Counting the zinc-proteins encoded in the human genome

被引:798
作者
Andreini, C
Banci, L
Bertini, I
Rosato, A
机构
[1] Univ Florence, Magnet Resonance Ctr, CERM, I-50019 Sesto Fiorentino, Italy
[2] Univ Florence, Dept Chem, I-50019 Sesto Fiorentino, Italy
[3] ProtEra Srl, I-50019 Sesto Fiorentino, Italy
关键词
zinc; metalloproteins; zinc finger; metalloprotease;
D O I
10.1021/pr050361j
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Metalloproteins are proteins capable of binding one or more metal ions, which may be required for their biological function, or for regulation of their activities or for structural purposes. Genome sequencing projects have provided a huge number of protein primary sequences, but, even though several different elaborate analyses and annotations have been enabled by a rich and ever-increasing portfolio of bioinformatic tools, metal-binding properties remain difficult to predict as well as to investigate experimentally. Consequently, the present knowledge about metalloproteins is only partial. The present bioinformatic research proposes a strategy to answer the question of how many and which proteins encoded in the human genome may require zinc for their physiological function. This is achieved by a combination of approaches, which include: (i) searching in the proteome for the zinc-binding patterns that, on their turn, are obtained from all available X-ray data; 00 using libraries of metal-binding protein domains based on multiple sequence alignments of known metalloproteins obtained from the Pfam database; and (iii) mining the annotations of human gene sequences, which are based on any type of information available. It is found that 1684 proteins in the human proteome are independently identified by all three approaches as zinc-proteins, 746 are identified by two, and 777 are identified by only one method. By assuming that all proteins identified by at least two approaches are truly zinc-binding and inspecting the proteins identified by a single method, it can be proposed that ca. 2800 human proteins are potentially zinc-binding in vivo, corresponding to 10% of the human proteome, with an uncertainty of 400 sequences. Available functional information suggests that the large majority of human zinc-binding proteins are involved in the regulation of gene expression. The most abundant class of zinc-binding proteins in humans is that of zinc-fingers, with Cys(4) and Cys(2)His(2) being the most common types of coordination environment.
引用
收藏
页码:196 / 201
页数:6
相关论文
共 39 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]   A hint to search for metalloproteins in gene banks [J].
Andreini, C ;
Bertini, I ;
Rosato, A .
BIOINFORMATICS, 2004, 20 (09) :1373-1380
[3]   Comparative analysis of the ADAM and ADAMTS families [J].
Andreini, C ;
Banci, L ;
Bertini, I ;
Elmi, S ;
Rosato, A .
JOURNAL OF PROTEOME RESEARCH, 2005, 4 (03) :881-888
[4]   Gene Ontology: tool for the unification of biology [J].
Ashburner, M ;
Ball, CA ;
Blake, JA ;
Botstein, D ;
Butler, H ;
Cherry, JM ;
Davis, AP ;
Dolinski, K ;
Dwight, SS ;
Eppig, JT ;
Harris, MA ;
Hill, DP ;
Issel-Tarver, L ;
Kasarskis, A ;
Lewis, S ;
Matese, JC ;
Richardson, JE ;
Ringwald, M ;
Rubin, GM ;
Sherlock, G .
NATURE GENETICS, 2000, 25 (01) :25-29
[5]   Structural genomics of proteins involved in copper homeostasis [J].
Banci, L ;
Rosato, A .
ACCOUNTS OF CHEMICAL RESEARCH, 2003, 36 (03) :215-221
[6]  
Bateman A, 2004, NUCLEIC ACIDS RES, V32, pD138, DOI [10.1093/nar/gkp985, 10.1093/nar/gkr1065, 10.1093/nar/gkh121]
[7]   The Protein Data Bank [J].
Berman, HM ;
Westbrook, J ;
Feng, Z ;
Gilliland, G ;
Bhat, TN ;
Weissig, H ;
Shindyalov, IN ;
Bourne, PE .
NUCLEIC ACIDS RESEARCH, 2000, 28 (01) :235-242
[8]   Copper modulates the degradation of copper chaperone for Cu,Zn superoxide dismutase by the 26 S proteosome [J].
Bertinato, J ;
L'Abbé, MR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (37) :35071-35078
[9]   Bioinorganic chemistry in the postgenomic era [J].
Bertini, I ;
Rosato, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (07) :3601-3604
[10]   Browsing gene banks for Fe2S2 ferredoxins and structural modeling of 88 plant-type sequences:: An analysis of fold and function [J].
Bertini, I ;
Luchinat, C ;
Provenzani, A ;
Rosato, A ;
Vasos, PR .
PROTEINS-STRUCTURE FUNCTION AND GENETICS, 2002, 46 (01) :110-127