Structure of PDB 5ah0 Chain B Binding Site BS01

Receptor Information
>5ah0 Chain B (length=387) Species: 1122947 (Pelosinus fermentans DSM 17108) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
MNSYPIVLVHGFMGWGRNEVLGLKYWGGITDYEQELSSYGYTAYTATVGP
VSSNWDRACELYAYIKGGTVDYGHAHSTQKGHSRYGRTYPGLYPEWGNLT
TEGKVNKIHLVAHSMGGQTVRTLVQLLKEGSEEERNTTPSQLSSLFAGGK
SWVHSITTIASPHDGTTLADGINIFGDFAKNLVASLASFTGAGEKLIYDF
KLDQWGLNRKSGESLTDYTNRVFNSAIWNSTNDLANWDLSTDGARVLNQW
VKAQSDIYYFSYSTCATVPSILTSNELPHVIYMTPLLYPFGRFIGSYTRN
EQGRVIIDNSWKPNDGVVNTISQNGPKIWSSDKIVNYNGVPQIGKWNSMP
LLDTIDHMDACGIGTNALTLSWYKGLAEKLSQLTISN
Ligand information
Ligand IDZN
InChIInChI=1S/Zn/q+2
InChIKeyPTFCDOFLOPIGGS-UHFFFAOYSA-N
SMILES
SoftwareSMILES
CACTVS 3.341[Zn++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Zn+2]
FormulaZn
NameZINC ION
ChEMBLCHEMBL1236970
DrugBankDB14532
ZINC
PDB chain5ah0 Chain B Residue 1403 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
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PDB5ah0 Characterization of a Poly(Butylene Adipate-Co-Terephthalate)-Hydrolyzing Lipase from Pelosinus Fermentans.
Resolution2.5 Å
Binding residue
(original residue number in PDB)
D71 H91 H97 D248
Binding residue
(residue number reindexed from 1)
D56 H76 H82 D233
Annotation score1
Enzymatic activity
Enzyme Commision number 3.1.1.3: triacylglycerol lipase.
Gene Ontology
Molecular Function
GO:0004806 triacylglycerol lipase activity
GO:0016787 hydrolase activity
GO:0046872 metal ion binding
Biological Process
GO:0016042 lipid catabolic process
Cellular Component
GO:0005576 extracellular region

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Molecular Function

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Biological Process

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Cellular Component
External links
PDB RCSB:5ah0, PDBe:5ah0, PDBj:5ah0
PDBsum5ah0
PubMed26490551
UniProtA0A0A0YMQ9

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