Structure of PDB 3g5a Chain A Binding Site BS01
Receptor Information
>3g5a Chain A (length=296) Species:
5478
(Nakaseomyces glabratus) [
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GAMVMRLGDAAELCYNLTSSYLQIAAESDSIIAQTQRAINTTKSILINET
FPKWSPLNGEISFSYNGGKDCQVLLLLYLSCLWEYYIVKLSLTKLPTVFI
DHDDTFKTLENFIEETSLRYSLSLYESDRDKCETMAEAFETFLQVFPETK
AIVIGIRHTDPFGEHLKPIQKTDANWPDFYRLQPLLHWNLANIWSFLLYS
NEPICELYRYGFTSLGNVEETLPNPHLRKDKNSTPLKLNFEWEIENRYKH
NEVTKAEPIPIADEDLVKIENLHEDYYPGWYLVDDKLERAGRIKKK
Ligand information
Ligand ID
APC
InChI
InChI=1S/C11H18N5O12P3/c12-9-6-10(14-2-13-9)16(3-15-6)11-8(18)7(17)5(27-11)1-26-29(19,20)4-30(21,22)28-31(23,24)25/h2-3,5,7-8,11,17-18H,1,4H2,(H,19,20)(H,21,22)(H2,12,13,14)(H2,23,24,25)/t5-,7-,8-,11-/m1/s1
InChIKey
CAWZRIXWFRFUQB-IOSLPCCCSA-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)(C[P@](=O)(O)OP(=O)(O)O)O)O)O)N
CACTVS 3.341
Nc1ncnc2n(cnc12)[C@@H]3O[C@H](CO[P@@](O)(=O)C[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)(CP(=O)(O)OP(=O)(O)O)O)O)O)N
ACDLabs 10.04
O=P(O)(O)OP(=O)(O)CP(=O)(O)OCC3OC(n2cnc1c(ncnc12)N)C(O)C3O
CACTVS 3.341
Nc1ncnc2n(cnc12)[CH]3O[CH](CO[P](O)(=O)C[P](O)(=O)O[P](O)(O)=O)[CH](O)[CH]3O
Formula
C11 H18 N5 O12 P3
Name
DIPHOSPHOMETHYLPHOSPHONIC ACID ADENOSYL ESTER;
ALPHA,BETA-METHYLENEADENOSINE-5'-TRIPHOSPHATE
ChEMBL
CHEMBL132722
DrugBank
DB02596
ZINC
ZINC000008295117
PDB chain
3g5a Chain A Residue 305 [
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Receptor-Ligand Complex Structure
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PDB
3g5a
Structure and mechanism of a eukaryotic FMN adenylyltransferase.
Resolution
1.95 Å
Binding residue
(original residue number in PDB)
S60 Y61 N62 G64 K65 D66 C67 F107 I108 I162 G163 Y216 L223
Binding residue
(residue number reindexed from 1)
S64 Y65 N66 G68 K69 D70 C71 F99 I100 I154 G155 Y208 L215
Annotation score
3
Enzymatic activity
Enzyme Commision number
2.7.7.2
: FAD synthase.
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0003824
catalytic activity
GO:0003919
FMN adenylyltransferase activity
GO:0005524
ATP binding
GO:0016779
nucleotidyltransferase activity
GO:0046872
metal ion binding
Biological Process
GO:0006747
FAD biosynthetic process
Cellular Component
GO:0005737
cytoplasm
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:3g5a
,
PDBe:3g5a
,
PDBj:3g5a
PDBsum
3g5a
PubMed
19375431
UniProt
Q6FNA9
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