Structure of PDB 2gt4 Chain C Binding Site BS01
Receptor Information
>2gt4 Chain C (length=160) Species:
83333
(Escherichia coli K-12) [
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MMFLRQEDFATVVRSTPLVSLDFIVENSRGEFLLGKRTNRPAQGYWFVPG
GRVQKDETLEAAFERLTMAELGLRLPITAGQFYGVWQHFYDDNFSGTDFT
THFVVLGFRFRVSEEELLLPDEQHDDYRWLTSDALLASDNVHANSRAYFL
AEKRTGVPGL
Ligand information
Ligand ID
BMA
InChI
InChI=1S/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2/t2-,3-,4+,5+,6-/m1/s1
InChIKey
WQZGKKKJIJFFOK-RWOPYEJCSA-N
SMILES
Software
SMILES
CACTVS 3.341
OC[C@H]1O[C@@H](O)[C@@H](O)[C@@H](O)[C@@H]1O
OpenEye OEToolkits 1.5.0
C(C1C(C(C(C(O1)O)O)O)O)O
CACTVS 3.341
OC[CH]1O[CH](O)[CH](O)[CH](O)[CH]1O
OpenEye OEToolkits 1.5.0
C([C@@H]1[C@H]([C@@H]([C@@H]([C@@H](O1)O)O)O)O)O
ACDLabs 10.04
OC1C(O)C(OC(O)C1O)CO
Formula
C6 H12 O6
Name
beta-D-mannopyranose;
beta-D-mannose;
D-mannose;
mannose
ChEMBL
DrugBank
ZINC
ZINC000003830679
PDB chain
2gt4 Chain C Residue 202 [
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Receptor-Ligand Complex Structure
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PDB
2gt4
X-ray, NMR, and mutational studies of the catalytic cycle of the GDP-mannose mannosyl hydrolase reaction.
Resolution
2.3 Å
Binding residue
(original residue number in PDB)
K36 R37 T38 N39
Binding residue
(residue number reindexed from 1)
K36 R37 T38 N39
Annotation score
5
Enzymatic activity
Enzyme Commision number
3.6.1.-
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0008727
GDP-mannose mannosyl hydrolase activity
GO:0016787
hydrolase activity
GO:0030145
manganese ion binding
GO:0042802
identical protein binding
GO:0042803
protein homodimerization activity
GO:0046872
metal ion binding
GO:0047917
GDP-glucosidase activity
Biological Process
GO:0009103
lipopolysaccharide biosynthetic process
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Molecular Function
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Biological Process
External links
PDB
RCSB:2gt4
,
PDBe:2gt4
,
PDBj:2gt4
PDBsum
2gt4
PubMed
16981689
UniProt
P32056
|GMM_ECOLI GDP-mannose mannosyl hydrolase (Gene Name=gmm)
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