Structure of PDB 6cqa Chain A Binding Site BS01
Receptor Information
>6cqa Chain A (length=159) Species:
562
(Escherichia coli) [
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MISLIAALAVDRVIGMENAMPWNLPADLAWFKRNTLNKPVIMGRHTWESI
GRPLPGRKNIILSSQPGTDDRVTWVKSVDEAIAACGDVPEIMVIGGGRVY
EQFLPKAQKLYLTHIDAEVEGDTHFPDYEPDDWESVFSEFHDADAQNSHS
YCFEILERR
Ligand information
Ligand ID
PQD
InChI
InChI=1S/C17H16N6/c18-11-3-1-2-10(8-11)9-23-7-6-12-14(23)5-4-13-15(12)16(19)22-17(20)21-13/h1-8H,9,18H2,(H4,19,20,21,22)
InChIKey
DNYUNVSBWOHMOD-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.385
Nc1cccc(Cn2ccc3c2ccc4nc(N)nc(N)c34)c1
OpenEye OEToolkits 2.0.6
c1cc(cc(c1)N)Cn2ccc3c2ccc4c3c(nc(n4)N)N
ACDLabs 12.01
c1c(N)cccc1Cn4c3ccc2nc(N)nc(c2c3cc4)N
Formula
C17 H16 N6
Name
7-[(3-aminophenyl)methyl]-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
ChEMBL
DrugBank
ZINC
PDB chain
6cqa Chain A Residue 203 [
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Receptor-Ligand Complex Structure
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PDB
6cqa
The crystal structure of a tetrahydrofolate-bound dihydrofolate reductase reveals the origin of slow product release.
Resolution
2.2 Å
Binding residue
(original residue number in PDB)
I5 A6 A7 M16 D27 F31 I50 I94
Binding residue
(residue number reindexed from 1)
I5 A6 A7 M16 D27 F31 I50 I94
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
I5 M20 W22 D27 L28 F31 L54 I91 T113
Catalytic site (residue number reindexed from 1)
I5 M20 W22 D27 L28 F31 L54 I91 T113
Enzyme Commision number
1.5.1.3
: dihydrofolate reductase.
Gene Ontology
Molecular Function
GO:0004146
dihydrofolate reductase activity
GO:0005515
protein binding
GO:0005542
folic acid binding
GO:0016491
oxidoreductase activity
GO:0050661
NADP binding
GO:0051870
methotrexate binding
GO:0051871
dihydrofolic acid binding
GO:0070401
NADP+ binding
GO:0070402
NADPH binding
Biological Process
GO:0006730
one-carbon metabolic process
GO:0009257
10-formyltetrahydrofolate biosynthetic process
GO:0009410
response to xenobiotic stimulus
GO:0031427
response to methotrexate
GO:0046452
dihydrofolate metabolic process
GO:0046654
tetrahydrofolate biosynthetic process
GO:0046655
folic acid metabolic 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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Cellular Component
External links
PDB
RCSB:6cqa
,
PDBe:6cqa
,
PDBj:6cqa
PDBsum
6cqa
PubMed
30564747
UniProt
P0ABQ4
|DYR_ECOLI Dihydrofolate reductase (Gene Name=folA)
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