Phycocyanobilin

Phycocyanobilin is a blue phycobilin, i.e., a tetrapyrrole chromophore found in cyanobacteria and in the chloroplasts of red algae, glaucophytes, and some cryptomonads. Phycocyanobilin is present only in the phycobiliproteins allophycocyanin and phycocyanin, of which it is the terminal acceptor of energy. It is covalently linked to these phycobiliproteins by a thioether bond.

Phycocyanobilin

Names
IUPAC name 3-[(2Z,5E)-2-[[3-(2-carboxyethyl)-5-[(Z)-[(3R,4R)-3-ethyl-4-methyl-5-oxopyrrolidin-2-ylidene]methyl]-4-methyl-1H-pyrrol-2-yl]methylidene]-5-[(4-ethyl-3-methyl-5-oxopyrrol-2-yl)methylidene]-4-methylpyrrol-3-yl]propanoic acid
Identifiers
CAS Number	20298-86-6 Y
3D model (JSmol)	Interactive image
Beilstein Reference	4285356
ChEBI	CHEBI:48863
ChemSpider	16736730
PubChem CID	5288007
UNII	36NUT04V2K Y
CompTox Dashboard (EPA)	DTXSID401107685
InChI InChI=1S/C33H40N4O6/c1-7-20-19(6)32(42)37-27(20)14-25-18(5)23(10-12-31(40)41)29(35-25)15-28-22(9-11-30(38)39)17(4)24(34-28)13-26-16(3)21(8-2)33(43)36-26/h13-15,19-20,34-35H,7-12H2,1-6H3,(H,37,42)(H,38,39)(H,40,41)/b24-13+,27-14-,28-15-/t19-,20-/m1/s1 Key: VUXLILWIGPBTLI-XPIJGMCFSA-N
SMILES CC[C@@H]\1[C@H](C(=O)N/C1=C\C2=C(C(=C(N2)/C=C\3/C(=C(/C(=C\C4=NC(=O)C(=C4C)CC)/N3)C)CCC(=O)O)CCC(=O)O)C)C
Properties
Chemical formula	C33H38N4O6
Molar mass	586.69 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Y verify (what is YN ?) Infobox references

Phycocyanobilin (PCB), has the ability to bind to human serum albumin (HSA), protein found mainly in the blood of humans. This PCB-HCA complex benefits the structure of HSA, increasing the thermal stability of HSA, as well as increasing its ability to prevent against proteolytic activity of other proteins.^[1]

Biosynthetic Pathway

Scheme illustrating the different steps of the biosynthesis of phycocyanobilin

The biosynthetic pathway of phycocyanobilin begins with 5-Aminolevulinic acid (5-ALA).^[2] Two molecules of 5-ALA undergo a condensation reaction catalyzed by Porphobilinogen (PBG) Synthase to yield a molecule of Porphobilinogen (PBG) (not shown).^[3] Four molecules of PBG are polymerized into a linear tetrapyrrole by Porphobilinogen deaminase. This reaction releases four ammonia molecules in the process. Completion of the tetrapyrrole is performed by Uroporphyrinogen III synthase which results in the macrocyclic Uroporphyrinogen III. Uroporphyrinogen III is then converted to a Heme by a Uroporphyrinogen III decarboxylase. The heme molecule is converted to Biliverdin IX α. Biliverdin is then finally reduced to Phycocyanobilin (PCB) by the Phycocyanin Ferredoxin Oxidoreductase PcyA. Literature circa 1989 includes phytochromobilin as an intermediate in this final conversion.^[2]