Structure of PDB 7oy1 Chain B Binding Site BS01
Receptor Information
>7oy1 Chain B (length=340) Species:
1924,1950,1114943
[
Search protein sequence
] [
Download receptor structure
] [
Download structure with residue number starting from 1
] [
View receptor structure
]
DALRTLIRLGSLHTPMVVRTAATLRLVDHILAGARTVKALAARTDTRPEA
LLRLIRHLVAIGLLEEDAPGEFVPTEVGELLADDHPAAQRAWHDLTQAVA
RADISFTRLPDAIRTGRPTYESIYGKPFYEDLAGRPDLRASFDSLMATEE
EAVDEAPAAAYDWTNVRHVLDVGGGNGGFAAAIARRAPHVSATVLEMAGT
VDTARSYLKDEGLSDRVDVVEGDFFEPLPRKADAIILSFVLLNWPDHDAV
RILTRCAEALEPGGRILIHERADVEGDGADRFFSTLLDLRMLVFLGGALR
TREKWDGLAASAGLVVEEVRGPLVSPNVPLDSSLLVLAPA
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
7oy1 Chain B Residue 400 [
Download ligand structure
] [
Download structure with residue number starting from 1
] [
View ligand structure
]
Receptor-Ligand Complex Structure
Global view
Local view
Structure summary
[
Spin on
] [
Spin off
] [
Reset
]
[
High quality
] [
Low quality
]
[
White background
] [
Black background
]
[
Spin on
] [
Spin off
] [
Reset
]
[
High quality
] [
Low quality
]
[
White background
] [
Black background
]
PDB
7oy1
Evolution-inspired engineering of anthracycline methyltransferases.
Resolution
2.39 Å
Binding residue
(original residue number in PDB)
Y143 R153 M160 G187 G188 E210 M211 G236 D237 F238 S252
Binding residue
(residue number reindexed from 1)
Y129 R139 M146 G173 G174 E196 M197 G222 D223 F224 S238
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:7oy1
,
PDBe:7oy1
,
PDBj:7oy1
PDBsum
7oy1
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)
[
Back to BioLiP
]