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4P8T

Crystal structure of M. tuberculosis DprE1 in complex with the non-covalent inhibitor QN129

Functional Information from GO Data
ChainGOidnamespacecontents
A0003885molecular_functionD-arabinono-1,4-lactone oxidase activity
A0005886cellular_componentplasma membrane
A0016020cellular_componentmembrane
A0016491molecular_functionoxidoreductase activity
A0035884biological_processarabinan biosynthetic process
A0042597cellular_componentperiplasmic space
A0045227biological_processcapsule polysaccharide biosynthetic process
A0046677biological_processresponse to antibiotic
A0050660molecular_functionflavin adenine dinucleotide binding
A0070592biological_processcell wall polysaccharide biosynthetic process
A0071555biological_processcell wall organization
A0071949molecular_functionFAD binding
B0003885molecular_functionD-arabinono-1,4-lactone oxidase activity
B0005886cellular_componentplasma membrane
B0016020cellular_componentmembrane
B0016491molecular_functionoxidoreductase activity
B0035884biological_processarabinan biosynthetic process
B0042597cellular_componentperiplasmic space
B0045227biological_processcapsule polysaccharide biosynthetic process
B0046677biological_processresponse to antibiotic
B0050660molecular_functionflavin adenine dinucleotide binding
B0070592biological_processcell wall polysaccharide biosynthetic process
B0071555biological_processcell wall organization
B0071949molecular_functionFAD binding
Functional Information from PDB Data
site_idAC1
Number of Residues33
Detailsbinding site for residue FAD A 501
ChainResidue
ATRP16
AASN63
AALA64
AMET74
AALA94
APRO116
AGLY117
ATHR118
AVAL121
ATHR122
AGLY124
AILE52
AGLY125
AALA128
ACYS129
AILE131
AHIS132
AASN178
AGLY179
AGLY182
AILE184
ATYR415
AALA53
AALA417
AR26502
AHOH630
AHOH644
AGLY55
ALEU56
AGLY57
AARG58
ASER59
ATYR60

site_idAC2
Number of Residues18
Detailsbinding site for residue R26 A 502
ChainResidue
ATYR60
AHIS132
AGLY133
ALYS134
ASER228
ATRP230
AARG325
AGLN334
AGLN336
ALEU363
AASN364
AVAL365
ALYS367
AASN385
ACYS387
ALYS418
AFAD501
A2J3504

site_idAC3
Number of Residues3
Detailsbinding site for residue IMD A 503
ChainResidue
ASER82
AASP84
BASP84

site_idAC4
Number of Residues8
Detailsbinding site for residue 2J3 A 504
ChainResidue
ALYS134
ASER228
AALA229
ATRP230
AALA244
ATYR314
APRO316
AR26502

site_idAC5
Number of Residues34
Detailsbinding site for residue FAD B 501
ChainResidue
BTRP16
BILE52
BALA53
BARG54
BGLY55
BLEU56
BGLY57
BARG58
BSER59
BTYR60
BASN63
BALA64
BMET74
BALA94
BPRO116
BGLY117
BTHR118
BVAL121
BTHR122
BGLY124
BGLY125
BALA128
BCYS129
BILE131
BHIS132
BASN178
BGLY179
BGLY182
BILE183
BILE184
BTYR415
BALA417
BR26502
BHOH618

site_idAC6
Number of Residues13
Detailsbinding site for residue R26 B 502
ChainResidue
BLYS134
BTRP230
BLEU363
BASN364
BVAL365
BLYS367
BASN385
BCYS387
BLYS418
BFAD501
BTYR60
BHIS132
BGLY133

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues2
DetailsBINDING: BINDING => ECO:0000269|PubMed:22733761, ECO:0000269|PubMed:23776209, ECO:0000269|PubMed:24500695, ECO:0000269|PubMed:25427196, ECO:0007744|PDB:4FDP, ECO:0007744|PDB:4NCR
ChainResidueDetails
AALA53
BALA53

site_idSWS_FT_FI2
Number of Residues10
DetailsBINDING: BINDING => ECO:0000269|PubMed:22733761, ECO:0000269|PubMed:23776209, ECO:0000269|PubMed:24500695, ECO:0000269|PubMed:25427196, ECO:0007744|PDB:4FDP, ECO:0007744|PDB:4KW5, ECO:0007744|PDB:4NCR
ChainResidueDetails
AGLY117
BTYR415
ATHR122
ACYS129
AILE184
ATYR415
BGLY117
BTHR122
BCYS129
BILE184

223166

PDB entries from 2024-07-31

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