1FX2

STRUCTURAL ANALYSIS OF ADENYLATE CYCLASES FROM TRYPANOSOMA BRUCEI IN THEIR MONOMERIC STATE

Summary for 1FX2

• Entry DOI: 10.2210/pdb1fx2/pdb
• Related: 1FX4
• Descriptor: RECEPTOR-TYPE ADENYLATE CYCLASE GRESAG 4.1, SULFATE ION, 2,3-DIHYDROXY-1,4-DITHIOBUTANE, ... (4 entities in total)
• Functional Keywords: camp, trypanosomes, adenylyl cyclases, monomer-dimer, catalysis, lyase
• Biological source: Trypanosoma brucei
• Cellular location: Membrane ; Multi-pass membrane protein : Q99279
• Total number of polymer chains: 1
• Total formula weight: 26755.05

Authors

Bieger, B.,Essen, L.-O. (deposition date: 2000-09-25, release date: 2001-02-28, Last modification date: 2024-02-07)

Primary citation

Bieger, B.,Essen, L.O.
Structural analysis of adenylate cyclases from Trypanosoma brucei in their monomeric state.
EMBO J., 20:433-445, 2001

PubMed Abstract: Cyclic AMP is a major trigger of the differentiation process of Trypanosoma brucei, a bloodstream parasite causing sleeping sickness. Its generation in trypanosomes is accomplished by a unique battery of membrane-bound adenylate cyclases (ACs). We have determined the high-resolution X-ray structures of the catalytic domains of two trypanosomal ACs (tACs), GRESAG4.1 and GRESAG4.3. The tAC domains are structurally highly related to the AC domains of higher eukaryotes, but also comprise a highly conserved structural element near the active site, the Delta-subdomain. A cavity below the Delta-subdomain might correspond to an allosteric regulator site as indicated by the stereospecific binding of a single (2S,3S)-1,4- dimercapto-2,3-butanediol molecule. In three different crystal forms, the tAC domains are exclusively observed in a monomeric, catalytically inactive state. Biochemical analysis and the mutagenesis profile of GRESAG4.1 confirmed a common catalytic mechanism of tACs that involves transient dimerization of the AC domain. A low dimerization tendency might play a regulatory role in T. brucei if the activation of tACs is similarly driven by ligand-induced dimerization as in membrane-bound guanylate cyclases.

PubMed: 11157750
DOI: 10.1093/emboj/20.3.433

Experimental method

X-RAY DIFFRACTION (1.46 Å)