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1HK8

STRUCTURAL BASIS FOR ALLOSTERIC SUBSTRATE SPECIFICITY REGULATION IN CLASS III RIBONUCLEOTIDE REDUCTASES: NRDD IN COMPLEX WITH DGTP

Replaces:  1H77
Functional Information from GO Data
ChainGOidnamespacecontents
A0003824molecular_functioncatalytic activity
A0004748molecular_functionribonucleoside-diphosphate reductase activity, thioredoxin disulfide as acceptor
A0006260biological_processDNA replication
A0008998molecular_functionribonucleoside-triphosphate reductase activity
A0009265biological_process2'-deoxyribonucleotide biosynthetic process
A0016491molecular_functionoxidoreductase activity
A0031250cellular_componentanaerobic ribonucleoside-triphosphate reductase complex
A0046872molecular_functionmetal ion binding
Functional Information from PDB Data
site_idAC1
Number of Residues4
DetailsBINDING SITE FOR RESIDUE ZN A1589
ChainResidue
ACYS543
ACYS546
ACYS561
ACYS564

site_idAC2
Number of Residues1
DetailsBINDING SITE FOR RESIDUE MN A1590
ChainResidue
ADGT1587

site_idAC3
Number of Residues18
DetailsBINDING SITE FOR RESIDUE DGT A1587
ChainResidue
AILE111
ALYS146
ALYS169
AASP173
AGLN176
AALA177
ATYR180
AGLU181
AMN1590
AHOH2077
AHOH2220
AHOH2221
AHOH2222
AHOH2223
AGLU100
APRO102
ALYS103
AVAL107

site_idAC4
Number of Residues11
DetailsBINDING SITE FOR RESIDUE DGT A1588
ChainResidue
AHIS64
AHIS66
AASP67
AGLU446
AASN447
ALEU448
AHOH2014
AHOH2224
AHOH2226
AHOH2227
AHOH2228

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues6
DetailsBINDING: BINDING => ECO:0000269|PubMed:12655046, ECO:0007744|PDB:1HK8
ChainResidueDetails
AHIS64
AHIS66
AASP67
ALYS103
AASN447
ALEU448

site_idSWS_FT_FI2
Number of Residues3
DetailsBINDING: BINDING => ECO:0000269|PubMed:11587648, ECO:0007744|PDB:1H79
ChainResidueDetails
AGLU100
AGLN114
ALYS146

site_idSWS_FT_FI3
Number of Residues1
DetailsBINDING: BINDING => ECO:0000269|PubMed:11587648, ECO:0007744|PDB:1H78
ChainResidueDetails
AALA445

site_idSWS_FT_FI4
Number of Residues4
DetailsBINDING: BINDING => ECO:0000269|PubMed:12655046, ECO:0000305|PubMed:11587648, ECO:0007744|PDB:1HK8
ChainResidueDetails
ACYS543
ACYS546
ACYS561
ACYS564

site_idSWS_FT_FI5
Number of Residues1
DetailsMOD_RES: Glycine radical => ECO:0000269|PubMed:8702830
ChainResidueDetails
AALA580

Catalytic Information from CSA
site_idMCSA1
Number of Residues9
DetailsM-CSA 416
ChainResidueDetails
AASN78activator, electrostatic stabiliser
ACYS79hydrogen radical relay
AMET288radical stabiliser
ACYS290hydrogen radical relay
ASER292electrostatic stabiliser
AASN311electrostatic stabiliser
ATYR441electrostatic stabiliser
AGLU446electrostatic stabiliser
AALA580hydrogen radical relay

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PDB entries from 2024-04-24

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