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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000323 | lytic vacuole | 6 | 1 |
GO:0005768 | endosome | 7 | 1 |
GO:0005773 | vacuole | 5 | 1 |
GO:0031410 | cytoplasmic vesicle | 6 | 1 |
GO:0031982 | vesicle | 4 | 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 |
GO:0097708 | intracellular vesicle | 5 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4I320
Term | Name | Level | Count |
---|---|---|---|
GO:0009987 | cellular process | 1 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022607 | cellular component assembly | 4 | 1 |
GO:0035493 | SNARE complex assembly | 6 | 1 |
GO:0043933 | protein-containing complex organization | 4 | 1 |
GO:0065003 | protein-containing complex assembly | 5 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000149 | SNARE binding | 3 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0005515 | protein binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 107 | 111 | PF00656 | 0.506 |
CLV_C14_Caspase3-7 | 494 | 498 | PF00656 | 0.569 |
CLV_NRD_NRD_1 | 326 | 328 | PF00675 | 0.593 |
CLV_NRD_NRD_1 | 378 | 380 | PF00675 | 0.506 |
CLV_NRD_NRD_1 | 498 | 500 | PF00675 | 0.487 |
CLV_NRD_NRD_1 | 537 | 539 | PF00675 | 0.517 |
CLV_PCSK_FUR_1 | 324 | 328 | PF00082 | 0.567 |
CLV_PCSK_FUR_1 | 376 | 380 | PF00082 | 0.449 |
CLV_PCSK_KEX2_1 | 326 | 328 | PF00082 | 0.593 |
CLV_PCSK_KEX2_1 | 378 | 380 | PF00082 | 0.506 |
CLV_PCSK_KEX2_1 | 537 | 539 | PF00082 | 0.517 |
CLV_PCSK_PC7_1 | 374 | 380 | PF00082 | 0.460 |
CLV_PCSK_SKI1_1 | 249 | 253 | PF00082 | 0.613 |
CLV_PCSK_SKI1_1 | 412 | 416 | PF00082 | 0.510 |
CLV_PCSK_SKI1_1 | 537 | 541 | PF00082 | 0.595 |
DEG_APCC_DBOX_1 | 148 | 156 | PF00400 | 0.595 |
DEG_APCC_DBOX_1 | 368 | 376 | PF00400 | 0.505 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.691 |
DOC_CYCLIN_RxL_1 | 376 | 388 | PF00134 | 0.519 |
DOC_CYCLIN_yCln2_LP_2 | 464 | 470 | PF00134 | 0.384 |
DOC_CYCLIN_yCln2_LP_2 | 489 | 495 | PF00134 | 0.650 |
DOC_MAPK_gen_1 | 376 | 385 | PF00069 | 0.518 |
DOC_MAPK_MEF2A_6 | 130 | 139 | PF00069 | 0.593 |
DOC_MAPK_MEF2A_6 | 292 | 300 | PF00069 | 0.504 |
DOC_MAPK_MEF2A_6 | 412 | 419 | PF00069 | 0.572 |
DOC_MAPK_MEF2A_6 | 545 | 554 | PF00069 | 0.434 |
DOC_PP1_RVXF_1 | 132 | 139 | PF00149 | 0.624 |
DOC_PP2B_LxvP_1 | 489 | 492 | PF13499 | 0.645 |
DOC_PP4_FxxP_1 | 10 | 13 | PF00568 | 0.576 |
DOC_PP4_FxxP_1 | 174 | 177 | PF00568 | 0.733 |
DOC_USP7_MATH_1 | 185 | 189 | PF00917 | 0.619 |
DOC_USP7_MATH_1 | 197 | 201 | PF00917 | 0.704 |
DOC_USP7_MATH_1 | 22 | 26 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 66 | 70 | PF00917 | 0.706 |
DOC_USP7_UBL2_3 | 530 | 534 | PF12436 | 0.522 |
DOC_WW_Pin1_4 | 344 | 349 | PF00397 | 0.602 |
DOC_WW_Pin1_4 | 477 | 482 | PF00397 | 0.475 |
DOC_WW_Pin1_4 | 69 | 74 | PF00397 | 0.734 |
DOC_WW_Pin1_4 | 9 | 14 | PF00397 | 0.672 |
LIG_14-3-3_CanoR_1 | 140 | 148 | PF00244 | 0.494 |
LIG_14-3-3_CanoR_1 | 170 | 175 | PF00244 | 0.741 |
LIG_14-3-3_CanoR_1 | 221 | 227 | PF00244 | 0.767 |
LIG_14-3-3_CanoR_1 | 23 | 28 | PF00244 | 0.627 |
LIG_14-3-3_CanoR_1 | 297 | 307 | PF00244 | 0.516 |
LIG_14-3-3_CanoR_1 | 355 | 359 | PF00244 | 0.594 |
LIG_BRCT_BRCA1_1 | 113 | 117 | PF00533 | 0.560 |
LIG_deltaCOP1_diTrp_1 | 2 | 10 | PF00928 | 0.678 |
LIG_EVH1_2 | 6 | 10 | PF00568 | 0.582 |
LIG_FHA_1 | 131 | 137 | PF00498 | 0.650 |
LIG_FHA_1 | 140 | 146 | PF00498 | 0.463 |
LIG_FHA_1 | 158 | 164 | PF00498 | 0.647 |
LIG_FHA_1 | 16 | 22 | PF00498 | 0.549 |
LIG_FHA_1 | 309 | 315 | PF00498 | 0.551 |
LIG_FHA_1 | 386 | 392 | PF00498 | 0.567 |
LIG_FHA_1 | 74 | 80 | PF00498 | 0.646 |
LIG_FHA_2 | 103 | 109 | PF00498 | 0.469 |
LIG_FHA_2 | 177 | 183 | PF00498 | 0.818 |
LIG_FHA_2 | 242 | 248 | PF00498 | 0.624 |
LIG_FHA_2 | 355 | 361 | PF00498 | 0.603 |
LIG_FHA_2 | 43 | 49 | PF00498 | 0.521 |
LIG_FHA_2 | 433 | 439 | PF00498 | 0.627 |
LIG_FHA_2 | 492 | 498 | PF00498 | 0.548 |
LIG_LIR_Apic_2 | 171 | 177 | PF02991 | 0.731 |
LIG_LIR_Apic_2 | 225 | 231 | PF02991 | 0.731 |
LIG_LIR_Apic_2 | 8 | 13 | PF02991 | 0.578 |
LIG_LIR_Gen_1 | 255 | 264 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 255 | 261 | PF02991 | 0.539 |
LIG_LIR_Nem_3 | 340 | 344 | PF02991 | 0.651 |
LIG_LYPXL_yS_3 | 466 | 469 | PF13949 | 0.479 |
LIG_NRBOX | 545 | 551 | PF00104 | 0.470 |
LIG_PCNA_yPIPBox_3 | 91 | 100 | PF02747 | 0.602 |
LIG_RPA_C_Fungi | 362 | 374 | PF08784 | 0.619 |
LIG_SH2_GRB2like | 395 | 398 | PF00017 | 0.660 |
LIG_SH2_STAP1 | 17 | 21 | PF00017 | 0.548 |
LIG_SH2_STAP1 | 387 | 391 | PF00017 | 0.514 |
LIG_SH2_STAP1 | 395 | 399 | PF00017 | 0.621 |
LIG_SH2_STAP1 | 460 | 464 | PF00017 | 0.508 |
LIG_SH2_STAT5 | 141 | 144 | PF00017 | 0.525 |
LIG_SH2_STAT5 | 17 | 20 | PF00017 | 0.513 |
LIG_SH2_STAT5 | 344 | 347 | PF00017 | 0.667 |
LIG_SH2_STAT5 | 387 | 390 | PF00017 | 0.560 |
LIG_SH2_STAT5 | 493 | 496 | PF00017 | 0.552 |
LIG_SH2_STAT5 | 53 | 56 | PF00017 | 0.498 |
LIG_SH3_3 | 142 | 148 | PF00018 | 0.427 |
LIG_SH3_CIN85_PxpxPR_1 | 232 | 237 | PF14604 | 0.696 |
LIG_SUMO_SIM_par_1 | 310 | 315 | PF11976 | 0.497 |
LIG_SUMO_SIM_par_1 | 387 | 393 | PF11976 | 0.550 |
LIG_SUMO_SIM_par_1 | 451 | 457 | PF11976 | 0.430 |
LIG_SUMO_SIM_par_1 | 466 | 472 | PF11976 | 0.449 |
LIG_TRAF2_1 | 105 | 108 | PF00917 | 0.579 |
LIG_TRAF2_1 | 213 | 216 | PF00917 | 0.766 |
LIG_TYR_ITIM | 464 | 469 | PF00017 | 0.483 |
LIG_Vh1_VBS_1 | 539 | 557 | PF01044 | 0.503 |
MOD_CK1_1 | 153 | 159 | PF00069 | 0.645 |
MOD_CK1_1 | 354 | 360 | PF00069 | 0.555 |
MOD_CK1_1 | 472 | 478 | PF00069 | 0.515 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.680 |
MOD_CK2_1 | 101 | 107 | PF00069 | 0.574 |
MOD_CK2_1 | 176 | 182 | PF00069 | 0.814 |
MOD_CK2_1 | 307 | 313 | PF00069 | 0.496 |
MOD_CK2_1 | 354 | 360 | PF00069 | 0.595 |
MOD_CK2_1 | 42 | 48 | PF00069 | 0.535 |
MOD_CK2_1 | 431 | 437 | PF00069 | 0.592 |
MOD_GlcNHglycan | 154 | 158 | PF01048 | 0.565 |
MOD_GlcNHglycan | 30 | 33 | PF01048 | 0.616 |
MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.535 |
MOD_GlcNHglycan | 471 | 474 | PF01048 | 0.518 |
MOD_GlcNHglycan | 483 | 486 | PF01048 | 0.555 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.696 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.700 |
MOD_GSK3_1 | 153 | 160 | PF00069 | 0.627 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.736 |
MOD_GSK3_1 | 198 | 205 | PF00069 | 0.724 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.591 |
MOD_GSK3_1 | 385 | 392 | PF00069 | 0.463 |
MOD_GSK3_1 | 454 | 461 | PF00069 | 0.510 |
MOD_GSK3_1 | 477 | 484 | PF00069 | 0.518 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.714 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.597 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.658 |
MOD_N-GLC_1 | 481 | 486 | PF02516 | 0.631 |
MOD_N-GLC_2 | 411 | 413 | PF02516 | 0.581 |
MOD_NEK2_1 | 241 | 246 | PF00069 | 0.751 |
MOD_NEK2_1 | 307 | 312 | PF00069 | 0.542 |
MOD_NEK2_1 | 431 | 436 | PF00069 | 0.639 |
MOD_NEK2_1 | 51 | 56 | PF00069 | 0.514 |
MOD_NEK2_1 | 64 | 69 | PF00069 | 0.673 |
MOD_PIKK_1 | 390 | 396 | PF00454 | 0.514 |
MOD_PIKK_1 | 42 | 48 | PF00454 | 0.553 |
MOD_PIKK_1 | 472 | 478 | PF00454 | 0.389 |
MOD_PKA_2 | 139 | 145 | PF00069 | 0.561 |
MOD_PKA_2 | 22 | 28 | PF00069 | 0.575 |
MOD_PKA_2 | 241 | 247 | PF00069 | 0.734 |
MOD_PKA_2 | 354 | 360 | PF00069 | 0.608 |
MOD_Plk_1 | 109 | 115 | PF00069 | 0.627 |
MOD_Plk_1 | 351 | 357 | PF00069 | 0.558 |
MOD_Plk_4 | 198 | 204 | PF00069 | 0.641 |
MOD_Plk_4 | 454 | 460 | PF00069 | 0.412 |
MOD_Plk_4 | 5 | 11 | PF00069 | 0.686 |
MOD_Plk_4 | 60 | 66 | PF00069 | 0.682 |
MOD_ProDKin_1 | 344 | 350 | PF00069 | 0.599 |
MOD_ProDKin_1 | 477 | 483 | PF00069 | 0.474 |
MOD_ProDKin_1 | 69 | 75 | PF00069 | 0.734 |
MOD_ProDKin_1 | 9 | 15 | PF00069 | 0.665 |
TRG_DiLeu_BaEn_4 | 441 | 447 | PF01217 | 0.500 |
TRG_ENDOCYTIC_2 | 466 | 469 | PF00928 | 0.479 |
TRG_ER_diArg_1 | 324 | 327 | PF00400 | 0.591 |
TRG_ER_diArg_1 | 365 | 368 | PF00400 | 0.600 |
TRG_ER_diArg_1 | 375 | 378 | PF00400 | 0.484 |
TRG_ER_diArg_1 | 537 | 539 | PF00400 | 0.534 |
TRG_NES_CRM1_1 | 382 | 394 | PF08389 | 0.534 |
TRG_NES_CRM1_1 | 544 | 558 | PF08389 | 0.505 |
TRG_Pf-PMV_PEXEL_1 | 326 | 331 | PF00026 | 0.589 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PG49 | Leptomonas seymouri | 57% | 73% |
A0A3S7X103 | Leishmania donovani | 100% | 100% |
A4HG01 | Leishmania braziliensis | 83% | 99% |
C9ZJJ3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 97% |
E9ACU1 | Leishmania major | 94% | 100% |
E9AZD0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
V5ANH3 | Trypanosoma cruzi | 25% | 100% |