Structure of PDB 2cja Chain A Binding Site BS02
Receptor Information
>2cja Chain A (length=477) Species:
269797
(Methanosarcina barkeri str. Fusaro) [
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SHMKLQFNLKAYFKKDAIAALFEEANSTLLTRGAPEGQGAKVTEWKLRIE
LTLQSGRYVRVHDAIFRLRKQLAEALGKKYKIGIRGIEVESFIIKVPADH
ELRMLKVPYIKSMENIEGGIQLELEVGEAEMKNRVPDRILTLLEEKIEAA
QYGAKAEHWNLLWQREPMEHPFKEDPTQAMMKEGWLKRGSSRGQWIHGPQ
SARIFRTFEKIVLEELLEPLGYREMIFPKLVTWEVWMKSGHAKGVYPEIY
YVCPPQTRDPDYWEEVADYYKVTHEVPTKLIKEKIAEPIGGMCYAQCPPF
WMYVAGETLPNEEIPVKVFDRSGTSHRYESGGIHGIERVDEFHRIEIVWI
GTKEEVLKCAEELHDRYMHIFNDILDIEWRKARVNTVGTTDYEACLPYRG
PDGEWLEFQNVSINGDKYPKGFNVKLQSGDELWSGCSGVGLERWAAVFLA
QKGLDPANWPEEFRNRVGEMPKGIRFL
Ligand information
Ligand ID
ATP
InChI
InChI=1S/C10H16N5O13P3/c11-8-5-9(13-2-12-8)15(3-14-5)10-7(17)6(16)4(26-10)1-25-30(21,22)28-31(23,24)27-29(18,19)20/h2-4,6-7,10,16-17H,1H2,(H,21,22)(H,23,24)(H2,11,12,13)(H2,18,19,20)/t4-,6-,7-,10-/m1/s1
InChIKey
ZKHQWZAMYRWXGA-KQYNXXCUSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)C3C(C(C(O3)COP(=O)(O)OP(=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[P](O)(O)=O)[CH](O)[CH]3O
ACDLabs 10.04
O=P(O)(O)OP(=O)(O)OP(=O)(O)OCC3OC(n2cnc1c(ncnc12)N)C(O)C3O
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)[C@H]3[C@@H]([C@@H]([C@H](O3)CO[P@@](=O)(O)O[P@](=O)(O)OP(=O)(O)O)O)O)N
CACTVS 3.341
Nc1ncnc2n(cnc12)[C@@H]3O[C@H](CO[P@](O)(=O)O[P@@](O)(=O)O[P](O)(O)=O)[C@@H](O)[C@H]3O
Formula
C10 H16 N5 O13 P3
Name
ADENOSINE-5'-TRIPHOSPHATE
ChEMBL
CHEMBL14249
DrugBank
DB00171
ZINC
ZINC000004261765
PDB chain
2cja Chain A Residue 1505 [
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Receptor-Ligand Complex Structure
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PDB
2cja
Structure of the Unusual Seryl-tRNA Synthetase Reveals a Distinct Zinc-Dependent Mode of Substrate Recognition
Resolution
2.2 Å
Binding residue
(original residue number in PDB)
H250 R336 E338 V348 F351 R353 E432 G465 R468
Binding residue
(residue number reindexed from 1)
H241 R327 E329 V339 F342 R344 E407 G440 R443
Annotation score
5
Enzymatic activity
Catalytic site (original residue number in PDB)
C306 R336 E338 R347 E355 D416 E432 N435 C461 R468
Catalytic site (residue number reindexed from 1)
C297 R327 E329 R338 E346 D391 E407 N410 C436 R443
Enzyme Commision number
6.1.1.11
: serine--tRNA ligase.
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0004812
aminoacyl-tRNA ligase activity
GO:0004828
serine-tRNA ligase activity
GO:0005524
ATP binding
GO:0008270
zinc ion binding
GO:0046872
metal ion binding
Biological Process
GO:0006412
translation
GO:0006434
seryl-tRNA aminoacylation
GO:0016260
selenocysteine biosynthetic process
Cellular Component
GO:0005737
cytoplasm
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:2cja
,
PDBe:2cja
,
PDBj:2cja
PDBsum
2cja
PubMed
16675947
UniProt
Q46AN5
|SYS2_METBF Type-2 serine--tRNA ligase (Gene Name=serS2)
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