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2QXU

Crystal Structure Analysis of the Bacillus subtilis lipase crystallized at pH 5.0

Functional Information from GO Data
ChainGOidnamespacecontents
A0004806molecular_functiontriacylglycerol lipase activity
A0005576cellular_componentextracellular region
A0016042biological_processlipid catabolic process
A0016298molecular_functionlipase activity
A0016787molecular_functionhydrolase activity
B0004806molecular_functiontriacylglycerol lipase activity
B0005576cellular_componentextracellular region
B0016042biological_processlipid catabolic process
B0016298molecular_functionlipase activity
B0016787molecular_functionhydrolase activity
C0004806molecular_functiontriacylglycerol lipase activity
C0005576cellular_componentextracellular region
C0016042biological_processlipid catabolic process
C0016298molecular_functionlipase activity
C0016787molecular_functionhydrolase activity
D0004806molecular_functiontriacylglycerol lipase activity
D0005576cellular_componentextracellular region
D0016042biological_processlipid catabolic process
D0016298molecular_functionlipase activity
D0016787molecular_functionhydrolase activity
E0004806molecular_functiontriacylglycerol lipase activity
E0005576cellular_componentextracellular region
E0016042biological_processlipid catabolic process
E0016298molecular_functionlipase activity
E0016787molecular_functionhydrolase activity
F0004806molecular_functiontriacylglycerol lipase activity
F0005576cellular_componentextracellular region
F0016042biological_processlipid catabolic process
F0016298molecular_functionlipase activity
F0016787molecular_functionhydrolase activity
G0004806molecular_functiontriacylglycerol lipase activity
G0005576cellular_componentextracellular region
G0016042biological_processlipid catabolic process
G0016298molecular_functionlipase activity
G0016787molecular_functionhydrolase activity
H0004806molecular_functiontriacylglycerol lipase activity
H0005576cellular_componentextracellular region
H0016042biological_processlipid catabolic process
H0016298molecular_functionlipase activity
H0016787molecular_functionhydrolase activity
Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues8
DetailsACT_SITE: Nucleophile => ECO:0000305|PubMed:11491291, ECO:0000305|PubMed:11583117, ECO:0000305|PubMed:12077437
ChainResidueDetails
ASER77
BSER77
CSER77
DSER77
ESER77
FSER77
GSER77
HSER77

site_idSWS_FT_FI2
Number of Residues16
DetailsACT_SITE: Charge relay system => ECO:0000305|PubMed:11491291, ECO:0000305|PubMed:11583117, ECO:0000305|PubMed:12077437
ChainResidueDetails
AASP133
EHIS156
FASP133
FHIS156
GASP133
GHIS156
HASP133
HHIS156
AHIS156
BASP133
BHIS156
CASP133
CHIS156
DASP133
DHIS156
EASP133

Catalytic Information from CSA
site_idCSA1
Number of Residues5
DetailsAnnotated By Reference To The Literature 1r4z
ChainResidueDetails
AASP133
AHIS156
AMET78
ASER77
AILE12

site_idCSA2
Number of Residues5
DetailsAnnotated By Reference To The Literature 1r4z
ChainResidueDetails
BASP133
BHIS156
BMET78
BSER77
BILE12

site_idCSA3
Number of Residues5
DetailsAnnotated By Reference To The Literature 1r4z
ChainResidueDetails
CASP133
CHIS156
CMET78
CSER77
CILE12

site_idCSA4
Number of Residues5
DetailsAnnotated By Reference To The Literature 1r4z
ChainResidueDetails
DASP133
DHIS156
DMET78
DSER77
DILE12

site_idCSA5
Number of Residues5
DetailsAnnotated By Reference To The Literature 1r4z
ChainResidueDetails
EASP133
EHIS156
EMET78
ESER77
EILE12

site_idCSA6
Number of Residues5
DetailsAnnotated By Reference To The Literature 1r4z
ChainResidueDetails
FASP133
FHIS156
FMET78
FSER77
FILE12

site_idCSA7
Number of Residues5
DetailsAnnotated By Reference To The Literature 1r4z
ChainResidueDetails
GASP133
GHIS156
GMET78
GSER77
GILE12

site_idCSA8
Number of Residues5
DetailsAnnotated By Reference To The Literature 1r4z
ChainResidueDetails
HASP133
HHIS156
HMET78
HSER77
HILE12

site_idMCSA1
Number of Residues5
DetailsM-CSA 518
ChainResidueDetails
AILE12electrostatic stabiliser
ASER77covalently attached, nucleofuge, nucleophile, proton acceptor, proton donor
AMET78electrostatic stabiliser
AASP133electrostatic stabiliser, increase basicity, modifies pKa
AHIS156proton acceptor, proton donor

site_idMCSA2
Number of Residues5
DetailsM-CSA 518
ChainResidueDetails
BILE12electrostatic stabiliser
BSER77covalently attached, nucleofuge, nucleophile, proton acceptor, proton donor
BMET78electrostatic stabiliser
BASP133electrostatic stabiliser, increase basicity, modifies pKa
BHIS156proton acceptor, proton donor

site_idMCSA3
Number of Residues5
DetailsM-CSA 518
ChainResidueDetails
CILE12electrostatic stabiliser
CSER77covalently attached, nucleofuge, nucleophile, proton acceptor, proton donor
CMET78electrostatic stabiliser
CASP133electrostatic stabiliser, increase basicity, modifies pKa
CHIS156proton acceptor, proton donor

site_idMCSA4
Number of Residues5
DetailsM-CSA 518
ChainResidueDetails
DILE12electrostatic stabiliser
DSER77covalently attached, nucleofuge, nucleophile, proton acceptor, proton donor
DMET78electrostatic stabiliser
DASP133electrostatic stabiliser, increase basicity, modifies pKa
DHIS156proton acceptor, proton donor

site_idMCSA5
Number of Residues5
DetailsM-CSA 518
ChainResidueDetails
EILE12electrostatic stabiliser
ESER77covalently attached, nucleofuge, nucleophile, proton acceptor, proton donor
EMET78electrostatic stabiliser
EASP133electrostatic stabiliser, increase basicity, modifies pKa
EHIS156proton acceptor, proton donor

site_idMCSA6
Number of Residues5
DetailsM-CSA 518
ChainResidueDetails
FILE12electrostatic stabiliser
FSER77covalently attached, nucleofuge, nucleophile, proton acceptor, proton donor
FMET78electrostatic stabiliser
FASP133electrostatic stabiliser, increase basicity, modifies pKa
FHIS156proton acceptor, proton donor

site_idMCSA7
Number of Residues5
DetailsM-CSA 518
ChainResidueDetails
GILE12electrostatic stabiliser
GSER77covalently attached, nucleofuge, nucleophile, proton acceptor, proton donor
GMET78electrostatic stabiliser
GASP133electrostatic stabiliser, increase basicity, modifies pKa
GHIS156proton acceptor, proton donor

site_idMCSA8
Number of Residues5
DetailsM-CSA 518
ChainResidueDetails
HILE12electrostatic stabiliser
HSER77covalently attached, nucleofuge, nucleophile, proton acceptor, proton donor
HMET78electrostatic stabiliser
HASP133electrostatic stabiliser, increase basicity, modifies pKa
HHIS156proton acceptor, proton donor

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PDB entries from 2024-10-30

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