Structure of PDB 7phf Chain B Binding Site BS01
Receptor Information
>7phf Chain B (length=270) Species:
1924,1950,1114943
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TVAARPQQIDALRTLIRLGSLHTPMVVRTAATLRLVDHILAGARTVKALA
ARTDTRPEALLRLIRHLVAIGLLEEDAPGEFVPTEVGELLADDHPAAQRA
WHDLTQAVARADISFTRLPDAIRTGRPTYESIYGKPFYEDLAGRPDLRAS
FDSLMTTTAFAAPARLDVVDVVDFFEPLRKADAIILSFVLLNWPDHDAVR
ILTRCAEALEILIHERDRFFSTLLDLRMLVFLGGALRTREKWDGLAASAG
LVVEVRLVPLDSCLLVLAPA
Ligand information
Ligand ID
SAH
InChI
InChI=1S/C14H20N6O5S/c15-6(14(23)24)1-2-26-3-7-9(21)10(22)13(25-7)20-5-19-8-11(16)17-4-18-12(8)20/h4-7,9-10,13,21-22H,1-3,15H2,(H,23,24)(H2,16,17,18)/t6-,7+,9+,10+,13+/m0/s1
InChIKey
ZJUKTBDSGOFHSH-WFMPWKQPSA-N
SMILES
Software
SMILES
CACTVS 3.341
N[CH](CCSC[CH]1O[CH]([CH](O)[CH]1O)n2cnc3c(N)ncnc23)C(O)=O
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)C3C(C(C(O3)CSCCC(C(=O)O)N)O)O)N
CACTVS 3.341
N[C@@H](CCSC[C@H]1O[C@H]([C@H](O)[C@@H]1O)n2cnc3c(N)ncnc23)C(O)=O
ACDLabs 10.04
O=C(O)C(N)CCSCC3OC(n2cnc1c(ncnc12)N)C(O)C3O
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)[C@H]3[C@@H]([C@@H]([C@H](O3)CSCC[C@@H](C(=O)O)N)O)O)N
Formula
C14 H20 N6 O5 S
Name
S-ADENOSYL-L-HOMOCYSTEINE
ChEMBL
CHEMBL418052
DrugBank
DB01752
ZINC
ZINC000004228232
PDB chain
7phf Chain B Residue 401 [
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Receptor-Ligand Complex Structure
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PDB
7phf
Evolution-inspired engineering of anthracycline methyltransferases.
Resolution
2.21 Å
Binding residue
(original residue number in PDB)
Y143 D237 F238 S252
Binding residue
(residue number reindexed from 1)
Y138 D173 F174 S187
Annotation score
5
Enzymatic activity
Enzyme Commision number
2.1.1.292
: carminomycin 4-O-methyltransferase.
4.1.1.-
Gene Ontology
Molecular Function
GO:0008168
methyltransferase activity
GO:0008171
O-methyltransferase activity
View graph for
Molecular Function
External links
PDB
RCSB:7phf
,
PDBe:7phf
,
PDBj:7phf
PDBsum
7phf
PubMed
36874276
UniProt
I2N5E8
;
Q06528
|DNRK_STRPE Carminomycin 4-O-methyltransferase DnrK (Gene Name=dnrK);
Q54527
|RDMB_STREF Aclacinomycin 10-hydroxylase RdmB (Gene Name=rdmB)
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