Structure of PDB 3p93 Chain H Binding Site BS02
Receptor Information
>3p93 Chain H (length=383) Species:
158080
() [
Search protein sequence
] [
Download receptor structure
] [
Download structure with residue number starting from 1
] [
View receptor structure
]
LKIRDAYTIVTCPGRNFVTLKIVTESGTHGIGDATLNGREMAVAAYLDEH
VVPALIGRDAGRIEDTWQYLYRGAYWRRGPVTMTAIAAVDMALWDIKAKA
AGMPLYQLLGGKSRERVMTYAHCTGQTIEDCLGEVARHVELGYRAVRVQS
GVPGSLPAEHVWSTEKYLNHAPKLFAAVRERFGDDLHVLHDVHHRLTPIE
AARLGKAVEPYHLFWLEDCVPAENQESLRLIREHTTTPLAIGEVFNSIHD
CRELIQNQWIDYIRMPLTHGGGITAMRRVADLASLYHVRTGFHGPTDLSP
VCLGAAIHFDTWVPNFGIQEHMPHTDETDAVFPHDYRFEDGHFLAGESPG
HGVDIDEELAAKYPYERASLPVNRLEDGTLWHW
Ligand information
Ligand ID
KDG
InChI
InChI=1S/C6H10O6/c7-2-5(10)3(8)1-4(9)6(11)12/h3,5,7-8,10H,1-2H2,(H,11,12)/t3-,5+/m0/s1
InChIKey
WPAMZTWLKIDIOP-WVZVXSGGSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
C([C@@H]([C@@H](CO)O)O)C(=O)C(=O)O
CACTVS 3.341
OC[C@@H](O)[C@@H](O)CC(=O)C(O)=O
ACDLabs 10.04
O=C(C(=O)O)CC(O)C(O)CO
CACTVS 3.341
OC[CH](O)[CH](O)CC(=O)C(O)=O
OpenEye OEToolkits 1.5.0
C(C(C(CO)O)O)C(=O)C(=O)O
Formula
C6 H10 O6
Name
2-KETO-3-DEOXYGLUCONATE
ChEMBL
DrugBank
ZINC
ZINC000001532568
PDB chain
3p93 Chain H Residue 407 [
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
3p93
CRYSTAL STRUCTURE OF D-MANNONATE DEHYDRATASE FROM CHROMOHALOBACTER SALEXIGENS complexed with MG,D-Mannonate and 2-keto-3-deoxy-D-Gluconate
Resolution
1.8 Å
Binding residue
(original residue number in PDB)
N39 H124 D213 H215 E265 H315 P317 D319 E342 W405
Binding residue
(residue number reindexed from 1)
N37 H122 D191 H193 E243 H293 P295 D297 E320 W383
Annotation score
5
Enzymatic activity
Catalytic site (original residue number in PDB)
H124 R149 Q151 D213 H215 E239 G264 E265 R286 P288 H315 G316 E342 W405
Catalytic site (residue number reindexed from 1)
H122 R147 Q149 D191 H193 E217 G242 E243 R264 P266 H293 G294 E320 W383
Enzyme Commision number
4.2.1.-
4.2.1.39
: gluconate dehydratase.
4.2.1.8
: mannonate dehydratase.
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0008927
mannonate dehydratase activity
GO:0016829
lyase activity
GO:0046872
metal ion binding
GO:0047929
gluconate dehydratase activity
Biological Process
GO:0009063
amino acid catabolic process
GO:0016052
carbohydrate catabolic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:3p93
,
PDBe:3p93
,
PDBj:3p93
PDBsum
3p93
PubMed
UniProt
Q1QT89
|DMGD_CHRSD D-galactonate dehydratase family member ManD (Gene Name=manD)
[
Back to BioLiP
]