Crystal structure of S-adenosyl-L-homocysteine hydrolase from P. aeruginosa in complex with fragment F2X-Entry F09
Malecki, P.H., Gawel, M., Stepniewska, M., Brzezinski, K.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 |
Adenosylhomocysteinase | 472 | Pseudomonas aeruginosa PAO1 | Mutation(s): 0  Gene Names: ahcY, sahH, PA0432 EC: 3.3.1.1 (PDB Primary Data), 3.13.2.1 (UniProt) | ||
UniProt | |||||
Find proteins for Q9I685 (Pseudomonas aeruginosa (strain ATCC 15692 / DSM 22644 / CIP 104116 / JCM 14847 / LMG 12228 / 1C / PRS 101 / PAO1)) Explore Q9I685  Go to UniProtKB:  Q9I685 | |||||
Entity Groups   | |||||
Sequence Clusters | 30% Identity50% Identity70% Identity90% Identity95% Identity100% Identity | ||||
UniProt Group | Q9I685 | ||||
Sequence AnnotationsExpand | |||||
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Ligands 7 Unique | |||||
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ID | Chains | Name / Formula / InChI Key | 2D Diagram | 3D Interactions | |
NAD Query on NAD | AA [auth C], E [auth A], IA [auth D], P [auth B] | NICOTINAMIDE-ADENINE-DINUCLEOTIDE C21 H27 N7 O14 P2 BAWFJGJZGIEFAR-NNYOXOHSSA-N | |||
UI4 (Subject of Investigation/LOI) Query on UI4 | CA [auth C], H [auth A], I [auth A], LA [auth D], T [auth B] | 4-pyridin-2-ylphenol C11 H9 N O VQHMPVXKDCHHSR-UHFFFAOYSA-N | |||
ADE Query on ADE | BA [auth C], F [auth A], JA [auth D], Q [auth B] | ADENINE C5 H5 N5 GFFGJBXGBJISGV-UHFFFAOYSA-N | |||
PO4 Query on PO4 | EA [auth C] FA [auth C] GA [auth C] HA [auth C] K [auth A] | PHOSPHATE ION O4 P NBIIXXVUZAFLBC-UHFFFAOYSA-K | |||
GOL Query on GOL | KA [auth D], O [auth B], R [auth B], S [auth B], U [auth B] | GLYCEROL C3 H8 O3 PEDCQBHIVMGVHV-UHFFFAOYSA-N | |||
DMS Query on DMS | G [auth A] | DIMETHYL SULFOXIDE C2 H6 O S IAZDPXIOMUYVGZ-UHFFFAOYSA-N | |||
K Query on K | DA [auth C], J [auth A], MA [auth D], V [auth B] | POTASSIUM ION K NPYPAHLBTDXSSS-UHFFFAOYSA-N |
Length ( Å ) | Angle ( ˚ ) |
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a = 73.83 | α = 90 |
b = 132.89 | β = 101.06 |
c = 98.71 | γ = 90 |
Software Name | Purpose |
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PHENIX | refinement |
XDS | data scaling |
XDS | data reduction |
REFMAC | phasing |
Funding Organization | Location | Grant Number |
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Polish National Science Centre | Poland | SONATA BIS 2018/30/E/NZ1/00729 |