Structure of PDB 1o88 Chain A Binding Site BS01
Receptor Information
>1o88 Chain A (length=352) Species:
556
(Dickeya chrysanthemi) [
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ATDTGGYAATAGGNVTGAVSKTATSMQDIVNIIDAARLDANGKKVKGGAY
PLVITYTGNEDSLINAAAANICGQWSKDPRGVEIKEFTKGITIIGANGSS
ANFGIWIKKSSDVVVQNMRIGYLPGGAKDGDMIRVDDSPNVWVDHNELFA
ANHECDGTPDNDTTFESAVDIKGASNTVTVSYNYIHGVKKVGLDGSSSSD
TGRNITYHHNYYNDVNARLPLQRGGLVHAYNNLYTNITGSGLNVRQNGQA
LIENNWFEKAINPVTSRYDGKNFGTWVLKGNNITKPADFSTYSITWTADT
KPYVNADSWTSTGTFPTVAYNYSPVSAQCVKDKLPGYAGVGKNLATLTST
AC
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
1o88 Chain A Residue 1353 [
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Receptor-Ligand Complex Structure
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PDB
1o88
Characterization and Implications of Ca2+ Binding to Pectate Lyase C
Resolution
2.2 Å
Binding residue
(original residue number in PDB)
D129 D131 E166 D170 C352
Binding residue
(residue number reindexed from 1)
D129 D131 E166 D170 C352
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
D129 D131 A151 E166 D170 A217 R218 P220
Catalytic site (residue number reindexed from 1)
D129 D131 A151 E166 D170 A217 R218 P220
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:1o88
,
PDBe:1o88
,
PDBj:1o88
PDBsum
1o88
PubMed
12540845
UniProt
P11073
|PLYC_DICCH Pectate lyase C (Gene Name=pelC)
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