Structural and functional roles of residues D95 and D97 in E. coli HPPK
Li, Y., Blaszczyk, J., Ji, X., Yan, H.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 |
2-amino-4-hydroxy-6-hydroxymethyldihydropteridine pyrophosphokinase | 158 | Escherichia coli K-12 | Mutation(s): 1  Gene Names: b0142, foIK, folK, JW0138 EC: 2.7.6.3 | ||
UniProt | |||||
Find proteins for P26281 (Escherichia coli (strain K12)) Explore P26281  Go to UniProtKB:  P26281 | |||||
Entity Groups   | |||||
Sequence Clusters | 30% Identity50% Identity70% Identity90% Identity95% Identity100% Identity | ||||
UniProt Group | P26281 | ||||
Sequence AnnotationsExpand | |||||
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Ligands 5 Unique | |||||
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ID | Chains | Name / Formula / InChI Key | 2D Diagram | 3D Interactions | |
APC Query on APC | C [auth A] | DIPHOSPHOMETHYLPHOSPHONIC ACID ADENOSYL ESTER C11 H18 N5 O12 P3 CAWZRIXWFRFUQB-IOSLPCCCSA-N | |||
PH2 Query on PH2 | D [auth A] | 2-AMINO-6-HYDROXYMETHYL-7,8-DIHYDRO-3H-PTERIDIN-4-ONE C7 H9 N5 O2 CQQNNQTXUGLUEV-UHFFFAOYSA-N | |||
ACT Query on ACT | F [auth A] | ACETATE ION C2 H3 O2 QTBSBXVTEAMEQO-UHFFFAOYSA-M | |||
CL Query on CL | E [auth A] | CHLORIDE ION Cl VEXZGXHMUGYJMC-UHFFFAOYSA-M | |||
MG Query on MG | B [auth A] | MAGNESIUM ION Mg JLVVSXFLKOJNIY-UHFFFAOYSA-N |
Length ( ? ) | Angle ( ? ) |
---|---|
a = 73.33 | ¦Á = 90 |
b = 38.29 | ¦Â = 117.01 |
c = 58.13 | ¦Ă = 90 |
Software Name | Purpose |
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DENZO | data reduction |
SCALEPACK | data scaling |
PHENIX | refinement |
PDB_EXTRACT | data extraction |
ADSC | data collection |
CNS | phasing |