Structure of PDB 4d5v Chain A Binding Site BS06
Receptor Information
>4d5v Chain A (length=434) Species:
51453
(Trichoderma reesei) [
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ESACTLQSETHPPLTWQKCSSGGTCTQQTGSVVIDANWRWTHATNSSTNC
YDGNTWSSTLCPDNETCAKNCCLDGAAYASTYGVTTSGNSLSIDFVTQSA
QKNVGARLYLMASDTTYQEFTLLGNEFSFDVDVSQLPCGLNGALYFVSMD
ADGGVSKYPTNTAGAKYGTGYCDSQCPRDLKFINGQANVEGWEPSSNNAN
TGIGGHGSCCSEMDIWQANSISEALTPHPCTTVGQEICEGDGCGGTYSDN
RYGGTCDPDGCDWNPYRLGNTSFYGPGSSFTLDTTKKLTVVTQFETSGAI
NRYYVQNGVTFQQPNAELGSYSGNELNDDYCTAEEAEFGGSSFSDKGGLT
QFKKATSGGMVLVMSLWDDYYANMLWLDSTYPTNETSSTPGAVRGSCSTS
SGVPAQVESQSPNAKVTFSNIKFGPIGSTGNPSG
Ligand information
Ligand ID
CO
InChI
InChI=1S/Co/q+2
InChIKey
XLJKHNWPARRRJB-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Co+2]
CACTVS 3.341
[Co++]
Formula
Co
Name
COBALT (II) ION
ChEMBL
DrugBank
DB14205
ZINC
PDB chain
4d5v Chain A Residue 1435 [
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Receptor-Ligand Complex Structure
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PDB
4d5v
Structural Insights Into the Inhibition of Cellobiohydrolase Cel7A by Xylooligosaccharides.
Resolution
1.62 Å
Binding residue
(original residue number in PDB)
E295 E325
Binding residue
(residue number reindexed from 1)
E295 E325
Annotation score
3
Enzymatic activity
Catalytic site (original residue number in PDB)
E212 D214 Q217 H228
Catalytic site (residue number reindexed from 1)
E212 D214 Q217 H228
Enzyme Commision number
3.2.1.91
: cellulose 1,4-beta-cellobiosidase (non-reducing end).
Gene Ontology
Molecular Function
GO:0004553
hydrolase activity, hydrolyzing O-glycosyl compounds
Biological Process
GO:0005975
carbohydrate metabolic process
View graph for
Molecular Function
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Biological Process
External links
PDB
RCSB:4d5v
,
PDBe:4d5v
,
PDBj:4d5v
PDBsum
4d5v
PubMed
25765184
UniProt
P62694
|GUX1_HYPJE Exoglucanase 1 (Gene Name=cbh1)
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