Structure of PDB 6fny Chain A

Receptor sequence
>6fnyA (length=515) Species: 266834 (Sinorhizobium meliloti 1021) [Search protein sequence]
GDPVTTGKPNILIIMVDQLNGKLFPDGPADFLHAPNLKALAKRSARFHNN
YTSSPLCAPARASFMAGQLPSRTRVYDNAAEYQSSIPTYAHHLRRAGYYT
ALSGKMHFVGPDQLHGFEERLTTDIYPADFGWTPDYRKPGERIDWWYHNL
GSVTGAGVAEITNQMEYDDEVAFLANQKLYQLSRENDDESRRPWCLTVSF
THPHDPYVARRKFWDLYEDCEHLTPEVGAIPLDEQDPHSQRIMLSCDYQN
FDVTEENVRRSRRAYFANISYLDEKVGELIDTLTRTRMLDDTLILFCSDH
GDMLGERGLWFKMNFFEGSARVPLMIAGPGIAPGLHLTPTSNLDVTPTLA
DLAGISLEEVRPWTDGVSLVPMVNGVERTEPVLMEYAAEASYAPLVAIRE
GKWKYVYCALDPEQLFDLEADPLELTNLAENPRGPVDQATLTAFRDMRAA
HWDMEAFDAAVRESQARRWVVYEALRNGAYYPWDHQPLQKASERYMRNHM
NLDTLEESKRYPRGE
3D structure
PDB6fny Structural and Mechanistic Analysis of the Choline Sulfatase from Sinorhizobium melliloti: A Class I Sulfatase Specific for an Alkyl Sulfate Ester.
ChainA
Resolution2.79 Å
3D
structure
Catalytic site residues are labeled in the structure
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Enzymatic activity
Catalytic site (original residue number in PDB) D14 Q15 C54 R58 K102 H104 T130 H201 D296 H297 K309
Catalytic site (residue number reindexed from 1) D17 Q18 C57 R61 K105 H107 T133 H204 D299 H300 K312
Enzyme Commision number 3.1.6.6: choline-sulfatase.
Interaction with ligand
Site
#
Ligand Ligand
chain
Binding residues on receptor
(original residue number in PDB)
Binding residues on receptor
(residue number reindexed from 1)
Binding affinity
BS01 CA A D14 C54 D296 H297 D17 C57 D299 H300
Gene Ontology
Molecular Function
GO:0008484 sulfuric ester hydrolase activity
GO:0016787 hydrolase activity
GO:0046872 metal ion binding
GO:0047753 choline-sulfatase activity
Biological Process
GO:0042425 choline biosynthetic process
Cellular Component
GO:0005737 cytoplasm

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Molecular Function

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Biological Process

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Cellular Component
External links
PDB RCSB:6fny, PDBe:6fny, PDBj:6fny
PDBsum6fny
PubMed29458126
UniProtO69787|BETC_RHIME Choline-sulfatase (Gene Name=betC)

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