Loading
PDBj
MenuPDBj@FacebookPDBj@TwitterPDBj@YouTubewwPDB FoundationwwPDB
RCSB PDBPDBeBMRBAdv. SearchSearch help

4HEJ

Discovery of Selective and Potent Inhibitors of Gram-positive Bacterial Thymidylate Kinase (TMK): Compund 16

Functional Information from GO Data
ChainGOidnamespacecontents
A0004798molecular_functionthymidylate kinase activity
A0005524molecular_functionATP binding
A0006233biological_processdTDP biosynthetic process
A0006235biological_processdTTP biosynthetic process
A0009165biological_processnucleotide biosynthetic process
A0016301molecular_functionkinase activity
A0046940biological_processnucleoside monophosphate phosphorylation
B0004798molecular_functionthymidylate kinase activity
B0005524molecular_functionATP binding
B0006233biological_processdTDP biosynthetic process
B0006235biological_processdTTP biosynthetic process
B0009165biological_processnucleotide biosynthetic process
B0016301molecular_functionkinase activity
B0046940biological_processnucleoside monophosphate phosphorylation
Functional Information from PDB Data
site_idAC1
Number of Residues16
DetailsBINDING SITE FOR RESIDUE 14D A 301
ChainResidue
AGLU37
AARG70
AARG92
ASER97
ATYR100
AGLN101
AHOH452
BHIS172
AGLY44
AILE47
AARG48
AVAL51
ALEU52
ALEU65
APHE66
ASER69

Functional Information from PROSITE/UniProt
site_idPS01331
Number of Residues13
DetailsTHYMIDYLATE_KINASE Thymidylate kinase signature. LCDRYidSSlAYQ
ChainResidueDetails
ALEU89-GLN101

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues2
DetailsBINDING: BINDING => ECO:0000255|HAMAP-Rule:MF_00165
ChainResidueDetails
AGLY9
BGLY9

223166

PDB entries from 2024-07-31

PDB statisticsPDBj update infoContact PDBjnumon