Structure of PDB 5ah0 Chain B Binding Site BS01
Receptor Information
>5ah0 Chain B (length=387) Species:
1122947
(Pelosinus fermentans DSM 17108) [
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MNSYPIVLVHGFMGWGRNEVLGLKYWGGITDYEQELSSYGYTAYTATVGP
VSSNWDRACELYAYIKGGTVDYGHAHSTQKGHSRYGRTYPGLYPEWGNLT
TEGKVNKIHLVAHSMGGQTVRTLVQLLKEGSEEERNTTPSQLSSLFAGGK
SWVHSITTIASPHDGTTLADGINIFGDFAKNLVASLASFTGAGEKLIYDF
KLDQWGLNRKSGESLTDYTNRVFNSAIWNSTNDLANWDLSTDGARVLNQW
VKAQSDIYYFSYSTCATVPSILTSNELPHVIYMTPLLYPFGRFIGSYTRN
EQGRVIIDNSWKPNDGVVNTISQNGPKIWSSDKIVNYNGVPQIGKWNSMP
LLDTIDHMDACGIGTNALTLSWYKGLAEKLSQLTISN
Ligand information
Ligand ID
ZN
InChI
InChI=1S/Zn/q+2
InChIKey
PTFCDOFLOPIGGS-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
[Zn++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Zn+2]
Formula
Zn
Name
ZINC ION
ChEMBL
CHEMBL1236970
DrugBank
DB14532
ZINC
PDB chain
5ah0 Chain B Residue 1403 [
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Receptor-Ligand Complex Structure
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PDB
5ah0
Characterization of a Poly(Butylene Adipate-Co-Terephthalate)-Hydrolyzing Lipase from Pelosinus Fermentans.
Resolution
2.5 Å
Binding residue
(original residue number in PDB)
D71 H91 H97 D248
Binding residue
(residue number reindexed from 1)
D56 H76 H82 D233
Annotation score
1
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
PDBsum
5ah0
PubMed
26490551
UniProt
A0A0A0YMQ9
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