes DCMA syndrome, a novel autosomal recessive

phospholipid translocation between two lipid compartments," the inner mitochondrial membrane and the outer membrane. Further experimental evidence suggests

1999.2751. PMID 10339406. "Entrez Gene: TIMM23 translocase of inner mitochondrial membrane 23 homolog (yeast)". Gerhard DS, Wagner L, Feingold EA, et al

1999.2751. PMID 10339406. "Entrez Gene: TIMM44 translocase of inner mitochondrial membrane 44 homolog (yeast)". Yuryev, Anton; Wennogle Lawrence P (Feb

the potential to be folded into an alpha helix spanning the inner mitochondrial membrane with a C-terminal hydrophilic domain interacting with globular

gradient when moving ATP (outward) and ADP (inward) across the inner mitochondrial membrane. The electroneutral symport of phosphate ion and H+ results in

that this segment mediates the association of CPT II with the inner mitochondrial membrane. Moreover, the insert might also facilitate the shuttling of

the potential to be folded into an alpha helix spanning the inner mitochondrial membrane with a C-terminal hydrophilic domain interacting with globular

Scythe. Together, the two do not affect the AIF attached to the inner mitochondrial membrane, however they influence the stability of AIF once it exits the

the potential to be folded into an alpha helix spanning the inner mitochondrial membrane with a C-terminal hydrophilic domain interacting with globular

bacterial cell membranes; and that cardiolipin is found only in the inner mitochondrial membrane and bacterial cell membranes. The Russian botanist Konstantin

TIM10B, Tim9b, translocase of inner mitochondrial membrane 10 homolog B (yeast), translocase of inner mitochondrial membrane 10B External IDs OMIM: 607388

the potential to be folded into an alpha helix spanning the inner mitochondrial membrane with a C-terminal hydrophilic domain interacting with globular

apoptosis. The calcium uniporter transports calcium across the inner mitochondrial membrane and is activated when calcium rises above a certain concentration

the potential to be folded into an alpha helix spanning the inner mitochondrial membrane with a C-terminal hydrophilic domain interacting with globular

1093/molbev/msm031. PMID 17329230. "Entrez Gene: TIMM13 translocase of inner mitochondrial membrane 13 homolog (yeast)". Ewing RM, Chu P, Elisma F, Li H, Taylor

the potential to be folded into an alpha helix spanning the inner mitochondrial membrane with a C-terminal hydrophilic domain interacting with globular

the potential to be folded into an alpha helix spanning the inner mitochondrial membrane with a C-terminal hydrophilic domain interacting with globular

the regulation of cholesterol transport from the outer to the inner mitochondrial membrane, the rate-determining step in steroid biosynthesis, has been

regenerate the NAD+ necessary for glycolysis to continue. However the inner mitochondrial membrane is impermeable to NADH and NAD+. Use is therefore made of two

the potential to be folded into an alpha helix spanning the inner mitochondrial membrane with a C-terminal hydrophilic domain interacting with globular

the potential to be folded into an alpha helix spanning the inner mitochondrial membrane with a C-terminal hydrophilic domain interacting with globular

the potential to be folded into an alpha helix spanning the inner mitochondrial membrane with a C-terminal hydrophilic domain interacting with globular

the potential to be folded into an alpha helix spanning the inner mitochondrial membrane with a C-terminal hydrophilic domain interacting with globular

center of the mitochondria and some proteins tethered to the inner mitochondrial membrane also help anchor the Z ring. The Z ring is anchored at the site

conductance potassium channel (BKCa++) opener. BKCa++ is found in the inner mitochondrial membrane of cardiomyocytes. Opening these channels is beneficial for post-ischemic

the potential to be folded into an alpha helix spanning the inner mitochondrial membrane with a C-terminal hydrophilic domain interacting with globular

the potential to be folded into an alpha helix spanning the inner mitochondrial membrane with a C-terminal hydrophilic domain interacting with globular

the potential to be folded into an alpha helix spanning the inner mitochondrial membrane with a C-terminal hydrophilic domain interacting with globular

the potential to be folded into an alpha helix spanning the inner mitochondrial membrane with a C-terminal hydrophilic domain interacting with globular

transport chain to ultimately form a proton gradient across the inner mitochondrial membrane. This gradient can then drive the production of ATP and H2O during

the potential to be folded into an alpha helix spanning the inner mitochondrial membrane with a C-terminal hydrophilic domain interacting with globular

the potential to be folded into an alpha helix spanning the inner mitochondrial membrane with a C-terminal hydrophilic domain interacting with globular

of components mediating preprotein translocation across the inner mitochondrial membrane". The EMBO Journal. 16 (9): 2205–16. doi:10.1093/emboj/16.9.2205

B. The enzyme is localized to the matrix-facing side of the inner mitochondrial membrane. Ferrochelatase is the best known member of a family of enzymes

the potential to be folded into an alpha helix spanning the inner mitochondrial membrane with a C-terminal hydrophilic domain interacting with globular

the potential to be folded into an alpha helix spanning the inner mitochondrial membrane with a C-terminal hydrophilic domain interacting with globular

the potential to be folded into an alpha helix spanning the inner mitochondrial membrane with a C-terminal hydrophilic domain interacting with globular

the potential to be folded into an alpha helix spanning the inner mitochondrial membrane with a C-terminal hydrophilic domain interacting with globular

the potential to be folded into an alpha helix spanning the inner mitochondrial membrane with a C-terminal hydrophilic domain interacting with globular

and partially through the inner mitochondrial membrane via the TIM complex, so it then spans the inner mitochondrial membrane. The process of import into

phosphorylation. They do this by increasing the permeability of the inner mitochondrial membrane, allowing protons that have been pumped into the intermembrane

in the assembly of the adenine nucleotide translocator in the inner mitochondrial membrane. Mutations in the AGK gene were the first to be implicated in

apoptosis cycle, an alteration of OPA1/Mgm1 activity within the inner mitochondrial membrane occurs. The role of the OPA1 protein is to protect cells against

the potential to be folded into an alpha helix spanning the inner mitochondrial membrane with a C-terminal hydrophilic domain interacting with globular

through carnitine-acylcarnitine translocase (CACT) located on the inner mitochondrial membrane. This antiporter returns one molecule of carnitine from the matrix

mitochondria. This protein forms a complex with mitofilin (IMMT) on the inner mitochondrial membrane, independent of MFN2. Mutations in the SLC25A46 gene, inherited

which naturally localise inside the mitochondria due to the inner mitochondrial membrane matrix-face's negative charge (as the fluorophores are cationic)

The protein is normally located on the outer surface of the inner mitochondrial membrane.[citation needed] A mutation in this gene was reported by Morgan

localized to two subcellular domains, the matrix side of the inner mitochondrial membrane where it is thought to be involved in the synthesis of phosphatidylglycerol

a lesser extent, the glycerol-phosphate shuttle) because the inner mitochondrial membrane is impermeable to NADH and NAD+. Instead of transferring the

a lesser extent, the glycerol-phosphate shuttle) because the inner mitochondrial membrane is impermeable to NADH and NAD+. Instead of transferring the

mitochondrial oxidative phosphorylation process takes place in the inner mitochondrial membrane of eukaryotic cells. This membrane is highly folded into structures

the cytosol is impossible, due to the impermeability of the inner mitochondrial membrane to NADH. Therefore, the malate-aspartate shuttle is needed to

stored as an electrochemical gradient of protons (H+) across the inner mitochondrial membrane is required to generate ATP from ADP and Pi (inorganic phosphate

protein THYN1: thymocyte nuclear protein 1 TIMM10: translocase of inner mitochondrial membrane 10 TIMM10B: Mitochondrial import inner membrane translocase subunit

acetyltransferase producing 3HIA-carnitine, which is transported across the inner mitochondrial membrane (and hence effectively out of the mitochondria) via carnitine-acylcarnitine

ancestral aerobic bacterium resembling P. denitrificans to the inner mitochondrial membrane, has been suggested. More recent phylogenetic analysis however

contributes to a proton electrochemical gradient across the inner mitochondrial membrane to drive ATP synthesis via protonmotive force. The mitochondrially-encoded

produce energy. This energy is used to shuttle protons across the inner mitochondrial membrane, from the mitochondrial matrix into the inner membrane space

transport of carnitine and carnitine/acylcarnitine exchange in the inner mitochondrial membrane, allowing the import of long-chain fatty acids into the mitochondria

is one of the cytochrome P450 oxidase enzymes located in the inner mitochondrial membrane of cells of the adrenal cortex. It is coded by a gene at 8q21-22

molecules produced by glycolysis are actively transported across the inner mitochondrial membrane, and into the matrix. Here they can be oxidized and combined

a Complete ATP Synthase Dimer Reveals the Molecular Basis of Inner Mitochondrial Membrane Morphology". Molecular Cell. 63 (3): 445–456. doi:10.1016/j.molcel

contributes to a proton electrochemical gradient across the inner mitochondrial membrane. The mitochondrially-encoded subunits perform the electron transfer

(PARG) gene and the common promoter sequence it shares with inner mitochondrial membrane translocase 23 (TIM23)". Gene. 314: 181–190. doi:10.1016/S0378-1119(03)00738-8

transport chain's ability to produce a proton gradient across the inner mitochondrial membrane. The ATP synthase complex exists within the mitochondrial membrane

transport cholesterol from the outer mitochondrial membrane to the inner mitochondrial membrane. The development of the corpus luteum is accompanied by an increase

Different pathways were investigated. So it could be shown that the inner mitochondrial membrane was damaged, and single strand DNA breaks were observed. The

acetyltransferase producing 3HIA-carnitine, which is transported across the inner mitochondrial membrane (and hence effectively out of the mitochondria) via carnitine-acylcarnitine

acid-carnitine complex. This complex is then transported through the inner mitochondrial membrane via a transporter protein called carnitine-acylcarnitine translocase

activity. As cardiolipin is synthesized in the luminal side of inner mitochondrial membrane, a major fraction of this newly synthesized pool of cardiolipin

the plasma membrane and stimulating the proton leak across the inner mitochondrial membrane. Hindered oxidative phosphorylation compromises ATP production

structure with 16–20 alternating Phb1 and Phb2 subunits in the inner mitochondrial membrane. The precise molecular function of the PHB complex is not clear

contributes to a proton electrochemical gradient across the inner mitochondrial membrane to drive ATP synthesis via protonmotive force. The mitochondrially-encoded

of cholesterol from the outer mitochondrial membrane to the inner mitochondrial membrane. Mutations in this gene are a cause of congenital lipoid adrenal

contributes to a proton electrochemical gradient across the inner mitochondrial membrane to drive ATP synthesis via protonmotive force. The mitochondrially-encoded

contributes to a proton electrochemical gradient across the inner mitochondrial membrane to drive ATP synthesis via protonmotive force. The mitochondrially-encoded

contributes to a proton electrochemical gradient across the inner mitochondrial membrane to drive ATP synthesis via protonmotive force. The mitochondrially-encoded

cytoplasmic protein HAP1; Huntingtin-associated protein 1, IMMT, an inner mitochondrial membrane protein, and PFN2; Profilin 2- ubiquitous actin monomer binding

transmembrane protein dimer with SDHC that anchors Complex II to the inner mitochondrial membrane. The SDHC/SDHD dimer provides binding sites for ubiquinone and

first identified in 1991 by single-channel recordings of the inner mitochondrial membrane. The molecular structure of mitoKATP is less clearly understood

staining. These are particles of 9 nm diameter that pepper the inner mitochondrial membrane. They were originally called elementary particles and were thought

transport chain, composed of four complexes embedded in the inner mitochondrial membrane. Complexes I, III, and IV pump protons from the matrix to the

transport chain, composed of four complexes embedded in the inner mitochondrial membrane. Complexes I, III, and IV pump protons from the matrix to the

AN, Koller A, Perkins GA, et al. (January 2011). "ChChd3, an inner mitochondrial membrane protein, is essential for maintaining crista integrity and mitochondrial

transported into mitochondrial matrix and is associated with the inner mitochondrial membrane. ClpP protease is a major contributor for mitochondrial protein

is an integral protein that enters cells' plasma membrane (or inner mitochondrial membrane). The plasma membrane is the site of the electron transport chain

Mootha VK, Tiranti V, Zeviani M (May 2006). "MPV17 encodes an inner mitochondrial membrane protein and is mutated in infantile hepatic mitochondrial DNA

of cytochrome c is indirectly mediated by the PT pore on the inner mitochondrial membrane, strong evidence suggest an earlier implication of the MAC pore

chain, resulting in the translocation of protons across the inner mitochondrial membrane. The NDUFAF2 gene encodes a complex I assembly factor, B17.2L

and Mfn2 (Mitofusins 1 and 2), and fusion at the level of the inner mitochondrial membrane is mediated by Opa1. Multiple research studies have observed

mitochondrial FAD by the glycerol phosphate shuttle located in the inner mitochondrial membrane. 2.5 in case of malate-aspartate shuttle transferring hydrogen

submitochondrial localization of RDH13 indicates its association with the inner mitochondrial membrane. The primary structure of RDH13 contains two hydrophobic segments

uses the reduction energy of NADH to move protons across the inner mitochondrial membrane against their concentration gradient. An example of primary active

coupled to the pumping of protons (hydrogen ions) across the inner mitochondrial membrane (chemiosmosis), which generates a proton motive force. Energy

mitochondria: in vivo transfer of a light-driven proton pump into the inner mitochondrial membrane of Schizosaccharomyces pombe". Proc. Natl. Acad. Sci. USA. 91

acetyltransferase producing 3HIA-carnitine, which is transported across the inner mitochondrial membrane (and hence effectively out of the mitochondria) via carnitine-acylcarnitine

I, Khalimonchuk O (September 2017). "Metalloproteases of the Inner Mitochondrial Membrane". Biochemistry. 56 (36): 4737–4746. doi:10.1021/acs.biochem.7b00663

gene T-urf 13, which encodes for a protein component of the inner mitochondrial membrane. T-toxin acts on this portion of the mitochondria. In a similar

is removed from the citric acid cycle and carried across the inner mitochondrial membrane into the cytosol. There it is cleaved by ATP citrate lyase into

induce the permeability transition pore (PTP). This PTP is an inner mitochondrial membrane (IMM) channel, whose opening leads to an increasing permeability

Reticulum-Resident Ubiquitin-Like Domain Member 2 Protein, Translocase of Inner Mitochondrial Membrane Domain-Containing Protein 1, Free Fatty Acid Receptor 2, Aquaporin

three glycerol groups that are particularly abundant in the inner mitochondrial membrane. They are believed to activate enzymes involved with oxidative

is removed from the citric acid cycle and carried across the inner mitochondrial membrane into the cytosol. There it is cleaved by ATP citrate lyase into

Succinate exits the mitochondrial matrix and passes through the inner mitochondrial membrane via dicarboxylate transporters, primarily SLC25A10, a succinate-fumarate/malate

Oxidase Assembly Factor 18 Integral membrane insertion into inner mitochondrial membrane 0.991 LAMA2 Laminin Subunit Alpha 2 Attachment to basement membrane

series of four large multienzyme complexes, all embedded in the inner mitochondrial membrane, to convert oxygen and simple sugars to energy. Mutations in

muscle cells. MPTP opening signifies a sudden change in the inner mitochondrial membrane permeability, allowing protons and other ions and solutes of

chaperonin 60. Paraplegin is a m-AAA metalloprotease of the inner mitochondrial membrane. It functions in ribosomal assembly and protein quality control

transfers them to ETF-ubiquinone oxidoreductases (ETF:QO) in the inner mitochondrial membrane. ETF:QO in turn relays them to ubiquinone from where they enter

into another translocase complex TIM17/23/44 located on the inner mitochondrial membrane. This is accompanied by the necessary release of the cytosolic

transfers them to ETF-ubiquinone oxidoreductases (ETF:QO) in the inner mitochondrial membrane. ETF:QO in turn relays them to ubiquinone from where they enter

enzymes reduces cellular functionality. Lipid peroxidation of the inner mitochondrial membrane reduces the electric potential and the ability to generate energy

involves the transport of protons (hydrogen ions) across the inner mitochondrial membrane by means of the electron transport chain. In the electron transport

phosphate for hydroxide ions. The protein is located in the inner mitochondrial membrane and transports phosphate ions for use in oxidative phosphorylation

includes two additional proteins. These proteins are located on the inner mitochondrial membrane. Israel reconstituted this system using proteins he purified

hypothalamus. ACTH increases the concentration of cholesterol in the inner mitochondrial membrane, via regulation of the steroidogenic acute regulatory protein

functionally substitute for its putative homologue Mrs2p in the yeast inner mitochondrial membrane". Journal of Biological Chemistry. 274 (29): 20438–20443. doi:10

acetyltransferase producing 3HIA-carnitine, which is transported across the inner mitochondrial membrane (and hence effectively out of the mitochondria) via carnitine-acylcarnitine

mitochondria: in vivo transfer of a light-driven proton pump into the inner mitochondrial membrane of Schizosaccharomyces pombe". Proceedings of the National Academy

of an F1-ATPase which uses the proton-motive force across the inner mitochondrial membrane to facilitate the synthesis of adenosine triphosphate (ATP).

administered before the injury. Bendavia binds to cardiolipin on the inner mitochondrial membrane and this inhibits cytochrome c peroxidase activity. This protects

functionally substitute for its putative homologue Mrs2p in the yeast inner mitochondrial membrane". The Journal of Biological Chemistry. 274 (29): 20438–43. doi:10

a complete ATP synthase dimer reveals the molecular basis of inner mitochondrial membrane morphology". Mol Cell. 63 (3): 445–56. doi:10.1016/j.molcel.2016