Structure of PDB 8cbo Chain E Binding Site BS02
Receptor Information
>8cbo Chain E (length=211) Species:
9606
(Homo sapiens) [
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KNFLFLRLWDRNMDIAMGWKGAQAMQFGQPLVFDMAYENYMKRKELQNTV
SQLLESEGWNRRNVDPFHIYFCNLKIDGALHRELVKRYQEKWDKLLLTST
EKSHVDLFPKDSIIYLTADSPNVMTTFRHDKVYVIGSFVDKSMQPGTSLA
KAKRLNLATECLPLDKYLQWEIGNKNLTLDQMIRILLCLKNNGNWQEALQ
FVPKRKHTGFL
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
8cbo Chain E Residue 401 [
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Receptor-Ligand Complex Structure
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PDB
8cbo
Structural basis for human mitochondrial tRNA maturation.
Resolution
3.2 Å
Binding residue
(original residue number in PDB)
L290 T291 A292 G310 F312 T321 S322 C335 L336 N350 L351 M356
Binding residue
(residue number reindexed from 1)
L116 T117 A118 G136 F138 T147 S148 C161 L162 N176 L177 M182
Annotation score
5
Enzymatic activity
Enzyme Commision number
2.1.1.-
2.1.1.218
: tRNA (adenine(9)-N(1))-methyltransferase.
2.1.1.221
: tRNA (guanine(9)-N(1))-methyltransferase.
External links
PDB
RCSB:8cbo
,
PDBe:8cbo
,
PDBj:8cbo
PDBsum
8cbo
PubMed
38824131
UniProt
Q7L0Y3
|TM10C_HUMAN tRNA methyltransferase 10 homolog C (Gene Name=TRMT10C)
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