Glyco-Enzyme Repository

Repository of Expression Constructs for Glycosylation Enzymes

Gateway® entry clones and mammalian, baculovirus and bacterial expression constructs for glycosyltransferases, glycoside hydrolases and glycan-modifying enzymes

aga27A

alpha-galactosidase · Cellvibrio japonicus Ueda107

Bacterial GT / GHClones available from DNASU

External resources

Identification and annotation

Gene symbolaga27A
Enzyme classBacterial GT / GH
CAZy familyNot assigned to a CAZy family
UniProt accessionB3PGJ1
NCBI GeneID6415039
DNA RefSeqNC_010995.1
Protein RefSeqYP_001980770
Source speciesCellvibrio japonicus Ueda107
Annotationalpha-galactosidase

Design strategy

How this coding region was truncated for soluble expression. See Construct Design for the strategy behind these choices.

Expressed residues24-404
Coding-region positions amplified70-1212

Gateway® entry clones

Coding regions captured in pDONR221 (or an equivalent synthesised donor). These transfer into any Gateway destination vector by LR recombination, including user-supplied vectors for custom projects.

Entry cloneFusion strategySequence filesDNASU clone ID
N-term pDONR221 capture cloneN-term fusionCjCD00405628

Expression constructs

Bacterial Expression

pET-based expression in E. coli. Clones are distributed by DNASU.

VectorFusion strategySequence filesDNASU clone ID
pET16-DESTN-term fusionCjCD00405570
pET32-DESTN-term fusionCjCD00405512
Ordering. Copy the DNASU clone ID and paste it into the DNASU clone search. Rows marked not yet assigned describe a construct design for which no distributable clone has been deposited. Baculovirus stocks are supplied by the Jarvis lab (dljarvis@uwyo.edu), never by DNASU. A step-by-step walkthrough is on the Tutorial page.