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2RE8

Glutaminyl-tRNA synthetase mutant C229R with bound analog 5'-O-[N-(L-GLUTAMYL)-SULFAMOYL]ADENOSINE

Functional Information from GO Data
ChainGOidnamespacecontents
A0000166molecular_functionnucleotide binding
A0004812molecular_functionaminoacyl-tRNA ligase activity
A0004819molecular_functionglutamine-tRNA ligase activity
A0005524molecular_functionATP binding
A0005737cellular_componentcytoplasm
A0005829cellular_componentcytosol
A0006412biological_processtranslation
A0006418biological_processtRNA aminoacylation for protein translation
A0006424biological_processglutamyl-tRNA aminoacylation
A0006425biological_processglutaminyl-tRNA aminoacylation
A0043039biological_processtRNA aminoacylation
Functional Information from PDB Data
site_idAC1
Number of Residues8
DetailsBINDING SITE FOR RESIDUE SO4 A 1394
ChainResidue
AHIS40
AHIS43
AARG260
AMET268
ASER269
ALYS270
AGSU998
AHOH1503

site_idAC2
Number of Residues6
DetailsBINDING SITE FOR RESIDUE SO4 A 1395
ChainResidue
AMET268
ASER269
ALYS272
AGLY482
AHOH1463
AVAL267

site_idAC3
Number of Residues17
DetailsBINDING SITE FOR RESIDUE GSU A 998
ChainResidue
AARG30
APRO32
APRO33
AGLU34
AGLY42
AHIS43
AASP66
ATYR211
AHIS215
AARG229
ATHR230
AARG260
ALEU261
ALYS270
ASO41394
AHOH1458
BA976

Functional Information from PROSITE/UniProt
site_idPS00178
Number of Residues12
DetailsAA_TRNA_LIGASE_I Aminoacyl-transfer RNA synthetases class-I signature. PepNGyLHIGHA
ChainResidueDetails
APRO33-ALA44

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues2
DetailsBINDING: BINDING => ECO:0000255|HAMAP-Rule:MF_00126, ECO:0000269|PubMed:23727144, ECO:0007744|PDB:4JXX, ECO:0007744|PDB:4JXZ, ECO:0007744|PDB:4JYZ
ChainResidueDetails
AGLU34
AHIS40

site_idSWS_FT_FI2
Number of Residues1
DetailsBINDING: BINDING => ECO:0000255|HAMAP-Rule:MF_00126, ECO:0000269|PubMed:12691748, ECO:0000269|PubMed:18477696, ECO:0000269|PubMed:9562563, ECO:0007744|PDB:1O0B
ChainResidueDetails
AASP66

site_idSWS_FT_FI3
Number of Residues1
DetailsBINDING: BINDING => ECO:0000255|HAMAP-Rule:MF_00126, ECO:0000269|PubMed:12691748, ECO:0000269|PubMed:15845536, ECO:0000269|PubMed:18477696, ECO:0000269|PubMed:9562563, ECO:0007744|PDB:1O0B, ECO:0007744|PDB:1ZJW
ChainResidueDetails
ATYR211

site_idSWS_FT_FI4
Number of Residues3
DetailsBINDING: BINDING => ECO:0000255|HAMAP-Rule:MF_00126, ECO:0000269|PubMed:18477696, ECO:0000269|PubMed:23727144, ECO:0000269|PubMed:9562563, ECO:0007744|PDB:4JXX, ECO:0007744|PDB:4JXZ, ECO:0007744|PDB:4JYZ
ChainResidueDetails
ATHR230
AARG260
AMET268

Catalytic Information from CSA
site_idCSA1
Number of Residues3
DetailsAnnotated By Reference To The Literature 1euy
ChainResidueDetails
AGLU34
ALYS270
AARG260

site_idCSA2
Number of Residues1
DetailsAnnotated By Reference To The Literature 1euy
ChainResidueDetails
ALYS270

site_idMCSA1
Number of Residues3
DetailsM-CSA 850
ChainResidueDetails
AGLU34proton shuttle (general acid/base)
AARG260electrostatic stabiliser
ALYS270electrostatic stabiliser

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PDB entries from 2024-10-30

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