Structure of PDB 2o1d Chain A Binding Site BS03
Receptor Information
>2o1d Chain A (length=399) Species:
1423
(Bacillus subtilis) [
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ADLGHQTLGSNDGWGAYSTGTTGGSKASSSNVYTVSNRNQLVSALGKETN
TTPKIIYIKGTIDMNVDDNLKPLGLNDYKDPEYDLDKYLKAYDPSTWGKK
EPSGTQEEARARSQKNQKARVMVDIPANTTIVGSGTNAKVVGGNFQIKSD
NVIIRNIEFQDAYDYFPQWDPTDGSSGNWNSQYDNITINGGTHIWIDHCT
FNDGSRPDSTSPKYYGRKYQHHDGQTDASNGANYITMSYNYYHDHDKSSI
FGSSDSKTSDDGKLKITLHHNRYKNIVQAAPRVRFGQVHVYNNYYEGSTS
SSSYPFSYAWGIGKSSKIYAQNNVIDVPGLSAAKTISVFSGGTALYDSGT
LLNGTQINASAANGLSSSVGWTPSLHGSIDASANVKSNVINQAGAGKLN
Ligand information
Ligand ID
CA
InChI
InChI=1S/Ca/q+2
InChIKey
BHPQYMZQTOCNFJ-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
[Ca++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Ca+2]
Formula
Ca
Name
CALCIUM ION
ChEMBL
DrugBank
DB14577
ZINC
PDB chain
2o1d Chain A Residue 403 [
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Receptor-Ligand Complex Structure
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PDB
2o1d
Structural insights into substrate specificity and the anti beta-elimination mechanism of pectate lyase.
Resolution
2.0 Å
Binding residue
(original residue number in PDB)
D184 D223 D227
Binding residue
(residue number reindexed from 1)
D184 D223 D227
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
D184 D223 D227 A279
Catalytic site (residue number reindexed from 1)
D184 D223 D227 A279
Enzyme Commision number
4.2.2.2
: pectate lyase.
Gene Ontology
Molecular Function
GO:0016829
lyase activity
GO:0030570
pectate lyase activity
GO:0046872
metal ion binding
Biological Process
GO:0045490
pectin 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:2o1d
,
PDBe:2o1d
,
PDBj:2o1d
PDBsum
2o1d
PubMed
20000851
UniProt
P39116
|PLY_BACSU Pectate lyase (Gene Name=pel)
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