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2BZ0

Crystal Structure of E. coli GTP cyclohydrolase II in complex with GTP analogue, GMPcPP, and Zinc

Summary for 2BZ0
Entry DOI10.2210/pdb2bz0/pdb
Related2BZ1
DescriptorGTP CYCLOHYDROLASE II, ZINC ION, MAGNESIUM ION, ... (5 entities in total)
Functional Keywordsriboflavin biosynthesis, gtp cyclohydrolase ii, catalytic zinc, gtp, hydrolase, magnesium
Biological sourceESCHERICHIA COLI
Total number of polymer chains2
Total formula weight44925.46
Authors
Ren, J.,Kotaka, M.,Lockyer, M.,Lamb, H.K.,Hawkins, A.R.,Stammers, D.K. (deposition date: 2005-08-09, release date: 2005-08-19, Last modification date: 2023-12-13)
Primary citationRen, J.,Kotaka, M.,Lockyer, M.,Lamb, H.K.,Hawkins, A.R.,Stammers, D.K.
GTP Cyclohydrolase II Structure and Mechanism.
J.Biol.Chem., 280:36912-, 2005
Cited by
PubMed Abstract: GTP cyclohydrolase II converts GTP to 2,5-diamino-6-beta-ribosyl-4(3H)-pyrimidinone 5'-phosphate, formate and pyrophosphate, the first step in riboflavin biosynthesis. The essential role of riboflavin in metabolism and the absence of GTP cyclohydrolase II in higher eukaryotes makes it a potential novel selective antimicrobial drug target. GTP cyclohydrolase II catalyzes a distinctive overall reaction from GTP cyclohydrolase I; the latter converts GTP to dihydroneopterin triphosphate, utilized in folate and tetrahydrobiopterin biosynthesis. The structure of GTP cyclohydrolase II determined at 1.54-A resolution reveals both a different protein fold to GTP cyclohydrolase I and distinctive molecular recognition determinants for GTP; although in both enzymes there is a bound catalytic zinc. The GTP cyclohydrolase II.GMPCPP complex structure shows Arg(128) interacting with the alpha-phosphonate, and thus in the case of GTP, Arg(128) is positioned to act as the nucleophile for pyrophosphate release and formation of the proposed covalent guanylyl-GTP cyclohydrolase II intermediate. Tyr(105) is identified as playing a key role in GTP ring opening; it is hydrogen-bonded to the zinc-activated water molecule, the latter being positioned for nucleophilic attack on the guanine C-8 atom. Although GTP cyclohydrolase I and GTP cyclohydrolase II both use a zinc ion for the GTP ring opening and formate release, different residues are utilized in each case to catalyze this reaction step.
PubMed: 16115872
DOI: 10.1074/JBC.M507725200
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.6 Å)
Structure validation

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