Loading
PDBj
MenuPDBj@FacebookPDBj@X(formerly Twitter)PDBj@BlueSkyPDBj@YouTubewwPDB FoundationwwPDBDonate
RCSB PDBPDBeBMRBAdv. SearchSearch help

5IBD

Crystal structure Mycobacterium tuberculosis CYP121 in complex with inhibitor fragment 24a

Functional Information from GO Data
ChainGOidnamespacecontents
A0004497molecular_functionmonooxygenase activity
A0005506molecular_functioniron ion binding
A0005737cellular_componentcytoplasm
A0009975molecular_functioncyclase activity
A0016491molecular_functionoxidoreductase activity
A0016705molecular_functionoxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen
A0016717molecular_functionoxidoreductase activity, acting on paired donors, with oxidation of a pair of donors resulting in the reduction of molecular oxygen to two molecules of water
A0020037molecular_functionheme binding
A0046872molecular_functionmetal ion binding
A0070025molecular_functioncarbon monoxide binding
Functional Information from PDB Data
site_idAC1
Number of Residues7
Detailsbinding site for residue SO4 A 401
ChainResidue
ALYS211
APRO330
AASN331
APRO332
ATHR333
ASER334
AHOH613

site_idAC2
Number of Residues5
Detailsbinding site for residue SO4 A 402
ChainResidue
AHOH502
AHOH589
AHOH593
ASER12
AARG17

site_idAC3
Number of Residues7
Detailsbinding site for residue SO4 A 403
ChainResidue
AARG58
ASER61
AMET62
ALYS63
AHIS343
AHOH553
AHOH567

site_idAC4
Number of Residues22
Detailsbinding site for residue HEM A 404
ChainResidue
AMET62
AMET86
AHIS146
APHE230
AGLY234
ASER237
APHE241
APHE280
ALEU284
AARG286
AALA337
APHE338
AGLY339
AHIS343
ACYS345
APRO346
AGGJ407
AHOH536
AHOH569
AHOH605
AHOH633
AHOH760

site_idAC5
Number of Residues8
Detailsbinding site for residue SO4 A 405
ChainResidue
AASN74
AGLN385
AGGJ407
AHOH517
AHOH625
AHOH660
AHOH701
AHOH838

site_idAC6
Number of Residues9
Detailsbinding site for residue SO4 A 406
ChainResidue
ASER219
AARG252
ASER324
AILE325
AHOH519
AHOH537
AHOH702
AHOH715
AHOH790

site_idAC7
Number of Residues16
Detailsbinding site for residue GGJ A 407
ChainResidue
ATHR77
AVAL78
AVAL82
AVAL83
AALA167
APHE168
AVAL228
AALA233
ASER237
APHE280
AARG386
AHEM404
ASO4405
AHOH549
AHOH660
AHOH808

Functional Information from PROSITE/UniProt
site_idPS00086
Number of Residues10
DetailsCYTOCHROME_P450 Cytochrome P450 cysteine heme-iron ligand signature. FGrGQHFCPG
ChainResidueDetails
APHE338-GLY347

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues4
DetailsBinding site: {"evidences":[{"source":"PubMed","id":"17028183","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"19416919","evidenceCode":"ECO:0000269"}]}
ChainResidueDetails

site_idSWS_FT_FI2
Number of Residues1
DetailsBinding site: {}
ChainResidueDetails

site_idSWS_FT_FI3
Number of Residues2
DetailsBinding site: {"evidences":[{"source":"PubMed","id":"12435731","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"17028183","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"18818197","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"19416919","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"22890978","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"23620594","evidenceCode":"ECO:0000269"}]}
ChainResidueDetails

site_idSWS_FT_FI4
Number of Residues1
DetailsBinding site: {"description":"axial binding residue"}
ChainResidueDetails

site_idSWS_FT_FI5
Number of Residues2
DetailsSite: {"description":"Participates in a stacking interactions with the tyrosyl of cYY"}
ChainResidueDetails

site_idSWS_FT_FI6
Number of Residues1
DetailsSite: {"description":"Important for the position of heme"}
ChainResidueDetails

242199

PDB entries from 2025-09-24

PDB statisticsPDBj update infoContact PDBjnumon