Structure of PDB 1rqp Chain B Binding Site BS01
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 A 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)
D210 F213 N215 W217 F254 S269 R270 R277 A279
Binding residue
(residue number reindexed from 1)
D203 F206 N208 W210 F247 S262 R263 R270 A272
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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