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1E2H

The nucleoside binding site of Herpes simplex type 1 thymidine kinase analyzed by X-ray crystallography

Functional Information from GO Data
ChainGOidnamespacecontents
A0004797molecular_functionthymidine kinase activity
A0005524molecular_functionATP binding
A0006230biological_processTMP biosynthetic process
B0004797molecular_functionthymidine kinase activity
B0005524molecular_functionATP binding
B0006230biological_processTMP biosynthetic process
Functional Information from PDB Data
site_idAC1
Number of Residues9
DetailsBINDING SITE FOR RESIDUE SO4 A 400
ChainResidue
AHIS58
AGLY59
AMET60
AGLY61
ALYS62
ATHR63
AARG220
AARG222
AHOH2143

site_idAC2
Number of Residues7
DetailsBINDING SITE FOR RESIDUE SO4 B 400
ChainResidue
BGLY59
BMET60
BGLY61
BLYS62
BTHR63
BHOH2004
BHOH2133

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 Residues4
DetailsAnnotated By Reference To The Literature 1kim
ChainResidueDetails
AGLU83
AARG222
AGLY59
AARG163

site_idCSA2
Number of Residues3
DetailsAnnotated By Reference To The Literature 1kim
ChainResidueDetails
BGLU83
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 Residues4
DetailsM-CSA 588
ChainResidueDetails
BLYS62electrostatic stabiliser, polar interaction
BGLU83proton acceptor, proton donor
BASP162metal ligand
BARG163electrostatic stabiliser, polar interaction

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PDB entries from 2025-06-11

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