about
Reductive evolution of the mitochondrial processing peptidases of the unicellular parasites trichomonas vaginalis and giardia intestinalisThe core components of organelle biogenesis and membrane transport in the hydrogenosomes of Trichomonas vaginalis.Hepcidin, the hormone of iron metabolism, is bound specifically to alpha-2-macroglobulin in blood.The minimal proteome in the reduced mitochondrion of the parasitic protist Giardia intestinalis.Efficacy of S-adenosylhomocysteine hydrolase inhibitors, D-eritadenine and (S)-DHPA, against the growth of Cryptosporidium parvum in vitro.Iron-induced changes in the proteome of Trichomonas vaginalis hydrogenosomes.Lateral gene transfer and gene duplication played a key role in the evolution of Mastigamoeba balamuthi hydrogenosomes.NIF-type iron-sulfur cluster assembly system is duplicated and distributed in the mitochondria and cytosol of Mastigamoeba balamuthi.Characterization of S-adenosylhomocysteine hydrolase from Cryptosporidium parvum.A nonmitochondrial hydrogen production in Naegleria gruberiN-Terminal Presequence-Independent Import of Phosphofructokinase into Hydrogenosomes of Trichomonas vaginalisAlternative pathway of metronidazole activation in Trichomonas vaginalis hydrogenosomes.Pyruvate decarboxylase, the target for omeprazole in metronidazole-resistant and iron-restricted Tritrichomonas foetus.High-molecular-mass complexes formed in vivo contain smHSPs and HSP70 and display chaperone-like activity.Novel functions of an iron-sulfur flavoprotein from Trichomonas vaginalis hydrogenosomesThe monothiol single-domain glutaredoxin is conserved in the highly reduced mitochondria of Giardia intestinalis.Giardia intestinalis incorporates heme into cytosolic cytochrome b₅.Flavodiiron protein from Trichomonas vaginalis hydrogenosomes: the terminal oxygen reductase.Frataxin, a conserved mitochondrial protein, in the hydrogenosome of Trichomonas vaginalis.Malic enzymes of Trichomonas vaginalis: two enzyme families, two distinct origins.Trichomonas hydrogenosomes contain the NADH dehydrogenase module of mitochondrial complex I.Engineering Escherichia coli for fermentative dihydrogen production: potential role of NADH-ferredoxin oxidoreductase from the hydrogenosome of anaerobic protozoa.Dynamic secretome of Trichomonas vaginalis: Case study of β-amylases.Sequence of a Giardia lamblia gene coding for the glycolytic enzyme, pyruvate,phosphate dikinase.OsmC and incomplete glycine decarboxylase complex mediate reductive detoxification of peroxides in hydrogenosomes of Trichomonas vaginalis.Identification, purification and separation of different isozymes of NADP-specific malic enzyme from Tritrichomonas foetus.Secondary alcohol dehydrogenase catalyzes the reduction of exogenous acetone to 2-propanol in Trichomonas vaginalisLateral gene transfer of p -cresol- and indole-producing enzymes from environmental bacteria to M astigamoeba balamuthiAlternative 2-keto acid oxidoreductases in Trichomonas vaginalis: Artifact of histochemical stainingKnock-downs of Iron-Sulfur Cluster Assembly Proteins IscS and IscU Down-regulate the Active Mitochondrion of ProcyclicTrypanosoma bruceiChaperone activity of tobacco HSP18, a small heat-shock protein, is inhibited by ATP
P50
Q28474319-C4B67134-58EE-4447-8B5E-16586551A939Q30155470-B748266B-8C96-4210-A1CC-0785BB4F62FCQ33432533-7060416F-9B99-42FC-964A-3E1BBA50EA52Q33842273-AA6FD2A4-D904-4AE9-9452-6D8026F0F780Q34039880-F91A0FA2-1B87-45AC-BE1D-BB18AAF84CD2Q34761263-AB7D7D0A-44F7-4D74-9AB0-7571E5E9912BQ35232380-26A4DA75-9A03-44D9-A5E8-4F3777E9C609Q36820121-21C0F972-C469-49D5-A8EA-447D716C6D81Q38957284-628EB899-68B6-4DEA-AEA4-6BD652786563Q39147890-6DCFE496-3F9B-4D60-B68E-0A8BC9DBE367Q40422464-B0A681AD-D71E-4B4F-AAE2-B4C8E586638EQ40667329-7CE90AE9-14DB-4507-AB3E-0201DBC7593FQ40882587-629D2321-3EE4-402F-81C4-3FF0384DC7AFQ40887941-4CB7380C-6A8B-4110-AD7E-1AE190C78840Q41076848-DC5AFC58-A9D5-4325-9D9A-9493C6969DC0Q41784612-0DCD1C5A-6B1C-4328-8A58-CCC1BBF6F4ACQ41831554-FA283EAF-4A90-436C-AEF0-5A2609983772Q41883584-DB4E9CE5-D13A-41E8-9D21-DC7CBBB41B67Q42263212-4AB5E0C3-F1B5-4CE8-98F5-E12A5D196AB2Q44807082-5F4AEB3F-6103-412C-9A76-3C3EB262C9BDQ45172271-0948DEA9-4742-484E-AE4F-F4B3ADE5B4F3Q46145351-42BC165D-5F3D-47A5-AC99-12A569D04F23Q47301010-BF403052-5297-41B6-942D-50F6A9DB2EB0Q48064291-F15B4E19-33F5-41E4-B370-E9B5E2387C44Q53800617-9BD2914F-5C11-46D2-8D99-183C182FADE3Q54248567-36E52FF1-0DE0-44A0-97BD-9135177D8A7EQ57809851-68563B5B-493D-4323-AEDC-58F7AF9E45C2Q57855707-57ABA72B-FA76-499A-9BEE-A9426025B250Q57855796-B584E38A-F3AA-49D4-B240-DBAF0F29F9ADQ58032914-26321986-C580-46BF-9F6E-16B0A0150C4DQ58032918-75C76258-0FF9-471C-803A-5762967A4648
P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
ricercatore
@it
հետազոտող
@hy
name
Ivan Hrdý
@ast
Ivan Hrdý
@cs
Ivan Hrdý
@en
Ivan Hrdý
@es
Ivan Hrdý
@nl
Ivan Hrdý
@sl
type
label
Ivan Hrdý
@ast
Ivan Hrdý
@cs
Ivan Hrdý
@en
Ivan Hrdý
@es
Ivan Hrdý
@nl
Ivan Hrdý
@sl
prefLabel
Ivan Hrdý
@ast
Ivan Hrdý
@cs
Ivan Hrdý
@en
Ivan Hrdý
@es
Ivan Hrdý
@nl
Ivan Hrdý
@sl
P214
P1053
K-8931-2017
P106
P21
P214
P31
P3829
P496
0000-0002-5595-9177
P569
1963-01-01T00:00:00Z
P691
mzk2008442773
P7859
viaf-84737986