Structure of PDB 3fl9 Chain B Binding Site BS01
Receptor Information
>3fl9 Chain B (length=158) Species:
1392
(Bacillus anthracis) [
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MIVSFMVAMDENRVIGKDNLPWRLPSELQYVKKTTMGHPLIMGRKNYEAI
GRPLPGRRNIIVTRNEGYHVEGCEVAHSVEEVFELCKNEEEIFIFGGAQI
YDLFLPYVDKLYITKIHHAFEGDTFFPEMDWKEVFVEKGLTDEKNPYTYY
YHVYEKQQ
Ligand information
Ligand ID
CA
InChI
InChI=1S/Ca/q+2
InChIKey
BHPQYMZQTOCNFJ-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
[Ca++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Ca+2]
Formula
Ca
Name
CALCIUM ION
ChEMBL
DrugBank
DB14577
ZINC
PDB chain
3fl9 Chain B Residue 300 [
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Receptor-Ligand Complex Structure
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PDB
3fl9
Crystal structure of Bacillus anthracis dihydrofolate reductase with the dihydrophthalazine-based trimethoprim derivative RAB1 provides a structural explanation of potency and selectivity.
Resolution
2.4 Å
Binding residue
(original residue number in PDB)
Y108 D110
Binding residue
(residue number reindexed from 1)
Y107 D109
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
M6 L21 W23 E28 L29 V32 L55 I93 T115
Catalytic site (residue number reindexed from 1)
M6 L20 W22 E27 L28 V31 L54 I92 T114
Enzyme Commision number
1.5.1.3
: dihydrofolate reductase.
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0004146
dihydrofolate reductase activity
GO:0016491
oxidoreductase activity
GO:0046872
metal ion binding
GO:0050661
NADP binding
Biological Process
GO:0006730
one-carbon metabolic process
GO:0046452
dihydrofolate metabolic process
GO:0046654
tetrahydrofolate biosynthetic process
GO:0046655
folic acid metabolic process
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:3fl9
,
PDBe:3fl9
,
PDBj:3fl9
PDBsum
3fl9
PubMed
19364848
UniProt
Q81R22
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