Crystal structure of Thiamine-monophosphate kinase from Stenotrophomonas maltophilia K279a
Abendroth, J., Horanyi, P.S., Lorimer, D.D., Edwards, T.E.To be published.
Experimental Data Snapshot
Starting Model: experimental
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Entity ID: 1 | |||||
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Molecule | Chains | Sequence Length | Organism | Details | Image |
Thiamine-monophosphate kinase | 328 | Stenotrophomonas maltophilia K279a | Mutation(s): 0  Gene Names: thiL, Smlt0731 EC: 2.7.4.16 | ||
UniProt | |||||
Find proteins for B2FNL5 (Stenotrophomonas maltophilia (strain K279a)) Explore B2FNL5  Go to UniProtKB:  B2FNL5 | |||||
Entity Groups   | |||||
Sequence Clusters | 30% Identity50% Identity70% Identity90% Identity95% Identity100% Identity | ||||
UniProt Group | B2FNL5 | ||||
Sequence AnnotationsExpand | |||||
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Ligands 2 Unique | |||||
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ID | Chains | Name / Formula / InChI Key | 2D Diagram | 3D Interactions | |
EDO Query on EDO | B [auth A], C [auth A] | 1,2-ETHANEDIOL C2 H6 O2 LYCAIKOWRPUZTN-UHFFFAOYSA-N | |||
NA Query on NA | D [auth A] | SODIUM ION Na FKNQFGJONOIPTF-UHFFFAOYSA-N |
Length ( Å ) | Angle ( ˚ ) |
---|---|
a = 80.44 | α = 90 |
b = 88.81 | β = 90 |
c = 44.27 | γ = 90 |
Software Name | Purpose |
---|---|
PHENIX | refinement |
XDS | data reduction |
XSCALE | data scaling |
PDB_EXTRACT | data extraction |
PHASER | phasing |
Coot | model building |
PHENIX | model building |