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1P7C

Crystal Structure of HSV1-TK complexed with TP5A

Functional Information from GO Data
ChainGOidnamespacecontents
A0004797molecular_functionthymidine kinase activity
A0005524molecular_functionATP binding
A0006230biological_processTMP biosynthetic process
A0009157biological_processdeoxyribonucleoside monophosphate biosynthetic process
A0016301molecular_functionkinase activity
A0071897biological_processDNA biosynthetic process
B0004797molecular_functionthymidine kinase activity
B0005524molecular_functionATP binding
B0006230biological_processTMP biosynthetic process
B0009157biological_processdeoxyribonucleoside monophosphate biosynthetic process
B0016301molecular_functionkinase activity
B0071897biological_processDNA biosynthetic process
Functional Information from PDB Data
site_idAC1
Number of Residues9
DetailsBINDING SITE FOR RESIDUE SO4 B 502
ChainResidue
BHIS58
BGLY59
BMET60
BGLY61
BLYS62
BTHR63
BARG220
BHOH519
BHOH540

site_idAC2
Number of Residues13
DetailsBINDING SITE FOR RESIDUE THM B 501
ChainResidue
BHIS58
BGLU83
BTRP88
BTYR101
BGLN125
BMET128
BARG163
BALA168
BTYR172
BGLU225
BHOH532
BHOH575
BHOH590

site_idAC3
Number of Residues33
DetailsBINDING SITE FOR RESIDUE T5A A 503
ChainResidue
AHIS58
AGLY59
AMET60
AGLY61
ALYS62
ATHR63
ATHR64
AGLU83
AILE97
AILE100
ATYR101
AGLN125
AMET128
ATYR132
AARG163
AALA168
ATYR172
AARG216
ALYS219
AARG220
AARG222
AGLU225
AGLN331
ASER332
APRO333
ACYS336
AHOH593
AHOH608
AHOH637
AHOH642
AHOH660
BGLN221
BASN376

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues2
DetailsACT_SITE: Proton acceptor => ECO:0000255|HAMAP-Rule:MF_04029
ChainResidueDetails
AGLU83
BGLU83

site_idSWS_FT_FI2
Number of Residues10
DetailsBINDING: BINDING => ECO:0000255|HAMAP-Rule:MF_04029
ChainResidueDetails
AGLY56
BARG222
ATYR101
AGLN125
AARG216
AARG222
BGLY56
BTYR101
BGLN125
BARG216

Catalytic Information from CSA
site_idCSA1
Number of Residues3
DetailsAnnotated By Reference To The Literature 1kim
ChainResidueDetails
AARG222
AGLY59
AARG163

site_idCSA2
Number of Residues4
DetailsAnnotated By Reference To The Literature 1kim
ChainResidueDetails
BGLU83
BARG222
BGLY59
BARG163

site_idMCSA1
Number of Residues7
DetailsM-CSA 588
ChainResidueDetails
ALYS62electrostatic stabiliser, polar interaction
AGLU83proton acceptor, proton donor
AASP162metal ligand
AARG163electrostatic stabiliser, polar interaction
AARG220electrostatic stabiliser, polar interaction
AARG222electrostatic stabiliser, polar interaction
AGLU225electrostatic stabiliser, polar interaction

site_idMCSA2
Number of Residues7
DetailsM-CSA 588
ChainResidueDetails
BLYS62electrostatic stabiliser, polar interaction
BGLU83proton acceptor, proton donor
BASP162metal ligand
BARG163electrostatic stabiliser, polar interaction
BARG220electrostatic stabiliser, polar interaction
BARG222electrostatic stabiliser, polar interaction
BGLU225electrostatic stabiliser, polar interaction

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PDB entries from 2024-05-01

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