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1E2K

Kinetics and crystal structure of the wild-type and the engineered Y101F mutant of Herpes simplex virus type 1 thymidine kinase interacting with (North)-methanocarba-thymidine

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 Residues10
DetailsBINDING SITE FOR RESIDUE SO4 A 400
ChainResidue
AHIS58
AHOH2179
AGLY59
AMET60
AGLY61
ALYS62
ATHR63
AARG220
AARG222
AHOH2005

site_idAC2
Number of Residues9
DetailsBINDING SITE FOR RESIDUE SO4 B 400
ChainResidue
BHIS58
BGLY59
BMET60
BGLY61
BLYS62
BTHR63
BHOH2074
BHOH2181
BHOH2182

site_idAC3
Number of Residues18
DetailsBINDING SITE FOR RESIDUE TMC A 500
ChainResidue
AHIS58
AGLU83
ATRP88
AILE97
AILE100
ATYR101
AGLN125
AMET128
ATYR132
AARG163
AALA168
ATYR172
AARG222
AHOH2011
AHOH2028
AHOH2178
AHOH2179
AHOH2180

site_idAC4
Number of Residues16
DetailsBINDING SITE FOR RESIDUE TMC B 500
ChainResidue
BHIS58
BGLU83
BILE97
BILE100
BTYR101
BGLN125
BMET128
BTYR132
BARG163
BALA168
BTYR172
BGLU225
BHOH2022
BHOH2074
BHOH2183
BHOH2184

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
AGLN125
AARG216
AARG222
BGLY56
BTYR101
BGLN125
BARG216
BARG222
AGLY56
ATYR101

Catalytic Information from CSA
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 2024-06-12

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