Structure of PDB 6c8r Chain A Binding Site BS01
Receptor Information
>6c8r Chain A (length=358) Species:
4058
(Catharanthus roseus) [
Search protein sequence
] [
Download receptor structure
] [
Download structure with residue number starting from 1
] [
View receptor structure
]
VEAHPMKGGDDSHSYSQNSCYQKGVIDAAKAVIVEAVNEKLDLENNPIFD
PIKPFRIADFGCSTGPNTFHAMQNIVESVETKYKSLQKTPEFHVFFNDHV
NNDFNVLFRSLPPNREFFAAGVPGSFYTRVFPKNSIHFAHCSYALHWLSK
VPKEIQDKNSLAYNKGRIHYTGTEKHVVKAYFGQFQRDFEGFLKARAQEI
VVGGLMVIQIPGLPSGEVLFSRTGAGLLHFLLGTSLMELVNKGIINEESV
DSFNLPQYHPSVEDLEMVIEMNDCFTIERVGTLPHPMKNLPFDVQRTSLQ
VRAIMECILTEHFGENILDPLFEIYTKNLQENFHVFDKEIRKDADLYLVL
KRKGNLEH
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
6c8r Chain A Residue 401 [
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
6c8r
Loganic Acid Methyltransferase: Insights into the Specificity of Methylation on an Iridoid Glycoside.
Resolution
1.951 Å
Binding residue
(original residue number in PDB)
P21 M22 Y31 G77 S79 N83 D114 H115 S141 F142 Y143 S158 Y159
Binding residue
(residue number reindexed from 1)
P5 M6 Y15 G61 S63 N67 D98 H99 S125 F126 Y127 S142 Y143
Annotation score
5
Enzymatic activity
Enzyme Commision number
2.1.1.50
: loganate O-methyltransferase.
Gene Ontology
Molecular Function
GO:0008168
methyltransferase activity
GO:0008757
S-adenosylmethionine-dependent methyltransferase activity
GO:0030749
loganate O-methyltransferase activity
GO:0046872
metal ion binding
Biological Process
GO:0032259
methylation
GO:0035834
indole alkaloid metabolic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:6c8r
,
PDBe:6c8r
,
PDBj:6c8r
PDBsum
6c8r
PubMed
29399933
UniProt
B2KPR3
|LAMT_CATRO Loganic acid O-methyltransferase (Gene Name=LAMT)
[
Back to BioLiP
]