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: 10 |
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: 8 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005741 | mitochondrial outer membrane | 5 | 1 |
GO:0005742 | mitochondrial outer membrane translocase complex | 4 | 1 |
GO:0016020 | membrane | 2 | 3 |
GO:0019867 | outer membrane | 3 | 1 |
GO:0031090 | organelle membrane | 3 | 1 |
GO:0031966 | mitochondrial membrane | 4 | 1 |
GO:0031968 | organelle outer membrane | 4 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0098588 | bounding membrane of organelle | 4 | 1 |
GO:0098796 | membrane protein complex | 2 | 1 |
GO:0098798 | mitochondrial protein-containing complex | 2 | 1 |
GO:0098799 | outer mitochondrial membrane protein complex | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
Related structures:
AlphaFold database: A4HGS1
Term | Name | Level | Count |
---|---|---|---|
GO:0006605 | protein targeting | 5 | 1 |
GO:0006626 | protein targeting to mitochondrion | 5 | 1 |
GO:0006810 | transport | 3 | 1 |
GO:0006839 | mitochondrial transport | 4 | 1 |
GO:0006886 | intracellular protein transport | 4 | 1 |
GO:0008104 | protein localization | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0015031 | protein transport | 4 | 1 |
GO:0030150 | protein import into mitochondrial matrix | 4 | 1 |
GO:0033036 | macromolecule localization | 2 | 1 |
GO:0033365 | protein localization to organelle | 5 | 1 |
GO:0044743 | protein transmembrane import into intracellular organelle | 4 | 1 |
GO:0045184 | establishment of protein localization | 3 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
GO:0055085 | transmembrane transport | 2 | 1 |
GO:0065002 | intracellular protein transmembrane transport | 4 | 1 |
GO:0070585 | protein localization to mitochondrion | 6 | 1 |
GO:0070727 | cellular macromolecule localization | 3 | 1 |
GO:0071702 | organic substance transport | 4 | 1 |
GO:0071705 | nitrogen compound transport | 4 | 1 |
GO:0071806 | protein transmembrane transport | 3 | 1 |
GO:0072594 | establishment of protein localization to organelle | 4 | 1 |
GO:0072655 | establishment of protein localization to mitochondrion | 5 | 1 |
GO:1990542 | mitochondrial transmembrane transport | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 224 | 228 | PF00656 | 0.577 |
CLV_C14_Caspase3-7 | 44 | 48 | PF00656 | 0.568 |
CLV_C14_Caspase3-7 | 475 | 479 | PF00656 | 0.582 |
CLV_C14_Caspase3-7 | 560 | 564 | PF00656 | 0.633 |
CLV_NRD_NRD_1 | 489 | 491 | PF00675 | 0.355 |
CLV_NRD_NRD_1 | 585 | 587 | PF00675 | 0.578 |
CLV_PCSK_KEX2_1 | 355 | 357 | PF00082 | 0.303 |
CLV_PCSK_KEX2_1 | 489 | 491 | PF00082 | 0.346 |
CLV_PCSK_KEX2_1 | 89 | 91 | PF00082 | 0.307 |
CLV_PCSK_PC1ET2_1 | 355 | 357 | PF00082 | 0.365 |
CLV_PCSK_PC1ET2_1 | 89 | 91 | PF00082 | 0.310 |
CLV_PCSK_SKI1_1 | 174 | 178 | PF00082 | 0.503 |
CLV_PCSK_SKI1_1 | 236 | 240 | PF00082 | 0.313 |
CLV_PCSK_SKI1_1 | 348 | 352 | PF00082 | 0.269 |
CLV_PCSK_SKI1_1 | 355 | 359 | PF00082 | 0.264 |
CLV_PCSK_SKI1_1 | 380 | 384 | PF00082 | 0.280 |
CLV_PCSK_SKI1_1 | 39 | 43 | PF00082 | 0.331 |
CLV_PCSK_SKI1_1 | 395 | 399 | PF00082 | 0.257 |
CLV_PCSK_SKI1_1 | 507 | 511 | PF00082 | 0.430 |
CLV_PCSK_SKI1_1 | 620 | 624 | PF00082 | 0.314 |
CLV_Separin_Metazoa | 486 | 490 | PF03568 | 0.655 |
CLV_Separin_Metazoa | 499 | 503 | PF03568 | 0.562 |
DEG_APCC_DBOX_1 | 120 | 128 | PF00400 | 0.556 |
DEG_APCC_KENBOX_2 | 181 | 185 | PF00400 | 0.592 |
DOC_CDC14_PxL_1 | 635 | 643 | PF14671 | 0.399 |
DOC_CYCLIN_yCln2_LP_2 | 615 | 621 | PF00134 | 0.317 |
DOC_MAPK_gen_1 | 118 | 126 | PF00069 | 0.579 |
DOC_MAPK_gen_1 | 210 | 216 | PF00069 | 0.540 |
DOC_MAPK_gen_1 | 37 | 45 | PF00069 | 0.495 |
DOC_MAPK_JIP1_4 | 37 | 43 | PF00069 | 0.546 |
DOC_MAPK_MEF2A_6 | 37 | 45 | PF00069 | 0.495 |
DOC_MAPK_MEF2A_6 | 489 | 496 | PF00069 | 0.531 |
DOC_PP1_RVXF_1 | 57 | 64 | PF00149 | 0.632 |
DOC_PP2B_LxvP_1 | 65 | 68 | PF13499 | 0.428 |
DOC_USP7_MATH_1 | 251 | 255 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 429 | 433 | PF00917 | 0.617 |
DOC_USP7_MATH_1 | 479 | 483 | PF00917 | 0.515 |
DOC_USP7_MATH_1 | 529 | 533 | PF00917 | 0.684 |
DOC_USP7_MATH_1 | 535 | 539 | PF00917 | 0.660 |
DOC_USP7_MATH_1 | 557 | 561 | PF00917 | 0.622 |
DOC_USP7_MATH_1 | 562 | 566 | PF00917 | 0.663 |
DOC_WW_Pin1_4 | 343 | 348 | PF00397 | 0.483 |
LIG_14-3-3_CanoR_1 | 118 | 128 | PF00244 | 0.582 |
LIG_14-3-3_CanoR_1 | 250 | 256 | PF00244 | 0.567 |
LIG_14-3-3_CanoR_1 | 414 | 422 | PF00244 | 0.488 |
LIG_14-3-3_CanoR_1 | 575 | 583 | PF00244 | 0.663 |
LIG_Actin_WH2_2 | 398 | 416 | PF00022 | 0.493 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.606 |
LIG_BRCT_BRCA1_1 | 449 | 453 | PF00533 | 0.463 |
LIG_BRCT_BRCA1_1 | 594 | 598 | PF00533 | 0.614 |
LIG_Clathr_ClatBox_1 | 213 | 217 | PF01394 | 0.460 |
LIG_EH1_1 | 616 | 624 | PF00400 | 0.317 |
LIG_FHA_1 | 301 | 307 | PF00498 | 0.515 |
LIG_FHA_1 | 332 | 338 | PF00498 | 0.499 |
LIG_FHA_1 | 4 | 10 | PF00498 | 0.615 |
LIG_FHA_1 | 40 | 46 | PF00498 | 0.482 |
LIG_FHA_1 | 547 | 553 | PF00498 | 0.633 |
LIG_FHA_1 | 56 | 62 | PF00498 | 0.506 |
LIG_FHA_2 | 13 | 19 | PF00498 | 0.558 |
LIG_FHA_2 | 175 | 181 | PF00498 | 0.729 |
LIG_FHA_2 | 20 | 26 | PF00498 | 0.519 |
LIG_FHA_2 | 222 | 228 | PF00498 | 0.602 |
LIG_FHA_2 | 229 | 235 | PF00498 | 0.571 |
LIG_FHA_2 | 264 | 270 | PF00498 | 0.480 |
LIG_FHA_2 | 539 | 545 | PF00498 | 0.644 |
LIG_FHA_2 | 574 | 580 | PF00498 | 0.640 |
LIG_LIR_LC3C_4 | 80 | 85 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 608 | 613 | PF02991 | 0.289 |
LIG_MLH1_MIPbox_1 | 449 | 453 | PF16413 | 0.477 |
LIG_MLH1_MIPbox_1 | 594 | 598 | PF16413 | 0.520 |
LIG_NRBOX | 164 | 170 | PF00104 | 0.565 |
LIG_PCNA_PIPBox_1 | 405 | 414 | PF02747 | 0.449 |
LIG_PCNA_yPIPBox_3 | 368 | 380 | PF02747 | 0.532 |
LIG_PDZ_Class_1 | 646 | 651 | PF00595 | 0.483 |
LIG_Pex14_2 | 382 | 386 | PF04695 | 0.449 |
LIG_Rb_pABgroove_1 | 369 | 377 | PF01858 | 0.527 |
LIG_SH2_CRK | 341 | 345 | PF00017 | 0.509 |
LIG_SH2_CRK | 628 | 632 | PF00017 | 0.426 |
LIG_SH2_CRK | 66 | 70 | PF00017 | 0.550 |
LIG_SH2_NCK_1 | 613 | 617 | PF00017 | 0.273 |
LIG_SH2_NCK_1 | 628 | 632 | PF00017 | 0.407 |
LIG_SH2_NCK_1 | 66 | 70 | PF00017 | 0.494 |
LIG_SH2_SRC | 476 | 479 | PF00017 | 0.626 |
LIG_SH2_SRC | 66 | 69 | PF00017 | 0.446 |
LIG_SH2_STAP1 | 613 | 617 | PF00017 | 0.259 |
LIG_SH2_STAT3 | 391 | 394 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 391 | 394 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 452 | 455 | PF00017 | 0.486 |
LIG_SH2_STAT5 | 476 | 479 | PF00017 | 0.527 |
LIG_SH2_STAT5 | 613 | 616 | PF00017 | 0.261 |
LIG_SH3_1 | 489 | 495 | PF00018 | 0.561 |
LIG_SH3_3 | 122 | 128 | PF00018 | 0.492 |
LIG_SH3_3 | 23 | 29 | PF00018 | 0.574 |
LIG_SH3_3 | 381 | 387 | PF00018 | 0.460 |
LIG_SH3_3 | 489 | 495 | PF00018 | 0.612 |
LIG_SH3_3 | 568 | 574 | PF00018 | 0.691 |
LIG_SUMO_SIM_anti_2 | 78 | 86 | PF11976 | 0.474 |
LIG_SUMO_SIM_par_1 | 212 | 217 | PF11976 | 0.499 |
LIG_SUMO_SIM_par_1 | 40 | 48 | PF11976 | 0.435 |
LIG_SUMO_SIM_par_1 | 78 | 86 | PF11976 | 0.460 |
LIG_TRAF2_1 | 290 | 293 | PF00917 | 0.521 |
LIG_TRAF2_1 | 423 | 426 | PF00917 | 0.625 |
LIG_UBA3_1 | 50 | 56 | PF00899 | 0.506 |
MOD_CDK_SPK_2 | 343 | 348 | PF00069 | 0.483 |
MOD_CK1_1 | 223 | 229 | PF00069 | 0.615 |
MOD_CK1_1 | 254 | 260 | PF00069 | 0.558 |
MOD_CK1_1 | 361 | 367 | PF00069 | 0.581 |
MOD_CK1_1 | 416 | 422 | PF00069 | 0.560 |
MOD_CK1_1 | 519 | 525 | PF00069 | 0.600 |
MOD_CK1_1 | 538 | 544 | PF00069 | 0.566 |
MOD_CK1_1 | 611 | 617 | PF00069 | 0.386 |
MOD_CK1_1 | 629 | 635 | PF00069 | 0.291 |
MOD_CK2_1 | 109 | 115 | PF00069 | 0.444 |
MOD_CK2_1 | 12 | 18 | PF00069 | 0.539 |
MOD_CK2_1 | 174 | 180 | PF00069 | 0.713 |
MOD_CK2_1 | 19 | 25 | PF00069 | 0.540 |
MOD_CK2_1 | 228 | 234 | PF00069 | 0.600 |
MOD_CK2_1 | 254 | 260 | PF00069 | 0.568 |
MOD_CK2_1 | 287 | 293 | PF00069 | 0.566 |
MOD_CK2_1 | 294 | 300 | PF00069 | 0.530 |
MOD_CK2_1 | 420 | 426 | PF00069 | 0.583 |
MOD_CK2_1 | 51 | 57 | PF00069 | 0.633 |
MOD_CK2_1 | 538 | 544 | PF00069 | 0.619 |
MOD_CK2_1 | 573 | 579 | PF00069 | 0.729 |
MOD_GlcNHglycan | 295 | 299 | PF01048 | 0.293 |
MOD_GlcNHglycan | 363 | 366 | PF01048 | 0.311 |
MOD_GlcNHglycan | 449 | 452 | PF01048 | 0.251 |
MOD_GlcNHglycan | 481 | 484 | PF01048 | 0.325 |
MOD_GlcNHglycan | 504 | 510 | PF01048 | 0.425 |
MOD_GlcNHglycan | 518 | 521 | PF01048 | 0.452 |
MOD_GlcNHglycan | 531 | 534 | PF01048 | 0.403 |
MOD_GlcNHglycan | 537 | 540 | PF01048 | 0.365 |
MOD_GlcNHglycan | 568 | 571 | PF01048 | 0.512 |
MOD_GlcNHglycan | 628 | 631 | PF01048 | 0.504 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.382 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.602 |
MOD_GSK3_1 | 226 | 233 | PF00069 | 0.619 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.528 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.568 |
MOD_GSK3_1 | 339 | 346 | PF00069 | 0.484 |
MOD_GSK3_1 | 413 | 420 | PF00069 | 0.473 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.551 |
MOD_GSK3_1 | 512 | 519 | PF00069 | 0.692 |
MOD_GSK3_1 | 529 | 536 | PF00069 | 0.625 |
MOD_GSK3_1 | 562 | 569 | PF00069 | 0.680 |
MOD_N-GLC_1 | 220 | 225 | PF02516 | 0.401 |
MOD_N-GLC_2 | 247 | 249 | PF02516 | 0.321 |
MOD_NEK2_1 | 109 | 114 | PF00069 | 0.485 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.542 |
MOD_NEK2_1 | 263 | 268 | PF00069 | 0.495 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.575 |
MOD_NEK2_1 | 413 | 418 | PF00069 | 0.447 |
MOD_NEK2_1 | 466 | 471 | PF00069 | 0.539 |
MOD_NEK2_1 | 51 | 56 | PF00069 | 0.548 |
MOD_NEK2_1 | 566 | 571 | PF00069 | 0.702 |
MOD_NEK2_1 | 626 | 631 | PF00069 | 0.506 |
MOD_NEK2_1 | 641 | 646 | PF00069 | 0.348 |
MOD_NEK2_2 | 605 | 610 | PF00069 | 0.414 |
MOD_NEK2_2 | 646 | 651 | PF00069 | 0.483 |
MOD_PIKK_1 | 119 | 125 | PF00454 | 0.601 |
MOD_PIKK_1 | 12 | 18 | PF00454 | 0.492 |
MOD_PIKK_1 | 251 | 257 | PF00454 | 0.530 |
MOD_PIKK_1 | 263 | 269 | PF00454 | 0.405 |
MOD_PIKK_1 | 339 | 345 | PF00454 | 0.499 |
MOD_PKA_1 | 140 | 146 | PF00069 | 0.567 |
MOD_PKA_2 | 12 | 18 | PF00069 | 0.509 |
MOD_PKA_2 | 413 | 419 | PF00069 | 0.450 |
MOD_PKB_1 | 37 | 45 | PF00069 | 0.537 |
MOD_Plk_1 | 19 | 25 | PF00069 | 0.539 |
MOD_Plk_1 | 216 | 222 | PF00069 | 0.598 |
MOD_Plk_1 | 330 | 336 | PF00069 | 0.471 |
MOD_Plk_1 | 358 | 364 | PF00069 | 0.522 |
MOD_Plk_1 | 39 | 45 | PF00069 | 0.491 |
MOD_Plk_1 | 562 | 568 | PF00069 | 0.574 |
MOD_Plk_2-3 | 287 | 293 | PF00069 | 0.569 |
MOD_Plk_4 | 331 | 337 | PF00069 | 0.471 |
MOD_Plk_4 | 417 | 423 | PF00069 | 0.516 |
MOD_Plk_4 | 605 | 611 | PF00069 | 0.331 |
MOD_ProDKin_1 | 343 | 349 | PF00069 | 0.479 |
MOD_SUMO_for_1 | 195 | 198 | PF00179 | 0.573 |
MOD_SUMO_for_1 | 460 | 463 | PF00179 | 0.507 |
MOD_SUMO_rev_2 | 233 | 238 | PF00179 | 0.598 |
MOD_SUMO_rev_2 | 40 | 48 | PF00179 | 0.435 |
MOD_SUMO_rev_2 | 499 | 509 | PF00179 | 0.611 |
TRG_DiLeu_BaEn_1 | 331 | 336 | PF01217 | 0.486 |
TRG_ENDOCYTIC_2 | 341 | 344 | PF00928 | 0.482 |
TRG_ENDOCYTIC_2 | 628 | 631 | PF00928 | 0.390 |
TRG_ENDOCYTIC_2 | 66 | 69 | PF00928 | 0.480 |
TRG_ER_diArg_1 | 36 | 39 | PF00400 | 0.587 |
TRG_ER_diArg_1 | 488 | 490 | PF00400 | 0.572 |
TRG_ER_diArg_1 | 583 | 586 | PF00400 | 0.682 |
TRG_NLS_MonoExtC_3 | 209 | 215 | PF00514 | 0.581 |
TRG_Pf-PMV_PEXEL_1 | 167 | 171 | PF00026 | 0.349 |
TRG_Pf-PMV_PEXEL_1 | 211 | 215 | PF00026 | 0.330 |
TRG_Pf-PMV_PEXEL_1 | 356 | 360 | PF00026 | 0.311 |
TRG_Pf-PMV_PEXEL_1 | 39 | 44 | PF00026 | 0.359 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HYF2 | Leptomonas seymouri | 72% | 100% |
A0A0S4IMM1 | Bodo saltans | 42% | 91% |
A0A1X0NQQ8 | Trypanosomatidae | 50% | 100% |
A0A3Q8IE19 | Leishmania donovani | 89% | 100% |
A0A3R7RF21 | Trypanosoma rangeli | 49% | 100% |
D0A915 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 51% | 96% |
E9B038 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
Q4Q848 | Leishmania major | 88% | 100% |
V5BCV7 | Trypanosoma cruzi | 49% | 100% |