Literature DB >> 1899708

Isolation, crystallization, crystal structure analysis and refinement of constitutive C-phycocyanin from the chromatically adapting cyanobacterium Fremyella diplosiphon at 1.66 A resolution.

M Duerring1, G B Schmidt, R Huber.   

Abstract

Constitutive phycocyanin from cyanobacterium Fremyella diplosiphon (Calothrix sp. PCC 7601) grown in green light, has been isolated and crystallized. The crystals belong to the space group R3 with cell constants a = b = 180.26 A, c = 61.24 A, alpha = beta = 90 degrees, gamma = 120 degrees. The crystal structure has been determined by Patterson search techniques using the molecular model of C-phycocyanin from the cyanobacterium Agmenellum quadruplicatum. The asymmetric unit of the crystal cell consists of two (alpha beta)-monomers related by a local dyad. Three asymmetric units are arranged around a crystallographic triad and form an (alpha beta)6-hexamer, the functional unit in the native antenna rod. The initial structure has been refined in a cyclic manner by energy-restrained crystallographic refinement and modelling until the conventional crystallographic R-factor converged at 18.1% with data to a resolution of 1.66 A. The molecular structure resembles closely the C-phycocyanins of Mastigocladus laminosus and A. quadruplicatum. The conformation and configuration of the alpha-84 and beta-84 chromophores is very similar to the corresponding chromophores in the trimeric C-phycocyanin of M. laminosus, whereas the beta-155 chromophore differs in configuration with C(4)-Z, C(10)-Z and C(15)-Z compared to C(4)-Z, C(10)-Z, C(15)-Z,E. The stereochemistry of the beta-155 chiral centres is C(2)-RC(3)-R and C(31)-S, respectively, whereas alpha-84 and beta-84 have C(2)-RC(3)-R and C(31)-R. The amino acid sequences of constitutive and inducible phycocyanin differ mainly in residues located on the surface of the beta-subunits that mediate the inter-hexameric contacts.

Entities:  

Mesh:

Substances:

Year:  1991        PMID: 1899708     DOI: 10.1016/0022-2836(91)90759-y

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   5.469


  29 in total

1.  Evolution of a light-harvesting protein by addition of new subunits and rearrangement of conserved elements: crystal structure of a cryptophyte phycoerythrin at 1.63-A resolution.

Authors:  K E Wilk; S J Harrop; L Jankova; D Edler; G Keenan; F Sharples; R G Hiller; P M Curmi
Journal:  Proc Natl Acad Sci U S A       Date:  1999-08-03       Impact factor: 11.205

2.  Significance of a two-domain structure in subunits of phycobiliproteins revealed by the normal mode analysis.

Authors:  H Kikuchi; H Wako; K Yura; M Go; M Mimuro
Journal:  Biophys J       Date:  2000-09       Impact factor: 4.033

3.  Finding important sites in protein sequences.

Authors:  Peter J Bickel; Katherina J Kechris; Philip C Spector; Gary J Wedemayer; Alexander N Glazer
Journal:  Proc Natl Acad Sci U S A       Date:  2002-11-04       Impact factor: 11.205

Review 4.  Elucidation of the molecular structures of components of the phycobilisome: reconstructing a giant.

Authors:  Noam Adir
Journal:  Photosynth Res       Date:  2005       Impact factor: 3.573

5.  CpeS is a lyase specific for attachment of 3Z-PEB to Cys82 of {beta}-phycoerythrin from Prochlorococcus marinus MED4.

Authors:  Jessica Wiethaus; Andrea W U Busch; Klaus Kock; Lars I Leichert; Christian Herrmann; Nicole Frankenberg-Dinkel
Journal:  J Biol Chem       Date:  2010-09-28       Impact factor: 5.157

6.  Distinct classes of red/far-red photochemistry within the phytochrome superfamily.

Authors:  Nathan C Rockwell; Lixia Shang; Shelley S Martin; J Clark Lagarias
Journal:  Proc Natl Acad Sci U S A       Date:  2009-04-01       Impact factor: 11.205

7.  Unusual spectral properties of bacteriophytochrome Agp2 result from a deprotonation of the chromophore in the red-absorbing form Pr.

Authors:  Benjamin Zienicke; Isabel Molina; René Glenz; Patrick Singer; Dorothee Ehmer; Francisco Velazquez Escobar; Peter Hildebrandt; Rolf Diller; Tilman Lamparter
Journal:  J Biol Chem       Date:  2013-09-13       Impact factor: 5.157

8.  Structural analysis at 2.2 A of orthorhombic crystals presents the asymmetry of the allophycocyanin-linker complex, AP.LC7.8, from phycobilisomes of Mastigocladus laminosus.

Authors:  W Reuter; G Wiegand; R Huber; M E Than
Journal:  Proc Natl Acad Sci U S A       Date:  1999-02-16       Impact factor: 11.205

9.  Subunit interactions and protein stability in the cyanobacterial light-harvesting proteins.

Authors:  T Plank; C Toole; L K Anderson
Journal:  J Bacteriol       Date:  1995-12       Impact factor: 3.490

10.  rpbA controls transcription of the constitutive phycocyanin gene set in Fremyella diplosiphon.

Authors:  K Kahn; M R Schaefer
Journal:  J Bacteriol       Date:  1997-12       Impact factor: 3.490

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.