Structure of PDB 5a88 Chain D Binding Site BS01
Receptor Information
>5a88 Chain D (length=137) Species:
1697
(Corynebacterium ammoniagenes) [
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HFYVTGPVVRGGFPTANQYFHDTVALPADGVYAGWLTILPTEAPVSGNME
PEVAYAAAISVGTNQRSVESFVLDRDADLYGHDVKVEFVDHVRAMEKFDS
VEQLLEVMAKDVQKTRTLLAQDVQAHKMAPETYFLQA
Ligand information
Ligand ID
ADP
InChI
InChI=1S/C10H15N5O10P2/c11-8-5-9(13-2-12-8)15(3-14-5)10-7(17)6(16)4(24-10)1-23-27(21,22)25-26(18,19)20/h2-4,6-7,10,16-17H,1H2,(H,21,22)(H2,11,12,13)(H2,18,19,20)/t4-,6-,7-,10-/m1/s1
InChIKey
XTWYTFMLZFPYCI-KQYNXXCUSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)[C@H]3[C@@H]([C@@H]([C@H](O3)CO[P@](=O)(O)OP(=O)(O)O)O)O)N
CACTVS 3.341
Nc1ncnc2n(cnc12)[CH]3O[CH](CO[P](O)(=O)O[P](O)(O)=O)[CH](O)[CH]3O
ACDLabs 10.04
O=P(O)(O)OP(=O)(O)OCC3OC(n2cnc1c(ncnc12)N)C(O)C3O
CACTVS 3.341
Nc1ncnc2n(cnc12)[C@@H]3O[C@H](CO[P@@](O)(=O)O[P](O)(O)=O)[C@@H](O)[C@H]3O
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)C3C(C(C(O3)COP(=O)(O)OP(=O)(O)O)O)O)N
Formula
C10 H15 N5 O10 P2
Name
ADENOSINE-5'-DIPHOSPHATE
ChEMBL
CHEMBL14830
DrugBank
DB16833
ZINC
ZINC000012360703
PDB chain
5a88 Chain D Residue 501 [
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Receptor-Ligand Complex Structure
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PDB
5a88
Structural Insights Into the Synthesis of Fmn in Prokaryotic Organisms.
Resolution
2.08 Å
Binding residue
(original residue number in PDB)
G196 T208 N210 V271 R274 D275 A276 L278 Y279
Binding residue
(residue number reindexed from 1)
G11 T15 N17 V72 R75 D76 A77 L79 Y80
Annotation score
5
Enzymatic activity
Enzyme Commision number
2.7.1.26
: riboflavin kinase.
2.7.7.2
: FAD synthase.
Gene Ontology
Molecular Function
GO:0008531
riboflavin kinase activity
Biological Process
GO:0009231
riboflavin biosynthetic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:5a88
,
PDBe:5a88
,
PDBj:5a88
PDBsum
5a88
PubMed
26627660
UniProt
Q59263
|RIBF_CORAM Bifunctional riboflavin kinase/FMN adenylyltransferase (Gene Name=ribF)
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