Structure of PDB 2ggx Chain B Binding Site BS04
Receptor Information
>2ggx Chain B (length=151) Species:
9606
(Homo sapiens) [
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ASLRQQVEALQGQVQHLQAAFSQYKKVELFPNGQSVGEKIFKTAGFVKPF
TEAQLLCTQAGGQLASPRSAAENAALQQLVVAKNEAAFLSMTDSKTEGKF
TYPTGESLVYSNWAPGEPNDDGGSEDCVEIFTNGKWNDRACGEKRLVVCE
F
Ligand information
Ligand ID
NPJ
InChI
InChI=1S/C18H25NO13/c20-5-9-11(22)12(23)14(25)18(30-9)32-16-10(6-21)31-17(15(26)13(16)24)29-8-3-1-7(2-4-8)19(27)28/h1-4,9-18,20-26H,5-6H2/t9-,10-,11-,12+,13-,14-,15-,16-,17+,18-/m1/s1
InChIKey
IAYJZWFYUSNIPN-LTHBGAKLSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
c1cc(ccc1[N+](=O)[O-])OC2C(C(C(C(O2)CO)OC3C(C(C(C(O3)CO)O)O)O)O)O
CACTVS 3.341
OC[CH]1O[CH](O[CH]2[CH](O)[CH](O)[CH](O[CH]2CO)Oc3ccc(cc3)[N+]([O-])=O)[CH](O)[CH](O)[CH]1O
ACDLabs 10.04
[O-][N+](=O)c3ccc(OC2OC(C(OC1OC(CO)C(O)C(O)C1O)C(O)C2O)CO)cc3
OpenEye OEToolkits 1.5.0
c1cc(ccc1[N+](=O)[O-])O[C@@H]2[C@@H]([C@H]([C@@H]([C@H](O2)CO)O[C@@H]3[C@@H]([C@H]([C@@H]([C@H](O3)CO)O)O)O)O)O
CACTVS 3.341
OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)[C@H](O[C@@H]2CO)Oc3ccc(cc3)[N+]([O-])=O)[C@H](O)[C@@H](O)[C@@H]1O
Formula
C18 H25 N O13
Name
4-NITROPHENYL 4-O-ALPHA-D-GLUCOPYRANOSYL-ALPHA-D-GALACTOPYRANOSIDE;
P-NITROPHENYL MALTOSIDE
ChEMBL
DrugBank
ZINC
ZINC000004282193
PDB chain
2ggx Chain B Residue 700 [
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Receptor-Ligand Complex Structure
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PDB
2ggx
Contributions of Phenylalanine 335 to Ligand Recognition by Human Surfactant Protein D: ring interactions with Sp-D ligands
Resolution
1.9 Å
Binding residue
(original residue number in PDB)
E321 N323 E329 F335 T336 N337 N341 R343
Binding residue
(residue number reindexed from 1)
E117 N119 E125 F131 T132 N133 N137 R139
Annotation score
1
Binding affinity
MOAD
: ic50=0.32mM
Enzymatic activity
Enzyme Commision number
?
External links
PDB
RCSB:2ggx
,
PDBe:2ggx
,
PDBj:2ggx
PDBsum
2ggx
PubMed
16636058
UniProt
P35247
|SFTPD_HUMAN Pulmonary surfactant-associated protein D (Gene Name=SFTPD)
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