| 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: 9 |
| NetGPI | no | yes: 0, no: 9 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005739 | mitochondrion | 5 | 2 |
| GO:0043226 | organelle | 2 | 2 |
| GO:0043227 | membrane-bounded organelle | 3 | 2 |
| GO:0043229 | intracellular organelle | 3 | 2 |
| GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
| GO:0110165 | cellular anatomical entity | 1 | 3 |
| GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: Q4Q3D0
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006091 | generation of precursor metabolites and energy | 3 | 2 |
| GO:0006120 | mitochondrial electron transport, NADH to ubiquinone | 7 | 2 |
| GO:0008152 | metabolic process | 1 | 2 |
| GO:0009060 | aerobic respiration | 6 | 2 |
| GO:0009987 | cellular process | 1 | 2 |
| GO:0010257 | NADH dehydrogenase complex assembly | 6 | 2 |
| GO:0015980 | energy derivation by oxidation of organic compounds | 4 | 2 |
| GO:0016043 | cellular component organization | 3 | 2 |
| GO:0019646 | aerobic electron transport chain | 6 | 2 |
| GO:0022607 | cellular component assembly | 4 | 2 |
| GO:0022900 | electron transport chain | 4 | 2 |
| GO:0022904 | respiratory electron transport chain | 5 | 2 |
| GO:0032981 | mitochondrial respiratory chain complex I assembly | 7 | 2 |
| GO:0033108 | mitochondrial respiratory chain complex assembly | 6 | 2 |
| GO:0043933 | protein-containing complex organization | 4 | 2 |
| GO:0044237 | cellular metabolic process | 2 | 2 |
| GO:0045333 | cellular respiration | 5 | 2 |
| GO:0065003 | protein-containing complex assembly | 5 | 2 |
| GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005488 | binding | 1 | 2 |
| GO:0005515 | protein binding | 2 | 2 |
| GO:0051082 | unfolded protein binding | 3 | 2 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 453 | 457 | PF00656 | 0.718 |
| CLV_NRD_NRD_1 | 112 | 114 | PF00675 | 0.459 |
| CLV_NRD_NRD_1 | 171 | 173 | PF00675 | 0.590 |
| CLV_NRD_NRD_1 | 267 | 269 | PF00675 | 0.591 |
| CLV_NRD_NRD_1 | 280 | 282 | PF00675 | 0.528 |
| CLV_NRD_NRD_1 | 306 | 308 | PF00675 | 0.465 |
| CLV_PCSK_KEX2_1 | 112 | 114 | PF00082 | 0.456 |
| CLV_PCSK_KEX2_1 | 158 | 160 | PF00082 | 0.614 |
| CLV_PCSK_KEX2_1 | 171 | 173 | PF00082 | 0.537 |
| CLV_PCSK_KEX2_1 | 267 | 269 | PF00082 | 0.593 |
| CLV_PCSK_KEX2_1 | 280 | 282 | PF00082 | 0.528 |
| CLV_PCSK_KEX2_1 | 306 | 308 | PF00082 | 0.469 |
| CLV_PCSK_PC1ET2_1 | 158 | 160 | PF00082 | 0.575 |
| CLV_PCSK_SKI1_1 | 128 | 132 | PF00082 | 0.438 |
| CLV_PCSK_SKI1_1 | 159 | 163 | PF00082 | 0.614 |
| CLV_PCSK_SKI1_1 | 175 | 179 | PF00082 | 0.522 |
| CLV_PCSK_SKI1_1 | 203 | 207 | PF00082 | 0.507 |
| CLV_PCSK_SKI1_1 | 306 | 310 | PF00082 | 0.514 |
| DEG_APCC_DBOX_1 | 202 | 210 | PF00400 | 0.520 |
| DEG_APCC_DBOX_1 | 377 | 385 | PF00400 | 0.445 |
| DOC_CKS1_1 | 7 | 12 | PF01111 | 0.673 |
| DOC_CYCLIN_RxL_1 | 122 | 136 | PF00134 | 0.536 |
| DOC_MAPK_gen_1 | 112 | 119 | PF00069 | 0.417 |
| DOC_MAPK_gen_1 | 126 | 134 | PF00069 | 0.436 |
| DOC_MAPK_gen_1 | 372 | 379 | PF00069 | 0.589 |
| DOC_MAPK_gen_1 | 400 | 410 | PF00069 | 0.603 |
| DOC_MAPK_MEF2A_6 | 112 | 119 | PF00069 | 0.417 |
| DOC_MAPK_MEF2A_6 | 126 | 134 | PF00069 | 0.436 |
| DOC_MAPK_MEF2A_6 | 403 | 412 | PF00069 | 0.492 |
| DOC_PP1_RVXF_1 | 64 | 71 | PF00149 | 0.616 |
| DOC_PP2B_LxvP_1 | 130 | 133 | PF13499 | 0.530 |
| DOC_PP4_FxxP_1 | 182 | 185 | PF00568 | 0.363 |
| DOC_USP7_MATH_1 | 196 | 200 | PF00917 | 0.715 |
| DOC_USP7_MATH_1 | 335 | 339 | PF00917 | 0.561 |
| DOC_USP7_MATH_1 | 83 | 87 | PF00917 | 0.638 |
| DOC_WW_Pin1_4 | 287 | 292 | PF00397 | 0.488 |
| DOC_WW_Pin1_4 | 297 | 302 | PF00397 | 0.527 |
| DOC_WW_Pin1_4 | 329 | 334 | PF00397 | 0.516 |
| DOC_WW_Pin1_4 | 372 | 377 | PF00397 | 0.568 |
| DOC_WW_Pin1_4 | 6 | 11 | PF00397 | 0.744 |
| LIG_14-3-3_CanoR_1 | 112 | 118 | PF00244 | 0.520 |
| LIG_14-3-3_CanoR_1 | 143 | 148 | PF00244 | 0.645 |
| LIG_14-3-3_CanoR_1 | 183 | 189 | PF00244 | 0.607 |
| LIG_14-3-3_CanoR_1 | 249 | 259 | PF00244 | 0.685 |
| LIG_14-3-3_CanoR_1 | 306 | 312 | PF00244 | 0.538 |
| LIG_14-3-3_CanoR_1 | 336 | 340 | PF00244 | 0.541 |
| LIG_14-3-3_CanoR_1 | 358 | 366 | PF00244 | 0.659 |
| LIG_14-3-3_CanoR_1 | 378 | 382 | PF00244 | 0.313 |
| LIG_14-3-3_CanoR_1 | 383 | 390 | PF00244 | 0.499 |
| LIG_Actin_WH2_2 | 435 | 451 | PF00022 | 0.607 |
| LIG_Actin_WH2_2 | 99 | 114 | PF00022 | 0.467 |
| LIG_APCC_ABBA_1 | 30 | 35 | PF00400 | 0.672 |
| LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.740 |
| LIG_BRCT_BRCA1_1 | 226 | 230 | PF00533 | 0.447 |
| LIG_deltaCOP1_diTrp_1 | 352 | 357 | PF00928 | 0.616 |
| LIG_eIF4E_1 | 303 | 309 | PF01652 | 0.571 |
| LIG_FHA_1 | 160 | 166 | PF00498 | 0.541 |
| LIG_FHA_1 | 214 | 220 | PF00498 | 0.574 |
| LIG_FHA_1 | 231 | 237 | PF00498 | 0.298 |
| LIG_FHA_1 | 90 | 96 | PF00498 | 0.447 |
| LIG_FHA_2 | 41 | 47 | PF00498 | 0.585 |
| LIG_FHA_2 | 7 | 13 | PF00498 | 0.668 |
| LIG_FHA_2 | 79 | 85 | PF00498 | 0.637 |
| LIG_GBD_Chelix_1 | 228 | 236 | PF00786 | 0.502 |
| LIG_Integrin_RGD_1 | 172 | 174 | PF01839 | 0.452 |
| LIG_LIR_Apic_2 | 181 | 185 | PF02991 | 0.359 |
| LIG_LIR_Gen_1 | 283 | 294 | PF02991 | 0.509 |
| LIG_LIR_Gen_1 | 462 | 470 | PF02991 | 0.664 |
| LIG_LIR_Nem_3 | 129 | 134 | PF02991 | 0.536 |
| LIG_LIR_Nem_3 | 146 | 152 | PF02991 | 0.678 |
| LIG_LIR_Nem_3 | 164 | 170 | PF02991 | 0.581 |
| LIG_LIR_Nem_3 | 253 | 259 | PF02991 | 0.448 |
| LIG_LIR_Nem_3 | 283 | 289 | PF02991 | 0.496 |
| LIG_LIR_Nem_3 | 300 | 305 | PF02991 | 0.581 |
| LIG_LIR_Nem_3 | 386 | 392 | PF02991 | 0.640 |
| LIG_LIR_Nem_3 | 462 | 467 | PF02991 | 0.657 |
| LIG_LIR_Nem_3 | 56 | 60 | PF02991 | 0.531 |
| LIG_LYPXL_yS_3 | 57 | 60 | PF13949 | 0.643 |
| LIG_SH2_CRK | 149 | 153 | PF00017 | 0.725 |
| LIG_SH2_CRK | 305 | 309 | PF00017 | 0.531 |
| LIG_SH2_STAT5 | 110 | 113 | PF00017 | 0.533 |
| LIG_SH2_STAT5 | 231 | 234 | PF00017 | 0.421 |
| LIG_SH2_STAT5 | 29 | 32 | PF00017 | 0.662 |
| LIG_SH2_STAT5 | 315 | 318 | PF00017 | 0.459 |
| LIG_SH2_STAT5 | 69 | 72 | PF00017 | 0.566 |
| LIG_SH3_3 | 185 | 191 | PF00018 | 0.644 |
| LIG_SH3_3 | 384 | 390 | PF00018 | 0.594 |
| LIG_SH3_3 | 4 | 10 | PF00018 | 0.751 |
| LIG_SUMO_SIM_anti_2 | 116 | 121 | PF11976 | 0.415 |
| LIG_SUMO_SIM_anti_2 | 90 | 97 | PF11976 | 0.473 |
| LIG_TRAF2_1 | 235 | 238 | PF00917 | 0.586 |
| LIG_WRC_WIRS_1 | 389 | 394 | PF05994 | 0.581 |
| MOD_CDC14_SPxK_1 | 375 | 378 | PF00782 | 0.555 |
| MOD_CDK_SPxK_1 | 372 | 378 | PF00069 | 0.557 |
| MOD_CDK_SPxxK_3 | 329 | 336 | PF00069 | 0.569 |
| MOD_CK1_1 | 192 | 198 | PF00069 | 0.712 |
| MOD_CK1_1 | 258 | 264 | PF00069 | 0.684 |
| MOD_CK1_1 | 297 | 303 | PF00069 | 0.517 |
| MOD_CK1_1 | 359 | 365 | PF00069 | 0.638 |
| MOD_CK2_1 | 151 | 157 | PF00069 | 0.565 |
| MOD_CK2_1 | 388 | 394 | PF00069 | 0.575 |
| MOD_CK2_1 | 40 | 46 | PF00069 | 0.571 |
| MOD_CK2_1 | 433 | 439 | PF00069 | 0.554 |
| MOD_CK2_1 | 78 | 84 | PF00069 | 0.626 |
| MOD_CMANNOS | 353 | 356 | PF00535 | 0.628 |
| MOD_Cter_Amidation | 265 | 268 | PF01082 | 0.656 |
| MOD_DYRK1A_RPxSP_1 | 6 | 10 | PF00069 | 0.688 |
| MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.642 |
| MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.734 |
| MOD_GlcNHglycan | 237 | 242 | PF01048 | 0.548 |
| MOD_GlcNHglycan | 252 | 255 | PF01048 | 0.673 |
| MOD_GlcNHglycan | 329 | 332 | PF01048 | 0.574 |
| MOD_GlcNHglycan | 84 | 88 | PF01048 | 0.726 |
| MOD_GSK3_1 | 192 | 199 | PF00069 | 0.692 |
| MOD_GSK3_1 | 325 | 332 | PF00069 | 0.628 |
| MOD_GSK3_1 | 356 | 363 | PF00069 | 0.510 |
| MOD_GSK3_1 | 433 | 440 | PF00069 | 0.511 |
| MOD_GSK3_1 | 79 | 86 | PF00069 | 0.634 |
| MOD_GSK3_1 | 87 | 94 | PF00069 | 0.536 |
| MOD_N-GLC_1 | 196 | 201 | PF02516 | 0.631 |
| MOD_NEK2_1 | 161 | 166 | PF00069 | 0.548 |
| MOD_NEK2_1 | 219 | 224 | PF00069 | 0.513 |
| MOD_NEK2_1 | 230 | 235 | PF00069 | 0.470 |
| MOD_NEK2_1 | 250 | 255 | PF00069 | 0.660 |
| MOD_NEK2_1 | 327 | 332 | PF00069 | 0.555 |
| MOD_NEK2_1 | 370 | 375 | PF00069 | 0.580 |
| MOD_NEK2_1 | 408 | 413 | PF00069 | 0.492 |
| MOD_NEK2_1 | 427 | 432 | PF00069 | 0.491 |
| MOD_NEK2_1 | 433 | 438 | PF00069 | 0.500 |
| MOD_NEK2_2 | 28 | 33 | PF00069 | 0.621 |
| MOD_PIKK_1 | 213 | 219 | PF00454 | 0.509 |
| MOD_PIKK_1 | 325 | 331 | PF00454 | 0.582 |
| MOD_PK_1 | 113 | 119 | PF00069 | 0.466 |
| MOD_PK_1 | 224 | 230 | PF00069 | 0.463 |
| MOD_PKA_2 | 250 | 256 | PF00069 | 0.688 |
| MOD_PKA_2 | 335 | 341 | PF00069 | 0.585 |
| MOD_PKA_2 | 359 | 365 | PF00069 | 0.703 |
| MOD_PKA_2 | 377 | 383 | PF00069 | 0.317 |
| MOD_PKB_1 | 358 | 366 | PF00069 | 0.520 |
| MOD_Plk_1 | 219 | 225 | PF00069 | 0.520 |
| MOD_Plk_1 | 322 | 328 | PF00069 | 0.548 |
| MOD_Plk_4 | 115 | 121 | PF00069 | 0.436 |
| MOD_Plk_4 | 126 | 132 | PF00069 | 0.426 |
| MOD_Plk_4 | 224 | 230 | PF00069 | 0.407 |
| MOD_Plk_4 | 258 | 264 | PF00069 | 0.648 |
| MOD_Plk_4 | 322 | 328 | PF00069 | 0.548 |
| MOD_Plk_4 | 40 | 46 | PF00069 | 0.617 |
| MOD_Plk_4 | 408 | 414 | PF00069 | 0.611 |
| MOD_Plk_4 | 433 | 439 | PF00069 | 0.569 |
| MOD_Plk_4 | 91 | 97 | PF00069 | 0.458 |
| MOD_ProDKin_1 | 287 | 293 | PF00069 | 0.491 |
| MOD_ProDKin_1 | 297 | 303 | PF00069 | 0.517 |
| MOD_ProDKin_1 | 329 | 335 | PF00069 | 0.518 |
| MOD_ProDKin_1 | 372 | 378 | PF00069 | 0.557 |
| MOD_ProDKin_1 | 6 | 12 | PF00069 | 0.739 |
| TRG_DiLeu_BaEn_1 | 91 | 96 | PF01217 | 0.531 |
| TRG_DiLeu_BaLyEn_6 | 304 | 309 | PF01217 | 0.626 |
| TRG_DiLeu_BaLyEn_6 | 418 | 423 | PF01217 | 0.571 |
| TRG_DiLeu_BaLyEn_6 | 63 | 68 | PF01217 | 0.622 |
| TRG_ENDOCYTIC_2 | 149 | 152 | PF00928 | 0.686 |
| TRG_ENDOCYTIC_2 | 167 | 170 | PF00928 | 0.577 |
| TRG_ENDOCYTIC_2 | 29 | 32 | PF00928 | 0.548 |
| TRG_ENDOCYTIC_2 | 305 | 308 | PF00928 | 0.512 |
| TRG_ENDOCYTIC_2 | 57 | 60 | PF00928 | 0.643 |
| TRG_ER_diArg_1 | 111 | 113 | PF00400 | 0.458 |
| TRG_ER_diArg_1 | 17 | 20 | PF00400 | 0.629 |
| TRG_ER_diArg_1 | 170 | 172 | PF00400 | 0.523 |
| TRG_ER_diArg_1 | 267 | 269 | PF00400 | 0.593 |
| TRG_ER_diArg_1 | 280 | 282 | PF00400 | 0.522 |
| TRG_ER_diArg_1 | 305 | 307 | PF00400 | 0.479 |
| TRG_ER_diArg_1 | 357 | 360 | PF00400 | 0.650 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1HZN2 | Leptomonas seymouri | 65% | 98% |
| A0A0S4IVY0 | Bodo saltans | 25% | 100% |
| A0A1X0P965 | Trypanosomatidae | 32% | 100% |
| A0A3Q8IIA0 | Leishmania donovani | 94% | 100% |
| A4HAI5 | Leishmania braziliensis | 78% | 100% |
| E9AHS6 | Leishmania infantum | 94% | 100% |
| E9B4P6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
| V5BEX5 | Trypanosoma cruzi | 34% | 100% |