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1KI6

CRYSTAL STRUCTURE OF THYMIDINE KINASE FROM HERPES SIMPLEX VIRUS TYPE I COMPLEXED WITH A 5-IODOURACIL ANHYDROHEXITOL NUCLEOSIDE

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 Residues8
DetailsBINDING SITE FOR RESIDUE SO4 A 3
ChainResidue
AHIS58
AGLY59
AMET60
AGLY61
ALYS62
ATHR63
AARG222
AHOH775

site_idAC2
Number of Residues10
DetailsBINDING SITE FOR RESIDUE SO4 B 4
ChainResidue
BGLY59
BMET60
BGLY61
BLYS62
BTHR63
BARG220
BARG222
BHOH675
BHOH766
BHIS58

site_idAC3
Number of Residues14
DetailsBINDING SITE FOR RESIDUE AHU A 1
ChainResidue
AHIS58
AILE97
AILE100
ATYR101
AGLN125
AMET128
ATYR132
AARG163
AALA168
ATYR172
AGLU225
AHOH564
AHOH566
AHOH775

site_idAC4
Number of Residues13
DetailsBINDING SITE FOR RESIDUE AHU B 2
ChainResidue
BHIS58
BGLU83
BTRP88
BILE97
BILE100
BTYR101
BGLN125
BMET128
BALA168
BTYR172
BGLU225
BHOH563
BHOH565

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues1
DetailsACT_SITE: Proton acceptor => ECO:0000255|HAMAP-Rule:MF_04029
ChainResidueDetails
BGLU83

site_idSWS_FT_FI2
Number of Residues5
DetailsBINDING: BINDING => ECO:0000255|HAMAP-Rule:MF_04029
ChainResidueDetails
BGLY56
BTYR101
BGLN125
BARG216
BARG222

Catalytic Information from CSA
site_idMCSA1
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

220113

PDB entries from 2024-05-22

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