Structure of PDB 2h00 Chain A Binding Site BS01
Receptor Information
>2h00 Chain A (length=225) Species:
9606
(Homo sapiens) [
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VSLNFKDPEAVRALTCTLLREDFGLSIDIPLERLIPTVPLRLNYIHWVED
LIGHQDSDKSTLRRGIDIGTGASCIYPLLGATLNGWYFLATEVDDMCFNY
AKKNVEQNNLSDLIKVVKVPQKTLLMDALKEESEIIYDFCMCNPPFFGIT
EIMAEGGELEFVKRIIHDSLQLKKRLRWYSCMLGKKCSLAPLKEELRIQG
VPKVTYTEFCQGRTMRWALAWSFYD
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
2h00 Chain A Residue 300 [
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Receptor-Ligand Complex Structure
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PDB
2h00
The Crystal Structure of Human methyltransferase 10 domain containing protein.
Resolution
2.0 Å
Binding residue
(original residue number in PDB)
L38 R45 G73 T74 E96 V97 Q125 N147 F151
Binding residue
(residue number reindexed from 1)
L34 R41 G69 T70 E92 V93 Q121 N143 F147
Annotation score
5
Enzymatic activity
Enzyme Commision number
2.1.1.346
: U6 snRNA m(6)A methyltransferase.
2.1.1.348
: mRNA m(6)A methyltransferase.
Gene Ontology
Molecular Function
GO:0008168
methyltransferase activity
View graph for
Molecular Function
External links
PDB
RCSB:2h00
,
PDBe:2h00
,
PDBj:2h00
PDBsum
2h00
PubMed
UniProt
Q86W50
|MET16_HUMAN RNA N6-adenosine-methyltransferase METTL16 (Gene Name=METTL16)
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