An unusual phylogenetic variation in the metal ion binding sites of porphobilinogen synthase

被引:59
作者
Jaffe, EK [1 ]
机构
[1] Fox Chase Canc Ctr, Inst Canc Res, Philadelphia, PA 19111 USA
来源
CHEMISTRY & BIOLOGY | 2003年 / 10卷 / 01期
关键词
D O I
10.1016/S1074-5521(02)00296-X
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Porphobilinogen synthase (PBGS), which catalyzes the first common step in tetrapyrrole biosynthesis contains a unique phylogenetic variation in the use of metal ions. Using sequence, structure, and enzymological information, this work codifies the phylogenetic segregation of metal utilization in PBGS from archaea, bacteria, and eucarya. All PBGS contain an active site metal binding sequence, determined herein to be either DXCXCX(Y/F)X(3)G(H/Q)CG or DXALDX(Y/F)X(3)G(H/Q)DG. The former dictates a requirement for zinc. Most PBGS that do not require zinc require magnesium and/or potassium instead. Most PBGS are also found to contain the binding determinants for an allosteric magnesium that resides outside the active site. The phylogenetic distribution of PBGS metal ion utilization suggests that the primordial PBGS required zinc and supports a hypothesis that the loss of the zinc site was concurrent with the advent of oxygenic photosynthesis.
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页码:25 / 34
页数:10
相关论文
共 33 条
[1]   Gapped BLAST and PSI-BLAST: a new generation of protein database search programs [J].
Altschul, SF ;
Madden, TL ;
Schaffer, AA ;
Zhang, JH ;
Zhang, Z ;
Miller, W ;
Lipman, DJ .
NUCLEIC ACIDS RESEARCH, 1997, 25 (17) :3389-3402
[2]   Insights into the evolutionary process of genome degradation [J].
Andersson, JO ;
Andersson, SGE .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 1999, 9 (06) :664-671
[3]   KINETICS OF INCORPORATION OF MAGNESIUM (2) INTO PORPHYRIN [J].
BAUM, SJ ;
PLANE, RA .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1966, 88 (05) :910-&
[4]   HYDRATION OF ZINC IONS - A COMPARISON WITH MAGNESIUM AND BERYLLIUM IONS [J].
BOCK, CW ;
KATZ, AK ;
GLUSKER, JP .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1995, 117 (13) :3754-3763
[5]  
BOESE QF, 1991, J BIOL CHEM, V266, P17060
[6]   Respiration capacity of the fermenting bacterium Lactococcus lactis and its positive effects on growth and survival [J].
Duwat, P ;
Sourice, S ;
Cesselin, B ;
Lamberet, G ;
Vido, K ;
Gaudu, P ;
Le Loir, Y ;
Violet, F ;
Loubière, P ;
Gruss, A .
JOURNAL OF BACTERIOLOGY, 2001, 183 (15) :4509-4516
[7]   X-ray structure of 5-aminolaevulinate dehydratase, a hybrid aldolase [J].
Erskine, PT ;
Senior, N ;
Awan, S ;
Lambert, R ;
Lewis, G ;
Tickle, LJ ;
Sarwar, M ;
Spencer, P ;
Thomas, P ;
Warren, MJ ;
ShoolinginJordan, PM ;
Wood, SP ;
Cooper, JB .
NATURE STRUCTURAL BIOLOGY, 1997, 4 (12) :1025-1031
[8]   The X-ray structure of yeast 5-aminolaevulinic acid dehydratase complexed with substrate and three inhibitors [J].
Erskine, PT ;
Newbold, R ;
Brindley, AA ;
Wood, SP ;
Shoolingin-Jordan, PM ;
Warren, MJ ;
Cooper, JB .
JOURNAL OF MOLECULAR BIOLOGY, 2001, 312 (01) :133-141
[9]   High resolution crystal structure of a Mg2+-dependent porphobilinogen synthase [J].
Frankenberg, N ;
Erskine, PT ;
Cooper, JB ;
Shoolingin-Jordan, PM ;
Jahn, D ;
Heinz, DW .
JOURNAL OF MOLECULAR BIOLOGY, 1999, 289 (03) :591-602
[10]   Pseudomonas aeruginosa contains a novel type V porphobilinogen synthase with no required catalytic metal ions [J].
Frankenberg, N ;
Jahn, D ;
Jaffe, EK .
BIOCHEMISTRY, 1999, 38 (42) :13976-13982