2HA7
Crystal structure of mutant S203A of mouse acetylcholinesterase complexed with butyrylthiocholine
Functional Information from GO Data
Chain | GOid | namespace | contents |
A | 0001919 | biological_process | regulation of receptor recycling |
A | 0002076 | biological_process | osteoblast development |
A | 0003990 | molecular_function | acetylcholinesterase activity |
A | 0004104 | molecular_function | cholinesterase activity |
A | 0005515 | molecular_function | protein binding |
A | 0005518 | molecular_function | collagen binding |
A | 0005576 | cellular_component | extracellular region |
A | 0005604 | cellular_component | basement membrane |
A | 0005615 | cellular_component | extracellular space |
A | 0005794 | cellular_component | Golgi apparatus |
A | 0005886 | cellular_component | plasma membrane |
A | 0006581 | biological_process | acetylcholine catabolic process |
A | 0007155 | biological_process | cell adhesion |
A | 0009986 | cellular_component | cell surface |
A | 0016020 | cellular_component | membrane |
A | 0016787 | molecular_function | hydrolase activity |
A | 0017171 | molecular_function | serine hydrolase activity |
A | 0031594 | cellular_component | neuromuscular junction |
A | 0031623 | biological_process | receptor internalization |
A | 0042166 | molecular_function | acetylcholine binding |
A | 0042802 | molecular_function | identical protein binding |
A | 0042803 | molecular_function | protein homodimerization activity |
A | 0043236 | molecular_function | laminin binding |
A | 0045202 | cellular_component | synapse |
A | 0048471 | cellular_component | perinuclear region of cytoplasm |
A | 0052689 | molecular_function | carboxylic ester hydrolase activity |
A | 0060041 | biological_process | retina development in camera-type eye |
A | 0095500 | biological_process | acetylcholine receptor signaling pathway |
A | 0098552 | cellular_component | side of membrane |
A | 0120162 | biological_process | positive regulation of cold-induced thermogenesis |
B | 0001919 | biological_process | regulation of receptor recycling |
B | 0002076 | biological_process | osteoblast development |
B | 0003990 | molecular_function | acetylcholinesterase activity |
B | 0004104 | molecular_function | cholinesterase activity |
B | 0005515 | molecular_function | protein binding |
B | 0005518 | molecular_function | collagen binding |
B | 0005576 | cellular_component | extracellular region |
B | 0005604 | cellular_component | basement membrane |
B | 0005615 | cellular_component | extracellular space |
B | 0005794 | cellular_component | Golgi apparatus |
B | 0005886 | cellular_component | plasma membrane |
B | 0006581 | biological_process | acetylcholine catabolic process |
B | 0007155 | biological_process | cell adhesion |
B | 0009986 | cellular_component | cell surface |
B | 0016020 | cellular_component | membrane |
B | 0016787 | molecular_function | hydrolase activity |
B | 0017171 | molecular_function | serine hydrolase activity |
B | 0031594 | cellular_component | neuromuscular junction |
B | 0031623 | biological_process | receptor internalization |
B | 0042166 | molecular_function | acetylcholine binding |
B | 0042802 | molecular_function | identical protein binding |
B | 0042803 | molecular_function | protein homodimerization activity |
B | 0043236 | molecular_function | laminin binding |
B | 0045202 | cellular_component | synapse |
B | 0048471 | cellular_component | perinuclear region of cytoplasm |
B | 0052689 | molecular_function | carboxylic ester hydrolase activity |
B | 0060041 | biological_process | retina development in camera-type eye |
B | 0095500 | biological_process | acetylcholine receptor signaling pathway |
B | 0098552 | cellular_component | side of membrane |
B | 0120162 | biological_process | positive regulation of cold-induced thermogenesis |
Functional Information from PDB Data
site_id | AC1 |
Number of Residues | 2 |
Details | BINDING SITE FOR RESIDUE IOD A 900 |
Chain | Residue |
A | PHE295 |
A | BCH910 |
site_id | AC2 |
Number of Residues | 1 |
Details | BINDING SITE FOR RESIDUE IOD A 902 |
Chain | Residue |
A | ARG245 |
site_id | AC3 |
Number of Residues | 3 |
Details | BINDING SITE FOR RESIDUE IOD A 903 |
Chain | Residue |
A | PRO290 |
A | GLN291 |
A | SER293 |
site_id | AC4 |
Number of Residues | 1 |
Details | BINDING SITE FOR RESIDUE IOD B 904 |
Chain | Residue |
B | ARG245 |
site_id | AC5 |
Number of Residues | 1 |
Details | BINDING SITE FOR RESIDUE IOD B 905 |
Chain | Residue |
B | SER293 |
site_id | AC6 |
Number of Residues | 1 |
Details | BINDING SITE FOR RESIDUE IOD B 906 |
Chain | Residue |
B | LYS332 |
site_id | AC7 |
Number of Residues | 2 |
Details | BINDING SITE FOR RESIDUE IOD A 907 |
Chain | Residue |
A | VAL255 |
A | ASP280 |
site_id | AC8 |
Number of Residues | 2 |
Details | BINDING SITE FOR RESIDUE IOD B 908 |
Chain | Residue |
B | LYS53 |
B | HOH966 |
site_id | AC9 |
Number of Residues | 1 |
Details | BINDING SITE FOR RESIDUE IOD B 909 |
Chain | Residue |
B | PHE295 |
site_id | BC1 |
Number of Residues | 8 |
Details | BINDING SITE FOR RESIDUE ETM A 908 |
Chain | Residue |
A | TRP86 |
A | GLY120 |
A | GLY121 |
A | GLU202 |
A | TYR337 |
A | HIS447 |
A | BUA909 |
A | HOH1001 |
site_id | BC2 |
Number of Residues | 7 |
Details | BINDING SITE FOR RESIDUE BUA A 909 |
Chain | Residue |
A | GLY121 |
A | GLY122 |
A | TYR124 |
A | ALA203 |
A | ALA204 |
A | HIS447 |
A | ETM908 |
site_id | BC3 |
Number of Residues | 6 |
Details | BINDING SITE FOR RESIDUE BCH A 910 |
Chain | Residue |
A | TYR72 |
A | TYR124 |
A | TRP286 |
A | TYR337 |
A | TYR341 |
A | IOD900 |
site_id | BC4 |
Number of Residues | 7 |
Details | BINDING SITE FOR RESIDUE ETM B 602 |
Chain | Residue |
B | TRP86 |
B | GLY120 |
B | GLY121 |
B | GLU202 |
B | TYR337 |
B | HIS447 |
B | BUA603 |
site_id | BC5 |
Number of Residues | 7 |
Details | BINDING SITE FOR RESIDUE BUA B 603 |
Chain | Residue |
B | GLY121 |
B | GLY122 |
B | TYR124 |
B | ALA203 |
B | ALA204 |
B | HIS447 |
B | ETM602 |
site_id | BC6 |
Number of Residues | 2 |
Details | BINDING SITE FOR RESIDUE BCH A 601 |
Chain | Residue |
A | ASP396 |
A | TRP442 |
site_id | BC7 |
Number of Residues | 10 |
Details | BINDING SITE FOR RESIDUE P6G A 901 |
Chain | Residue |
A | LEU380 |
A | HIS381 |
A | GLN527 |
A | PHE535 |
A | HOH913 |
B | ALA377 |
B | LEU380 |
B | HIS381 |
B | PHE531 |
B | PHE535 |
Functional Information from PROSITE/UniProt
site_id | PS00941 |
Number of Residues | 11 |
Details | CARBOXYLESTERASE_B_2 Carboxylesterases type-B signature 2. EDCLYLNVWtP |
Chain | Residue | Details |
A | GLU94-PRO104 |
Functional Information from SwissProt/UniProt
site_id | SWS_FT_FI1 |
Number of Residues | 2 |
Details | ACT_SITE: Acyl-ester intermediate |
Chain | Residue | Details |
A | ALA203 | |
B | ALA203 |
site_id | SWS_FT_FI2 |
Number of Residues | 4 |
Details | ACT_SITE: Charge relay system |
Chain | Residue | Details |
A | GLU334 | |
A | HIS447 | |
B | GLU334 | |
B | HIS447 |
site_id | SWS_FT_FI3 |
Number of Residues | 2 |
Details | CARBOHYD: N-linked (GlcNAc...) asparagine => ECO:0000255 |
Chain | Residue | Details |
A | ASN265 | |
B | ASN265 |
site_id | SWS_FT_FI4 |
Number of Residues | 4 |
Details | CARBOHYD: N-linked (GlcNAc...) asparagine |
Chain | Residue | Details |
A | ASN350 | |
A | ASN464 | |
B | ASN350 | |
B | ASN464 |