Search Results - "Fenton, W A"
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GroEL‐Mediated protein folding
Published in Protein science (01-04-1997)“…I Architecture of GroEL and GroES and the reaction pathway A. Architecture of the chaperonins B. Reaction pathway of GroEL‐GroES‐mediated folding II…”
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2
Residues in chaperonin GroEL required for polypeptide binding and release
Published in Nature (London) (13-10-1994)“…Chaperonins are ring-shaped protein complexes that are essential in the cell, mediating ATP-dependent polypeptide folding in a variety of compartments. Recent…”
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3
Clinical heterogeneity and prognosis in combined methylmalonic aciduria and homocystinuria (cblC)
Published in Journal of inherited metabolic disease (01-08-1997)“…The clbC form of methylmalonic acidaemia is a rare and poorly understood condition which results from impaired biosynthesis of methylcobalamin and…”
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4
Distinct actions of cis and trans ATP within the double ring of the chaperonin GroEL
Published in Nature (London) (21-08-1997)“…The chaperonin GroEL is a double-ring structure with a central cavity in each ring that provides an environment for the efficient folding of proteins when…”
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5
Folding in vivo of bacterial cytoplasmic proteins: role of GroEL
Published in Cell (10-09-1993)“…A general role for chaperonin ring structures in mediating folding of newly translated proteins has been suggested. Here we have directly examined the role of…”
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6
Release of both native and non-native proteins from a cis -only GroEL ternary complex
Published in Nature (London) (05-09-1996)“…Protein folding by the double-ring chaperonin GroEL is initiated in cis ternary complexes, in which polypeptide is sequestered in the central channel of a…”
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7
Stable transformation of CHO Cells and human NARP cybrids confers oligomycin resistance (oli(r)) following transfer of a mitochondrial DNA-encoded oli(r) ATPase6 gene to the nuclear genome: a model system for mtDNA gene therapy
Published in Rejuvenation research (01-03-2005)“…Point and deletion mutations and a general depletion of mammalian mitochondrial DNA (mtDNA) give rise to a wide variety of medical syndromes that are…”
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8
Cleavage of Precursors by the Mitochondrial Processing Peptidase Requires a Compatible Mature Protein or an Intermediate Octapeptide
Published in The Journal of cell biology (01-04-1991)“…Many precursors of mitochondrial proteins are processed in two successive steps by independent matrix peptidases (MPP and MIP), whereas others are cleaved in a…”
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9
Expression and Kinetic Characterization of Methylmalonyl-CoA Mutase from Patients with the Mut− Phenotype: Evidence for Naturally Occurring Interallelic Complementation
Published in Human molecular genetics (01-09-1997)“…l-Methylmalonyl-CoA mutase (MUT) is an adenosylcobalamin (AdoCbl)-requiring mitochondrial matrix enzyme that catalyzes the isomerization of l-methylmalonyl-CoA…”
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10
Citrate inhibition of snake venom proteases
Published in Toxicon (Oxford) (01-12-1998)“…Thirty snake venoms had a citrate content of 2.3 to 12.9%, dry basis, by an aconitase–isocitric dehydrogenase coupled enzyme assay. This is a venom…”
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11
GroEL, GroES, and ATP-dependent folding and spontaneous assembly of ornithine transcarbamylase
Published in The Journal of biological chemistry (05-04-1993)“…When purified rat liver ornithine transcarbamylase (OTC), a trimer of 36 kDa subunits, was denatured in 6 M guanidine hydrochloride and then diluted…”
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12
Mitochondrial protein transport--a system in search of mutations
Published in American journal of human genetics (01-08-1995)“…After years of searching in the cDNA of patients with defects in specific mitochondrial proteins and, with somewhat less diligence, in patients with undefined…”
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13
The venomous hair structure, venom and life cycle of Lagoa crispata, a puss caterpillar of Oklahoma
Published in Toxicon (Oxford) (01-09-2000)“…The presence of a unique population of Lagoa crispata, puss caterpillar, in western Oklahoma is reported. A detailed microscopic examination shows the…”
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14
The β Subunit of the Mitochondrial Processing Peptidase From Rat Liver: Cloning and Sequencing of a cDNA and Comparison With a Proposed Family of Metallopeptidases
Published in Proceedings of the National Academy of Sciences - PNAS (01-06-1993)“…Most nuclearly encoded mitochondrial proteins are synthesized with amino-terminal leader peptides that are removed by the mitochondrial processing peptidase…”
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15
ATP-Bound States of GroEL Captured by Cryo-Electron Microscopy
Published in Cell (28-12-2001)“…The chaperonin GroEL drives its protein-folding cycle by cooperatively binding ATP to one of its two rings, priming that ring to become folding-active upon…”
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16
Orthotopic liver transplantation for urea cycle enzyme deficiency
Published in Hepatology (Baltimore, Md.) (01-03-1992)“…Hyperammonemia, abnormalities in plasma amino acids and abnormalities of standard liver functions were corrected by orthotopic liver transplantation in a…”
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17
GroEL-GroES Cycling: ATP and Nonnative Polypeptide Direct Alternation of Folding-Active Rings
Published in Cell (30-04-1999)“…The double-ring chaperonin GroEL mediates protein folding in the central cavity of a ring bound by ATP and GroES, but it is unclear how GroEL cycles from one…”
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18
GroEL/GroES-Mediated Folding of a Protein Too Large to Be Encapsulated
Published in Cell (19-10-2001)“…The chaperonin GroEL binds nonnative proteins too large to fit inside the productive GroEL-GroES cis cavity, but whether and how it assists their folding has…”
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Journal Article -
19
STRUCTURE AND FUNCTION IN GroEL-MEDIATED PROTEIN FOLDING
Published in Annual review of biochemistry (01-01-1998)“…Recent structural and biochemical investigations have come together to allow a better understanding of the mechanism of chaperonin (GroEL, Hsp60)-mediated…”
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20
Identification of RNA splicing errors resulting in human ornithine transcarbamylase deficiency
Published in American journal of human genetics (01-06-1991)“…Ornithine transcarbamylase (OTC) is an X-linked, liver-specific enzyme that catalyzes the second step of the urea cycle. In humans, inherited deficiency of OTC…”
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