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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000421 | autophagosome membrane | 6 | 2 |
GO:0005774 | vacuolar membrane | 5 | 2 |
GO:0005840 | ribosome | 5 | 11 |
GO:0016020 | membrane | 2 | 2 |
GO:0031090 | organelle membrane | 3 | 2 |
GO:0032991 | protein-containing complex | 1 | 11 |
GO:0043226 | organelle | 2 | 11 |
GO:0043228 | non-membrane-bounded organelle | 3 | 11 |
GO:0043229 | intracellular organelle | 3 | 11 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 11 |
GO:0098588 | bounding membrane of organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
GO:1990904 | ribonucleoprotein complex | 2 | 11 |
Related structures:
AlphaFold database: Q4Q446
Term | Name | Level | Count |
---|---|---|---|
GO:0000045 | autophagosome assembly | 6 | 11 |
GO:0006996 | organelle organization | 4 | 11 |
GO:0007033 | vacuole organization | 5 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016043 | cellular component organization | 3 | 11 |
GO:0022607 | cellular component assembly | 4 | 11 |
GO:0070925 | organelle assembly | 5 | 11 |
GO:0071840 | cellular component organization or biogenesis | 2 | 11 |
GO:1905037 | autophagosome organization | 6 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 466 | 470 | PF00656 | 0.473 |
CLV_C14_Caspase3-7 | 527 | 531 | PF00656 | 0.750 |
CLV_NRD_NRD_1 | 207 | 209 | PF00675 | 0.500 |
CLV_NRD_NRD_1 | 391 | 393 | PF00675 | 0.460 |
CLV_NRD_NRD_1 | 428 | 430 | PF00675 | 0.463 |
CLV_PCSK_KEX2_1 | 207 | 209 | PF00082 | 0.505 |
CLV_PCSK_KEX2_1 | 226 | 228 | PF00082 | 0.574 |
CLV_PCSK_KEX2_1 | 293 | 295 | PF00082 | 0.196 |
CLV_PCSK_KEX2_1 | 390 | 392 | PF00082 | 0.494 |
CLV_PCSK_KEX2_1 | 428 | 430 | PF00082 | 0.463 |
CLV_PCSK_PC1ET2_1 | 226 | 228 | PF00082 | 0.726 |
CLV_PCSK_PC1ET2_1 | 293 | 295 | PF00082 | 0.196 |
CLV_PCSK_SKI1_1 | 130 | 134 | PF00082 | 0.404 |
CLV_PCSK_SKI1_1 | 180 | 184 | PF00082 | 0.491 |
CLV_PCSK_SKI1_1 | 195 | 199 | PF00082 | 0.506 |
CLV_PCSK_SKI1_1 | 293 | 297 | PF00082 | 0.312 |
CLV_PCSK_SKI1_1 | 396 | 400 | PF00082 | 0.439 |
CLV_PCSK_SKI1_1 | 429 | 433 | PF00082 | 0.564 |
CLV_PCSK_SKI1_1 | 442 | 446 | PF00082 | 0.291 |
CLV_PCSK_SKI1_1 | 471 | 475 | PF00082 | 0.484 |
CLV_PCSK_SKI1_1 | 539 | 543 | PF00082 | 0.535 |
CLV_PCSK_SKI1_1 | 99 | 103 | PF00082 | 0.591 |
DEG_APCC_DBOX_1 | 391 | 399 | PF00400 | 0.511 |
DEG_SPOP_SBC_1 | 277 | 281 | PF00917 | 0.396 |
DOC_CYCLIN_RxL_1 | 471 | 479 | PF00134 | 0.531 |
DOC_MAPK_DCC_7 | 475 | 485 | PF00069 | 0.429 |
DOC_MAPK_gen_1 | 183 | 192 | PF00069 | 0.491 |
DOC_MAPK_MEF2A_6 | 509 | 518 | PF00069 | 0.462 |
DOC_USP7_MATH_1 | 265 | 269 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 277 | 281 | PF00917 | 0.530 |
DOC_USP7_MATH_1 | 36 | 40 | PF00917 | 0.571 |
DOC_USP7_MATH_1 | 431 | 435 | PF00917 | 0.543 |
DOC_USP7_MATH_1 | 504 | 508 | PF00917 | 0.507 |
DOC_USP7_MATH_1 | 528 | 532 | PF00917 | 0.744 |
DOC_USP7_MATH_1 | 543 | 547 | PF00917 | 0.583 |
DOC_USP7_MATH_1 | 575 | 579 | PF00917 | 0.484 |
DOC_USP7_MATH_1 | 82 | 86 | PF00917 | 0.602 |
DOC_WW_Pin1_4 | 239 | 244 | PF00397 | 0.777 |
DOC_WW_Pin1_4 | 246 | 251 | PF00397 | 0.737 |
DOC_WW_Pin1_4 | 256 | 261 | PF00397 | 0.499 |
DOC_WW_Pin1_4 | 308 | 313 | PF00397 | 0.351 |
DOC_WW_Pin1_4 | 531 | 536 | PF00397 | 0.710 |
DOC_WW_Pin1_4 | 8 | 13 | PF00397 | 0.671 |
LIG_14-3-3_CanoR_1 | 167 | 173 | PF00244 | 0.591 |
LIG_14-3-3_CanoR_1 | 195 | 200 | PF00244 | 0.540 |
LIG_14-3-3_CanoR_1 | 442 | 449 | PF00244 | 0.437 |
LIG_14-3-3_CanoR_1 | 509 | 516 | PF00244 | 0.537 |
LIG_14-3-3_CanoR_1 | 68 | 78 | PF00244 | 0.583 |
LIG_Actin_WH2_2 | 165 | 182 | PF00022 | 0.557 |
LIG_Actin_WH2_2 | 19 | 37 | PF00022 | 0.600 |
LIG_CaM_IQ_9 | 148 | 164 | PF13499 | 0.554 |
LIG_DLG_GKlike_1 | 391 | 398 | PF00625 | 0.507 |
LIG_FHA_1 | 146 | 152 | PF00498 | 0.604 |
LIG_FHA_1 | 187 | 193 | PF00498 | 0.467 |
LIG_FHA_1 | 358 | 364 | PF00498 | 0.501 |
LIG_FHA_1 | 381 | 387 | PF00498 | 0.473 |
LIG_FHA_1 | 44 | 50 | PF00498 | 0.420 |
LIG_FHA_1 | 472 | 478 | PF00498 | 0.560 |
LIG_FHA_1 | 508 | 514 | PF00498 | 0.494 |
LIG_FHA_1 | 70 | 76 | PF00498 | 0.510 |
LIG_FHA_2 | 169 | 175 | PF00498 | 0.591 |
LIG_FHA_2 | 182 | 188 | PF00498 | 0.519 |
LIG_FHA_2 | 196 | 202 | PF00498 | 0.445 |
LIG_FHA_2 | 401 | 407 | PF00498 | 0.410 |
LIG_FHA_2 | 422 | 428 | PF00498 | 0.486 |
LIG_FHA_2 | 54 | 60 | PF00498 | 0.576 |
LIG_FHA_2 | 87 | 93 | PF00498 | 0.550 |
LIG_LIR_Gen_1 | 157 | 165 | PF02991 | 0.458 |
LIG_LIR_Gen_1 | 42 | 52 | PF02991 | 0.557 |
LIG_LIR_Nem_3 | 114 | 120 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 157 | 161 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 163 | 168 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 39 | 44 | PF02991 | 0.579 |
LIG_NRBOX | 394 | 400 | PF00104 | 0.501 |
LIG_Pex14_2 | 564 | 568 | PF04695 | 0.494 |
LIG_SH2_CRK | 117 | 121 | PF00017 | 0.458 |
LIG_SH2_CRK | 158 | 162 | PF00017 | 0.455 |
LIG_SH2_CRK | 165 | 169 | PF00017 | 0.467 |
LIG_SH2_CRK | 44 | 48 | PF00017 | 0.555 |
LIG_SH2_STAP1 | 91 | 95 | PF00017 | 0.403 |
LIG_SH2_STAT3 | 551 | 554 | PF00017 | 0.580 |
LIG_SH2_STAT5 | 158 | 161 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 178 | 181 | PF00017 | 0.604 |
LIG_SH2_STAT5 | 317 | 320 | PF00017 | 0.501 |
LIG_SH2_STAT5 | 333 | 336 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 44 | 47 | PF00017 | 0.557 |
LIG_SH3_3 | 6 | 12 | PF00018 | 0.670 |
LIG_SUMO_SIM_anti_2 | 510 | 517 | PF11976 | 0.458 |
LIG_SUMO_SIM_par_1 | 195 | 202 | PF11976 | 0.432 |
LIG_SUMO_SIM_par_1 | 462 | 469 | PF11976 | 0.478 |
LIG_SUMO_SIM_par_1 | 575 | 580 | PF11976 | 0.473 |
LIG_TRAF2_1 | 125 | 128 | PF00917 | 0.510 |
LIG_UBA3_1 | 132 | 139 | PF00899 | 0.605 |
MOD_CK1_1 | 11 | 17 | PF00069 | 0.639 |
MOD_CK1_1 | 249 | 255 | PF00069 | 0.678 |
MOD_CK1_1 | 268 | 274 | PF00069 | 0.563 |
MOD_CK1_1 | 319 | 325 | PF00069 | 0.444 |
MOD_CK1_1 | 379 | 385 | PF00069 | 0.330 |
MOD_CK1_1 | 394 | 400 | PF00069 | 0.377 |
MOD_CK1_1 | 43 | 49 | PF00069 | 0.592 |
MOD_CK1_1 | 507 | 513 | PF00069 | 0.462 |
MOD_CK1_1 | 531 | 537 | PF00069 | 0.662 |
MOD_CK1_1 | 546 | 552 | PF00069 | 0.596 |
MOD_CK1_1 | 556 | 562 | PF00069 | 0.590 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.614 |
MOD_CK1_1 | 86 | 92 | PF00069 | 0.486 |
MOD_CK2_1 | 168 | 174 | PF00069 | 0.558 |
MOD_CK2_1 | 181 | 187 | PF00069 | 0.525 |
MOD_CK2_1 | 86 | 92 | PF00069 | 0.554 |
MOD_Cter_Amidation | 291 | 294 | PF01082 | 0.224 |
MOD_GlcNHglycan | 297 | 300 | PF01048 | 0.359 |
MOD_GlcNHglycan | 370 | 373 | PF01048 | 0.314 |
MOD_GlcNHglycan | 415 | 418 | PF01048 | 0.327 |
MOD_GlcNHglycan | 433 | 436 | PF01048 | 0.426 |
MOD_GlcNHglycan | 449 | 452 | PF01048 | 0.286 |
MOD_GlcNHglycan | 498 | 501 | PF01048 | 0.499 |
MOD_GlcNHglycan | 506 | 509 | PF01048 | 0.510 |
MOD_GlcNHglycan | 530 | 533 | PF01048 | 0.657 |
MOD_GlcNHglycan | 555 | 558 | PF01048 | 0.654 |
MOD_GSK3_1 | 239 | 246 | PF00069 | 0.722 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.669 |
MOD_GSK3_1 | 268 | 275 | PF00069 | 0.546 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.591 |
MOD_GSK3_1 | 376 | 383 | PF00069 | 0.312 |
MOD_GSK3_1 | 427 | 434 | PF00069 | 0.529 |
MOD_GSK3_1 | 492 | 499 | PF00069 | 0.462 |
MOD_GSK3_1 | 504 | 511 | PF00069 | 0.457 |
MOD_GSK3_1 | 526 | 533 | PF00069 | 0.747 |
MOD_GSK3_1 | 543 | 550 | PF00069 | 0.506 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.634 |
MOD_LATS_1 | 440 | 446 | PF00433 | 0.421 |
MOD_N-GLC_1 | 546 | 551 | PF02516 | 0.632 |
MOD_N-GLC_1 | 83 | 88 | PF02516 | 0.604 |
MOD_NEK2_1 | 244 | 249 | PF00069 | 0.689 |
MOD_NEK2_1 | 295 | 300 | PF00069 | 0.345 |
MOD_NEK2_1 | 318 | 323 | PF00069 | 0.469 |
MOD_NEK2_1 | 327 | 332 | PF00069 | 0.344 |
MOD_NEK2_1 | 354 | 359 | PF00069 | 0.382 |
MOD_NEK2_1 | 368 | 373 | PF00069 | 0.275 |
MOD_NEK2_1 | 399 | 404 | PF00069 | 0.410 |
MOD_NEK2_1 | 455 | 460 | PF00069 | 0.420 |
MOD_NEK2_1 | 47 | 52 | PF00069 | 0.503 |
MOD_NEK2_1 | 473 | 478 | PF00069 | 0.353 |
MOD_NEK2_1 | 66 | 71 | PF00069 | 0.623 |
MOD_NEK2_2 | 36 | 41 | PF00069 | 0.570 |
MOD_NEK2_2 | 410 | 415 | PF00069 | 0.443 |
MOD_PIKK_1 | 34 | 40 | PF00454 | 0.544 |
MOD_PKA_1 | 391 | 397 | PF00069 | 0.476 |
MOD_PKA_2 | 111 | 117 | PF00069 | 0.506 |
MOD_PKA_2 | 168 | 174 | PF00069 | 0.558 |
MOD_PKA_2 | 391 | 397 | PF00069 | 0.477 |
MOD_PKA_2 | 427 | 433 | PF00069 | 0.451 |
MOD_PKA_2 | 447 | 453 | PF00069 | 0.494 |
MOD_PKA_2 | 492 | 498 | PF00069 | 0.393 |
MOD_PKA_2 | 508 | 514 | PF00069 | 0.430 |
MOD_PKA_2 | 69 | 75 | PF00069 | 0.628 |
MOD_Plk_1 | 156 | 162 | PF00069 | 0.542 |
MOD_Plk_1 | 186 | 192 | PF00069 | 0.380 |
MOD_Plk_1 | 380 | 386 | PF00069 | 0.312 |
MOD_Plk_1 | 405 | 411 | PF00069 | 0.475 |
MOD_Plk_1 | 546 | 552 | PF00069 | 0.518 |
MOD_Plk_1 | 66 | 72 | PF00069 | 0.593 |
MOD_Plk_1 | 83 | 89 | PF00069 | 0.497 |
MOD_Plk_4 | 268 | 274 | PF00069 | 0.515 |
MOD_Plk_4 | 36 | 42 | PF00069 | 0.544 |
MOD_Plk_4 | 410 | 416 | PF00069 | 0.390 |
MOD_Plk_4 | 47 | 53 | PF00069 | 0.516 |
MOD_Plk_4 | 473 | 479 | PF00069 | 0.519 |
MOD_ProDKin_1 | 239 | 245 | PF00069 | 0.779 |
MOD_ProDKin_1 | 246 | 252 | PF00069 | 0.738 |
MOD_ProDKin_1 | 256 | 262 | PF00069 | 0.495 |
MOD_ProDKin_1 | 308 | 314 | PF00069 | 0.343 |
MOD_ProDKin_1 | 531 | 537 | PF00069 | 0.693 |
MOD_ProDKin_1 | 8 | 14 | PF00069 | 0.670 |
MOD_SUMO_for_1 | 214 | 217 | PF00179 | 0.594 |
MOD_SUMO_rev_2 | 121 | 126 | PF00179 | 0.460 |
MOD_SUMO_rev_2 | 176 | 185 | PF00179 | 0.565 |
MOD_SUMO_rev_2 | 290 | 295 | PF00179 | 0.387 |
TRG_DiLeu_BaEn_1 | 23 | 28 | PF01217 | 0.596 |
TRG_DiLeu_BaEn_4 | 128 | 134 | PF01217 | 0.450 |
TRG_ENDOCYTIC_2 | 117 | 120 | PF00928 | 0.456 |
TRG_ENDOCYTIC_2 | 158 | 161 | PF00928 | 0.434 |
TRG_ENDOCYTIC_2 | 165 | 168 | PF00928 | 0.446 |
TRG_ENDOCYTIC_2 | 44 | 47 | PF00928 | 0.544 |
TRG_ER_diArg_1 | 133 | 136 | PF00400 | 0.363 |
TRG_ER_diArg_1 | 167 | 170 | PF00400 | 0.563 |
TRG_ER_diArg_1 | 206 | 208 | PF00400 | 0.549 |
TRG_ER_diArg_1 | 389 | 392 | PF00400 | 0.477 |
TRG_ER_diArg_1 | 61 | 64 | PF00400 | 0.574 |
TRG_ER_diArg_1 | 68 | 71 | PF00400 | 0.572 |
TRG_Pf-PMV_PEXEL_1 | 118 | 122 | PF00026 | 0.474 |
TRG_Pf-PMV_PEXEL_1 | 177 | 181 | PF00026 | 0.530 |
TRG_Pf-PMV_PEXEL_1 | 208 | 212 | PF00026 | 0.598 |
TRG_Pf-PMV_PEXEL_1 | 396 | 401 | PF00026 | 0.513 |
TRG_Pf-PMV_PEXEL_1 | 76 | 80 | PF00026 | 0.524 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAK2 | Leptomonas seymouri | 68% | 100% |
A0A0S4IUZ3 | Bodo saltans | 24% | 100% |
A0A0S4JA64 | Bodo saltans | 21% | 99% |
A0A1X0NWL7 | Trypanosomatidae | 36% | 100% |
A0A3R7NP23 | Trypanosoma rangeli | 21% | 99% |
A0A3S7X6T5 | Leishmania donovani | 93% | 100% |
A0A422NYX2 | Trypanosoma rangeli | 35% | 100% |
A4HLK2 | Leishmania braziliensis | 81% | 100% |
A4I913 | Leishmania infantum | 93% | 100% |
D0A054 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 22% | 100% |
D0A7L8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
E9B3X8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
O15736 | Dictyostelium discoideum | 23% | 96% |
Q5RAC9 | Pongo abelii | 26% | 97% |
Q676U5 | Homo sapiens | 26% | 97% |
Q6NNP0 | Arabidopsis thaliana | 27% | 100% |
Q8C0J2 | Mus musculus | 25% | 97% |
V5BW76 | Trypanosoma cruzi | 39% | 100% |