Structure of PDB 5eeh Chain B Binding Site BS02
Receptor Information
>5eeh Chain B (length=340) Species:
1950
(Streptomyces peucetius) [
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QIDALRTLIRLGSLHTPMVVRTAATLRLVDHILAGARTVKALAARTDTRP
EALLRLIRHLVAIGLLEEDAPGEFVPTEVGELLADDHPAAQRAWHDLTQA
VARADISFTRLPDAIRTGRPTYESIYGKPFYEDLAGRPDLRASFDSLLAC
DQDVAFDAPAAAYDWTNVRHVLDVGGGKGGFAAAIARRAPHVSATVLEMA
GTVDTARSYLKDEGLSDRVDVVEGDFFEPLPRKADAIILSFVLLNWPDHD
AVRILTRCAEALEPGGRILIHERDDLHENSFNEQFTELDLRMLVFLGGAL
RTREKWDGLAASAGLVVEEVRQLPSPTIPYDLSLLVLAPA
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
5eeh Chain B Residue 402 [
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Receptor-Ligand Complex Structure
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PDB
5eeh
Functional AdoMet Isosteres Resistant to Classical AdoMet Degradation Pathways.
Resolution
1.82 Å
Binding residue
(original residue number in PDB)
Y143 R153 G187 E210 M211 G236 D237 F238 S252
Binding residue
(residue number reindexed from 1)
Y131 R141 G175 E198 M199 G224 D225 F226 S240
Annotation score
5
Enzymatic activity
Catalytic site (original residue number in PDB)
L256 N257 E284 L312
Catalytic site (residue number reindexed from 1)
L244 N245 E272 L300
Enzyme Commision number
2.1.1.292
: carminomycin 4-O-methyltransferase.
Gene Ontology
Molecular Function
GO:0008168
methyltransferase activity
GO:0008171
O-methyltransferase activity
Biological Process
GO:0017000
antibiotic biosynthetic process
GO:0032259
methylation
GO:1901771
daunorubicin biosynthetic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:5eeh
,
PDBe:5eeh
,
PDBj:5eeh
PDBsum
5eeh
PubMed
27351335
UniProt
Q06528
|DNRK_STRPE Carminomycin 4-O-methyltransferase DnrK (Gene Name=dnrK)
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