Structure of PDB 3okc Chain A Binding Site BS01
Receptor Information
>3okc Chain A (length=378) Species:
1718
(Corynebacterium glutamicum) [
Search protein sequence
] [
Download receptor structure
] [
Download structure with residue number starting from 1
] [
View receptor structure
]
SRKTLVVTNDFPPRIGGIQSYLRDFIATQDPESIVVFASTQNAEEAHAYD
KTLDYEVIRWPRSVMLPTPTTAHAMAEIIREREIDNVWFGAAAPLALMAG
TAKQAGASKVIASTHGHEVGWSMLPGSRQSLRKIGTEVDVLTYISQYTLR
RFKSAFGSHPTFEHLPSGVDVKRFTPATPEDKSATRKKLGFTDTTPVIAC
NSRLVPRKGQDSLIKAMPQVIAARPDAQLLIVGSGRYESTLRRLATDVSQ
NVKFLGRLEYQDMINTLAAADIFAMPARTRGGGLDVEGLGIVYLEAQACG
VPVIAGTSGGAPETVTPATGLVVEGSDVDKLSELLIELLDDPIRRAAMGA
AGRAHVEAEWSWEIMGERLTNILQSEPR
Ligand information
Ligand ID
GDP
InChI
InChI=1S/C10H15N5O11P2/c11-10-13-7-4(8(18)14-10)12-2-15(7)9-6(17)5(16)3(25-9)1-24-28(22,23)26-27(19,20)21/h2-3,5-6,9,16-17H,1H2,(H,22,23)(H2,19,20,21)(H3,11,13,14,18)/t3-,5-,6-,9-/m1/s1
InChIKey
QGWNDRXFNXRZMB-UUOKFMHZSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.7.6
c1nc2c(n1C3C(C(C(O3)COP(=O)(O)OP(=O)(O)O)O)O)N=C(NC2=O)N
CACTVS 3.385
NC1=Nc2n(cnc2C(=O)N1)[C@@H]3O[C@H](CO[P](O)(=O)O[P](O)(O)=O)[C@@H](O)[C@H]3O
CACTVS 3.385
NC1=Nc2n(cnc2C(=O)N1)[CH]3O[CH](CO[P](O)(=O)O[P](O)(O)=O)[CH](O)[CH]3O
ACDLabs 12.01
O=P(O)(O)OP(=O)(O)OCC3OC(n2cnc1c2N=C(N)NC1=O)C(O)C3O
OpenEye OEToolkits 1.7.6
c1nc2c(n1[C@H]3[C@@H]([C@@H]([C@H](O3)CO[P@](=O)(O)OP(=O)(O)O)O)O)N=C(NC2=O)N
Formula
C10 H15 N5 O11 P2
Name
GUANOSINE-5'-DIPHOSPHATE
ChEMBL
CHEMBL384759
DrugBank
DB04315
ZINC
ZINC000008215481
PDB chain
3okc Chain A Residue 601 [
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
3okc
Acceptor substrate discrimination in phosphatidyl-myo-inositol mannoside synthesis: structural and mutational analysis of mannosyltransferase Corynebacterium glutamicum PimB'.
Resolution
2.4 Å
Binding residue
(original residue number in PDB)
K211 R260 L261 M266 I294 V295 E298
Binding residue
(residue number reindexed from 1)
K208 R257 L258 M263 I291 V292 E295
Annotation score
4
Binding affinity
MOAD
: Kd=36.5uM
PDBbind-CN
: -logKd/Ki=4.44,Kd=36.5uM
Enzymatic activity
Enzyme Commision number
2.4.1.346
: phosphatidyl-myo-inositol dimannoside synthase.
Gene Ontology
Molecular Function
GO:0016757
glycosyltransferase activity
GO:0016758
hexosyltransferase activity
GO:0033164
glycolipid 1,6-alpha-mannosyltransferase activity
GO:0043750
phosphatidylinositol alpha-mannosyltransferase activity
Biological Process
GO:0008654
phospholipid biosynthetic process
GO:0009247
glycolipid biosynthetic process
GO:0046488
phosphatidylinositol metabolic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:3okc
,
PDBe:3okc
,
PDBj:3okc
PDBsum
3okc
PubMed
20843801
UniProt
Q8NNK8
|PIMB_CORGL GDP-mannose-dependent monoacylated alpha-(1-6)-phosphatidylinositol monomannoside mannosyltransferase (Gene Name=pimB)
[
Back to BioLiP
]