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: 6 |
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: 16 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9ATU8
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 9 |
GO:0006886 | intracellular protein transport | 4 | 9 |
GO:0007034 | vacuolar transport | 4 | 9 |
GO:0008104 | protein localization | 4 | 9 |
GO:0009987 | cellular process | 1 | 9 |
GO:0015031 | protein transport | 4 | 9 |
GO:0016192 | vesicle-mediated transport | 4 | 9 |
GO:0016197 | endosomal transport | 4 | 9 |
GO:0032509 | endosome transport via multivesicular body sorting pathway | 5 | 9 |
GO:0032511 | late endosome to vacuole transport via multivesicular body sorting pathway | 6 | 9 |
GO:0033036 | macromolecule localization | 2 | 9 |
GO:0033365 | protein localization to organelle | 5 | 9 |
GO:0043328 | protein transport to vacuole involved in ubiquitin-dependent protein catabolic process via the multivesicular body sorting pathway | 5 | 9 |
GO:0045184 | establishment of protein localization | 3 | 9 |
GO:0045324 | late endosome to vacuole transport | 5 | 9 |
GO:0046907 | intracellular transport | 3 | 9 |
GO:0051179 | localization | 1 | 9 |
GO:0051234 | establishment of localization | 2 | 9 |
GO:0051641 | cellular localization | 2 | 9 |
GO:0051649 | establishment of localization in cell | 3 | 9 |
GO:0070727 | cellular macromolecule localization | 3 | 9 |
GO:0071702 | organic substance transport | 4 | 9 |
GO:0071705 | nitrogen compound transport | 4 | 9 |
GO:0071985 | multivesicular body sorting pathway | 5 | 9 |
GO:0072594 | establishment of protein localization to organelle | 4 | 9 |
GO:0072665 | protein localization to vacuole | 6 | 9 |
GO:0072666 | establishment of protein localization to vacuole | 5 | 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 9 |
GO:0005515 | protein binding | 2 | 9 |
GO:0005543 | phospholipid binding | 3 | 9 |
GO:0008289 | lipid binding | 2 | 9 |
GO:0032182 | ubiquitin-like protein binding | 3 | 9 |
GO:0035091 | phosphatidylinositol binding | 4 | 9 |
GO:0043130 | ubiquitin binding | 4 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 291 | 295 | PF00656 | 0.447 |
CLV_NRD_NRD_1 | 187 | 189 | PF00675 | 0.726 |
CLV_NRD_NRD_1 | 65 | 67 | PF00675 | 0.314 |
CLV_PCSK_FUR_1 | 210 | 214 | PF00082 | 0.635 |
CLV_PCSK_KEX2_1 | 187 | 189 | PF00082 | 0.747 |
CLV_PCSK_KEX2_1 | 212 | 214 | PF00082 | 0.756 |
CLV_PCSK_KEX2_1 | 64 | 66 | PF00082 | 0.314 |
CLV_PCSK_PC1ET2_1 | 212 | 214 | PF00082 | 0.653 |
CLV_PCSK_PC7_1 | 61 | 67 | PF00082 | 0.314 |
CLV_PCSK_SKI1_1 | 101 | 105 | PF00082 | 0.314 |
CLV_PCSK_SKI1_1 | 286 | 290 | PF00082 | 0.464 |
CLV_PCSK_SKI1_1 | 75 | 79 | PF00082 | 0.326 |
DEG_APCC_DBOX_1 | 285 | 293 | PF00400 | 0.427 |
DEG_COP1_1 | 415 | 425 | PF00400 | 0.503 |
DEG_SCF_FBW7_1 | 417 | 424 | PF00400 | 0.502 |
DOC_CKS1_1 | 378 | 383 | PF01111 | 0.658 |
DOC_CYCLIN_RxL_1 | 98 | 106 | PF00134 | 0.369 |
DOC_MAPK_gen_1 | 172 | 180 | PF00069 | 0.569 |
DOC_MAPK_gen_1 | 51 | 59 | PF00069 | 0.432 |
DOC_MAPK_MEF2A_6 | 124 | 132 | PF00069 | 0.360 |
DOC_MAPK_MEF2A_6 | 172 | 180 | PF00069 | 0.563 |
DOC_MAPK_MEF2A_6 | 268 | 276 | PF00069 | 0.515 |
DOC_PP2B_LxvP_1 | 34 | 37 | PF13499 | 0.406 |
DOC_PP2B_LxvP_1 | 356 | 359 | PF13499 | 0.619 |
DOC_USP7_MATH_1 | 123 | 127 | PF00917 | 0.442 |
DOC_USP7_MATH_1 | 316 | 320 | PF00917 | 0.679 |
DOC_USP7_MATH_1 | 321 | 325 | PF00917 | 0.632 |
DOC_USP7_MATH_1 | 402 | 406 | PF00917 | 0.703 |
DOC_USP7_MATH_1 | 440 | 444 | PF00917 | 0.754 |
DOC_USP7_MATH_1 | 456 | 460 | PF00917 | 0.759 |
DOC_USP7_MATH_1 | 471 | 475 | PF00917 | 0.652 |
DOC_WW_Pin1_4 | 312 | 317 | PF00397 | 0.627 |
DOC_WW_Pin1_4 | 371 | 376 | PF00397 | 0.676 |
DOC_WW_Pin1_4 | 377 | 382 | PF00397 | 0.681 |
DOC_WW_Pin1_4 | 406 | 411 | PF00397 | 0.598 |
DOC_WW_Pin1_4 | 417 | 422 | PF00397 | 0.685 |
DOC_WW_Pin1_4 | 426 | 431 | PF00397 | 0.705 |
DOC_WW_Pin1_4 | 436 | 441 | PF00397 | 0.805 |
DOC_WW_Pin1_4 | 444 | 449 | PF00397 | 0.546 |
DOC_WW_Pin1_4 | 461 | 466 | PF00397 | 0.517 |
LIG_14-3-3_CanoR_1 | 290 | 299 | PF00244 | 0.593 |
LIG_Actin_WH2_2 | 275 | 292 | PF00022 | 0.444 |
LIG_Actin_WH2_2 | 3 | 18 | PF00022 | 0.293 |
LIG_BH_BH3_1 | 141 | 157 | PF00452 | 0.478 |
LIG_BIR_III_2 | 313 | 317 | PF00653 | 0.659 |
LIG_BRCT_BRCA1_1 | 134 | 138 | PF00533 | 0.371 |
LIG_BRCT_BRCA1_1 | 89 | 93 | PF00533 | 0.432 |
LIG_FHA_1 | 129 | 135 | PF00498 | 0.438 |
LIG_FHA_1 | 273 | 279 | PF00498 | 0.494 |
LIG_FHA_1 | 378 | 384 | PF00498 | 0.660 |
LIG_FHA_1 | 401 | 407 | PF00498 | 0.535 |
LIG_FHA_1 | 486 | 492 | PF00498 | 0.586 |
LIG_FHA_1 | 54 | 60 | PF00498 | 0.469 |
LIG_FHA_1 | 76 | 82 | PF00498 | 0.314 |
LIG_FHA_2 | 149 | 155 | PF00498 | 0.380 |
LIG_FHA_2 | 236 | 242 | PF00498 | 0.458 |
LIG_FHA_2 | 246 | 252 | PF00498 | 0.491 |
LIG_FHA_2 | 289 | 295 | PF00498 | 0.455 |
LIG_GBD_Chelix_1 | 215 | 223 | PF00786 | 0.647 |
LIG_HCF-1_HBM_1 | 270 | 273 | PF13415 | 0.475 |
LIG_LIR_Gen_1 | 21 | 26 | PF02991 | 0.339 |
LIG_LIR_Gen_1 | 270 | 278 | PF02991 | 0.482 |
LIG_LIR_Gen_1 | 38 | 45 | PF02991 | 0.386 |
LIG_LIR_Gen_1 | 496 | 502 | PF02991 | 0.604 |
LIG_LIR_Nem_3 | 21 | 25 | PF02991 | 0.348 |
LIG_LIR_Nem_3 | 238 | 242 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 270 | 276 | PF02991 | 0.510 |
LIG_LIR_Nem_3 | 38 | 42 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 496 | 501 | PF02991 | 0.604 |
LIG_SH2_GRB2like | 242 | 245 | PF00017 | 0.423 |
LIG_SH2_PTP2 | 22 | 25 | PF00017 | 0.246 |
LIG_SH2_PTP2 | 273 | 276 | PF00017 | 0.515 |
LIG_SH2_SRC | 22 | 25 | PF00017 | 0.364 |
LIG_SH2_SRC | 39 | 42 | PF00017 | 0.324 |
LIG_SH2_STAT3 | 263 | 266 | PF00017 | 0.520 |
LIG_SH2_STAT5 | 147 | 150 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 22 | 25 | PF00017 | 0.290 |
LIG_SH2_STAT5 | 242 | 245 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 263 | 266 | PF00017 | 0.538 |
LIG_SH2_STAT5 | 273 | 276 | PF00017 | 0.433 |
LIG_SH3_3 | 177 | 183 | PF00018 | 0.616 |
LIG_SH3_3 | 375 | 381 | PF00018 | 0.733 |
LIG_SH3_3 | 404 | 410 | PF00018 | 0.792 |
LIG_SH3_3 | 419 | 425 | PF00018 | 0.643 |
LIG_SH3_3 | 481 | 487 | PF00018 | 0.711 |
LIG_SUMO_SIM_anti_2 | 21 | 28 | PF11976 | 0.253 |
LIG_SUMO_SIM_anti_2 | 56 | 61 | PF11976 | 0.406 |
LIG_SUMO_SIM_par_1 | 274 | 280 | PF11976 | 0.442 |
LIG_SUMO_SIM_par_1 | 409 | 416 | PF11976 | 0.512 |
LIG_TRAF2_1 | 142 | 145 | PF00917 | 0.524 |
LIG_TRAF2_1 | 346 | 349 | PF00917 | 0.695 |
LIG_TRAF2_1 | 413 | 416 | PF00917 | 0.631 |
LIG_TRAF2_1 | 455 | 458 | PF00917 | 0.569 |
LIG_TRAF2_2 | 190 | 195 | PF00917 | 0.682 |
LIG_UBA3_1 | 6 | 13 | PF00899 | 0.388 |
LIG_UBA3_1 | 81 | 87 | PF00899 | 0.354 |
LIG_WW_3 | 357 | 361 | PF00397 | 0.724 |
MOD_CK1_1 | 191 | 197 | PF00069 | 0.579 |
MOD_CK1_1 | 262 | 268 | PF00069 | 0.518 |
MOD_CK2_1 | 2 | 8 | PF00069 | 0.456 |
MOD_CK2_1 | 245 | 251 | PF00069 | 0.422 |
MOD_CK2_1 | 410 | 416 | PF00069 | 0.755 |
MOD_CK2_1 | 456 | 462 | PF00069 | 0.647 |
MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.453 |
MOD_GlcNHglycan | 229 | 232 | PF01048 | 0.490 |
MOD_GlcNHglycan | 296 | 299 | PF01048 | 0.457 |
MOD_GlcNHglycan | 319 | 322 | PF01048 | 0.666 |
MOD_GlcNHglycan | 323 | 326 | PF01048 | 0.637 |
MOD_GlcNHglycan | 332 | 335 | PF01048 | 0.626 |
MOD_GlcNHglycan | 340 | 343 | PF01048 | 0.620 |
MOD_GlcNHglycan | 344 | 347 | PF01048 | 0.586 |
MOD_GlcNHglycan | 364 | 367 | PF01048 | 0.713 |
MOD_GlcNHglycan | 397 | 400 | PF01048 | 0.715 |
MOD_GlcNHglycan | 457 | 461 | PF01048 | 0.789 |
MOD_GlcNHglycan | 473 | 476 | PF01048 | 0.734 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.451 |
MOD_GSK3_1 | 223 | 230 | PF00069 | 0.524 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.483 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.358 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.586 |
MOD_GSK3_1 | 326 | 333 | PF00069 | 0.635 |
MOD_GSK3_1 | 334 | 341 | PF00069 | 0.647 |
MOD_GSK3_1 | 402 | 409 | PF00069 | 0.628 |
MOD_GSK3_1 | 417 | 424 | PF00069 | 0.694 |
MOD_GSK3_1 | 434 | 441 | PF00069 | 0.673 |
MOD_N-GLC_1 | 132 | 137 | PF02516 | 0.355 |
MOD_N-GLC_1 | 87 | 92 | PF02516 | 0.193 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.373 |
MOD_NEK2_1 | 232 | 237 | PF00069 | 0.441 |
MOD_NEK2_1 | 277 | 282 | PF00069 | 0.519 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.513 |
MOD_NEK2_1 | 330 | 335 | PF00069 | 0.721 |
MOD_NEK2_1 | 435 | 440 | PF00069 | 0.728 |
MOD_NEK2_1 | 45 | 50 | PF00069 | 0.319 |
MOD_NEK2_1 | 81 | 86 | PF00069 | 0.406 |
MOD_PIKK_1 | 188 | 194 | PF00454 | 0.762 |
MOD_PIKK_1 | 262 | 268 | PF00454 | 0.492 |
MOD_PIKK_1 | 292 | 298 | PF00454 | 0.444 |
MOD_PIKK_1 | 96 | 102 | PF00454 | 0.314 |
MOD_PKA_2 | 227 | 233 | PF00069 | 0.502 |
MOD_PKA_2 | 368 | 374 | PF00069 | 0.512 |
MOD_Plk_1 | 132 | 138 | PF00069 | 0.352 |
MOD_Plk_1 | 303 | 309 | PF00069 | 0.516 |
MOD_Plk_1 | 342 | 348 | PF00069 | 0.655 |
MOD_Plk_1 | 53 | 59 | PF00069 | 0.369 |
MOD_Plk_4 | 132 | 138 | PF00069 | 0.380 |
MOD_Plk_4 | 18 | 24 | PF00069 | 0.391 |
MOD_Plk_4 | 2 | 8 | PF00069 | 0.421 |
MOD_Plk_4 | 259 | 265 | PF00069 | 0.561 |
MOD_Plk_4 | 272 | 278 | PF00069 | 0.402 |
MOD_Plk_4 | 326 | 332 | PF00069 | 0.680 |
MOD_Plk_4 | 81 | 87 | PF00069 | 0.334 |
MOD_ProDKin_1 | 312 | 318 | PF00069 | 0.628 |
MOD_ProDKin_1 | 371 | 377 | PF00069 | 0.672 |
MOD_ProDKin_1 | 406 | 412 | PF00069 | 0.600 |
MOD_ProDKin_1 | 417 | 423 | PF00069 | 0.684 |
MOD_ProDKin_1 | 426 | 432 | PF00069 | 0.708 |
MOD_ProDKin_1 | 436 | 442 | PF00069 | 0.806 |
MOD_ProDKin_1 | 444 | 450 | PF00069 | 0.541 |
MOD_ProDKin_1 | 461 | 467 | PF00069 | 0.510 |
MOD_SUMO_for_1 | 176 | 179 | PF00179 | 0.595 |
MOD_SUMO_for_1 | 301 | 304 | PF00179 | 0.551 |
TRG_DiLeu_BaEn_1 | 125 | 130 | PF01217 | 0.456 |
TRG_DiLeu_BaEn_2 | 39 | 45 | PF01217 | 0.406 |
TRG_DiLeu_BaEn_4 | 144 | 150 | PF01217 | 0.514 |
TRG_DiLeu_BaLyEn_6 | 13 | 18 | PF01217 | 0.335 |
TRG_ENDOCYTIC_2 | 22 | 25 | PF00928 | 0.381 |
TRG_ENDOCYTIC_2 | 273 | 276 | PF00928 | 0.489 |
TRG_ENDOCYTIC_2 | 39 | 42 | PF00928 | 0.452 |
TRG_ER_diArg_1 | 63 | 66 | PF00400 | 0.314 |
TRG_Pf-PMV_PEXEL_1 | 43 | 47 | PF00026 | 0.406 |
TRG_Pf-PMV_PEXEL_1 | 65 | 69 | PF00026 | 0.292 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PB53 | Leptomonas seymouri | 63% | 94% |
A0A3Q8IJX3 | Leishmania donovani | 85% | 98% |
A0A3R7M014 | Trypanosoma rangeli | 36% | 100% |
A4HQ30 | Leishmania braziliensis | 69% | 100% |
A4IDT6 | Leishmania infantum | 85% | 98% |
Q4Q0P8 | Leishmania major | 80% | 100% |
V5BM99 | Trypanosoma cruzi | 36% | 100% |