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1ZOT

crystal structure analysis of the CyaA/C-Cam with PMEAPP

Summary for 1ZOT
Entry DOI10.2210/pdb1zot/pdb
DescriptorCyaA with C-terminal Calmodulin, Calmodulin, MAGNESIUM ION, ... (6 entities in total)
Functional Keywordscyaa, adenylyl cyclase toxin, pmeapp, atp, calmodulin-binding, lyase
Biological sourceBordetella pertussis
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Cellular locationSecreted: P15318
Cytoplasm, cytoskeleton, spindle: P62158
Total number of polymer chains2
Total formula weight47188.83
Authors
Guo, Q.,Tang, W.J. (deposition date: 2005-05-13, release date: 2005-08-09, Last modification date: 2024-02-14)
Primary citationGuo, Q.,Shen, Y.,Lee, Y.S.,Gibbs, C.S.,Mrksich, M.,Tang, W.J.
Structural basis for the interaction of Bordetella pertussis adenylyl cyclase toxin with calmodulin.
Embo J., 24:3190-3201, 2005
Cited by
PubMed Abstract: CyaA is crucial for colonization by Bordetella pertussis, the etiologic agent of whooping cough. Here we report crystal structures of the adenylyl cyclase domain (ACD) of CyaA with the C-terminal domain of calmodulin. Four discrete regions of CyaA bind calcium-loaded calmodulin with a large buried contact surface. Of those, a tryptophan residue (W242) at an alpha-helix of CyaA makes extensive contacts with the calcium-induced, hydrophobic pocket of calmodulin. Mutagenic analyses show that all four regions of CyaA contribute to calmodulin binding and the calmodulin-induced conformational change of CyaA is crucial for catalytic activation. A crystal structure of CyaA-calmodulin with adefovir diphosphate, the metabolite of an approved antiviral drug, reveals the location of catalytic site of CyaA and how adefovir diphosphate tightly binds CyaA. The ACD of CyaA shares a similar structure and mechanism of activation with anthrax edema factor (EF). However, the interactions of CyaA with calmodulin completely diverge from those of EF. This provides molecular details of how two structurally homologous bacterial toxins evolved divergently to bind calmodulin, an evolutionarily conserved calcium sensor.
PubMed: 16138079
DOI: 10.1038/sj.emboj.7600800
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.2 Å)
Structure validation

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数据于2024-10-30公开中

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