Structure of PDB 5v96 Chain D Binding Site BS02
Receptor Information
>5v96 Chain D (length=465) Species:
5763
(Naegleria fowleri) [
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TIEYQVKDMSLASLGRKRIEMAEKEMPGLMACRAKYGEEKPLNGVRITGS
LHMTVETAVLIETLKAIGGNIRWCSCNIFSTQDDAAAAIAAANTPVFAWK
GETLVEYWECTWKAIRFGPYQGPQLIVDDGGDATLLIHRGFQAEKEPSIL
DEDGGVEELRIVNNLLKRILKEEPGFFSKIVPDIKGVSEETTTGVHRLYA
MQKQGTLLFPAINVNDSVTKSKFDNIYGCRHSLLDGLNRATDVMLAGKEC
VICGFGDVGKGCAEALKGQGARVIVTEIDPINALQACMAGYTVKTVEDCL
ATADIYVTATGNKDIITLDHMKKMKDMAIICNIGHFDNEIDVLGLKTCEG
VKEINIKPQVDQFLFPDGHSIILLAQGRLVNLGCATGHPAFVMSASFTNQ
TLAQISLWKDKYEIGVYTLPKVLDEEVARLHLEKLGAKLTKLTTSQADYI
GVNANGPYKADHYRY
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
5v96 Chain D Residue 501 [
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Receptor-Ligand Complex Structure
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PDB
5v96
Crystal Structure of S-adenosyl-l-homocysteine Hydrolase from Naegleria fowleri with bound NAD and Adenosine
Resolution
2.0 Å
Binding residue
(original residue number in PDB)
T198 T199 T200 N232 G261 G263 D264 V265 E284 I285 N289 T317 N319 I322 I340 G341 N388 H395
Binding residue
(residue number reindexed from 1)
T191 T192 T193 N225 G254 G256 D257 V258 E277 I278 N282 T310 N312 I315 I333 G334 N381 H388
Annotation score
2
Enzymatic activity
Catalytic site (original residue number in PDB)
E197 N222 K227 D231 N232 C236 H342 H395 S403 Q407
Catalytic site (residue number reindexed from 1)
E190 N215 K220 D224 N225 C229 H335 H388 S396 Q400
Enzyme Commision number
3.13.2.1
: adenosylhomocysteinase.
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0004013
adenosylhomocysteinase activity
GO:0016787
hydrolase activity
Biological Process
GO:0006730
one-carbon metabolic process
GO:0033353
S-adenosylmethionine cycle
Cellular Component
GO:0005829
cytosol
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:5v96
,
PDBe:5v96
,
PDBj:5v96
PDBsum
5v96
PubMed
UniProt
A0A1Z0YU84
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