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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 10 |
GO:0031207 | Sec62/Sec63 complex | 3 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0098796 | membrane protein complex | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
GO:0140534 | endoplasmic reticulum protein-containing complex | 2 | 2 |
Related structures:
AlphaFold database: E9AFU0
Term | Name | Level | Count |
---|---|---|---|
GO:0006605 | protein targeting | 5 | 2 |
GO:0006612 | protein targeting to membrane | 5 | 2 |
GO:0006613 | cotranslational protein targeting to membrane | 6 | 2 |
GO:0006614 | SRP-dependent cotranslational protein targeting to membrane | 7 | 2 |
GO:0006620 | post-translational protein targeting to endoplasmic reticulum membrane | 6 | 2 |
GO:0006810 | transport | 3 | 11 |
GO:0006886 | intracellular protein transport | 4 | 11 |
GO:0008104 | protein localization | 4 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0015031 | protein transport | 4 | 11 |
GO:0031204 | post-translational protein targeting to membrane, translocation | 5 | 11 |
GO:0033036 | macromolecule localization | 2 | 11 |
GO:0033365 | protein localization to organelle | 5 | 2 |
GO:0045047 | protein targeting to ER | 6 | 2 |
GO:0045184 | establishment of protein localization | 3 | 11 |
GO:0046907 | intracellular transport | 3 | 11 |
GO:0051179 | localization | 1 | 11 |
GO:0051234 | establishment of localization | 2 | 11 |
GO:0051641 | cellular localization | 2 | 11 |
GO:0051649 | establishment of localization in cell | 3 | 11 |
GO:0051668 | localization within membrane | 3 | 2 |
GO:0055085 | transmembrane transport | 2 | 11 |
GO:0065002 | intracellular protein transmembrane transport | 4 | 11 |
GO:0070727 | cellular macromolecule localization | 3 | 11 |
GO:0070972 | protein localization to endoplasmic reticulum | 6 | 2 |
GO:0071702 | organic substance transport | 4 | 11 |
GO:0071705 | nitrogen compound transport | 4 | 11 |
GO:0071806 | protein transmembrane transport | 3 | 11 |
GO:0072594 | establishment of protein localization to organelle | 4 | 2 |
GO:0072599 | establishment of protein localization to endoplasmic reticulum | 5 | 2 |
GO:0072657 | protein localization to membrane | 4 | 2 |
GO:0090150 | establishment of protein localization to membrane | 4 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 2 |
GO:0008320 | protein transmembrane transporter activity | 3 | 2 |
GO:0022857 | transmembrane transporter activity | 2 | 2 |
GO:0022884 | macromolecule transmembrane transporter activity | 3 | 2 |
GO:0140318 | protein transporter activity | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 452 | 456 | PF00656 | 0.563 |
CLV_MEL_PAP_1 | 446 | 452 | PF00089 | 0.370 |
CLV_NRD_NRD_1 | 150 | 152 | PF00675 | 0.571 |
CLV_NRD_NRD_1 | 179 | 181 | PF00675 | 0.495 |
CLV_NRD_NRD_1 | 278 | 280 | PF00675 | 0.344 |
CLV_NRD_NRD_1 | 282 | 284 | PF00675 | 0.324 |
CLV_NRD_NRD_1 | 38 | 40 | PF00675 | 0.433 |
CLV_PCSK_KEX2_1 | 159 | 161 | PF00082 | 0.496 |
CLV_PCSK_KEX2_1 | 179 | 181 | PF00082 | 0.350 |
CLV_PCSK_KEX2_1 | 278 | 280 | PF00082 | 0.360 |
CLV_PCSK_KEX2_1 | 282 | 284 | PF00082 | 0.324 |
CLV_PCSK_KEX2_1 | 38 | 40 | PF00082 | 0.406 |
CLV_PCSK_PC1ET2_1 | 159 | 161 | PF00082 | 0.513 |
CLV_PCSK_PC7_1 | 155 | 161 | PF00082 | 0.496 |
CLV_PCSK_PC7_1 | 278 | 284 | PF00082 | 0.354 |
CLV_PCSK_SKI1_1 | 103 | 107 | PF00082 | 0.373 |
CLV_PCSK_SKI1_1 | 112 | 116 | PF00082 | 0.335 |
CLV_PCSK_SKI1_1 | 188 | 192 | PF00082 | 0.593 |
CLV_PCSK_SKI1_1 | 210 | 214 | PF00082 | 0.599 |
CLV_PCSK_SKI1_1 | 283 | 287 | PF00082 | 0.400 |
CLV_PCSK_SKI1_1 | 383 | 387 | PF00082 | 0.344 |
CLV_PCSK_SKI1_1 | 39 | 43 | PF00082 | 0.435 |
CLV_PCSK_SKI1_1 | 412 | 416 | PF00082 | 0.403 |
CLV_PCSK_SKI1_1 | 93 | 97 | PF00082 | 0.355 |
DEG_APCC_DBOX_1 | 111 | 119 | PF00400 | 0.546 |
DEG_APCC_DBOX_1 | 282 | 290 | PF00400 | 0.568 |
DOC_CYCLIN_RxL_1 | 322 | 333 | PF00134 | 0.628 |
DOC_CYCLIN_RxL_1 | 35 | 46 | PF00134 | 0.661 |
DOC_CYCLIN_RxL_1 | 380 | 390 | PF00134 | 0.553 |
DOC_CYCLIN_RxL_1 | 410 | 420 | PF00134 | 0.635 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 413 | 421 | PF00134 | 0.606 |
DOC_CYCLIN_yCln2_LP_2 | 28 | 34 | PF00134 | 0.378 |
DOC_MAPK_DCC_7 | 110 | 120 | PF00069 | 0.558 |
DOC_MAPK_gen_1 | 110 | 117 | PF00069 | 0.465 |
DOC_MAPK_gen_1 | 244 | 255 | PF00069 | 0.621 |
DOC_MAPK_gen_1 | 278 | 288 | PF00069 | 0.513 |
DOC_MAPK_gen_1 | 434 | 443 | PF00069 | 0.646 |
DOC_MAPK_MEF2A_6 | 106 | 115 | PF00069 | 0.578 |
DOC_MAPK_MEF2A_6 | 282 | 290 | PF00069 | 0.517 |
DOC_MAPK_MEF2A_6 | 395 | 404 | PF00069 | 0.666 |
DOC_PP1_RVXF_1 | 101 | 108 | PF00149 | 0.571 |
DOC_PP1_RVXF_1 | 246 | 252 | PF00149 | 0.579 |
DOC_PP1_RVXF_1 | 91 | 97 | PF00149 | 0.553 |
DOC_PP2B_LxvP_1 | 139 | 142 | PF13499 | 0.334 |
DOC_PP2B_LxvP_1 | 28 | 31 | PF13499 | 0.378 |
DOC_PP4_FxxP_1 | 267 | 270 | PF00568 | 0.568 |
DOC_USP7_MATH_1 | 19 | 23 | PF00917 | 0.335 |
DOC_USP7_MATH_1 | 339 | 343 | PF00917 | 0.553 |
DOC_USP7_MATH_1 | 360 | 364 | PF00917 | 0.682 |
DOC_WW_Pin1_4 | 53 | 58 | PF00397 | 0.615 |
LIG_14-3-3_CanoR_1 | 151 | 155 | PF00244 | 0.330 |
LIG_14-3-3_CanoR_1 | 449 | 457 | PF00244 | 0.595 |
LIG_Actin_WH2_2 | 90 | 108 | PF00022 | 0.568 |
LIG_APCC_ABBA_1 | 415 | 420 | PF00400 | 0.558 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.489 |
LIG_BRCT_BRCA1_1 | 129 | 133 | PF00533 | 0.585 |
LIG_BRCT_BRCA1_1 | 14 | 18 | PF00533 | 0.355 |
LIG_FHA_1 | 145 | 151 | PF00498 | 0.282 |
LIG_FHA_1 | 19 | 25 | PF00498 | 0.432 |
LIG_FHA_1 | 380 | 386 | PF00498 | 0.563 |
LIG_FHA_1 | 388 | 394 | PF00498 | 0.532 |
LIG_FHA_2 | 196 | 202 | PF00498 | 0.490 |
LIG_FHA_2 | 211 | 217 | PF00498 | 0.357 |
LIG_FHA_2 | 45 | 51 | PF00498 | 0.653 |
LIG_LIR_Gen_1 | 10 | 20 | PF02991 | 0.282 |
LIG_LIR_Gen_1 | 125 | 135 | PF02991 | 0.461 |
LIG_LIR_Gen_1 | 173 | 182 | PF02991 | 0.313 |
LIG_LIR_Gen_1 | 342 | 351 | PF02991 | 0.642 |
LIG_LIR_Gen_1 | 369 | 379 | PF02991 | 0.627 |
LIG_LIR_Gen_1 | 419 | 430 | PF02991 | 0.541 |
LIG_LIR_Nem_3 | 10 | 16 | PF02991 | 0.282 |
LIG_LIR_Nem_3 | 125 | 131 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 153 | 157 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 173 | 178 | PF02991 | 0.150 |
LIG_LIR_Nem_3 | 342 | 346 | PF02991 | 0.654 |
LIG_LIR_Nem_3 | 369 | 374 | PF02991 | 0.592 |
LIG_LIR_Nem_3 | 419 | 425 | PF02991 | 0.535 |
LIG_NRBOX | 221 | 227 | PF00104 | 0.335 |
LIG_NRBOX | 420 | 426 | PF00104 | 0.596 |
LIG_Pex14_1 | 119 | 123 | PF04695 | 0.355 |
LIG_Pex14_1 | 251 | 255 | PF04695 | 0.559 |
LIG_Pex14_2 | 263 | 267 | PF04695 | 0.568 |
LIG_REV1ctd_RIR_1 | 93 | 101 | PF16727 | 0.555 |
LIG_SH2_CRK | 128 | 132 | PF00017 | 0.525 |
LIG_SH2_CRK | 154 | 158 | PF00017 | 0.295 |
LIG_SH2_CRK | 182 | 186 | PF00017 | 0.282 |
LIG_SH2_CRK | 343 | 347 | PF00017 | 0.606 |
LIG_SH2_GRB2like | 472 | 475 | PF00017 | 0.647 |
LIG_SH2_NCK_1 | 355 | 359 | PF00017 | 0.619 |
LIG_SH2_NCK_1 | 73 | 77 | PF00017 | 0.650 |
LIG_SH2_PTP2 | 175 | 178 | PF00017 | 0.296 |
LIG_SH2_STAT3 | 384 | 387 | PF00017 | 0.608 |
LIG_SH2_STAT3 | 472 | 475 | PF00017 | 0.582 |
LIG_SH2_STAT5 | 175 | 178 | PF00017 | 0.282 |
LIG_SH2_STAT5 | 235 | 238 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 275 | 278 | PF00017 | 0.554 |
LIG_SH2_STAT5 | 29 | 32 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 384 | 387 | PF00017 | 0.521 |
LIG_SH2_STAT5 | 429 | 432 | PF00017 | 0.638 |
LIG_SH2_STAT5 | 67 | 70 | PF00017 | 0.582 |
LIG_SH3_3 | 105 | 111 | PF00018 | 0.661 |
LIG_SH3_3 | 203 | 209 | PF00018 | 0.463 |
LIG_SH3_3 | 267 | 273 | PF00018 | 0.545 |
LIG_SH3_4 | 434 | 441 | PF00018 | 0.618 |
LIG_SUMO_SIM_anti_2 | 21 | 28 | PF11976 | 0.358 |
LIG_SUMO_SIM_par_1 | 288 | 293 | PF11976 | 0.519 |
LIG_TRAF2_1 | 190 | 193 | PF00917 | 0.386 |
LIG_TRAF2_1 | 198 | 201 | PF00917 | 0.427 |
LIG_TRAF2_1 | 396 | 399 | PF00917 | 0.620 |
LIG_UBA3_1 | 249 | 257 | PF00899 | 0.627 |
LIG_UBA3_1 | 326 | 335 | PF00899 | 0.656 |
LIG_WRC_WIRS_1 | 13 | 18 | PF05994 | 0.355 |
MOD_CK1_1 | 143 | 149 | PF00069 | 0.328 |
MOD_CK1_1 | 53 | 59 | PF00069 | 0.613 |
MOD_CK1_1 | 9 | 15 | PF00069 | 0.403 |
MOD_CK2_1 | 143 | 149 | PF00069 | 0.280 |
MOD_CK2_1 | 195 | 201 | PF00069 | 0.492 |
MOD_CK2_1 | 210 | 216 | PF00069 | 0.357 |
MOD_CK2_1 | 44 | 50 | PF00069 | 0.624 |
MOD_GlcNHglycan | 124 | 127 | PF01048 | 0.355 |
MOD_GlcNHglycan | 143 | 146 | PF01048 | 0.496 |
MOD_GlcNHglycan | 376 | 379 | PF01048 | 0.380 |
MOD_GlcNHglycan | 409 | 412 | PF01048 | 0.375 |
MOD_GlcNHglycan | 63 | 66 | PF01048 | 0.449 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.310 |
MOD_N-GLC_1 | 165 | 170 | PF02516 | 0.482 |
MOD_NEK2_1 | 122 | 127 | PF00069 | 0.351 |
MOD_NEK2_1 | 18 | 23 | PF00069 | 0.430 |
MOD_NEK2_1 | 61 | 66 | PF00069 | 0.583 |
MOD_PK_1 | 442 | 448 | PF00069 | 0.465 |
MOD_PKA_1 | 278 | 284 | PF00069 | 0.538 |
MOD_PKA_2 | 150 | 156 | PF00069 | 0.378 |
MOD_PKA_2 | 278 | 284 | PF00069 | 0.538 |
MOD_PKA_2 | 379 | 385 | PF00069 | 0.600 |
MOD_PKA_2 | 448 | 454 | PF00069 | 0.601 |
MOD_Plk_1 | 200 | 206 | PF00069 | 0.420 |
MOD_Plk_1 | 9 | 15 | PF00069 | 0.403 |
MOD_Plk_2-3 | 195 | 201 | PF00069 | 0.467 |
MOD_Plk_4 | 19 | 25 | PF00069 | 0.335 |
MOD_Plk_4 | 290 | 296 | PF00069 | 0.567 |
MOD_Plk_4 | 339 | 345 | PF00069 | 0.612 |
MOD_Plk_4 | 63 | 69 | PF00069 | 0.560 |
MOD_Plk_4 | 78 | 84 | PF00069 | 0.519 |
MOD_Plk_4 | 9 | 15 | PF00069 | 0.411 |
MOD_ProDKin_1 | 53 | 59 | PF00069 | 0.615 |
MOD_SUMO_rev_2 | 189 | 198 | PF00179 | 0.360 |
MOD_SUMO_rev_2 | 363 | 368 | PF00179 | 0.648 |
TRG_DiLeu_BaEn_1 | 216 | 221 | PF01217 | 0.428 |
TRG_DiLeu_BaEn_1 | 420 | 425 | PF01217 | 0.512 |
TRG_DiLeu_BaEn_2 | 91 | 97 | PF01217 | 0.590 |
TRG_DiLeu_BaLyEn_6 | 245 | 250 | PF01217 | 0.620 |
TRG_DiLeu_BaLyEn_6 | 306 | 311 | PF01217 | 0.468 |
TRG_ENDOCYTIC_2 | 128 | 131 | PF00928 | 0.482 |
TRG_ENDOCYTIC_2 | 154 | 157 | PF00928 | 0.295 |
TRG_ENDOCYTIC_2 | 175 | 178 | PF00928 | 0.282 |
TRG_ENDOCYTIC_2 | 182 | 185 | PF00928 | 0.282 |
TRG_ENDOCYTIC_2 | 343 | 346 | PF00928 | 0.608 |
TRG_ENDOCYTIC_2 | 422 | 425 | PF00928 | 0.569 |
TRG_ER_diArg_1 | 109 | 112 | PF00400 | 0.665 |
TRG_ER_diArg_1 | 178 | 180 | PF00400 | 0.293 |
TRG_ER_diArg_1 | 38 | 40 | PF00400 | 0.622 |
TRG_NES_CRM1_1 | 419 | 433 | PF08389 | 0.595 |
TRG_Pf-PMV_PEXEL_1 | 172 | 177 | PF00026 | 0.549 |
TRG_Pf-PMV_PEXEL_1 | 283 | 287 | PF00026 | 0.340 |
TRG_Pf-PMV_PEXEL_1 | 328 | 333 | PF00026 | 0.435 |
TRG_Pf-PMV_PEXEL_1 | 383 | 387 | PF00026 | 0.335 |
TRG_Pf-PMV_PEXEL_1 | 395 | 399 | PF00026 | 0.329 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1ICG5 | Leptomonas seymouri | 80% | 100% |
A0A0S4JR42 | Bodo saltans | 48% | 99% |
A0A1X0P4Z0 | Trypanosomatidae | 61% | 100% |
A0A3R7RRP5 | Trypanosoma rangeli | 58% | 100% |
A0A3S7X9X2 | Leishmania donovani | 96% | 100% |
A4HND0 | Leishmania braziliensis | 88% | 100% |
A4IC02 | Leishmania infantum | 97% | 100% |
C9ZYK3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 50% | 100% |
E9B6Z2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |