Structure of PDB 2bb3 Chain B Binding Site BS01
Receptor Information
>2bb3 Chain B (length=192) Species:
224325
(Archaeoglobus fulgidus DSM 4304) [
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GHMIWIVGSGTCRGQTTERAKEIIERAEVIYGSRRALELAGVVDDSRARI
LRSFKGDEIRRIMEEGREREVAVISTGDPMVAGLGRVLREIAEDVEIKIE
PAISSVQVALARLKVDLSEVAVVDCHAELTELLKYRHLLILADSHFPLER
LGKRRVVLLENLCMEGERIREGNADSIELESDYTIIFVEREV
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
2bb3 Chain B Residue 203 [
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Receptor-Ligand Complex Structure
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PDB
2bb3
Crystal Structure of Cobalamin Biosynthesis Precorrin-6Y Methylase (cbiE) from Archaeoglobus fulgidus
Resolution
2.27 Å
Binding residue
(original residue number in PDB)
T74 G75 D76 V79 A80 S102 S103 L144 A145 L165 M167 D185 Y186 I188
Binding residue
(residue number reindexed from 1)
T76 G77 D78 V81 A82 S104 S105 L141 A142 L162 M164 D182 Y183 I185
Annotation score
4
Enzymatic activity
Enzyme Commision number
2.1.1.-
Gene Ontology
Molecular Function
GO:0008168
methyltransferase activity
GO:0008276
protein methyltransferase activity
Biological Process
GO:0009236
cobalamin biosynthetic process
GO:0032259
methylation
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:2bb3
,
PDBe:2bb3
,
PDBj:2bb3
PDBsum
2bb3
PubMed
UniProt
O29536
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