Loading
PDBj
MenuPDBj@FacebookPDBj@X(formerly Twitter)PDBj@BlueSkyPDBj@YouTubewwPDB FoundationwwPDBDonate
RCSB PDBPDBeBMRBAdv. SearchSearch help

4PVA

Crystal structure of GH62 hydrolase from thermophilic fungus Scytalidium thermophilum

Summary for 4PVA
Entry DOI10.2210/pdb4pva/pdb
Related4PVI
DescriptorGH62 hydrolase, GLYCEROL, PHOSPHATE ION, ... (4 entities in total)
Functional Keywordsarabinofuranosidase, arabinofuranohydrolase, gh62 hydrolase, fungal genomics, arabinoxylan, lignocellulose degradation, hydrolase
Biological sourceScytalidium thermophilum
Total number of polymer chains1
Total formula weight39765.48
Authors
Nocek, B.,Kaur, A.P.,Xu, X.,Cui, H.,Savchenko, A. (deposition date: 2014-03-15, release date: 2014-11-19, Last modification date: 2024-11-06)
Primary citationKaur, A.P.,Nocek, B.P.,Xu, X.,Lowden, M.J.,Leyva, J.F.,Stogios, P.J.,Cui, H.,Di Leo, R.,Powlowski, J.,Tsang, A.,Savchenko, A.
Functional and structural diversity in GH62 alpha-L-arabinofuranosidases from the thermophilic fungus Scytalidium thermophilum.
Microb Biotechnol, 8:419-433, 2015
Cited by
PubMed Abstract: The genome of the thermophilic fungus Scytalidium thermophilum (strain CBS 625.91) harbours a wide range of genes involved in carbohydrate degradation, including three genes, abf62A, abf62B and abf62C, predicted to encode glycoside hydrolase family 62 (GH62) enzymes. Transcriptome analysis showed that only abf62A and abf62C are actively expressed during growth on diverse substrates including straws from barley, alfalfa, triticale and canola. The abf62A and abf62C genes were expressed in Escherichia coli and the resulting recombinant proteins were characterized. Calcium-free crystal structures of Abf62C in apo and xylotriose bound forms were determined to 1.23 and 1.48 Å resolution respectively. Site-directed mutagenesis confirmed Asp55, Asp171 and Glu230 as catalytic triad residues, and revealed the critical role of non-catalytic residues Asp194, Trp229 and Tyr338 in positioning the scissile α-L-arabinofuranoside bond at the catalytic site. Further, the +2R substrate-binding site residues Tyr168 and Asn339, as well as the +2NR residue Tyr226, are involved in accommodating long-chain xylan polymers. Overall, our structural and functional analysis highlights characteristic differences between Abf62A and Abf62C, which represent divergent subgroups in the GH62 family.
PubMed: 25267315
DOI: 10.1111/1751-7915.12168
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.23 Å)
Structure validation

246704

PDB entries from 2025-12-24

PDB statisticsPDBj update infoContact PDBjnumon