Structure of PDB 5dm3 Chain B Binding Site BS01
Receptor Information
>5dm3 Chain B (length=385) Species:
290398
(Chromohalobacter israelensis DSM 3043) [
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NTLALDDLKTRVESGEIDTVLVCIVDMQGRLMGKRLHARHFVDHGWEETH
CCYIMKPDLATLRCVPWLEGTAMVLCDLLDHAEVPHAPRAILKRQLARLE
AMGLEAIMATELEFFLFEKSLDETTKEEHVLRPLRNHLHAAGIPVEGTKG
EAGQEELNIRCAKALDTADYHTIAKHATKEIAWQQGRAVTFLSKWHHAHA
GSSSHIHQSLWKQGLPAFHDERDALGMSALMKHYLAGLLKYAPDYTYFLA
PYLNSYKRFQKGTFAPTRTVWSVDNRTAGFRLCAEGTRAVRIECRIGGSD
LNPYLAMAGQLAAGIKGIEECLALPPPAGLIPQNLRDAMEALRGSTMLRE
AMGEDVVDHYVRAAEVELEDFQRVVSDYEVARGFE
Ligand information
Ligand ID
ADP
InChI
InChI=1S/C10H15N5O10P2/c11-8-5-9(13-2-12-8)15(3-14-5)10-7(17)6(16)4(24-10)1-23-27(21,22)25-26(18,19)20/h2-4,6-7,10,16-17H,1H2,(H,21,22)(H2,11,12,13)(H2,18,19,20)/t4-,6-,7-,10-/m1/s1
InChIKey
XTWYTFMLZFPYCI-KQYNXXCUSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)[C@H]3[C@@H]([C@@H]([C@H](O3)CO[P@](=O)(O)OP(=O)(O)O)O)O)N
CACTVS 3.341
Nc1ncnc2n(cnc12)[CH]3O[CH](CO[P](O)(=O)O[P](O)(O)=O)[CH](O)[CH]3O
ACDLabs 10.04
O=P(O)(O)OP(=O)(O)OCC3OC(n2cnc1c(ncnc12)N)C(O)C3O
CACTVS 3.341
Nc1ncnc2n(cnc12)[C@@H]3O[C@H](CO[P@@](O)(=O)O[P](O)(O)=O)[C@@H](O)[C@H]3O
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)C3C(C(C(O3)COP(=O)(O)OP(=O)(O)O)O)O)N
Formula
C10 H15 N5 O10 P2
Name
ADENOSINE-5'-DIPHOSPHATE
ChEMBL
CHEMBL14830
DrugBank
DB16833
ZINC
ZINC000012360703
PDB chain
5dm3 Chain B Residue 501 [
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Receptor-Ligand Complex Structure
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PDB
5dm3
Crystal Structure of Glutamine Synthetase from Chromohalobacter salexigens DSM 3043(Csal_0679, TARGET EFI-550015) with bound ADP
Resolution
2.6 Å
Binding residue
(original residue number in PDB)
I139 A141 E201 R217 C218 H264 S266 R348
Binding residue
(residue number reindexed from 1)
I107 A109 E146 R160 C161 H207 S209 R291
Annotation score
5
Enzymatic activity
Catalytic site (original residue number in PDB)
E143 E145 E206 E213 H262 R333 E350 R352
Catalytic site (residue number reindexed from 1)
E111 E113 E151 E156 H205 R276 E293 R295
Enzyme Commision number
6.3.1.2
: glutamine synthetase.
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0003824
catalytic activity
GO:0004356
glutamine synthetase activity
GO:0016874
ligase activity
GO:0016879
ligase activity, forming carbon-nitrogen bonds
Biological Process
GO:0006542
glutamine biosynthetic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:5dm3
,
PDBe:5dm3
,
PDBj:5dm3
PDBsum
5dm3
PubMed
UniProt
Q1QZR8
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