標(biāo)題: Titlebook: Biochemistry of Vitamin B6; Proceedings of the 7 Timo K. Korpela,Philipp Christen Conference proceedings 1987 Birkh?user Verlag Basel 1987 [打印本頁] 作者: Extraneous 時(shí)間: 2025-3-21 19:54
書目名稱Biochemistry of Vitamin B6影響因子(影響力)
書目名稱Biochemistry of Vitamin B6影響因子(影響力)學(xué)科排名
書目名稱Biochemistry of Vitamin B6網(wǎng)絡(luò)公開度
書目名稱Biochemistry of Vitamin B6網(wǎng)絡(luò)公開度學(xué)科排名
書目名稱Biochemistry of Vitamin B6被引頻次
書目名稱Biochemistry of Vitamin B6被引頻次學(xué)科排名
書目名稱Biochemistry of Vitamin B6年度引用
書目名稱Biochemistry of Vitamin B6年度引用學(xué)科排名
書目名稱Biochemistry of Vitamin B6讀者反饋
書目名稱Biochemistry of Vitamin B6讀者反饋學(xué)科排名
作者: 不透明 時(shí)間: 2025-3-21 20:15 作者: LEER 時(shí)間: 2025-3-22 04:14
Closing Remarksl?, Dr. Timo Korpela, Dr. Seppo Sarimo and all of those who have helped them to make this a pleasant and productive symposium. Their young helpers in the blue and white shirts have charmed us all. Their efforts, the friendliness of the people of Turku, and the beautiful midsummer nights have combine作者: STALE 時(shí)間: 2025-3-22 04:53
Genes, Biosynthesis, and Intracellular Processing of the Iso-Enzymes of Aspartate Aminotransferasegenes, and are synthesized on free polysomes. The precursor contains a basic NH.-terminal prepiece. The genes of the two homologous isoenzymes possess similarly positioned exon-intron boundaries. The prepiece of mAspAT is encoded by one (or more) separate exon(s). Pre-mAspAT cDNA and mAspAT cDNA hav作者: 客觀 時(shí)間: 2025-3-22 11:34
Structure-Function Relation of the Presequence of a Precursor to Pig Mitochondrial Aspartate Aminotrithin its presequence were tested. The amino-terminal portion is essential for mitochondrial uptake and processing. The presence of two positively charged residues, Hisl8 and Arg28, may not be requisite for the uptake, but the processing efficiency was reduced by the single amino acid change, Arg28 作者: 掙扎 時(shí)間: 2025-3-22 15:47
D-Amino Acid Aminotransferase from a Thermophile, , SP. YM-1: Enzymological Properties, Cloning of tbacterium (. sp. YM-1) showed a very high activity of D-amino acid aminotransferase. The enzyme purified to homogeneity from cell extracts of YM-1 has a molecular weight of about 62,000, and is composed of two subunits identical in molecular weight (30,000). The D-amino acid aminotransferase gene wa作者: 利用 時(shí)間: 2025-3-22 20:44 作者: iodides 時(shí)間: 2025-3-22 22:12 作者: Herbivorous 時(shí)間: 2025-3-23 05:08 作者: SEED 時(shí)間: 2025-3-23 09:00
Mechanistic Analysis of the Aspartate Aminotransferase Active Site Mutants—Y70F, K258A, and R292Dt Y70 is not an . amino acid for catalysis. Rather, this residue does provide an important functional role in substantially reducing the rate constant for cofactor dissociation from the enzyme. The PMP form of K258A reacts with α-ketoglutarate to give the ketimine as a stable final product. The corr作者: 草率男 時(shí)間: 2025-3-23 10:57
Bacterial Tryptophan Synthase: A Multienzyme Complex Which Contains Pyridoxal Phosphater oligonucleotide-directed site-specific mutagenesis of the . and . genes of .. has been developed to examine the role of specific amino acid residues in the two subunits. It has been found that changing arginine-179 of the a subunit to leucine does not inactivate the enzyme, but does cause marked a作者: 孵卵器 時(shí)間: 2025-3-23 14:25 作者: 招致 時(shí)間: 2025-3-23 21:50 作者: 漫不經(jīng)心 時(shí)間: 2025-3-23 22:24
Tarife der Kraftfahrtversicherung,; however, no general agreement has yet been reached concerning the site(s) at which the presequence is cleaved off during maturation of the enzyme (Simmaco et al., 1986). In order to gain further Insight into this interesting problem, we undertook the protein structural analysis of the crystalline OATase from pig kidney.作者: 使增至最大 時(shí)間: 2025-3-24 04:22 作者: Pageant 時(shí)間: 2025-3-24 09:27 作者: 我怕被刺穿 時(shí)間: 2025-3-24 12:57 作者: 懲罰 時(shí)間: 2025-3-24 17:26
Mechanistic Analysis of the Aspartate Aminotransferase Active Site Mutants—Y70F, K258A, and R292Dphic analysis showed that the dicarboxylic amino acid substrate specificity is dictated by ion pairing with R292. The mutation R292D converts the title enzyme to a cationic amino acid transaminase, which preferentially catalyzes the transamination of Arg or Lys over Asp or Glu.作者: SPALL 時(shí)間: 2025-3-24 20:16 作者: quiet-sleep 時(shí)間: 2025-3-25 02:20
,Beispiele ausgeführter KWK-Anlagen,hout the world. I knew Prof. Braunstein personally from the 1950’s, and enjoyed our close professional and personal relationship for a period of more than three decades. I am very pleased to be asked to participate in the opening session of this conference*.作者: Juvenile 時(shí)間: 2025-3-25 04:58 作者: hankering 時(shí)間: 2025-3-25 10:52
https://doi.org/10.1007/978-3-663-13222-6fe in vivo. Components of ai hepatic system that reversibly inactivates TyrAT in the presence of L-cysteine are described. An additional, soluble factor irreversibly inactivates TyrAT during incubation at pH 8.作者: penance 時(shí)間: 2025-3-25 14:12 作者: 香料 時(shí)間: 2025-3-25 17:33
Closing Remarksthe blue and white shirts have charmed us all. Their efforts, the friendliness of the people of Turku, and the beautiful midsummer nights have combined to make our week of work together here unforgettable.作者: Eeg332 時(shí)間: 2025-3-25 23:54 作者: 謙卑 時(shí)間: 2025-3-26 00:16
Anlagenauswahl und Dimensionierung,ic acid. Instead, she observed the accumulation of succinate. She had surmised that “possibly a combination of the amino group with some reactive carbohydrate residue takes place; then when splitting and oxidation occur the amino group is retained in the form of a new amino acid”.作者: 放棄 時(shí)間: 2025-3-26 08:07 作者: Chronological 時(shí)間: 2025-3-26 11:01
Tarife der Kraftfahrtversicherung,oxal 5′-phosphate was determined from the nucleotide sequence of the gene and the amino acid sequences of tryptic peptides. The primary structure of D- amino acid aminotransferase shows high sequence homology with that of branched-chain amino acid aminotransferase of .. . (the . gene product).作者: Expurgate 時(shí)間: 2025-3-26 13:39 作者: 人類學(xué)家 時(shí)間: 2025-3-26 20:30
Genes, Biosynthesis, and Intracellular Processing of the Iso-Enzymes of Aspartate Aminotransferaseurs with t. ～0.5 min; it can be blocked by dissipating the mitochondrial membrane potential. The ensuing accumulation of the precursor in the cytosol is limited by its rapid proteolytic degradation (t. ～5 min). Extensive inhibitor studies indicated that the bulk of accumulated pre-mAspAT is degraded作者: Uncultured 時(shí)間: 2025-3-27 00:08 作者: 阻礙 時(shí)間: 2025-3-27 04:17 作者: Host142 時(shí)間: 2025-3-27 08:21 作者: 開始發(fā)作 時(shí)間: 2025-3-27 12:46
Anlagenauswahl und Dimensionierung,, it was more or less accidental and unpredictable. It was preceded by reports concerning two unrelated processes of tissue metabolism. In 1929–1932 J. Parnas and P. Ostern inferred from their studies of the resynthesis of adenylic acid from inosine monophosphate in muscle that this reaction does no作者: 租約 時(shí)間: 2025-3-27 13:49 作者: 搜集 時(shí)間: 2025-3-27 21:51 作者: depreciate 時(shí)間: 2025-3-28 00:55 作者: 遺產(chǎn) 時(shí)間: 2025-3-28 05:39
,Haupts?tze der Kr?fte- und Bewegungslehre,ithin its presequence were tested. The amino-terminal portion is essential for mitochondrial uptake and processing. The presence of two positively charged residues, Hisl8 and Arg28, may not be requisite for the uptake, but the processing efficiency was reduced by the single amino acid change, Arg28 作者: 符合你規(guī)定 時(shí)間: 2025-3-28 06:43 作者: 亞麻制品 時(shí)間: 2025-3-28 13:50
Tarife der Kraftfahrtversicherung,h is then Imported into the mitochondrial matrix and matures therein as a result of proteolytic removal of the presequence. Recently, the complete amino acid sequences of rat (Mueckler & Pitot, 1985) and human (Inana et al., 1986) liver pre-OATases were deduced from the cloned cDNA (complementary DN作者: 嚙齒動(dòng)物 時(shí)間: 2025-3-28 16:59
https://doi.org/10.1007/978-3-663-13222-6T possesses a proteolytically-sensitive site beginning at Arg 27, and an extensive region near the carboxylic terminal that may confer a short half-life in vivo. Components of ai hepatic system that reversibly inactivates TyrAT in the presence of L-cysteine are described. An additional, soluble fact作者: BACLE 時(shí)間: 2025-3-28 19:59
System der Pflichtversicherung,, a specific anti-rat histidine decarboxylase (HDC) antibody which reacted only with HDC-containing cells in rat tissues immunostained DDC-containing cells also in guinea-pig tissues. On immunoblotting, anti-rat HDC antibody recognized not only rat HDC but also guinea-pig DDC.作者: CON 時(shí)間: 2025-3-28 23:14
Sonderformen der Kraftfahrtversicherung,t Y70 is not an . amino acid for catalysis. Rather, this residue does provide an important functional role in substantially reducing the rate constant for cofactor dissociation from the enzyme. The PMP form of K258A reacts with α-ketoglutarate to give the ketimine as a stable final product. The corr作者: 等待 時(shí)間: 2025-3-29 05:28 作者: 發(fā)生 時(shí)間: 2025-3-29 08:38 作者: Campaign 時(shí)間: 2025-3-29 14:20 作者: 過度 時(shí)間: 2025-3-29 17:20 作者: 陳舊 時(shí)間: 2025-3-29 19:50
Demonstration of Immunochemical Cross-Reactivity of Dopa Decarboxylase and Histidine Decarboxylase U, a specific anti-rat histidine decarboxylase (HDC) antibody which reacted only with HDC-containing cells in rat tissues immunostained DDC-containing cells also in guinea-pig tissues. On immunoblotting, anti-rat HDC antibody recognized not only rat HDC but also guinea-pig DDC.作者: FLOUR 時(shí)間: 2025-3-30 00:37
Site-Specific Mutations in E. coli Maltodextrin Phosphorylase With Differential Effects on Substratephorylase activity. Mutagenesis of Lys533 and Glu637 affect K. and k. values to a different extent. The results suggest that Lys533 together wTtri pyridoxal phosphate are part of a proton transfer relay and Glu637 modifies phosphate binding in the ground and transition state.作者: Omniscient 時(shí)間: 2025-3-30 04:09 作者: 1分開 時(shí)間: 2025-3-30 12:09 作者: 不給啤 時(shí)間: 2025-3-30 13:30 作者: COLON 時(shí)間: 2025-3-30 17:28 作者: 恩惠 時(shí)間: 2025-3-30 23:56 作者: vasospasm 時(shí)間: 2025-3-31 01:09 作者: eardrum 時(shí)間: 2025-3-31 05:03
978-3-0348-9989-5Birkh?user Verlag Basel 1987作者: 同位素 時(shí)間: 2025-3-31 09:11
Overview: 978-3-0348-9989-5978-3-0348-9308-4
