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4MQK

Carbonmonoxy Structure of the Human Fetal Hemoglobin Mutant HbF Toms River alphawtgammaV67M

Functional Information from GO Data
ChainGOidnamespacecontents
A0004601molecular_functionperoxidase activity
A0005344molecular_functionoxygen carrier activity
A0005506molecular_functioniron ion binding
A0005515molecular_functionprotein binding
A0005576cellular_componentextracellular region
A0005615cellular_componentextracellular space
A0005829cellular_componentcytosol
A0005833cellular_componenthemoglobin complex
A0006954biological_processinflammatory response
A0015670biological_processcarbon dioxide transport
A0015671biological_processoxygen transport
A0016020cellular_componentmembrane
A0019825molecular_functionoxygen binding
A0020037molecular_functionheme binding
A0030185biological_processnitric oxide transport
A0031720molecular_functionhaptoglobin binding
A0031838cellular_componenthaptoglobin-hemoglobin complex
A0042542biological_processresponse to hydrogen peroxide
A0042744biological_processhydrogen peroxide catabolic process
A0046872molecular_functionmetal ion binding
A0048821biological_processerythrocyte development
A0070062cellular_componentextracellular exosome
A0071682cellular_componentendocytic vesicle lumen
A0072562cellular_componentblood microparticle
A0098869biological_processcellular oxidant detoxification
B0005344molecular_functionoxygen carrier activity
B0005515molecular_functionprotein binding
B0005829cellular_componentcytosol
B0005833cellular_componenthemoglobin complex
B0015670biological_processcarbon dioxide transport
B0015671biological_processoxygen transport
B0019825molecular_functionoxygen binding
B0020037molecular_functionheme binding
B0031721molecular_functionhemoglobin alpha binding
B0031838cellular_componenthaptoglobin-hemoglobin complex
B0046872molecular_functionmetal ion binding
B0048821biological_processerythrocyte development
B0072562cellular_componentblood microparticle
C0004601molecular_functionperoxidase activity
C0005344molecular_functionoxygen carrier activity
C0005506molecular_functioniron ion binding
C0005515molecular_functionprotein binding
C0005576cellular_componentextracellular region
C0005615cellular_componentextracellular space
C0005829cellular_componentcytosol
C0005833cellular_componenthemoglobin complex
C0006954biological_processinflammatory response
C0015670biological_processcarbon dioxide transport
C0015671biological_processoxygen transport
C0016020cellular_componentmembrane
C0019825molecular_functionoxygen binding
C0020037molecular_functionheme binding
C0030185biological_processnitric oxide transport
C0031720molecular_functionhaptoglobin binding
C0031838cellular_componenthaptoglobin-hemoglobin complex
C0042542biological_processresponse to hydrogen peroxide
C0042744biological_processhydrogen peroxide catabolic process
C0046872molecular_functionmetal ion binding
C0048821biological_processerythrocyte development
C0070062cellular_componentextracellular exosome
C0071682cellular_componentendocytic vesicle lumen
C0072562cellular_componentblood microparticle
C0098869biological_processcellular oxidant detoxification
D0005344molecular_functionoxygen carrier activity
D0005515molecular_functionprotein binding
D0005829cellular_componentcytosol
D0005833cellular_componenthemoglobin complex
D0015670biological_processcarbon dioxide transport
D0015671biological_processoxygen transport
D0019825molecular_functionoxygen binding
D0020037molecular_functionheme binding
D0031721molecular_functionhemoglobin alpha binding
D0031838cellular_componenthaptoglobin-hemoglobin complex
D0046872molecular_functionmetal ion binding
D0048821biological_processerythrocyte development
D0072562cellular_componentblood microparticle
E0004601molecular_functionperoxidase activity
E0005344molecular_functionoxygen carrier activity
E0005506molecular_functioniron ion binding
E0005515molecular_functionprotein binding
E0005576cellular_componentextracellular region
E0005615cellular_componentextracellular space
E0005829cellular_componentcytosol
E0005833cellular_componenthemoglobin complex
E0006954biological_processinflammatory response
E0015670biological_processcarbon dioxide transport
E0015671biological_processoxygen transport
E0016020cellular_componentmembrane
E0019825molecular_functionoxygen binding
E0020037molecular_functionheme binding
E0030185biological_processnitric oxide transport
E0031720molecular_functionhaptoglobin binding
E0031838cellular_componenthaptoglobin-hemoglobin complex
E0042542biological_processresponse to hydrogen peroxide
E0042744biological_processhydrogen peroxide catabolic process
E0046872molecular_functionmetal ion binding
E0048821biological_processerythrocyte development
E0070062cellular_componentextracellular exosome
E0071682cellular_componentendocytic vesicle lumen
E0072562cellular_componentblood microparticle
E0098869biological_processcellular oxidant detoxification
F0005344molecular_functionoxygen carrier activity
F0005515molecular_functionprotein binding
F0005829cellular_componentcytosol
F0005833cellular_componenthemoglobin complex
F0015670biological_processcarbon dioxide transport
F0015671biological_processoxygen transport
F0019825molecular_functionoxygen binding
F0020037molecular_functionheme binding
F0031721molecular_functionhemoglobin alpha binding
F0031838cellular_componenthaptoglobin-hemoglobin complex
F0046872molecular_functionmetal ion binding
F0048821biological_processerythrocyte development
F0072562cellular_componentblood microparticle
G0004601molecular_functionperoxidase activity
G0005344molecular_functionoxygen carrier activity
G0005506molecular_functioniron ion binding
G0005515molecular_functionprotein binding
G0005576cellular_componentextracellular region
G0005615cellular_componentextracellular space
G0005829cellular_componentcytosol
G0005833cellular_componenthemoglobin complex
G0006954biological_processinflammatory response
G0015670biological_processcarbon dioxide transport
G0015671biological_processoxygen transport
G0016020cellular_componentmembrane
G0019825molecular_functionoxygen binding
G0020037molecular_functionheme binding
G0030185biological_processnitric oxide transport
G0031720molecular_functionhaptoglobin binding
G0031838cellular_componenthaptoglobin-hemoglobin complex
G0042542biological_processresponse to hydrogen peroxide
G0042744biological_processhydrogen peroxide catabolic process
G0046872molecular_functionmetal ion binding
G0048821biological_processerythrocyte development
G0070062cellular_componentextracellular exosome
G0071682cellular_componentendocytic vesicle lumen
G0072562cellular_componentblood microparticle
G0098869biological_processcellular oxidant detoxification
H0005344molecular_functionoxygen carrier activity
H0005515molecular_functionprotein binding
H0005829cellular_componentcytosol
H0005833cellular_componenthemoglobin complex
H0015670biological_processcarbon dioxide transport
H0015671biological_processoxygen transport
H0019825molecular_functionoxygen binding
H0020037molecular_functionheme binding
H0031721molecular_functionhemoglobin alpha binding
H0031838cellular_componenthaptoglobin-hemoglobin complex
H0046872molecular_functionmetal ion binding
H0048821biological_processerythrocyte development
H0072562cellular_componentblood microparticle
Functional Information from PDB Data
site_idAC1
Number of Residues20
DetailsBINDING SITE FOR RESIDUE HEM A 201
ChainResidue
ATYR42
APHE98
ALEU101
ALEU136
ACMO202
AHOH310
AHOH312
AHOH318
GSER3
GALA5
HSER50
APHE43
HSER52
AHIS58
ALYS61
ALEU86
AHIS87
ALEU91
AVAL93
AASN97

site_idAC2
Number of Residues3
DetailsBINDING SITE FOR RESIDUE CMO A 202
ChainResidue
AHIS58
AVAL62
AHEM201

site_idAC3
Number of Residues15
DetailsBINDING SITE FOR RESIDUE HEM B 201
ChainResidue
BPHE41
BPHE42
BHIS63
BLYS66
BMET67
BSER70
BLEU91
BHIS92
BLEU96
BASN102
BLEU106
BVAL137
BLEU141
BCMO202
DLYS65

site_idAC4
Number of Residues3
DetailsBINDING SITE FOR RESIDUE CMO B 202
ChainResidue
BHIS63
BMET67
BHEM201

site_idAC5
Number of Residues22
DetailsBINDING SITE FOR RESIDUE HEM C 201
ChainResidue
CTYR42
CPHE43
CPHE46
CHIS58
CLYS61
CLEU83
CLEU86
CHIS87
CLEU91
CASN97
CPHE98
CLEU101
CLEU136
CCMO202
CHOH315
CHOH329
CHOH343
ESER3
EALA5
FSER50
FSER52
FHOH306

site_idAC6
Number of Residues4
DetailsBINDING SITE FOR RESIDUE CMO C 202
ChainResidue
CLEU29
CHIS58
CVAL62
CHEM201

site_idAC7
Number of Residues14
DetailsBINDING SITE FOR RESIDUE HEM D 201
ChainResidue
DPHE41
DPHE42
DHIS63
DLYS66
DMET67
DLEU91
DHIS92
DLEU96
DASN102
DPHE103
DLEU106
DVAL137
DLEU141
DCMO202

site_idAC8
Number of Residues3
DetailsBINDING SITE FOR RESIDUE CMO D 202
ChainResidue
DHIS63
DMET67
DHEM201

site_idAC9
Number of Residues13
DetailsBINDING SITE FOR RESIDUE HEM E 201
ChainResidue
ETYR42
EPHE43
EPHE46
EHIS58
ELYS61
EHIS87
ELEU91
EASN97
EPHE98
ELEU101
EVAL132
EHOH325
FLYS76

site_idBC1
Number of Residues15
DetailsBINDING SITE FOR RESIDUE HEM F 201
ChainResidue
FHIS63
FLYS66
FSER70
FLEU88
FLEU91
FHIS92
FLEU96
FASN102
FPHE103
FLEU106
FVAL137
FLEU141
FCMO202
FPHE41
FPHE42

site_idBC2
Number of Residues3
DetailsBINDING SITE FOR RESIDUE CMO F 202
ChainResidue
FHIS63
FMET67
FHEM201

site_idBC3
Number of Residues15
DetailsBINDING SITE FOR RESIDUE HEM G 201
ChainResidue
GTYR42
GPHE43
GPHE46
GHIS58
GLYS61
GLEU83
GLEU86
GHIS87
GASN97
GPHE98
GLEU101
GLEU136
GHOH329
GHOH330
HHIS77

site_idBC4
Number of Residues16
DetailsBINDING SITE FOR RESIDUE HEM H 201
ChainResidue
GASN78
HPHE41
HPHE42
HHIS63
HLYS66
HMET67
HSER70
HLEU88
HLEU91
HHIS92
HLYS95
HLEU96
HASN102
HLEU106
HLEU141
HCMO202

site_idBC5
Number of Residues3
DetailsBINDING SITE FOR RESIDUE CMO H 202
ChainResidue
HHIS63
HMET67
HHEM201

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues32
DetailsPeptide: {"description":"Hemopressin","featureId":"PRO_0000455882","evidences":[{"source":"PubMed","id":"18077343","evidenceCode":"ECO:0000305"}]}
ChainResidueDetails

site_idSWS_FT_FI2
Number of Residues856
DetailsDomain: {"description":"Globin","evidences":[{"source":"PROSITE-ProRule","id":"PRU00238","evidenceCode":"ECO:0000255"}]}
ChainResidueDetails

site_idSWS_FT_FI3
Number of Residues4
DetailsBinding site: {"evidences":[{"source":"PROSITE-ProRule","id":"PRU00238","evidenceCode":"ECO:0000255"}]}
ChainResidueDetails

site_idSWS_FT_FI4
Number of Residues4
DetailsBinding site: {"description":"proximal binding residue","evidences":[{"source":"PROSITE-ProRule","id":"PRU00238","evidenceCode":"ECO:0000255"}]}
ChainResidueDetails

site_idSWS_FT_FI5
Number of Residues56
DetailsSite: {"description":"(Microbial infection) Cleavage; by N.americanus apr-2","evidences":[{"source":"PubMed","id":"12552433","evidenceCode":"ECO:0000269"}]}
ChainResidueDetails

site_idSWS_FT_FI6
Number of Residues20
DetailsSite: {"description":"Not glycated","evidences":[{"source":"PubMed","id":"7358733","evidenceCode":"ECO:0000269"}]}
ChainResidueDetails

site_idSWS_FT_FI7
Number of Residues12
DetailsModified residue: {"description":"Phosphoserine","evidences":[{"source":"PubMed","id":"24275569","evidenceCode":"ECO:0007744"}]}
ChainResidueDetails

site_idSWS_FT_FI8
Number of Residues12
DetailsModified residue: {"description":"N6-succinyllysine; alternate","evidences":[{"source":"UniProtKB","id":"P01942","evidenceCode":"ECO:0000250"}]}
ChainResidueDetails

site_idSWS_FT_FI9
Number of Residues4
DetailsModified residue: {"description":"Phosphothreonine","evidences":[{"source":"PubMed","id":"24275569","evidenceCode":"ECO:0007744"}]}
ChainResidueDetails

site_idSWS_FT_FI10
Number of Residues4
DetailsModified residue: {"description":"N6-succinyllysine","evidences":[{"source":"UniProtKB","id":"P01942","evidenceCode":"ECO:0000250"}]}
ChainResidueDetails

site_idSWS_FT_FI11
Number of Residues4
DetailsModified residue: {"description":"Phosphotyrosine","evidences":[{"source":"PubMed","id":"24275569","evidenceCode":"ECO:0007744"}]}
ChainResidueDetails

site_idSWS_FT_FI12
Number of Residues16
DetailsModified residue: {"description":"Phosphoserine","evidences":[{"source":"UniProtKB","id":"P01942","evidenceCode":"ECO:0000250"}]}
ChainResidueDetails

site_idSWS_FT_FI13
Number of Residues12
DetailsModified residue: {"description":"Phosphothreonine","evidences":[{"source":"UniProtKB","id":"P01942","evidenceCode":"ECO:0000250"}]}
ChainResidueDetails

site_idSWS_FT_FI14
Number of Residues12
DetailsGlycosylation: {"description":"N-linked (Glc) (glycation) lysine; alternate","evidences":[{"source":"PubMed","id":"7358733","evidenceCode":"ECO:0000269"}]}
ChainResidueDetails

site_idSWS_FT_FI15
Number of Residues4
DetailsGlycosylation: {"description":"N-linked (Glc) (glycation) lysine","evidences":[{"source":"PubMed","id":"7358733","evidenceCode":"ECO:0000269"}]}
ChainResidueDetails

site_idSWS_FT_FI16
Number of Residues4
DetailsBinding site: {"description":"distal binding residue","evidences":[{"source":"UniProtKB","id":"P80044","evidenceCode":"ECO:0000250"}]}
ChainResidueDetails

site_idSWS_FT_FI17
Number of Residues4
DetailsBinding site: {"description":"proximal binding residue","evidences":[{"source":"PubMed","id":"881729","evidenceCode":"ECO:0000269"},{"source":"PDB","id":"1FDH","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"4MQJ","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"4MQK","evidenceCode":"ECO:0007744"}]}
ChainResidueDetails

site_idSWS_FT_FI18
Number of Residues4
DetailsModified residue: {"description":"Phosphothreonine","evidences":[{"source":"UniProtKB","id":"P68871","evidenceCode":"ECO:0000250"}]}
ChainResidueDetails

site_idSWS_FT_FI19
Number of Residues24
DetailsModified residue: {"description":"Phosphoserine","evidences":[{"source":"PubMed","id":"23186163","evidenceCode":"ECO:0007744"}]}
ChainResidueDetails

site_idSWS_FT_FI20
Number of Residues8
DetailsModified residue: {"description":"N6-acetyllysine","evidences":[{"source":"UniProtKB","id":"P68871","evidenceCode":"ECO:0000250"}]}
ChainResidueDetails

site_idSWS_FT_FI21
Number of Residues4
DetailsModified residue: {"description":"S-nitrosocysteine","evidences":[{"source":"UniProtKB","id":"P68871","evidenceCode":"ECO:0000250"}]}
ChainResidueDetails

239492

PDB entries from 2025-07-30

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