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

4O1B

The crystal structure of a mutant NAMPT (G217R) in complex with an inhibitor APO866

Functional Information from GO Data
ChainGOidnamespacecontents
A0005125molecular_functioncytokine activity
A0005515molecular_functionprotein binding
A0005576cellular_componentextracellular region
A0005615cellular_componentextracellular space
A0005634cellular_componentnucleus
A0005737cellular_componentcytoplasm
A0005829cellular_componentcytosol
A0007165biological_processsignal transduction
A0007267biological_processcell-cell signaling
A0007623biological_processcircadian rhythm
A0008284biological_processpositive regulation of cell population proliferation
A0008286biological_processinsulin receptor signaling pathway
A0009435biological_processNAD biosynthetic process
A0016607cellular_componentnuclear speck
A0016757molecular_functionglycosyltransferase activity
A0019363biological_processpyridine nucleotide biosynthetic process
A0030054cellular_componentcell junction
A0032922biological_processcircadian regulation of gene expression
A0034356biological_processNAD biosynthesis via nicotinamide riboside salvage pathway
A0042802molecular_functionidentical protein binding
A0045944biological_processpositive regulation of transcription by RNA polymerase II
A0047280molecular_functionnicotinamide phosphoribosyltransferase activity
A0048511biological_processrhythmic process
A0051770biological_processpositive regulation of nitric-oxide synthase biosynthetic process
A0060612biological_processadipose tissue development
A0070062cellular_componentextracellular exosome
B0005125molecular_functioncytokine activity
B0005515molecular_functionprotein binding
B0005576cellular_componentextracellular region
B0005615cellular_componentextracellular space
B0005634cellular_componentnucleus
B0005737cellular_componentcytoplasm
B0005829cellular_componentcytosol
B0007165biological_processsignal transduction
B0007267biological_processcell-cell signaling
B0007623biological_processcircadian rhythm
B0008284biological_processpositive regulation of cell population proliferation
B0008286biological_processinsulin receptor signaling pathway
B0009435biological_processNAD biosynthetic process
B0016607cellular_componentnuclear speck
B0016757molecular_functionglycosyltransferase activity
B0019363biological_processpyridine nucleotide biosynthetic process
B0030054cellular_componentcell junction
B0032922biological_processcircadian regulation of gene expression
B0034356biological_processNAD biosynthesis via nicotinamide riboside salvage pathway
B0042802molecular_functionidentical protein binding
B0045944biological_processpositive regulation of transcription by RNA polymerase II
B0047280molecular_functionnicotinamide phosphoribosyltransferase activity
B0048511biological_processrhythmic process
B0051770biological_processpositive regulation of nitric-oxide synthase biosynthetic process
B0060612biological_processadipose tissue development
B0070062cellular_componentextracellular exosome
Functional Information from PDB Data
site_idAC1
Number of Residues15
DetailsBINDING SITE FOR RESIDUE DGB A 601
ChainResidue
AGLY185
AARG311
AILE378
AALA379
AHOH754
AHOH893
BTYR18
ALYS189
APHE193
AARG196
AARG217
AASP219
AVAL242
AALA244
ASER275

site_idAC2
Number of Residues9
DetailsBINDING SITE FOR RESIDUE PO4 A 602
ChainResidue
AARG392
ASER398
ALYS400
AEDO606
AHOH744
AHOH763
AHOH767
AHOH1086
BARG196

site_idAC3
Number of Residues10
DetailsBINDING SITE FOR RESIDUE PO4 A 603
ChainResidue
AARG196
AGLU246
AHIS247
AARG311
AASP313
AHOH824
AHOH917
BTYR18
BHOH738
BHOH823

site_idAC4
Number of Residues9
DetailsBINDING SITE FOR RESIDUE EDO A 604
ChainResidue
AASP354
AGLY355
AGLY383
AGLY384
AHOH829
AHOH847
AHOH944
AHOH1001
AHOH1122

site_idAC5
Number of Residues5
DetailsBINDING SITE FOR RESIDUE EDO A 605
ChainResidue
AGLY315
APRO317
AASP354
AHOH1137
BHOH934

site_idAC6
Number of Residues8
DetailsBINDING SITE FOR RESIDUE EDO A 606
ChainResidue
AARG40
AARG392
AASP393
AASN396
ACYS397
ASER398
APO4602
AHOH1056

site_idAC7
Number of Residues4
DetailsBINDING SITE FOR RESIDUE EDO A 607
ChainResidue
APHE123
AVAL124
AARG434
AASN479

site_idAC8
Number of Residues2
DetailsBINDING SITE FOR RESIDUE EDO A 608
ChainResidue
AGLY181
AASN182

site_idAC9
Number of Residues13
DetailsBINDING SITE FOR RESIDUE DGB B 601
ChainResidue
ATYR18
BGLY185
BLYS189
BPHE193
BARG196
BASP219
BALA244
BSER275
BARG311
BILE378
BALA379
BHOH735
BHOH898

site_idBC1
Number of Residues9
DetailsBINDING SITE FOR RESIDUE PO4 B 602
ChainResidue
AARG196
AHOH917
BARG392
BSER398
BLYS400
BEDO604
BHOH728
BHOH823
BHOH1037

site_idBC2
Number of Residues10
DetailsBINDING SITE FOR RESIDUE PO4 B 603
ChainResidue
ATYR18
AHOH741
AHOH763
BARG196
BGLU246
BHIS247
BARG311
BASP313
BHOH766
BHOH851

site_idBC3
Number of Residues7
DetailsBINDING SITE FOR RESIDUE EDO B 604
ChainResidue
BSER398
BPO4602
BARG40
BARG392
BASP393
BASN396
BCYS397

site_idBC4
Number of Residues7
DetailsBINDING SITE FOR RESIDUE EDO B 605
ChainResidue
ALYS400
ACYS401
APHE414
BHIS247
BSER248
BTHR251
BHOH727

site_idBC5
Number of Residues7
DetailsBINDING SITE FOR RESIDUE EDO B 606
ChainResidue
AHOH948
BGLY315
BASP354
BGLY355
BHOH958
BHOH1167
BHOH1223

site_idBC6
Number of Residues3
DetailsBINDING SITE FOR RESIDUE EDO B 607
ChainResidue
BARG217
BTYR240
BSER241

site_idBC7
Number of Residues8
DetailsBINDING SITE FOR RESIDUE EDO B 608
ChainResidue
AHOH1262
BSER382
BGLY383
BGLY384
BHOH840
BHOH848
BHOH1105
BHOH1132

site_idBC8
Number of Residues7
DetailsBINDING SITE FOR RESIDUE EDO B 609
ChainResidue
BLYS117
BASP456
BLEU458
BHOH774
BHOH906
BHOH991
BHOH1219

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues14
DetailsBINDING:
ChainResidueDetails
AARG196
BHIS247
BARG311
BGLY353
BGLY384
BARG392
AASP219
AHIS247
AARG311
AGLY353
AGLY384
AARG392
BARG196
BASP219

site_idSWS_FT_FI2
Number of Residues2
DetailsMOD_RES: N-acetylmethionine => ECO:0007744|PubMed:22223895
ChainResidueDetails
AMET1
BMET1

site_idSWS_FT_FI3
Number of Residues2
DetailsMOD_RES: Phosphotyrosine => ECO:0007744|PubMed:15592455
ChainResidueDetails
ATYR188
BTYR188

site_idSWS_FT_FI4
Number of Residues2
DetailsMOD_RES: Phosphoserine => ECO:0007744|PubMed:23186163
ChainResidueDetails
ASER472
BSER472

222415

PDB entries from 2024-07-10

PDB statisticsPDBj update infoContact PDBjnumon