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1 l as cell-free experiments with uroporphyrin/coproporphyrin.
2 ar porphyrins, such as protoporphyrin IX and coproporphyrin.
3 rphyrins, but, unlike PCT, these were mainly coproporphyrin.
4 s was undertaken in a search for accumulated coproporphyrin, a red autofluorescent byproduct of heme
5 ts studied so far excrete copious amounts of coproporphyrin and protoporphyrin when grown on enriched
6 alysis of extracted dense particles revealed coproporphyrin as the sole porphyrin present.
7 rin intermediates including uroporphyrin and coproporphyrin, based on HPLC analysis of cell lysates a
8 ultraperformance liquid chromatography, with coproporphyrin being the most abundant species in all N.
9 xposed, cooperative interactions between the coproporphyrin carboxylates.
10 les using a model system involving free-base coproporphyrin (COP) complexed with horse heart cytochro
11 edly elevated urinary uroporphyrin (URO) and coproporphyrin (COPRO) consistent with CEP.
12 proporphyrin, insert ferrous iron to make Fe-coproporphyrin (coproheme), and then decarboxylate copro
13 WCNTs with heme (FePP), protoporphyrin (PP), coproporphyrin (CP), and uroporphyrin (UP).
14 dified with a spin-label ([MAL-6-alpha2]), a coproporphyrin ([CP-alpha2]) and a coproporphyrin plus a
15     Because some organisms that possess this coproporphyrin-dependent branch are major causes of huma
16                                              Coproporphyrin exhibits bathochromic shifts in both the
17             As neither protoporphyrin IX nor coproporphyrin export improved with extracellular hemope
18  to a cysteine in the hydrophobic core and a coproporphyrin I (CP) appended on the N-terminus of a sy
19 etic disorder leading to accumulation of uro/coproporphyrin-I in tissues due to inhibition of uroporp
20  AhbD, transform didecarboxysirohaem into Fe-coproporphyrin III and haem respectively.
21   Activation of CgoX induces accumulation of coproporphyrin III and leads to photosensitization of Gr
22 he conversion of coproporphyrinogen III into coproporphyrin III by coproporphyrin synthase HemY, inse
23  to provide rapid and accurate annotation of coproporphyrin III directly from a bacterial-fungal cocu
24           In contrast, the Q0,0 band of zinc coproporphyrin III in a glassy solvent (dimethylformamid
25 se HemH, and oxidative decarboxylation of Fe-coproporphyrin III into protohaem IX by Fe-coproporphyri
26 phyrin synthase HemY, insertion of iron into coproporphyrin III via ferrochelatase HemH, and oxidativ
27   BfrB binds iron-free protoporphyrin IX and coproporphyrin III, whereas BfrC does not bind porphyrin
28 mice lack mitochondrial ATP-driven import of coproporphyrin III.
29  Instead, they oxidize coproporphyrinogen to coproporphyrin, insert ferrous iron to make Fe-coproporp
30 e-coproporphyrin III into protohaem IX by Fe-coproporphyrin oxidase/dehydrogenase HemQ.
31 pha2]), a coproporphyrin ([CP-alpha2]) and a coproporphyrin plus a spin-label ([CP-MAL-6-alpha2]) sel
32            Both the spectral properties of a coproporphyrin probe appended to the loop region and the
33                                          The coproporphyrin probes covalently attached to the N-termi
34             The DeltahemQ mutant accumulates coproporphyrin specifically under aerobic conditions.
35 porphyrinogen III into coproporphyrin III by coproporphyrin synthase HemY, insertion of iron into cop
36 c metabolites including the orange-pigmented coproporphyrin, the antibiotic chloramphenicol, and the
37                           The observation of coproporphyrin within lipofuscin granules, previously un