spacer
spacer

PDBsum entry 1x1c

Go to PDB code: 
Top Page protein ligands metals links
Transferase PDB id
1x1c
Contents
Protein chain
337 a.a.
Ligands
SO4
SAH
GOL
Metals
_ZN ×5
Waters ×20

References listed in PDB file
Key reference
Title Crystal structures of bchu, A methyltransferase involved in bacteriochlorophyll c biosynthesis, And its complex with s-Adenosylhomocysteine: implications for reaction mechanism.
Authors K.Wada, H.Yamaguchi, J.Harada, K.Niimi, S.Osumi, Y.Saga, H.Oh-Oka, H.Tamiaki, K.Fukuyama.
Ref. J Mol Biol, 2006, 360, 839-849. [DOI no: 10.1016/j.jmb.2006.05.057]
PubMed id 16797589
Abstract
BchU plays a role in bacteriochlorophyll c biosynthesis by catalyzing methylation at the C-20 position of cyclic tetrapyrrole chlorin using S-adenosylmethionine (SAM) as a methyl source. This methylation causes red-shifts of the electronic absorption spectrum of the light-harvesting pigment, allowing green photosynthetic bacteria to adapt to low-light environments. We have determined the crystal structures of BchU and its complex with S-adenosylhomocysteine (SAH). BchU forms a dimer and each subunit consists of two domains, an N-terminal domain and a C-terminal domain. Dimerization occurs through interactions between the N-terminal domains and the residues responsible for the catalytic reaction are in the C-terminal domain. The binding site of SAH is located in a large cavity between the two domains, where SAH is specifically recognized by many hydrogen bonds and a salt-bridge. The electron density map of BchU in complex with an analog of bacteriochlorophyll c located its central metal near the SAH-binding site, but the tetrapyrrole ring was invisible, suggesting that binding of the ring to BchU is loose and/or occupancy of the ring is low. It is likely that His290 acts as a ligand for the central metal of the substrate. The orientation of the substrate was predicted by simulation, and allows us to propose a mechanism for the BchU directed methylation: the strictly conserved Tyr246 residue acts catalytically in the direct transfer of the methyl group from SAM to the substrate through an S(N)2-like mechanism.
Figure 1.
Figure 1. Methylation catalyzed by Chl. tepidum BchU. Compounds: 1, 8-ethyl-12-methyl-bacteriochlorophyllide d; 2, 8-ethyl-12-methyl-bacteriochlorophyllide c.
Figure 9.
Figure 9. A proposed reaction mechanism for C-20 methylation of Zn BChlid d to Zn-BChlid c by SAM and BchU.
The above figures are reprinted by permission from Elsevier: J Mol Biol (2006, 360, 839-849) copyright 2006.
PROCHECK
Go to PROCHECK summary
 Headers

 

spacer

spacer