Structure of PDB 5jra Chain A Binding Site BS02
Receptor Information
>5jra Chain A (length=126) Species:
85698
(Achromobacter xylosoxidans) [
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PFAKPEDAVKYRQSAVTLMASHFGRMTPVVKGQAPYDAAQIKANVEVLKT
LSALPWAAFGPGTEGGDARPEIWSDAASFKQKQQAFQDNIVKLSAAADAG
DLDKLRAAFGDVGASCKACHDAYRKK
Ligand information
Ligand ID
ASC
InChI
InChI=1S/C6H8O6/c7-1-2(8)5-3(9)4(10)6(11)12-5/h2,5,7-10H,1H2/t2-,5+/m0/s1
InChIKey
CIWBSHSKHKDKBQ-JLAZNSOCSA-N
SMILES
Software
SMILES
CACTVS 3.341
OC[CH](O)[CH]1OC(=O)C(=C1O)O
OpenEye OEToolkits 1.5.0
C(C(C1C(=C(C(=O)O1)O)O)O)O
OpenEye OEToolkits 1.5.0
C([C@@H]([C@@H]1C(=C(C(=O)O1)O)O)O)O
CACTVS 3.341
OC[C@H](O)[C@H]1OC(=O)C(=C1O)O
ACDLabs 10.04
O=C1OC(C(O)=C1O)C(O)CO
Formula
C6 H8 O6
Name
ASCORBIC ACID;
Vitamin C
ChEMBL
CHEMBL196
DrugBank
DB00126
ZINC
ZINC000100006770
PDB chain
5jra Chain A Residue 202 [
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Receptor-Ligand Complex Structure
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PDB
5jra
Engineering proximal vs. distal heme-NO coordination via dinitrosyl dynamics: implications for NO sensor design.
Resolution
1.38 Å
Binding residue
(original residue number in PDB)
F23 G113
Binding residue
(residue number reindexed from 1)
F23 G113
Annotation score
3
Enzymatic activity
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0005506
iron ion binding
GO:0009055
electron transfer activity
GO:0020037
heme binding
GO:0046872
metal ion binding
Biological Process
GO:0022900
electron transport chain
Cellular Component
GO:0042597
periplasmic space
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Molecular Function
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Cellular Component
External links
PDB
RCSB:5jra
,
PDBe:5jra
,
PDBj:5jra
PDBsum
5jra
PubMed
28451315
UniProt
P00138
|CYCP_ALCXX Cytochrome c'
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