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6W4X

Holocomplex of E. coli class Ia ribonucleotide reductase with GDP and TTP

Functional Information from GO Data
ChainGOidnamespacecontents
A0004748molecular_functionribonucleoside-diphosphate reductase activity, thioredoxin disulfide as acceptor
A0005515molecular_functionprotein binding
A0005524molecular_functionATP binding
A0005829cellular_componentcytosol
A0005971cellular_componentribonucleoside-diphosphate reductase complex
A0006457biological_processprotein folding
A0009185biological_processribonucleoside diphosphate metabolic process
A0009263biological_processdeoxyribonucleotide biosynthetic process
A0009265biological_process2'-deoxyribonucleotide biosynthetic process
A0015949biological_processnucleobase-containing small molecule interconversion
A0016491molecular_functionoxidoreductase activity
A0042802molecular_functionidentical protein binding
A0044183molecular_functionprotein folding chaperone
B0004748molecular_functionribonucleoside-diphosphate reductase activity, thioredoxin disulfide as acceptor
B0005515molecular_functionprotein binding
B0005524molecular_functionATP binding
B0005829cellular_componentcytosol
B0005971cellular_componentribonucleoside-diphosphate reductase complex
B0006457biological_processprotein folding
B0009185biological_processribonucleoside diphosphate metabolic process
B0009263biological_processdeoxyribonucleotide biosynthetic process
B0009265biological_process2'-deoxyribonucleotide biosynthetic process
B0015949biological_processnucleobase-containing small molecule interconversion
B0016491molecular_functionoxidoreductase activity
B0042802molecular_functionidentical protein binding
B0044183molecular_functionprotein folding chaperone
C0004748molecular_functionribonucleoside-diphosphate reductase activity, thioredoxin disulfide as acceptor
C0005506molecular_functioniron ion binding
C0005515molecular_functionprotein binding
C0005737cellular_componentcytoplasm
C0005829cellular_componentcytosol
C0005971cellular_componentribonucleoside-diphosphate reductase complex
C0009185biological_processribonucleoside diphosphate metabolic process
C0009263biological_processdeoxyribonucleotide biosynthetic process
C0009265biological_process2'-deoxyribonucleotide biosynthetic process
C0015949biological_processnucleobase-containing small molecule interconversion
C0016491molecular_functionoxidoreductase activity
C0042802molecular_functionidentical protein binding
C0046872molecular_functionmetal ion binding
D0004748molecular_functionribonucleoside-diphosphate reductase activity, thioredoxin disulfide as acceptor
D0005506molecular_functioniron ion binding
D0005515molecular_functionprotein binding
D0005737cellular_componentcytoplasm
D0005829cellular_componentcytosol
D0005971cellular_componentribonucleoside-diphosphate reductase complex
D0009185biological_processribonucleoside diphosphate metabolic process
D0009263biological_processdeoxyribonucleotide biosynthetic process
D0009265biological_process2'-deoxyribonucleotide biosynthetic process
D0015949biological_processnucleobase-containing small molecule interconversion
D0016491molecular_functionoxidoreductase activity
D0042802molecular_functionidentical protein binding
D0046872molecular_functionmetal ion binding
Functional Information from PDB Data
site_idAC1
Number of Residues11
Detailsbinding site for residue TTP A 801
ChainResidue
AASP232
BSER249
BCYS292
ASER233
ALEU234
AILE237
AARG262
AILE268
AARG269
APHE281
AMG802

site_idAC2
Number of Residues1
Detailsbinding site for residue MG A 802
ChainResidue
ATTP801

site_idAC3
Number of Residues16
Detailsbinding site for residue GDP B 801
ChainResidue
BPRO208
BTHR209
BSER224
BGLY253
BARG298
BGLY299
BALA301
BASN437
BLEU438
BCYS439
BGLU441
BLEU464
BSER622
BGLU623
BTHR624
BSER625

site_idAC4
Number of Residues15
Detailsbinding site for residue TTP B 802
ChainResidue
ASER249
AARG251
ACYS292
BASP232
BSER233
BLEU234
BILE237
BILE261
BARG262
BILE268
BARG269
BGLY270
BHIS275
BPHE281
BMG803

site_idAC5
Number of Residues2
Detailsbinding site for residue MG B 803
ChainResidue
BARG262
BTTP802

site_idAC6
Number of Residues8
Detailsbinding site for residue FEO C 501
ChainResidue
CASP84
CGLU115
CHIS118
CGLU204
CGLU238
CHIS241
CHOH601
CHOH602

site_idAC7
Number of Residues8
Detailsbinding site for residue FEO D 501
ChainResidue
DASP84
DGLU115
DHIS118
DGLU204
DGLU238
DHIS241
DHOH601
DHOH602

Functional Information from PROSITE/UniProt
site_idPS00089
Number of Residues23
DetailsRIBORED_LARGE Ribonucleotide reductase large subunit signature. WeaLresikthGLRNstlSAlmP
ChainResidueDetails
ATRP599-PRO621

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues2
DetailsACT_SITE:
ChainResidueDetails
CFY3122
DFY3122
BASN437
BGLU441

site_idSWS_FT_FI2
Number of Residues12
DetailsBINDING:
ChainResidueDetails
CASP84
DGLU204
DGLU238
DHIS241
CGLU115
CHIS118
CGLU204
CGLU238
CHIS241
DASP84
DGLU115
DHIS118

site_idSWS_FT_FI3
Number of Residues8
DetailsBINDING: BINDING => ECO:0000269|PubMed:9309223, ECO:0007744|PDB:3R1R
ChainResidueDetails
ALYS9
AGLU15
ATHR55
ALYS91
BLYS9
BGLU15
BTHR55
BLYS91

site_idSWS_FT_FI4
Number of Residues14
DetailsBINDING: BINDING => ECO:0000269|PubMed:9309223, ECO:0007744|PDB:4R1R
ChainResidueDetails
ATHR209
BARG262
BARG269
BASN437
BGLU441
BGLU623
AASP232
AARG262
AARG269
AASN437
AGLU441
AGLU623
BTHR209
BASP232

site_idSWS_FT_FI5
Number of Residues4
DetailsSITE: Important for hydrogen atom transfer
ChainResidueDetails
ACYS225
ACYS462
BCYS225
BCYS462

site_idSWS_FT_FI6
Number of Residues4
DetailsSITE: Important for electron transfer
ChainResidueDetails
ATYR730
ATYR731
BTYR730
BTYR731

site_idSWS_FT_FI7
Number of Residues4
DetailsSITE: Interacts with thioredoxin/glutaredoxin
ChainResidueDetails
ACYS754
ACYS759
BCYS754
BCYS759

site_idSWS_FT_FI8
Number of Residues2
DetailsMOD_RES: N6-acetyllysine => ECO:0000269|PubMed:18723842
ChainResidueDetails
ALYS283
BLYS283

Catalytic Information from CSA
site_idMCSA1
Number of Residues2
DetailsM-CSA 918
ChainResidueDetails
CFY3122pi-pi interaction, single electron relay
CASP237
ACYS439hydrogen radical acceptor, hydrogen radical donor, single electron acceptor
AGLU441proton acceptor
ACYS462
ATYR730pi-pi interaction, single electron relay
ATYR731pi-pi interaction, single electron relay

site_idMCSA2
Number of Residues2
DetailsM-CSA 918
ChainResidueDetails
DFY3122pi-pi interaction, single electron relay
DASP237
BCYS439hydrogen radical acceptor, hydrogen radical donor, single electron acceptor
BGLU441proton acceptor
BCYS462
BTYR730pi-pi interaction, single electron relay
BTYR731pi-pi interaction, single electron relay

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PDB entries from 2024-07-24

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