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: 5 |
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: 8 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | yes | yes: 5, no: 6 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000139 | Golgi membrane | 5 | 2 |
GO:0005737 | cytoplasm | 2 | 2 |
GO:0005789 | endoplasmic reticulum membrane | 4 | 2 |
GO:0005793 | endoplasmic reticulum-Golgi intermediate compartment | 5 | 2 |
GO:0016020 | membrane | 2 | 10 |
GO:0030134 | COPII-coated ER to Golgi transport vesicle | 8 | 2 |
GO:0030135 | coated vesicle | 7 | 2 |
GO:0031090 | organelle membrane | 3 | 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:0098588 | bounding membrane of organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
Related structures:
AlphaFold database: Q4QJ95
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 2 |
GO:0006888 | endoplasmic reticulum to Golgi vesicle-mediated transport | 4 | 2 |
GO:0006996 | organelle organization | 4 | 2 |
GO:0007029 | endoplasmic reticulum organization | 5 | 2 |
GO:0007030 | Golgi organization | 5 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0016192 | vesicle-mediated transport | 4 | 2 |
GO:0046907 | intracellular transport | 3 | 2 |
GO:0048193 | Golgi vesicle transport | 5 | 2 |
GO:0051179 | localization | 1 | 2 |
GO:0051234 | establishment of localization | 2 | 2 |
GO:0051641 | cellular localization | 2 | 2 |
GO:0051649 | establishment of localization in cell | 3 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 3 |
GO:0005537 | mannose binding | 4 | 2 |
GO:0030246 | carbohydrate binding | 2 | 3 |
GO:0036094 | small molecule binding | 2 | 2 |
GO:0048029 | monosaccharide binding | 3 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 163 | 167 | PF00656 | 0.631 |
CLV_NRD_NRD_1 | 209 | 211 | PF00675 | 0.564 |
CLV_NRD_NRD_1 | 214 | 216 | PF00675 | 0.548 |
CLV_NRD_NRD_1 | 363 | 365 | PF00675 | 0.410 |
CLV_NRD_NRD_1 | 371 | 373 | PF00675 | 0.398 |
CLV_NRD_NRD_1 | 432 | 434 | PF00675 | 0.565 |
CLV_NRD_NRD_1 | 435 | 437 | PF00675 | 0.583 |
CLV_NRD_NRD_1 | 490 | 492 | PF00675 | 0.482 |
CLV_PCSK_FUR_1 | 433 | 437 | PF00082 | 0.566 |
CLV_PCSK_KEX2_1 | 209 | 211 | PF00082 | 0.527 |
CLV_PCSK_KEX2_1 | 214 | 216 | PF00082 | 0.530 |
CLV_PCSK_KEX2_1 | 226 | 228 | PF00082 | 0.510 |
CLV_PCSK_KEX2_1 | 363 | 365 | PF00082 | 0.405 |
CLV_PCSK_KEX2_1 | 371 | 373 | PF00082 | 0.400 |
CLV_PCSK_KEX2_1 | 377 | 379 | PF00082 | 0.496 |
CLV_PCSK_KEX2_1 | 434 | 436 | PF00082 | 0.578 |
CLV_PCSK_KEX2_1 | 490 | 492 | PF00082 | 0.478 |
CLV_PCSK_PC1ET2_1 | 214 | 216 | PF00082 | 0.554 |
CLV_PCSK_PC1ET2_1 | 226 | 228 | PF00082 | 0.495 |
CLV_PCSK_PC1ET2_1 | 363 | 365 | PF00082 | 0.446 |
CLV_PCSK_PC1ET2_1 | 377 | 379 | PF00082 | 0.538 |
CLV_PCSK_PC1ET2_1 | 434 | 436 | PF00082 | 0.601 |
CLV_PCSK_PC7_1 | 210 | 216 | PF00082 | 0.583 |
CLV_PCSK_SKI1_1 | 210 | 214 | PF00082 | 0.564 |
CLV_PCSK_SKI1_1 | 222 | 226 | PF00082 | 0.489 |
CLV_PCSK_SKI1_1 | 346 | 350 | PF00082 | 0.558 |
CLV_PCSK_SKI1_1 | 364 | 368 | PF00082 | 0.288 |
CLV_PCSK_SKI1_1 | 428 | 432 | PF00082 | 0.655 |
CLV_PCSK_SKI1_1 | 439 | 443 | PF00082 | 0.617 |
CLV_PCSK_SKI1_1 | 448 | 452 | PF00082 | 0.509 |
CLV_Separin_Metazoa | 395 | 399 | PF03568 | 0.489 |
DEG_APCC_DBOX_1 | 434 | 442 | PF00400 | 0.665 |
DEG_APCC_DBOX_1 | 459 | 467 | PF00400 | 0.344 |
DOC_CYCLIN_RxL_1 | 216 | 229 | PF00134 | 0.606 |
DOC_MAPK_gen_1 | 236 | 245 | PF00069 | 0.488 |
DOC_MAPK_gen_1 | 360 | 370 | PF00069 | 0.348 |
DOC_MAPK_gen_1 | 447 | 455 | PF00069 | 0.617 |
DOC_MAPK_gen_1 | 490 | 496 | PF00069 | 0.598 |
DOC_MAPK_MEF2A_6 | 236 | 245 | PF00069 | 0.488 |
DOC_MAPK_MEF2A_6 | 363 | 370 | PF00069 | 0.342 |
DOC_PP1_RVXF_1 | 104 | 110 | PF00149 | 0.231 |
DOC_PP1_RVXF_1 | 491 | 497 | PF00149 | 0.538 |
DOC_PP2B_LxvP_1 | 289 | 292 | PF13499 | 0.439 |
DOC_PP4_FxxP_1 | 50 | 53 | PF00568 | 0.244 |
DOC_SPAK_OSR1_1 | 108 | 112 | PF12202 | 0.244 |
DOC_USP7_MATH_1 | 21 | 25 | PF00917 | 0.667 |
DOC_USP7_MATH_1 | 437 | 441 | PF00917 | 0.693 |
DOC_USP7_MATH_1 | 53 | 57 | PF00917 | 0.264 |
DOC_USP7_UBL2_3 | 222 | 226 | PF12436 | 0.610 |
DOC_WW_Pin1_4 | 154 | 159 | PF00397 | 0.651 |
DOC_WW_Pin1_4 | 313 | 318 | PF00397 | 0.394 |
LIG_14-3-3_CanoR_1 | 227 | 232 | PF00244 | 0.536 |
LIG_14-3-3_CanoR_1 | 321 | 325 | PF00244 | 0.560 |
LIG_14-3-3_CanoR_1 | 364 | 369 | PF00244 | 0.280 |
LIG_14-3-3_CanoR_1 | 436 | 442 | PF00244 | 0.627 |
LIG_14-3-3_CanoR_1 | 80 | 86 | PF00244 | 0.267 |
LIG_deltaCOP1_diTrp_1 | 101 | 109 | PF00928 | 0.338 |
LIG_deltaCOP1_diTrp_1 | 168 | 176 | PF00928 | 0.597 |
LIG_FHA_1 | 280 | 286 | PF00498 | 0.499 |
LIG_FHA_1 | 3 | 9 | PF00498 | 0.559 |
LIG_FHA_1 | 343 | 349 | PF00498 | 0.370 |
LIG_FHA_1 | 365 | 371 | PF00498 | 0.411 |
LIG_FHA_1 | 389 | 395 | PF00498 | 0.546 |
LIG_FHA_1 | 476 | 482 | PF00498 | 0.646 |
LIG_FHA_1 | 81 | 87 | PF00498 | 0.275 |
LIG_FHA_1 | 93 | 99 | PF00498 | 0.275 |
LIG_FHA_2 | 194 | 200 | PF00498 | 0.670 |
LIG_FHA_2 | 227 | 233 | PF00498 | 0.519 |
LIG_FHA_2 | 347 | 353 | PF00498 | 0.415 |
LIG_FHA_2 | 397 | 403 | PF00498 | 0.462 |
LIG_FHA_2 | 449 | 455 | PF00498 | 0.479 |
LIG_FHA_2 | 80 | 86 | PF00498 | 0.343 |
LIG_LIR_Apic_2 | 47 | 53 | PF02991 | 0.244 |
LIG_LIR_Gen_1 | 284 | 292 | PF02991 | 0.504 |
LIG_LIR_Gen_1 | 449 | 458 | PF02991 | 0.523 |
LIG_LIR_Gen_1 | 76 | 86 | PF02991 | 0.275 |
LIG_LIR_LC3C_4 | 11 | 15 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 218 | 224 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 284 | 289 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 449 | 453 | PF02991 | 0.531 |
LIG_LIR_Nem_3 | 76 | 81 | PF02991 | 0.275 |
LIG_PDZ_Class_3 | 504 | 509 | PF00595 | 0.620 |
LIG_Pex14_2 | 221 | 225 | PF04695 | 0.608 |
LIG_Pex14_2 | 248 | 252 | PF04695 | 0.419 |
LIG_PTB_Apo_2 | 72 | 79 | PF02174 | 0.257 |
LIG_SH2_STAP1 | 152 | 156 | PF00017 | 0.616 |
LIG_SH2_STAP1 | 400 | 404 | PF00017 | 0.486 |
LIG_SH2_STAP1 | 475 | 479 | PF00017 | 0.518 |
LIG_SH2_STAT3 | 137 | 140 | PF00017 | 0.257 |
LIG_SH2_STAT3 | 334 | 337 | PF00017 | 0.536 |
LIG_SH2_STAT5 | 137 | 140 | PF00017 | 0.244 |
LIG_SH2_STAT5 | 286 | 289 | PF00017 | 0.492 |
LIG_SH2_STAT5 | 400 | 403 | PF00017 | 0.402 |
LIG_SH3_1 | 498 | 504 | PF00018 | 0.534 |
LIG_SH3_3 | 330 | 336 | PF00018 | 0.607 |
LIG_SH3_3 | 498 | 504 | PF00018 | 0.534 |
LIG_SUMO_SIM_anti_2 | 11 | 16 | PF11976 | 0.415 |
LIG_SUMO_SIM_anti_2 | 352 | 359 | PF11976 | 0.338 |
LIG_SUMO_SIM_anti_2 | 391 | 399 | PF11976 | 0.496 |
LIG_TRAF2_1 | 196 | 199 | PF00917 | 0.578 |
LIG_TRAF2_1 | 350 | 353 | PF00917 | 0.454 |
LIG_TRAF2_1 | 49 | 52 | PF00917 | 0.294 |
LIG_UBA3_1 | 220 | 226 | PF00899 | 0.608 |
MOD_CDK_SPxxK_3 | 154 | 161 | PF00069 | 0.647 |
MOD_CK1_1 | 298 | 304 | PF00069 | 0.575 |
MOD_CK1_1 | 422 | 428 | PF00069 | 0.418 |
MOD_CK2_1 | 193 | 199 | PF00069 | 0.645 |
MOD_CK2_1 | 227 | 233 | PF00069 | 0.507 |
MOD_CK2_1 | 346 | 352 | PF00069 | 0.484 |
MOD_CK2_1 | 396 | 402 | PF00069 | 0.471 |
MOD_CK2_1 | 46 | 52 | PF00069 | 0.359 |
MOD_GlcNHglycan | 297 | 300 | PF01048 | 0.680 |
MOD_GlcNHglycan | 421 | 424 | PF01048 | 0.371 |
MOD_GlcNHglycan | 70 | 73 | PF01048 | 0.453 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.663 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.504 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.591 |
MOD_GSK3_1 | 342 | 349 | PF00069 | 0.579 |
MOD_GSK3_1 | 384 | 391 | PF00069 | 0.603 |
MOD_GSK3_1 | 396 | 403 | PF00069 | 0.434 |
MOD_N-GLC_1 | 120 | 125 | PF02516 | 0.526 |
MOD_N-GLC_1 | 292 | 297 | PF02516 | 0.572 |
MOD_NEK2_1 | 120 | 125 | PF00069 | 0.345 |
MOD_NEK2_1 | 3 | 8 | PF00069 | 0.637 |
MOD_NEK2_1 | 419 | 424 | PF00069 | 0.375 |
MOD_NEK2_1 | 473 | 478 | PF00069 | 0.501 |
MOD_NEK2_1 | 494 | 499 | PF00069 | 0.618 |
MOD_NEK2_1 | 79 | 84 | PF00069 | 0.347 |
MOD_NEK2_2 | 437 | 442 | PF00069 | 0.574 |
MOD_PK_1 | 227 | 233 | PF00069 | 0.544 |
MOD_PKA_1 | 216 | 222 | PF00069 | 0.475 |
MOD_PKA_1 | 226 | 232 | PF00069 | 0.503 |
MOD_PKA_1 | 364 | 370 | PF00069 | 0.298 |
MOD_PKA_2 | 107 | 113 | PF00069 | 0.244 |
MOD_PKA_2 | 216 | 222 | PF00069 | 0.450 |
MOD_PKA_2 | 226 | 232 | PF00069 | 0.485 |
MOD_PKA_2 | 320 | 326 | PF00069 | 0.503 |
MOD_PKA_2 | 79 | 85 | PF00069 | 0.267 |
MOD_Plk_1 | 378 | 384 | PF00069 | 0.540 |
MOD_Plk_1 | 46 | 52 | PF00069 | 0.257 |
MOD_Plk_2-3 | 193 | 199 | PF00069 | 0.655 |
MOD_Plk_2-3 | 379 | 385 | PF00069 | 0.453 |
MOD_Plk_4 | 216 | 222 | PF00069 | 0.375 |
MOD_Plk_4 | 281 | 287 | PF00069 | 0.460 |
MOD_Plk_4 | 298 | 304 | PF00069 | 0.551 |
MOD_Plk_4 | 364 | 370 | PF00069 | 0.371 |
MOD_Plk_4 | 379 | 385 | PF00069 | 0.480 |
MOD_Plk_4 | 8 | 14 | PF00069 | 0.554 |
MOD_ProDKin_1 | 154 | 160 | PF00069 | 0.648 |
MOD_ProDKin_1 | 313 | 319 | PF00069 | 0.396 |
MOD_SUMO_for_1 | 376 | 379 | PF00179 | 0.492 |
MOD_SUMO_rev_2 | 440 | 450 | PF00179 | 0.528 |
MOD_SUMO_rev_2 | 465 | 473 | PF00179 | 0.391 |
TRG_DiLeu_BaEn_1 | 353 | 358 | PF01217 | 0.415 |
TRG_DiLeu_BaLyEn_6 | 40 | 45 | PF01217 | 0.431 |
TRG_ENDOCYTIC_2 | 286 | 289 | PF00928 | 0.492 |
TRG_ER_diArg_1 | 106 | 109 | PF00400 | 0.248 |
TRG_ER_diArg_1 | 370 | 372 | PF00400 | 0.397 |
TRG_ER_diArg_1 | 433 | 436 | PF00400 | 0.617 |
TRG_NES_CRM1_1 | 457 | 469 | PF08389 | 0.533 |
TRG_NLS_MonoCore_2 | 212 | 217 | PF00514 | 0.599 |
TRG_NLS_MonoCore_2 | 432 | 437 | PF00514 | 0.602 |
TRG_NLS_MonoExtC_3 | 212 | 217 | PF00514 | 0.616 |
TRG_NLS_MonoExtC_3 | 432 | 437 | PF00514 | 0.592 |
TRG_NLS_MonoExtN_4 | 210 | 217 | PF00514 | 0.622 |
TRG_NLS_MonoExtN_4 | 360 | 367 | PF00514 | 0.323 |
TRG_NLS_MonoExtN_4 | 431 | 438 | PF00514 | 0.667 |
TRG_Pf-PMV_PEXEL_1 | 464 | 469 | PF00026 | 0.325 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IIA0 | Leptomonas seymouri | 78% | 100% |
A0A1X0NKB0 | Trypanosomatidae | 42% | 79% |
A0A3R7LT82 | Trypanosoma rangeli | 47% | 93% |
A0A3S5H5L7 | Leishmania donovani | 96% | 84% |
A4H4F2 | Leishmania braziliensis | 87% | 100% |
A4HSM9 | Leishmania infantum | 96% | 98% |
C9ZU67 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 82% |
E8NHN5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 83% |
E9AKL4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 98% |
V5ARI9 | Trypanosoma cruzi | 47% | 87% |