about
Identification and structure of a novel archaeal HypB for [NiFe] hydrogenase maturationCrystal structures of chitin binding domains of chitinase from Thermococcus kodakarensis KOD1Crystal structure of a [NiFe] hydrogenase maturation protease HybD from Thermococcus kodakarensis KOD1A regulatory factor, Fil1p, involved in derepression of the isocitrate lyase gene in Saccharomyces cerevisiae--a possible mitochondrial protein necessary for protein synthesis in mitochondria.Dual biosynthesis pathway for longer-chain polyamines in the hyperthermophilic archaeon Thermococcus kodakarensisSodium-driven energy conversion for flagellar rotation of the earliest divergent hyperthermophilic bacterium.Polymorphobacter multimanifer gen. nov., sp. nov., a polymorphic bacterium isolated from Antarctic white rock.A Structurally Novel Chitinase from the Chitin-Degrading Hyperthermophilic Archaeon Thermococcus chitonophagus.Protein synthesis in giant liposomes using the in vitro translation system of Thermococcus kodakaraensis.A novel candidate for the true fructose-1,6-bisphosphatase in archaea.Structural basis of a Ni acquisition cycle for [NiFe] hydrogenase by Ni-metallochaperone HypA and its enhancer.The X-ray crystal structure of the euryarchaeal RNA polymerase in an open-clamp configuration.Archaeal RNA polymerase subunits E and F are not required for transcription in vitro, but a Thermococcus kodakarensis mutant lacking subunit F is temperature-sensitiveAnalysis of carbon source-regulated gene expression by the upstream region of the Candida tropicalis malate synthase gene in Saccharomyces cerevisiae.Characterization of a cytosolic NiFe-hydrogenase from the hyperthermophilic archaeon Thermococcus kodakaraensis KOD1.Pseudouridine at position 55 in tRNA controls the contents of other modified nucleotides for low-temperature adaptation in the extreme-thermophilic eubacterium Thermus thermophilusOverproduction of the membrane-bound [NiFe]-hydrogenase in Thermococcus kodakarensis and its effect on hydrogen productionAn archaeal RNA binding protein, FAU-1, is a novel ribonuclease related to rRNA stability in Pyrococcus and Thermococcus.An archaeal histone is required for transformation of Thermococcus kodakarensis.A novel branching enzyme of the GH-57 family in the hyperthermophilic archaeon Thermococcus kodakaraensis KOD1.Distinct physiological roles of the three [NiFe]-hydrogenase orthologs in the hyperthermophilic archaeon Thermococcus kodakarensis.Genetic studies on the virus-like regions in the genome of hyperthermophilic archaeon, Thermococcus kodakarensis.Different roles of two transcription factor B proteins in the hyperthermophilic archaeon Thermococcus kodakarensis.Genetic analyses of the functions of [NiFe]-hydrogenase maturation endopeptidases in the hyperthermophilic archaeon Thermococcus kodakarensis.Gene regulation of two ferredoxin:NADP+ oxidoreductases by the redox-responsive regulator SurR in Thermococcus kodakarensis.Pcal_1311, an alcohol dehydrogenase homologue from Pyrobaculum calidifontis, displays NADH-dependent high aldehyde reductase activity.Novel and convenient methods for Candida tropicalis gene disruption using a mutated hygromycin B resistance gene.Expression profiles and physiological roles of two types of prefoldins from the hyperthermophilic archaeon Thermococcus kodakaraensis.Stabilization of tRNA (mG37) methyltransferase [TrmD] from Aquifex aeolicus by an intersubunit disulfide bond formation.Continuous hydrogen production by the hyperthermophilic archaeon, Thermococcus kodakaraensis KOD1.Expression of acetylcholine (ACh) and ACh-synthesizing activity in Archaea.Effective approaches for the production of heterologous proteins using the Thermococcus kodakaraensis-based translation system.The Cdc45/RecJ-like protein forms a complex with GINS and MCM, and is important for DNA replication in Thermococcus kodakarensis.Possible function of the second RecJ-like protein in stalled replication fork repair by interacting with Hef.Identification of the glucosamine kinase in the chitinolytic pathway of Thermococcus kodakarensis.The Fur iron regulator-like protein is cryptic in the hyperthermophilic archaeon Thermococcus kodakaraensis.The upstream region of the isocitrate lyase gene (UPR-ICL) of Candida tropicalis induces gene expression in both Saccharomyces cerevisiae and Escherichia coli by acetate via two distinct promoters.Engineering of a hyperthermophilic archaeon, Thermococcus kodakarensis, that displays chitin-dependent hydrogen production.A highly productive system for cell-free protein synthesis using a lysate of the hyperthermophilic archaeon, Thermococcus kodakaraensis.Cell-free protein synthesis at high temperatures using the lysate of a hyperthermophile.
P50
Q27683973-F34D541D-5CEB-458B-947E-74620281E161Q27703750-A026A25D-3F0E-46BC-BFA1-A2F0C024BD16Q27704892-DC32A460-1B28-4E90-819B-E3F62A094546Q27936540-941C5550-3B68-43EA-A885-CA20ED9C22DDQ28485553-186B1B62-BE57-457F-A1A8-D93E75CC5A67Q30659981-A6286549-0473-4C9F-A059-56ABCFDC5B53Q30781954-88EAFA95-D54C-44EB-8993-90B6D6BEF15BQ31072260-DDF54961-0063-4D4F-8E79-61CC0FAEDF50Q33514585-FFEF100D-DA96-4D7C-9256-106543599E7EQ33959692-C25A6FAD-7735-422B-95E2-2973420171B7Q35796174-3A667787-244D-4CDC-B998-D9D42BE95CBCQ36311478-5C78055F-BCA7-46F9-B3B1-44E94738F5B0Q37080464-CAE62C5C-04B6-42E6-AAA8-CAAB76A777CEQ38349463-29E8282C-EA4D-448F-B34B-E0013CB9348FQ39726103-33C0E8B6-C354-4028-AC8B-9D990B85BB7EQ42056393-75F58C14-2AD0-4E68-87E1-7A069BE3ACF1Q42244642-D803CFE4-D96E-4758-91AC-78B9174DE450Q42281351-7C8FC6F3-2AD0-4553-BE69-98CA2382B81BQ42371623-AE984F03-77A0-429D-AC6F-805B5EF82A74Q42577922-C3068B17-5641-4999-8B09-5933B6A6B4DAQ42793303-762D431F-54BF-4EFE-9CFD-7EC256399A74Q43017223-73ABBBB6-873D-4FA2-8FA5-0470A0257D6BQ43021127-21E5A276-534C-4F45-8AAD-357C0F6226EFQ43028820-33A3CA72-D06F-48D2-8162-F94B77104237Q43031339-E078DADD-0946-4504-92DB-5BFF73B7AAEAQ43032967-32F4F72E-8125-4DC5-A446-BAC9852710BAQ43794868-5B1853B9-0AD6-4A17-A666-F2B7A58DA9ACQ44082759-E43FE814-19DB-4E11-8B51-C83201CA7142Q44794796-26DA5026-7D45-412B-A160-4550A1D1FCA8Q45262431-90F511B8-F001-4CFC-A446-7E9F4DF66E0CQ46528775-3784D2B8-576A-4272-A6F1-1604ACF401D8Q46963645-22846728-4ED4-48CC-A98D-B957DAE23337Q47099421-7F7914EE-43D8-4638-AE3E-9694903B4295Q47138433-5BD602D5-62A6-4E71-907A-48CD376342B3Q47340452-31F24B80-89D6-4A0B-9C9C-850E4406B044Q47682886-69F08393-65B1-4669-924B-E66C8F42E22AQ48073804-79278AF2-CB7E-4A9F-87C1-841E6C5D0AB1Q48791808-0E9D8859-5FB9-4BCC-B786-6BE270EE3508Q51094469-7DBF9B41-CA3E-4660-9A1A-5A701D1C6CD4Q51191840-8FFC9788-9B6A-45F8-9E1F-C9A1144F830C
P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Tamotsu Kanai
@ast
Tamotsu Kanai
@en
Tamotsu Kanai
@es
Tamotsu Kanai
@nl
Tamotsu Kanai
@sl
type
label
Tamotsu Kanai
@ast
Tamotsu Kanai
@en
Tamotsu Kanai
@es
Tamotsu Kanai
@nl
Tamotsu Kanai
@sl
prefLabel
Tamotsu Kanai
@ast
Tamotsu Kanai
@en
Tamotsu Kanai
@es
Tamotsu Kanai
@nl
Tamotsu Kanai
@sl
P1053
I-5842-2012
P106
P108
P21
P31
P3829
P496
0000-0003-3537-2114
P569
2000-01-01T00:00:00Z