Structure of PDB 1chm Chain A Binding Site BS02
Receptor Information
>1chm Chain A (length=401) Species:
303
(Pseudomonas putida) [
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QMPKTLRIRNGDKVRSTFSAQEYANRQARLRAHLAAENIDAAIFTSYHNI
NYYSDFLYCSFGRPYALVVTEDDVISISANIDGGQPWRRTVGTDNIVYTD
WQRDNYFAAIQQALPKARRIGIEHDHLNLQNRDKLAARYPDAELVDVAAA
CMRMRMIKSAEEHVMIRHGARIADIGGAAVVEALGDQVPEYEVALHATQA
MVRAIADTFEDVELMDTWTWFQSGINTDGAHNPVTTRKVNKGDILSLNCF
PMIAGYYTALERTLFLDHCSDDHLRLWQVNVEVHEAGLKLIKPGARCSDI
ARELNEIFLKHDVLQYRTFGYGHSFGTLSHYYGREAGLELREDIDTVLEP
GMVVSMEPMIMLPEGLPGAGGYREHDILIVNENGAENITKFPYGPEKNII
R
Ligand information
Ligand ID
CMS
InChI
InChI=1S/C4H8N2O3/c1-6(4(5)9)2-3(7)8/h2H2,1H3,(H2,5,9)(H,7,8)
InChIKey
SREKYKXYSQMOIB-UHFFFAOYSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
CN(CC(=O)O)C(=O)N
CACTVS 3.341
CN(CC(O)=O)C(N)=O
ACDLabs 10.04
O=C(O)CN(C(=O)N)C
Formula
C4 H8 N2 O3
Name
CARBAMOYL SARCOSINE
ChEMBL
DrugBank
ZINC
ZINC000040165548
PDB chain
1chm Chain B Residue 404 [
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Receptor-Ligand Complex Structure
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PDB
1chm
Enzymatic mechanism of creatine amidinohydrolase as deduced from crystal structures.
Resolution
1.9 Å
Binding residue
(original residue number in PDB)
F62 R64 I82
Binding residue
(residue number reindexed from 1)
F61 R63 I81
Annotation score
2
Binding affinity
MOAD
: Ki=0.22mM
Enzymatic activity
Catalytic site (original residue number in PDB)
H232 E262 E358
Catalytic site (residue number reindexed from 1)
H231 E261 E357
Enzyme Commision number
3.5.3.3
: creatinase.
Gene Ontology
Molecular Function
GO:0016787
hydrolase activity
GO:0016980
creatinase activity
View graph for
Molecular Function
External links
PDB
RCSB:1chm
,
PDBe:1chm
,
PDBj:1chm
PDBsum
1chm
PubMed
1696320
UniProt
P38488
|CREA_PSEPU Creatinase
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