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4FF6

Mycobacterium tuberculosis DprE1 in complex with CT325 - monoclinic crystal form

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 Residues34
DetailsBINDING SITE FOR RESIDUE FAD A 501
ChainResidue
ATRP16
ATYR60
AASN63
AALA64
AMET74
AALA94
APRO116
AGLY117
ATHR118
AVAL121
ATHR122
AILE52
AGLY124
AGLY125
AALA128
ACYS129
AILE131
AHIS132
AASN178
AGLY179
AGLY182
AILE184
AALA53
ATYR415
AALA417
A0T4502
AHOH608
AHOH611
AARG54
AGLY55
ALEU56
AGLY57
AARG58
ASER59

site_idAC2
Number of Residues11
DetailsBINDING SITE FOR RESIDUE 0T4 A 502
ChainResidue
AGLY117
AGLY133
ALYS134
ATRP230
AGLN336
AVAL365
AASN385
AILE386
ACYS387
AFAD501
AHOH655

site_idAC3
Number of Residues4
DetailsBINDING SITE FOR RESIDUE IMD A 503
ChainResidue
ASER82
AASP84
BSER82
BASP84

site_idAC4
Number of Residues6
DetailsBINDING SITE FOR RESIDUE IMD A 504
ChainResidue
AMET102
AALA105
ALEU106
ALEU110
ATRP111
AVAL112

site_idAC5
Number of Residues31
DetailsBINDING SITE FOR RESIDUE FAD B 501
ChainResidue
BTRP16
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
BILE184
BTYR415
BALA417
B0T4502

site_idAC6
Number of Residues11
DetailsBINDING SITE FOR RESIDUE 0T4 B 502
ChainResidue
BGLY117
BHIS132
BGLY133
BLYS134
BGLN336
BVAL365
BLYS367
BASN385
BILE386
BCYS387
BFAD501

site_idAC7
Number of Residues6
DetailsBINDING SITE FOR RESIDUE IMD B 503
ChainResidue
BLEU110
BTRP111
BVAL112
BMET191
BMET102
BLEU106

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
ATYR415
BGLY117
BTHR122
BCYS129
BILE184
BTYR415
ACYS129
AILE184
AGLY117
ATHR122

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PDB entries from 2024-06-12

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