10LI | pdb_000010li

D-Ornithine/D-lysine decarboxylase complexed with putrescine and agmatine


Experimental Data Snapshot

  • Method: X-RAY DIFFRACTION
  • Resolution: 1.67 Å
  • R-Value Free: 
    0.180 (Depositor), 0.181 (DCC) 
  • R-Value Work: 
    0.141 (Depositor), 0.141 (DCC) 
  • R-Value Observed: 
    0.143 (Depositor) 

Starting Model: experimental
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Ligand Structure Quality Assessment 


This is version 1.0 of the entry. See complete history


Literature

D-Ornithine/D-lysine decarboxylase complexed with putrescine and agmatine

Phillips, R.S.Blankenship, S.

To be published.

Macromolecules
Find similar proteins by:  (by identity cutoff)  |  3D Structure
Entity ID: 1
MoleculeChains Sequence LengthOrganismDetailsImage
Diaminopimelate decarboxylase478Salmonella enterica subsp. enterica serovar TyphimuriumMutation(s): 0 
Gene Names: 
UniProt
Find proteins for A0A0D6FAR3 (Salmonella typhimurium)
Explore A0A0D6FAR3 
Go to UniProtKB:  A0A0D6FAR3
Entity Groups  
Sequence Clusters30% Identity50% Identity70% Identity90% Identity95% Identity100% Identity
UniProt GroupA0A0D6FAR3
Sequence Annotations
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  • Reference Sequence
Small Molecules
Ligands 7 Unique
IDChains Name / Formula / InChI Key2D Diagram3D Interactions
AG2 (Subject of Investigation/LOI)
Query on AG2

Download Ideal Coordinates CCD File 
J [auth A]AGMATINE
C5 H14 N4
QYPPJABKJHAVHS-UHFFFAOYSA-N
PUT (Subject of Investigation/LOI)
Query on PUT

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B [auth A],
I [auth A]
1,4-DIAMINOBUTANE
C4 H12 N2
KIDHWZJUCRJVML-UHFFFAOYSA-N
DMS
Query on DMS

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D [auth A],
F [auth A],
G [auth A]
DIMETHYL SULFOXIDE
C2 H6 O S
IAZDPXIOMUYVGZ-UHFFFAOYSA-N
EDO
Query on EDO

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C [auth A],
H [auth A]
1,2-ETHANEDIOL
C2 H6 O2
LYCAIKOWRPUZTN-UHFFFAOYSA-N
ACT
Query on ACT

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E [auth A]ACETATE ION
C2 H3 O2
QTBSBXVTEAMEQO-UHFFFAOYSA-M
CL
Query on CL

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K [auth A],
L [auth A],
M [auth A],
N [auth A],
O [auth A]
CHLORIDE ION
Cl
VEXZGXHMUGYJMC-UHFFFAOYSA-M
NA
Query on NA

Download Ideal Coordinates CCD File 
P [auth A]SODIUM ION
Na
FKNQFGJONOIPTF-UHFFFAOYSA-N
Modified Residues  1 Unique
IDChains TypeFormula2D DiagramParent
LLP
Query on LLP
A
L-PEPTIDE LINKINGC14 H22 N3 O7 PLYS
Experimental Data & Validation

Experimental Data

  • Method: X-RAY DIFFRACTION
  • Resolution: 1.67 Å
  • R-Value Free:  0.180 (Depositor), 0.181 (DCC) 
  • R-Value Work:  0.141 (Depositor), 0.141 (DCC) 
  • R-Value Observed: 0.143 (Depositor) 
Space Group: C 1 2 1
Unit Cell:
Length ( Å )Angle ( ˚ )
a = 139.413α = 90
b = 50.556β = 120.692
c = 73.281γ = 90
Software Package:
Software NamePurpose
PHENIXrefinement
autoPROCdata reduction
Aimlessdata scaling
PHASERphasing

Structure Validation

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Ligand Structure Quality Assessment 


Entry History & Funding Information

Deposition Data


Funding OrganizationLocationGrant Number
National Institutes of Health/National Institute of General Medical Sciences (NIH/NIGMS)United StatesGM137008

Revision History  (Full details and data files)

  • Version 1.0: 2026-02-11
    Type: Initial release