Structure of PDB 2ewe Chain A Binding Site BS06
Receptor Information
>2ewe Chain A (length=352) Species:
556
(Dickeya chrysanthemi) [
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ATDTGGYAATAGGNVTGAVSKTATSMQDIVNIIDAARLDANGKKVKGGAY
PLVITYTGNEDSLINAAAANICGQWSKDPRGVEIKEFTKGITIIGANGSS
ANFGIWIKKSSDVVVQNMRIGYLPGGAKDGDMIRVDDSPNVWVDHNELFA
ANHECDGTPDNDTTFESAVDIKGASNTVTVSYNYIHGVKKVGLDGSSSSD
TGRNITYHHNYYNDVNAKLPLQRGGLVHAYNNLYTNITGSGLNVRQNGQA
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
2ewe Chain A Residue 704 [
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Receptor-Ligand Complex Structure
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PDB
2ewe
Structure of a Plant Cell Wall Fragment Complexed to Pectate Lyase C
Resolution
2.2 Å
Binding residue
(original residue number in PDB)
K218 Y268
Binding residue
(residue number reindexed from 1)
K218 Y268
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
D129 D131 A151 E166 D170 A217 K218 P220
Catalytic site (residue number reindexed from 1)
D129 D131 A151 E166 D170 A217 K218 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:2ewe
,
PDBe:2ewe
,
PDBj:2ewe
PDBsum
2ewe
PubMed
10368179
UniProt
P11073
|PLYC_DICCH Pectate lyase C (Gene Name=pelC)
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