2QXU
Crystal Structure Analysis of the Bacillus subtilis lipase crystallized at pH 5.0
Functional Information from GO Data
Chain | GOid | namespace | contents |
A | 0004806 | molecular_function | triacylglycerol lipase activity |
A | 0005576 | cellular_component | extracellular region |
A | 0016042 | biological_process | lipid catabolic process |
A | 0016298 | molecular_function | lipase activity |
A | 0016787 | molecular_function | hydrolase activity |
B | 0004806 | molecular_function | triacylglycerol lipase activity |
B | 0005576 | cellular_component | extracellular region |
B | 0016042 | biological_process | lipid catabolic process |
B | 0016298 | molecular_function | lipase activity |
B | 0016787 | molecular_function | hydrolase activity |
C | 0004806 | molecular_function | triacylglycerol lipase activity |
C | 0005576 | cellular_component | extracellular region |
C | 0016042 | biological_process | lipid catabolic process |
C | 0016298 | molecular_function | lipase activity |
C | 0016787 | molecular_function | hydrolase activity |
D | 0004806 | molecular_function | triacylglycerol lipase activity |
D | 0005576 | cellular_component | extracellular region |
D | 0016042 | biological_process | lipid catabolic process |
D | 0016298 | molecular_function | lipase activity |
D | 0016787 | molecular_function | hydrolase activity |
E | 0004806 | molecular_function | triacylglycerol lipase activity |
E | 0005576 | cellular_component | extracellular region |
E | 0016042 | biological_process | lipid catabolic process |
E | 0016298 | molecular_function | lipase activity |
E | 0016787 | molecular_function | hydrolase activity |
F | 0004806 | molecular_function | triacylglycerol lipase activity |
F | 0005576 | cellular_component | extracellular region |
F | 0016042 | biological_process | lipid catabolic process |
F | 0016298 | molecular_function | lipase activity |
F | 0016787 | molecular_function | hydrolase activity |
G | 0004806 | molecular_function | triacylglycerol lipase activity |
G | 0005576 | cellular_component | extracellular region |
G | 0016042 | biological_process | lipid catabolic process |
G | 0016298 | molecular_function | lipase activity |
G | 0016787 | molecular_function | hydrolase activity |
H | 0004806 | molecular_function | triacylglycerol lipase activity |
H | 0005576 | cellular_component | extracellular region |
H | 0016042 | biological_process | lipid catabolic process |
H | 0016298 | molecular_function | lipase activity |
H | 0016787 | molecular_function | hydrolase activity |
Functional Information from SwissProt/UniProt
site_id | SWS_FT_FI1 |
Number of Residues | 8 |
Details | ACT_SITE: Nucleophile => ECO:0000305|PubMed:11491291, ECO:0000305|PubMed:11583117, ECO:0000305|PubMed:12077437 |
Chain | Residue | Details |
A | SER77 | |
B | SER77 | |
C | SER77 | |
D | SER77 | |
E | SER77 | |
F | SER77 | |
G | SER77 | |
H | SER77 |
site_id | SWS_FT_FI2 |
Number of Residues | 16 |
Details | ACT_SITE: Charge relay system => ECO:0000305|PubMed:11491291, ECO:0000305|PubMed:11583117, ECO:0000305|PubMed:12077437 |
Chain | Residue | Details |
A | ASP133 | |
E | HIS156 | |
F | ASP133 | |
F | HIS156 | |
G | ASP133 | |
G | HIS156 | |
H | ASP133 | |
H | HIS156 | |
A | HIS156 | |
B | ASP133 | |
B | HIS156 | |
C | ASP133 | |
C | HIS156 | |
D | ASP133 | |
D | HIS156 | |
E | ASP133 |
Catalytic Information from CSA
site_id | CSA1 |
Number of Residues | 5 |
Details | Annotated By Reference To The Literature 1r4z |
Chain | Residue | Details |
A | ASP133 | |
A | HIS156 | |
A | MET78 | |
A | SER77 | |
A | ILE12 |
site_id | CSA2 |
Number of Residues | 5 |
Details | Annotated By Reference To The Literature 1r4z |
Chain | Residue | Details |
B | ASP133 | |
B | HIS156 | |
B | MET78 | |
B | SER77 | |
B | ILE12 |
site_id | CSA3 |
Number of Residues | 5 |
Details | Annotated By Reference To The Literature 1r4z |
Chain | Residue | Details |
C | ASP133 | |
C | HIS156 | |
C | MET78 | |
C | SER77 | |
C | ILE12 |
site_id | CSA4 |
Number of Residues | 5 |
Details | Annotated By Reference To The Literature 1r4z |
Chain | Residue | Details |
D | ASP133 | |
D | HIS156 | |
D | MET78 | |
D | SER77 | |
D | ILE12 |
site_id | CSA5 |
Number of Residues | 5 |
Details | Annotated By Reference To The Literature 1r4z |
Chain | Residue | Details |
E | ASP133 | |
E | HIS156 | |
E | MET78 | |
E | SER77 | |
E | ILE12 |
site_id | CSA6 |
Number of Residues | 5 |
Details | Annotated By Reference To The Literature 1r4z |
Chain | Residue | Details |
F | ASP133 | |
F | HIS156 | |
F | MET78 | |
F | SER77 | |
F | ILE12 |
site_id | CSA7 |
Number of Residues | 5 |
Details | Annotated By Reference To The Literature 1r4z |
Chain | Residue | Details |
G | ASP133 | |
G | HIS156 | |
G | MET78 | |
G | SER77 | |
G | ILE12 |
site_id | CSA8 |
Number of Residues | 5 |
Details | Annotated By Reference To The Literature 1r4z |
Chain | Residue | Details |
H | ASP133 | |
H | HIS156 | |
H | MET78 | |
H | SER77 | |
H | ILE12 |
site_id | MCSA1 |
Number of Residues | 5 |
Details | M-CSA 518 |
Chain | Residue | Details |
A | ILE12 | electrostatic stabiliser |
A | SER77 | covalently attached, nucleofuge, nucleophile, proton acceptor, proton donor |
A | MET78 | electrostatic stabiliser |
A | ASP133 | electrostatic stabiliser, increase basicity, modifies pKa |
A | HIS156 | proton acceptor, proton donor |
site_id | MCSA2 |
Number of Residues | 5 |
Details | M-CSA 518 |
Chain | Residue | Details |
B | ILE12 | electrostatic stabiliser |
B | SER77 | covalently attached, nucleofuge, nucleophile, proton acceptor, proton donor |
B | MET78 | electrostatic stabiliser |
B | ASP133 | electrostatic stabiliser, increase basicity, modifies pKa |
B | HIS156 | proton acceptor, proton donor |
site_id | MCSA3 |
Number of Residues | 5 |
Details | M-CSA 518 |
Chain | Residue | Details |
C | ILE12 | electrostatic stabiliser |
C | SER77 | covalently attached, nucleofuge, nucleophile, proton acceptor, proton donor |
C | MET78 | electrostatic stabiliser |
C | ASP133 | electrostatic stabiliser, increase basicity, modifies pKa |
C | HIS156 | proton acceptor, proton donor |
site_id | MCSA4 |
Number of Residues | 5 |
Details | M-CSA 518 |
Chain | Residue | Details |
D | ILE12 | electrostatic stabiliser |
D | SER77 | covalently attached, nucleofuge, nucleophile, proton acceptor, proton donor |
D | MET78 | electrostatic stabiliser |
D | ASP133 | electrostatic stabiliser, increase basicity, modifies pKa |
D | HIS156 | proton acceptor, proton donor |
site_id | MCSA5 |
Number of Residues | 5 |
Details | M-CSA 518 |
Chain | Residue | Details |
E | ILE12 | electrostatic stabiliser |
E | SER77 | covalently attached, nucleofuge, nucleophile, proton acceptor, proton donor |
E | MET78 | electrostatic stabiliser |
E | ASP133 | electrostatic stabiliser, increase basicity, modifies pKa |
E | HIS156 | proton acceptor, proton donor |
site_id | MCSA6 |
Number of Residues | 5 |
Details | M-CSA 518 |
Chain | Residue | Details |
F | ILE12 | electrostatic stabiliser |
F | SER77 | covalently attached, nucleofuge, nucleophile, proton acceptor, proton donor |
F | MET78 | electrostatic stabiliser |
F | ASP133 | electrostatic stabiliser, increase basicity, modifies pKa |
F | HIS156 | proton acceptor, proton donor |
site_id | MCSA7 |
Number of Residues | 5 |
Details | M-CSA 518 |
Chain | Residue | Details |
G | ILE12 | electrostatic stabiliser |
G | SER77 | covalently attached, nucleofuge, nucleophile, proton acceptor, proton donor |
G | MET78 | electrostatic stabiliser |
G | ASP133 | electrostatic stabiliser, increase basicity, modifies pKa |
G | HIS156 | proton acceptor, proton donor |
site_id | MCSA8 |
Number of Residues | 5 |
Details | M-CSA 518 |
Chain | Residue | Details |
H | ILE12 | electrostatic stabiliser |
H | SER77 | covalently attached, nucleofuge, nucleophile, proton acceptor, proton donor |
H | MET78 | electrostatic stabiliser |
H | ASP133 | electrostatic stabiliser, increase basicity, modifies pKa |
H | HIS156 | proton acceptor, proton donor |