Structure of PDB 3qlr Chain A Binding Site BS03
Receptor Information
>3qlr Chain A (length=192) Species:
5476
(Candida albicans) [
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MLKPNVAIIVAALKPALGIGYKGKMPWRLRKEIRYFKDVTTRTTKPNTRN
AVIMGRKTWESIPQKFRPLPDRLNIILSRSYENEIIDDNIIHASSIESSL
NLVSDVERVFIIGGAEIYNELINNSLVSHLLITEIEHPSPESIEMDTFLK
FPLESWTKQPKSELQKFVGDTVLEDDIKEGDFTYNYTLWTRK
Ligand information
Ligand ID
GLY
InChI
InChI=1S/C2H5NO2/c3-1-2(4)5/h1,3H2,(H,4,5)
InChIKey
DHMQDGOQFOQNFH-UHFFFAOYSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
C(C(=O)O)N
CACTVS 3.341
NCC(O)=O
ACDLabs 10.04
O=C(O)CN
Formula
C2 H5 N O2
Name
GLYCINE
ChEMBL
CHEMBL773
DrugBank
DB00145
ZINC
ZINC000004658552
PDB chain
3qlr Chain A Residue 804 [
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Receptor-Ligand Complex Structure
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PDB
3qlr
Crystal Structures of Candida albicans Dihydrofolate Reductase Bound to Propargyl-Linked Antifolates Reveal the Flexibility of Active Site Loop Residues Critical for Ligand Potency and Selectivity.
Resolution
2.149 Å
Binding residue
(original residue number in PDB)
N5 R108 V109
Binding residue
(residue number reindexed from 1)
N5 R108 V109
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
M25 W27 E32 I33 F36 L69 V109 T133
Catalytic site (residue number reindexed from 1)
M25 W27 E32 I33 F36 L69 V109 T133
Enzyme Commision number
1.5.1.3
: dihydrofolate reductase.
Gene Ontology
Molecular Function
GO:0004146
dihydrofolate reductase activity
GO:0016491
oxidoreductase activity
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:0005739
mitochondrion
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:3qlr
,
PDBe:3qlr
,
PDBj:3qlr
PDBsum
3qlr
PubMed
21726415
UniProt
P22906
|DYR_CANAX Dihydrofolate reductase (Gene Name=DFR1)
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