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 | 2 |
GO:0005768 | endosome | 7 | 2 |
GO:0005773 | vacuole | 5 | 2 |
GO:0031410 | cytoplasmic vesicle | 6 | 2 |
GO:0031982 | vesicle | 4 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0097708 | intracellular vesicle | 5 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: E9ACU1
Term | Name | Level | Count |
---|---|---|---|
GO:0009987 | cellular process | 1 | 2 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0022607 | cellular component assembly | 4 | 2 |
GO:0035493 | SNARE complex assembly | 6 | 2 |
GO:0043933 | protein-containing complex organization | 4 | 2 |
GO:0065003 | protein-containing complex assembly | 5 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000149 | SNARE binding | 3 | 2 |
GO:0005488 | binding | 1 | 2 |
GO:0005515 | protein binding | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 107 | 111 | PF00656 | 0.506 |
CLV_C14_Caspase3-7 | 492 | 496 | PF00656 | 0.574 |
CLV_NRD_NRD_1 | 324 | 326 | PF00675 | 0.590 |
CLV_NRD_NRD_1 | 376 | 378 | PF00675 | 0.510 |
CLV_NRD_NRD_1 | 496 | 498 | PF00675 | 0.492 |
CLV_NRD_NRD_1 | 535 | 537 | PF00675 | 0.526 |
CLV_PCSK_FUR_1 | 322 | 326 | PF00082 | 0.565 |
CLV_PCSK_FUR_1 | 374 | 378 | PF00082 | 0.456 |
CLV_PCSK_KEX2_1 | 324 | 326 | PF00082 | 0.590 |
CLV_PCSK_KEX2_1 | 376 | 378 | PF00082 | 0.510 |
CLV_PCSK_KEX2_1 | 535 | 537 | PF00082 | 0.526 |
CLV_PCSK_PC7_1 | 372 | 378 | PF00082 | 0.463 |
CLV_PCSK_SKI1_1 | 247 | 251 | PF00082 | 0.607 |
CLV_PCSK_SKI1_1 | 535 | 539 | PF00082 | 0.604 |
DEG_APCC_DBOX_1 | 146 | 154 | PF00400 | 0.597 |
DEG_APCC_DBOX_1 | 234 | 242 | PF00400 | 0.473 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.704 |
DOC_CYCLIN_RxL_1 | 374 | 386 | PF00134 | 0.523 |
DOC_CYCLIN_yCln2_LP_2 | 462 | 468 | PF00134 | 0.389 |
DOC_CYCLIN_yCln2_LP_2 | 487 | 493 | PF00134 | 0.659 |
DOC_MAPK_gen_1 | 374 | 383 | PF00069 | 0.523 |
DOC_MAPK_MEF2A_6 | 128 | 137 | PF00069 | 0.591 |
DOC_MAPK_MEF2A_6 | 410 | 417 | PF00069 | 0.583 |
DOC_MAPK_MEF2A_6 | 543 | 552 | PF00069 | 0.441 |
DOC_PP1_RVXF_1 | 130 | 137 | PF00149 | 0.629 |
DOC_PP2B_LxvP_1 | 487 | 490 | PF13499 | 0.658 |
DOC_USP7_MATH_1 | 22 | 26 | PF00917 | 0.665 |
DOC_USP7_MATH_1 | 66 | 70 | PF00917 | 0.706 |
DOC_USP7_UBL2_3 | 528 | 532 | PF12436 | 0.522 |
DOC_WW_Pin1_4 | 342 | 347 | PF00397 | 0.615 |
DOC_WW_Pin1_4 | 475 | 480 | PF00397 | 0.494 |
DOC_WW_Pin1_4 | 69 | 74 | PF00397 | 0.732 |
DOC_WW_Pin1_4 | 9 | 14 | PF00397 | 0.664 |
LIG_14-3-3_CanoR_1 | 138 | 146 | PF00244 | 0.500 |
LIG_14-3-3_CanoR_1 | 168 | 173 | PF00244 | 0.727 |
LIG_14-3-3_CanoR_1 | 219 | 225 | PF00244 | 0.766 |
LIG_14-3-3_CanoR_1 | 23 | 28 | PF00244 | 0.626 |
LIG_14-3-3_CanoR_1 | 295 | 305 | PF00244 | 0.524 |
LIG_BRCT_BRCA1_1 | 113 | 117 | PF00533 | 0.566 |
LIG_FHA_1 | 129 | 135 | PF00498 | 0.646 |
LIG_FHA_1 | 138 | 144 | PF00498 | 0.468 |
LIG_FHA_1 | 156 | 162 | PF00498 | 0.640 |
LIG_FHA_1 | 16 | 22 | PF00498 | 0.549 |
LIG_FHA_1 | 196 | 202 | PF00498 | 0.570 |
LIG_FHA_1 | 307 | 313 | PF00498 | 0.553 |
LIG_FHA_1 | 384 | 390 | PF00498 | 0.571 |
LIG_FHA_1 | 74 | 80 | PF00498 | 0.643 |
LIG_FHA_1 | 9 | 15 | PF00498 | 0.505 |
LIG_FHA_2 | 175 | 181 | PF00498 | 0.788 |
LIG_FHA_2 | 240 | 246 | PF00498 | 0.613 |
LIG_FHA_2 | 353 | 359 | PF00498 | 0.615 |
LIG_FHA_2 | 43 | 49 | PF00498 | 0.538 |
LIG_FHA_2 | 431 | 437 | PF00498 | 0.635 |
LIG_FHA_2 | 490 | 496 | PF00498 | 0.556 |
LIG_LIR_Apic_2 | 223 | 229 | PF02991 | 0.729 |
LIG_LIR_Gen_1 | 253 | 262 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 253 | 259 | PF02991 | 0.540 |
LIG_LIR_Nem_3 | 338 | 342 | PF02991 | 0.648 |
LIG_LIR_Nem_3 | 461 | 467 | PF02991 | 0.351 |
LIG_LYPXL_yS_3 | 464 | 467 | PF13949 | 0.486 |
LIG_NRBOX | 543 | 549 | PF00104 | 0.478 |
LIG_PCNA_yPIPBox_3 | 91 | 100 | PF02747 | 0.604 |
LIG_RPA_C_Fungi | 285 | 297 | PF08784 | 0.367 |
LIG_RPA_C_Fungi | 360 | 372 | PF08784 | 0.631 |
LIG_SH2_GRB2like | 393 | 396 | PF00017 | 0.713 |
LIG_SH2_NCK_1 | 41 | 45 | PF00017 | 0.383 |
LIG_SH2_STAP1 | 17 | 21 | PF00017 | 0.540 |
LIG_SH2_STAP1 | 385 | 389 | PF00017 | 0.518 |
LIG_SH2_STAP1 | 393 | 397 | PF00017 | 0.667 |
LIG_SH2_STAP1 | 458 | 462 | PF00017 | 0.512 |
LIG_SH2_STAT5 | 139 | 142 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 17 | 20 | PF00017 | 0.507 |
LIG_SH2_STAT5 | 342 | 345 | PF00017 | 0.676 |
LIG_SH2_STAT5 | 385 | 388 | PF00017 | 0.563 |
LIG_SH2_STAT5 | 491 | 494 | PF00017 | 0.560 |
LIG_SH2_STAT5 | 53 | 56 | PF00017 | 0.508 |
LIG_SH3_3 | 140 | 146 | PF00018 | 0.435 |
LIG_SH3_3 | 7 | 13 | PF00018 | 0.619 |
LIG_SH3_CIN85_PxpxPR_1 | 230 | 235 | PF14604 | 0.687 |
LIG_Sin3_3 | 157 | 164 | PF02671 | 0.487 |
LIG_SUMO_SIM_par_1 | 308 | 313 | PF11976 | 0.501 |
LIG_SUMO_SIM_par_1 | 385 | 391 | PF11976 | 0.558 |
LIG_SUMO_SIM_par_1 | 449 | 455 | PF11976 | 0.429 |
LIG_SUMO_SIM_par_1 | 464 | 470 | PF11976 | 0.451 |
LIG_TRAF2_1 | 211 | 214 | PF00917 | 0.764 |
LIG_TRAF2_1 | 356 | 359 | PF00917 | 0.521 |
LIG_TYR_ITIM | 462 | 467 | PF00017 | 0.490 |
LIG_Vh1_VBS_1 | 537 | 555 | PF01044 | 0.508 |
MOD_CK1_1 | 151 | 157 | PF00069 | 0.640 |
MOD_CK1_1 | 352 | 358 | PF00069 | 0.568 |
MOD_CK1_1 | 470 | 476 | PF00069 | 0.517 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.680 |
MOD_CK2_1 | 101 | 107 | PF00069 | 0.571 |
MOD_CK2_1 | 174 | 180 | PF00069 | 0.788 |
MOD_CK2_1 | 305 | 311 | PF00069 | 0.498 |
MOD_CK2_1 | 352 | 358 | PF00069 | 0.608 |
MOD_CK2_1 | 42 | 48 | PF00069 | 0.550 |
MOD_CK2_1 | 429 | 435 | PF00069 | 0.603 |
MOD_GlcNHglycan | 152 | 156 | PF01048 | 0.558 |
MOD_GlcNHglycan | 30 | 33 | PF01048 | 0.606 |
MOD_GlcNHglycan | 469 | 472 | PF01048 | 0.513 |
MOD_GlcNHglycan | 481 | 484 | PF01048 | 0.588 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.698 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.667 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.621 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.776 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.592 |
MOD_GSK3_1 | 383 | 390 | PF00069 | 0.466 |
MOD_GSK3_1 | 452 | 459 | PF00069 | 0.507 |
MOD_GSK3_1 | 475 | 482 | PF00069 | 0.539 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.709 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.604 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.659 |
MOD_N-GLC_1 | 479 | 484 | PF02516 | 0.665 |
MOD_N-GLC_2 | 409 | 411 | PF02516 | 0.587 |
MOD_NEK2_1 | 239 | 244 | PF00069 | 0.738 |
MOD_NEK2_1 | 305 | 310 | PF00069 | 0.546 |
MOD_NEK2_1 | 370 | 375 | PF00069 | 0.563 |
MOD_NEK2_1 | 429 | 434 | PF00069 | 0.652 |
MOD_NEK2_1 | 51 | 56 | PF00069 | 0.521 |
MOD_NEK2_1 | 64 | 69 | PF00069 | 0.675 |
MOD_PIKK_1 | 388 | 394 | PF00454 | 0.546 |
MOD_PIKK_1 | 42 | 48 | PF00454 | 0.568 |
MOD_PKA_2 | 137 | 143 | PF00069 | 0.567 |
MOD_PKA_2 | 174 | 180 | PF00069 | 0.658 |
MOD_PKA_2 | 22 | 28 | PF00069 | 0.581 |
MOD_PKA_2 | 239 | 245 | PF00069 | 0.720 |
MOD_PKA_2 | 352 | 358 | PF00069 | 0.621 |
MOD_Plk_1 | 109 | 115 | PF00069 | 0.631 |
MOD_Plk_4 | 182 | 188 | PF00069 | 0.557 |
MOD_Plk_4 | 196 | 202 | PF00069 | 0.649 |
MOD_Plk_4 | 452 | 458 | PF00069 | 0.408 |
MOD_Plk_4 | 5 | 11 | PF00069 | 0.682 |
MOD_Plk_4 | 60 | 66 | PF00069 | 0.688 |
MOD_ProDKin_1 | 342 | 348 | PF00069 | 0.614 |
MOD_ProDKin_1 | 475 | 481 | PF00069 | 0.494 |
MOD_ProDKin_1 | 69 | 75 | PF00069 | 0.734 |
MOD_ProDKin_1 | 9 | 15 | PF00069 | 0.655 |
TRG_DiLeu_BaEn_4 | 439 | 445 | PF01217 | 0.502 |
TRG_ENDOCYTIC_2 | 464 | 467 | PF00928 | 0.486 |
TRG_ER_diArg_1 | 322 | 325 | PF00400 | 0.591 |
TRG_ER_diArg_1 | 363 | 366 | PF00400 | 0.615 |
TRG_ER_diArg_1 | 374 | 377 | PF00400 | 0.493 |
TRG_ER_diArg_1 | 535 | 537 | PF00400 | 0.542 |
TRG_NES_CRM1_1 | 380 | 392 | PF08389 | 0.541 |
TRG_NES_CRM1_1 | 542 | 556 | PF08389 | 0.510 |
TRG_Pf-PMV_PEXEL_1 | 324 | 329 | PF00026 | 0.589 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PG49 | Leptomonas seymouri | 56% | 72% |
A0A3S7X103 | Leishmania donovani | 94% | 100% |
A4HG01 | Leishmania braziliensis | 83% | 100% |
A4I320 | Leishmania infantum | 94% | 100% |
C9ZJJ3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 97% |
E9AZD0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
V5ANH3 | Trypanosoma cruzi | 26% | 100% |