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

5X8A

Crystal structure of ATP bound thymidylate kinase from thermus thermophilus HB8

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 Residues2
Detailsbinding site for residue MG A 201
ChainResidue
AVAL175
BHOH335

site_idAC2
Number of Residues3
Detailsbinding site for residue CL A 202
ChainResidue
AGLU169
AGLY171
AARG172

site_idAC3
Number of Residues4
Detailsbinding site for residue CL A 203
ChainResidue
AGLY13
AGLY15
ALYS16
ATHR17

site_idAC4
Number of Residues1
Detailsbinding site for residue CL A 204
ChainResidue
ALYS123

site_idAC5
Number of Residues4
Detailsbinding site for residue CL A 205
ChainResidue
AARG22
AARG139
AHOH301
AHOH323

site_idAC6
Number of Residues23
Detailsbinding site for residue ATP B 201
ChainResidue
BPRO2
BLEU11
BASP12
BGLY13
BSER14
BGLY15
BLYS16
BTHR17
BTHR18
BGLU28
BGLY31
BARG91
BARG140
BVAL141
BLEU180
BPRO181
BGLU182
BILE185
BMG202
BPEG206
BHOH301
BHOH304
BHOH322

site_idAC7
Number of Residues3
Detailsbinding site for residue MG B 202
ChainResidue
BTHR17
BATP201
BHOH301

site_idAC8
Number of Residues3
Detailsbinding site for residue MG B 203
ChainResidue
BPHE65
BSER96
BGLN100

site_idAC9
Number of Residues4
Detailsbinding site for residue CL B 204
ChainResidue
AHOH335
BGLU169
BGLY171
BARG172

site_idAD1
Number of Residues3
Detailsbinding site for residue PEG B 205
ChainResidue
BGLU113
BARG116
BGLU117

site_idAD2
Number of Residues5
Detailsbinding site for residue PEG B 206
ChainResidue
BGLU28
BARG32
BVAL34
BGLU182
BATP201

Functional Information from PROSITE/UniProt
site_idPS01331
Number of Residues13
DetailsTHYMIDYLATE_KINASE Thymidylate kinase signature. ISDRYldSSlAYQ
ChainResidueDetails
AILE88-GLN100

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues2
DetailsBINDING: BINDING => ECO:0000255|HAMAP-Rule:MF_00165
ChainResidueDetails
AGLY10
BGLY10

222415

PDB entries from 2024-07-10

PDB statisticsPDBj update infoContact PDBjnumon