Electron Transport Chain (see tricarboxylic acid section for Complex II), cytochrome c oxidase assembly factor
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 15 |
NetGPI | no | yes: 0, no: 15 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005743 | mitochondrial inner membrane | 5 | 10 |
GO:0016020 | membrane | 2 | 15 |
GO:0019866 | organelle inner membrane | 4 | 10 |
GO:0031090 | organelle membrane | 3 | 10 |
GO:0031966 | mitochondrial membrane | 4 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 15 |
GO:0005737 | cytoplasm | 2 | 2 |
GO:0005739 | mitochondrion | 5 | 1 |
GO:0031974 | membrane-enclosed lumen | 2 | 1 |
GO:0031981 | nuclear lumen | 5 | 1 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0043233 | organelle lumen | 3 | 1 |
GO:0070013 | intracellular organelle lumen | 4 | 1 |
GO:0097014 | ciliary plasm | 5 | 1 |
GO:0099568 | cytoplasmic region | 3 | 1 |
Related structures:
AlphaFold database: A4HSB1
Term | Name | Level | Count |
---|---|---|---|
GO:0006873 | intracellular monoatomic ion homeostasis | 4 | 10 |
GO:0006875 | obsolete intracellular metal ion homeostasis | 6 | 10 |
GO:0006878 | intracellular copper ion homeostasis | 8 | 10 |
GO:0008535 | respiratory chain complex IV assembly | 7 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016043 | cellular component organization | 3 | 11 |
GO:0017004 | cytochrome complex assembly | 6 | 11 |
GO:0019725 | cellular homeostasis | 2 | 10 |
GO:0022607 | cellular component assembly | 4 | 11 |
GO:0030003 | intracellular monoatomic cation homeostasis | 5 | 10 |
GO:0042592 | homeostatic process | 3 | 10 |
GO:0043933 | protein-containing complex organization | 4 | 11 |
GO:0046916 | obsolete intracellular transition metal ion homeostasis | 7 | 10 |
GO:0048878 | chemical homeostasis | 4 | 10 |
GO:0050801 | monoatomic ion homeostasis | 5 | 10 |
GO:0055065 | obsolete metal ion homeostasis | 7 | 10 |
GO:0055070 | copper ion homeostasis | 9 | 10 |
GO:0055076 | obsolete transition metal ion homeostasis | 8 | 10 |
GO:0055080 | monoatomic cation homeostasis | 6 | 10 |
GO:0055082 | intracellular chemical homeostasis | 3 | 10 |
GO:0065003 | protein-containing complex assembly | 5 | 11 |
GO:0065007 | biological regulation | 1 | 10 |
GO:0065008 | regulation of biological quality | 2 | 10 |
GO:0071840 | cellular component organization or biogenesis | 2 | 11 |
GO:0098771 | inorganic ion homeostasis | 6 | 10 |
GO:0033108 | mitochondrial respiratory chain complex assembly | 6 | 2 |
GO:0033617 | mitochondrial cytochrome c oxidase assembly | 7 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 5 |
GO:0005488 | binding | 1 | 10 |
GO:0005507 | copper ion binding | 6 | 10 |
GO:0016491 | oxidoreductase activity | 2 | 5 |
GO:0016530 | metallochaperone activity | 2 | 10 |
GO:0016531 | copper chaperone activity | 3 | 10 |
GO:0043167 | ion binding | 2 | 10 |
GO:0043169 | cation binding | 3 | 10 |
GO:0046872 | metal ion binding | 4 | 10 |
GO:0046914 | transition metal ion binding | 5 | 10 |
GO:0140104 | molecular carrier activity | 1 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 208 | 210 | PF00675 | 0.433 |
CLV_NRD_NRD_1 | 35 | 37 | PF00675 | 0.415 |
CLV_NRD_NRD_1 | 62 | 64 | PF00675 | 0.499 |
CLV_PCSK_KEX2_1 | 117 | 119 | PF00082 | 0.564 |
CLV_PCSK_KEX2_1 | 208 | 210 | PF00082 | 0.503 |
CLV_PCSK_KEX2_1 | 35 | 37 | PF00082 | 0.415 |
CLV_PCSK_KEX2_1 | 62 | 64 | PF00082 | 0.519 |
CLV_PCSK_PC1ET2_1 | 117 | 119 | PF00082 | 0.499 |
CLV_PCSK_PC7_1 | 113 | 119 | PF00082 | 0.549 |
CLV_PCSK_SKI1_1 | 113 | 117 | PF00082 | 0.609 |
CLV_PCSK_SKI1_1 | 135 | 139 | PF00082 | 0.540 |
CLV_PCSK_SKI1_1 | 288 | 292 | PF00082 | 0.559 |
CLV_PCSK_SKI1_1 | 3 | 7 | PF00082 | 0.496 |
CLV_PCSK_SKI1_1 | 62 | 66 | PF00082 | 0.469 |
DEG_APCC_DBOX_1 | 208 | 216 | PF00400 | 0.222 |
DOC_CKS1_1 | 230 | 235 | PF01111 | 0.222 |
DOC_CYCLIN_yCln2_LP_2 | 138 | 144 | PF00134 | 0.222 |
DOC_MAPK_DCC_7 | 193 | 203 | PF00069 | 0.222 |
DOC_PP1_RVXF_1 | 274 | 281 | PF00149 | 0.270 |
DOC_USP7_MATH_1 | 122 | 126 | PF00917 | 0.418 |
DOC_USP7_MATH_1 | 239 | 243 | PF00917 | 0.222 |
DOC_USP7_MATH_1 | 39 | 43 | PF00917 | 0.635 |
DOC_WW_Pin1_4 | 229 | 234 | PF00397 | 0.249 |
DOC_WW_Pin1_4 | 35 | 40 | PF00397 | 0.676 |
DOC_WW_Pin1_4 | 53 | 58 | PF00397 | 0.721 |
LIG_14-3-3_CanoR_1 | 127 | 131 | PF00244 | 0.437 |
LIG_14-3-3_CanoR_1 | 181 | 189 | PF00244 | 0.317 |
LIG_AP2alpha_1 | 277 | 281 | PF02296 | 0.251 |
LIG_BRCT_BRCA1_1 | 159 | 163 | PF00533 | 0.253 |
LIG_deltaCOP1_diTrp_1 | 304 | 310 | PF00928 | 0.292 |
LIG_eIF4E_1 | 19 | 25 | PF01652 | 0.575 |
LIG_FHA_1 | 289 | 295 | PF00498 | 0.275 |
LIG_FHA_2 | 145 | 151 | PF00498 | 0.234 |
LIG_FHA_2 | 249 | 255 | PF00498 | 0.313 |
LIG_LIR_Gen_1 | 160 | 168 | PF02991 | 0.251 |
LIG_LIR_Gen_1 | 216 | 226 | PF02991 | 0.256 |
LIG_LIR_Gen_1 | 85 | 96 | PF02991 | 0.605 |
LIG_LIR_Nem_3 | 160 | 166 | PF02991 | 0.224 |
LIG_LIR_Nem_3 | 216 | 221 | PF02991 | 0.236 |
LIG_LIR_Nem_3 | 225 | 229 | PF02991 | 0.204 |
LIG_LIR_Nem_3 | 242 | 246 | PF02991 | 0.168 |
LIG_LIR_Nem_3 | 85 | 91 | PF02991 | 0.622 |
LIG_LIR_Nem_3 | 93 | 97 | PF02991 | 0.362 |
LIG_Pex14_1 | 161 | 165 | PF04695 | 0.265 |
LIG_Pex14_2 | 157 | 161 | PF04695 | 0.222 |
LIG_Pex14_2 | 164 | 168 | PF04695 | 0.222 |
LIG_Pex14_2 | 222 | 226 | PF04695 | 0.222 |
LIG_Pex14_2 | 277 | 281 | PF04695 | 0.251 |
LIG_REV1ctd_RIR_1 | 278 | 288 | PF16727 | 0.277 |
LIG_SH2_CRK | 247 | 251 | PF00017 | 0.222 |
LIG_SH2_CRK | 94 | 98 | PF00017 | 0.302 |
LIG_SH2_NCK_1 | 247 | 251 | PF00017 | 0.222 |
LIG_SH2_STAT5 | 119 | 122 | PF00017 | 0.342 |
LIG_SH2_STAT5 | 165 | 168 | PF00017 | 0.262 |
LIG_SH2_STAT5 | 218 | 221 | PF00017 | 0.265 |
LIG_SH2_STAT5 | 260 | 263 | PF00017 | 0.238 |
LIG_SH3_3 | 218 | 224 | PF00018 | 0.249 |
LIG_SH3_3 | 227 | 233 | PF00018 | 0.196 |
LIG_SH3_3 | 70 | 76 | PF00018 | 0.585 |
LIG_TRAF2_1 | 250 | 253 | PF00917 | 0.297 |
LIG_TRAF2_1 | 255 | 258 | PF00917 | 0.293 |
LIG_TRAF2_2 | 233 | 238 | PF00917 | 0.222 |
MOD_CDK_SPK_2 | 229 | 234 | PF00069 | 0.249 |
MOD_CK1_1 | 129 | 135 | PF00069 | 0.418 |
MOD_CK1_1 | 18 | 24 | PF00069 | 0.717 |
MOD_CK1_1 | 248 | 254 | PF00069 | 0.215 |
MOD_CK1_1 | 42 | 48 | PF00069 | 0.701 |
MOD_CK2_1 | 11 | 17 | PF00069 | 0.554 |
MOD_CK2_1 | 144 | 150 | PF00069 | 0.218 |
MOD_CMANNOS | 307 | 310 | PF00535 | 0.493 |
MOD_GlcNHglycan | 123 | 127 | PF01048 | 0.580 |
MOD_GlcNHglycan | 41 | 44 | PF01048 | 0.465 |
MOD_GSK3_1 | 11 | 18 | PF00069 | 0.646 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.400 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.698 |
MOD_N-GLC_1 | 51 | 56 | PF02516 | 0.430 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.672 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.292 |
MOD_NEK2_1 | 15 | 20 | PF00069 | 0.627 |
MOD_NEK2_1 | 157 | 162 | PF00069 | 0.233 |
MOD_NEK2_1 | 166 | 171 | PF00069 | 0.271 |
MOD_NEK2_1 | 58 | 63 | PF00069 | 0.653 |
MOD_PIKK_1 | 150 | 156 | PF00454 | 0.227 |
MOD_PKA_1 | 208 | 214 | PF00069 | 0.222 |
MOD_PKA_2 | 126 | 132 | PF00069 | 0.401 |
MOD_PKA_2 | 180 | 186 | PF00069 | 0.221 |
MOD_PKA_2 | 208 | 214 | PF00069 | 0.218 |
MOD_Plk_1 | 262 | 268 | PF00069 | 0.265 |
MOD_Plk_1 | 51 | 57 | PF00069 | 0.542 |
MOD_Plk_4 | 104 | 110 | PF00069 | 0.318 |
MOD_Plk_4 | 11 | 17 | PF00069 | 0.554 |
MOD_Plk_4 | 217 | 223 | PF00069 | 0.264 |
MOD_ProDKin_1 | 229 | 235 | PF00069 | 0.249 |
MOD_ProDKin_1 | 35 | 41 | PF00069 | 0.675 |
MOD_ProDKin_1 | 53 | 59 | PF00069 | 0.722 |
TRG_DiLeu_BaEn_1 | 46 | 51 | PF01217 | 0.554 |
TRG_ENDOCYTIC_2 | 165 | 168 | PF00928 | 0.253 |
TRG_ENDOCYTIC_2 | 218 | 221 | PF00928 | 0.253 |
TRG_ENDOCYTIC_2 | 246 | 249 | PF00928 | 0.253 |
TRG_ENDOCYTIC_2 | 94 | 97 | PF00928 | 0.277 |
TRG_ER_diArg_1 | 133 | 136 | PF00400 | 0.335 |
TRG_ER_diArg_1 | 207 | 209 | PF00400 | 0.222 |
TRG_ER_diArg_1 | 25 | 28 | PF00400 | 0.623 |
TRG_ER_diArg_1 | 34 | 36 | PF00400 | 0.600 |
TRG_NES_CRM1_1 | 210 | 225 | PF08389 | 0.279 |
TRG_NLS_MonoExtN_4 | 113 | 120 | PF00514 | 0.292 |
TRG_Pf-PMV_PEXEL_1 | 288 | 292 | PF00026 | 0.559 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2G6 | Leptomonas seymouri | 36% | 72% |
A0A0N0P3R3 | Leptomonas seymouri | 76% | 100% |
A0A0N1I6S1 | Leptomonas seymouri | 30% | 100% |
A0A0S4J8R8 | Bodo saltans | 74% | 100% |
A0A0S4KH84 | Bodo saltans | 27% | 95% |
A0A1X0NLN8 | Trypanosomatidae | 74% | 100% |
A0A1X0NWD3 | Trypanosomatidae | 30% | 100% |
A0A3Q8ID19 | Leishmania donovani | 38% | 72% |
A0A3S5H5E9 | Leishmania donovani | 100% | 100% |
A0A3S5H786 | Leishmania donovani | 30% | 100% |
A4H427 | Leishmania braziliensis | 88% | 100% |
A4HF41 | Leishmania braziliensis | 38% | 100% |
A4HYS6 | Leishmania infantum | 30% | 100% |
A4I2C5 | Leishmania infantum | 39% | 72% |
A6H784 | Bos taurus | 36% | 100% |
C9ZYA3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 79% | 100% |
E9AID5 | Leishmania braziliensis | 30% | 100% |
E9AK94 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
E9AUM2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E9AYH7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 39% | 100% |
O43819 | Homo sapiens | 37% | 100% |
O97196 | Leishmania major | 92% | 100% |
Q4Q8Z5 | Leishmania major | 39% | 100% |
Q4QCW2 | Leishmania major | 30% | 100% |
Q5RH02 | Danio rerio | 34% | 100% |
Q8VCL2 | Mus musculus | 34% | 100% |
V5BI84 | Trypanosoma cruzi | 75% | 100% |