Structure of PDB 1t6y Chain B Binding Site BS01
Receptor Information
>1t6y Chain B (length=270) Species:
2336
(Thermotoga maritima) [
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VVSIGVFDGVHIGHQKVLRTMKEIAFFRKDDSLIYTISYPPEYFLPDFPG
LLMTVESRVEMLSRYARTVVLDFFRIKDLTPEGFVERYLSGVSAVVVGRD
FRFGKNASGNASFLRKKGVEVYEIEDVVVQGKRVSSSLIRNLVQEGRVEE
IPAYLGRYFEIEGIVHFPTANIDRGNEKLVDLKRGVYLVRVHLPDGKKKF
GVMNVGFNVKYEVYILDFEGDLYGQRLKLEVLKFMRDEKKFDSIEELKAA
IDQDVKSARNMIDDIINSKF
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
1t6y Chain B Residue 594 [
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Receptor-Ligand Complex Structure
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PDB
1t6y
Crystal structure of ADP bound FAD synthetase
Resolution
2.8 Å
Binding residue
(original residue number in PDB)
P479 T480 A481 Y533 I534 G539 L541
Binding residue
(residue number reindexed from 1)
P168 T169 A170 Y214 I215 G220 L222
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:0003919
FMN adenylyltransferase activity
GO:0005524
ATP binding
GO:0008531
riboflavin kinase activity
GO:0016301
kinase activity
GO:0016779
nucleotidyltransferase activity
GO:0046872
metal ion binding
Biological Process
GO:0006747
FAD biosynthetic process
GO:0006771
riboflavin metabolic process
GO:0009231
riboflavin biosynthetic process
GO:0009398
FMN biosynthetic process
GO:0016310
phosphorylation
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Molecular Function
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Biological Process
External links
PDB
RCSB:1t6y
,
PDBe:1t6y
,
PDBj:1t6y
PDBsum
1t6y
PubMed
UniProt
Q9WZW1
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