Evidence map›Paper›PMID 30644839›Full record

ArticleActa crystallographica. Section D, Structural biology2019

The structure of the AliC GH13 α-amylase from Alicyclobacillus sp. reveals the accommodation of starch branching points in the α-amylase family.

Jon Agirre, Olga Moroz, Sebastian Meier, Jesper Brask, Astrid Munch, Tine Hoff, Carsten Andersen, Keith S Wilson, Gideon J Davies

Open access · greenAbstract read
In one paragraph

Article in Acta crystallographica. Section D, Structural biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Crystal Structure of 4,6-α-Glucanotransferase GtfC-ΔC from ThermophilicJournal of agricultural and food chemistry · 2022
    Article
  5. Review
  6. Article
  7. 3D-Printed Protein Models as an Educational Tool in Biochemistry Outreach.Biochemistry and molecular biology education : a bimonthly publication of the International Union of Biochemistry and Molecular Biology
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 2 countries.

Jon AgirreYork Structural Biology Laboratory, Department of Chemistry, The University of York, York YO10 5DD, England.ORCID 0000-0002-1086-0253
Olga MorozYork Structural Biology Laboratory, Department of Chemistry, The University of York, York YO10 5DD, England.ORCID 0000-0002-0354-6119
Sebastian MeierDepartment of Chemistry, Technical University of Denmark, 2800 Lyngby, Denmark.ORCID 0000-0003-3761-3217
Jesper BraskNovozymes A/S, Krogshoejvej 36, 2880 Bagsvaerd, Denmark.
Astrid MunchNovozymes A/S, Krogshoejvej 36, 2880 Bagsvaerd, Denmark.ORCID 0000-0002-3650-8143
Tine HoffNovozymes A/S, Krogshoejvej 36, 2880 Bagsvaerd, Denmark.
Carsten AndersenNovozymes A/S, Krogshoejvej 36, 2880 Bagsvaerd, Denmark.
Keith S WilsonYork Structural Biology Laboratory, Department of Chemistry, The University of York, York YO10 5DD, England.ORCID 0000-0002-3581-2194
Gideon J DaviesYork Structural Biology Laboratory, Department of Chemistry, The University of York, York YO10 5DD, England.ORCID 0000-0002-7343-776X
Novozymes (Denmark) · DKUniversity of York · GBTechnical University of Denmark · DK

Funding

Royal Society Ken Murray Research ProfessorshipRoyal Society UF160039
6 · The paper itself

Abstract

α-Amylases are glycoside hydrolases that break the α-1,4 bonds in starch and related glycans. The degradation of starch is rendered difficult by the presence of varying degrees of α-1,6 branch points and their possible accommodation within the active centre of α-amylase enzymes. Given the myriad industrial uses for starch and thus also for α-amylase-catalysed starch degradation and modification, there is considerable interest in how different α-amylases might accommodate these branches, thus impacting on the potential processing of highly branched post-hydrolysis remnants (known as limit dextrins) and societal applications. Here, it was sought to probe the branch-point accommodation of the Alicyclobacillus sp. CAZy family GH13 α-amylase AliC, prompted by the observation of a molecule of glucose in a position that may represent a branch point in an acarbose complex solved at 2.1 Å resolution. Limit digest analysis by two-dimensional NMR using both pullulan (a regular linear polysaccharide of α-1,4, α-1,4, α-1,6 repeating trisaccharides) and amylopectin starch showed how the Alicyclobacillus sp. enzyme could accept α-1,6 branches in at least the -2, +1 and +2 subsites, consistent with the three-dimensional structures with glucosyl moieties in the +1 and +2 subsites and the solvent-exposure of the -2 subsite 6-hydroxyl group. Together, the work provides a rare insight into branch-point acceptance in these industrial catalysts.

Indexed as

AcarboseAlicyclobacillusalpha-AmylasesGlycoside Hydrolase InhibitorsMagnetic Resonance SpectroscopyStarchSubstrate SpecificityAcarbosealpha-AmylasesGlycoside Hydrolase InhibitorsStarchAliC GH13 α-amylaseAlicyclobacilluscarbohydrate-active enzymesglycoside hydrolasespullulanstarch branching points

Identifiers

PMID30644839
PMCPMC6333287
OpenAlexW2906820189

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.