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6LKM

Crystal structure of Ribonucleotide reductase R1 subunit, RRM1 in complex with 5-chloro-N-((1S,2R)-2-(6-fluoro-2,3-dimethylphenyl)-1-(5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)propyl)-4-methyl-3,4-dihydro-2H-benzo[b][1,4]oxazine-8-sulfonamide

Functional Information from GO Data
ChainGOidnamespacecontents
A0004748molecular_functionribonucleoside-diphosphate reductase activity, thioredoxin disulfide as acceptor
A0005524molecular_functionATP binding
A0009263biological_processdeoxyribonucleotide biosynthetic process
B0004748molecular_functionribonucleoside-diphosphate reductase activity, thioredoxin disulfide as acceptor
B0005524molecular_functionATP binding
B0009263biological_processdeoxyribonucleotide biosynthetic process
Functional Information from PDB Data
site_idAC1
Number of Residues1
Detailsbinding site for residue MG A 801
ChainResidue
ATTP802

site_idAC2
Number of Residues16
Detailsbinding site for residue TTP A 802
ChainResidue
ASER269
AASN270
AMG801
BLYS243
BTYR285
BVAL286
BASP287
BGLY289
AASP226
ASER227
AILE228
AILE255
AARG256
AILE262
AALA263
AGLY264

site_idAC3
Number of Residues6
Detailsbinding site for residue EJ6 A 803
ChainResidue
ASER687
AGLN688
ALYS689
ALYS719
ASER722
AMET723

site_idAC4
Number of Residues2
Detailsbinding site for residue MG B 801
ChainResidue
BTTP802
BHOH904

site_idAC5
Number of Residues18
Detailsbinding site for residue TTP B 802
ChainResidue
ALYS243
ATYR285
AVAL286
AASP287
AGLN288
BASP226
BSER227
BILE228
BARG256
BILE262
BALA263
BGLY264
BTHR265
BSER269
BASN270
BMG801
BHOH904
BHOH907

site_idAC6
Number of Residues6
Detailsbinding site for residue EJ6 B 803
ChainResidue
BILE686
BSER687
BGLN688
BLYS689
BLYS719
BMET723

Functional Information from PROSITE/UniProt
site_idPS00089
Number of Residues23
DetailsRIBORED_LARGE Ribonucleotide reductase large subunit signature. WkvLkekiakyGIRNsllIApmP
ChainResidueDetails
ATRP581-PRO603

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues4
DetailsActive site: {"description":"Proton acceptor","evidences":[{"evidenceCode":"ECO:0000250"}]}
ChainResidueDetails

site_idSWS_FT_FI2
Number of Residues2
DetailsActive site: {"description":"Cysteine radical intermediate","evidences":[{"evidenceCode":"ECO:0000250"}]}
ChainResidueDetails

site_idSWS_FT_FI3
Number of Residues14
DetailsBinding site: {"evidences":[{"source":"PDB","id":"3HND","evidenceCode":"ECO:0007744"}]}
ChainResidueDetails

site_idSWS_FT_FI4
Number of Residues10
DetailsBinding site: {"evidences":[{"source":"PDB","id":"3HNE","evidenceCode":"ECO:0007744"}]}
ChainResidueDetails

site_idSWS_FT_FI5
Number of Residues4
DetailsSite: {"description":"Important for hydrogen atom transfer","evidences":[{"evidenceCode":"ECO:0000250"}]}
ChainResidueDetails

site_idSWS_FT_FI6
Number of Residues4
DetailsSite: {"description":"Important for electron transfer","evidences":[{"evidenceCode":"ECO:0000250"}]}
ChainResidueDetails

site_idSWS_FT_FI7
Number of Residues2
DetailsModified residue: {"description":"N6-acetyllysine","evidences":[{"source":"PubMed","id":"19608861","evidenceCode":"ECO:0007744"}]}
ChainResidueDetails

247947

PDB entries from 2026-01-21

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