5YQT
Crystal Structure of the L74F/M78V/I80V/L114F mutant of LEH complexed with cyclopentene oxide
Functional Information from GO Data
Chain | GOid | namespace | contents |
A | 0016787 | molecular_function | hydrolase activity |
A | 0018744 | molecular_function | limonene-1,2-epoxide hydrolase activity |
B | 0016787 | molecular_function | hydrolase activity |
B | 0018744 | molecular_function | limonene-1,2-epoxide hydrolase activity |
C | 0016787 | molecular_function | hydrolase activity |
C | 0018744 | molecular_function | limonene-1,2-epoxide hydrolase activity |
D | 0016787 | molecular_function | hydrolase activity |
D | 0018744 | molecular_function | limonene-1,2-epoxide hydrolase activity |
E | 0016787 | molecular_function | hydrolase activity |
E | 0018744 | molecular_function | limonene-1,2-epoxide hydrolase activity |
F | 0016787 | molecular_function | hydrolase activity |
F | 0018744 | molecular_function | limonene-1,2-epoxide hydrolase activity |
G | 0016787 | molecular_function | hydrolase activity |
G | 0018744 | molecular_function | limonene-1,2-epoxide hydrolase activity |
H | 0016787 | molecular_function | hydrolase activity |
H | 0018744 | molecular_function | limonene-1,2-epoxide hydrolase activity |
Functional Information from PDB Data
site_id | AC1 |
Number of Residues | 9 |
Details | binding site for residue 3ZS C 201 |
Chain | Residue |
C | LEU35 |
C | TYR53 |
C | LEU71 |
C | PHE74 |
C | PHE75 |
C | VAL80 |
C | ASP101 |
C | LEU103 |
C | HOH305 |
site_id | AC2 |
Number of Residues | 5 |
Details | binding site for residue 3ZS D 201 |
Chain | Residue |
D | LEU35 |
D | TYR53 |
D | LEU71 |
D | PHE74 |
D | VAL80 |
site_id | AC3 |
Number of Residues | 4 |
Details | binding site for residue 3ZS A 201 |
Chain | Residue |
A | TYR53 |
A | PHE74 |
A | VAL80 |
A | HOH306 |
site_id | AC4 |
Number of Residues | 5 |
Details | binding site for residue 3ZS B 201 |
Chain | Residue |
B | TYR53 |
B | PHE74 |
B | VAL80 |
B | ASP101 |
B | HOH307 |
site_id | AC5 |
Number of Residues | 3 |
Details | binding site for residue 3ZS H 201 |
Chain | Residue |
H | TYR53 |
H | ASP101 |
H | HOH304 |
Functional Information from SwissProt/UniProt
site_id | SWS_FT_FI1 |
Number of Residues | 8 |
Details | ACT_SITE: Proton donor => ECO:0000305 |
Chain | Residue | Details |
C | ASP101 | |
D | ASP101 | |
A | ASP101 | |
B | ASP101 | |
E | ASP101 | |
F | ASP101 | |
G | ASP101 | |
H | ASP101 |
site_id | SWS_FT_FI2 |
Number of Residues | 8 |
Details | ACT_SITE: Proton acceptor => ECO:0000305 |
Chain | Residue | Details |
C | ASP132 | |
D | ASP132 | |
A | ASP132 | |
B | ASP132 | |
E | ASP132 | |
F | ASP132 | |
G | ASP132 | |
H | ASP132 |
Catalytic Information from CSA
site_id | MCSA1 |
Number of Residues | 5 |
Details | M-CSA 644 |
Chain | Residue | Details |
C | TYR53 | electrostatic stabiliser |
C | ASN55 | electrostatic stabiliser |
C | ARG99 | electrostatic stabiliser, proton acceptor, proton donor, proton relay |
C | ASP101 | proton acceptor, proton donor |
C | ASP132 | activator, proton acceptor, proton donor |
site_id | MCSA2 |
Number of Residues | 5 |
Details | M-CSA 644 |
Chain | Residue | Details |
D | TYR53 | electrostatic stabiliser |
D | ASN55 | electrostatic stabiliser |
D | ARG99 | electrostatic stabiliser, proton acceptor, proton donor, proton relay |
D | ASP101 | proton acceptor, proton donor |
D | ASP132 | activator, proton acceptor, proton donor |
site_id | MCSA3 |
Number of Residues | 5 |
Details | M-CSA 644 |
Chain | Residue | Details |
A | TYR53 | electrostatic stabiliser |
A | ASN55 | electrostatic stabiliser |
A | ARG99 | electrostatic stabiliser, proton acceptor, proton donor, proton relay |
A | ASP101 | proton acceptor, proton donor |
A | ASP132 | activator, proton acceptor, proton donor |
site_id | MCSA4 |
Number of Residues | 5 |
Details | M-CSA 644 |
Chain | Residue | Details |
B | TYR53 | electrostatic stabiliser |
B | ASN55 | electrostatic stabiliser |
B | ARG99 | electrostatic stabiliser, proton acceptor, proton donor, proton relay |
B | ASP101 | proton acceptor, proton donor |
B | ASP132 | activator, proton acceptor, proton donor |
site_id | MCSA5 |
Number of Residues | 5 |
Details | M-CSA 644 |
Chain | Residue | Details |
E | TYR53 | electrostatic stabiliser |
E | ASN55 | electrostatic stabiliser |
E | ARG99 | electrostatic stabiliser, proton acceptor, proton donor, proton relay |
E | ASP101 | proton acceptor, proton donor |
E | ASP132 | activator, proton acceptor, proton donor |
site_id | MCSA6 |
Number of Residues | 5 |
Details | M-CSA 644 |
Chain | Residue | Details |
F | TYR53 | electrostatic stabiliser |
F | ASN55 | electrostatic stabiliser |
F | ARG99 | electrostatic stabiliser, proton acceptor, proton donor, proton relay |
F | ASP101 | proton acceptor, proton donor |
F | ASP132 | activator, proton acceptor, proton donor |
site_id | MCSA7 |
Number of Residues | 5 |
Details | M-CSA 644 |
Chain | Residue | Details |
G | TYR53 | electrostatic stabiliser |
G | ASN55 | electrostatic stabiliser |
G | ARG99 | electrostatic stabiliser, proton acceptor, proton donor, proton relay |
G | ASP101 | proton acceptor, proton donor |
G | ASP132 | activator, proton acceptor, proton donor |
site_id | MCSA8 |
Number of Residues | 5 |
Details | M-CSA 644 |
Chain | Residue | Details |
H | TYR53 | electrostatic stabiliser |
H | ASN55 | electrostatic stabiliser |
H | ARG99 | electrostatic stabiliser, proton acceptor, proton donor, proton relay |
H | ASP101 | proton acceptor, proton donor |
H | ASP132 | activator, proton acceptor, proton donor |