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

5KNP

Crystal structure of Mycobacterium tuberculosis hypoxanthine guanine phosphoribosyltransferase in complex with [3S,4R]-(4-(Hypoxanthin-9-yl)pyrrolidin-3-yl)-oxymethanephosphonic acid

Functional Information from GO Data
ChainGOidnamespacecontents
A0000166molecular_functionnucleotide binding
A0000287molecular_functionmagnesium ion binding
A0004422molecular_functionhypoxanthine phosphoribosyltransferase activity
A0005737cellular_componentcytoplasm
A0005829cellular_componentcytosol
A0006166biological_processpurine ribonucleoside salvage
A0006177biological_processGMP biosynthetic process
A0006178biological_processguanine salvage
A0006188biological_processIMP biosynthetic process
A0016757molecular_functionglycosyltransferase activity
A0032263biological_processGMP salvage
A0032264biological_processIMP salvage
A0043101biological_processpurine-containing compound salvage
A0046100biological_processhypoxanthine metabolic process
A0046872molecular_functionmetal ion binding
A0052657molecular_functionguanine phosphoribosyltransferase activity
B0000166molecular_functionnucleotide binding
B0000287molecular_functionmagnesium ion binding
B0004422molecular_functionhypoxanthine phosphoribosyltransferase activity
B0005737cellular_componentcytoplasm
B0005829cellular_componentcytosol
B0006166biological_processpurine ribonucleoside salvage
B0006177biological_processGMP biosynthetic process
B0006178biological_processguanine salvage
B0006188biological_processIMP biosynthetic process
B0016757molecular_functionglycosyltransferase activity
B0032263biological_processGMP salvage
B0032264biological_processIMP salvage
B0043101biological_processpurine-containing compound salvage
B0046100biological_processhypoxanthine metabolic process
B0046872molecular_functionmetal ion binding
B0052657molecular_functionguanine phosphoribosyltransferase activity
C0000166molecular_functionnucleotide binding
C0000287molecular_functionmagnesium ion binding
C0004422molecular_functionhypoxanthine phosphoribosyltransferase activity
C0005737cellular_componentcytoplasm
C0005829cellular_componentcytosol
C0006166biological_processpurine ribonucleoside salvage
C0006177biological_processGMP biosynthetic process
C0006178biological_processguanine salvage
C0006188biological_processIMP biosynthetic process
C0016757molecular_functionglycosyltransferase activity
C0032263biological_processGMP salvage
C0032264biological_processIMP salvage
C0043101biological_processpurine-containing compound salvage
C0046100biological_processhypoxanthine metabolic process
C0046872molecular_functionmetal ion binding
C0052657molecular_functionguanine phosphoribosyltransferase activity
D0000166molecular_functionnucleotide binding
D0000287molecular_functionmagnesium ion binding
D0004422molecular_functionhypoxanthine phosphoribosyltransferase activity
D0005737cellular_componentcytoplasm
D0005829cellular_componentcytosol
D0006166biological_processpurine ribonucleoside salvage
D0006177biological_processGMP biosynthetic process
D0006178biological_processguanine salvage
D0006188biological_processIMP biosynthetic process
D0016757molecular_functionglycosyltransferase activity
D0032263biological_processGMP salvage
D0032264biological_processIMP salvage
D0043101biological_processpurine-containing compound salvage
D0046100biological_processhypoxanthine metabolic process
D0046872molecular_functionmetal ion binding
D0052657molecular_functionguanine phosphoribosyltransferase activity
Functional Information from PDB Data
site_idAC1
Number of Residues14
Detailsbinding site for residue 6W7 A 301
ChainResidue
AVAL124
APOP304
AHOH409
AHOH419
AHOH423
AHOH429
AVAL125
AASP126
ASER127
AGLY128
ALYS154
APHE175
AVAL176
AASP182

site_idAC2
Number of Residues5
Detailsbinding site for residue MG A 302
ChainResidue
AASP182
APOP304
AHOH406
AHOH407
AHOH419

site_idAC3
Number of Residues6
Detailsbinding site for residue MG A 303
ChainResidue
AGLU122
AASP123
AHOH402
AHOH410
AHOH428
AHOH445

site_idAC4
Number of Residues13
Detailsbinding site for residue POP A 304
ChainResidue
ALEU65
ALYS66
AGLY67
AASP182
AARG188
A6W7301
AMG302
AHOH406
AHOH410
AHOH413
AHOH419
AHOH424
AHOH428

site_idAC5
Number of Residues12
Detailsbinding site for residue 6W7 B 301
ChainResidue
BVAL124
BVAL125
BASP126
BSER127
BGLY128
BLYS154
BPHE175
BVAL176
BPOP304
BHOH410
BHOH412
BHOH419

site_idAC6
Number of Residues5
Detailsbinding site for residue MG B 302
ChainResidue
BASP182
BPOP304
BHOH409
BHOH412
BHOH424

site_idAC7
Number of Residues5
Detailsbinding site for residue MG B 303
ChainResidue
BGLU122
BASP123
BHOH401
BHOH417
BHOH427

site_idAC8
Number of Residues13
Detailsbinding site for residue POP B 304
ChainResidue
BLEU65
BLYS66
BGLY67
BASP182
BARG188
B6W7301
BMG302
BHOH404
BHOH409
BHOH412
BHOH420
BHOH427
BHOH434

site_idAC9
Number of Residues13
Detailsbinding site for residue 6W7 C 301
ChainResidue
CVAL124
CASP126
CSER127
CGLY128
CTHR130
CLYS154
CPHE175
CVAL176
CASP182
CPOP304
CHOH403
CHOH406
CHOH428

site_idAD1
Number of Residues5
Detailsbinding site for residue MG C 302
ChainResidue
CASP182
CPOP304
CHOH401
CHOH414
CHOH427

site_idAD2
Number of Residues6
Detailsbinding site for residue MG C 303
ChainResidue
CGLU122
CASP123
CHOH419
CHOH429
CHOH430
CHOH438

site_idAD3
Number of Residues11
Detailsbinding site for residue POP C 304
ChainResidue
CGLY67
CASP182
CARG188
C6W7301
CMG302
CHOH401
CHOH413
CHOH427
CHOH432
CLEU65
CLYS66

site_idAD4
Number of Residues12
Detailsbinding site for residue 6W7 D 301
ChainResidue
DVAL124
DVAL125
DASP126
DSER127
DGLY128
DLYS154
DASP174
DPHE175
DVAL176
DPOP304
DHOH404
DHOH430

site_idAD5
Number of Residues5
Detailsbinding site for residue MG D 302
ChainResidue
DASP182
DPOP304
DHOH409
DHOH411
DHOH417

site_idAD6
Number of Residues6
Detailsbinding site for residue MG D 303
ChainResidue
DGLU122
DASP123
DHOH405
DHOH418
DHOH429
DHOH431

site_idAD7
Number of Residues11
Detailsbinding site for residue POP D 304
ChainResidue
DLEU65
DLYS66
DGLY67
DASP182
DARG188
D6W7301
DMG302
DHOH403
DHOH409
DHOH417
DHOH429

Functional Information from PROSITE/UniProt
site_idPS00103
Number of Residues13
DetailsPUR_PYR_PR_TRANSFER Purine/pyrimidine phosphoribosyl transferases signature. VLIVEDVVDSGlT
ChainResidueDetails
AVAL118-THR130

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues4
DetailsACT_SITE: Proton acceptor => ECO:0000250|UniProtKB:P0A9M2
ChainResidueDetails
AASP126
CASP126
DASP126
BASP126

site_idSWS_FT_FI2
Number of Residues12
DetailsBINDING: BINDING => ECO:0000269|PubMed:25915781, ECO:0007744|PDB:4RHT, ECO:0007744|PDB:5KNP
ChainResidueDetails
BGLY67
BARG188
CLYS66
CGLY67
CARG188
DLYS66
DGLY67
DARG188
ALYS66
AGLY67
AARG188
BLYS66

site_idSWS_FT_FI3
Number of Residues20
DetailsBINDING: BINDING => ECO:0000269|PubMed:25915781, ECO:0007744|PDB:4RHT
ChainResidueDetails
AASP182
BGLU122
BASP123
BLYS154
BPHE175
BASP182
CGLU122
CASP123
CLYS154
CPHE175
CASP182
DGLU122
DASP123
DLYS154
DPHE175
DASP182
AGLU122
AASP123
ALYS154
APHE175

219869

PDB entries from 2024-05-15

PDB statisticsPDBj update infoContact PDBjnumon