Structure of PDB 2vef Chain A Binding Site BS01
Receptor Information
>2vef Chain A (length=279) Species:
1313
(Streptococcus pneumoniae) [
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HAKTVICGIINVTPFALEQALQQARKLIAEGASMLDIGGESSYVEIEEEI
QRVVPVIKAIRKESDVLISIDTWKSQVAEAALAAGADLVNDITGLMGDEK
MPHVVAEARAQVVIMFNPVMARPQHPSSLIFPHFGFAFTELADFETLPIE
ELMEAFFERALARAAEAGIAPENILLDPGIGFGLTKKENLLLLRDLDKLH
QKGYPIFLGVSRKRFVINILEENGFEVNPETELGFRNRDTASAHVTSIAA
RQGVEVVRVHDVASHRMAVEIASAIRLAD
Ligand information
Ligand ID
PO4
InChI
InChI=1S/H3O4P/c1-5(2,3)4/h(H3,1,2,3,4)/p-3
InChIKey
NBIIXXVUZAFLBC-UHFFFAOYSA-K
SMILES
Software
SMILES
CACTVS 3.341
[O-][P]([O-])([O-])=O
ACDLabs 10.04
[O-]P([O-])([O-])=O
OpenEye OEToolkits 1.5.0
[O-]P(=O)([O-])[O-]
Formula
O4 P
Name
PHOSPHATE ION
ChEMBL
DrugBank
DB14523
ZINC
PDB chain
2vef Chain A Residue 1304 [
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Receptor-Ligand Complex Structure
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PDB
2vef
Dihydropteroate Synthase from Streptococcus Pneumoniae: Structure, Ligand Recognition and Mechanism of Sulfonamide Resistance.
Resolution
1.8 Å
Binding residue
(original residue number in PDB)
A44 E45 R290
Binding residue
(residue number reindexed from 1)
A29 E30 R266
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
K237 R282
Catalytic site (residue number reindexed from 1)
K213 R258
Enzyme Commision number
2.5.1.15
: dihydropteroate synthase.
Gene Ontology
Molecular Function
GO:0004156
dihydropteroate synthase activity
GO:0016740
transferase activity
GO:0046872
metal ion binding
Biological Process
GO:0009396
folic acid-containing compound biosynthetic process
GO:0042558
pteridine-containing compound metabolic process
GO:0044237
cellular metabolic process
GO:0046654
tetrahydrofolate biosynthetic process
GO:0046656
folic acid biosynthetic process
GO:0046677
response to antibiotic
Cellular Component
GO:0005829
cytosol
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:2vef
,
PDBe:2vef
,
PDBj:2vef
PDBsum
2vef
PubMed
18321242
UniProt
P59655
|DHPS_STRR6 Dihydropteroate synthase (Gene Name=sulA)
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