Structure of PDB 1m2o Chain B Binding Site BS02
Receptor Information
>1m2o Chain B (length=164) Species:
4932
(Saccharomyces cerevisiae) [
Search protein sequence
] [
Download receptor structure
] [
Download structure with residue number starting from 1
] [
View receptor structure
]
GKLLFLGLDNAGKTTLLHMLKNDRLATLQPTWHPTSEELAIGNIKFTTFD
LGGHIQARRLWKDYFPEVNGIVFLVDAADPERFDEARVELDALFNIAELK
DVPFVILGNKIDAPNAVSEAELRSALGLLNTTGIEGQRPVEVFMCSVVMR
NGYLEAFQWLSQYI
Ligand information
Ligand ID
GNP
InChI
InChI=1S/C10H17N6O13P3/c11-10-13-7-4(8(19)14-10)12-2-16(7)9-6(18)5(17)3(28-9)1-27-32(25,26)29-31(23,24)15-30(20,21)22/h2-3,5-6,9,17-18H,1H2,(H,25,26)(H3,11,13,14,19)(H4,15,20,21,22,23,24)/t3-,5-,6-,9-/m1/s1
InChIKey
UQABYHGXWYXDTK-UUOKFMHZSA-N
SMILES
Software
SMILES
ACDLabs 10.04
O=P(O)(O)NP(=O)(O)OP(=O)(O)OCC3OC(n2cnc1c2N=C(N)NC1=O)C(O)C3O
OpenEye OEToolkits 1.5.0
c1nc2c(n1[C@H]3[C@@H]([C@@H]([C@H](O3)CO[P@](=O)(O)O[P@@](=O)(NP(=O)(O)O)O)O)O)N=C(NC2=O)N
OpenEye OEToolkits 1.5.0
c1nc2c(n1C3C(C(C(O3)COP(=O)(O)OP(=O)(NP(=O)(O)O)O)O)O)N=C(NC2=O)N
CACTVS 3.341
NC1=Nc2n(cnc2C(=O)N1)[C@@H]3O[C@H](CO[P@@](O)(=O)O[P@@](O)(=O)N[P](O)(O)=O)[C@@H](O)[C@H]3O
CACTVS 3.341
NC1=Nc2n(cnc2C(=O)N1)[CH]3O[CH](CO[P](O)(=O)O[P](O)(=O)N[P](O)(O)=O)[CH](O)[CH]3O
Formula
C10 H17 N6 O13 P3
Name
PHOSPHOAMINOPHOSPHONIC ACID-GUANYLATE ESTER
ChEMBL
CHEMBL1233085
DrugBank
DB02082
ZINC
ZINC000037868676
PDB chain
1m2o Chain B Residue 5200 [
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
1m2o
Structure of the Sec23/24-Sar1 pre-budding complex of the COPII vesicle coat
Resolution
2.5 Å
Binding residue
(original residue number in PDB)
D32 N33 G35 K36 T37 T38 T54 G76 N132 K133 D135 S172 V173 V174
Binding residue
(residue number reindexed from 1)
D9 N10 G12 K13 T14 T15 T31 G53 N109 K110 D112 S146 V147 V148
Annotation score
3
Enzymatic activity
Catalytic site (original residue number in PDB)
H77
Catalytic site (residue number reindexed from 1)
H54
Enzyme Commision number
3.6.5.-
Gene Ontology
Molecular Function
GO:0003924
GTPase activity
GO:0005515
protein binding
GO:0005525
GTP binding
GO:0016787
hydrolase activity
Biological Process
GO:0000266
mitochondrial fission
GO:0003400
regulation of COPII vesicle coating
GO:0006886
intracellular protein transport
GO:0006888
endoplasmic reticulum to Golgi vesicle-mediated transport
GO:0006998
nuclear envelope organization
GO:0007006
mitochondrial membrane organization
GO:0015031
protein transport
GO:0016050
vesicle organization
GO:0016192
vesicle-mediated transport
GO:0061024
membrane organization
GO:0070863
positive regulation of protein exit from endoplasmic reticulum
GO:1902953
positive regulation of ER to Golgi vesicle-mediated transport
Cellular Component
GO:0000139
Golgi membrane
GO:0005739
mitochondrion
GO:0005783
endoplasmic reticulum
GO:0005789
endoplasmic reticulum membrane
GO:0005794
Golgi apparatus
GO:0012507
ER to Golgi transport vesicle membrane
GO:0016020
membrane
GO:0030127
COPII vesicle coat
GO:0031410
cytoplasmic vesicle
GO:0044233
mitochondria-associated endoplasmic reticulum membrane contact site
GO:0070971
endoplasmic reticulum exit site
View graph for
Molecular Function
View graph for
Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:1m2o
,
PDBe:1m2o
,
PDBj:1m2o
PDBsum
1m2o
PubMed
12239560
UniProt
P20606
|SAR1_YEAST Small COPII coat GTPase SAR1 (Gene Name=SAR1)
[
Back to BioLiP
]