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 | 2 |
GO:0031090 | organelle membrane | 3 | 2 |
Related structures:
AlphaFold database: A0A3Q8IEM5
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 2 |
GO:0006996 | organelle organization | 4 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0022607 | cellular component assembly | 4 | 2 |
GO:0034389 | lipid droplet organization | 5 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0070925 | organelle assembly | 5 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
GO:0140042 | lipid droplet formation | 6 | 2 |
GO:0140694 | non-membrane-bounded organelle assembly | 6 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 476 | 478 | PF00675 | 0.534 |
CLV_NRD_NRD_1 | 494 | 496 | PF00675 | 0.389 |
CLV_NRD_NRD_1 | 6 | 8 | PF00675 | 0.582 |
CLV_PCSK_KEX2_1 | 476 | 478 | PF00082 | 0.524 |
CLV_PCSK_KEX2_1 | 494 | 496 | PF00082 | 0.389 |
CLV_PCSK_KEX2_1 | 6 | 8 | PF00082 | 0.576 |
CLV_PCSK_SKI1_1 | 383 | 387 | PF00082 | 0.590 |
CLV_PCSK_SKI1_1 | 397 | 401 | PF00082 | 0.641 |
DEG_APCC_DBOX_1 | 66 | 74 | PF00400 | 0.611 |
DOC_MAPK_gen_1 | 160 | 169 | PF00069 | 0.438 |
DOC_MAPK_gen_1 | 303 | 313 | PF00069 | 0.399 |
DOC_MAPK_gen_1 | 378 | 387 | PF00069 | 0.403 |
DOC_MAPK_MEF2A_6 | 338 | 346 | PF00069 | 0.426 |
DOC_MAPK_MEF2A_6 | 349 | 356 | PF00069 | 0.348 |
DOC_PP1_RVXF_1 | 301 | 308 | PF00149 | 0.381 |
DOC_PP1_RVXF_1 | 381 | 388 | PF00149 | 0.392 |
DOC_PP2B_LxvP_1 | 9 | 12 | PF13499 | 0.693 |
DOC_PP4_FxxP_1 | 146 | 149 | PF00568 | 0.499 |
DOC_PP4_FxxP_1 | 309 | 312 | PF00568 | 0.362 |
DOC_PP4_FxxP_1 | 350 | 353 | PF00568 | 0.329 |
DOC_PP4_FxxP_1 | 456 | 459 | PF00568 | 0.728 |
DOC_PP4_MxPP_1 | 470 | 473 | PF00568 | 0.678 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.746 |
DOC_USP7_MATH_1 | 268 | 272 | PF00917 | 0.443 |
DOC_USP7_MATH_1 | 333 | 337 | PF00917 | 0.453 |
DOC_USP7_MATH_1 | 419 | 423 | PF00917 | 0.485 |
DOC_USP7_MATH_1 | 442 | 446 | PF00917 | 0.668 |
DOC_USP7_MATH_1 | 53 | 57 | PF00917 | 0.668 |
DOC_WW_Pin1_4 | 208 | 213 | PF00397 | 0.476 |
DOC_WW_Pin1_4 | 348 | 353 | PF00397 | 0.429 |
DOC_WW_Pin1_4 | 455 | 460 | PF00397 | 0.613 |
DOC_WW_Pin1_4 | 499 | 504 | PF00397 | 0.730 |
DOC_WW_Pin1_4 | 7 | 12 | PF00397 | 0.710 |
LIG_14-3-3_CanoR_1 | 202 | 212 | PF00244 | 0.494 |
LIG_14-3-3_CanoR_1 | 250 | 255 | PF00244 | 0.427 |
LIG_14-3-3_CanoR_1 | 397 | 404 | PF00244 | 0.432 |
LIG_14-3-3_CanoR_1 | 476 | 485 | PF00244 | 0.785 |
LIG_14-3-3_CanoR_1 | 494 | 500 | PF00244 | 0.597 |
LIG_14-3-3_CanoR_1 | 58 | 63 | PF00244 | 0.688 |
LIG_Actin_WH2_2 | 481 | 496 | PF00022 | 0.722 |
LIG_Actin_WH2_2 | 56 | 73 | PF00022 | 0.636 |
LIG_BRCT_BRCA1_1 | 327 | 331 | PF00533 | 0.461 |
LIG_BRCT_BRCA1_1 | 480 | 484 | PF00533 | 0.659 |
LIG_BRCT_BRCA1_1 | 495 | 499 | PF00533 | 0.746 |
LIG_CtBP_PxDLS_1 | 472 | 476 | PF00389 | 0.616 |
LIG_DLG_GKlike_1 | 163 | 170 | PF00625 | 0.454 |
LIG_FHA_1 | 114 | 120 | PF00498 | 0.447 |
LIG_FHA_1 | 14 | 20 | PF00498 | 0.573 |
LIG_FHA_1 | 151 | 157 | PF00498 | 0.548 |
LIG_FHA_1 | 159 | 165 | PF00498 | 0.514 |
LIG_FHA_1 | 195 | 201 | PF00498 | 0.376 |
LIG_FHA_1 | 234 | 240 | PF00498 | 0.368 |
LIG_FHA_1 | 287 | 293 | PF00498 | 0.369 |
LIG_FHA_1 | 349 | 355 | PF00498 | 0.423 |
LIG_FHA_1 | 387 | 393 | PF00498 | 0.382 |
LIG_FHA_1 | 404 | 410 | PF00498 | 0.230 |
LIG_FHA_1 | 488 | 494 | PF00498 | 0.719 |
LIG_FHA_2 | 59 | 65 | PF00498 | 0.643 |
LIG_GBD_Chelix_1 | 87 | 95 | PF00786 | 0.362 |
LIG_LIR_Apic_2 | 145 | 149 | PF02991 | 0.498 |
LIG_LIR_Apic_2 | 366 | 371 | PF02991 | 0.397 |
LIG_LIR_Apic_2 | 454 | 459 | PF02991 | 0.722 |
LIG_LIR_Gen_1 | 179 | 189 | PF02991 | 0.451 |
LIG_LIR_Gen_1 | 295 | 305 | PF02991 | 0.360 |
LIG_LIR_Gen_1 | 315 | 323 | PF02991 | 0.356 |
LIG_LIR_Gen_1 | 345 | 354 | PF02991 | 0.369 |
LIG_LIR_Gen_1 | 405 | 415 | PF02991 | 0.344 |
LIG_LIR_Gen_1 | 483 | 493 | PF02991 | 0.702 |
LIG_LIR_Gen_1 | 57 | 64 | PF02991 | 0.627 |
LIG_LIR_Nem_3 | 179 | 185 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 295 | 300 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 315 | 319 | PF02991 | 0.334 |
LIG_LIR_Nem_3 | 328 | 334 | PF02991 | 0.339 |
LIG_LIR_Nem_3 | 345 | 350 | PF02991 | 0.253 |
LIG_LIR_Nem_3 | 405 | 410 | PF02991 | 0.310 |
LIG_LIR_Nem_3 | 483 | 488 | PF02991 | 0.681 |
LIG_LIR_Nem_3 | 498 | 504 | PF02991 | 0.752 |
LIG_LIR_Nem_3 | 57 | 63 | PF02991 | 0.656 |
LIG_LIR_Nem_3 | 66 | 72 | PF02991 | 0.609 |
LIG_NRBOX | 425 | 431 | PF00104 | 0.425 |
LIG_PALB2_WD40_1 | 292 | 300 | PF16756 | 0.305 |
LIG_Pex14_1 | 314 | 318 | PF04695 | 0.434 |
LIG_Pex14_1 | 398 | 402 | PF04695 | 0.425 |
LIG_SH2_CRK | 501 | 505 | PF00017 | 0.604 |
LIG_SH2_PTP2 | 72 | 75 | PF00017 | 0.362 |
LIG_SH2_PTP2 | 77 | 80 | PF00017 | 0.310 |
LIG_SH2_SRC | 72 | 75 | PF00017 | 0.250 |
LIG_SH2_STAP1 | 235 | 239 | PF00017 | 0.325 |
LIG_SH2_STAP1 | 316 | 320 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 235 | 238 | PF00017 | 0.389 |
LIG_SH2_STAT5 | 318 | 321 | PF00017 | 0.408 |
LIG_SH2_STAT5 | 60 | 63 | PF00017 | 0.665 |
LIG_SH2_STAT5 | 69 | 72 | PF00017 | 0.589 |
LIG_SH2_STAT5 | 77 | 80 | PF00017 | 0.401 |
LIG_SH3_3 | 206 | 212 | PF00018 | 0.423 |
LIG_SH3_3 | 327 | 333 | PF00018 | 0.431 |
LIG_SH3_3 | 370 | 376 | PF00018 | 0.334 |
LIG_SH3_3 | 8 | 14 | PF00018 | 0.722 |
LIG_Sin3_3 | 82 | 89 | PF02671 | 0.362 |
LIG_SUMO_SIM_anti_2 | 165 | 171 | PF11976 | 0.449 |
LIG_SUMO_SIM_anti_2 | 339 | 345 | PF11976 | 0.339 |
LIG_SUMO_SIM_anti_2 | 405 | 412 | PF11976 | 0.356 |
LIG_SUMO_SIM_par_1 | 297 | 302 | PF11976 | 0.365 |
LIG_SUMO_SIM_par_1 | 419 | 425 | PF11976 | 0.387 |
LIG_SUMO_SIM_par_1 | 84 | 90 | PF11976 | 0.401 |
LIG_TRAF2_1 | 244 | 247 | PF00917 | 0.419 |
LIG_TRFH_1 | 222 | 226 | PF08558 | 0.467 |
LIG_TYR_ITIM | 70 | 75 | PF00017 | 0.503 |
LIG_WRC_WIRS_1 | 404 | 409 | PF05994 | 0.287 |
LIG_WRC_WIRS_1 | 443 | 448 | PF05994 | 0.608 |
LIG_WRC_WIRS_1 | 59 | 64 | PF05994 | 0.646 |
LIG_WW_2 | 11 | 14 | PF00397 | 0.672 |
MOD_CDC14_SPxK_1 | 502 | 505 | PF00782 | 0.678 |
MOD_CDK_SPK_2 | 208 | 213 | PF00069 | 0.487 |
MOD_CDK_SPK_2 | 455 | 460 | PF00069 | 0.613 |
MOD_CDK_SPxK_1 | 499 | 505 | PF00069 | 0.731 |
MOD_CDK_SPxxK_3 | 499 | 506 | PF00069 | 0.652 |
MOD_CK1_1 | 183 | 189 | PF00069 | 0.440 |
MOD_CK1_1 | 422 | 428 | PF00069 | 0.419 |
MOD_CK1_1 | 487 | 493 | PF00069 | 0.722 |
MOD_CK1_1 | 98 | 104 | PF00069 | 0.405 |
MOD_CK2_1 | 2 | 8 | PF00069 | 0.742 |
MOD_CK2_1 | 333 | 339 | PF00069 | 0.461 |
MOD_CK2_1 | 442 | 448 | PF00069 | 0.669 |
MOD_CK2_1 | 477 | 483 | PF00069 | 0.684 |
MOD_CK2_1 | 58 | 64 | PF00069 | 0.604 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.704 |
MOD_GlcNHglycan | 257 | 260 | PF01048 | 0.546 |
MOD_GlcNHglycan | 320 | 323 | PF01048 | 0.632 |
MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.619 |
MOD_GlcNHglycan | 447 | 453 | PF01048 | 0.397 |
MOD_GlcNHglycan | 90 | 94 | PF01048 | 0.474 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.345 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.350 |
MOD_GSK3_1 | 386 | 393 | PF00069 | 0.358 |
MOD_GSK3_1 | 484 | 491 | PF00069 | 0.723 |
MOD_GSK3_1 | 495 | 502 | PF00069 | 0.699 |
MOD_GSK3_1 | 54 | 61 | PF00069 | 0.653 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.495 |
MOD_N-GLC_1 | 292 | 297 | PF02516 | 0.512 |
MOD_N-GLC_1 | 363 | 368 | PF02516 | 0.503 |
MOD_N-GLC_1 | 499 | 504 | PF02516 | 0.530 |
MOD_NEK2_1 | 156 | 161 | PF00069 | 0.473 |
MOD_NEK2_1 | 188 | 193 | PF00069 | 0.363 |
MOD_NEK2_1 | 279 | 284 | PF00069 | 0.360 |
MOD_NEK2_1 | 292 | 297 | PF00069 | 0.372 |
MOD_NEK2_1 | 363 | 368 | PF00069 | 0.346 |
MOD_NEK2_1 | 386 | 391 | PF00069 | 0.353 |
MOD_NEK2_1 | 488 | 493 | PF00069 | 0.718 |
MOD_NEK2_1 | 62 | 67 | PF00069 | 0.650 |
MOD_NEK2_1 | 95 | 100 | PF00069 | 0.423 |
MOD_NEK2_2 | 194 | 199 | PF00069 | 0.421 |
MOD_PIKK_1 | 158 | 164 | PF00454 | 0.564 |
MOD_PIKK_1 | 488 | 494 | PF00454 | 0.719 |
MOD_PK_1 | 281 | 287 | PF00069 | 0.377 |
MOD_PKA_2 | 150 | 156 | PF00069 | 0.484 |
MOD_PKA_2 | 478 | 484 | PF00069 | 0.678 |
MOD_PKA_2 | 493 | 499 | PF00069 | 0.732 |
MOD_Plk_1 | 138 | 144 | PF00069 | 0.476 |
MOD_Plk_1 | 292 | 298 | PF00069 | 0.309 |
MOD_Plk_1 | 31 | 37 | PF00069 | 0.616 |
MOD_Plk_1 | 363 | 369 | PF00069 | 0.303 |
MOD_Plk_1 | 488 | 494 | PF00069 | 0.700 |
MOD_Plk_4 | 165 | 171 | PF00069 | 0.472 |
MOD_Plk_4 | 217 | 223 | PF00069 | 0.429 |
MOD_Plk_4 | 250 | 256 | PF00069 | 0.303 |
MOD_Plk_4 | 403 | 409 | PF00069 | 0.284 |
MOD_Plk_4 | 422 | 428 | PF00069 | 0.367 |
MOD_Plk_4 | 58 | 64 | PF00069 | 0.699 |
MOD_ProDKin_1 | 208 | 214 | PF00069 | 0.477 |
MOD_ProDKin_1 | 348 | 354 | PF00069 | 0.431 |
MOD_ProDKin_1 | 455 | 461 | PF00069 | 0.614 |
MOD_ProDKin_1 | 499 | 505 | PF00069 | 0.731 |
MOD_ProDKin_1 | 7 | 13 | PF00069 | 0.708 |
MOD_SUMO_for_1 | 231 | 234 | PF00179 | 0.436 |
MOD_SUMO_for_1 | 244 | 247 | PF00179 | 0.293 |
MOD_SUMO_for_1 | 504 | 507 | PF00179 | 0.663 |
TRG_DiLeu_BaEn_1 | 152 | 157 | PF01217 | 0.457 |
TRG_DiLeu_BaLyEn_6 | 380 | 385 | PF01217 | 0.359 |
TRG_ENDOCYTIC_2 | 316 | 319 | PF00928 | 0.371 |
TRG_ENDOCYTIC_2 | 347 | 350 | PF00928 | 0.320 |
TRG_ENDOCYTIC_2 | 485 | 488 | PF00928 | 0.709 |
TRG_ENDOCYTIC_2 | 501 | 504 | PF00928 | 0.567 |
TRG_ENDOCYTIC_2 | 60 | 63 | PF00928 | 0.646 |
TRG_ENDOCYTIC_2 | 72 | 75 | PF00928 | 0.168 |
TRG_ENDOCYTIC_2 | 77 | 80 | PF00928 | 0.310 |
TRG_ER_diArg_1 | 358 | 361 | PF00400 | 0.339 |
TRG_ER_diArg_1 | 475 | 477 | PF00400 | 0.797 |
TRG_ER_diArg_1 | 493 | 495 | PF00400 | 0.574 |
TRG_ER_diLys_1 | 505 | 508 | PF00400 | 0.653 |
TRG_NES_CRM1_1 | 24 | 38 | PF08389 | 0.648 |
TRG_Pf-PMV_PEXEL_1 | 135 | 139 | PF00026 | 0.694 |
TRG_Pf-PMV_PEXEL_1 | 154 | 158 | PF00026 | 0.652 |
TRG_Pf-PMV_PEXEL_1 | 397 | 401 | PF00026 | 0.620 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8U6 | Leptomonas seymouri | 56% | 100% |
A0A0S4J1Q7 | Bodo saltans | 22% | 100% |
A0A1X0NJH4 | Trypanosomatidae | 36% | 100% |
A4HIZ2 | Leishmania braziliensis | 74% | 100% |
A4I6A9 | Leishmania infantum | 99% | 100% |
E9B1G5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q4Q6P7 | Leishmania major | 93% | 100% |
V5BN41 | Trypanosoma cruzi | 40% | 100% |