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9F2F

Carbonic anhydrase II variant with bound iron complex in space group R3 (ArPase)

This is a non-PDB format compatible entry.
Functional Information from GO Data
ChainGOidnamespacecontents
A0002009biological_processmorphogenesis of an epithelium
A0004064molecular_functionarylesterase activity
A0004089molecular_functioncarbonate dehydratase activity
A0005515molecular_functionprotein binding
A0005737cellular_componentcytoplasm
A0005829cellular_componentcytosol
A0005886cellular_componentplasma membrane
A0008270molecular_functionzinc ion binding
A0015670biological_processcarbon dioxide transport
A0016020cellular_componentmembrane
A0016829molecular_functionlyase activity
A0018820molecular_functioncyanamide hydratase activity
A0032230biological_processpositive regulation of synaptic transmission, GABAergic
A0032849biological_processpositive regulation of cellular pH reduction
A0038166biological_processangiotensin-activated signaling pathway
A0043209cellular_componentmyelin sheath
A0044070biological_processregulation of monoatomic anion transport
A0045177cellular_componentapical part of cell
A0046872molecular_functionmetal ion binding
A0046903biological_processsecretion
A0051453biological_processregulation of intracellular pH
A0070050biological_processneuron cellular homeostasis
A0070062cellular_componentextracellular exosome
A2001150biological_processpositive regulation of dipeptide transmembrane transport
A2001225biological_processregulation of chloride transport
B0002009biological_processmorphogenesis of an epithelium
B0004064molecular_functionarylesterase activity
B0004089molecular_functioncarbonate dehydratase activity
B0005515molecular_functionprotein binding
B0005737cellular_componentcytoplasm
B0005829cellular_componentcytosol
B0005886cellular_componentplasma membrane
B0008270molecular_functionzinc ion binding
B0015670biological_processcarbon dioxide transport
B0016020cellular_componentmembrane
B0016829molecular_functionlyase activity
B0018820molecular_functioncyanamide hydratase activity
B0032230biological_processpositive regulation of synaptic transmission, GABAergic
B0032849biological_processpositive regulation of cellular pH reduction
B0038166biological_processangiotensin-activated signaling pathway
B0043209cellular_componentmyelin sheath
B0044070biological_processregulation of monoatomic anion transport
B0045177cellular_componentapical part of cell
B0046872molecular_functionmetal ion binding
B0046903biological_processsecretion
B0051453biological_processregulation of intracellular pH
B0070050biological_processneuron cellular homeostasis
B0070062cellular_componentextracellular exosome
B2001150biological_processpositive regulation of dipeptide transmembrane transport
B2001225biological_processregulation of chloride transport
C0002009biological_processmorphogenesis of an epithelium
C0004064molecular_functionarylesterase activity
C0004089molecular_functioncarbonate dehydratase activity
C0005515molecular_functionprotein binding
C0005737cellular_componentcytoplasm
C0005829cellular_componentcytosol
C0005886cellular_componentplasma membrane
C0008270molecular_functionzinc ion binding
C0015670biological_processcarbon dioxide transport
C0016020cellular_componentmembrane
C0016829molecular_functionlyase activity
C0018820molecular_functioncyanamide hydratase activity
C0032230biological_processpositive regulation of synaptic transmission, GABAergic
C0032849biological_processpositive regulation of cellular pH reduction
C0038166biological_processangiotensin-activated signaling pathway
C0043209cellular_componentmyelin sheath
C0044070biological_processregulation of monoatomic anion transport
C0045177cellular_componentapical part of cell
C0046872molecular_functionmetal ion binding
C0046903biological_processsecretion
C0051453biological_processregulation of intracellular pH
C0070050biological_processneuron cellular homeostasis
C0070062cellular_componentextracellular exosome
C2001150biological_processpositive regulation of dipeptide transmembrane transport
C2001225biological_processregulation of chloride transport
D0002009biological_processmorphogenesis of an epithelium
D0004064molecular_functionarylesterase activity
D0004089molecular_functioncarbonate dehydratase activity
D0005515molecular_functionprotein binding
D0005737cellular_componentcytoplasm
D0005829cellular_componentcytosol
D0005886cellular_componentplasma membrane
D0008270molecular_functionzinc ion binding
D0015670biological_processcarbon dioxide transport
D0016020cellular_componentmembrane
D0016829molecular_functionlyase activity
D0018820molecular_functioncyanamide hydratase activity
D0032230biological_processpositive regulation of synaptic transmission, GABAergic
D0032849biological_processpositive regulation of cellular pH reduction
D0038166biological_processangiotensin-activated signaling pathway
D0043209cellular_componentmyelin sheath
D0044070biological_processregulation of monoatomic anion transport
D0045177cellular_componentapical part of cell
D0046872molecular_functionmetal ion binding
D0046903biological_processsecretion
D0051453biological_processregulation of intracellular pH
D0070050biological_processneuron cellular homeostasis
D0070062cellular_componentextracellular exosome
D2001150biological_processpositive regulation of dipeptide transmembrane transport
D2001225biological_processregulation of chloride transport
Functional Information from PROSITE/UniProt
site_idPS00162
Number of Residues17
DetailsALPHA_CA_1 Alpha-carbonic anhydrases signature. SEHtVdkkkYaaELHLV
ChainResidueDetails
ASER105-VAL121

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues4
DetailsACT_SITE: Proton donor/acceptor => ECO:0000305|PubMed:15667203, ECO:0000305|PubMed:17330962
ChainResidueDetails
AHIS64
BHIS64
CHIS64
DHIS64

site_idSWS_FT_FI2
Number of Residues4
DetailsBINDING: BINDING => ECO:0000269|PubMed:11076507, ECO:0000269|PubMed:12499545, ECO:0000269|PubMed:1336460, ECO:0000269|PubMed:1433293, ECO:0000269|PubMed:1909891, ECO:0000269|PubMed:19583303, ECO:0000269|PubMed:3151019, ECO:0000269|PubMed:3151020, ECO:0000269|PubMed:4621826, ECO:0000269|PubMed:7761440, ECO:0000269|PubMed:7803386, ECO:0000269|PubMed:7901850, ECO:0000269|PubMed:8218160, ECO:0000269|PubMed:8262987, ECO:0000269|PubMed:8331673, ECO:0000269|PubMed:8399159, ECO:0000269|PubMed:8431430, ECO:0000269|PubMed:8451242, ECO:0000269|PubMed:8482389, ECO:0000269|PubMed:8639494, ECO:0000269|PubMed:8987974, ECO:0000269|PubMed:9398308, ECO:0000269|PubMed:9865942
ChainResidueDetails
AHIS94
BHIS94
CHIS94
DHIS94

site_idSWS_FT_FI3
Number of Residues8
DetailsBINDING: BINDING => ECO:0000269|PubMed:11076507, ECO:0000269|PubMed:12499545, ECO:0000269|PubMed:1336460, ECO:0000269|PubMed:1433293, ECO:0000269|PubMed:1909891, ECO:0000269|PubMed:19583303, ECO:0000269|PubMed:3151019, ECO:0000269|PubMed:3151020, ECO:0000269|PubMed:7761440, ECO:0000269|PubMed:7803386, ECO:0000269|PubMed:7901850, ECO:0000269|PubMed:8218160, ECO:0000269|PubMed:8262987, ECO:0000269|PubMed:8331673, ECO:0000269|PubMed:8399159, ECO:0000269|PubMed:8431430, ECO:0000269|PubMed:8451242, ECO:0000269|PubMed:8482389, ECO:0000269|PubMed:8639494, ECO:0000269|PubMed:8987974, ECO:0000269|PubMed:9398308, ECO:0000269|PubMed:9865942
ChainResidueDetails
AHIS96
AHIS119
BHIS96
BHIS119
CHIS96
CHIS119
DHIS96
DHIS119

site_idSWS_FT_FI4
Number of Residues4
DetailsBINDING: BINDING => ECO:0000269|PubMed:10550681, ECO:0000269|PubMed:19520834
ChainResidueDetails
ATHR198
BTHR198
CTHR198
DTHR198

site_idSWS_FT_FI5
Number of Residues4
DetailsSITE: Fine-tunes the proton-transfer properties of H-64 => ECO:0000305|PubMed:17330962
ChainResidueDetails
ATYR7
BTYR7
CTYR7
DTYR7

site_idSWS_FT_FI6
Number of Residues8
DetailsSITE: Fine-tunes the proton-transfer properties of H-64; involved in the binding of some activators, including histamine and L-histidine => ECO:0000269|PubMed:16214338, ECO:0000269|PubMed:9265618, ECO:0000305|PubMed:17330962
ChainResidueDetails
AASN62
AASN67
BASN62
BASN67
CASN62
CASN67
DASN62
DASN67

site_idSWS_FT_FI7
Number of Residues4
DetailsSITE: Involved in the binding of some activators, including histamine and L-histidine => ECO:0000269|PubMed:16214338, ECO:0000269|PubMed:9265618, ECO:0000305|PubMed:17330962
ChainResidueDetails
AGLN92
BGLN92
CGLN92
DGLN92

site_idSWS_FT_FI8
Number of Residues4
DetailsMOD_RES: Phosphoserine => ECO:0000250|UniProtKB:P27139
ChainResidueDetails
AALA2
BALA2
CALA2
DALA2

site_idSWS_FT_FI9
Number of Residues8
DetailsMOD_RES: Phosphoserine => ECO:0007744|PubMed:24275569
ChainResidueDetails
ASER165
ASER172
BSER165
BSER172
CSER165
CSER172
DSER165
DSER172

Catalytic Information from CSA
site_idMCSA1
Number of Residues6
DetailsM-CSA 216
ChainResidueDetails
AHIS64hydrogen bond acceptor, hydrogen bond donor, proton acceptor, proton donor
AHIS94metal ligand
AHIS96metal ligand
AGLU106activator, electrostatic stabiliser, hydrogen bond acceptor
AHIS119metal ligand
ATHR198activator, electrostatic stabiliser, hydrogen bond acceptor, hydrogen bond donor, increase nucleophilicity

site_idMCSA2
Number of Residues6
DetailsM-CSA 216
ChainResidueDetails
BHIS64hydrogen bond acceptor, hydrogen bond donor, proton acceptor, proton donor
BHIS94metal ligand
BHIS96metal ligand
BGLU106activator, electrostatic stabiliser, hydrogen bond acceptor
BHIS119metal ligand
BTHR198activator, electrostatic stabiliser, hydrogen bond acceptor, hydrogen bond donor, increase nucleophilicity

site_idMCSA3
Number of Residues6
DetailsM-CSA 216
ChainResidueDetails
CHIS64hydrogen bond acceptor, hydrogen bond donor, proton acceptor, proton donor
CHIS94metal ligand
CHIS96metal ligand
CGLU106activator, electrostatic stabiliser, hydrogen bond acceptor
CHIS119metal ligand
CTHR198activator, electrostatic stabiliser, hydrogen bond acceptor, hydrogen bond donor, increase nucleophilicity

site_idMCSA4
Number of Residues6
DetailsM-CSA 216
ChainResidueDetails
DHIS64hydrogen bond acceptor, hydrogen bond donor, proton acceptor, proton donor
DHIS94metal ligand
DHIS96metal ligand
DGLU106activator, electrostatic stabiliser, hydrogen bond acceptor
DHIS119metal ligand
DTHR198activator, electrostatic stabiliser, hydrogen bond acceptor, hydrogen bond donor, increase nucleophilicity

237992

PDB entries from 2025-06-25

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