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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005747 | mitochondrial respiratory chain complex I | 4 | 1 |
GO:0030964 | NADH dehydrogenase complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0045271 | respiratory chain complex I | 4 | 1 |
GO:0098796 | membrane protein complex | 2 | 1 |
GO:0098798 | mitochondrial protein-containing complex | 2 | 1 |
GO:0098800 | inner mitochondrial membrane protein complex | 3 | 1 |
GO:0098803 | respiratory chain complex | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1902495 | transmembrane transporter complex | 3 | 1 |
GO:1990204 | oxidoreductase complex | 3 | 1 |
GO:1990351 | transporter complex | 2 | 1 |
GO:0005739 | mitochondrion | 5 | 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 |
Related structures:
AlphaFold database: A4HBP0
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 10 |
GO:0004324 | ferredoxin-NADP+ reductase activity | 6 | 5 |
GO:0008937 | ferredoxin-NAD(P) reductase activity | 5 | 5 |
GO:0016491 | oxidoreductase activity | 2 | 10 |
GO:0016730 | oxidoreductase activity, acting on iron-sulfur proteins as donors | 3 | 7 |
GO:0016731 | oxidoreductase activity, acting on iron-sulfur proteins as donors, NAD or NADP as acceptor | 4 | 7 |
GO:0015039 | NADPH-adrenodoxin reductase activity | 5 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 172 | 176 | PF00656 | 0.425 |
CLV_C14_Caspase3-7 | 498 | 502 | PF00656 | 0.401 |
CLV_C14_Caspase3-7 | 539 | 543 | PF00656 | 0.451 |
CLV_NRD_NRD_1 | 272 | 274 | PF00675 | 0.400 |
CLV_NRD_NRD_1 | 427 | 429 | PF00675 | 0.494 |
CLV_NRD_NRD_1 | 75 | 77 | PF00675 | 0.489 |
CLV_PCSK_FUR_1 | 219 | 223 | PF00082 | 0.496 |
CLV_PCSK_KEX2_1 | 221 | 223 | PF00082 | 0.459 |
CLV_PCSK_KEX2_1 | 272 | 274 | PF00082 | 0.400 |
CLV_PCSK_KEX2_1 | 322 | 324 | PF00082 | 0.420 |
CLV_PCSK_KEX2_1 | 74 | 76 | PF00082 | 0.536 |
CLV_PCSK_PC1ET2_1 | 221 | 223 | PF00082 | 0.459 |
CLV_PCSK_PC1ET2_1 | 322 | 324 | PF00082 | 0.420 |
CLV_PCSK_PC1ET2_1 | 74 | 76 | PF00082 | 0.599 |
CLV_PCSK_SKI1_1 | 286 | 290 | PF00082 | 0.388 |
CLV_PCSK_SKI1_1 | 621 | 625 | PF00082 | 0.416 |
CLV_PCSK_SKI1_1 | 641 | 645 | PF00082 | 0.612 |
CLV_PCSK_SKI1_1 | 655 | 659 | PF00082 | 0.555 |
DEG_APCC_DBOX_1 | 395 | 403 | PF00400 | 0.394 |
DEG_Nend_UBRbox_4 | 1 | 3 | PF02207 | 0.443 |
DEG_SCF_FBW7_1 | 643 | 648 | PF00400 | 0.662 |
DEG_SPOP_SBC_1 | 536 | 540 | PF00917 | 0.681 |
DOC_ANK_TNKS_1 | 221 | 228 | PF00023 | 0.470 |
DOC_CYCLIN_RxL_1 | 19 | 27 | PF00134 | 0.440 |
DOC_CYCLIN_RxL_1 | 652 | 662 | PF00134 | 0.617 |
DOC_CYCLIN_yClb1_LxF_4 | 390 | 395 | PF00134 | 0.265 |
DOC_CYCLIN_yCln2_LP_2 | 110 | 116 | PF00134 | 0.311 |
DOC_MAPK_DCC_7 | 394 | 404 | PF00069 | 0.397 |
DOC_MAPK_gen_1 | 219 | 226 | PF00069 | 0.478 |
DOC_MAPK_gen_1 | 290 | 300 | PF00069 | 0.275 |
DOC_MAPK_gen_1 | 319 | 327 | PF00069 | 0.443 |
DOC_MAPK_gen_1 | 385 | 395 | PF00069 | 0.416 |
DOC_MAPK_gen_1 | 586 | 593 | PF00069 | 0.384 |
DOC_MAPK_gen_1 | 74 | 81 | PF00069 | 0.440 |
DOC_MAPK_gen_1 | 97 | 106 | PF00069 | 0.295 |
DOC_MAPK_MEF2A_6 | 293 | 300 | PF00069 | 0.273 |
DOC_MAPK_MEF2A_6 | 621 | 628 | PF00069 | 0.412 |
DOC_MAPK_MEF2A_6 | 74 | 81 | PF00069 | 0.526 |
DOC_MAPK_MEF2A_6 | 97 | 106 | PF00069 | 0.295 |
DOC_PP1_RVXF_1 | 13 | 19 | PF00149 | 0.448 |
DOC_PP1_RVXF_1 | 141 | 147 | PF00149 | 0.371 |
DOC_PP1_RVXF_1 | 390 | 396 | PF00149 | 0.322 |
DOC_PP2B_LxvP_1 | 110 | 113 | PF13499 | 0.311 |
DOC_PP2B_LxvP_1 | 180 | 183 | PF13499 | 0.408 |
DOC_PP2B_LxvP_1 | 26 | 29 | PF13499 | 0.436 |
DOC_USP7_MATH_1 | 174 | 178 | PF00917 | 0.440 |
DOC_USP7_MATH_1 | 367 | 371 | PF00917 | 0.669 |
DOC_USP7_MATH_1 | 47 | 51 | PF00917 | 0.741 |
DOC_USP7_MATH_1 | 535 | 539 | PF00917 | 0.643 |
DOC_USP7_MATH_1 | 58 | 62 | PF00917 | 0.738 |
DOC_USP7_MATH_1 | 63 | 67 | PF00917 | 0.722 |
DOC_USP7_MATH_1 | 645 | 649 | PF00917 | 0.632 |
DOC_USP7_MATH_1 | 684 | 688 | PF00917 | 0.641 |
DOC_USP7_UBL2_3 | 257 | 261 | PF12436 | 0.503 |
DOC_USP7_UBL2_3 | 293 | 297 | PF12436 | 0.448 |
DOC_USP7_UBL2_3 | 472 | 476 | PF12436 | 0.506 |
DOC_USP7_UBL2_3 | 488 | 492 | PF12436 | 0.263 |
DOC_USP7_UBL2_3 | 612 | 616 | PF12436 | 0.396 |
DOC_WW_Pin1_4 | 119 | 124 | PF00397 | 0.428 |
DOC_WW_Pin1_4 | 206 | 211 | PF00397 | 0.448 |
DOC_WW_Pin1_4 | 362 | 367 | PF00397 | 0.723 |
DOC_WW_Pin1_4 | 397 | 402 | PF00397 | 0.450 |
DOC_WW_Pin1_4 | 641 | 646 | PF00397 | 0.666 |
LIG_14-3-3_CanoR_1 | 143 | 147 | PF00244 | 0.351 |
LIG_14-3-3_CanoR_1 | 244 | 254 | PF00244 | 0.370 |
LIG_BIR_III_2 | 545 | 549 | PF00653 | 0.472 |
LIG_BIR_III_4 | 348 | 352 | PF00653 | 0.663 |
LIG_BIR_III_4 | 433 | 437 | PF00653 | 0.347 |
LIG_BRCT_BRCA1_1 | 208 | 212 | PF00533 | 0.458 |
LIG_BRCT_BRCA1_1 | 86 | 90 | PF00533 | 0.418 |
LIG_CtBP_PxDLS_1 | 607 | 612 | PF00389 | 0.433 |
LIG_eIF4E_1 | 413 | 419 | PF01652 | 0.517 |
LIG_FHA_1 | 21 | 27 | PF00498 | 0.710 |
LIG_FHA_1 | 3 | 9 | PF00498 | 0.540 |
LIG_FHA_1 | 569 | 575 | PF00498 | 0.425 |
LIG_FHA_1 | 583 | 589 | PF00498 | 0.500 |
LIG_FHA_2 | 170 | 176 | PF00498 | 0.401 |
LIG_FHA_2 | 332 | 338 | PF00498 | 0.496 |
LIG_FHA_2 | 372 | 378 | PF00498 | 0.763 |
LIG_FHA_2 | 420 | 426 | PF00498 | 0.545 |
LIG_FHA_2 | 617 | 623 | PF00498 | 0.511 |
LIG_HP1_1 | 548 | 552 | PF01393 | 0.481 |
LIG_LIR_Apic_2 | 17 | 21 | PF02991 | 0.445 |
LIG_LIR_Gen_1 | 105 | 114 | PF02991 | 0.295 |
LIG_LIR_Gen_1 | 198 | 207 | PF02991 | 0.464 |
LIG_LIR_Gen_1 | 435 | 445 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 105 | 110 | PF02991 | 0.311 |
LIG_LIR_Nem_3 | 195 | 199 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 209 | 215 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 242 | 246 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 282 | 288 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 299 | 305 | PF02991 | 0.396 |
LIG_LIR_Nem_3 | 435 | 440 | PF02991 | 0.482 |
LIG_NRBOX | 653 | 659 | PF00104 | 0.499 |
LIG_SH2_CRK | 165 | 169 | PF00017 | 0.317 |
LIG_SH2_CRK | 200 | 204 | PF00017 | 0.434 |
LIG_SH2_CRK | 207 | 211 | PF00017 | 0.500 |
LIG_SH2_CRK | 437 | 441 | PF00017 | 0.519 |
LIG_SH2_GRB2like | 199 | 202 | PF00017 | 0.330 |
LIG_SH2_STAP1 | 165 | 169 | PF00017 | 0.317 |
LIG_SH2_STAT5 | 245 | 248 | PF00017 | 0.390 |
LIG_SH2_STAT5 | 302 | 305 | PF00017 | 0.404 |
LIG_SH2_STAT5 | 413 | 416 | PF00017 | 0.498 |
LIG_SH2_STAT5 | 437 | 440 | PF00017 | 0.467 |
LIG_SH2_STAT5 | 482 | 485 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 582 | 585 | PF00017 | 0.412 |
LIG_SH2_STAT5 | 653 | 656 | PF00017 | 0.498 |
LIG_SH2_STAT5 | 94 | 97 | PF00017 | 0.195 |
LIG_SH3_3 | 120 | 126 | PF00018 | 0.295 |
LIG_SH3_3 | 349 | 355 | PF00018 | 0.595 |
LIG_SH3_3 | 363 | 369 | PF00018 | 0.648 |
LIG_SH3_3 | 516 | 522 | PF00018 | 0.601 |
LIG_SUMO_SIM_anti_2 | 265 | 271 | PF11976 | 0.476 |
LIG_SUMO_SIM_anti_2 | 400 | 407 | PF11976 | 0.493 |
LIG_SUMO_SIM_anti_2 | 547 | 553 | PF11976 | 0.733 |
LIG_SUMO_SIM_par_1 | 22 | 27 | PF11976 | 0.564 |
LIG_SUMO_SIM_par_1 | 4 | 9 | PF11976 | 0.433 |
LIG_SUMO_SIM_par_1 | 547 | 553 | PF11976 | 0.617 |
LIG_TRAF2_1 | 334 | 337 | PF00917 | 0.586 |
LIG_TRFH_1 | 397 | 401 | PF08558 | 0.395 |
LIG_TYR_ITIM | 300 | 305 | PF00017 | 0.256 |
LIG_UBA3_1 | 651 | 655 | PF00899 | 0.636 |
LIG_WRC_WIRS_1 | 551 | 556 | PF05994 | 0.736 |
MOD_CDK_SPxK_1 | 641 | 647 | PF00069 | 0.671 |
MOD_CK1_1 | 192 | 198 | PF00069 | 0.446 |
MOD_CK1_1 | 335 | 341 | PF00069 | 0.579 |
MOD_CK1_1 | 40 | 46 | PF00069 | 0.705 |
MOD_CK1_1 | 553 | 559 | PF00069 | 0.668 |
MOD_CK1_1 | 56 | 62 | PF00069 | 0.673 |
MOD_CK1_1 | 84 | 90 | PF00069 | 0.295 |
MOD_CK2_1 | 192 | 198 | PF00069 | 0.459 |
MOD_CK2_1 | 331 | 337 | PF00069 | 0.522 |
MOD_CK2_1 | 362 | 368 | PF00069 | 0.680 |
MOD_CK2_1 | 371 | 377 | PF00069 | 0.650 |
MOD_CK2_1 | 419 | 425 | PF00069 | 0.544 |
MOD_CK2_1 | 47 | 53 | PF00069 | 0.677 |
MOD_Cter_Amidation | 610 | 613 | PF01082 | 0.443 |
MOD_Cter_Amidation | 632 | 635 | PF01082 | 0.520 |
MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.408 |
MOD_GlcNHglycan | 26 | 29 | PF01048 | 0.697 |
MOD_GlcNHglycan | 276 | 280 | PF01048 | 0.382 |
MOD_GlcNHglycan | 368 | 372 | PF01048 | 0.734 |
MOD_GlcNHglycan | 539 | 542 | PF01048 | 0.677 |
MOD_GlcNHglycan | 555 | 558 | PF01048 | 0.710 |
MOD_GlcNHglycan | 56 | 59 | PF01048 | 0.683 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.636 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.313 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.574 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.671 |
MOD_GSK3_1 | 275 | 282 | PF00069 | 0.465 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.691 |
MOD_GSK3_1 | 331 | 338 | PF00069 | 0.556 |
MOD_GSK3_1 | 358 | 365 | PF00069 | 0.677 |
MOD_GSK3_1 | 367 | 374 | PF00069 | 0.617 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.686 |
MOD_GSK3_1 | 553 | 560 | PF00069 | 0.681 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.628 |
MOD_GSK3_1 | 641 | 648 | PF00069 | 0.643 |
MOD_N-GLC_1 | 148 | 153 | PF02516 | 0.410 |
MOD_N-GLC_1 | 397 | 402 | PF02516 | 0.485 |
MOD_N-GLC_1 | 40 | 45 | PF02516 | 0.705 |
MOD_N-GLC_1 | 53 | 58 | PF02516 | 0.724 |
MOD_N-GLC_1 | 557 | 562 | PF02516 | 0.686 |
MOD_NEK2_1 | 217 | 222 | PF00069 | 0.530 |
MOD_NEK2_1 | 239 | 244 | PF00069 | 0.355 |
MOD_NEK2_1 | 24 | 29 | PF00069 | 0.655 |
MOD_NEK2_1 | 419 | 424 | PF00069 | 0.507 |
MOD_NEK2_1 | 444 | 449 | PF00069 | 0.417 |
MOD_NEK2_1 | 6 | 11 | PF00069 | 0.444 |
MOD_NEK2_1 | 90 | 95 | PF00069 | 0.381 |
MOD_PIKK_1 | 677 | 683 | PF00454 | 0.407 |
MOD_PK_1 | 452 | 458 | PF00069 | 0.456 |
MOD_PKA_2 | 142 | 148 | PF00069 | 0.357 |
MOD_PKA_2 | 536 | 542 | PF00069 | 0.562 |
MOD_Plk_1 | 148 | 154 | PF00069 | 0.405 |
MOD_Plk_1 | 275 | 281 | PF00069 | 0.421 |
MOD_Plk_4 | 142 | 148 | PF00069 | 0.363 |
MOD_Plk_4 | 495 | 501 | PF00069 | 0.429 |
MOD_Plk_4 | 505 | 511 | PF00069 | 0.349 |
MOD_Plk_4 | 569 | 575 | PF00069 | 0.557 |
MOD_Plk_4 | 90 | 96 | PF00069 | 0.175 |
MOD_ProDKin_1 | 119 | 125 | PF00069 | 0.428 |
MOD_ProDKin_1 | 206 | 212 | PF00069 | 0.451 |
MOD_ProDKin_1 | 362 | 368 | PF00069 | 0.725 |
MOD_ProDKin_1 | 397 | 403 | PF00069 | 0.449 |
MOD_ProDKin_1 | 641 | 647 | PF00069 | 0.667 |
MOD_SUMO_for_1 | 296 | 299 | PF00179 | 0.473 |
TRG_ENDOCYTIC_2 | 165 | 168 | PF00928 | 0.319 |
TRG_ENDOCYTIC_2 | 200 | 203 | PF00928 | 0.454 |
TRG_ENDOCYTIC_2 | 243 | 246 | PF00928 | 0.386 |
TRG_ENDOCYTIC_2 | 302 | 305 | PF00928 | 0.404 |
TRG_ENDOCYTIC_2 | 437 | 440 | PF00928 | 0.509 |
TRG_ENDOCYTIC_2 | 577 | 580 | PF00928 | 0.374 |
TRG_ER_diArg_1 | 392 | 395 | PF00400 | 0.484 |
TRG_ER_diArg_1 | 75 | 77 | PF00400 | 0.541 |
TRG_NLS_MonoExtN_4 | 73 | 78 | PF00514 | 0.576 |
TRG_Pf-PMV_PEXEL_1 | 100 | 105 | PF00026 | 0.341 |
TRG_Pf-PMV_PEXEL_1 | 598 | 603 | PF00026 | 0.435 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDQ8 | Leptomonas seymouri | 64% | 98% |
A0A0S4J2F1 | Bodo saltans | 43% | 100% |
A0A1X0NYU3 | Trypanosomatidae | 50% | 100% |
A0A3S5H794 | Leishmania donovani | 85% | 99% |
A0A422MZJ3 | Trypanosoma rangeli | 48% | 100% |
A4HZ41 | Leishmania infantum | 85% | 99% |
D0A1P2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 49% | 100% |
E9AV09 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 98% |
O33064 | Mycobacterium leprae (strain TN) | 29% | 100% |
P48360 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 30% | 100% |
P56522 | Rattus norvegicus | 33% | 100% |
P65529 | Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) | 31% | 100% |
P82861 | Salvelinus fontinalis | 30% | 100% |
P9WJI0 | Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) | 31% | 100% |
P9WJI1 | Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) | 31% | 100% |
Q4QCH3 | Leishmania major | 84% | 100% |
Q54KG7 | Dictyostelium discoideum | 28% | 100% |
Q61578 | Mus musculus | 32% | 100% |
Q9V3T9 | Drosophila melanogaster | 30% | 100% |
V5BQ55 | Trypanosoma cruzi | 52% | 100% |