Structure of PDB 5o5k Chain I Binding Site BS04
Receptor Information
>5o5k Chain I (length=216) Species:
1299331
(Mycobacterium intracellulare 1956) [
Search protein sequence
] [
Download receptor structure
] [
Download structure with residue number starting from 1
] [
View receptor structure
]
AVMEAEYERSEALLANMLPGSIAERLKSSSRSVIADKYDEVSVLFADIVG
FTERASTTTPADLVRFLNRLYGAFDELVDKHGLEKIKVSGDSYMVVSGVP
RARPDHAFALADFALDMANVAAALKDPHGDPVPLRMGMACGPVVAGVVGS
RRFFYDVWGDAVNVASRMESTDSVGRIQVPEAMYERLKNEFVLQERGRIE
VKGKGVMRTWYLIGRK
Ligand information
Ligand ID
ONM
InChI
InChI=1S/C18H23N6O15P3/c1-20-9-5-3-2-4-8(9)17(27)37-13-10(6-35-41(31,32)39-42(33,34)38-40(28,29)30)36-16(12(13)25)24-7-21-11-14(24)22-18(19)23-15(11)26/h2-5,7,10,12-13,16,20,25H,6H2,1H3,(H,31,32)(H,33,34)(H2,28,29,30)(H3,19,22,23,26)/t10-,12-,13-,16-/m1/s1
InChIKey
DSPRYHPLXXUNHS-XNIJJKJLSA-N
SMILES
Software
SMILES
CACTVS 3.341
CNc1ccccc1C(=O)O[C@H]2[C@@H](O)[C@@H](O[C@@H]2CO[P@](O)(=O)O[P@@](O)(=O)O[P](O)(O)=O)n3cnc4C(=O)NC(=Nc34)N
ACDLabs 10.04
O=P(O)(O)OP(=O)(O)OP(=O)(O)OCC4OC(n2cnc1c2N=C(N)NC1=O)C(O)C4OC(=O)c3ccccc3NC
CACTVS 3.341
CNc1ccccc1C(=O)O[CH]2[CH](O)[CH](O[CH]2CO[P](O)(=O)O[P](O)(=O)O[P](O)(O)=O)n3cnc4C(=O)NC(=Nc34)N
OpenEye OEToolkits 1.5.0
CNc1ccccc1C(=O)OC2C(OC(C2O)n3cnc4c3N=C(NC4=O)N)COP(=O)(O)OP(=O)(O)OP(=O)(O)O
OpenEye OEToolkits 1.5.0
CNc1ccccc1C(=O)O[C@@H]2[C@H](O[C@H]([C@@H]2O)n3cnc4c3N=C(NC4=O)N)CO[P@@](=O)(O)O[P@](=O)(O)OP(=O)(O)O
Formula
C18 H23 N6 O15 P3
Name
3'-O-(N-METHYLANTHRANILOYL)-GUANOSINE-5'-TRIPHOSPHATE
ChEMBL
CHEMBL403351
DrugBank
ZINC
ZINC000049792258
PDB chain
5o5k Chain J Residue 501 [
Download ligand structure
] [
Download structure with residue number starting from 1
] [
View ligand structure
]
Receptor-Ligand Complex Structure
Global view
Local view
Structure summary
[
Spin on
] [
Spin off
] [
Reset
]
[
High quality
] [
Low quality
]
[
White background
] [
Black background
]
[
Spin on
] [
Spin off
] [
Reset
]
[
High quality
] [
Low quality
]
[
White background
] [
Black background
]
PDB
5o5k
Role of the nucleotidyl cyclase helical domain in catalytically active dimer formation.
Resolution
3.4 Å
Binding residue
(original residue number in PDB)
F254 K296 M303 W367 G368 D369 V371 N372 S375
Binding residue
(residue number reindexed from 1)
F45 K87 M94 W158 G159 D160 V162 N163 S166
Annotation score
2
Enzymatic activity
Catalytic site (original residue number in PDB)
D256 I257 D300 R376 K411
Catalytic site (residue number reindexed from 1)
D47 I48 D91 R167 K202
Enzyme Commision number
4.6.1.1
: adenylate cyclase.
Gene Ontology
Molecular Function
GO:0016849
phosphorus-oxygen lyase activity
Biological Process
GO:0009190
cyclic nucleotide biosynthetic process
GO:0035556
intracellular signal transduction
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:5o5k
,
PDBe:5o5k
,
PDBj:5o5k
PDBsum
5o5k
PubMed
29087332
UniProt
X8CHM4
[
Back to BioLiP
]