Structure of PDB 4bc0 Chain A Binding Site BS01

Receptor Information
>4bc0 Chain A (length=542) Species: 10090 (Mus musculus) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
GREDPQLLVRVRGGQLRGIRLKAPGGPVSAFLGIPFAEPPVGSRRFMPPE
PKRPWSGVLDATTFQNVCYQYVDTLYPGFEGTEMWNPNRELSEDCLYLNV
WTPYPRPASPTPVLIWIYGGGFYSGAASLDVYDGRFLAQVEGAVLVSMNY
RVGTFGFLALPGSREAPGNVGLLDQRLALQWVQENIAAFGGDPMSVTLFG
ESAGAASVGMHILSLPSRSLFHRAVLQSGTPNGPWATVSAGEARRRATLL
ARLVGCPPGGAGGNDTELIACLRTRPAQDLVDHEWHVLPQESIFRFSFVP
VVDGDFLSDTPEALINTGDFQDLQVLVGVVKDEGSYFLVYGVPGFSKDNE
SLISRAQFLAGVRIGVPQASDLAAEAVVLHYTDWLHPEDPTHLRDAMSAV
VGDHNVVCPVAQLAGRLAAQGARVYAYIFEHRASTLTWPLWMGVPHGYEI
EFIFGLPLDPSLNYTTEERIFAQRLMKYWTNFARTGDPNDPRDSKSPQWP
PYTTAAQQYVSLNLKPLEVRRGLRAQTCAFWNRFLPKLLSAT
Ligand information
Ligand ID4OJ
InChIInChI=1S/C7H9O4P/c1-6-4-2-3-5-7(6)11-12(8,9)10/h2-5H,1H3,(H2,8,9,10)
InChIKeyHUJOGFUFUMBXPL-UHFFFAOYSA-N
SMILES
SoftwareSMILES
ACDLabs 12.01O=P(O)(Oc1ccccc1C)O
CACTVS 3.385Cc1ccccc1O[P](O)(O)=O
OpenEye OEToolkits 1.9.2Cc1ccccc1OP(=O)(O)O
FormulaC7 H9 O4 P
Name(2-methylphenyl) dihydrogen phosphate;
o-cresyl-phosphate
ChEMBL
DrugBank
ZINCZINC000039189548
PDB chain4bc0 Chain A Residue 600 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
Global viewLocal viewStructure summary

[Spin on] [Spin off] [Reset]
[High quality] [Low quality]
[White background] [Black background]
[Spin on] [Spin off] [Reset]
[High quality] [Low quality]
[White background] [Black background]
PDB4bc0 Inhibition Pathways of the Potent Organophosphate Cbdp with Cholinesterases Revealed by X-Ray Crystallographic Snapshots and Mass Spectrometry
Resolution3.35 Å
Binding residue
(original residue number in PDB)		W86 G121 G122 S203 A204
Binding residue
(residue number reindexed from 1)		W85 G120 G121 S202 A203
Annotation score1
Enzymatic activity
Catalytic site (original residue number in PDB) G121 G122 G154 S203 A204 G242 F297 F299 E334 H447
Catalytic site (residue number reindexed from 1) G120 G121 G153 S202 A203 G241 F296 F298 E333 H446
Enzyme Commision number 3.1.1.7: acetylcholinesterase.
Gene Ontology
Molecular Function
GO:0003990 acetylcholinesterase activity
GO:0004104 cholinesterase activity
GO:0005515 protein binding
GO:0005518 collagen binding
GO:0016787 hydrolase activity
GO:0017171 serine hydrolase activity
GO:0042166 acetylcholine binding
GO:0042802 identical protein binding
GO:0042803 protein homodimerization activity
GO:0043236 laminin binding
GO:0052689 carboxylic ester hydrolase activity
Biological Process
GO:0001919 regulation of receptor recycling
GO:0002076 osteoblast development
GO:0006581 acetylcholine catabolic process
GO:0007155 cell adhesion
GO:0031623 receptor internalization
GO:0060041 retina development in camera-type eye
GO:0095500 acetylcholine receptor signaling pathway
GO:0120162 positive regulation of cold-induced thermogenesis
Cellular Component
GO:0005576 extracellular region
GO:0005604 basement membrane
GO:0005615 extracellular space
GO:0005794 Golgi apparatus
GO:0005886 plasma membrane
GO:0009986 cell surface
GO:0016020 membrane
GO:0031594 neuromuscular junction
GO:0045202 synapse
GO:0048471 perinuclear region of cytoplasm
GO:0098552 side of membrane

View graph for
Molecular Function
View graph for
Biological Process
View graph for
Cellular Component
External links
PDB RCSB:4bc0, PDBe:4bc0, PDBj:4bc0
PDBsum4bc0
PubMed23339663
UniProtP21836|ACES_MOUSE Acetylcholinesterase (Gene Name=Ache)

[Back to BioLiP]