Structure of PDB 3amq Chain C Binding Site BS01
Receptor Information
>3amq Chain C (length=256) Species:
2336
(Thermotoga maritima) [
Search protein sequence
] [
Download receptor structure
] [
Download structure with residue number starting from 1
] [
View receptor structure
]
MVLMTKPGTSDFVWNGIPLSMELNLWNIKEYSGSVAMKFDGEKITFDADI
QNLSPKEPERYVLGYPEFYYGYKPWENHTAEGSKLPVPVSSMKSFSVEVS
FDIHHEPSLPLNFAMETWLTREKYQTEASIGDVCIMVWFYFNNLTPGGEK
IEEFTIPFVLNGESVEGTWELWLAEWGWDYLAFRLKDPVKKGRVKFDVRH
FLDAAGKALSSSARVKDFEDLYFTVWEIGTEFGSPETKSAQFGWKFENFS
IDLEVR
Ligand information
Ligand ID
GLC
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-DVKNGEFBSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
C(C1C(C(C(C(O1)O)O)O)O)O
OpenEye OEToolkits 1.5.0
C([C@@H]1[C@H]([C@@H]([C@H]([C@H](O1)O)O)O)O)O
CACTVS 3.341
OC[CH]1O[CH](O)[CH](O)[CH](O)[CH]1O
CACTVS 3.341
OC[C@H]1O[C@H](O)[C@H](O)[C@@H](O)[C@@H]1O
ACDLabs 10.04
OC1C(O)C(OC(O)C1O)CO
Formula
C6 H12 O6
Name
alpha-D-glucopyranose;
alpha-D-glucose;
D-glucose;
glucose
ChEMBL
CHEMBL423707
DrugBank
ZINC
ZINC000003861213
PDB chain
3amq Chain G Residue 1 [
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
3amq
Crystal structure and substrate-binding mode of cellulase 12A from Thermotoga maritima
Resolution
1.8 Å
Binding residue
(original residue number in PDB)
W26 Y65 E116 W118 M136 E231
Binding residue
(residue number reindexed from 1)
W26 Y65 E116 W118 M136 E231
Annotation score
4
Enzymatic activity
Enzyme Commision number
3.2.1.4
: cellulase.
Gene Ontology
Molecular Function
GO:0004553
hydrolase activity, hydrolyzing O-glycosyl compounds
GO:0008810
cellulase activity
GO:0016798
hydrolase activity, acting on glycosyl bonds
Biological Process
GO:0000272
polysaccharide catabolic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:3amq
,
PDBe:3amq
,
PDBj:3amq
PDBsum
3amq
PubMed
21268113
UniProt
Q60032
[
Back to BioLiP
]