Loading
PDBj
MenuPDBj@FacebookPDBj@TwitterPDBj@YouTubewwPDB FoundationwwPDB
RCSB PDBPDBeBMRBAdv. SearchSearch help

5UPV

Crystal Structure of the Catalytic Domain of the Inosine Monophosphate Dehydrogenase from Mycobacterium tuberculosis In the presence of G36

Functional Information from GO Data
ChainGOidnamespacecontents
A0003824molecular_functioncatalytic activity
A0003938molecular_functionIMP dehydrogenase activity
A0006164biological_processpurine nucleotide biosynthetic process
A0016491molecular_functionoxidoreductase activity
Functional Information from PDB Data
site_idAC1
Number of Residues26
Detailsbinding site for residue IMP A 601
ChainResidue
ASER83
AGLY376
AMET395
AGLY397
ASER398
ATYR421
AGLY423
AMET424
AGLY425
AGLU458
AGLY459
AMET85
A8KV602
AEDO607
AHOH719
AHOH749
AHOH756
AHOH775
AHOH816
AASN313
AGLY338
ASER339
AILE340
ACYS341
AASP374
AGLY375

site_idAC2
Number of Residues9
Detailsbinding site for residue 8KV A 602
ChainResidue
APRO61
AMET424
AGLY425
ALEU455
AVAL456
AGLU458
ATYR487
AIMP601
AFMT603

site_idAC3
Number of Residues4
Detailsbinding site for residue FMT A 603
ChainResidue
ATHR284
AALA285
A8KV602
AHOH758

site_idAC4
Number of Residues8
Detailsbinding site for residue EDO A 604
ChainResidue
ALEU53
AALA315
AALA351
AALA356
AGLU359
AHOH710
AHOH745
AHOH807

site_idAC5
Number of Residues3
Detailsbinding site for residue FMT A 605
ChainResidue
AASP36
AGLN498
AHOH798

site_idAC6
Number of Residues7
Detailsbinding site for residue EDO A 606
ChainResidue
AALA56
ASER57
AASP58
AHIS288
AASN289
AARG290
ALEU293

site_idAC7
Number of Residues9
Detailsbinding site for residue EDO A 607
ChainResidue
AALA285
AASN313
AGLY334
AVAL335
AGLY336
ACYS341
AIMP601
AHOH714
AHOH787

site_idAC8
Number of Residues5
Detailsbinding site for residue FMT A 608
ChainResidue
AARG92
AALA404
AGLU405
AALA406
AHOH827

Functional Information from PROSITE/UniProt
site_idPS00487
Number of Residues13
DetailsIMP_DH_GMP_RED IMP dehydrogenase / GMP reductase signature. VKVGVGpGSICtT
ChainResidueDetails
AVAL331-THR343

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues1
DetailsACT_SITE: Thioimidate intermediate => ECO:0000255|HAMAP-Rule:MF_01964, ECO:0000305|PubMed:26440283
ChainResidueDetails
ACYS341

site_idSWS_FT_FI2
Number of Residues1
DetailsACT_SITE: Proton acceptor => ECO:0000255|HAMAP-Rule:MF_01964, ECO:0000305|PubMed:26440283
ChainResidueDetails
AARG443

site_idSWS_FT_FI3
Number of Residues8
DetailsBINDING: BINDING => ECO:0000255|HAMAP-Rule:MF_01964, ECO:0000269|PubMed:26440283
ChainResidueDetails
AASP283
ASER339
AASP374
AGLY397
ATYR421
AGLU511
ASER512
AHIS513

site_idSWS_FT_FI4
Number of Residues3
DetailsBINDING: BINDING => ECO:0000269|PubMed:26440283
ChainResidueDetails
AASN289
ATHR343
AGLU458

site_idSWS_FT_FI5
Number of Residues1
DetailsBINDING: BINDING => ECO:0000255|HAMAP-Rule:MF_01964
ChainResidueDetails
AGLY334

site_idSWS_FT_FI6
Number of Residues3
DetailsBINDING: in other chain => ECO:0000255|HAMAP-Rule:MF_01964, ECO:0000269|PubMed:26440283
ChainResidueDetails
AGLY336
AGLY338
ACYS341

227111

PDB entries from 2024-11-06

PDB statisticsPDBj update infoContact PDBjnumon