Structure of PDB 5n5s Chain D Binding Site BS01
Receptor Information
>5n5s Chain D (length=480) Species:
3218
(Physcomitrium patens) [
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TPKKYNIFLASKPVDGDRKWLDVTNKYTNDVAAKVPQATHKDIDDAIDAA
VAAAPAMAAMGAYERKAVLEKVVAELKNRFEEIAQTLTMESGKPIKDARG
EVTRTIDTFQVAAEESVRIYGEHIPLDISARNKGLQGIVKKFPIGPVSMV
SPWNFPLNLVAHKVAPAIAVGCPFVLKPASRTPLSALILGEILHKIEELP
LGAFSILPVSREDADMFTVDERFKLLTFTGSGPIGWDMKARAGKKKVVME
LGGNAPCIVDDYVPDLDYTIQRLINGGFYQGGQSCIHMQRLYVHERLYDE
VKEGFVAAVKKLKMGNPFEEDTYLGPMISESAAKGIEDWVKEAVAKGGKL
LTGGNRKGAFIEPTVIEDVPIEANARKEEIFGPVVLLYKYSDFKEAVKEC
NNTHYGLQSGIFTKDLNKAFYAFEHMEVGGVILNDSPALRVDSQPYGGLK
DSGIQREGVKYAMDDMLETKVLVMRNVGTL
Ligand information
Ligand ID
NAP
InChI
InChI=1S/C21H28N7O17P3/c22-17-12-19(25-7-24-17)28(8-26-12)21-16(44-46(33,34)35)14(30)11(43-21)6-41-48(38,39)45-47(36,37)40-5-10-13(29)15(31)20(42-10)27-3-1-2-9(4-27)18(23)32/h1-4,7-8,10-11,13-16,20-21,29-31H,5-6H2,(H7-,22,23,24,25,32,33,34,35,36,37,38,39)/t10-,11-,13-,14-,15-,16-,20-,21-/m1/s1
InChIKey
XJLXINKUBYWONI-NNYOXOHSSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
c1cc(c[n+](c1)C2C(C(C(O2)COP(=O)([O-])OP(=O)(O)OCC3C(C(C(O3)n4cnc5c4ncnc5N)OP(=O)(O)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[P](O)(O)=O)[CH]3O)n4cnc5c(N)ncnc45)[CH](O)[CH]2O
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[P](O)(O)=O)[C@@H]3O)n4cnc5c(N)ncnc45)[C@@H](O)[C@H]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)OP(=O)(O)O)O)O)O)C(=O)N
Formula
C21 H28 N7 O17 P3
Name
NADP NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE;
2'-MONOPHOSPHOADENOSINE 5'-DIPHOSPHORIBOSE
ChEMBL
CHEMBL295069
DrugBank
DB03461
ZINC
PDB chain
5n5s Chain D Residue 503 [
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Receptor-Ligand Complex Structure
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PDB
5n5s
The ALDH21 gene found in lower plants and some vascular plants codes for a NADP(+) -dependent succinic semialdehyde dehydrogenase.
Resolution
2.3 Å
Binding residue
(original residue number in PDB)
V167 S168 P169 W170 N171 L176 K194 S197 R228 A231 T246 G247 S248 I251 E267 L268 C302 E396 F398 Y463
Binding residue
(residue number reindexed from 1)
V150 S151 P152 W153 N154 L159 K177 S180 R211 A214 T229 G230 S231 I234 E250 L251 C285 E379 F381 Y446
Annotation score
3
Binding affinity
MOAD
: Kd=31uM
Enzymatic activity
Catalytic site (original residue number in PDB)
N171 K194 E267 C302 E396 E474
Catalytic site (residue number reindexed from 1)
N154 K177 E250 C285 E379 E457
Enzyme Commision number
1.2.1.9
: glyceraldehyde-3-phosphate dehydrogenase (NADP(+)).
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0008911
lactaldehyde dehydrogenase (NAD+) activity
GO:0016491
oxidoreductase activity
GO:0016620
oxidoreductase activity, acting on the aldehyde or oxo group of donors, NAD or NADP as acceptor
View graph for
Molecular Function
External links
PDB
RCSB:5n5s
,
PDBe:5n5s
,
PDBj:5n5s
PDBsum
5n5s
PubMed
28749584
UniProt
A9SS48
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