Sequence homologies between guanylyl cyclases and structural analogies to other signal‐transducing proteins

FEBS Letters

Böhme, Eycke¹  Koesling, Doris¹  Schultz, Günter¹ 

[1] Institut für Pharmakologie, Freie Universität Berlin, Thielallee 67-73, D-1000 Berlin 33, Germany

关键词: Guanylyl cyclase;    Protein-tyrosine kinase;    Protein-tyrosine phosphatase;    Adenyl cyclase;    Transmembrane signalling;   

DOI  :  10.1016/0014-5793(91)80317-V

学科分类：生物化学/生物物理

来源: John Wiley & Sons Ltd.

【 摘 要 】

The cyclic GMP-forming enzyme guanylyl cyclase exists in cytosolic and in membrane-bound forms differing in structure and regulations. Determination of the primary structures of the guanylyl cyclases revealed that the cytosolic enzyme form consists of two similar subunits and that membrane-bound guanylyl cyclases represent enzyme forms in which the catalytic part is located in an intracellular, C-terminal domain and is regulated by an extracelluar, N-terminal receptor domain. A domain of 250 amino acids conserved in all guanylyl cyclases appears to be required for the formation of cyclic nucleotide, as this homologous domain is also found in the cytosolic regions of the adenylyl cyclase. The general structures of guanylyl cyclases shows similarities with other signal transducing enzymes such as protein-tyrosine phosphatases and protein-tyrosine kinases. which also exist in cytosolic and receptor-linked forms.

【 授权许可】

Unknown