Structure of a stable form of sulfheme.

Abstract:

:A stable green heme was extracted from ferric cyanosulfmyoglobin after it had undergone an internal conversion reaction. After iron removal and conversion to the methyl ester, the resulting green porphyrin was purified by high-pressure liquid chromatography. Visible, 1H NMR, and mass spectrometric studies provided evidence to identify the substituents of the porphyrin. Nuclear Overhauser enhancements enabled an assignment of the single modified pyrrole. Substituent positions 1, 2, 5, 6, 7, and 8 have the original protoporphyrin IX substituents. At ring B, the 4-vinyl group has cyclized with a single sulfur atom to form a fifth ring with a 2,5-dihydrothiophene type of structure.

journal_name

Biochemistry

journal_title

Biochemistry

authors

Bondoc LL,Chau MH,Price MA,Timkovich R

doi

10.1021/bi00374a021

subject

Has Abstract

pub_date

1986-12-30 00:00:00

pages

8458-66

issue

26

eissn

0006-2960

issn

1520-4995

journal_volume

25

pub_type

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