戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 yrrole groups of uroporphyrinogen to produce coproporphyrinogen.
2 r acetate groups of uroporphyrinogen to form coproporphyrinogen.
3 etic pathway, converting uroporphyrinogen to coproporphyrinogen by decarboxylating the four acetate s
4  erythrocytes by measuring the production of coproporphyrinogen I or III.
5 microM and an apparent Kcat of 16 min-1 with coproporphyrinogen III as substrate.
6 osed to regulate heme synthesis by shuttling coproporphyrinogen III from the cytoplasm into the mitoc
7 formation of haem involves the conversion of coproporphyrinogen III into coproporphyrin III by coprop
8 II oxidase (CPO) catalyzes the conversion of coproporphyrinogen III into protoporphyrinogen IX in thi
9           Loss of AtHEMN1 function increased coproporphyrinogen III level and reduced protoporphyrino
10                         The cpx genes encode coproporphyrinogen III oxidase ('coprogen oxidase'), whi
11                                              Coproporphyrinogen III oxidase (CPO) catalyzes the conve
12 es uroporphyrinogen decarboxylase (UROD) and coproporphyrinogen III oxidase (CPO) in the heme biosynt
13 way: ferrochelatase (HemH) and an isozyme of coproporphyrinogen III oxidase (HemF).
14 and the recently resolved X-ray structure of coproporphyrinogen III oxidase (HemN) was used as the co
15     However, the Apo strain showed increased coproporphyrinogen III oxidase and ferrochelatase levels
16 r high oxygen tension because of the aerobic coproporphyrinogen III oxidase HemF.
17 at TspO negatively regulates the activity of coproporphyrinogen III oxidase in this bacterium.
18      hemN, encoding one of the isoenzymes of coproporphyrinogen III oxidase of R. sphaeroides, provid
19 stitute for copper-containing plastocyanin), coproporphyrinogen III oxidase, and Mg-protoporphyrin IX
20                                              Coproporphyrinogen III oxidase, encoded by a single nucl
21 is predicted to code for an oxygen-dependent coproporphyrinogen III oxidase.
22 or the two-step decarboxylative oxidation of coproporphyrinogen III to protoporphyrinogen IX catalyze
23 nthetic pathway, catalyzes the conversion of coproporphyrinogen III to protoporphyrinogen IX.
24 s heme to form biliverdin, and HemF oxidizes coproporphyrinogen III to protoporphyrinogen IX.
25 inetics of its proposed endogenous substrate coproporphyrinogen III, and (iii) transport kinetics of
26 zyme utilizes protoporphyrinogen IX, but not coproporphyrinogen III, as substrate and produces 3 mol
27 l and accumulates the biosynthetic precursor coproporphyrinogen III; a suppressor mutant of this stra
28 rboxylation of two propionate side chains on coproporphyrinogen-III to produce protoporphyrinogen-IX.
29  monovinyl intermediate in the metabolism of coproporphyrinogen-IV, was shown to be an equally good s
30 ntification of a small-molecule activator of coproporphyrinogen oxidase (CgoX) from Gram-positive bac
31                                              Coproporphyrinogen oxidase (copro'gen oxidase) catalyses
32                                              Coproporphyrinogen oxidase (CPO) (EC 1.3.3.3), the antep
33                                              Coproporphyrinogen oxidase (CPO) is an essential enzyme
34 r resulting from the half-normal activity of coproporphyrinogen oxidase (CPO), a mitochondrial enzyme
35 hyrinogens were prepared to probe the enzyme coproporphyrinogen oxidase (CPO).
36 tly decreased transcripts were mitochondrial coproporphyrinogen oxidase (CPOX) of the heme pathway an
37 xpression of the porphyrin-synthesis enzymes coproporphyrinogen oxidase (increased) and ferrochelatas
38 px1, Cyc6, and Crd1, encoding, respectively, coproporphyrinogen oxidase, cytochrome c(6), and a novel
39 regulated in a p53-dependent manner included coproporphyrinogen oxidase, ICErel-II cysteine protease,
40 g Cyc6 and Cpx1 encoding cytochrome c(6) and coproporphyrinogen oxidase, respectively.
41 f URO-D in complex with the I and III isomer coproporphyrinogen products.
42                        Instead, they oxidize coproporphyrinogen to coproporphyrin, insert ferrous iro
43 inding cassette transporter, which regulates coproporphyrinogen transport from the cytoplasm into the