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6UB7

Crystal structure of a GH128 (subgroup V) exo-beta-1,3-glucanase from Cryptococcus neoformans (CnGH128_V)

Summary for 6UB7
Entry DOI10.2210/pdb6ub7/pdb
DescriptorGlyco_hydro_cc domain-containing protein, POTASSIUM ION (3 entities in total)
Functional Keywordsglycosyl hydrolase, carbohydrate, hydrolase
Biological sourceCryptococcus neoformans
Total number of polymer chains1
Total formula weight32813.25
Authors
Santos, C.R.,Costa, P.A.C.R.,Murakami, M.T. (deposition date: 2019-09-11, release date: 2020-05-20, Last modification date: 2024-03-13)
Primary citationSantos, C.R.,Costa, P.A.C.R.,Vieira, P.S.,Gonzalez, S.E.T.,Correa, T.L.R.,Lima, E.A.,Mandelli, F.,Pirolla, R.A.S.,Domingues, M.N.,Cabral, L.,Martins, M.P.,Cordeiro, R.L.,Junior, A.T.,Souza, B.P.,Prates, E.T.,Gozzo, F.C.,Persinoti, G.F.,Skaf, M.S.,Murakami, M.T.
Structural insights into beta-1,3-glucan cleavage by a glycoside hydrolase family.
Nat.Chem.Biol., 16:920-929, 2020
Cited by
PubMed Abstract: The fundamental and assorted roles of β-1,3-glucans in nature are underpinned on diverse chemistry and molecular structures, demanding sophisticated and intricate enzymatic systems for their processing. In this work, the selectivity and modes of action of a glycoside hydrolase family active on β-1,3-glucans were systematically investigated combining sequence similarity network, phylogeny, X-ray crystallography, enzyme kinetics, mutagenesis and molecular dynamics. This family exhibits a minimalist and versatile (α/β)-barrel scaffold, which can harbor distinguishing exo or endo modes of action, including an ancillary-binding site for the anchoring of triple-helical β-1,3-glucans. The substrate binding occurs via a hydrophobic knuckle complementary to the canonical curved conformation of β-1,3-glucans or through a substrate conformational change imposed by the active-site topology of some fungal enzymes. Together, these findings expand our understanding of the enzymatic arsenal of bacteria and fungi for the breakdown and modification of β-1,3-glucans, which can be exploited for biotechnological applications.
PubMed: 32451508
DOI: 10.1038/s41589-020-0554-5
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.8 Å)
Structure validation

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