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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
GO:0005789 | endoplasmic reticulum membrane | 4 | 1 |
GO:0031090 | organelle membrane | 3 | 1 |
Related structures:
AlphaFold database: E9B1G5
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022607 | cellular component assembly | 4 | 1 |
GO:0034389 | lipid droplet organization | 5 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0070925 | organelle assembly | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0140042 | lipid droplet formation | 6 | 1 |
GO:0140694 | non-membrane-bounded organelle assembly | 6 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 476 | 478 | PF00675 | 0.562 |
CLV_NRD_NRD_1 | 494 | 496 | PF00675 | 0.425 |
CLV_NRD_NRD_1 | 6 | 8 | PF00675 | 0.582 |
CLV_PCSK_FUR_1 | 4 | 8 | PF00082 | 0.391 |
CLV_PCSK_FUR_1 | 474 | 478 | PF00082 | 0.456 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.526 |
CLV_PCSK_KEX2_1 | 476 | 478 | PF00082 | 0.554 |
CLV_PCSK_KEX2_1 | 494 | 496 | PF00082 | 0.425 |
CLV_PCSK_KEX2_1 | 6 | 8 | PF00082 | 0.536 |
CLV_PCSK_PC1ET2_1 | 3 | 5 | PF00082 | 0.397 |
CLV_PCSK_SKI1_1 | 250 | 254 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 383 | 387 | PF00082 | 0.576 |
CLV_PCSK_SKI1_1 | 397 | 401 | PF00082 | 0.653 |
CLV_PCSK_SKI1_1 | 71 | 75 | PF00082 | 0.247 |
DEG_APCC_DBOX_1 | 249 | 257 | PF00400 | 0.227 |
DEG_APCC_DBOX_1 | 293 | 301 | PF00400 | 0.335 |
DEG_APCC_DBOX_1 | 66 | 74 | PF00400 | 0.603 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.736 |
DOC_MAPK_gen_1 | 303 | 313 | PF00069 | 0.406 |
DOC_MAPK_gen_1 | 378 | 387 | PF00069 | 0.364 |
DOC_MAPK_MEF2A_6 | 294 | 301 | PF00069 | 0.372 |
DOC_MAPK_MEF2A_6 | 338 | 346 | PF00069 | 0.435 |
DOC_MAPK_MEF2A_6 | 349 | 356 | PF00069 | 0.399 |
DOC_MAPK_NFAT4_5 | 294 | 302 | PF00069 | 0.422 |
DOC_PP1_RVXF_1 | 301 | 308 | PF00149 | 0.406 |
DOC_PP1_RVXF_1 | 381 | 388 | PF00149 | 0.433 |
DOC_PP2B_LxvP_1 | 9 | 12 | PF13499 | 0.725 |
DOC_PP4_FxxP_1 | 146 | 149 | PF00568 | 0.508 |
DOC_PP4_FxxP_1 | 309 | 312 | PF00568 | 0.394 |
DOC_PP4_FxxP_1 | 350 | 353 | PF00568 | 0.355 |
DOC_PP4_FxxP_1 | 455 | 458 | PF00568 | 0.730 |
DOC_USP7_MATH_1 | 268 | 272 | PF00917 | 0.484 |
DOC_USP7_MATH_1 | 333 | 337 | PF00917 | 0.465 |
DOC_USP7_MATH_1 | 419 | 423 | PF00917 | 0.491 |
DOC_USP7_MATH_1 | 442 | 446 | PF00917 | 0.708 |
DOC_USP7_MATH_1 | 53 | 57 | PF00917 | 0.708 |
DOC_WW_Pin1_4 | 208 | 213 | PF00397 | 0.490 |
DOC_WW_Pin1_4 | 348 | 353 | PF00397 | 0.420 |
DOC_WW_Pin1_4 | 469 | 474 | PF00397 | 0.635 |
DOC_WW_Pin1_4 | 499 | 504 | PF00397 | 0.790 |
DOC_WW_Pin1_4 | 7 | 12 | PF00397 | 0.758 |
LIG_14-3-3_CanoR_1 | 202 | 212 | PF00244 | 0.469 |
LIG_14-3-3_CanoR_1 | 397 | 404 | PF00244 | 0.461 |
LIG_14-3-3_CanoR_1 | 476 | 484 | PF00244 | 0.800 |
LIG_14-3-3_CanoR_1 | 494 | 500 | PF00244 | 0.636 |
LIG_14-3-3_CanoR_1 | 58 | 63 | PF00244 | 0.639 |
LIG_Actin_WH2_2 | 481 | 496 | PF00022 | 0.756 |
LIG_Actin_WH2_2 | 56 | 73 | PF00022 | 0.689 |
LIG_BRCT_BRCA1_1 | 327 | 331 | PF00533 | 0.513 |
LIG_BRCT_BRCA1_1 | 480 | 484 | PF00533 | 0.704 |
LIG_BRCT_BRCA1_1 | 495 | 499 | PF00533 | 0.778 |
LIG_Clathr_ClatBox_1 | 253 | 257 | PF01394 | 0.224 |
LIG_DLG_GKlike_1 | 163 | 170 | PF00625 | 0.473 |
LIG_eIF4E_1 | 69 | 75 | PF01652 | 0.520 |
LIG_FHA_1 | 114 | 120 | PF00498 | 0.424 |
LIG_FHA_1 | 151 | 157 | PF00498 | 0.501 |
LIG_FHA_1 | 159 | 165 | PF00498 | 0.483 |
LIG_FHA_1 | 195 | 201 | PF00498 | 0.390 |
LIG_FHA_1 | 287 | 293 | PF00498 | 0.401 |
LIG_FHA_1 | 349 | 355 | PF00498 | 0.466 |
LIG_FHA_1 | 387 | 393 | PF00498 | 0.399 |
LIG_FHA_1 | 404 | 410 | PF00498 | 0.196 |
LIG_FHA_1 | 43 | 49 | PF00498 | 0.702 |
LIG_FHA_1 | 488 | 494 | PF00498 | 0.752 |
LIG_FHA_2 | 59 | 65 | PF00498 | 0.662 |
LIG_GBD_Chelix_1 | 297 | 305 | PF00786 | 0.593 |
LIG_GBD_Chelix_1 | 87 | 95 | PF00786 | 0.408 |
LIG_LIR_Apic_2 | 145 | 149 | PF02991 | 0.510 |
LIG_LIR_Apic_2 | 366 | 371 | PF02991 | 0.411 |
LIG_LIR_Apic_2 | 452 | 458 | PF02991 | 0.745 |
LIG_LIR_Gen_1 | 179 | 189 | PF02991 | 0.471 |
LIG_LIR_Gen_1 | 295 | 304 | PF02991 | 0.379 |
LIG_LIR_Gen_1 | 315 | 323 | PF02991 | 0.363 |
LIG_LIR_Gen_1 | 345 | 354 | PF02991 | 0.371 |
LIG_LIR_Gen_1 | 405 | 415 | PF02991 | 0.383 |
LIG_LIR_Nem_3 | 179 | 185 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 295 | 299 | PF02991 | 0.384 |
LIG_LIR_Nem_3 | 315 | 319 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 328 | 334 | PF02991 | 0.365 |
LIG_LIR_Nem_3 | 345 | 350 | PF02991 | 0.284 |
LIG_LIR_Nem_3 | 405 | 410 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 66 | 72 | PF02991 | 0.551 |
LIG_NRBOX | 425 | 431 | PF00104 | 0.484 |
LIG_Pex14_1 | 314 | 318 | PF04695 | 0.485 |
LIG_Pex14_1 | 398 | 402 | PF04695 | 0.452 |
LIG_Pex14_2 | 275 | 279 | PF04695 | 0.378 |
LIG_SH2_CRK | 77 | 81 | PF00017 | 0.194 |
LIG_SH2_PTP2 | 72 | 75 | PF00017 | 0.408 |
LIG_SH2_STAP1 | 235 | 239 | PF00017 | 0.355 |
LIG_SH2_STAP1 | 316 | 320 | PF00017 | 0.410 |
LIG_SH2_STAP1 | 77 | 81 | PF00017 | 0.358 |
LIG_SH2_STAT5 | 235 | 238 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 318 | 321 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 60 | 63 | PF00017 | 0.678 |
LIG_SH2_STAT5 | 69 | 72 | PF00017 | 0.620 |
LIG_SH2_STAT5 | 77 | 80 | PF00017 | 0.344 |
LIG_SH3_3 | 206 | 212 | PF00018 | 0.422 |
LIG_SH3_3 | 327 | 333 | PF00018 | 0.453 |
LIG_SH3_3 | 8 | 14 | PF00018 | 0.764 |
LIG_Sin3_3 | 82 | 89 | PF02671 | 0.408 |
LIG_SUMO_SIM_anti_2 | 165 | 171 | PF11976 | 0.470 |
LIG_SUMO_SIM_anti_2 | 251 | 258 | PF11976 | 0.273 |
LIG_SUMO_SIM_anti_2 | 295 | 302 | PF11976 | 0.327 |
LIG_SUMO_SIM_anti_2 | 339 | 345 | PF11976 | 0.346 |
LIG_SUMO_SIM_anti_2 | 405 | 412 | PF11976 | 0.370 |
LIG_SUMO_SIM_par_1 | 251 | 258 | PF11976 | 0.389 |
LIG_SUMO_SIM_par_1 | 295 | 302 | PF11976 | 0.402 |
LIG_SUMO_SIM_par_1 | 84 | 90 | PF11976 | 0.431 |
LIG_TRAF2_1 | 244 | 247 | PF00917 | 0.463 |
LIG_TRAF2_1 | 451 | 454 | PF00917 | 0.581 |
LIG_TRFH_1 | 222 | 226 | PF08558 | 0.482 |
LIG_TYR_ITIM | 70 | 75 | PF00017 | 0.536 |
LIG_WRC_WIRS_1 | 404 | 409 | PF05994 | 0.380 |
LIG_WRC_WIRS_1 | 443 | 448 | PF05994 | 0.650 |
LIG_WRC_WIRS_1 | 59 | 64 | PF05994 | 0.694 |
LIG_WW_2 | 11 | 14 | PF00397 | 0.716 |
LIG_WW_3 | 457 | 461 | PF00397 | 0.642 |
MOD_CDC14_SPxK_1 | 502 | 505 | PF00782 | 0.733 |
MOD_CDK_SPK_2 | 208 | 213 | PF00069 | 0.495 |
MOD_CDK_SPK_2 | 469 | 474 | PF00069 | 0.580 |
MOD_CDK_SPxK_1 | 499 | 505 | PF00069 | 0.791 |
MOD_CDK_SPxxK_3 | 469 | 476 | PF00069 | 0.637 |
MOD_CK1_1 | 469 | 475 | PF00069 | 0.618 |
MOD_CK1_1 | 98 | 104 | PF00069 | 0.420 |
MOD_CK2_1 | 2 | 8 | PF00069 | 0.762 |
MOD_CK2_1 | 333 | 339 | PF00069 | 0.445 |
MOD_CK2_1 | 442 | 448 | PF00069 | 0.714 |
MOD_CK2_1 | 58 | 64 | PF00069 | 0.642 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.708 |
MOD_GlcNHglycan | 257 | 260 | PF01048 | 0.583 |
MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.707 |
MOD_GlcNHglycan | 417 | 420 | PF01048 | 0.382 |
MOD_GlcNHglycan | 90 | 94 | PF01048 | 0.487 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.370 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.366 |
MOD_GSK3_1 | 386 | 393 | PF00069 | 0.348 |
MOD_GSK3_1 | 415 | 422 | PF00069 | 0.342 |
MOD_GSK3_1 | 462 | 469 | PF00069 | 0.603 |
MOD_GSK3_1 | 484 | 491 | PF00069 | 0.755 |
MOD_GSK3_1 | 495 | 502 | PF00069 | 0.738 |
MOD_GSK3_1 | 58 | 65 | PF00069 | 0.636 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.481 |
MOD_N-GLC_1 | 363 | 368 | PF02516 | 0.533 |
MOD_N-GLC_1 | 499 | 504 | PF02516 | 0.590 |
MOD_NEK2_1 | 156 | 161 | PF00069 | 0.480 |
MOD_NEK2_1 | 188 | 193 | PF00069 | 0.413 |
MOD_NEK2_1 | 279 | 284 | PF00069 | 0.362 |
MOD_NEK2_1 | 292 | 297 | PF00069 | 0.365 |
MOD_NEK2_1 | 363 | 368 | PF00069 | 0.404 |
MOD_NEK2_1 | 386 | 391 | PF00069 | 0.361 |
MOD_NEK2_1 | 415 | 420 | PF00069 | 0.371 |
MOD_NEK2_1 | 488 | 493 | PF00069 | 0.751 |
MOD_NEK2_1 | 62 | 67 | PF00069 | 0.612 |
MOD_NEK2_1 | 95 | 100 | PF00069 | 0.439 |
MOD_NEK2_2 | 194 | 199 | PF00069 | 0.439 |
MOD_NEK2_2 | 42 | 47 | PF00069 | 0.672 |
MOD_NEK2_2 | 53 | 58 | PF00069 | 0.495 |
MOD_PIKK_1 | 158 | 164 | PF00454 | 0.489 |
MOD_PIKK_1 | 488 | 494 | PF00454 | 0.752 |
MOD_PK_1 | 281 | 287 | PF00069 | 0.416 |
MOD_PKA_2 | 150 | 156 | PF00069 | 0.516 |
MOD_PKA_2 | 478 | 484 | PF00069 | 0.719 |
MOD_PKA_2 | 493 | 499 | PF00069 | 0.766 |
MOD_Plk_1 | 138 | 144 | PF00069 | 0.505 |
MOD_Plk_1 | 363 | 369 | PF00069 | 0.332 |
MOD_Plk_1 | 488 | 494 | PF00069 | 0.737 |
MOD_Plk_1 | 63 | 69 | PF00069 | 0.570 |
MOD_Plk_2-3 | 448 | 454 | PF00069 | 0.740 |
MOD_Plk_4 | 165 | 171 | PF00069 | 0.470 |
MOD_Plk_4 | 403 | 409 | PF00069 | 0.373 |
MOD_Plk_4 | 462 | 468 | PF00069 | 0.725 |
MOD_Plk_4 | 58 | 64 | PF00069 | 0.675 |
MOD_Plk_4 | 75 | 81 | PF00069 | 0.267 |
MOD_ProDKin_1 | 208 | 214 | PF00069 | 0.490 |
MOD_ProDKin_1 | 348 | 354 | PF00069 | 0.421 |
MOD_ProDKin_1 | 469 | 475 | PF00069 | 0.636 |
MOD_ProDKin_1 | 499 | 505 | PF00069 | 0.791 |
MOD_ProDKin_1 | 7 | 13 | PF00069 | 0.756 |
MOD_SUMO_for_1 | 231 | 234 | PF00179 | 0.472 |
MOD_SUMO_for_1 | 244 | 247 | PF00179 | 0.298 |
TRG_DiLeu_BaEn_1 | 152 | 157 | PF01217 | 0.477 |
TRG_DiLeu_BaLyEn_6 | 380 | 385 | PF01217 | 0.391 |
TRG_ENDOCYTIC_2 | 316 | 319 | PF00928 | 0.388 |
TRG_ENDOCYTIC_2 | 347 | 350 | PF00928 | 0.346 |
TRG_ENDOCYTIC_2 | 60 | 63 | PF00928 | 0.672 |
TRG_ENDOCYTIC_2 | 72 | 75 | PF00928 | 0.410 |
TRG_ENDOCYTIC_2 | 77 | 80 | PF00928 | 0.369 |
TRG_ER_diArg_1 | 358 | 361 | PF00400 | 0.367 |
TRG_ER_diArg_1 | 4 | 7 | PF00400 | 0.727 |
TRG_ER_diArg_1 | 473 | 476 | PF00400 | 0.778 |
TRG_ER_diArg_1 | 493 | 495 | PF00400 | 0.603 |
TRG_NES_CRM1_1 | 24 | 39 | PF08389 | 0.700 |
TRG_NLS_MonoExtC_3 | 2 | 7 | PF00514 | 0.595 |
TRG_Pf-PMV_PEXEL_1 | 135 | 139 | PF00026 | 0.741 |
TRG_Pf-PMV_PEXEL_1 | 154 | 158 | PF00026 | 0.667 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8U6 | Leptomonas seymouri | 57% | 100% |
A0A1X0NJH4 | Trypanosomatidae | 36% | 100% |
A0A3Q8IEM5 | Leishmania donovani | 90% | 100% |
A4HIZ2 | Leishmania braziliensis | 74% | 100% |
A4I6A9 | Leishmania infantum | 90% | 100% |
C9ZN36 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
Q4Q6P7 | Leishmania major | 90% | 100% |
V5BN41 | Trypanosoma cruzi | 40% | 100% |