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:0110165 | cellular anatomical entity | 1 | 10 |
GO:0031207 | Sec62/Sec63 complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0098796 | membrane protein complex | 2 | 1 |
GO:0140534 | endoplasmic reticulum protein-containing complex | 2 | 1 |
Related structures:
AlphaFold database: E9B6Z2
Term | Name | Level | Count |
---|---|---|---|
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: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:0055085 | transmembrane transport | 2 | 11 |
GO:0065002 | intracellular protein transmembrane transport | 4 | 11 |
GO:0070727 | cellular macromolecule localization | 3 | 11 |
GO:0071702 | organic substance transport | 4 | 11 |
GO:0071705 | nitrogen compound transport | 4 | 11 |
GO:0071806 | protein transmembrane transport | 3 | 11 |
GO:0006605 | protein targeting | 5 | 1 |
GO:0006612 | protein targeting to membrane | 5 | 1 |
GO:0006613 | cotranslational protein targeting to membrane | 6 | 1 |
GO:0006614 | SRP-dependent cotranslational protein targeting to membrane | 7 | 1 |
GO:0006620 | post-translational protein targeting to endoplasmic reticulum membrane | 6 | 1 |
GO:0033365 | protein localization to organelle | 5 | 1 |
GO:0045047 | protein targeting to ER | 6 | 1 |
GO:0051668 | localization within membrane | 3 | 1 |
GO:0070972 | protein localization to endoplasmic reticulum | 6 | 1 |
GO:0072594 | establishment of protein localization to organelle | 4 | 1 |
GO:0072599 | establishment of protein localization to endoplasmic reticulum | 5 | 1 |
GO:0072657 | protein localization to membrane | 4 | 1 |
GO:0090150 | establishment of protein localization to membrane | 4 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 1 |
GO:0008320 | protein transmembrane transporter activity | 3 | 1 |
GO:0022857 | transmembrane transporter activity | 2 | 1 |
GO:0022884 | macromolecule transmembrane transporter activity | 3 | 1 |
GO:0140318 | protein transporter activity | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 452 | 456 | PF00656 | 0.540 |
CLV_MEL_PAP_1 | 446 | 452 | PF00089 | 0.335 |
CLV_NRD_NRD_1 | 150 | 152 | PF00675 | 0.562 |
CLV_NRD_NRD_1 | 179 | 181 | PF00675 | 0.478 |
CLV_NRD_NRD_1 | 278 | 280 | PF00675 | 0.331 |
CLV_NRD_NRD_1 | 282 | 284 | PF00675 | 0.316 |
CLV_NRD_NRD_1 | 38 | 40 | PF00675 | 0.405 |
CLV_PCSK_KEX2_1 | 159 | 161 | PF00082 | 0.481 |
CLV_PCSK_KEX2_1 | 179 | 181 | PF00082 | 0.416 |
CLV_PCSK_KEX2_1 | 278 | 280 | PF00082 | 0.331 |
CLV_PCSK_KEX2_1 | 282 | 284 | PF00082 | 0.316 |
CLV_PCSK_KEX2_1 | 38 | 40 | PF00082 | 0.373 |
CLV_PCSK_PC1ET2_1 | 159 | 161 | PF00082 | 0.490 |
CLV_PCSK_PC7_1 | 155 | 161 | PF00082 | 0.472 |
CLV_PCSK_PC7_1 | 278 | 284 | PF00082 | 0.338 |
CLV_PCSK_SKI1_1 | 103 | 107 | PF00082 | 0.344 |
CLV_PCSK_SKI1_1 | 112 | 116 | PF00082 | 0.302 |
CLV_PCSK_SKI1_1 | 188 | 192 | PF00082 | 0.576 |
CLV_PCSK_SKI1_1 | 210 | 214 | PF00082 | 0.599 |
CLV_PCSK_SKI1_1 | 283 | 287 | PF00082 | 0.391 |
CLV_PCSK_SKI1_1 | 383 | 387 | PF00082 | 0.326 |
CLV_PCSK_SKI1_1 | 39 | 43 | PF00082 | 0.412 |
CLV_PCSK_SKI1_1 | 412 | 416 | PF00082 | 0.377 |
CLV_PCSK_SKI1_1 | 93 | 97 | PF00082 | 0.332 |
DEG_APCC_DBOX_1 | 282 | 290 | PF00400 | 0.555 |
DOC_CYCLIN_RxL_1 | 322 | 333 | PF00134 | 0.629 |
DOC_CYCLIN_RxL_1 | 35 | 46 | PF00134 | 0.609 |
DOC_CYCLIN_RxL_1 | 380 | 390 | PF00134 | 0.537 |
DOC_CYCLIN_RxL_1 | 410 | 420 | PF00134 | 0.594 |
DOC_CYCLIN_yClb3_PxF_3 | 308 | 316 | PF00134 | 0.503 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 413 | 421 | PF00134 | 0.593 |
DOC_CYCLIN_yCln2_LP_2 | 28 | 34 | PF00134 | 0.346 |
DOC_MAPK_gen_1 | 110 | 117 | PF00069 | 0.442 |
DOC_MAPK_gen_1 | 244 | 255 | PF00069 | 0.610 |
DOC_MAPK_gen_1 | 434 | 443 | PF00069 | 0.632 |
DOC_MAPK_MEF2A_6 | 106 | 115 | PF00069 | 0.547 |
DOC_MAPK_MEF2A_6 | 287 | 294 | PF00069 | 0.576 |
DOC_MAPK_MEF2A_6 | 395 | 404 | PF00069 | 0.666 |
DOC_MAPK_NFAT4_5 | 287 | 295 | PF00069 | 0.449 |
DOC_PP1_RVXF_1 | 101 | 108 | PF00149 | 0.541 |
DOC_PP1_RVXF_1 | 246 | 252 | PF00149 | 0.560 |
DOC_PP1_RVXF_1 | 91 | 97 | PF00149 | 0.530 |
DOC_PP2B_LxvP_1 | 139 | 142 | PF13499 | 0.314 |
DOC_PP2B_LxvP_1 | 28 | 31 | PF13499 | 0.346 |
DOC_PP4_FxxP_1 | 267 | 270 | PF00568 | 0.551 |
DOC_USP7_MATH_1 | 19 | 23 | PF00917 | 0.302 |
DOC_USP7_MATH_1 | 277 | 281 | PF00917 | 0.424 |
DOC_USP7_MATH_1 | 339 | 343 | PF00917 | 0.528 |
DOC_USP7_MATH_1 | 360 | 364 | PF00917 | 0.652 |
DOC_WW_Pin1_4 | 53 | 58 | PF00397 | 0.579 |
LIG_14-3-3_CanoR_1 | 151 | 155 | PF00244 | 0.304 |
LIG_14-3-3_CanoR_1 | 278 | 286 | PF00244 | 0.427 |
LIG_14-3-3_CanoR_1 | 449 | 457 | PF00244 | 0.590 |
LIG_Actin_WH2_2 | 90 | 108 | PF00022 | 0.540 |
LIG_APCC_ABBA_1 | 415 | 420 | PF00400 | 0.537 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.470 |
LIG_BRCT_BRCA1_1 | 129 | 133 | PF00533 | 0.568 |
LIG_BRCT_BRCA1_1 | 14 | 18 | PF00533 | 0.321 |
LIG_EVH1_1 | 307 | 311 | PF00568 | 0.522 |
LIG_FHA_1 | 145 | 151 | PF00498 | 0.259 |
LIG_FHA_1 | 19 | 25 | PF00498 | 0.409 |
LIG_FHA_1 | 380 | 386 | PF00498 | 0.546 |
LIG_FHA_1 | 388 | 394 | PF00498 | 0.516 |
LIG_FHA_2 | 196 | 202 | PF00498 | 0.477 |
LIG_FHA_2 | 211 | 217 | PF00498 | 0.347 |
LIG_FHA_2 | 45 | 51 | PF00498 | 0.629 |
LIG_LIR_Gen_1 | 10 | 20 | PF02991 | 0.258 |
LIG_LIR_Gen_1 | 125 | 135 | PF02991 | 0.428 |
LIG_LIR_Gen_1 | 173 | 182 | PF02991 | 0.290 |
LIG_LIR_Gen_1 | 342 | 351 | PF02991 | 0.601 |
LIG_LIR_Gen_1 | 369 | 379 | PF02991 | 0.615 |
LIG_LIR_Gen_1 | 419 | 430 | PF02991 | 0.519 |
LIG_LIR_Nem_3 | 10 | 16 | PF02991 | 0.258 |
LIG_LIR_Nem_3 | 125 | 131 | PF02991 | 0.302 |
LIG_LIR_Nem_3 | 153 | 157 | PF02991 | 0.348 |
LIG_LIR_Nem_3 | 173 | 178 | PF02991 | 0.150 |
LIG_LIR_Nem_3 | 342 | 346 | PF02991 | 0.651 |
LIG_LIR_Nem_3 | 369 | 374 | PF02991 | 0.581 |
LIG_LIR_Nem_3 | 419 | 425 | PF02991 | 0.513 |
LIG_NRBOX | 221 | 227 | PF00104 | 0.302 |
LIG_NRBOX | 420 | 426 | PF00104 | 0.584 |
LIG_Pex14_1 | 119 | 123 | PF04695 | 0.321 |
LIG_Pex14_1 | 251 | 255 | PF04695 | 0.543 |
LIG_Pex14_2 | 263 | 267 | PF04695 | 0.550 |
LIG_REV1ctd_RIR_1 | 93 | 101 | PF16727 | 0.528 |
LIG_SH2_CRK | 128 | 132 | PF00017 | 0.497 |
LIG_SH2_CRK | 154 | 158 | PF00017 | 0.271 |
LIG_SH2_CRK | 182 | 186 | PF00017 | 0.258 |
LIG_SH2_CRK | 343 | 347 | PF00017 | 0.593 |
LIG_SH2_GRB2like | 472 | 475 | PF00017 | 0.635 |
LIG_SH2_NCK_1 | 355 | 359 | PF00017 | 0.590 |
LIG_SH2_NCK_1 | 73 | 77 | PF00017 | 0.636 |
LIG_SH2_PTP2 | 175 | 178 | PF00017 | 0.272 |
LIG_SH2_STAT3 | 384 | 387 | PF00017 | 0.599 |
LIG_SH2_STAT3 | 472 | 475 | PF00017 | 0.561 |
LIG_SH2_STAT5 | 175 | 178 | PF00017 | 0.258 |
LIG_SH2_STAT5 | 235 | 238 | PF00017 | 0.420 |
LIG_SH2_STAT5 | 275 | 278 | PF00017 | 0.540 |
LIG_SH2_STAT5 | 29 | 32 | PF00017 | 0.302 |
LIG_SH2_STAT5 | 384 | 387 | PF00017 | 0.515 |
LIG_SH2_STAT5 | 429 | 432 | PF00017 | 0.624 |
LIG_SH2_STAT5 | 67 | 70 | PF00017 | 0.554 |
LIG_SH3_3 | 105 | 111 | PF00018 | 0.641 |
LIG_SH3_3 | 203 | 209 | PF00018 | 0.461 |
LIG_SH3_3 | 267 | 273 | PF00018 | 0.535 |
LIG_SH3_3 | 305 | 311 | PF00018 | 0.514 |
LIG_SH3_4 | 434 | 441 | PF00018 | 0.596 |
LIG_SUMO_SIM_anti_2 | 21 | 28 | PF11976 | 0.324 |
LIG_SUMO_SIM_anti_2 | 78 | 84 | PF11976 | 0.501 |
LIG_TRAF2_1 | 190 | 193 | PF00917 | 0.369 |
LIG_TRAF2_1 | 198 | 201 | PF00917 | 0.409 |
LIG_TRAF2_1 | 362 | 365 | PF00917 | 0.528 |
LIG_TRAF2_1 | 396 | 399 | PF00917 | 0.615 |
LIG_UBA3_1 | 249 | 257 | PF00899 | 0.586 |
LIG_UBA3_1 | 326 | 335 | PF00899 | 0.619 |
LIG_WRC_WIRS_1 | 13 | 18 | PF05994 | 0.321 |
LIG_WW_2 | 308 | 311 | PF00397 | 0.587 |
MOD_CK1_1 | 143 | 149 | PF00069 | 0.316 |
MOD_CK1_1 | 53 | 59 | PF00069 | 0.577 |
MOD_CK1_1 | 9 | 15 | PF00069 | 0.377 |
MOD_CK2_1 | 143 | 149 | PF00069 | 0.256 |
MOD_CK2_1 | 195 | 201 | PF00069 | 0.472 |
MOD_CK2_1 | 210 | 216 | PF00069 | 0.352 |
MOD_CK2_1 | 359 | 365 | PF00069 | 0.658 |
MOD_CK2_1 | 44 | 50 | PF00069 | 0.595 |
MOD_GlcNHglycan | 124 | 127 | PF01048 | 0.321 |
MOD_GlcNHglycan | 143 | 146 | PF01048 | 0.472 |
MOD_GlcNHglycan | 376 | 379 | PF01048 | 0.365 |
MOD_GlcNHglycan | 409 | 412 | PF01048 | 0.353 |
MOD_GlcNHglycan | 63 | 66 | PF01048 | 0.435 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.301 |
MOD_N-GLC_1 | 165 | 170 | PF02516 | 0.458 |
MOD_NEK2_1 | 122 | 127 | PF00069 | 0.318 |
MOD_NEK2_1 | 18 | 23 | PF00069 | 0.406 |
MOD_NEK2_1 | 61 | 66 | PF00069 | 0.553 |
MOD_PKA_1 | 278 | 284 | PF00069 | 0.520 |
MOD_PKA_2 | 150 | 156 | PF00069 | 0.300 |
MOD_PKA_2 | 277 | 283 | PF00069 | 0.522 |
MOD_PKA_2 | 379 | 385 | PF00069 | 0.590 |
MOD_PKA_2 | 448 | 454 | PF00069 | 0.584 |
MOD_Plk_1 | 200 | 206 | PF00069 | 0.401 |
MOD_Plk_1 | 9 | 15 | PF00069 | 0.377 |
MOD_Plk_2-3 | 195 | 201 | PF00069 | 0.440 |
MOD_Plk_4 | 19 | 25 | PF00069 | 0.302 |
MOD_Plk_4 | 339 | 345 | PF00069 | 0.636 |
MOD_Plk_4 | 50 | 56 | PF00069 | 0.635 |
MOD_Plk_4 | 63 | 69 | PF00069 | 0.533 |
MOD_Plk_4 | 78 | 84 | PF00069 | 0.496 |
MOD_Plk_4 | 9 | 15 | PF00069 | 0.385 |
MOD_ProDKin_1 | 53 | 59 | PF00069 | 0.579 |
MOD_SUMO_rev_2 | 189 | 198 | PF00179 | 0.345 |
MOD_SUMO_rev_2 | 362 | 368 | PF00179 | 0.637 |
TRG_DiLeu_BaEn_1 | 216 | 221 | PF01217 | 0.412 |
TRG_DiLeu_BaEn_1 | 420 | 425 | PF01217 | 0.492 |
TRG_DiLeu_BaEn_2 | 91 | 97 | PF01217 | 0.570 |
TRG_DiLeu_BaLyEn_6 | 245 | 250 | PF01217 | 0.610 |
TRG_ENDOCYTIC_2 | 128 | 131 | PF00928 | 0.452 |
TRG_ENDOCYTIC_2 | 154 | 157 | PF00928 | 0.271 |
TRG_ENDOCYTIC_2 | 175 | 178 | PF00928 | 0.258 |
TRG_ENDOCYTIC_2 | 182 | 185 | PF00928 | 0.258 |
TRG_ENDOCYTIC_2 | 343 | 346 | PF00928 | 0.593 |
TRG_ENDOCYTIC_2 | 422 | 425 | PF00928 | 0.550 |
TRG_ER_diArg_1 | 109 | 112 | PF00400 | 0.648 |
TRG_ER_diArg_1 | 178 | 180 | PF00400 | 0.278 |
TRG_ER_diArg_1 | 38 | 40 | PF00400 | 0.592 |
TRG_NES_CRM1_1 | 419 | 433 | PF08389 | 0.577 |
TRG_Pf-PMV_PEXEL_1 | 172 | 177 | PF00026 | 0.548 |
TRG_Pf-PMV_PEXEL_1 | 328 | 333 | PF00026 | 0.436 |
TRG_Pf-PMV_PEXEL_1 | 383 | 387 | PF00026 | 0.318 |
TRG_Pf-PMV_PEXEL_1 | 395 | 399 | PF00026 | 0.314 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1ICG5 | Leptomonas seymouri | 81% | 100% |
A0A0S4JR42 | Bodo saltans | 48% | 99% |
A0A1X0P4Z0 | Trypanosomatidae | 61% | 100% |
A0A3R7RRP5 | Trypanosoma rangeli | 58% | 100% |
A0A3S7X9X2 | Leishmania donovani | 96% | 100% |
A4HND0 | Leishmania braziliensis | 89% | 100% |
A4IC02 | Leishmania infantum | 96% | 100% |
C9ZYK3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 50% | 100% |
E9AFU0 | Leishmania major | 96% | 100% |