Structure of PDB 5axb Chain A Binding Site BS01
Receptor Information
>5axb Chain A (length=429) Species:
10090
(Mus musculus) [
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KLPYKVADIGLAAWGRKALDIAENEMPGLMRMREMYSASKPLKGARIAGC
LHMTVETAVLIETLVALGAEVRWSSCNIFSTQDHAAAAIAKAGIPVFAWK
GETDEEYLWCIEQTLHFKDGPLNMILDDGGDLTNLIHTKYPQLLSGIRGI
SEETTTGVHNLYKMMSNGILKVPAINVNDSVTKSKFDNLYGCRESLIDGI
KRATDVMIAGKVAVVAGYGDVGKGCAQALRGFGARVIITEIDPINALQAA
MEGYEVTTMDEACKEGNIFVTTTGCVDIILGRHFEQMKDDAIVCNIGHFD
VEIDVKWLNENAVEKVNIKPQVDRYWLKNGRRIILLAEGRLVNLGCAMGH
PSFVMSNSFTNQVMAQIELWTHPDKYPVGVHFLPKKLDEAVAEAHLGKLN
VKLTKLTEKQAQYLGMPINGPFKPDHYRY
Ligand information
Ligand ID
NAD
InChI
InChI=1S/C21H27N7O14P2/c22-17-12-19(25-7-24-17)28(8-26-12)21-16(32)14(30)11(41-21)6-39-44(36,37)42-43(34,35)38-5-10-13(29)15(31)20(40-10)27-3-1-2-9(4-27)18(23)33/h1-4,7-8,10-11,13-16,20-21,29-32H,5-6H2,(H5-,22,23,24,25,33,34,35,36,37)/t10-,11-,13-,14-,15-,16-,20-,21-/m1/s1
InChIKey
BAWFJGJZGIEFAR-NNYOXOHSSA-N
SMILES
Software
SMILES
CACTVS 3.341
NC(=O)c1ccc[n+](c1)[C@@H]2O[C@H](CO[P]([O-])(=O)O[P@](O)(=O)OC[C@H]3O[C@H]([C@H](O)[C@@H]3O)n4cnc5c(N)ncnc45)[C@@H](O)[C@H]2O
OpenEye OEToolkits 1.5.0
c1cc(c[n+](c1)C2C(C(C(O2)COP(=O)([O-])OP(=O)(O)OCC3C(C(C(O3)n4cnc5c4ncnc5N)O)O)O)O)C(=O)N
CACTVS 3.341
NC(=O)c1ccc[n+](c1)[CH]2O[CH](CO[P]([O-])(=O)O[P](O)(=O)OC[CH]3O[CH]([CH](O)[CH]3O)n4cnc5c(N)ncnc45)[CH](O)[CH]2O
OpenEye OEToolkits 1.5.0
c1cc(c[n+](c1)[C@H]2[C@@H]([C@@H]([C@H](O2)CO[P@@](=O)([O-])O[P@@](=O)(O)OC[C@@H]3[C@H]([C@H]([C@@H](O3)n4cnc5c4ncnc5N)O)O)O)O)C(=O)N
Formula
C21 H27 N7 O14 P2
Name
NICOTINAMIDE-ADENINE-DINUCLEOTIDE
ChEMBL
CHEMBL1234613
DrugBank
DB14128
ZINC
PDB chain
5axb Chain A Residue 501 [
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Receptor-Ligand Complex Structure
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PDB
5axb
Crystal structure of mouse SAHH complexed with noraristeromycin
Resolution
1.65 Å
Binding residue
(original residue number in PDB)
T157 T158 T159 N191 G222 D223 V224 T242 E243 I244 N248 T275 T276 I281 I299 G300 N346 H353
Binding residue
(residue number reindexed from 1)
T154 T155 T156 N188 G219 D220 V221 T239 E240 I241 N245 T272 T273 I278 I296 G297 N343 H350
Annotation score
2
Enzymatic activity
Catalytic site (original residue number in PDB)
H55 S78 S83 D131 E156 N181 K186 D190 N191 C195 H301 H353 S361 Q365
Catalytic site (residue number reindexed from 1)
H52 S75 S80 D128 E153 N178 K183 D187 N188 C192 H298 H350 S358 Q362
Enzyme Commision number
3.13.2.1
: adenosylhomocysteinase.
Gene Ontology
Molecular Function
GO:0004013
adenosylhomocysteinase activity
GO:0005507
copper ion binding
GO:0005515
protein binding
GO:0016787
hydrolase activity
GO:0042802
identical protein binding
GO:0051287
NAD binding
Biological Process
GO:0006730
one-carbon metabolic process
GO:0019510
S-adenosylhomocysteine catabolic process
Cellular Component
GO:0005634
nucleus
GO:0005737
cytoplasm
GO:0005783
endoplasmic reticulum
GO:0005829
cytosol
GO:0042470
melanosome
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:5axb
,
PDBe:5axb
,
PDBj:5axb
PDBsum
5axb
PubMed
UniProt
P50247
|SAHH_MOUSE Adenosylhomocysteinase (Gene Name=Ahcy)
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