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5FV9

Crystal structure of GalNAc-T2 in complex with compound 16d

Functional Information from GO Data
ChainGOidnamespacecontents
A0000139cellular_componentGolgi membrane
A0002639biological_processpositive regulation of immunoglobulin production
A0004653molecular_functionpolypeptide N-acetylgalactosaminyltransferase activity
A0005515molecular_functionprotein binding
A0005576cellular_componentextracellular region
A0005789cellular_componentendoplasmic reticulum membrane
A0005794cellular_componentGolgi apparatus
A0005795cellular_componentGolgi stack
A0006486biological_processobsolete protein glycosylation
A0006493biological_processprotein O-linked glycosylation
A0016020cellular_componentmembrane
A0016266biological_processprotein O-linked glycosylation via N-acetyl-galactosamine
A0016740molecular_functiontransferase activity
A0016757molecular_functionglycosyltransferase activity
A0018243biological_processobsolete protein O-linked glycosylation via threonine
A0030145molecular_functionmanganese ion binding
A0030246molecular_functioncarbohydrate binding
A0032580cellular_componentGolgi cisterna membrane
A0046872molecular_functionmetal ion binding
A0048471cellular_componentperinuclear region of cytoplasm
A0051604biological_processprotein maturation
B0000139cellular_componentGolgi membrane
B0002639biological_processpositive regulation of immunoglobulin production
B0004653molecular_functionpolypeptide N-acetylgalactosaminyltransferase activity
B0005515molecular_functionprotein binding
B0005576cellular_componentextracellular region
B0005789cellular_componentendoplasmic reticulum membrane
B0005794cellular_componentGolgi apparatus
B0005795cellular_componentGolgi stack
B0006486biological_processobsolete protein glycosylation
B0006493biological_processprotein O-linked glycosylation
B0016020cellular_componentmembrane
B0016266biological_processprotein O-linked glycosylation via N-acetyl-galactosamine
B0016740molecular_functiontransferase activity
B0016757molecular_functionglycosyltransferase activity
B0018243biological_processobsolete protein O-linked glycosylation via threonine
B0030145molecular_functionmanganese ion binding
B0030246molecular_functioncarbohydrate binding
B0032580cellular_componentGolgi cisterna membrane
B0046872molecular_functionmetal ion binding
B0048471cellular_componentperinuclear region of cytoplasm
B0051604biological_processprotein maturation
C0000139cellular_componentGolgi membrane
C0002639biological_processpositive regulation of immunoglobulin production
C0004653molecular_functionpolypeptide N-acetylgalactosaminyltransferase activity
C0005515molecular_functionprotein binding
C0005576cellular_componentextracellular region
C0005789cellular_componentendoplasmic reticulum membrane
C0005794cellular_componentGolgi apparatus
C0005795cellular_componentGolgi stack
C0006486biological_processobsolete protein glycosylation
C0006493biological_processprotein O-linked glycosylation
C0016020cellular_componentmembrane
C0016266biological_processprotein O-linked glycosylation via N-acetyl-galactosamine
C0016740molecular_functiontransferase activity
C0016757molecular_functionglycosyltransferase activity
C0018243biological_processobsolete protein O-linked glycosylation via threonine
C0030145molecular_functionmanganese ion binding
C0030246molecular_functioncarbohydrate binding
C0032580cellular_componentGolgi cisterna membrane
C0046872molecular_functionmetal ion binding
C0048471cellular_componentperinuclear region of cytoplasm
C0051604biological_processprotein maturation
D0000139cellular_componentGolgi membrane
D0002639biological_processpositive regulation of immunoglobulin production
D0004653molecular_functionpolypeptide N-acetylgalactosaminyltransferase activity
D0005515molecular_functionprotein binding
D0005576cellular_componentextracellular region
D0005789cellular_componentendoplasmic reticulum membrane
D0005794cellular_componentGolgi apparatus
D0005795cellular_componentGolgi stack
D0006486biological_processobsolete protein glycosylation
D0006493biological_processprotein O-linked glycosylation
D0016020cellular_componentmembrane
D0016266biological_processprotein O-linked glycosylation via N-acetyl-galactosamine
D0016740molecular_functiontransferase activity
D0016757molecular_functionglycosyltransferase activity
D0018243biological_processobsolete protein O-linked glycosylation via threonine
D0030145molecular_functionmanganese ion binding
D0030246molecular_functioncarbohydrate binding
D0032580cellular_componentGolgi cisterna membrane
D0046872molecular_functionmetal ion binding
D0048471cellular_componentperinuclear region of cytoplasm
D0051604biological_processprotein maturation
E0000139cellular_componentGolgi membrane
E0002639biological_processpositive regulation of immunoglobulin production
E0004653molecular_functionpolypeptide N-acetylgalactosaminyltransferase activity
E0005515molecular_functionprotein binding
E0005576cellular_componentextracellular region
E0005789cellular_componentendoplasmic reticulum membrane
E0005794cellular_componentGolgi apparatus
E0005795cellular_componentGolgi stack
E0006486biological_processobsolete protein glycosylation
E0006493biological_processprotein O-linked glycosylation
E0016020cellular_componentmembrane
E0016266biological_processprotein O-linked glycosylation via N-acetyl-galactosamine
E0016740molecular_functiontransferase activity
E0016757molecular_functionglycosyltransferase activity
E0018243biological_processobsolete protein O-linked glycosylation via threonine
E0030145molecular_functionmanganese ion binding
E0030246molecular_functioncarbohydrate binding
E0032580cellular_componentGolgi cisterna membrane
E0046872molecular_functionmetal ion binding
E0048471cellular_componentperinuclear region of cytoplasm
E0051604biological_processprotein maturation
F0000139cellular_componentGolgi membrane
F0002639biological_processpositive regulation of immunoglobulin production
F0004653molecular_functionpolypeptide N-acetylgalactosaminyltransferase activity
F0005515molecular_functionprotein binding
F0005576cellular_componentextracellular region
F0005789cellular_componentendoplasmic reticulum membrane
F0005794cellular_componentGolgi apparatus
F0005795cellular_componentGolgi stack
F0006486biological_processobsolete protein glycosylation
F0006493biological_processprotein O-linked glycosylation
F0016020cellular_componentmembrane
F0016266biological_processprotein O-linked glycosylation via N-acetyl-galactosamine
F0016740molecular_functiontransferase activity
F0016757molecular_functionglycosyltransferase activity
F0018243biological_processobsolete protein O-linked glycosylation via threonine
F0030145molecular_functionmanganese ion binding
F0030246molecular_functioncarbohydrate binding
F0032580cellular_componentGolgi cisterna membrane
F0046872molecular_functionmetal ion binding
F0048471cellular_componentperinuclear region of cytoplasm
F0051604biological_processprotein maturation
Functional Information from PDB Data
site_idAC1
Number of Residues14
DetailsBINDING SITE FOR RESIDUE UDP A 1570
ChainResidue
ATHR143
AARG362
AMN1571
AHOH2084
AHOH2164
AHOH2166
AHIS145
AASP176
AARG201
ALEU204
AASP224
AHIS226
AVAL330
AHIS359

site_idAC2
Number of Residues4
DetailsBINDING SITE FOR RESIDUE MN A 1571
ChainResidue
AASP224
AHIS226
AHIS359
AUDP1570

site_idAC3
Number of Residues3
DetailsBINDING SITE FOR RESIDUE EDO A 1572
ChainResidue
AGLY535
ASER536
AASN537

site_idAC4
Number of Residues3
DetailsBINDING SITE FOR RESIDUE EDO A 1573
ChainResidue
ATYR177
ASER178
AASN179

site_idAC5
Number of Residues3
DetailsBINDING SITE FOR RESIDUE GOL A 1575
ChainResidue
ATYR99
ALYS103
AHOH2024

site_idAC6
Number of Residues14
DetailsBINDING SITE FOR RESIDUE Y6W B 1570
ChainResidue
BTHR143
BHIS145
BASP176
BARG201
BLEU204
BSER207
BASP224
BHIS226
BVAL330
BGLU334
BARG362
BMN1571
BUDP1572
BHOH2168

site_idAC7
Number of Residues5
DetailsBINDING SITE FOR RESIDUE MN B 1571
ChainResidue
BASP224
BHIS226
BHIS359
BY6W1570
BUDP1572

site_idAC8
Number of Residues13
DetailsBINDING SITE FOR RESIDUE UDP B 1572
ChainResidue
BTHR143
BPHE144
BHIS145
BASP176
BARG201
BLEU204
BASP224
BHIS226
BHIS359
BARG362
BY6W1570
BMN1571
BHOH2051

site_idAC9
Number of Residues2
DetailsBINDING SITE FOR RESIDUE EDO B 1573
ChainResidue
BTYR408
BGLY409

site_idBC1
Number of Residues4
DetailsBINDING SITE FOR RESIDUE EDO B 1574
ChainResidue
BGLU481
BALA483
BLYS491
BMET493

site_idBC2
Number of Residues15
DetailsBINDING SITE FOR RESIDUE UDP C 1570
ChainResidue
CTHR143
CHIS145
CASP176
CARG201
CLEU204
CSER207
CASP224
CHIS226
CVAL330
CHIS359
CARG362
CMN1571
CHOH2058
CHOH2059
CHOH2132

site_idBC3
Number of Residues4
DetailsBINDING SITE FOR RESIDUE MN C 1571
ChainResidue
CASP224
CHIS226
CHIS359
CUDP1570

site_idBC4
Number of Residues3
DetailsBINDING SITE FOR RESIDUE EDO C 1572
ChainResidue
CLYS271
CLYS302
CVAL433

site_idBC5
Number of Residues3
DetailsBINDING SITE FOR RESIDUE EDO C 1573
ChainResidue
CASP517
CSER518
CARG519

site_idBC6
Number of Residues5
DetailsBINDING SITE FOR RESIDUE GOL C 1574
ChainResidue
CTYR408
CGLY409
CHOH2303
CHOH2304
FGLN412

site_idBC7
Number of Residues17
DetailsBINDING SITE FOR RESIDUE UDP D 1555
ChainResidue
DARG201
DGLY203
DLEU204
DSER207
DASP224
DHIS226
DVAL330
DGLU334
DHIS359
DARG362
DMN1556
DHOH2055
DHOH2180
DTHR143
DPHE144
DHIS145
DASP176

site_idBC8
Number of Residues4
DetailsBINDING SITE FOR RESIDUE MN D 1556
ChainResidue
DASP224
DHIS226
DHIS359
DUDP1555

site_idBC9
Number of Residues16
DetailsBINDING SITE FOR RESIDUE UDP E 1570
ChainResidue
ETHR143
EHIS145
EASP176
EARG201
ELEU204
ESER207
EASP224
EHIS226
EVAL330
EHIS359
EARG362
EMN1571
EY6W1572
EHOH2053
EHOH2054
EHOH2121

site_idCC1
Number of Residues5
DetailsBINDING SITE FOR RESIDUE MN E 1571
ChainResidue
EASP224
EHIS226
EHIS359
EUDP1570
EY6W1572

site_idCC2
Number of Residues14
DetailsBINDING SITE FOR RESIDUE Y6W E 1572
ChainResidue
ETHR143
EPHE144
EHIS145
EASP176
EARG201
ESER207
EHIS226
EVAL330
EGLU334
EARG362
EUDP1570
EMN1571
EHOH2109
EHOH2181

site_idCC3
Number of Residues7
DetailsBINDING SITE FOR RESIDUE EDO E 1573
ChainResidue
AHOH2158
EASN198
EASP199
EARG200
EGLU202
EARG210
EHOH2101

site_idCC4
Number of Residues2
DetailsBINDING SITE FOR RESIDUE EDO E 1574
ChainResidue
ETRP343
EASN432

site_idCC5
Number of Residues3
DetailsBINDING SITE FOR RESIDUE EDO E 1575
ChainResidue
ETYR177
ESER178
EASN179

site_idCC6
Number of Residues4
DetailsBINDING SITE FOR RESIDUE EDO E 1576
ChainResidue
EGLU481
ELYS491
EHIS492
EMET493

site_idCC7
Number of Residues13
DetailsBINDING SITE FOR RESIDUE UDP F 1570
ChainResidue
FTHR143
FPHE144
FHIS145
FASP176
FARG201
FLEU204
FASP224
FHIS226
FHIS359
FARG362
FMN1571
FY6W1572
FHOH2063

site_idCC8
Number of Residues5
DetailsBINDING SITE FOR RESIDUE MN F 1571
ChainResidue
FASP224
FHIS226
FHIS359
FUDP1570
FY6W1572

site_idCC9
Number of Residues12
DetailsBINDING SITE FOR RESIDUE Y6W F 1572
ChainResidue
FTHR143
FPHE144
FASP176
FARG201
FASP224
FHIS226
FVAL330
FGLU334
FARG362
FUDP1570
FMN1571
FHOH2097

site_idDC1
Number of Residues4
DetailsBINDING SITE FOR RESIDUE EDO F 1573
ChainResidue
FARG502
FSER536
FASN537
FHOH2199

site_idDC2
Number of Residues4
DetailsBINDING SITE FOR RESIDUE EDO F 1574
ChainResidue
FPRO407
FTYR408
FGLY409
FHOH2200

site_idDC3
Number of Residues4
DetailsBINDING SITE FOR RESIDUE EDO F 1575
ChainResidue
FARG514
FASP517
FSER518
FARG519

site_idDC4
Number of Residues4
DetailsBINDING SITE FOR RESIDUE GOL F 1576
ChainResidue
FASP199
FGLU202
FARG210
FHOH2202

site_idDC5
Number of Residues3
DetailsBINDING SITE FOR RESIDUE GOL F 1577
ChainResidue
EARG514
EASP517
EARG519

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues615
DetailsDomain: {"description":"Ricin B-type lectin","evidences":[{"source":"PROSITE-ProRule","id":"PRU00174","evidenceCode":"ECO:0000255"}]}
ChainResidueDetails

site_idSWS_FT_FI2
Number of Residues630
DetailsRegion: {"description":"Catalytic subdomain A"}
ChainResidueDetails

site_idSWS_FT_FI3
Number of Residues372
DetailsRegion: {"description":"Catalytic subdomain B"}
ChainResidueDetails

site_idSWS_FT_FI4
Number of Residues36
DetailsBinding site: {"evidences":[{"source":"PubMed","id":"16434399","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"24954443","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"25939779","evidenceCode":"ECO:0000269"},{"source":"PDB","id":"2FFU","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"2FFV","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"4D0T","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"4D11","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"5AJP","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"5FV9","evidenceCode":"ECO:0007744"}]}
ChainResidueDetails

site_idSWS_FT_FI5
Number of Residues18
DetailsBinding site: {"evidences":[{"source":"PubMed","id":"16434399","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"24954443","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"25939779","evidenceCode":"ECO:0000269"},{"source":"PDB","id":"2FFU","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"2FFV","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"4D0T","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"4D0Z","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"4D11","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"5AJP","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"5FV9","evidenceCode":"ECO:0007744"}]}
ChainResidueDetails

site_idSWS_FT_FI6
Number of Residues6
DetailsSite: {"description":"Not glycosylated"}
ChainResidueDetails

site_idSWS_FT_FI7
Number of Residues5
DetailsModified residue: {"description":"Phosphoserine","evidences":[{"source":"PubMed","id":"23186163","evidenceCode":"ECO:0007744"}]}
ChainResidueDetails

247536

PDB entries from 2026-01-14

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