Structure of PDB 3fcx Chain A Binding Site BS01
Receptor Information
>3fcx Chain A (length=268) Species:
9606
(Homo sapiens) [
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MALKQISSNKCFGGLQKVFEHDSVELNCKMKFAVYLPPKAETGKCPALYW
LSGLTCTEQNFISKSGYHQSASEHGLVVIAPDTSPRGCNIFGTGAGFYVD
ATEDPWKTNYRMYSYVTEELPQLINANFPVDPQRMSIFGHSMGGHGALIC
ALKNPGKYKSVSAFAPICNPVLCPWGKKAFSGYLGSKWKAYDATHLVKSY
PLDILIDQGKDDQFLLDGQLLPDNFIAACTEKKIPVVFRLQEDYDHSYYF
IATFITDHIRHHAKYLNA
Ligand information
Ligand ID
MG
InChI
InChI=1S/Mg/q+2
InChIKey
JLVVSXFLKOJNIY-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Mg+2]
CACTVS 3.341
[Mg++]
Formula
Mg
Name
MAGNESIUM ION
ChEMBL
DrugBank
DB01378
ZINC
PDB chain
3fcx Chain A Residue 283 [
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Receptor-Ligand Complex Structure
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PDB
3fcx
Crystal structure of human esterase D: a potential genetic marker of retinoblastoma
Resolution
1.5 Å
Binding residue
(original residue number in PDB)
H153 P178 D203 A204
Binding residue
(residue number reindexed from 1)
H145 P170 D192 A193
Annotation score
1
Enzymatic activity
Enzyme Commision number
3.1.1.56
: methylumbelliferyl-acetate deacetylase.
3.1.2.12
: S-formylglutathione hydrolase.
Gene Ontology
Molecular Function
GO:0005515
protein binding
GO:0016788
hydrolase activity, acting on ester bonds
GO:0018738
S-formylglutathione hydrolase activity
GO:0042802
identical protein binding
GO:0047374
methylumbelliferyl-acetate deacetylase activity
GO:0052689
carboxylic ester hydrolase activity
Biological Process
GO:0008150
biological_process
GO:0046294
formaldehyde catabolic process
Cellular Component
GO:0005737
cytoplasm
GO:0005788
endoplasmic reticulum lumen
GO:0005829
cytosol
GO:0031410
cytoplasmic vesicle
GO:0070062
extracellular exosome
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:3fcx
,
PDBe:3fcx
,
PDBj:3fcx
PDBsum
3fcx
PubMed
19126594
UniProt
P10768
|ESTD_HUMAN S-formylglutathione hydrolase (Gene Name=ESD)
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