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4IVQ

Crystal structure of thymidine kinase from Herpes simplex virus type 1 in complex with IN43/5

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 Residues13
DetailsBINDING SITE FOR RESIDUE I43 A 501
ChainResidue
AHIS58
AARG176
AMET231
AHOH673
AHOH674
AGLU83
ATRP88
AILE97
ATYR101
AGLN125
AMET128
AARG163
ATYR172

site_idAC2
Number of Residues8
DetailsBINDING SITE FOR RESIDUE SO4 A 502
ChainResidue
AHIS58
AGLY59
AMET60
AGLY61
ALYS62
ATHR63
AARG216
AHOH669

site_idAC3
Number of Residues4
DetailsBINDING SITE FOR RESIDUE SO4 A 503
ChainResidue
ALYS317
AARG320
AHOH608
AHOH692

site_idAC4
Number of Residues14
DetailsBINDING SITE FOR RESIDUE I43 B 401
ChainResidue
BHIS58
BGLU83
BTRP88
BILE97
BTYR101
BGLN125
BMET128
BARG163
BTYR172
BARG176
BARG222
BMET231
BHOH556
BHOH589

site_idAC5
Number of Residues6
DetailsBINDING SITE FOR RESIDUE SO4 B 402
ChainResidue
BHIS58
BGLY59
BGLY61
BARG220
BARG222
BHOH583

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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