9DTP | pdb_00009dtp

GlfT2 from Nocardia brasiliensis


Experimental Data Snapshot

  • Method: X-RAY DIFFRACTION
  • Resolution: 3.11 Å
  • R-Value Free: 
    0.258 (Depositor), 0.257 (DCC) 
  • R-Value Work: 
    0.221 (Depositor), 0.221 (DCC) 
  • R-Value Observed: 
    0.222 (Depositor) 

Starting Model: in silico
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wwPDB Validation   3D Report Full Report


Ligand Structure Quality Assessment 


This is version 1.0 of the entry. See complete history


Literature

GlfT2 from Nocardia brasiliensis

Carter, A.W.Dodge, G.J.Keys, A.M.Justen, A.M.Taylor, K.I.Imperiali, B.Kulik, H.J.Kiessling, L.L.

To be published.

Macromolecules
Find similar proteins by:  (by identity cutoff)  |  3D Structure
Entity ID: 1
MoleculeChains Sequence LengthOrganismDetailsImage
Galactofuranosyltransferase
A, B, C, D, E
A, B, C, D, E, F, G, H
666Nocardia brasiliensis ATCC 700358Mutation(s): 0 
Gene Names: O3I_000690
UniProt
Find proteins for K0EQQ2 (Nocardia brasiliensis (strain ATCC 700358 / HUJEG-1))
Explore K0EQQ2 
Go to UniProtKB:  K0EQQ2
Entity Groups  
Sequence Clusters30% Identity50% Identity70% Identity90% Identity95% Identity100% Identity
UniProt GroupK0EQQ2
Sequence Annotations
Expand
  • Reference Sequence
Small Molecules
Ligands 3 Unique
IDChains Name / Formula / InChI Key2D Diagram3D Interactions
TRT
Query on TRT

Download Ideal Coordinates CCD File 
DA [auth F]
HA [auth G]
J [auth A]
KA [auth H]
N [auth B]
DA [auth F],
HA [auth G],
J [auth A],
KA [auth H],
N [auth B],
R [auth C],
V [auth D],
Z [auth E]
FRAGMENT OF TRITON X-100
C21 H36 O4
HEUDUECKTWTQQR-UHFFFAOYSA-N
GOL
Query on GOL

Download Ideal Coordinates CCD File 
AA [auth E]
BA [auth E]
EA [auth F]
FA [auth F]
IA [auth G]
AA [auth E],
BA [auth E],
EA [auth F],
FA [auth F],
IA [auth G],
K [auth A],
L [auth A],
LA [auth H],
MA [auth H],
O [auth B],
P [auth B],
S [auth C],
T [auth C],
W [auth D],
X [auth D]
GLYCEROL
C3 H8 O3
PEDCQBHIVMGVHV-UHFFFAOYSA-N
MG
Query on MG

Download Ideal Coordinates CCD File 
CA [auth F]
GA [auth G]
I [auth A]
JA [auth H]
M [auth B]
CA [auth F],
GA [auth G],
I [auth A],
JA [auth H],
M [auth B],
Q [auth C],
U [auth D],
Y [auth E]
MAGNESIUM ION
Mg
JLVVSXFLKOJNIY-UHFFFAOYSA-N
Experimental Data & Validation

Experimental Data

  • Method: X-RAY DIFFRACTION
  • Resolution: 3.11 Å
  • R-Value Free:  0.258 (Depositor), 0.257 (DCC) 
  • R-Value Work:  0.221 (Depositor), 0.221 (DCC) 
  • R-Value Observed: 0.222 (Depositor) 
Space Group: P 21 21 21
Unit Cell:
Length ( Å )Angle ( ˚ )
a = 107.026α = 90
b = 205.045β = 90
c = 295.32γ = 90
Software Package:
Software NamePurpose
PHENIXrefinement
JBluIce-EPICSdata collection
XDSdata reduction
XDSdata scaling
PHENIXphasing
Cootmodel building

Structure Validation

View Full Validation Report



Ligand Structure Quality Assessment 


Entry History & Funding Information

Deposition Data


Funding OrganizationLocationGrant Number
National Institutes of Health/National Institute Of Allergy and Infectious Diseases (NIH/NIAID)United States5R01 AI126592-09
National Institutes of Health/National Institute of General Medical Sciences (NIH/NIGMS)United States1F31 GM148069

Revision History  (Full details and data files)

  • Version 1.0: 2025-10-08
    Type: Initial release