Structure of PDB 5ecc Chain B Binding Site BS02
Receptor Information
>5ecc Chain B (length=157) Species:
573
(Klebsiella pneumoniae) [
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MKLSLMVAISKNGVIGNGPDIPWSAKGEQLLFKAITYNQWLLVGRKTFES
MGALPNRKYAVVTRSSFTSDNENVLIFPSIKDALTNLKKITDHVIVSGGG
EIYKSLIDQVDTLHISTIDIEPEGDVYFPEIPSNFRPVFTQDFASNINYS
YQIWQKG
Ligand information
Ligand ID
6DR
InChI
InChI=1S/C21H21N5O/c1-3-18-17(20(22)26-21(23)25-18)6-4-5-16-13-15(7-8-19(16)27-2)14-9-11-24-12-10-14/h7-13H,3,5H2,1-2H3,(H4,22,23,25,26)
InChIKey
CZCHMGRCEXJPTP-UHFFFAOYSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.7.2
CCc1c(c(nc(n1)N)N)C#CCc2cc(ccc2OC)c3ccncc3
ACDLabs 12.01
n3c(c(C#CCc2cc(c1ccncc1)ccc2OC)c(nc3N)N)CC
CACTVS 3.370
CCc1nc(N)nc(N)c1C#CCc2cc(ccc2OC)c3ccncc3
Formula
C21 H21 N5 O
Name
6-ethyl-5-{3-[2-methoxy-5-(pyridin-4-yl)phenyl]prop-1-yn-1-yl}pyrimidine-2,4-diamine
ChEMBL
CHEMBL3526249
DrugBank
ZINC
ZINC000095921195
PDB chain
5ecc Chain B Residue 202 [
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Receptor-Ligand Complex Structure
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PDB
5ecc
Crystal Structures of Trimethoprim-Resistant DfrA1 Rationalize Potent Inhibition by Propargyl-Linked Antifolates.
Resolution
1.87 Å
Binding residue
(original residue number in PDB)
M5 V6 I20 E27 Q28 F31 M50
Binding residue
(residue number reindexed from 1)
M6 V7 I21 E28 Q29 F32 M51
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
M5 I20 W22 E27 Q28 F31 L53 V93 S115
Catalytic site (residue number reindexed from 1)
M6 I21 W23 E28 Q29 F32 L54 V94 S116
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:0050661
NADP binding
Biological Process
GO:0046452
dihydrofolate metabolic process
GO:0046654
tetrahydrofolate biosynthetic process
GO:0046655
folic acid metabolic process
View graph for
Molecular Function
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Biological Process
External links
PDB
RCSB:5ecc
,
PDBe:5ecc
,
PDBj:5ecc
PDBsum
5ecc
PubMed
27624966
UniProt
A4GRC7
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