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: 6 |
NetGPI | no | yes: 0, no: 6 |
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: A4HG01
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 | 43 | 47 | PF00656 | 0.604 |
CLV_NRD_NRD_1 | 470 | 472 | PF00675 | 0.583 |
CLV_PCSK_KEX2_1 | 219 | 221 | PF00082 | 0.432 |
CLV_PCSK_KEX2_1 | 470 | 472 | PF00082 | 0.583 |
CLV_PCSK_PC1ET2_1 | 219 | 221 | PF00082 | 0.432 |
CLV_PCSK_SKI1_1 | 211 | 215 | PF00082 | 0.475 |
CLV_PCSK_SKI1_1 | 345 | 349 | PF00082 | 0.534 |
CLV_PCSK_SKI1_1 | 470 | 474 | PF00082 | 0.619 |
DEG_APCC_DBOX_1 | 82 | 90 | PF00400 | 0.685 |
DOC_CYCLIN_RxL_1 | 309 | 321 | PF00134 | 0.517 |
DOC_CYCLIN_RxL_1 | 48 | 56 | PF00134 | 0.453 |
DOC_CYCLIN_yCln2_LP_2 | 397 | 403 | PF00134 | 0.408 |
DOC_CYCLIN_yCln2_LP_2 | 422 | 428 | PF00134 | 0.675 |
DOC_MAPK_gen_1 | 201 | 209 | PF00069 | 0.612 |
DOC_MAPK_gen_1 | 309 | 318 | PF00069 | 0.605 |
DOC_MAPK_MEF2A_6 | 170 | 178 | PF00069 | 0.515 |
DOC_MAPK_MEF2A_6 | 201 | 209 | PF00069 | 0.428 |
DOC_MAPK_MEF2A_6 | 345 | 352 | PF00069 | 0.599 |
DOC_MAPK_MEF2A_6 | 478 | 487 | PF00069 | 0.475 |
DOC_MAPK_MEF2A_6 | 64 | 73 | PF00069 | 0.745 |
DOC_PP1_RVXF_1 | 66 | 73 | PF00149 | 0.719 |
DOC_PP2B_LxvP_1 | 422 | 425 | PF13499 | 0.668 |
DOC_PP4_FxxP_1 | 108 | 111 | PF00568 | 0.731 |
DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.555 |
DOC_USP7_MATH_1 | 200 | 204 | PF00917 | 0.423 |
DOC_USP7_UBL2_3 | 463 | 467 | PF12436 | 0.588 |
DOC_WW_Pin1_4 | 11 | 16 | PF00397 | 0.666 |
DOC_WW_Pin1_4 | 118 | 123 | PF00397 | 0.641 |
DOC_WW_Pin1_4 | 410 | 415 | PF00397 | 0.551 |
DOC_WW_Pin1_4 | 5 | 10 | PF00397 | 0.741 |
LIG_14-3-3_CanoR_1 | 104 | 109 | PF00244 | 0.777 |
LIG_14-3-3_CanoR_1 | 154 | 160 | PF00244 | 0.780 |
LIG_14-3-3_CanoR_1 | 175 | 179 | PF00244 | 0.494 |
LIG_14-3-3_CanoR_1 | 230 | 240 | PF00244 | 0.633 |
LIG_14-3-3_CanoR_1 | 74 | 82 | PF00244 | 0.565 |
LIG_Actin_WH2_2 | 475 | 490 | PF00022 | 0.318 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.574 |
LIG_FHA_1 | 164 | 170 | PF00498 | 0.535 |
LIG_FHA_1 | 319 | 325 | PF00498 | 0.588 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.735 |
LIG_FHA_1 | 74 | 80 | PF00498 | 0.532 |
LIG_FHA_1 | 92 | 98 | PF00498 | 0.685 |
LIG_FHA_2 | 111 | 117 | PF00498 | 0.774 |
LIG_FHA_2 | 143 | 149 | PF00498 | 0.511 |
LIG_FHA_2 | 175 | 181 | PF00498 | 0.641 |
LIG_FHA_2 | 288 | 294 | PF00498 | 0.668 |
LIG_FHA_2 | 366 | 372 | PF00498 | 0.658 |
LIG_FHA_2 | 39 | 45 | PF00498 | 0.606 |
LIG_FHA_2 | 425 | 431 | PF00498 | 0.670 |
LIG_LIR_Apic_2 | 105 | 111 | PF02991 | 0.727 |
LIG_LIR_Apic_2 | 158 | 164 | PF02991 | 0.786 |
LIG_LIR_Gen_1 | 188 | 197 | PF02991 | 0.583 |
LIG_LIR_Nem_3 | 188 | 194 | PF02991 | 0.592 |
LIG_LIR_Nem_3 | 273 | 277 | PF02991 | 0.665 |
LIG_LYPXL_yS_3 | 399 | 402 | PF13949 | 0.555 |
LIG_LYPXL_yS_3 | 434 | 437 | PF13949 | 0.311 |
LIG_NRBOX | 478 | 484 | PF00104 | 0.464 |
LIG_PCNA_yPIPBox_3 | 27 | 36 | PF02747 | 0.735 |
LIG_RPA_C_Fungi | 295 | 307 | PF08784 | 0.648 |
LIG_SH2_GRB2like | 328 | 331 | PF00017 | 0.728 |
LIG_SH2_STAP1 | 320 | 324 | PF00017 | 0.584 |
LIG_SH2_STAP1 | 328 | 332 | PF00017 | 0.599 |
LIG_SH2_STAP1 | 393 | 397 | PF00017 | 0.479 |
LIG_SH2_STAT5 | 277 | 280 | PF00017 | 0.660 |
LIG_SH2_STAT5 | 320 | 323 | PF00017 | 0.579 |
LIG_SH2_STAT5 | 426 | 429 | PF00017 | 0.585 |
LIG_Sin3_3 | 93 | 100 | PF02671 | 0.538 |
LIG_SUMO_SIM_par_1 | 320 | 326 | PF11976 | 0.599 |
LIG_SUMO_SIM_par_1 | 384 | 390 | PF11976 | 0.544 |
LIG_SUMO_SIM_par_1 | 399 | 405 | PF11976 | 0.306 |
LIG_TRAF2_1 | 146 | 149 | PF00917 | 0.769 |
LIG_TRAF2_1 | 235 | 238 | PF00917 | 0.367 |
LIG_TRAF2_1 | 291 | 294 | PF00917 | 0.514 |
LIG_TRAF2_1 | 41 | 44 | PF00917 | 0.675 |
LIG_TYR_ITIM | 397 | 402 | PF00017 | 0.557 |
LIG_Vh1_VBS_1 | 472 | 490 | PF01044 | 0.574 |
MOD_CK1_1 | 405 | 411 | PF00069 | 0.588 |
MOD_CK1_1 | 5 | 11 | PF00069 | 0.757 |
MOD_CK1_1 | 87 | 93 | PF00069 | 0.690 |
MOD_CK2_1 | 110 | 116 | PF00069 | 0.776 |
MOD_CK2_1 | 142 | 148 | PF00069 | 0.505 |
MOD_CK2_1 | 240 | 246 | PF00069 | 0.566 |
MOD_CK2_1 | 287 | 293 | PF00069 | 0.593 |
MOD_CK2_1 | 364 | 370 | PF00069 | 0.584 |
MOD_CK2_1 | 37 | 43 | PF00069 | 0.711 |
MOD_CK2_1 | 424 | 430 | PF00069 | 0.426 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.551 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.515 |
MOD_GlcNHglycan | 242 | 245 | PF01048 | 0.453 |
MOD_GlcNHglycan | 404 | 407 | PF01048 | 0.573 |
MOD_GlcNHglycan | 416 | 419 | PF01048 | 0.574 |
MOD_GlcNHglycan | 88 | 92 | PF01048 | 0.606 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.688 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.774 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.520 |
MOD_GSK3_1 | 355 | 362 | PF00069 | 0.507 |
MOD_GSK3_1 | 387 | 394 | PF00069 | 0.481 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.804 |
MOD_GSK3_1 | 405 | 412 | PF00069 | 0.266 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.691 |
MOD_LATS_1 | 268 | 274 | PF00433 | 0.399 |
MOD_N-GLC_1 | 414 | 419 | PF02516 | 0.663 |
MOD_N-GLC_2 | 344 | 346 | PF02516 | 0.601 |
MOD_NEK2_1 | 127 | 132 | PF00069 | 0.533 |
MOD_NEK2_1 | 174 | 179 | PF00069 | 0.750 |
MOD_NEK2_1 | 240 | 245 | PF00069 | 0.618 |
MOD_NEK2_1 | 305 | 310 | PF00069 | 0.498 |
MOD_NEK2_1 | 364 | 369 | PF00069 | 0.672 |
MOD_NEK2_1 | 402 | 407 | PF00069 | 0.593 |
MOD_PIKK_1 | 323 | 329 | PF00454 | 0.571 |
MOD_PKA_2 | 174 | 180 | PF00069 | 0.747 |
MOD_PKA_2 | 200 | 206 | PF00069 | 0.542 |
MOD_PKA_2 | 287 | 293 | PF00069 | 0.623 |
MOD_PKA_2 | 73 | 79 | PF00069 | 0.687 |
MOD_Plk_1 | 45 | 51 | PF00069 | 0.694 |
MOD_Plk_4 | 387 | 393 | PF00069 | 0.462 |
MOD_ProDKin_1 | 118 | 124 | PF00069 | 0.642 |
MOD_ProDKin_1 | 410 | 416 | PF00069 | 0.551 |
MOD_ProDKin_1 | 5 | 11 | PF00069 | 0.742 |
TRG_DiLeu_BaEn_4 | 374 | 380 | PF01217 | 0.571 |
TRG_ENDOCYTIC_2 | 399 | 402 | PF00928 | 0.555 |
TRG_ENDOCYTIC_2 | 434 | 437 | PF00928 | 0.311 |
TRG_ER_diArg_1 | 298 | 301 | PF00400 | 0.602 |
TRG_ER_diArg_1 | 470 | 472 | PF00400 | 0.607 |
TRG_NES_CRM1_1 | 315 | 327 | PF08389 | 0.608 |
TRG_NES_CRM1_1 | 477 | 491 | PF08389 | 0.577 |
TRG_Pf-PMV_PEXEL_1 | 259 | 264 | PF00026 | 0.657 |
TRG_Pf-PMV_PEXEL_1 | 51 | 56 | PF00026 | 0.457 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7X103 | Leishmania donovani | 83% | 88% |
A4I320 | Leishmania infantum | 83% | 88% |
E9ACU1 | Leishmania major | 83% | 100% |
E9AZD0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 88% |
V5ANH3 | Trypanosoma cruzi | 27% | 90% |