Porphyrin

Porphyrin structure

A porphyrin is a heterocyclic macrocycle made from 4 pyrrole subunits linked on opposite sides through 4 methine bridges. The macrocycle, therefore, is completely aromatic, unlike the related corrins or chlorins.

Contents

Types of porphyrins and related molecules

Porphyrins combine readily with metals, coordinating with them in the central cavity. Iron-, zinc-, copper-, nickel-, and cobalt-containing porphyrins are known, and many other metals can be inserted. A porphyrin in which no metal is inserted in its cavity is called a "free base".

Some iron containing porphyrins are called hemes, and heme-containing proteins, or hemoproteins, are found extensively in biochemistry such as haemoglobin.

If one of the four pyrrole subunits is reduced, a chlorin is produced, the ring structure found in chlorophyll. If two of the four pyrrole subunits are reduced, then either a bacteriochlorin (as found in some photosynthetic bacteria), or an isobacteriochlorin, depending on the relative positions of the reduced pyrroles, is formed.

Porphyrin synthesis

Table

This is a schematic representation of porphyrin biosynthesis, with references by EC number and the OMIM database. The porphyria associated with the deficiency of each enzyme is also shown:

Enzyme substrate Product Chromosome EC OMIM porphyria
ALA synthase Glycine, succinyl CoA D-Aminolevulinic acid 3p21.1 2.3.1.37 (http://www.expasy.org/cgi-bin/nicezyme.pl?2.3.1.37) 125290 (http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=125290) none
ALA dehydratase D-Aminolevulinic acid Porphobilinogen 9q34 4.2.1.24 (http://www.expasy.org/cgi-bin/nicezyme.pl?4.2.1.24) 125270 (http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=125270) acute hepatic
PBG deaminase Porphobilinogen Hydroxymethyl bilane 11q23.3 2.5.1.61 (http://www.expasy.org/cgi-bin/nicezyme.pl?2.5.1.61) 176000 (http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=176000) acute intermittent
Uroporphyrinogen III synthase Hydroxymethyl bilane Uroporphyrinogen III 10q25.2-q26.3 4.2.1.75 (http://www.expasy.org/cgi-bin/nicezyme.pl?4.2.1.75) 606938 (http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=606938) congenital erythropoietic
Uroporphyrinogen III decarboxylase Uroporphyrinogen III Coproporphyrinogen III 1q34 4.1.1.37 (http://www.expasy.org/cgi-bin/nicezyme.pl?4.1.1.37) 176100 (http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=176100) cutanea tarda
Coproporphyrinogen III oxidase Coproporphyrinogen III Protoporphyrinogen IX 3q12 1.3.3.3 (http://www.expasy.org/cgi-bin/nicezyme.pl?1.3.3.3) 121300 (http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=121300) coproporphyria
Protoporphyrinogen oxidase Protoporphyrinogen IX Protoporphyrin IX 1q22 1.3.3.4 (http://www.expasy.org/cgi-bin/nicezyme.pl?1.3.3.4) 600923 (http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600923) variegate
Ferrochelatase Protoporphyrin IX Heme 18q21.3 4.99.1.1 (http://www.expasy.org/cgi-bin/nicezyme.pl?4.99.1.1) 177000 (http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=177000) protoporphyria

In brief

Please see the articles on individual enzymes

Missing image
Heme_synthesis.png
Heme synthesis - note that some reactions occur in the cytoplasm and some in the mitochondrion (yellow)

The committed step for porphyrin synthesis is the formation of D-Aminolevulinic acid from glycine (an abundant amino acid) and succinyl-CoA (from the citric acid cycle). Two dALA molecules are combined into porphobilinogen (PBG), which contains the pyrrole ring. Four PBGs are then combined through deamination into hydroxymethyl bilane (HMB), which is hydrolysed to form the circular tetrapyrrole uroporphyrinogen III. This molecule undergoes a number of further modifications. Intermediates are used in different species to form particular substances, but in humans, the main end product protoporphyrin IX is combined with iron to form heme.

See also

External links

fr:Porphyrine io:Porfirino pl:Porfiryna

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