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6Q94

Crystal structure of human GDP-D-mannose 4,6-dehydratase (S156D) in complex with GDP-Man

Functional Information from GO Data
ChainGOidnamespacecontents
A0005515molecular_functionprotein binding
A0005737cellular_componentcytoplasm
A0005829cellular_componentcytosol
A0007219biological_processNotch signaling pathway
A0008446molecular_functionGDP-mannose 4,6-dehydratase activity
A0016829molecular_functionlyase activity
A0019673biological_processGDP-mannose metabolic process
A0042350biological_processGDP-L-fucose biosynthetic process
A0042351biological_process'de novo' GDP-L-fucose biosynthetic process
A0042802molecular_functionidentical protein binding
A0070062cellular_componentextracellular exosome
A0070401molecular_functionNADP+ binding
B0005515molecular_functionprotein binding
B0005737cellular_componentcytoplasm
B0005829cellular_componentcytosol
B0007219biological_processNotch signaling pathway
B0008446molecular_functionGDP-mannose 4,6-dehydratase activity
B0016829molecular_functionlyase activity
B0019673biological_processGDP-mannose metabolic process
B0042350biological_processGDP-L-fucose biosynthetic process
B0042351biological_process'de novo' GDP-L-fucose biosynthetic process
B0042802molecular_functionidentical protein binding
B0070062cellular_componentextracellular exosome
B0070401molecular_functionNADP+ binding
C0005515molecular_functionprotein binding
C0005737cellular_componentcytoplasm
C0005829cellular_componentcytosol
C0007219biological_processNotch signaling pathway
C0008446molecular_functionGDP-mannose 4,6-dehydratase activity
C0016829molecular_functionlyase activity
C0019673biological_processGDP-mannose metabolic process
C0042350biological_processGDP-L-fucose biosynthetic process
C0042351biological_process'de novo' GDP-L-fucose biosynthetic process
C0042802molecular_functionidentical protein binding
C0070062cellular_componentextracellular exosome
C0070401molecular_functionNADP+ binding
D0005515molecular_functionprotein binding
D0005737cellular_componentcytoplasm
D0005829cellular_componentcytosol
D0007219biological_processNotch signaling pathway
D0008446molecular_functionGDP-mannose 4,6-dehydratase activity
D0016829molecular_functionlyase activity
D0019673biological_processGDP-mannose metabolic process
D0042350biological_processGDP-L-fucose biosynthetic process
D0042351biological_process'de novo' GDP-L-fucose biosynthetic process
D0042802molecular_functionidentical protein binding
D0070062cellular_componentextracellular exosome
D0070401molecular_functionNADP+ binding
E0005515molecular_functionprotein binding
E0005737cellular_componentcytoplasm
E0005829cellular_componentcytosol
E0007219biological_processNotch signaling pathway
E0008446molecular_functionGDP-mannose 4,6-dehydratase activity
E0016829molecular_functionlyase activity
E0019673biological_processGDP-mannose metabolic process
E0042350biological_processGDP-L-fucose biosynthetic process
E0042351biological_process'de novo' GDP-L-fucose biosynthetic process
E0042802molecular_functionidentical protein binding
E0070062cellular_componentextracellular exosome
E0070401molecular_functionNADP+ binding
F0005515molecular_functionprotein binding
F0005737cellular_componentcytoplasm
F0005829cellular_componentcytosol
F0007219biological_processNotch signaling pathway
F0008446molecular_functionGDP-mannose 4,6-dehydratase activity
F0016829molecular_functionlyase activity
F0019673biological_processGDP-mannose metabolic process
F0042350biological_processGDP-L-fucose biosynthetic process
F0042351biological_process'de novo' GDP-L-fucose biosynthetic process
F0042802molecular_functionidentical protein binding
F0070062cellular_componentextracellular exosome
F0070401molecular_functionNADP+ binding
G0005515molecular_functionprotein binding
G0005737cellular_componentcytoplasm
G0005829cellular_componentcytosol
G0007219biological_processNotch signaling pathway
G0008446molecular_functionGDP-mannose 4,6-dehydratase activity
G0016829molecular_functionlyase activity
G0019673biological_processGDP-mannose metabolic process
G0042350biological_processGDP-L-fucose biosynthetic process
G0042351biological_process'de novo' GDP-L-fucose biosynthetic process
G0042802molecular_functionidentical protein binding
G0070062cellular_componentextracellular exosome
G0070401molecular_functionNADP+ binding
H0005515molecular_functionprotein binding
H0005737cellular_componentcytoplasm
H0005829cellular_componentcytosol
H0007219biological_processNotch signaling pathway
H0008446molecular_functionGDP-mannose 4,6-dehydratase activity
H0016829molecular_functionlyase activity
H0019673biological_processGDP-mannose metabolic process
H0042350biological_processGDP-L-fucose biosynthetic process
H0042351biological_process'de novo' GDP-L-fucose biosynthetic process
H0042802molecular_functionidentical protein binding
H0070062cellular_componentextracellular exosome
H0070401molecular_functionNADP+ binding
Functional Information from PDB Data
site_idAC1
Number of Residues22
Detailsbinding site for residue NAP B 401
ChainResidue
AARG56
BASN61
BASP86
BLEU87
BLEU108
BGLY109
BALA110
BSER112
BTYR123
BALA153
BTYR179
ASER57
BLYS183
BARG214
BGDD402
ASER58
BGLY30
BTHR32
BGLY33
BGLN34
BASP35
BARG55

site_idAC2
Number of Residues20
Detailsbinding site for residue GDD B 402
ChainResidue
BSER112
BHIS113
BVAL114
BTHR155
BTYR179
BASN208
BARG214
BASN217
BPHE218
BVAL219
BLYS222
BLEU240
BGLY241
BASN242
BALA245
BARG247
BVAL281
BARG325
BGLU328
BNAP401

site_idAC3
Number of Residues22
Detailsbinding site for residue NAP A 401
ChainResidue
AGLY30
ATHR32
AGLY33
AGLN34
AASP35
AARG55
AASN61
AASP86
ALEU87
ALEU108
AGLY109
AALA110
ASER112
ATYR123
AVAL127
AALA153
ATYR179
ALYS183
AGDD402
BARG56
BSER57
BSER58

site_idAC4
Number of Residues21
Detailsbinding site for residue GDD A 402
ChainResidue
ASER112
ATHR155
AASP156
AGLU157
ATYR179
APHE207
AASN208
AARG214
AASN217
APHE218
AVAL219
ALYS222
ALEU240
AGLY241
AASN242
AALA245
AARG247
ATYR323
AARG325
AGLU328
ANAP401

site_idAC5
Number of Residues20
Detailsbinding site for residue NAP C 401
ChainResidue
CALA153
CTYR179
CLYS183
CGDD402
EARG56
ESER58
CGLY30
CTHR32
CGLY33
CGLN34
CASP35
CARG55
CASP86
CLEU87
CLEU108
CGLY109
CALA110
CSER112
CTYR123
CVAL127

site_idAC6
Number of Residues22
Detailsbinding site for residue GDD C 402
ChainResidue
CSER112
CVAL114
CTHR155
CASP156
CGLU157
CTYR179
CLEU206
CPHE207
CASN208
CARG214
CASN217
CPHE218
CVAL219
CLYS222
CGLY241
CASN242
CALA245
CARG247
CVAL281
CARG325
CGLU328
CNAP401

site_idAC7
Number of Residues23
Detailsbinding site for residue NAP D 401
ChainResidue
DGLY30
DTHR32
DGLY33
DGLN34
DASP35
DARG55
DASN61
DASP86
DLEU87
DLEU108
DGLY109
DALA110
DSER112
DTYR123
DALA153
DTHR155
DTYR179
DLYS183
DARG214
DGDD402
FARG56
FSER57
FSER58

site_idAC8
Number of Residues22
Detailsbinding site for residue GDD D 402
ChainResidue
DSER112
DVAL114
DTHR155
DASP156
DGLU157
DTYR179
DPHE207
DASN208
DARG214
DASN217
DPHE218
DVAL219
DLYS222
DLEU240
DGLY241
DASN242
DALA245
DARG247
DVAL281
DARG325
DGLU328
DNAP401

site_idAC9
Number of Residues3
Detailsbinding site for residue EDO D 403
ChainResidue
DTYR84
FASN217
FTYR323

site_idAD1
Number of Residues1
Detailsbinding site for residue EDO D 404
ChainResidue
DASN217

site_idAD2
Number of Residues21
Detailsbinding site for residue NAP E 401
ChainResidue
CARG56
CSER57
CSER58
EGLY30
ETHR32
EGLY33
EGLN34
EASP35
EARG55
EASP86
ELEU87
ELEU108
EGLY109
EALA110
ESER112
ETYR123
EVAL127
EALA153
ETYR179
ELYS183
EGDD402

site_idAD3
Number of Residues21
Detailsbinding site for residue GDD E 402
ChainResidue
ESER112
EVAL114
ETHR155
EASP156
ETYR179
EPHE207
EASN208
EARG214
EASN217
EPHE218
EVAL219
ELYS222
ELEU240
EGLY241
EASN242
EALA245
EARG247
EVAL281
EARG325
EGLU328
ENAP401

site_idAD4
Number of Residues21
Detailsbinding site for residue GDD F 401
ChainResidue
FSER112
FVAL114
FTHR155
FASP156
FTYR179
FLEU206
FPHE207
FASN208
FARG214
FASN217
FPHE218
FVAL219
FLYS222
FGLY241
FASN242
FALA245
FARG247
FVAL281
FARG325
FGLU328
FNAP402

site_idAD5
Number of Residues22
Detailsbinding site for residue NAP F 402
ChainResidue
DARG56
DSER57
DSER58
FGLY30
FTHR32
FGLY33
FGLN34
FASP35
FARG55
FASN61
FASP86
FLEU87
FLEU108
FGLY109
FALA110
FSER112
FTYR123
FVAL127
FALA153
FTYR179
FLYS183
FGDD401

site_idAD6
Number of Residues22
Detailsbinding site for residue NAP G 401
ChainResidue
GGLY30
GTHR32
GGLY33
GGLN34
GASP35
GARG55
GASN61
GASP86
GLEU87
GLEU108
GGLY109
GALA110
GSER112
GTYR123
GVAL127
GALA153
GTYR179
GLYS183
GGDD402
HARG56
HSER57
HSER58

site_idAD7
Number of Residues21
Detailsbinding site for residue GDD G 402
ChainResidue
GSER112
GHIS113
GVAL114
GTHR155
GASP156
GTYR179
GPHE207
GASN208
GARG214
GASN217
GPHE218
GVAL219
GLYS222
GLEU240
GGLY241
GASN242
GALA245
GARG247
GARG325
GGLU328
GNAP401

site_idAD8
Number of Residues2
Detailsbinding site for residue EDO G 403
ChainResidue
GPHE60
GHIS75

site_idAD9
Number of Residues20
Detailsbinding site for residue NAP H 401
ChainResidue
GARG56
GSER58
HGLY30
HTHR32
HGLY33
HGLN34
HASP35
HARG55
HASP86
HLEU87
HLEU108
HGLY109
HALA110
HSER112
HTYR123
HVAL127
HTHR155
HTYR179
HLYS183
HGDD402

site_idAE1
Number of Residues20
Detailsbinding site for residue GDD H 402
ChainResidue
HSER112
HVAL114
HTHR155
HASP156
HTYR179
HASN208
HARG214
HASN217
HPHE218
HVAL219
HLYS222
HLEU240
HGLY241
HASN242
HALA245
HARG247
HTYR323
HARG325
HGLU328
HNAP401

site_idAE2
Number of Residues1
Detailsbinding site for residue EDO H 403
ChainResidue
HTYR323

Functional Information from PROSITE/UniProt
site_idPS00061
Number of Residues29
DetailsADH_SHORT Short-chain dehydrogenases/reductases family signature. PqkettpfypRspYGAAKLYAyWIVvNFR
ChainResidueDetails
BPRO166-ARG194

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues8
DetailsActive site: {"evidences":[{"evidenceCode":"ECO:0000250"}]}
ChainResidueDetails

site_idSWS_FT_FI2
Number of Residues16
DetailsActive site: {"description":"Nucleophile","evidences":[{"evidenceCode":"ECO:0000250"}]}
ChainResidueDetails

site_idSWS_FT_FI3
Number of Residues136
DetailsBinding site: {"evidences":[{"source":"Reference","evidenceCode":"ECO:0000269","citation":{"citationType":"submission","publicationDate":"APR-2004","submissionDatabase":"PDB data bank","title":"Crystal structure and biophysical characterization of human GDP-D-mannose 4,6-dehydratase.","authors":["Vedadi M.","Walker J.R.","Sharma S.","Houston S.","Wasney G.","Loppnau P.","Oppermann U."]}}]}
ChainResidueDetails

site_idSWS_FT_FI4
Number of Residues8
DetailsModified residue: {"description":"Phosphotyrosine","evidences":[{"source":"PubMed","id":"23186163","evidenceCode":"ECO:0007744"}]}
ChainResidueDetails

246704

PDB entries from 2025-12-24

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