Structure of PDB 5ugh Chain B Binding Site BS01
Receptor Information
>5ugh Chain B (length=365) Species:
9606
(Homo sapiens) [
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AFIEEGTFLFTSESVGEGHPDKICDQISDAVLDAHLQQDPDAKVACETVA
KTGMILLAGEITSRAAVDYQKVVREAVKHIGYDDSSKGFDYKTCNVLVAL
EQQSPDQGLMFGYATDETEECMPLTIVLAHKLNAKLAELRRNGTLPWLRP
DSKTQVTVQYMQDRGAVLPIRVHTIVISVQHDEEVCLDEMRDALKEKVIK
AVVPAKYLDEDTIYHLQPSGRFVIGGPDAGLTGRKIIVDTYGGWGAHGGG
AFSGKDYTKVDRSAAYAARWVAKSLVKGGLCRRVLVQVSYAIGVSHPLSI
SIFHYGTSQKSERELLEIVKKNFDLRPGVIVRDLDLKKPIYQRTAAYGHF
GRDSFPWEVPKKLKY
Ligand information
Ligand ID
8AJ
InChI
InChI=1S/C20H19ClN4/c1-24(2)11-10-19-22-23-20-13-16(14-6-4-3-5-7-14)17-12-15(21)8-9-18(17)25(19)20/h3-9,12-13H,10-11H2,1-2H3
InChIKey
LYLASWLQCMKZAT-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 12.01
c4c(Cl)cc1c(n3c(cc1c2ccccc2)nnc3CCN(C)C)c4
OpenEye OEToolkits 2.0.6
CN(C)CCc1nnc2n1c3ccc(cc3c(c2)c4ccccc4)Cl
CACTVS 3.385
CN(C)CCc1nnc2cc(c3ccccc3)c4cc(Cl)ccc4n12
Formula
C20 H19 Cl N4
Name
2-(7-chloro-5-phenyl[1,2,4]triazolo[4,3-a]quinolin-1-yl)-N,N-dimethylethan-1-amine;
PF-02929366
ChEMBL
CHEMBL337420
DrugBank
ZINC
ZINC000027329107
PDB chain
5ugh Chain B Residue 401 [
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Receptor-Ligand Complex Structure
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PDB
5ugh
Targeting S-adenosylmethionine biosynthesis with a novel allosteric inhibitor of Mat2A.
Resolution
2.062 Å
Binding residue
(original residue number in PDB)
L315 S331 I332 F333 E342
Binding residue
(residue number reindexed from 1)
L285 S301 I302 F303 E312
Annotation score
1
Binding affinity
MOAD
: Kd=170nM
Enzymatic activity
Catalytic site (original residue number in PDB)
H29 D31 K32 E57 E70 K181 F250 D258 A259 R264 K265 K285 K289 D291
Catalytic site (residue number reindexed from 1)
H19 D21 K22 E47 E60 K153 F222 D228 A229 R234 K235 K255 K259 D261
Enzyme Commision number
2.5.1.6
: methionine adenosyltransferase.
Gene Ontology
Molecular Function
GO:0004478
methionine adenosyltransferase activity
GO:0005515
protein binding
GO:0005524
ATP binding
GO:0016740
transferase activity
GO:0036094
small molecule binding
GO:0042802
identical protein binding
GO:0046872
metal ion binding
Biological Process
GO:0006556
S-adenosylmethionine biosynthetic process
GO:0006730
one-carbon metabolic process
GO:0034214
protein hexamerization
GO:0051291
protein heterooligomerization
GO:0061431
cellular response to methionine
GO:1904263
positive regulation of TORC1 signaling
GO:1990830
cellular response to leukemia inhibitory factor
Cellular Component
GO:0005829
cytosol
GO:0048269
methionine adenosyltransferase complex
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:5ugh
,
PDBe:5ugh
,
PDBj:5ugh
PDBsum
5ugh
PubMed
28553945
UniProt
P31153
|METK2_HUMAN S-adenosylmethionine synthase isoform type-2 (Gene Name=MAT2A)
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