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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 18 |
NetGPI | no | yes: 0, no: 18 |
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: A4HNQ4
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 19 |
GO:0016192 | vesicle-mediated transport | 4 | 19 |
GO:0051179 | localization | 1 | 19 |
GO:0051234 | establishment of localization | 2 | 19 |
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_C14_Caspase3-7 | 274 | 278 | PF00656 | 0.301 |
CLV_NRD_NRD_1 | 13 | 15 | PF00675 | 0.487 |
CLV_NRD_NRD_1 | 195 | 197 | PF00675 | 0.273 |
CLV_NRD_NRD_1 | 240 | 242 | PF00675 | 0.394 |
CLV_NRD_NRD_1 | 343 | 345 | PF00675 | 0.282 |
CLV_NRD_NRD_1 | 574 | 576 | PF00675 | 0.261 |
CLV_PCSK_FUR_1 | 11 | 15 | PF00082 | 0.539 |
CLV_PCSK_KEX2_1 | 13 | 15 | PF00082 | 0.487 |
CLV_PCSK_KEX2_1 | 195 | 197 | PF00082 | 0.283 |
CLV_PCSK_SKI1_1 | 35 | 39 | PF00082 | 0.302 |
CLV_PCSK_SKI1_1 | 367 | 371 | PF00082 | 0.304 |
CLV_PCSK_SKI1_1 | 390 | 394 | PF00082 | 0.356 |
CLV_PCSK_SKI1_1 | 515 | 519 | PF00082 | 0.378 |
CLV_PCSK_SKI1_1 | 571 | 575 | PF00082 | 0.186 |
DEG_APCC_DBOX_1 | 389 | 397 | PF00400 | 0.395 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.566 |
DOC_CKS1_1 | 245 | 250 | PF01111 | 0.313 |
DOC_CKS1_1 | 286 | 291 | PF01111 | 0.359 |
DOC_CYCLIN_yCln2_LP_2 | 249 | 255 | PF00134 | 0.286 |
DOC_CYCLIN_yCln2_LP_2 | 518 | 524 | PF00134 | 0.165 |
DOC_MAPK_DCC_7 | 241 | 251 | PF00069 | 0.395 |
DOC_MAPK_gen_1 | 322 | 330 | PF00069 | 0.282 |
DOC_MAPK_gen_1 | 531 | 540 | PF00069 | 0.224 |
DOC_MAPK_MEF2A_6 | 206 | 215 | PF00069 | 0.442 |
DOC_MAPK_MEF2A_6 | 230 | 239 | PF00069 | 0.290 |
DOC_MAPK_MEF2A_6 | 531 | 540 | PF00069 | 0.281 |
DOC_PP2B_LxvP_1 | 249 | 252 | PF13499 | 0.307 |
DOC_USP7_MATH_1 | 231 | 235 | PF00917 | 0.282 |
DOC_USP7_MATH_1 | 27 | 31 | PF00917 | 0.232 |
DOC_USP7_MATH_1 | 355 | 359 | PF00917 | 0.370 |
DOC_USP7_MATH_1 | 596 | 600 | PF00917 | 0.410 |
DOC_USP7_UBL2_3 | 206 | 210 | PF12436 | 0.282 |
DOC_USP7_UBL2_3 | 318 | 322 | PF12436 | 0.179 |
DOC_USP7_UBL2_3 | 471 | 475 | PF12436 | 0.282 |
DOC_WW_Pin1_4 | 153 | 158 | PF00397 | 0.363 |
DOC_WW_Pin1_4 | 244 | 249 | PF00397 | 0.310 |
DOC_WW_Pin1_4 | 285 | 290 | PF00397 | 0.357 |
LIG_14-3-3_CanoR_1 | 181 | 189 | PF00244 | 0.283 |
LIG_14-3-3_CanoR_1 | 218 | 223 | PF00244 | 0.398 |
LIG_14-3-3_CanoR_1 | 299 | 306 | PF00244 | 0.224 |
LIG_14-3-3_CanoR_1 | 325 | 331 | PF00244 | 0.282 |
LIG_14-3-3_CanoR_1 | 371 | 375 | PF00244 | 0.307 |
LIG_14-3-3_CanoR_1 | 463 | 470 | PF00244 | 0.312 |
LIG_Actin_WH2_2 | 141 | 156 | PF00022 | 0.282 |
LIG_Actin_WH2_2 | 215 | 232 | PF00022 | 0.368 |
LIG_BIR_III_2 | 277 | 281 | PF00653 | 0.301 |
LIG_BRCT_BRCA1_1 | 607 | 611 | PF00533 | 0.228 |
LIG_Clathr_ClatBox_1 | 236 | 240 | PF01394 | 0.293 |
LIG_deltaCOP1_diTrp_1 | 18 | 28 | PF00928 | 0.448 |
LIG_eIF4E_1 | 51 | 57 | PF01652 | 0.263 |
LIG_FHA_1 | 109 | 115 | PF00498 | 0.342 |
LIG_FHA_1 | 143 | 149 | PF00498 | 0.295 |
LIG_FHA_1 | 164 | 170 | PF00498 | 0.346 |
LIG_FHA_1 | 230 | 236 | PF00498 | 0.336 |
LIG_FHA_1 | 245 | 251 | PF00498 | 0.211 |
LIG_FHA_1 | 29 | 35 | PF00498 | 0.364 |
LIG_FHA_1 | 325 | 331 | PF00498 | 0.355 |
LIG_FHA_1 | 355 | 361 | PF00498 | 0.426 |
LIG_FHA_1 | 487 | 493 | PF00498 | 0.282 |
LIG_FHA_1 | 504 | 510 | PF00498 | 0.282 |
LIG_FHA_1 | 572 | 578 | PF00498 | 0.249 |
LIG_FHA_1 | 589 | 595 | PF00498 | 0.260 |
LIG_FHA_1 | 601 | 607 | PF00498 | 0.205 |
LIG_FHA_2 | 223 | 229 | PF00498 | 0.395 |
LIG_FHA_2 | 314 | 320 | PF00498 | 0.351 |
LIG_FHA_2 | 399 | 405 | PF00498 | 0.321 |
LIG_FHA_2 | 542 | 548 | PF00498 | 0.292 |
LIG_FHA_2 | 583 | 589 | PF00498 | 0.165 |
LIG_Integrin_isoDGR_2 | 365 | 367 | PF01839 | 0.282 |
LIG_LIR_Gen_1 | 107 | 118 | PF02991 | 0.375 |
LIG_LIR_Gen_1 | 145 | 155 | PF02991 | 0.290 |
LIG_LIR_Gen_1 | 18 | 28 | PF02991 | 0.315 |
LIG_LIR_Gen_1 | 254 | 263 | PF02991 | 0.282 |
LIG_LIR_Gen_1 | 93 | 103 | PF02991 | 0.295 |
LIG_LIR_Nem_3 | 100 | 106 | PF02991 | 0.318 |
LIG_LIR_Nem_3 | 107 | 112 | PF02991 | 0.333 |
LIG_LIR_Nem_3 | 145 | 150 | PF02991 | 0.290 |
LIG_LIR_Nem_3 | 18 | 24 | PF02991 | 0.318 |
LIG_LIR_Nem_3 | 225 | 229 | PF02991 | 0.282 |
LIG_LIR_Nem_3 | 301 | 306 | PF02991 | 0.282 |
LIG_LIR_Nem_3 | 93 | 98 | PF02991 | 0.315 |
LIG_MYND_1 | 248 | 252 | PF01753 | 0.365 |
LIG_NRBOX | 33 | 39 | PF00104 | 0.281 |
LIG_PCNA_yPIPBox_3 | 60 | 72 | PF02747 | 0.282 |
LIG_Pex14_2 | 336 | 340 | PF04695 | 0.263 |
LIG_PTB_Apo_2 | 22 | 29 | PF02174 | 0.452 |
LIG_PTB_Apo_2 | 497 | 504 | PF02174 | 0.263 |
LIG_PTB_Phospho_1 | 497 | 503 | PF10480 | 0.263 |
LIG_REV1ctd_RIR_1 | 292 | 301 | PF16727 | 0.165 |
LIG_SH2_GRB2like | 138 | 141 | PF00017 | 0.423 |
LIG_SH2_GRB2like | 23 | 26 | PF00017 | 0.466 |
LIG_SH2_NCK_1 | 417 | 421 | PF00017 | 0.309 |
LIG_SH2_SRC | 138 | 141 | PF00017 | 0.292 |
LIG_SH2_STAP1 | 106 | 110 | PF00017 | 0.268 |
LIG_SH2_STAP1 | 255 | 259 | PF00017 | 0.263 |
LIG_SH2_STAP1 | 417 | 421 | PF00017 | 0.285 |
LIG_SH2_STAT3 | 451 | 454 | PF00017 | 0.395 |
LIG_SH2_STAT5 | 109 | 112 | PF00017 | 0.311 |
LIG_SH2_STAT5 | 138 | 141 | PF00017 | 0.282 |
LIG_SH2_STAT5 | 23 | 26 | PF00017 | 0.295 |
LIG_SH2_STAT5 | 539 | 542 | PF00017 | 0.368 |
LIG_SH2_STAT5 | 543 | 546 | PF00017 | 0.363 |
LIG_SH3_1 | 242 | 248 | PF00018 | 0.395 |
LIG_SH3_3 | 242 | 248 | PF00018 | 0.342 |
LIG_SH3_3 | 283 | 289 | PF00018 | 0.347 |
LIG_SH3_3 | 393 | 399 | PF00018 | 0.276 |
LIG_SH3_3 | 80 | 86 | PF00018 | 0.395 |
LIG_SUMO_SIM_anti_2 | 232 | 240 | PF11976 | 0.285 |
LIG_SUMO_SIM_anti_2 | 370 | 376 | PF11976 | 0.295 |
LIG_SUMO_SIM_anti_2 | 534 | 539 | PF11976 | 0.274 |
LIG_SUMO_SIM_par_1 | 232 | 240 | PF11976 | 0.283 |
LIG_SUMO_SIM_par_1 | 326 | 332 | PF11976 | 0.395 |
LIG_SUMO_SIM_par_1 | 505 | 510 | PF11976 | 0.395 |
LIG_SUMO_SIM_par_1 | 60 | 65 | PF11976 | 0.277 |
LIG_TRAF2_1 | 68 | 71 | PF00917 | 0.261 |
LIG_UBA3_1 | 150 | 154 | PF00899 | 0.261 |
LIG_UBA3_1 | 411 | 419 | PF00899 | 0.263 |
LIG_UBA3_1 | 424 | 429 | PF00899 | 0.313 |
MOD_CDK_SPxxK_3 | 153 | 160 | PF00069 | 0.355 |
MOD_CK1_1 | 156 | 162 | PF00069 | 0.326 |
MOD_CK1_1 | 163 | 169 | PF00069 | 0.377 |
MOD_CK1_1 | 205 | 211 | PF00069 | 0.424 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.671 |
MOD_CK1_1 | 599 | 605 | PF00069 | 0.397 |
MOD_CK1_1 | 87 | 93 | PF00069 | 0.382 |
MOD_CK2_1 | 313 | 319 | PF00069 | 0.314 |
MOD_CK2_1 | 326 | 332 | PF00069 | 0.282 |
MOD_CK2_1 | 370 | 376 | PF00069 | 0.307 |
MOD_CK2_1 | 541 | 547 | PF00069 | 0.282 |
MOD_CK2_1 | 582 | 588 | PF00069 | 0.165 |
MOD_Cter_Amidation | 11 | 14 | PF01082 | 0.427 |
MOD_GlcNHglycan | 346 | 349 | PF01048 | 0.355 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.647 |
MOD_GlcNHglycan | 86 | 89 | PF01048 | 0.336 |
MOD_GSK3_1 | 114 | 121 | PF00069 | 0.355 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.287 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.367 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.357 |
MOD_GSK3_1 | 218 | 225 | PF00069 | 0.316 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.329 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.286 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.250 |
MOD_GSK3_1 | 576 | 583 | PF00069 | 0.352 |
MOD_GSK3_1 | 584 | 591 | PF00069 | 0.252 |
MOD_GSK3_1 | 596 | 603 | PF00069 | 0.269 |
MOD_N-GLC_1 | 367 | 372 | PF02516 | 0.291 |
MOD_N-GLC_1 | 383 | 388 | PF02516 | 0.172 |
MOD_N-GLC_1 | 503 | 508 | PF02516 | 0.263 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.588 |
MOD_NEK2_1 | 113 | 118 | PF00069 | 0.322 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.293 |
MOD_NEK2_1 | 313 | 318 | PF00069 | 0.320 |
MOD_NEK2_1 | 462 | 467 | PF00069 | 0.276 |
MOD_NEK2_1 | 582 | 587 | PF00069 | 0.405 |
MOD_NEK2_1 | 600 | 605 | PF00069 | 0.228 |
MOD_NEK2_1 | 611 | 616 | PF00069 | 0.233 |
MOD_PIKK_1 | 169 | 175 | PF00454 | 0.299 |
MOD_PIKK_1 | 486 | 492 | PF00454 | 0.286 |
MOD_PIKK_1 | 49 | 55 | PF00454 | 0.293 |
MOD_PK_1 | 218 | 224 | PF00069 | 0.386 |
MOD_PKA_1 | 344 | 350 | PF00069 | 0.263 |
MOD_PKA_2 | 180 | 186 | PF00069 | 0.302 |
MOD_PKA_2 | 298 | 304 | PF00069 | 0.224 |
MOD_PKA_2 | 324 | 330 | PF00069 | 0.309 |
MOD_PKA_2 | 370 | 376 | PF00069 | 0.335 |
MOD_PKA_2 | 462 | 468 | PF00069 | 0.291 |
MOD_PKA_2 | 84 | 90 | PF00069 | 0.358 |
MOD_PKB_1 | 200 | 208 | PF00069 | 0.395 |
MOD_Plk_1 | 114 | 120 | PF00069 | 0.429 |
MOD_Plk_1 | 367 | 373 | PF00069 | 0.311 |
MOD_Plk_1 | 386 | 392 | PF00069 | 0.456 |
MOD_Plk_2-3 | 175 | 181 | PF00069 | 0.307 |
MOD_Plk_2-3 | 398 | 404 | PF00069 | 0.282 |
MOD_Plk_4 | 114 | 120 | PF00069 | 0.436 |
MOD_Plk_4 | 231 | 237 | PF00069 | 0.288 |
MOD_Plk_4 | 370 | 376 | PF00069 | 0.261 |
MOD_Plk_4 | 596 | 602 | PF00069 | 0.276 |
MOD_Plk_4 | 90 | 96 | PF00069 | 0.205 |
MOD_ProDKin_1 | 153 | 159 | PF00069 | 0.363 |
MOD_ProDKin_1 | 244 | 250 | PF00069 | 0.310 |
MOD_ProDKin_1 | 285 | 291 | PF00069 | 0.357 |
MOD_SUMO_for_1 | 278 | 281 | PF00179 | 0.307 |
MOD_SUMO_for_1 | 428 | 431 | PF00179 | 0.355 |
MOD_SUMO_for_1 | 592 | 595 | PF00179 | 0.395 |
MOD_SUMO_rev_2 | 274 | 280 | PF00179 | 0.261 |
MOD_SUMO_rev_2 | 394 | 401 | PF00179 | 0.282 |
TRG_DiLeu_BaEn_1 | 146 | 151 | PF01217 | 0.261 |
TRG_DiLeu_BaEn_1 | 387 | 392 | PF01217 | 0.395 |
TRG_DiLeu_BaEn_1 | 440 | 445 | PF01217 | 0.342 |
TRG_DiLeu_BaEn_2 | 331 | 337 | PF01217 | 0.263 |
TRG_DiLeu_BaLyEn_6 | 245 | 250 | PF01217 | 0.323 |
TRG_DiLeu_BaLyEn_6 | 444 | 449 | PF01217 | 0.342 |
TRG_ENDOCYTIC_2 | 255 | 258 | PF00928 | 0.282 |
TRG_ENDOCYTIC_2 | 317 | 320 | PF00928 | 0.355 |
TRG_ENDOCYTIC_2 | 95 | 98 | PF00928 | 0.321 |
TRG_ER_diArg_1 | 11 | 14 | PF00400 | 0.430 |
TRG_ER_diArg_1 | 195 | 197 | PF00400 | 0.188 |
TRG_ER_diArg_1 | 199 | 202 | PF00400 | 0.167 |
TRG_Pf-PMV_PEXEL_1 | 575 | 580 | PF00026 | 0.261 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7D5 | Leptomonas seymouri | 83% | 100% |
A0A0N0P7P1 | Leptomonas seymouri | 31% | 100% |
A0A0S4JI94 | Bodo saltans | 50% | 94% |
A0A1X0P7Y3 | Trypanosomatidae | 29% | 100% |
A0A1X0P895 | Trypanosomatidae | 66% | 100% |
A0A3Q8IG36 | Leishmania donovani | 33% | 100% |
A0A3R7MWF2 | Trypanosoma rangeli | 21% | 93% |
A0A3S7XAA1 | Leishmania donovani | 90% | 100% |
A0A422P2E3 | Trypanosoma rangeli | 65% | 100% |
A4HP92 | Leishmania braziliensis | 32% | 100% |
A4ICU1 | Leishmania infantum | 91% | 100% |
A4IDJ7 | Leishmania infantum | 33% | 100% |
D0A395 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
E9ASG3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
E9AT00 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
O08700 | Rattus norvegicus | 30% | 100% |
O18637 | Drosophila virilis | 20% | 94% |
O49048 | Arabidopsis thaliana | 30% | 100% |
O74534 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 21% | 97% |
P22213 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 22% | 93% |
P38932 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 28% | 100% |
P97390 | Mus musculus | 30% | 100% |
Q09805 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 27% | 100% |
Q24179 | Drosophila melanogaster | 21% | 97% |
Q4Q1J8 | Leishmania major | 33% | 100% |
Q4Q232 | Leishmania major | 90% | 100% |
Q54GE3 | Dictyostelium discoideum | 28% | 100% |
Q54QC8 | Dictyostelium discoideum | 20% | 100% |
Q5VNU3 | Oryza sativa subsp. japonica | 21% | 94% |
Q60770 | Mus musculus | 22% | 100% |
Q62991 | Rattus norvegicus | 21% | 97% |
Q64324 | Mus musculus | 21% | 100% |
Q7XWP3 | Oryza sativa subsp. japonica | 21% | 93% |
Q851W1 | Oryza sativa subsp. japonica | 21% | 99% |
Q8BRF7 | Mus musculus | 21% | 97% |
Q8WVM8 | Homo sapiens | 21% | 96% |
Q9C5P7 | Arabidopsis thaliana | 22% | 92% |
Q9C5X3 | Arabidopsis thaliana | 20% | 93% |
Q9NRW7 | Homo sapiens | 29% | 100% |
Q9SZ77 | Arabidopsis thaliana | 21% | 93% |
V5BV59 | Trypanosoma cruzi | 65% | 100% |
V5DCK0 | Trypanosoma cruzi | 31% | 100% |