6APJ

Crystal Structure of human ST6GALNAC2


Experimental Data Snapshot

  • Method: X-RAY DIFFRACTION
  • Resolution: 3.10 Å
  • R-Value Free: 0.252 
  • R-Value Work: 0.201 
  • R-Value Observed: 0.206 

wwPDB Validation   3D Report Full Report


Ligand Structure Quality Assessment 


This is version 1.4 of the entry. See complete history


Literature

Expression system for structural and functional studies of human glycosylation enzymes.

Moremen, K.W.Ramiah, A.Stuart, M.Steel, J.Meng, L.Forouhar, F.Moniz, H.A.Gahlay, G.Gao, Z.Chapla, D.Wang, S.Yang, J.Y.Prabhakar, P.K.Johnson, R.Rosa, M.D.Geisler, C.Nairn, A.V.Seetharaman, J.Wu, S.C.Tong, L.Gilbert, H.J.LaBaer, J.Jarvis, D.L.

(2018) Nat Chem Biol 14: 156-162

  • DOI: https://doi.org/10.1038/nchembio.2539
  • Primary Citation of Related Structures:  
    6APJ, 6APL

  • PubMed Abstract: 

    Vertebrate glycoproteins and glycolipids are synthesized in complex biosynthetic pathways localized predominantly within membrane compartments of the secretory pathway. The enzymes that catalyze these reactions are exquisitely specific, yet few have been extensively characterized because of challenges associated with their recombinant expression as functional products. We used a modular approach to create an expression vector library encoding all known human glycosyltransferases, glycoside hydrolases, and sulfotransferases, as well as other glycan-modifying enzymes. We then expressed the enzymes as secreted catalytic domain fusion proteins in mammalian and insect cell hosts, purified and characterized a subset of the enzymes, and determined the structure of one enzyme, the sialyltransferase ST6GalNAcII. Many enzymes were produced at high yields and at similar levels in both hosts, but individual protein expression levels varied widely. This expression vector library will be a transformative resource for recombinant enzyme production, broadly enabling structure-function studies and expanding applications of these enzymes in glycochemistry and glycobiology.


  • Organizational Affiliation

    Complex Carbohydrate Research Center, University of Georgia, Athens, Georgia, USA.


Macromolecules
Find similar proteins by:  (by identity cutoff)  |  3D Structure
Entity ID: 1
MoleculeChains Sequence LengthOrganismDetailsImage
Alpha-N-acetylgalactosaminide alpha-2,6-sialyltransferase 2
A, B, C, D, E
A, B, C, D, E, F
374Homo sapiensMutation(s): 0 
Gene Names: ST6GALNAC2SIAT7BSIATL1STHM
EC: 2.4.99
UniProt & NIH Common Fund Data Resources
Find proteins for Q9UJ37 (Homo sapiens)
Explore Q9UJ37 
Go to UniProtKB:  Q9UJ37
PHAROS:  Q9UJ37
GTEx:  ENSG00000070731 
Entity Groups  
Sequence Clusters30% Identity50% Identity70% Identity90% Identity95% Identity100% Identity
UniProt GroupQ9UJ37
Sequence Annotations
Expand
  • Reference Sequence
Small Molecules
Modified Residues  1 Unique
IDChains TypeFormula2D DiagramParent
MSE
Query on MSE
A, B, C, D, E
A, B, C, D, E, F
L-PEPTIDE LINKINGC5 H11 N O2 SeMET
Experimental Data & Validation

Experimental Data

  • Method: X-RAY DIFFRACTION
  • Resolution: 3.10 Å
  • R-Value Free: 0.252 
  • R-Value Work: 0.201 
  • R-Value Observed: 0.206 
  • Space Group: P 1
Unit Cell:
Length ( Å )Angle ( ˚ )
a = 71.346α = 98.78
b = 71.803β = 101.92
c = 134.246γ = 103.48
Software Package:
Software NamePurpose
PHENIXrefinement
REFMACrefinement
CNSrefinement
XDSdata reduction
XDSdata scaling
SHELXCDphasing

Structure Validation

View Full Validation Report



Ligand Structure Quality Assessment 


Entry History 

Deposition Data

Revision History  (Full details and data files)

  • Version 1.0: 2017-12-20
    Type: Initial release
  • Version 1.1: 2018-01-03
    Changes: Database references
  • Version 1.2: 2018-01-24
    Changes: Database references
  • Version 1.3: 2019-07-17
    Changes: Data collection, Refinement description
  • Version 1.4: 2020-07-29
    Type: Remediation
    Reason: Carbohydrate remediation
    Changes: Data collection, Derived calculations, Structure summary