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<entry dataset="Swiss-Prot" created="2003-11-21" modified="2026-09-02" version="142" xmlns="http://uniprot.org/uniprot">
  <accession>Q9T9W1</accession>
  <name>COX1_PANTR</name>
  <protein>
    <recommendedName>
      <fullName>Cytochrome c oxidase subunit 1</fullName>
      <ecNumber>7.1.1.9</ecNumber>
    </recommendedName>
    <alternativeName>
      <fullName>Cytochrome c oxidase polypeptide I</fullName>
    </alternativeName>
  </protein>
  <gene>
    <name type="primary">MT-CO1</name>
    <name type="synonym">COI</name>
    <name type="synonym">COXI</name>
    <name type="synonym">MTCO1</name>
  </gene>
  <organism>
    <name type="scientific">Pan troglodytes</name>
    <name type="common">Chimpanzee</name>
    <dbReference type="NCBI Taxonomy" id="9598"/>
    <lineage>
      <taxon>Eukaryota</taxon>
      <taxon>Metazoa</taxon>
      <taxon>Chordata</taxon>
      <taxon>Craniata</taxon>
      <taxon>Vertebrata</taxon>
      <taxon>Euteleostomi</taxon>
      <taxon>Mammalia</taxon>
      <taxon>Eutheria</taxon>
      <taxon>Euarchontoglires</taxon>
      <taxon>Primates</taxon>
      <taxon>Haplorrhini</taxon>
      <taxon>Catarrhini</taxon>
      <taxon>Hominidae</taxon>
      <taxon>Pan</taxon>
    </lineage>
  </organism>
  <geneLocation type="mitochondrion"/>
  <reference key="1">
    <citation type="journal article" date="1995" name="Proc. Natl. Acad. Sci. U.S.A." volume="92" first="532" last="536">
      <title>Recent African origin of modern humans revealed by complete sequences of hominoid mitochondrial DNAs.</title>
      <authorList>
        <person name="Horai S."/>
        <person name="Hayasaka K."/>
        <person name="Kondo R."/>
        <person name="Tsugane K."/>
        <person name="Takahata N."/>
      </authorList>
      <dbReference type="PubMed" id="7530363"/>
      <dbReference type="DOI" id="10.1073/pnas.92.2.532"/>
    </citation>
    <scope>NUCLEOTIDE SEQUENCE [GENOMIC DNA]</scope>
  </reference>
  <comment type="function">
    <text evidence="3">Component of the cytochrome c oxidase, the last enzyme in the mitochondrial electron transport chain which drives oxidative phosphorylation. The respiratory chain contains 3 multisubunit complexes succinate dehydrogenase (complex II, CII), ubiquinol-cytochrome c oxidoreductase (cytochrome b-c1 complex, complex III, CIII) and cytochrome c oxidase (complex IV, CIV), that cooperate to transfer electrons derived from NADH and succinate to molecular oxygen, creating an electrochemical gradient over the inner membrane that drives transmembrane transport and the ATP synthase. Cytochrome c oxidase is the component of the respiratory chain that catalyzes the reduction of oxygen to water. Electrons originating from reduced cytochrome c in the intermembrane space (IMS) are transferred via the dinuclear copper A center (CU(A)) of subunit 2 and heme A of subunit 1 to the active site in subunit 1, a binuclear center (BNC) formed by heme A3 and copper B (CU(B)). The BNC reduces molecular oxygen to 2 water molecules using 4 electrons from cytochrome c in the IMS and 4 protons from the mitochondrial matrix.</text>
  </comment>
  <comment type="catalytic activity">
    <reaction evidence="3">
      <text>4 Fe(II)-[cytochrome c] + O2 + 8 H(+)(in) = 4 Fe(III)-[cytochrome c] + 2 H2O + 4 H(+)(out)</text>
      <dbReference type="Rhea" id="RHEA:11436"/>
      <dbReference type="Rhea" id="RHEA-COMP:10350"/>
      <dbReference type="Rhea" id="RHEA-COMP:14399"/>
      <dbReference type="ChEBI" id="CHEBI:15377"/>
      <dbReference type="ChEBI" id="CHEBI:15378"/>
      <dbReference type="ChEBI" id="CHEBI:15379"/>
      <dbReference type="ChEBI" id="CHEBI:29033"/>
      <dbReference type="ChEBI" id="CHEBI:29034"/>
      <dbReference type="EC" id="7.1.1.9"/>
    </reaction>
    <physiologicalReaction direction="left-to-right" evidence="3">
      <dbReference type="Rhea" id="RHEA:11437"/>
    </physiologicalReaction>
  </comment>
  <comment type="cofactor">
    <cofactor evidence="2">
      <name>heme</name>
      <dbReference type="ChEBI" id="CHEBI:30413"/>
    </cofactor>
    <text evidence="2">Binds 2 heme A groups non-covalently per subunit.</text>
  </comment>
  <comment type="cofactor">
    <cofactor evidence="2">
      <name>Cu cation</name>
      <dbReference type="ChEBI" id="CHEBI:23378"/>
    </cofactor>
    <text evidence="2">Binds a copper B center.</text>
  </comment>
  <comment type="pathway">
    <text evidence="3">Energy metabolism; oxidative phosphorylation.</text>
  </comment>
  <comment type="subunit">
    <text evidence="1 2">Component of the cytochrome c oxidase (complex IV, CIV), a multisubunit enzyme composed of 14 subunits. The complex is composed of a catalytic core of 3 subunits MT-CO1, MT-CO2 and MT-CO3, encoded in the mitochondrial DNA, and 11 supernumerary subunits COX4I, COX5A, COX5B, COX6A, COX6B, COX6C, COX7A, COX7B, COX7C, COX8 and COXFA4, which are encoded in the nuclear genome. The complex exists as a monomer or a dimer and forms supercomplexes (SCs) in the inner mitochondrial membrane with NADH-ubiquinone oxidoreductase (complex I, CI) and ubiquinol-cytochrome c oxidoreductase (cytochrome b-c1 complex, complex III, CIII), resulting in different assemblies (supercomplex SCI(1)III(2)IV(1) and megacomplex MCI(2)III(2)IV(2)) (By similarity). As a newly synthesized protein, rapidly incorporates into a multi-subunit assembly intermediate in the inner membrane, called MITRAC (mitochondrial translation regulation assembly intermediate of cytochrome c oxidase) complex, whose core components are COA3/MITRAC12 and COX14. Within the MITRAC complex, interacts with COA3 and with SMIM20/MITRAC7; the interaction with SMIM20 stabilizes the newly synthesized MT-CO1 and prevents its premature turnover. Interacts with TMEM177 in a COX20-dependent manner (By similarity).</text>
  </comment>
  <comment type="subcellular location">
    <subcellularLocation>
      <location evidence="2">Mitochondrion inner membrane</location>
      <topology evidence="2">Multi-pass membrane protein</topology>
    </subcellularLocation>
  </comment>
  <comment type="similarity">
    <text evidence="4">Belongs to the heme-copper respiratory oxidase family.</text>
  </comment>
  <dbReference type="EC" id="7.1.1.9"/>
  <dbReference type="EMBL" id="D38113">
    <property type="protein sequence ID" value="BAA85270.1"/>
    <property type="molecule type" value="Genomic_DNA"/>
  </dbReference>
  <dbReference type="AlphaFoldDB" id="Q9T9W1"/>
  <dbReference type="SMR" id="Q9T9W1"/>
  <dbReference type="FunCoup" id="Q9T9W1">
    <property type="interactions" value="218"/>
  </dbReference>
  <dbReference type="STRING" id="9598.ENSPTRP00000061408"/>
  <dbReference type="PaxDb" id="9598-ENSPTRP00000061408"/>
  <dbReference type="Ensembl" id="ENSPTRT00000076402.1">
    <property type="protein sequence ID" value="ENSPTRP00000061408.1"/>
    <property type="gene ID" value="ENSPTRG00000042657.1"/>
  </dbReference>
  <dbReference type="KEGG" id="ptr:807866"/>
  <dbReference type="VGNC" id="VGNC:11714">
    <property type="gene designation" value="MT-CO1"/>
  </dbReference>
  <dbReference type="eggNOG" id="KOG4769">
    <property type="taxonomic scope" value="Eukaryota"/>
  </dbReference>
  <dbReference type="GeneTree" id="ENSGT00390000001518"/>
  <dbReference type="HOGENOM" id="CLU_011899_7_3_1"/>
  <dbReference type="InParanoid" id="Q9T9W1"/>
  <dbReference type="OMA" id="WAMMSIG"/>
  <dbReference type="UniPathway" id="UPA00705"/>
  <dbReference type="Proteomes" id="UP000002277">
    <property type="component" value="Mitochondrion"/>
  </dbReference>
  <dbReference type="Bgee" id="ENSPTRG00000042657">
    <property type="expression patterns" value="Expressed in hindlimb stylopod muscle and 20 other cell types or tissues"/>
  </dbReference>
  <dbReference type="GO" id="GO:0005743">
    <property type="term" value="C:mitochondrial inner membrane"/>
    <property type="evidence" value="ECO:0000250"/>
    <property type="project" value="UniProtKB"/>
  </dbReference>
  <dbReference type="GO" id="GO:0045277">
    <property type="term" value="C:respiratory chain complex IV"/>
    <property type="evidence" value="ECO:0000250"/>
    <property type="project" value="UniProtKB"/>
  </dbReference>
  <dbReference type="GO" id="GO:0004129">
    <property type="term" value="F:cytochrome-c oxidase activity"/>
    <property type="evidence" value="ECO:0000250"/>
    <property type="project" value="UniProtKB"/>
  </dbReference>
  <dbReference type="GO" id="GO:0020037">
    <property type="term" value="F:heme binding"/>
    <property type="evidence" value="ECO:0000501"/>
    <property type="project" value="InterPro"/>
  </dbReference>
  <dbReference type="GO" id="GO:0009060">
    <property type="term" value="P:aerobic respiration"/>
    <property type="evidence" value="ECO:0000318"/>
    <property type="project" value="GO_Central"/>
  </dbReference>
  <dbReference type="GO" id="GO:0006119">
    <property type="term" value="P:oxidative phosphorylation"/>
    <property type="evidence" value="ECO:0000501"/>
    <property type="project" value="UniProtKB-UniPathway"/>
  </dbReference>
  <dbReference type="GO" id="GO:0022904">
    <property type="term" value="P:respiratory electron transport chain"/>
    <property type="evidence" value="ECO:0000318"/>
    <property type="project" value="GO_Central"/>
  </dbReference>
  <dbReference type="CDD" id="cd01663">
    <property type="entry name" value="Cyt_c_Oxidase_I"/>
    <property type="match status" value="1"/>
  </dbReference>
  <dbReference type="FunFam" id="1.20.210.10:FF:000001">
    <property type="entry name" value="Cytochrome c oxidase subunit 1"/>
    <property type="match status" value="1"/>
  </dbReference>
  <dbReference type="Gene3D" id="1.20.210.10">
    <property type="entry name" value="Cytochrome c oxidase-like, subunit I domain"/>
    <property type="match status" value="1"/>
  </dbReference>
  <dbReference type="InterPro" id="IPR023616">
    <property type="entry name" value="Cyt_c_oxase-like_su1_dom"/>
  </dbReference>
  <dbReference type="InterPro" id="IPR036927">
    <property type="entry name" value="Cyt_c_oxase-like_su1_sf"/>
  </dbReference>
  <dbReference type="InterPro" id="IPR000883">
    <property type="entry name" value="Cyt_C_Oxase_1"/>
  </dbReference>
  <dbReference type="InterPro" id="IPR023615">
    <property type="entry name" value="Cyt_c_Oxase_su1_BS"/>
  </dbReference>
  <dbReference type="InterPro" id="IPR033944">
    <property type="entry name" value="Cyt_c_oxase_su1_dom"/>
  </dbReference>
  <dbReference type="PANTHER" id="PTHR10422">
    <property type="entry name" value="CYTOCHROME C OXIDASE SUBUNIT 1"/>
    <property type="match status" value="1"/>
  </dbReference>
  <dbReference type="PANTHER" id="PTHR10422:SF18">
    <property type="entry name" value="CYTOCHROME C OXIDASE SUBUNIT 1"/>
    <property type="match status" value="1"/>
  </dbReference>
  <dbReference type="Pfam" id="PF00115">
    <property type="entry name" value="COX1"/>
    <property type="match status" value="1"/>
  </dbReference>
  <dbReference type="PRINTS" id="PR01165">
    <property type="entry name" value="CYCOXIDASEI"/>
  </dbReference>
  <dbReference type="SUPFAM" id="SSF81442">
    <property type="entry name" value="Cytochrome c oxidase subunit I-like"/>
    <property type="match status" value="1"/>
  </dbReference>
  <dbReference type="PROSITE" id="PS50855">
    <property type="entry name" value="COX1"/>
    <property type="match status" value="1"/>
  </dbReference>
  <dbReference type="PROSITE" id="PS00077">
    <property type="entry name" value="COX1_CUB"/>
    <property type="match status" value="1"/>
  </dbReference>
  <proteinExistence type="inferred from homology"/>
  <keyword id="KW-0106">Calcium</keyword>
  <keyword id="KW-0186">Copper</keyword>
  <keyword id="KW-0249">Electron transport</keyword>
  <keyword id="KW-0349">Heme</keyword>
  <keyword id="KW-0408">Iron</keyword>
  <keyword id="KW-0460">Magnesium</keyword>
  <keyword id="KW-0472">Membrane</keyword>
  <keyword id="KW-0479">Metal-binding</keyword>
  <keyword id="KW-0496">Mitochondrion</keyword>
  <keyword id="KW-0999">Mitochondrion inner membrane</keyword>
  <keyword id="KW-1185">Reference proteome</keyword>
  <keyword id="KW-0679">Respiratory chain</keyword>
  <keyword id="KW-0915">Sodium</keyword>
  <keyword id="KW-1278">Translocase</keyword>
  <keyword id="KW-0812">Transmembrane</keyword>
  <keyword id="KW-1133">Transmembrane helix</keyword>
  <keyword id="KW-0813">Transport</keyword>
  <feature type="chain" id="PRO_0000183379" description="Cytochrome c oxidase subunit 1">
    <location>
      <begin position="1"/>
      <end position="513"/>
    </location>
  </feature>
  <feature type="topological domain" description="Mitochondrial matrix" evidence="2">
    <location>
      <begin position="1"/>
      <end position="11"/>
    </location>
  </feature>
  <feature type="transmembrane region" description="Helical; Name=I" evidence="2">
    <location>
      <begin position="12"/>
      <end position="40"/>
    </location>
  </feature>
  <feature type="topological domain" description="Mitochondrial intermembrane" evidence="2">
    <location>
      <begin position="41"/>
      <end position="50"/>
    </location>
  </feature>
  <feature type="transmembrane region" description="Helical; Name=II" evidence="2">
    <location>
      <begin position="51"/>
      <end position="86"/>
    </location>
  </feature>
  <feature type="topological domain" description="Mitochondrial matrix" evidence="2">
    <location>
      <begin position="87"/>
      <end position="94"/>
    </location>
  </feature>
  <feature type="transmembrane region" description="Helical; Name=III" evidence="2">
    <location>
      <begin position="95"/>
      <end position="117"/>
    </location>
  </feature>
  <feature type="topological domain" description="Mitochondrial intermembrane" evidence="2">
    <location>
      <begin position="118"/>
      <end position="140"/>
    </location>
  </feature>
  <feature type="transmembrane region" description="Helical; Name=IV" evidence="2">
    <location>
      <begin position="141"/>
      <end position="170"/>
    </location>
  </feature>
  <feature type="topological domain" description="Mitochondrial matrix" evidence="2">
    <location>
      <begin position="171"/>
      <end position="182"/>
    </location>
  </feature>
  <feature type="transmembrane region" description="Helical; Name=V" evidence="2">
    <location>
      <begin position="183"/>
      <end position="212"/>
    </location>
  </feature>
  <feature type="topological domain" description="Mitochondrial intermembrane" evidence="2">
    <location>
      <begin position="213"/>
      <end position="227"/>
    </location>
  </feature>
  <feature type="transmembrane region" description="Helical; Name=VI" evidence="2">
    <location>
      <begin position="228"/>
      <end position="261"/>
    </location>
  </feature>
  <feature type="topological domain" description="Mitochondrial matrix" evidence="2">
    <location>
      <begin position="262"/>
      <end position="269"/>
    </location>
  </feature>
  <feature type="transmembrane region" description="Helical; Name=VII" evidence="2">
    <location>
      <begin position="270"/>
      <end position="286"/>
    </location>
  </feature>
  <feature type="topological domain" description="Mitochondrial intermembrane" evidence="2">
    <location>
      <begin position="287"/>
      <end position="298"/>
    </location>
  </feature>
  <feature type="transmembrane region" description="Helical; Name=VIII" evidence="2">
    <location>
      <begin position="299"/>
      <end position="327"/>
    </location>
  </feature>
  <feature type="topological domain" description="Mitochondrial matrix" evidence="2">
    <location>
      <begin position="328"/>
      <end position="335"/>
    </location>
  </feature>
  <feature type="transmembrane region" description="Helical; Name=IX" evidence="2">
    <location>
      <begin position="336"/>
      <end position="357"/>
    </location>
  </feature>
  <feature type="topological domain" description="Mitochondrial intermembrane" evidence="2">
    <location>
      <begin position="358"/>
      <end position="370"/>
    </location>
  </feature>
  <feature type="transmembrane region" description="Helical; Name=X" evidence="2">
    <location>
      <begin position="371"/>
      <end position="400"/>
    </location>
  </feature>
  <feature type="topological domain" description="Mitochondrial matrix" evidence="2">
    <location>
      <begin position="401"/>
      <end position="406"/>
    </location>
  </feature>
  <feature type="transmembrane region" description="Helical; Name=XI" evidence="2">
    <location>
      <begin position="407"/>
      <end position="433"/>
    </location>
  </feature>
  <feature type="topological domain" description="Mitochondrial intermembrane" evidence="2">
    <location>
      <begin position="434"/>
      <end position="446"/>
    </location>
  </feature>
  <feature type="transmembrane region" description="Helical; Name=XII" evidence="2">
    <location>
      <begin position="447"/>
      <end position="478"/>
    </location>
  </feature>
  <feature type="topological domain" description="Mitochondrial matrix" evidence="2">
    <location>
      <begin position="479"/>
      <end position="513"/>
    </location>
  </feature>
  <feature type="binding site" evidence="2">
    <location>
      <position position="40"/>
    </location>
    <ligand>
      <name>Na(+)</name>
      <dbReference type="ChEBI" id="CHEBI:29101"/>
    </ligand>
  </feature>
  <feature type="binding site" evidence="2">
    <location>
      <position position="45"/>
    </location>
    <ligand>
      <name>Na(+)</name>
      <dbReference type="ChEBI" id="CHEBI:29101"/>
    </ligand>
  </feature>
  <feature type="binding site" description="axial binding residue" evidence="2">
    <location>
      <position position="61"/>
    </location>
    <ligand>
      <name>Fe(II)-heme a</name>
      <dbReference type="ChEBI" id="CHEBI:61715"/>
      <note>low-spin</note>
    </ligand>
    <ligandPart>
      <name>Fe</name>
      <dbReference type="ChEBI" id="CHEBI:18248"/>
    </ligandPart>
  </feature>
  <feature type="binding site" evidence="2">
    <location>
      <position position="240"/>
    </location>
    <ligand>
      <name>Cu cation</name>
      <dbReference type="ChEBI" id="CHEBI:23378"/>
      <label>B</label>
    </ligand>
  </feature>
  <feature type="binding site" evidence="2">
    <location>
      <position position="244"/>
    </location>
    <ligand>
      <name>O2</name>
      <dbReference type="ChEBI" id="CHEBI:15379"/>
    </ligand>
  </feature>
  <feature type="binding site" evidence="2">
    <location>
      <position position="290"/>
    </location>
    <ligand>
      <name>Cu cation</name>
      <dbReference type="ChEBI" id="CHEBI:23378"/>
      <label>B</label>
    </ligand>
  </feature>
  <feature type="binding site" evidence="2">
    <location>
      <position position="291"/>
    </location>
    <ligand>
      <name>Cu cation</name>
      <dbReference type="ChEBI" id="CHEBI:23378"/>
      <label>B</label>
    </ligand>
  </feature>
  <feature type="binding site" evidence="2">
    <location>
      <position position="368"/>
    </location>
    <ligand>
      <name>Mg(2+)</name>
      <dbReference type="ChEBI" id="CHEBI:18420"/>
      <note>ligand shared with MT-CO2</note>
    </ligand>
  </feature>
  <feature type="binding site" evidence="2">
    <location>
      <position position="369"/>
    </location>
    <ligand>
      <name>Mg(2+)</name>
      <dbReference type="ChEBI" id="CHEBI:18420"/>
      <note>ligand shared with MT-CO2</note>
    </ligand>
  </feature>
  <feature type="binding site" description="axial binding residue" evidence="2">
    <location>
      <position position="376"/>
    </location>
    <ligand>
      <name>heme a3</name>
      <dbReference type="ChEBI" id="CHEBI:83282"/>
      <note>high-spin</note>
    </ligand>
    <ligandPart>
      <name>Fe</name>
      <dbReference type="ChEBI" id="CHEBI:18248"/>
    </ligandPart>
  </feature>
  <feature type="binding site" description="axial binding residue" evidence="2">
    <location>
      <position position="378"/>
    </location>
    <ligand>
      <name>Fe(II)-heme a</name>
      <dbReference type="ChEBI" id="CHEBI:61715"/>
      <note>low-spin</note>
    </ligand>
    <ligandPart>
      <name>Fe</name>
      <dbReference type="ChEBI" id="CHEBI:18248"/>
    </ligandPart>
  </feature>
  <feature type="binding site" evidence="2">
    <location>
      <position position="441"/>
    </location>
    <ligand>
      <name>Na(+)</name>
      <dbReference type="ChEBI" id="CHEBI:29101"/>
    </ligand>
  </feature>
  <feature type="cross-link" description="1'-histidyl-3'-tyrosine (His-Tyr)" evidence="2">
    <location>
      <begin position="240"/>
      <end position="244"/>
    </location>
  </feature>
  <evidence type="ECO:0000250" key="1">
    <source>
      <dbReference type="UniProtKB" id="P00395"/>
    </source>
  </evidence>
  <evidence type="ECO:0000250" key="2">
    <source>
      <dbReference type="UniProtKB" id="P00396"/>
    </source>
  </evidence>
  <evidence type="ECO:0000250" key="3">
    <source>
      <dbReference type="UniProtKB" id="P00401"/>
    </source>
  </evidence>
  <evidence type="ECO:0000305" key="4"/>
  <sequence length="513" mass="56972" checksum="0C4EC1613FCD9E80" modified="2000-05-01" version="1">MFTDRWLFSTNHKDIGTLYLLFGAWAGVLGTALSLLIRAELGQPGNLLGNDHIYNVIVTAHAFVMIFFMVMPIMIGGFGNWLVPLMIGAPDMAFPRMNNMSFWLLPPSLLLLLASAMVEAGAGTGWTVYPPLAGNYSHPGASVDLTIFSLHLAGISSILGAINFITTIINMKPPAMTQYQTPLFVWSVLITAVLLLLSLPVLAAGITMLLTDRNLNTTFFDPAGGGDPILYQHLFWFFGHPEVYILILPGFGMISHIVTYYSGKKEPFGYMGMVWAMMSIGFLGFIVWAHHMFTVGMDVDTRAYFTSATMIIAIPTGVKVFSWLATLHGSNMKWSAAVLWALGFIFLFTVGGLTGIVLANSSLDIVLHDTYYVVAHFHYVLSMGAVFAIMGGFIHWFPLFSGYTLDQTYAKIQFAIMFIGVNLTFFPQHFLGLSGMPRRYSDYPDAYTTWNVLSSVGSFISLTAVMLMIFMIWEAFASKRKVLMVEEPSANLEWLYGCPPPYHTFEEPVYMKS</sequence>
</entry>
<copyright>
Copyrighted by the UniProt Consortium, see https://www.uniprot.org/terms Distributed under the Creative Commons Attribution (CC BY 4.0) License
</copyright>
</uniprot>