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1KZI

Crystal Structure of EcTS/dUMP/THF Complex

Functional Information from GO Data
ChainGOidnamespacecontents
A0000287molecular_functionmagnesium ion binding
A0003723molecular_functionRNA binding
A0004799molecular_functionthymidylate synthase activity
A0005737cellular_componentcytoplasm
A0005829cellular_componentcytosol
A0006231biological_processdTMP biosynthetic process
A0006235biological_processdTTP biosynthetic process
A0006417biological_processregulation of translation
A0008168molecular_functionmethyltransferase activity
A0009165biological_processnucleotide biosynthetic process
A0009314biological_processresponse to radiation
A0016741molecular_functiontransferase activity, transferring one-carbon groups
A0032259biological_processmethylation
A0042803molecular_functionprotein homodimerization activity
B0000287molecular_functionmagnesium ion binding
B0003723molecular_functionRNA binding
B0004799molecular_functionthymidylate synthase activity
B0005737cellular_componentcytoplasm
B0005829cellular_componentcytosol
B0006231biological_processdTMP biosynthetic process
B0006235biological_processdTTP biosynthetic process
B0006417biological_processregulation of translation
B0008168molecular_functionmethyltransferase activity
B0009165biological_processnucleotide biosynthetic process
B0009314biological_processresponse to radiation
B0016741molecular_functiontransferase activity, transferring one-carbon groups
B0032259biological_processmethylation
B0042803molecular_functionprotein homodimerization activity
Functional Information from PDB Data
site_idAC1
Number of Residues3
DetailsBINDING SITE FOR RESIDUE CO3 A 803
ChainResidue
AARG99
AHOH558
AHOH738

site_idAC2
Number of Residues3
DetailsBINDING SITE FOR RESIDUE CO3 A 804
ChainResidue
AARG49
AGLY257
AHOH493

site_idAC3
Number of Residues4
DetailsBINDING SITE FOR RESIDUE CO3 A 805
ChainResidue
AHOH744
AGLU223
AARG225
AHIS255

site_idAC4
Number of Residues18
DetailsBINDING SITE FOR RESIDUE UMP A 302
ChainResidue
AARG21
ATYR94
ACYS146
AHIS147
AGLN165
AARG166
ASER167
ACYS168
AASP169
AASN177
AHIS207
ATYR209
ATHG303
AHOH412
AHOH432
AHOH658
BARG126
BARG127

site_idAC5
Number of Residues21
DetailsBINDING SITE FOR RESIDUE THG A 303
ChainResidue
AHIS51
AILE79
ATRP80
ATRP83
ALEU143
AASP169
AGLY173
APHE176
AVAL262
AALA263
AUMP302
AHOH419
AHOH442
AHOH448
AHOH467
AHOH551
AHOH575
AHOH597
AHOH615
AHOH625
AHOH646

site_idAC6
Number of Residues4
DetailsBINDING SITE FOR RESIDUE DTU A 800
ChainResidue
ALEU116
ALYS120
AGLN191
ACYS192

site_idAC7
Number of Residues16
DetailsBINDING SITE FOR RESIDUE UMP B 304
ChainResidue
AARG126
AARG127
BARG21
BCYS146
BHIS147
BGLN165
BARG166
BSER167
BCYS168
BASP169
BASN177
BHIS207
BTYR209
BTHG305
BHOH439
BHOH509

site_idAC8
Number of Residues13
DetailsBINDING SITE FOR RESIDUE THG B 305
ChainResidue
BILE79
BTRP83
BLEU143
BASP169
BGLY173
BVAL262
BALA263
BUMP304
BHOH461
BHOH480
BHOH569
BHOH737
BHOH749

site_idAC9
Number of Residues8
DetailsBINDING SITE FOR RESIDUE DTT B 802
ChainResidue
BPRO224
BARG225
BPRO226
BARG234
BARG243
BGLU245
BASP246
BHOH735

site_idBC1
Number of Residues4
DetailsBINDING SITE FOR RESIDUE GOL A 801
ChainResidue
AGLN9
AGLN64
AARG99
AHOH599

Functional Information from PROSITE/UniProt
site_idPS00091
Number of Residues29
DetailsTHYMIDYLATE_SYNTHASE Thymidylate synthase active site. RriIvsaWNvgeldkma.....LaPCHaffQFyV
ChainResidueDetails
AARG126-VAL154

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues2
DetailsACT_SITE: Nucleophile => ECO:0000255|HAMAP-Rule:MF_00008, ECO:0000269|PubMed:2223754, ECO:0000269|PubMed:8973201, ECO:0000269|PubMed:9416600
ChainResidueDetails
ACYS146
BCYS146

site_idSWS_FT_FI2
Number of Residues8
DetailsBINDING: in other chain => ECO:0000269|PubMed:2223754, ECO:0000269|PubMed:8973201, ECO:0007744|PDB:1KCE, ECO:0007744|PDB:2TSC
ChainResidueDetails
BARG21
BARG166
BASN177
BHIS207
AARG21
AARG166
AASN177
AHIS207

site_idSWS_FT_FI3
Number of Residues6
DetailsBINDING: BINDING => ECO:0000305|PubMed:8312270, ECO:0007744|PDB:1TYS
ChainResidueDetails
AALA263
BHIS51
BASP169
BALA263
AHIS51
AASP169

site_idSWS_FT_FI4
Number of Residues2
DetailsBINDING: BINDING => ECO:0000269|PubMed:2223754, ECO:0000269|PubMed:8973201, ECO:0007744|PDB:1KCE, ECO:0007744|PDB:2TSC
ChainResidueDetails
AARG126
BARG126

221051

PDB entries from 2024-06-12

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