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1P62

Structure of human dCK complexed with gemcitabine and ADP-MG

Functional Information from GO Data
ChainGOidnamespacecontents
B0004136molecular_functiondeoxyadenosine kinase activity
B0004137molecular_functiondeoxycytidine kinase activity
B0004138molecular_functiondeoxyguanosine kinase activity
B0005515molecular_functionprotein binding
B0005524molecular_functionATP binding
B0005634cellular_componentnucleus
B0005654cellular_componentnucleoplasm
B0005737cellular_componentcytoplasm
B0005739cellular_componentmitochondrion
B0005829cellular_componentcytosol
B0006139biological_processnucleobase-containing compound metabolic process
B0006220biological_processpyrimidine nucleotide metabolic process
B0008144molecular_functionobsolete drug binding
B0009224biological_processCMP biosynthetic process
B0016301molecular_functionkinase activity
B0016310biological_processphosphorylation
B0019136molecular_functiondeoxynucleoside kinase activity
B0042803molecular_functionprotein homodimerization activity
B0043771molecular_functioncytidine kinase activity
B0106383biological_processdAMP salvage
B1901135biological_processcarbohydrate derivative metabolic process
B1901293biological_processnucleoside phosphate biosynthetic process
Functional Information from PDB Data
site_idAC1
Number of Residues6
DetailsBINDING SITE FOR RESIDUE MG B 401
ChainResidue
BSER35
BGLU127
BADP301
BHOH543
BHOH544
BHOH545

site_idAC2
Number of Residues25
DetailsBINDING SITE FOR RESIDUE ADP B 301
ChainResidue
BLYS34
BSER35
BTHR36
BGLU127
BARG188
BLEU191
BARG192
BTYR210
BHIS218
BVAL238
BGLU240
BASP241
BPHE242
BMG401
BHOH420
BHOH422
BHOH437
BHOH452
BHOH506
BHOH532
BHOH544
BHOH545
BALA31
BALA32
BGLY33

site_idAC3
Number of Residues13
DetailsBINDING SITE FOR RESIDUE GEO B 302
ChainResidue
BILE30
BGLU53
BTRP58
BMET85
BTYR86
BPHE96
BGLN97
BARG128
BASP133
BPHE137
BGLU197
BHOH414
BHOH416

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues1
DetailsACT_SITE: Proton acceptor => ECO:0000255
ChainResidueDetails
BGLU127

site_idSWS_FT_FI2
Number of Residues9
DetailsBINDING:
ChainResidueDetails
BGLY28
BGLU53
BTYR86
BGLN97
BARG128
BASP133
BARG188
BGLU197
BGLU240

site_idSWS_FT_FI3
Number of Residues2
DetailsMOD_RES: Phosphoserine; by CK1 => ECO:0000305|PubMed:20637175
ChainResidueDetails
BSER11
BSER15

site_idSWS_FT_FI4
Number of Residues1
DetailsMOD_RES: Phosphothreonine; by CK1 => ECO:0000305|PubMed:20637175
ChainResidueDetails
BTHR72

site_idSWS_FT_FI5
Number of Residues1
DetailsMOD_RES: Phosphoserine => ECO:0000269|PubMed:20637175, ECO:0007744|PubMed:18669648, ECO:0007744|PubMed:20068231, ECO:0007744|PubMed:23186163
ChainResidueDetails
BSER74

Catalytic Information from CSA
site_idCSA1
Number of Residues2
DetailsAnnotated By Reference To The Literature 2ocp
ChainResidueDetails
BGLU53
BARG128

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PDB entries from 2024-08-21

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