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1KI4

CRYSTAL STRUCTURE OF THYMIDINE KINASE FROM HERPES SIMPLEX VIRUS TYPE I COMPLEXED WITH 5-BROMOTHIENYLDEOXYURIDINE

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 Residues7
DetailsBINDING SITE FOR RESIDUE SO4 A 3
ChainResidue
AGLY59
AMET60
AGLY61
ALYS62
ATHR63
AARG222
AHOH657

site_idAC2
Number of Residues8
DetailsBINDING SITE FOR RESIDUE SO4 B 4
ChainResidue
BMET60
BGLY61
BLYS62
BTHR63
BARG222
BHOH569
BHIS58
BGLY59

site_idAC3
Number of Residues18
DetailsBINDING SITE FOR RESIDUE BTD A 1
ChainResidue
AHIS58
AGLU83
ATRP88
AILE97
AILE100
ATYR101
AGLN125
AMET128
ATYR132
AARG163
AHIS164
AALA167
AALA168
ATYR172
AARG222
AGLU225
AHOH570
AHOH572

site_idAC4
Number of Residues16
DetailsBINDING SITE FOR RESIDUE BTD B 2
ChainResidue
BHIS58
BGLU83
BTRP88
BILE97
BTYR101
BGLN125
BMET128
BTYR132
BARG163
BHIS164
BALA167
BALA168
BTYR172
BARG222
BGLU225
BHOH567

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_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 2024-04-24

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