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

3PI8

Site-specific Glycosylation of Hemoglobin Utilizing Oxime Ligation Chemistry as a Viable Alternative to PEGylation

Functional Information from GO Data
ChainGOidnamespacecontents
A0004601molecular_functionperoxidase activity
A0005344molecular_functionoxygen carrier activity
A0005506molecular_functioniron ion binding
A0005515molecular_functionprotein binding
A0005833cellular_componenthemoglobin complex
A0015671biological_processoxygen transport
A0019825molecular_functionoxygen binding
A0020037molecular_functionheme binding
A0031720molecular_functionhaptoglobin binding
A0031838cellular_componenthaptoglobin-hemoglobin complex
A0042744biological_processhydrogen peroxide catabolic process
A0043177molecular_functionorganic acid binding
A0046872molecular_functionmetal ion binding
A0098869biological_processcellular oxidant detoxification
B0004601molecular_functionperoxidase activity
B0005344molecular_functionoxygen carrier activity
B0005833cellular_componenthemoglobin complex
B0015671biological_processoxygen transport
B0019825molecular_functionoxygen binding
B0020037molecular_functionheme binding
B0031720molecular_functionhaptoglobin binding
B0031721molecular_functionhemoglobin alpha binding
B0031838cellular_componenthaptoglobin-hemoglobin complex
B0042744biological_processhydrogen peroxide catabolic process
B0043177molecular_functionorganic acid binding
B0046872molecular_functionmetal ion binding
B0098869biological_processcellular oxidant detoxification
C0004601molecular_functionperoxidase activity
C0005344molecular_functionoxygen carrier activity
C0005506molecular_functioniron ion binding
C0005515molecular_functionprotein binding
C0005833cellular_componenthemoglobin complex
C0015671biological_processoxygen transport
C0019825molecular_functionoxygen binding
C0020037molecular_functionheme binding
C0031720molecular_functionhaptoglobin binding
C0031838cellular_componenthaptoglobin-hemoglobin complex
C0042744biological_processhydrogen peroxide catabolic process
C0043177molecular_functionorganic acid binding
C0046872molecular_functionmetal ion binding
C0098869biological_processcellular oxidant detoxification
D0004601molecular_functionperoxidase activity
D0005344molecular_functionoxygen carrier activity
D0005833cellular_componenthemoglobin complex
D0015671biological_processoxygen transport
D0019825molecular_functionoxygen binding
D0020037molecular_functionheme binding
D0031720molecular_functionhaptoglobin binding
D0031721molecular_functionhemoglobin alpha binding
D0031838cellular_componenthaptoglobin-hemoglobin complex
D0042744biological_processhydrogen peroxide catabolic process
D0043177molecular_functionorganic acid binding
D0046872molecular_functionmetal ion binding
D0098869biological_processcellular oxidant detoxification
Functional Information from PDB Data
site_idAC1
Number of Residues15
DetailsBINDING SITE FOR RESIDUE HEM A 142
ChainResidue
ATYR42
AASN97
APHE98
ALEU101
ALEU136
ACMO143
AHOH433
APHE43
AHIS45
AHIS58
ALYS61
ALEU83
ALEU86
AHIS87
ALEU91

site_idAC2
Number of Residues5
DetailsBINDING SITE FOR RESIDUE CMO A 143
ChainResidue
ALEU29
APHE43
AHIS58
AVAL62
AHEM142

site_idAC3
Number of Residues13
DetailsBINDING SITE FOR RESIDUE HEM B 147
ChainResidue
BTHR38
BPHE41
BHIS63
BLYS66
BSER70
BLEU88
BHIS92
BLEU96
BASN102
BPHE103
BCMO148
BHOH154
BHOH172

site_idAC4
Number of Residues5
DetailsBINDING SITE FOR RESIDUE CMO B 148
ChainResidue
BLEU28
BPHE42
BHIS63
BVAL67
BHEM147

site_idAC5
Number of Residues16
DetailsBINDING SITE FOR RESIDUE HEM C 142
ChainResidue
AALA12
ALYS16
CTYR42
CHIS45
CHIS58
CLYS61
CLEU83
CLEU86
CHIS87
CLEU91
CVAL93
CASN97
CPHE98
CLEU101
CCMO143
CHOH163

site_idAC6
Number of Residues5
DetailsBINDING SITE FOR RESIDUE CMO C 143
ChainResidue
CLEU29
CPHE43
CHIS58
CVAL62
CHEM142

site_idAC7
Number of Residues16
DetailsBINDING SITE FOR RESIDUE HEM D 147
ChainResidue
DPHE41
DPHE42
DHIS63
DVAL67
DSER70
DPHE71
DLEU88
DLEU91
DHIS92
DLEU96
DVAL98
DASN102
DPHE103
DLEU106
DLEU141
DCMO148

site_idAC8
Number of Residues4
DetailsBINDING SITE FOR RESIDUE CMO D 148
ChainResidue
DLEU28
DHIS63
DVAL67
DHEM147

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues2
DetailsBINDING: distal binding residue
ChainResidueDetails
BHIS63
DHIS63

site_idSWS_FT_FI2
Number of Residues2
DetailsBINDING: proximal binding residue
ChainResidueDetails
BHIS92
DHIS92

site_idSWS_FT_FI3
Number of Residues2
DetailsMOD_RES: Phosphothreonine => ECO:0000250|UniProtKB:P68871
ChainResidueDetails
BTHR12
DTHR12
ASER49
CSER3
CSER35
CSER49

site_idSWS_FT_FI4
Number of Residues2
DetailsMOD_RES: Phosphoserine => ECO:0000250|UniProtKB:P68871
ChainResidueDetails
BSER44
DSER44
ALYS40
CLYS7
CLYS11
CLYS40

site_idSWS_FT_FI5
Number of Residues4
DetailsMOD_RES: N6-acetyllysine => ECO:0000250|UniProtKB:P68871
ChainResidueDetails
BLYS59
BLYS82
DLYS59
DLYS82

site_idSWS_FT_FI6
Number of Residues2
DetailsMOD_RES: S-nitrosocysteine => ECO:0000250|UniProtKB:P68871
ChainResidueDetails
BCYS93
DCYS93

site_idSWS_FT_FI7
Number of Residues6
DetailsMOD_RES: Phosphoserine => ECO:0000250|UniProtKB:P01942
ChainResidueDetails
ASER102
ASER124
ASER138
CSER102
CSER124
CSER138

site_idSWS_FT_FI8
Number of Residues6
DetailsMOD_RES: Phosphothreonine => ECO:0000250|UniProtKB:P01942
ChainResidueDetails
ATHR108
ATHR134
ATHR137
CTHR108
CTHR134
CTHR137

223790

PDB entries from 2024-08-14

PDB statisticsPDBj update infoContact PDBjnumon