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. | yes | 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 | 2 |
GO:0005742 | mitochondrial outer membrane translocase complex | 4 | 2 |
GO:0016020 | membrane | 2 | 4 |
GO:0019867 | outer membrane | 3 | 2 |
GO:0031090 | organelle membrane | 3 | 2 |
GO:0031966 | mitochondrial membrane | 4 | 2 |
GO:0031968 | organelle outer membrane | 4 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0098588 | bounding membrane of organelle | 4 | 2 |
GO:0098796 | membrane protein complex | 2 | 2 |
GO:0098798 | mitochondrial protein-containing complex | 2 | 2 |
GO:0098799 | outer mitochondrial membrane protein complex | 3 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 4 |
Related structures:
AlphaFold database: Q4Q848
Term | Name | Level | Count |
---|---|---|---|
GO:0006605 | protein targeting | 5 | 2 |
GO:0006626 | protein targeting to mitochondrion | 5 | 2 |
GO:0006810 | transport | 3 | 2 |
GO:0006839 | mitochondrial transport | 4 | 2 |
GO:0006886 | intracellular protein transport | 4 | 2 |
GO:0008104 | protein localization | 4 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0015031 | protein transport | 4 | 2 |
GO:0030150 | protein import into mitochondrial matrix | 4 | 2 |
GO:0033036 | macromolecule localization | 2 | 2 |
GO:0033365 | protein localization to organelle | 5 | 2 |
GO:0044743 | protein transmembrane import into intracellular organelle | 4 | 2 |
GO:0045184 | establishment of protein localization | 3 | 2 |
GO:0046907 | intracellular transport | 3 | 2 |
GO:0051179 | localization | 1 | 2 |
GO:0051234 | establishment of localization | 2 | 2 |
GO:0051641 | cellular localization | 2 | 2 |
GO:0051649 | establishment of localization in cell | 3 | 2 |
GO:0055085 | transmembrane transport | 2 | 2 |
GO:0065002 | intracellular protein transmembrane transport | 4 | 2 |
GO:0070585 | protein localization to mitochondrion | 6 | 2 |
GO:0070727 | cellular macromolecule localization | 3 | 2 |
GO:0071702 | organic substance transport | 4 | 2 |
GO:0071705 | nitrogen compound transport | 4 | 2 |
GO:0071806 | protein transmembrane transport | 3 | 2 |
GO:0072594 | establishment of protein localization to organelle | 4 | 2 |
GO:0072655 | establishment of protein localization to mitochondrion | 5 | 2 |
GO:1990542 | mitochondrial transmembrane transport | 3 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 475 | 479 | PF00656 | 0.620 |
CLV_NRD_NRD_1 | 489 | 491 | PF00675 | 0.394 |
CLV_NRD_NRD_1 | 585 | 587 | PF00675 | 0.616 |
CLV_PCSK_KEX2_1 | 355 | 357 | PF00082 | 0.348 |
CLV_PCSK_KEX2_1 | 489 | 491 | PF00082 | 0.385 |
CLV_PCSK_PC1ET2_1 | 355 | 357 | PF00082 | 0.408 |
CLV_PCSK_SKI1_1 | 174 | 178 | PF00082 | 0.519 |
CLV_PCSK_SKI1_1 | 179 | 183 | PF00082 | 0.587 |
CLV_PCSK_SKI1_1 | 236 | 240 | PF00082 | 0.349 |
CLV_PCSK_SKI1_1 | 348 | 352 | PF00082 | 0.310 |
CLV_PCSK_SKI1_1 | 355 | 359 | PF00082 | 0.307 |
CLV_PCSK_SKI1_1 | 380 | 384 | PF00082 | 0.320 |
CLV_PCSK_SKI1_1 | 39 | 43 | PF00082 | 0.348 |
CLV_PCSK_SKI1_1 | 395 | 399 | PF00082 | 0.299 |
CLV_PCSK_SKI1_1 | 414 | 418 | PF00082 | 0.397 |
CLV_PCSK_SKI1_1 | 507 | 511 | PF00082 | 0.482 |
CLV_PCSK_SKI1_1 | 620 | 624 | PF00082 | 0.357 |
CLV_Separin_Metazoa | 486 | 490 | PF03568 | 0.690 |
DEG_APCC_DBOX_1 | 120 | 128 | PF00400 | 0.599 |
DEG_SCF_FBW7_2 | 109 | 115 | PF00400 | 0.551 |
DEG_SPOP_SBC_1 | 519 | 523 | PF00917 | 0.689 |
DOC_CDC14_PxL_1 | 635 | 643 | PF14671 | 0.434 |
DOC_CKS1_1 | 109 | 114 | PF01111 | 0.553 |
DOC_CYCLIN_yCln2_LP_2 | 532 | 538 | PF00134 | 0.802 |
DOC_CYCLIN_yCln2_LP_2 | 615 | 621 | PF00134 | 0.359 |
DOC_MAPK_gen_1 | 118 | 126 | PF00069 | 0.605 |
DOC_MAPK_gen_1 | 37 | 45 | PF00069 | 0.548 |
DOC_MAPK_JIP1_4 | 37 | 43 | PF00069 | 0.598 |
DOC_MAPK_MEF2A_6 | 37 | 45 | PF00069 | 0.548 |
DOC_MAPK_MEF2A_6 | 489 | 496 | PF00069 | 0.570 |
DOC_PP1_RVXF_1 | 57 | 64 | PF00149 | 0.662 |
DOC_PP2B_LxvP_1 | 532 | 535 | PF13499 | 0.675 |
DOC_PP2B_LxvP_1 | 99 | 102 | PF13499 | 0.506 |
DOC_USP7_MATH_1 | 181 | 185 | PF00917 | 0.701 |
DOC_USP7_MATH_1 | 251 | 255 | PF00917 | 0.628 |
DOC_USP7_MATH_1 | 416 | 420 | PF00917 | 0.610 |
DOC_USP7_MATH_1 | 429 | 433 | PF00917 | 0.639 |
DOC_USP7_MATH_1 | 479 | 483 | PF00917 | 0.554 |
DOC_USP7_MATH_1 | 562 | 566 | PF00917 | 0.703 |
DOC_USP7_MATH_1 | 67 | 71 | PF00917 | 0.637 |
DOC_WW_Pin1_4 | 108 | 113 | PF00397 | 0.648 |
DOC_WW_Pin1_4 | 343 | 348 | PF00397 | 0.523 |
DOC_WW_Pin1_4 | 515 | 520 | PF00397 | 0.710 |
LIG_14-3-3_CanoR_1 | 118 | 128 | PF00244 | 0.603 |
LIG_14-3-3_CanoR_1 | 250 | 256 | PF00244 | 0.607 |
LIG_14-3-3_CanoR_1 | 414 | 422 | PF00244 | 0.525 |
LIG_14-3-3_CanoR_1 | 575 | 583 | PF00244 | 0.702 |
LIG_Actin_WH2_2 | 398 | 416 | PF00022 | 0.533 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.656 |
LIG_BRCT_BRCA1_1 | 449 | 453 | PF00533 | 0.503 |
LIG_BRCT_BRCA1_1 | 567 | 571 | PF00533 | 0.689 |
LIG_BRCT_BRCA1_1 | 594 | 598 | PF00533 | 0.655 |
LIG_EH1_1 | 616 | 624 | PF00400 | 0.359 |
LIG_FHA_1 | 301 | 307 | PF00498 | 0.555 |
LIG_FHA_1 | 332 | 338 | PF00498 | 0.542 |
LIG_FHA_1 | 4 | 10 | PF00498 | 0.662 |
LIG_FHA_1 | 40 | 46 | PF00498 | 0.550 |
LIG_FHA_1 | 547 | 553 | PF00498 | 0.695 |
LIG_FHA_1 | 56 | 62 | PF00498 | 0.548 |
LIG_FHA_2 | 13 | 19 | PF00498 | 0.607 |
LIG_FHA_2 | 175 | 181 | PF00498 | 0.759 |
LIG_FHA_2 | 20 | 26 | PF00498 | 0.573 |
LIG_FHA_2 | 222 | 228 | PF00498 | 0.662 |
LIG_FHA_2 | 229 | 235 | PF00498 | 0.628 |
LIG_FHA_2 | 264 | 270 | PF00498 | 0.545 |
LIG_Integrin_RGD_1 | 104 | 106 | PF01839 | 0.321 |
LIG_LIR_Nem_3 | 608 | 613 | PF02991 | 0.331 |
LIG_MLH1_MIPbox_1 | 449 | 453 | PF16413 | 0.517 |
LIG_NRBOX | 164 | 170 | PF00104 | 0.607 |
LIG_PCNA_PIPBox_1 | 405 | 414 | PF02747 | 0.487 |
LIG_PCNA_yPIPBox_3 | 368 | 380 | PF02747 | 0.574 |
LIG_PDZ_Class_1 | 646 | 651 | PF00595 | 0.519 |
LIG_Pex14_2 | 382 | 386 | PF04695 | 0.488 |
LIG_Rb_pABgroove_1 | 369 | 377 | PF01858 | 0.569 |
LIG_SH2_CRK | 341 | 345 | PF00017 | 0.549 |
LIG_SH2_CRK | 628 | 632 | PF00017 | 0.383 |
LIG_SH2_CRK | 66 | 70 | PF00017 | 0.583 |
LIG_SH2_NCK_1 | 613 | 617 | PF00017 | 0.315 |
LIG_SH2_NCK_1 | 628 | 632 | PF00017 | 0.370 |
LIG_SH2_NCK_1 | 66 | 70 | PF00017 | 0.526 |
LIG_SH2_SRC | 476 | 479 | PF00017 | 0.660 |
LIG_SH2_STAP1 | 613 | 617 | PF00017 | 0.300 |
LIG_SH2_STAT3 | 391 | 394 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 391 | 394 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 452 | 455 | PF00017 | 0.528 |
LIG_SH2_STAT5 | 476 | 479 | PF00017 | 0.566 |
LIG_SH2_STAT5 | 613 | 616 | PF00017 | 0.302 |
LIG_SH3_1 | 489 | 495 | PF00018 | 0.608 |
LIG_SH3_3 | 122 | 128 | PF00018 | 0.538 |
LIG_SH3_3 | 23 | 29 | PF00018 | 0.631 |
LIG_SH3_3 | 381 | 387 | PF00018 | 0.499 |
LIG_SH3_3 | 489 | 495 | PF00018 | 0.650 |
LIG_TRAF2_1 | 423 | 426 | PF00917 | 0.669 |
LIG_TRAF2_1 | 511 | 514 | PF00917 | 0.702 |
LIG_UBA3_1 | 50 | 56 | PF00899 | 0.561 |
MOD_CDK_SPK_2 | 343 | 348 | PF00069 | 0.523 |
MOD_CK1_1 | 223 | 229 | PF00069 | 0.674 |
MOD_CK1_1 | 254 | 260 | PF00069 | 0.597 |
MOD_CK1_1 | 361 | 367 | PF00069 | 0.629 |
MOD_CK1_1 | 420 | 426 | PF00069 | 0.632 |
MOD_CK1_1 | 565 | 571 | PF00069 | 0.705 |
MOD_CK1_1 | 611 | 617 | PF00069 | 0.427 |
MOD_CK1_1 | 629 | 635 | PF00069 | 0.327 |
MOD_CK2_1 | 12 | 18 | PF00069 | 0.587 |
MOD_CK2_1 | 130 | 136 | PF00069 | 0.696 |
MOD_CK2_1 | 174 | 180 | PF00069 | 0.747 |
MOD_CK2_1 | 181 | 187 | PF00069 | 0.796 |
MOD_CK2_1 | 19 | 25 | PF00069 | 0.592 |
MOD_CK2_1 | 221 | 227 | PF00069 | 0.682 |
MOD_CK2_1 | 228 | 234 | PF00069 | 0.654 |
MOD_CK2_1 | 254 | 260 | PF00069 | 0.614 |
MOD_CK2_1 | 287 | 293 | PF00069 | 0.607 |
MOD_CK2_1 | 420 | 426 | PF00069 | 0.631 |
MOD_CK2_1 | 51 | 57 | PF00069 | 0.668 |
MOD_GlcNHglycan | 142 | 145 | PF01048 | 0.593 |
MOD_GlcNHglycan | 359 | 363 | PF01048 | 0.409 |
MOD_GlcNHglycan | 449 | 452 | PF01048 | 0.291 |
MOD_GlcNHglycan | 481 | 484 | PF01048 | 0.363 |
MOD_GlcNHglycan | 504 | 510 | PF01048 | 0.469 |
MOD_GlcNHglycan | 565 | 568 | PF01048 | 0.525 |
MOD_GlcNHglycan | 579 | 582 | PF01048 | 0.478 |
MOD_GlcNHglycan | 590 | 593 | PF01048 | 0.441 |
MOD_GlcNHglycan | 628 | 631 | PF01048 | 0.638 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.402 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.679 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.662 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.566 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.607 |
MOD_GSK3_1 | 339 | 346 | PF00069 | 0.531 |
MOD_GSK3_1 | 416 | 423 | PF00069 | 0.536 |
MOD_GSK3_1 | 505 | 512 | PF00069 | 0.674 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.583 |
MOD_GSK3_1 | 514 | 521 | PF00069 | 0.738 |
MOD_GSK3_1 | 571 | 578 | PF00069 | 0.792 |
MOD_GSK3_1 | 588 | 595 | PF00069 | 0.695 |
MOD_N-GLC_1 | 220 | 225 | PF02516 | 0.472 |
MOD_N-GLC_1 | 296 | 301 | PF02516 | 0.403 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.585 |
MOD_NEK2_1 | 263 | 268 | PF00069 | 0.538 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.636 |
MOD_NEK2_1 | 466 | 471 | PF00069 | 0.577 |
MOD_NEK2_1 | 51 | 56 | PF00069 | 0.577 |
MOD_NEK2_1 | 571 | 576 | PF00069 | 0.716 |
MOD_NEK2_1 | 626 | 631 | PF00069 | 0.545 |
MOD_NEK2_1 | 641 | 646 | PF00069 | 0.385 |
MOD_NEK2_2 | 605 | 610 | PF00069 | 0.453 |
MOD_NEK2_2 | 646 | 651 | PF00069 | 0.519 |
MOD_PIKK_1 | 119 | 125 | PF00454 | 0.629 |
MOD_PIKK_1 | 12 | 18 | PF00454 | 0.540 |
MOD_PIKK_1 | 244 | 250 | PF00454 | 0.599 |
MOD_PIKK_1 | 251 | 257 | PF00454 | 0.567 |
MOD_PIKK_1 | 263 | 269 | PF00454 | 0.443 |
MOD_PIKK_1 | 339 | 345 | PF00454 | 0.539 |
MOD_PIKK_1 | 509 | 515 | PF00454 | 0.671 |
MOD_PK_1 | 46 | 52 | PF00069 | 0.636 |
MOD_PKA_2 | 12 | 18 | PF00069 | 0.557 |
MOD_PKB_1 | 37 | 45 | PF00069 | 0.590 |
MOD_Plk_1 | 19 | 25 | PF00069 | 0.592 |
MOD_Plk_1 | 216 | 222 | PF00069 | 0.643 |
MOD_Plk_1 | 330 | 336 | PF00069 | 0.511 |
MOD_Plk_1 | 39 | 45 | PF00069 | 0.513 |
MOD_Plk_2-3 | 132 | 138 | PF00069 | 0.656 |
MOD_Plk_2-3 | 20 | 26 | PF00069 | 0.604 |
MOD_Plk_2-3 | 287 | 293 | PF00069 | 0.606 |
MOD_Plk_4 | 331 | 337 | PF00069 | 0.511 |
MOD_Plk_4 | 417 | 423 | PF00069 | 0.553 |
MOD_Plk_4 | 46 | 52 | PF00069 | 0.534 |
MOD_Plk_4 | 605 | 611 | PF00069 | 0.373 |
MOD_ProDKin_1 | 108 | 114 | PF00069 | 0.651 |
MOD_ProDKin_1 | 343 | 349 | PF00069 | 0.518 |
MOD_ProDKin_1 | 515 | 521 | PF00069 | 0.709 |
MOD_SUMO_for_1 | 195 | 198 | PF00179 | 0.612 |
MOD_SUMO_for_1 | 460 | 463 | PF00179 | 0.546 |
MOD_SUMO_rev_2 | 175 | 184 | PF00179 | 0.773 |
MOD_SUMO_rev_2 | 499 | 509 | PF00179 | 0.652 |
MOD_SUMO_rev_2 | 86 | 91 | PF00179 | 0.661 |
TRG_DiLeu_BaEn_1 | 331 | 336 | PF01217 | 0.526 |
TRG_ENDOCYTIC_2 | 341 | 344 | PF00928 | 0.521 |
TRG_ENDOCYTIC_2 | 628 | 631 | PF00928 | 0.357 |
TRG_ENDOCYTIC_2 | 66 | 69 | PF00928 | 0.517 |
TRG_ER_diArg_1 | 36 | 39 | PF00400 | 0.635 |
TRG_ER_diArg_1 | 488 | 490 | PF00400 | 0.619 |
TRG_ER_diArg_1 | 583 | 586 | PF00400 | 0.726 |
TRG_NLS_MonoExtC_3 | 209 | 215 | PF00514 | 0.622 |
TRG_Pf-PMV_PEXEL_1 | 167 | 171 | PF00026 | 0.412 |
TRG_Pf-PMV_PEXEL_1 | 211 | 215 | PF00026 | 0.370 |
TRG_Pf-PMV_PEXEL_1 | 356 | 360 | PF00026 | 0.354 |
TRG_Pf-PMV_PEXEL_1 | 39 | 44 | PF00026 | 0.413 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HYF2 | Leptomonas seymouri | 73% | 100% |
A0A0S4IMM1 | Bodo saltans | 43% | 91% |
A0A1X0NQQ8 | Trypanosomatidae | 49% | 100% |
A0A3Q8IE19 | Leishmania donovani | 98% | 100% |
A0A3R7RF21 | Trypanosoma rangeli | 49% | 100% |
A4HGS1 | Leishmania braziliensis | 88% | 100% |
D0A915 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 96% |
E9B038 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
V5BCV7 | Trypanosoma cruzi | 48% | 100% |