Structure of PDB 5ybh Chain B Binding Site BS02
Receptor Information
>5ybh Chain B (length=340) Species:
623
(Shigella flexneri) [
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GSHMHTQVGRGLLGAVVNPLGEVTDKFAVTDNSEILYRPVDNAPPLYSER
AAIEKPFLTGIKVIDSLLTCGEGQRMGIFASAGCGKTFLMNMLIEHSGAD
IYVIGLIGERGREVTETVDYLKNSEKKSRCVLVYATSDYSSVDRCNAAYI
ATAIAEFFRTEGHKVALFIDSLTRYARALRDVALAAGESPARRGYPVSVF
DSLPRLLERPGKLKAGGSITAFYTVLLEDDDFADPLAEEVRSILDGHIYL
SRNLAQKGQFPAIDSLKSISRVFTQVVDEKHRIMAAAFRELLSEIEELRT
IISQDKIYNKISVVESFLKQDYRLGFTYEQTMELIGETIR
Ligand information
Ligand ID
MG
InChI
InChI=1S/Mg/q+2
InChIKey
JLVVSXFLKOJNIY-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Mg+2]
CACTVS 3.341
[Mg++]
Formula
Mg
Name
MAGNESIUM ION
ChEMBL
DrugBank
DB01378
ZINC
PDB chain
5ybh Chain B Residue 504 [
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Receptor-Ligand Complex Structure
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PDB
5ybh
Structural Insight Into Conformational Changes Induced by ATP Binding in a Type III Secretion-Associated ATPase FromShigella flexneri
Resolution
2.5 Å
Binding residue
(original residue number in PDB)
I186 S250 R253
Binding residue
(residue number reindexed from 1)
I107 S171 R174
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
K165 E188 R189 R350
Catalytic site (residue number reindexed from 1)
K86 E109 R110 R271
Enzyme Commision number
7.4.2.8
: protein-secreting ATPase.
Gene Ontology
Molecular Function
GO:0005524
ATP binding
GO:0016887
ATP hydrolysis activity
Biological Process
GO:0009058
biosynthetic process
GO:0030254
protein secretion by the type III secretion system
Cellular Component
GO:0005737
cytoplasm
GO:0030257
type III protein secretion system complex
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:5ybh
,
PDBe:5ybh
,
PDBj:5ybh
PDBsum
5ybh
PubMed
30013545
UniProt
P0A1C1
|SCTN_SHIFL Type 3 secretion system ATPase (Gene Name=sctN)
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