Vesicle mediated transport, Vacuolar sorting-associated 45-like
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: 15 |
NetGPI | no | yes: 0, no: 15 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000139 | Golgi membrane | 5 | 2 |
GO:0016020 | membrane | 2 | 2 |
GO:0031090 | organelle membrane | 3 | 2 |
GO:0098588 | bounding membrane of organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: A4IDJ7
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 16 |
GO:0016192 | vesicle-mediated transport | 4 | 16 |
GO:0051179 | localization | 1 | 16 |
GO:0051234 | establishment of localization | 2 | 16 |
GO:0006886 | intracellular protein transport | 4 | 2 |
GO:0008104 | protein localization | 4 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0015031 | protein transport | 4 | 2 |
GO:0033036 | macromolecule localization | 2 | 2 |
GO:0045184 | establishment of protein localization | 3 | 2 |
GO:0046907 | intracellular transport | 3 | 2 |
GO:0051641 | cellular localization | 2 | 2 |
GO:0051649 | establishment of localization in cell | 3 | 2 |
GO:0070727 | cellular macromolecule localization | 3 | 2 |
GO:0071702 | organic substance transport | 4 | 2 |
GO:0071705 | nitrogen compound transport | 4 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 149 | 151 | PF00675 | 0.362 |
CLV_NRD_NRD_1 | 164 | 166 | PF00675 | 0.280 |
CLV_NRD_NRD_1 | 333 | 335 | PF00675 | 0.337 |
CLV_PCSK_KEX2_1 | 149 | 151 | PF00082 | 0.337 |
CLV_PCSK_KEX2_1 | 163 | 165 | PF00082 | 0.290 |
CLV_PCSK_KEX2_1 | 332 | 334 | PF00082 | 0.308 |
CLV_PCSK_KEX2_1 | 453 | 455 | PF00082 | 0.308 |
CLV_PCSK_PC1ET2_1 | 332 | 334 | PF00082 | 0.308 |
CLV_PCSK_PC1ET2_1 | 453 | 455 | PF00082 | 0.308 |
CLV_PCSK_SKI1_1 | 12 | 16 | PF00082 | 0.322 |
CLV_PCSK_SKI1_1 | 125 | 129 | PF00082 | 0.348 |
CLV_PCSK_SKI1_1 | 285 | 289 | PF00082 | 0.413 |
CLV_PCSK_SKI1_1 | 311 | 315 | PF00082 | 0.272 |
CLV_PCSK_SKI1_1 | 334 | 338 | PF00082 | 0.361 |
CLV_PCSK_SKI1_1 | 433 | 437 | PF00082 | 0.308 |
CLV_PCSK_SKI1_1 | 78 | 82 | PF00082 | 0.345 |
DEG_APCC_DBOX_1 | 332 | 340 | PF00400 | 0.337 |
DEG_APCC_DBOX_1 | 63 | 71 | PF00400 | 0.366 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.387 |
DEG_SCF_FBW7_1 | 213 | 219 | PF00400 | 0.275 |
DEG_SPOP_SBC_1 | 475 | 479 | PF00917 | 0.302 |
DOC_ANK_TNKS_1 | 148 | 155 | PF00023 | 0.413 |
DOC_CKS1_1 | 130 | 135 | PF01111 | 0.413 |
DOC_CKS1_1 | 213 | 218 | PF01111 | 0.324 |
DOC_CYCLIN_RxL_1 | 331 | 340 | PF00134 | 0.332 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 49 | 57 | PF00134 | 0.413 |
DOC_CYCLIN_yCln2_LP_2 | 217 | 223 | PF00134 | 0.318 |
DOC_CYCLIN_yCln2_LP_2 | 238 | 244 | PF00134 | 0.308 |
DOC_MAPK_gen_1 | 332 | 341 | PF00069 | 0.308 |
DOC_MAPK_gen_1 | 433 | 441 | PF00069 | 0.308 |
DOC_MAPK_gen_1 | 55 | 63 | PF00069 | 0.322 |
DOC_MAPK_gen_1 | 81 | 89 | PF00069 | 0.413 |
DOC_MAPK_MEF2A_6 | 200 | 207 | PF00069 | 0.331 |
DOC_MAPK_MEF2A_6 | 332 | 341 | PF00069 | 0.308 |
DOC_MAPK_MEF2A_6 | 490 | 498 | PF00069 | 0.349 |
DOC_PP2B_LxvP_1 | 238 | 241 | PF13499 | 0.366 |
DOC_USP7_MATH_1 | 366 | 370 | PF00917 | 0.374 |
DOC_USP7_MATH_1 | 475 | 479 | PF00917 | 0.255 |
DOC_USP7_MATH_1 | 529 | 533 | PF00917 | 0.403 |
DOC_WW_Pin1_4 | 129 | 134 | PF00397 | 0.361 |
DOC_WW_Pin1_4 | 171 | 176 | PF00397 | 0.413 |
DOC_WW_Pin1_4 | 212 | 217 | PF00397 | 0.316 |
DOC_WW_Pin1_4 | 554 | 559 | PF00397 | 0.441 |
LIG_14-3-3_CanoR_1 | 234 | 239 | PF00244 | 0.342 |
LIG_14-3-3_CanoR_1 | 292 | 298 | PF00244 | 0.314 |
LIG_14-3-3_CanoR_1 | 358 | 363 | PF00244 | 0.303 |
LIG_14-3-3_CanoR_1 | 365 | 373 | PF00244 | 0.269 |
LIG_14-3-3_CanoR_1 | 419 | 425 | PF00244 | 0.386 |
LIG_Actin_RPEL_3 | 44 | 63 | PF02755 | 0.413 |
LIG_Actin_WH2_2 | 437 | 455 | PF00022 | 0.308 |
LIG_Actin_WH2_2 | 50 | 66 | PF00022 | 0.383 |
LIG_APCC_ABBA_1 | 393 | 398 | PF00400 | 0.308 |
LIG_Clathr_ClatBox_1 | 204 | 208 | PF01394 | 0.327 |
LIG_eIF4E_1 | 82 | 88 | PF01652 | 0.194 |
LIG_FHA_1 | 200 | 206 | PF00498 | 0.355 |
LIG_FHA_1 | 213 | 219 | PF00498 | 0.222 |
LIG_FHA_1 | 235 | 241 | PF00498 | 0.413 |
LIG_FHA_1 | 29 | 35 | PF00498 | 0.336 |
LIG_FHA_1 | 292 | 298 | PF00498 | 0.350 |
LIG_FHA_1 | 308 | 314 | PF00498 | 0.328 |
LIG_FHA_1 | 322 | 328 | PF00498 | 0.400 |
LIG_FHA_1 | 419 | 425 | PF00498 | 0.279 |
LIG_FHA_2 | 294 | 300 | PF00498 | 0.288 |
LIG_FHA_2 | 366 | 372 | PF00498 | 0.424 |
LIG_FHA_2 | 435 | 441 | PF00498 | 0.324 |
LIG_FHA_2 | 444 | 450 | PF00498 | 0.256 |
LIG_FHA_2 | 501 | 507 | PF00498 | 0.341 |
LIG_FHA_2 | 91 | 97 | PF00498 | 0.266 |
LIG_GBD_Chelix_1 | 151 | 159 | PF00786 | 0.366 |
LIG_LIR_Gen_1 | 115 | 123 | PF02991 | 0.295 |
LIG_LIR_Gen_1 | 222 | 231 | PF02991 | 0.315 |
LIG_LIR_Gen_1 | 353 | 363 | PF02991 | 0.266 |
LIG_LIR_Gen_1 | 402 | 411 | PF02991 | 0.413 |
LIG_LIR_Gen_1 | 437 | 445 | PF02991 | 0.366 |
LIG_LIR_Gen_1 | 546 | 556 | PF02991 | 0.308 |
LIG_LIR_Gen_1 | 84 | 92 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 115 | 120 | PF02991 | 0.295 |
LIG_LIR_Nem_3 | 353 | 359 | PF02991 | 0.266 |
LIG_LIR_Nem_3 | 402 | 407 | PF02991 | 0.413 |
LIG_LIR_Nem_3 | 437 | 441 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 466 | 472 | PF02991 | 0.312 |
LIG_LIR_Nem_3 | 546 | 552 | PF02991 | 0.332 |
LIG_LIR_Nem_3 | 84 | 88 | PF02991 | 0.374 |
LIG_LYPXL_yS_3 | 469 | 472 | PF13949 | 0.308 |
LIG_MYND_1 | 216 | 220 | PF01753 | 0.361 |
LIG_PCNA_yPIPBox_3 | 136 | 150 | PF02747 | 0.308 |
LIG_PCNA_yPIPBox_3 | 49 | 57 | PF02747 | 0.411 |
LIG_PTB_Apo_2 | 261 | 268 | PF02174 | 0.308 |
LIG_SH2_CRK | 195 | 199 | PF00017 | 0.413 |
LIG_SH2_CRK | 404 | 408 | PF00017 | 0.413 |
LIG_SH2_NCK_1 | 384 | 388 | PF00017 | 0.347 |
LIG_SH2_PTP2 | 60 | 63 | PF00017 | 0.413 |
LIG_SH2_SRC | 195 | 198 | PF00017 | 0.413 |
LIG_SH2_STAP1 | 404 | 408 | PF00017 | 0.413 |
LIG_SH2_STAT3 | 280 | 283 | PF00017 | 0.413 |
LIG_SH2_STAT3 | 460 | 463 | PF00017 | 0.385 |
LIG_SH2_STAT3 | 471 | 474 | PF00017 | 0.359 |
LIG_SH2_STAT5 | 252 | 255 | PF00017 | 0.288 |
LIG_SH2_STAT5 | 280 | 283 | PF00017 | 0.308 |
LIG_SH2_STAT5 | 326 | 329 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 39 | 42 | PF00017 | 0.308 |
LIG_SH2_STAT5 | 396 | 399 | PF00017 | 0.364 |
LIG_SH2_STAT5 | 445 | 448 | PF00017 | 0.308 |
LIG_SH2_STAT5 | 471 | 474 | PF00017 | 0.308 |
LIG_SH2_STAT5 | 502 | 505 | PF00017 | 0.399 |
LIG_SH2_STAT5 | 60 | 63 | PF00017 | 0.413 |
LIG_SH3_1 | 384 | 390 | PF00018 | 0.277 |
LIG_SH3_3 | 210 | 216 | PF00018 | 0.383 |
LIG_SH3_3 | 384 | 390 | PF00018 | 0.246 |
LIG_SUMO_SIM_anti_2 | 201 | 208 | PF11976 | 0.314 |
LIG_SUMO_SIM_anti_2 | 338 | 343 | PF11976 | 0.343 |
LIG_SUMO_SIM_anti_2 | 548 | 554 | PF11976 | 0.301 |
LIG_SUMO_SIM_par_1 | 12 | 18 | PF11976 | 0.288 |
LIG_SUMO_SIM_par_1 | 201 | 208 | PF11976 | 0.312 |
LIG_SUMO_SIM_par_1 | 335 | 340 | PF11976 | 0.308 |
LIG_TRAF2_1 | 247 | 250 | PF00917 | 0.361 |
LIG_TRAF2_1 | 296 | 299 | PF00917 | 0.413 |
LIG_TRAF2_1 | 368 | 371 | PF00917 | 0.266 |
LIG_TRAF2_1 | 503 | 506 | PF00917 | 0.308 |
LIG_TYR_ITAM | 401 | 417 | PF00017 | 0.266 |
LIG_UBA3_1 | 378 | 386 | PF00899 | 0.290 |
LIG_WRC_WIRS_1 | 139 | 144 | PF05994 | 0.308 |
LIG_WRC_WIRS_1 | 359 | 364 | PF05994 | 0.344 |
LIG_WRC_WIRS_1 | 435 | 440 | PF05994 | 0.332 |
MOD_CK1_1 | 137 | 143 | PF00069 | 0.394 |
MOD_CK1_1 | 350 | 356 | PF00069 | 0.330 |
MOD_CK1_1 | 361 | 367 | PF00069 | 0.318 |
MOD_CK1_1 | 43 | 49 | PF00069 | 0.470 |
MOD_CK1_1 | 548 | 554 | PF00069 | 0.415 |
MOD_CK1_1 | 66 | 72 | PF00069 | 0.407 |
MOD_CK2_1 | 105 | 111 | PF00069 | 0.271 |
MOD_CK2_1 | 26 | 32 | PF00069 | 0.413 |
MOD_CK2_1 | 293 | 299 | PF00069 | 0.316 |
MOD_CK2_1 | 337 | 343 | PF00069 | 0.307 |
MOD_CK2_1 | 365 | 371 | PF00069 | 0.396 |
MOD_CK2_1 | 443 | 449 | PF00069 | 0.304 |
MOD_CK2_1 | 500 | 506 | PF00069 | 0.341 |
MOD_CK2_1 | 90 | 96 | PF00069 | 0.449 |
MOD_GlcNHglycan | 143 | 146 | PF01048 | 0.284 |
MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.279 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.413 |
MOD_GlcNHglycan | 460 | 463 | PF01048 | 0.308 |
MOD_GlcNHglycan | 478 | 481 | PF01048 | 0.308 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.342 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.385 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.259 |
MOD_GSK3_1 | 307 | 314 | PF00069 | 0.307 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.321 |
MOD_GSK3_1 | 346 | 353 | PF00069 | 0.300 |
MOD_GSK3_1 | 361 | 368 | PF00069 | 0.332 |
MOD_GSK3_1 | 530 | 537 | PF00069 | 0.366 |
MOD_N-GLC_1 | 105 | 110 | PF02516 | 0.358 |
MOD_NEK2_1 | 138 | 143 | PF00069 | 0.351 |
MOD_NEK2_1 | 23 | 28 | PF00069 | 0.296 |
MOD_NEK2_1 | 313 | 318 | PF00069 | 0.281 |
MOD_NEK2_1 | 337 | 342 | PF00069 | 0.270 |
MOD_NEK2_1 | 40 | 45 | PF00069 | 0.204 |
MOD_NEK2_1 | 425 | 430 | PF00069 | 0.324 |
MOD_NEK2_1 | 452 | 457 | PF00069 | 0.332 |
MOD_NEK2_1 | 492 | 497 | PF00069 | 0.437 |
MOD_NEK2_2 | 530 | 535 | PF00069 | 0.308 |
MOD_PIKK_1 | 143 | 149 | PF00454 | 0.387 |
MOD_PIKK_1 | 26 | 32 | PF00454 | 0.314 |
MOD_PIKK_1 | 366 | 372 | PF00454 | 0.413 |
MOD_PIKK_1 | 388 | 394 | PF00454 | 0.421 |
MOD_PIKK_1 | 443 | 449 | PF00454 | 0.332 |
MOD_PKA_2 | 199 | 205 | PF00069 | 0.315 |
MOD_PKA_2 | 291 | 297 | PF00069 | 0.327 |
MOD_PKA_2 | 364 | 370 | PF00069 | 0.353 |
MOD_PKA_2 | 418 | 424 | PF00069 | 0.349 |
MOD_PKA_2 | 63 | 69 | PF00069 | 0.401 |
MOD_Plk_1 | 105 | 111 | PF00069 | 0.421 |
MOD_Plk_1 | 337 | 343 | PF00069 | 0.339 |
MOD_Plk_1 | 371 | 377 | PF00069 | 0.413 |
MOD_Plk_1 | 492 | 498 | PF00069 | 0.215 |
MOD_Plk_2-3 | 105 | 111 | PF00069 | 0.413 |
MOD_Plk_4 | 105 | 111 | PF00069 | 0.358 |
MOD_Plk_4 | 134 | 140 | PF00069 | 0.379 |
MOD_Plk_4 | 154 | 160 | PF00069 | 0.266 |
MOD_Plk_4 | 199 | 205 | PF00069 | 0.329 |
MOD_Plk_4 | 322 | 328 | PF00069 | 0.300 |
MOD_Plk_4 | 434 | 440 | PF00069 | 0.311 |
MOD_Plk_4 | 492 | 498 | PF00069 | 0.365 |
MOD_Plk_4 | 545 | 551 | PF00069 | 0.349 |
MOD_ProDKin_1 | 129 | 135 | PF00069 | 0.361 |
MOD_ProDKin_1 | 171 | 177 | PF00069 | 0.413 |
MOD_ProDKin_1 | 212 | 218 | PF00069 | 0.316 |
MOD_SUMO_rev_2 | 298 | 303 | PF00179 | 0.421 |
TRG_DiLeu_BaEn_1 | 505 | 510 | PF01217 | 0.308 |
TRG_DiLeu_BaEn_3 | 298 | 304 | PF01217 | 0.413 |
TRG_DiLeu_BaLyEn_6 | 213 | 218 | PF01217 | 0.327 |
TRG_ENDOCYTIC_2 | 223 | 226 | PF00928 | 0.302 |
TRG_ENDOCYTIC_2 | 404 | 407 | PF00928 | 0.366 |
TRG_ENDOCYTIC_2 | 414 | 417 | PF00928 | 0.366 |
TRG_ENDOCYTIC_2 | 469 | 472 | PF00928 | 0.308 |
TRG_ENDOCYTIC_2 | 60 | 63 | PF00928 | 0.400 |
TRG_ENDOCYTIC_2 | 85 | 88 | PF00928 | 0.376 |
TRG_ER_diArg_1 | 148 | 150 | PF00400 | 0.348 |
TRG_ER_diArg_1 | 163 | 165 | PF00400 | 0.216 |
TRG_ER_diArg_1 | 166 | 169 | PF00400 | 0.201 |
TRG_Pf-PMV_PEXEL_1 | 149 | 153 | PF00026 | 0.413 |
TRG_Pf-PMV_PEXEL_1 | 3 | 8 | PF00026 | 0.477 |
TRG_Pf-PMV_PEXEL_1 | 334 | 338 | PF00026 | 0.308 |
TRG_Pf-PMV_PEXEL_1 | 454 | 458 | PF00026 | 0.296 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7D5 | Leptomonas seymouri | 31% | 91% |
A0A0N0P7P1 | Leptomonas seymouri | 81% | 93% |
A0A0N1HUY7 | Leptomonas seymouri | 22% | 77% |
A0A0S4JI94 | Bodo saltans | 32% | 85% |
A0A1X0P7Y3 | Trypanosomatidae | 54% | 93% |
A0A1X0P895 | Trypanosomatidae | 32% | 91% |
A0A3Q8IG36 | Leishmania donovani | 100% | 100% |
A0A3R7NER3 | Trypanosoma rangeli | 55% | 100% |
A0A3S7XAA1 | Leishmania donovani | 32% | 91% |
A0A422P2E3 | Trypanosoma rangeli | 31% | 91% |
A4HNQ4 | Leishmania braziliensis | 33% | 100% |
A4HP92 | Leishmania braziliensis | 89% | 100% |
A4ICU1 | Leishmania infantum | 32% | 100% |
C9ZX51 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 21% | 87% |
D0A395 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 51% | 95% |
E9ASG3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
E9AT00 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 97% | 100% |
E9AYK6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 20% | 76% |
O08599 | Mus musculus | 21% | 94% |
O08700 | Rattus norvegicus | 32% | 98% |
O49048 | Arabidopsis thaliana | 30% | 98% |
O74534 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 23% | 87% |
O94590 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 22% | 81% |
P38932 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 29% | 97% |
P61763 | Bos taurus | 21% | 94% |
P61764 | Homo sapiens | 21% | 94% |
P61765 | Rattus norvegicus | 21% | 94% |
P97390 | Mus musculus | 32% | 98% |
Q07327 | Drosophila melanogaster | 22% | 94% |
Q09805 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 28% | 100% |
Q4Q1J8 | Leishmania major | 96% | 100% |
Q4Q232 | Leishmania major | 33% | 100% |
Q54GE3 | Dictyostelium discoideum | 30% | 99% |
Q54QC8 | Dictyostelium discoideum | 23% | 93% |
Q5R6D2 | Pongo abelii | 21% | 94% |
Q5VNU3 | Oryza sativa subsp. japonica | 21% | 85% |
Q62753 | Rattus norvegicus | 21% | 94% |
Q64324 | Mus musculus | 21% | 94% |
Q6R748 | Gallus gallus | 20% | 94% |
Q7XWP3 | Oryza sativa subsp. japonica | 20% | 84% |
Q851W1 | Oryza sativa subsp. japonica | 25% | 90% |
Q9C5X3 | Arabidopsis thaliana | 22% | 84% |
Q9NRW7 | Homo sapiens | 32% | 98% |
Q9SL48 | Arabidopsis thaliana | 20% | 89% |
V5BV59 | Trypanosoma cruzi | 32% | 90% |
V5DCK0 | Trypanosoma cruzi | 55% | 98% |