Structure of PDB 1rqp Chain B Binding Site BS02
Receptor Information
>1rqp Chain B (length=291) Species:
29303
(Streptantibioticus cattleyicolor) [
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RPIIAFMSDLGTTDDSVAQCKGLMYSICPDVTVVDVCHSMTPWDVEEGAR
YIVDLPRFFPEGTVFATTTYPATGTTTRSVAVRIKQAAKGGARGQWAGSG
AGFERAEGSYIYIAPNNGLLTTVLEEHGYLEAYEVTSPKVIPEQPEPTFY
SREMVAIPSAHLAAGFPLSEVGRPLEDHEIVRFNRPAVEQDGEALVGVVS
AIDHPFGNVWTNIHRTDLEKAGIGYGARLRLTLDGVLPFEAPLTPTFADA
GEIGNIAIYLNSRGYLSIARNAASLAYPYHLKEGMSARVEA
Ligand information
Ligand ID
SAM
InChI
InChI=1S/C15H22N6O5S/c1-27(3-2-7(16)15(24)25)4-8-10(22)11(23)14(26-8)21-6-20-9-12(17)18-5-19-13(9)21/h5-8,10-11,14,22-23H,2-4,16H2,1H3,(H2-,17,18,19,24,25)/t7-,8+,10+,11+,14+,27-/m0/s1
InChIKey
MEFKEPWMEQBLKI-FCKMPRQPSA-N
SMILES
Software
SMILES
CACTVS 3.341
C[S@@+](CC[C@H](N)C([O-])=O)C[C@H]1O[C@H]([C@H](O)[C@@H]1O)n2cnc3c(N)ncnc23
OpenEye OEToolkits 1.5.0
C[S+](CCC(C(=O)[O-])N)CC1C(C(C(O1)n2cnc3c2ncnc3N)O)O
CACTVS 3.341
C[S+](CC[CH](N)C([O-])=O)C[CH]1O[CH]([CH](O)[CH]1O)n2cnc3c(N)ncnc23
OpenEye OEToolkits 1.5.0
C[S@@+](CC[C@@H](C(=O)[O-])N)C[C@@H]1[C@H]([C@H]([C@@H](O1)n2cnc3c2ncnc3N)O)O
ACDLabs 10.04
[O-]C(=O)C(N)CC[S+](C)CC3OC(n2cnc1c(ncnc12)N)C(O)C3O
Formula
C15 H22 N6 O5 S
Name
S-ADENOSYLMETHIONINE
ChEMBL
CHEMBL1235831
DrugBank
ZINC
PDB chain
1rqp Chain B Residue 500 [
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Receptor-Ligand Complex Structure
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PDB
1rqp
Crystal structure and mechanism of a bacterial fluorinating enzyme
Resolution
1.8 Å
Binding residue
(original residue number in PDB)
D16 L17 S23 W50 Y77 P78 T155 F156 S158
Binding residue
(residue number reindexed from 1)
D9 L10 S16 W43 Y70 P71 T148 F149 S151
Annotation score
5
Enzymatic activity
Enzyme Commision number
2.5.1.63
: adenosyl-fluoride synthase.
Gene Ontology
Molecular Function
GO:0016740
transferase activity
GO:0033846
adenosyl-fluoride synthase activity
View graph for
Molecular Function
External links
PDB
RCSB:1rqp
,
PDBe:1rqp
,
PDBj:1rqp
PDBsum
1rqp
PubMed
14765200
UniProt
Q70GK9
|FLA_STRCT Fluorinase (Gene Name=flA)
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