Structure of PDB 3kpd Chain B Binding Site BS01
Receptor Information
>3kpd Chain B (length=121) Species:
2190
(Methanocaldococcus jannaschii) [
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TLVKDILSKPPITAHSNISIMEAAKILIKHNINHLPIVDEHGKLVGIITS
WDIAKALAQNKKTIEEIMTRNVITAHEDEPVDHVAIKMSKYNISGVPVVD
DYRRVVGIVTSEDISRLFGGK
Ligand information
Ligand ID
SAM
InChI
InChI=1S/C15H22N6O5S/c1-27(3-2-7(16)15(24)25)4-8-10(22)11(23)14(26-8)21-6-20-9-12(17)18-5-19-13(9)21/h5-8,10-11,14,22-23H,2-4,16H2,1H3,(H2-,17,18,19,24,25)/t7-,8+,10+,11+,14+,27-/m0/s1
InChIKey
MEFKEPWMEQBLKI-FCKMPRQPSA-N
SMILES
Software
SMILES
CACTVS 3.341
C[S@@+](CC[C@H](N)C([O-])=O)C[C@H]1O[C@H]([C@H](O)[C@@H]1O)n2cnc3c(N)ncnc23
OpenEye OEToolkits 1.5.0
C[S+](CCC(C(=O)[O-])N)CC1C(C(C(O1)n2cnc3c2ncnc3N)O)O
CACTVS 3.341
C[S+](CC[CH](N)C([O-])=O)C[CH]1O[CH]([CH](O)[CH]1O)n2cnc3c(N)ncnc23
OpenEye OEToolkits 1.5.0
C[S@@+](CC[C@@H](C(=O)[O-])N)C[C@@H]1[C@H]([C@H]([C@@H](O1)n2cnc3c2ncnc3N)O)O
ACDLabs 10.04
[O-]C(=O)C(N)CC[S+](C)CC3OC(n2cnc1c(ncnc12)N)C(O)C3O
Formula
C15 H22 N6 O5 S
Name
S-ADENOSYLMETHIONINE
ChEMBL
CHEMBL1235831
DrugBank
ZINC
PDB chain
3kpd Chain B Residue 1000 [
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Receptor-Ligand Complex Structure
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PDB
3kpd
Binding of S-Methyl-5'-Thioadenosine and S-Adenosyl-l-Methionine to Protein MJ0100 Triggers an Open-to-Closed Conformational Change in Its CBS Motif Pair.
Resolution
2.91 Å
Binding residue
(original residue number in PDB)
I434 T436 W438 D439 T456 V459 I460 N479 I480 S481 G482
Binding residue
(residue number reindexed from 1)
I47 T49 W51 D52 T69 V72 I73 N92 I93 S94 G95
Annotation score
1
Enzymatic activity
Enzyme Commision number
2.8.1.16
: L-aspartate semialdehyde sulfurtransferase.
External links
PDB
RCSB:3kpd
,
PDBe:3kpd
,
PDBj:3kpd
PDBsum
3kpd
PubMed
20026078
UniProt
Q57564
|ASST_METJA L-aspartate semialdehyde sulfurtransferase (Gene Name=MJ0100)
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