Structure of PDB 4r3n Chain B Binding Site BS02
Receptor Information
>4r3n Chain B (length=347) Species:
1313
(Streptococcus pneumoniae) [
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GYTVAVVGATGAVGAQMIKMLEESTLPIDKIRYLASARSAGKSLKFKDQD
ITIEETTETAFEGVDIALFSAGSSTSAKYAPYAVKAGVVVVDNTSYFRQN
PDVPLVVPEVNAHALDAHNGIIACPNCSTIQMMVALEPVRQKWGLDRIIV
STYQAVSGAGMGAILETQRELREVLNDGVKPCDLHAEILPSGGDKKHYPI
AFNALPQIDVFTDNDYTYEEMKMTKETKKIMEDDSIAVSATCVRIPVLSA
HSESVYIETKEVAPIEEVKAAIAAFPGAVLEDDVAHQIYPQAINAVGSRD
TFVGRIRKDLDAEKGIHMWVVSDNLLKGAAWNSVQIAETLHERGLVR
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
4r3n Chain B Residue 403 [
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Receptor-Ligand Complex Structure
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PDB
4r3n
A cautionary tale of structure-guided inhibitor development against an essential enzyme in the aspartate-biosynthetic pathway.
Resolution
1.35 Å
Binding residue
(original residue number in PDB)
G9 T11 G12 A13 V14 A36 S37 S40 S71 A72 G73 T76 T95 N127 C128 G161 M162 G329
Binding residue
(residue number reindexed from 1)
G8 T10 G11 A12 V13 A35 S36 S39 S70 A71 G72 T75 T94 N126 C127 G160 M161 G328
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
C128 Q155 R245 H252
Catalytic site (residue number reindexed from 1)
C127 Q154 R244 H251
Enzyme Commision number
1.2.1.11
: aspartate-semialdehyde dehydrogenase.
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0004073
aspartate-semialdehyde dehydrogenase activity
GO:0016491
oxidoreductase activity
GO:0016620
oxidoreductase activity, acting on the aldehyde or oxo group of donors, NAD or NADP as acceptor
GO:0046983
protein dimerization activity
GO:0050661
NADP binding
GO:0051287
NAD binding
Biological Process
GO:0008652
amino acid biosynthetic process
GO:0009085
lysine biosynthetic process
GO:0009086
methionine biosynthetic process
GO:0009088
threonine biosynthetic process
GO:0009089
lysine biosynthetic process via diaminopimelate
GO:0009097
isoleucine biosynthetic process
GO:0019877
diaminopimelate biosynthetic process
GO:0071266
'de novo' L-methionine biosynthetic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:4r3n
,
PDBe:4r3n
,
PDBj:4r3n
PDBsum
4r3n
PubMed
25478842
UniProt
Q8DQ00
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