| 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: 3 |
| 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: 10 |
| NetGPI | no | yes: 0, no: 10 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005737 | cytoplasm | 2 | 11 |
| GO:0110165 | cellular anatomical entity | 1 | 11 |
Related structures:
AlphaFold database: A4HL26
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0000045 | autophagosome assembly | 6 | 11 |
| GO:0006508 | proteolysis | 4 | 11 |
| GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
| GO:0006810 | transport | 3 | 11 |
| GO:0006996 | organelle organization | 4 | 11 |
| GO:0007033 | vacuole organization | 5 | 11 |
| GO:0008104 | protein localization | 4 | 11 |
| GO:0008152 | metabolic process | 1 | 11 |
| GO:0009987 | cellular process | 1 | 11 |
| GO:0015031 | protein transport | 4 | 11 |
| GO:0016043 | cellular component organization | 3 | 11 |
| GO:0019538 | protein metabolic process | 3 | 11 |
| GO:0022607 | cellular component assembly | 4 | 11 |
| GO:0033036 | macromolecule localization | 2 | 11 |
| GO:0036211 | protein modification process | 4 | 11 |
| GO:0043170 | macromolecule metabolic process | 3 | 11 |
| GO:0043412 | macromolecule modification | 4 | 11 |
| GO:0044238 | primary metabolic process | 2 | 11 |
| GO:0045184 | establishment of protein localization | 3 | 11 |
| GO:0051179 | localization | 1 | 11 |
| GO:0051234 | establishment of localization | 2 | 11 |
| GO:0051641 | cellular localization | 2 | 11 |
| GO:0051697 | protein delipidation | 5 | 11 |
| GO:0070727 | cellular macromolecule localization | 3 | 11 |
| GO:0070925 | organelle assembly | 5 | 11 |
| GO:0071702 | organic substance transport | 4 | 11 |
| GO:0071704 | organic substance metabolic process | 2 | 11 |
| GO:0071705 | nitrogen compound transport | 4 | 11 |
| GO:0071840 | cellular component organization or biogenesis | 2 | 11 |
| GO:1901564 | organonitrogen compound metabolic process | 3 | 11 |
| GO:1905037 | autophagosome organization | 6 | 11 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0003824 | catalytic activity | 1 | 11 |
| GO:0004175 | endopeptidase activity | 4 | 11 |
| GO:0004197 | cysteine-type endopeptidase activity | 5 | 11 |
| GO:0008233 | peptidase activity | 3 | 11 |
| GO:0008234 | cysteine-type peptidase activity | 4 | 11 |
| GO:0016787 | hydrolase activity | 2 | 11 |
| GO:0140096 | catalytic activity, acting on a protein | 2 | 11 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_NRD_NRD_1 | 263 | 265 | PF00675 | 0.183 |
| CLV_NRD_NRD_1 | 296 | 298 | PF00675 | 0.304 |
| CLV_NRD_NRD_1 | 40 | 42 | PF00675 | 0.629 |
| CLV_PCSK_SKI1_1 | 264 | 268 | PF00082 | 0.340 |
| CLV_PCSK_SKI1_1 | 381 | 385 | PF00082 | 0.486 |
| CLV_PCSK_SKI1_1 | 71 | 75 | PF00082 | 0.286 |
| DEG_ODPH_VHL_1 | 224 | 236 | PF01847 | 0.564 |
| DOC_CKS1_1 | 36 | 41 | PF01111 | 0.641 |
| DOC_CYCLIN_RxL_1 | 68 | 77 | PF00134 | 0.387 |
| DOC_CYCLIN_yCln2_LP_2 | 216 | 222 | PF00134 | 0.460 |
| DOC_MAPK_gen_1 | 297 | 305 | PF00069 | 0.557 |
| DOC_MAPK_MEF2A_6 | 230 | 238 | PF00069 | 0.459 |
| DOC_MAPK_MEF2A_6 | 298 | 307 | PF00069 | 0.564 |
| DOC_MAPK_MEF2A_6 | 381 | 390 | PF00069 | 0.485 |
| DOC_PP1_RVXF_1 | 262 | 269 | PF00149 | 0.540 |
| DOC_PP1_RVXF_1 | 70 | 77 | PF00149 | 0.512 |
| DOC_PP2B_LxvP_1 | 216 | 219 | PF13499 | 0.453 |
| DOC_PP4_FxxP_1 | 268 | 271 | PF00568 | 0.491 |
| DOC_PP4_FxxP_1 | 36 | 39 | PF00568 | 0.647 |
| DOC_USP7_MATH_1 | 277 | 281 | PF00917 | 0.512 |
| DOC_USP7_MATH_1 | 86 | 90 | PF00917 | 0.528 |
| DOC_USP7_UBL2_3 | 156 | 160 | PF12436 | 0.564 |
| DOC_USP7_UBL2_3 | 42 | 46 | PF12436 | 0.337 |
| DOC_WW_Pin1_4 | 163 | 168 | PF00397 | 0.479 |
| DOC_WW_Pin1_4 | 341 | 346 | PF00397 | 0.673 |
| DOC_WW_Pin1_4 | 35 | 40 | PF00397 | 0.622 |
| DOC_WW_Pin1_4 | 388 | 393 | PF00397 | 0.694 |
| DOC_WW_Pin1_4 | 44 | 49 | PF00397 | 0.528 |
| LIG_14-3-3_CanoR_1 | 100 | 106 | PF00244 | 0.564 |
| LIG_14-3-3_CanoR_1 | 350 | 355 | PF00244 | 0.768 |
| LIG_14-3-3_CanoR_1 | 61 | 68 | PF00244 | 0.278 |
| LIG_BRCT_BRCA1_1 | 133 | 137 | PF00533 | 0.484 |
| LIG_BRCT_BRCA1_1 | 32 | 36 | PF00533 | 0.635 |
| LIG_EH_1 | 373 | 377 | PF12763 | 0.524 |
| LIG_EVH1_1 | 82 | 86 | PF00568 | 0.564 |
| LIG_FHA_1 | 100 | 106 | PF00498 | 0.506 |
| LIG_FHA_1 | 328 | 334 | PF00498 | 0.309 |
| LIG_FHA_1 | 45 | 51 | PF00498 | 0.479 |
| LIG_FHA_1 | 61 | 67 | PF00498 | 0.300 |
| LIG_FHA_2 | 309 | 315 | PF00498 | 0.540 |
| LIG_Integrin_RGD_1 | 291 | 293 | PF01839 | 0.211 |
| LIG_LIR_Apic_2 | 33 | 39 | PF02991 | 0.649 |
| LIG_LIR_Gen_1 | 134 | 145 | PF02991 | 0.513 |
| LIG_LIR_Gen_1 | 228 | 239 | PF02991 | 0.471 |
| LIG_LIR_Gen_1 | 62 | 73 | PF02991 | 0.522 |
| LIG_LIR_Nem_3 | 134 | 140 | PF02991 | 0.513 |
| LIG_LIR_Nem_3 | 255 | 259 | PF02991 | 0.407 |
| LIG_LIR_Nem_3 | 313 | 318 | PF02991 | 0.474 |
| LIG_LIR_Nem_3 | 330 | 334 | PF02991 | 0.299 |
| LIG_LIR_Nem_3 | 80 | 85 | PF02991 | 0.471 |
| LIG_LIR_Nem_3 | 92 | 98 | PF02991 | 0.510 |
| LIG_PTAP_UEV_1 | 140 | 145 | PF05743 | 0.460 |
| LIG_SH2_PTP2 | 119 | 122 | PF00017 | 0.564 |
| LIG_SH2_STAP1 | 161 | 165 | PF00017 | 0.540 |
| LIG_SH2_STAP1 | 231 | 235 | PF00017 | 0.474 |
| LIG_SH2_STAT5 | 119 | 122 | PF00017 | 0.510 |
| LIG_SH2_STAT5 | 273 | 276 | PF00017 | 0.501 |
| LIG_SH2_STAT5 | 278 | 281 | PF00017 | 0.505 |
| LIG_SH2_STAT5 | 308 | 311 | PF00017 | 0.449 |
| LIG_SH2_STAT5 | 75 | 78 | PF00017 | 0.487 |
| LIG_SH3_3 | 138 | 144 | PF00018 | 0.460 |
| LIG_SH3_3 | 326 | 332 | PF00018 | 0.484 |
| LIG_SH3_3 | 392 | 398 | PF00018 | 0.716 |
| LIG_SH3_3 | 80 | 86 | PF00018 | 0.540 |
| LIG_SUMO_SIM_anti_2 | 320 | 327 | PF11976 | 0.298 |
| LIG_SUMO_SIM_anti_2 | 47 | 54 | PF11976 | 0.495 |
| LIG_SUMO_SIM_par_1 | 47 | 54 | PF11976 | 0.495 |
| LIG_UBA3_1 | 234 | 242 | PF00899 | 0.560 |
| LIG_UBA3_1 | 67 | 72 | PF00899 | 0.205 |
| LIG_WW_2 | 83 | 86 | PF00397 | 0.564 |
| MOD_CDK_SPxK_1 | 35 | 41 | PF00069 | 0.644 |
| MOD_CDK_SPxxK_3 | 35 | 42 | PF00069 | 0.642 |
| MOD_CK1_1 | 163 | 169 | PF00069 | 0.527 |
| MOD_CK1_1 | 280 | 286 | PF00069 | 0.495 |
| MOD_CK1_1 | 327 | 333 | PF00069 | 0.407 |
| MOD_CK1_1 | 337 | 343 | PF00069 | 0.507 |
| MOD_CK1_1 | 77 | 83 | PF00069 | 0.531 |
| MOD_CK2_1 | 163 | 169 | PF00069 | 0.528 |
| MOD_Cter_Amidation | 262 | 265 | PF01082 | 0.183 |
| MOD_GlcNHglycan | 141 | 144 | PF01048 | 0.262 |
| MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.651 |
| MOD_GlcNHglycan | 359 | 362 | PF01048 | 0.636 |
| MOD_GlcNHglycan | 53 | 56 | PF01048 | 0.408 |
| MOD_GlcNHglycan | 57 | 60 | PF01048 | 0.424 |
| MOD_GSK3_1 | 276 | 283 | PF00069 | 0.465 |
| MOD_GSK3_1 | 334 | 341 | PF00069 | 0.453 |
| MOD_GSK3_1 | 51 | 58 | PF00069 | 0.460 |
| MOD_GSK3_1 | 86 | 93 | PF00069 | 0.499 |
| MOD_N-GLC_1 | 131 | 136 | PF02516 | 0.183 |
| MOD_N-GLC_1 | 386 | 391 | PF02516 | 0.482 |
| MOD_N-GLC_1 | 86 | 91 | PF02516 | 0.270 |
| MOD_NEK2_1 | 105 | 110 | PF00069 | 0.520 |
| MOD_NEK2_1 | 386 | 391 | PF00069 | 0.482 |
| MOD_NEK2_1 | 74 | 79 | PF00069 | 0.460 |
| MOD_NEK2_1 | 98 | 103 | PF00069 | 0.490 |
| MOD_PIKK_1 | 99 | 105 | PF00454 | 0.540 |
| MOD_PKA_2 | 60 | 66 | PF00069 | 0.435 |
| MOD_PKA_2 | 99 | 105 | PF00069 | 0.538 |
| MOD_Plk_1 | 131 | 137 | PF00069 | 0.383 |
| MOD_Plk_1 | 386 | 392 | PF00069 | 0.479 |
| MOD_Plk_4 | 160 | 166 | PF00069 | 0.500 |
| MOD_Plk_4 | 21 | 27 | PF00069 | 0.585 |
| MOD_Plk_4 | 230 | 236 | PF00069 | 0.432 |
| MOD_Plk_4 | 252 | 258 | PF00069 | 0.540 |
| MOD_Plk_4 | 283 | 289 | PF00069 | 0.514 |
| MOD_Plk_4 | 324 | 330 | PF00069 | 0.449 |
| MOD_ProDKin_1 | 163 | 169 | PF00069 | 0.479 |
| MOD_ProDKin_1 | 341 | 347 | PF00069 | 0.674 |
| MOD_ProDKin_1 | 35 | 41 | PF00069 | 0.618 |
| MOD_ProDKin_1 | 388 | 394 | PF00069 | 0.691 |
| MOD_ProDKin_1 | 44 | 50 | PF00069 | 0.521 |
| MOD_SUMO_rev_2 | 123 | 131 | PF00179 | 0.383 |
| TRG_DiLeu_BaLyEn_6 | 329 | 334 | PF01217 | 0.385 |
| TRG_ENDOCYTIC_2 | 161 | 164 | PF00928 | 0.540 |
| TRG_ENDOCYTIC_2 | 231 | 234 | PF00928 | 0.460 |
| TRG_ENDOCYTIC_2 | 315 | 318 | PF00928 | 0.564 |
| TRG_NES_CRM1_1 | 128 | 139 | PF08389 | 0.542 |
| TRG_Pf-PMV_PEXEL_1 | 197 | 201 | PF00026 | 0.364 |
| TRG_Pf-PMV_PEXEL_1 | 41 | 45 | PF00026 | 0.337 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A098DRK7 | Gibberella zeae (strain ATCC MYA-4620 / CBS 123657 / FGSC 9075 / NRRL 31084 / PH-1) | 22% | 85% |
| A0A0N1IIY5 | Leptomonas seymouri | 67% | 100% |
| A0A0S4JSC7 | Bodo saltans | 27% | 100% |
| A0A1X0NS04 | Trypanosomatidae | 37% | 100% |
| A0A1X0P2H1 | Trypanosomatidae | 25% | 100% |
| A0A3S7X6B3 | Leishmania donovani | 77% | 100% |
| A0A422NI42 | Trypanosoma rangeli | 40% | 100% |
| A1CJ08 | Aspergillus clavatus (strain ATCC 1007 / CBS 513.65 / DSM 816 / NCTC 3887 / NRRL 1 / QM 1276 / 107) | 24% | 100% |
| A2Q1V6 | Medicago truncatula | 23% | 82% |
| A2QY50 | Aspergillus niger (strain CBS 513.88 / FGSC A1513) | 25% | 99% |
| A2XHJ5 | Oryza sativa subsp. indica | 22% | 84% |
| A4I8K7 | Leishmania infantum | 77% | 100% |
| A5DEF7 | Meyerozyma guilliermondii (strain ATCC 6260 / CBS 566 / DSM 6381 / JCM 1539 / NBRC 10279 / NRRL Y-324) | 26% | 99% |
| A5DSB4 | Lodderomyces elongisporus (strain ATCC 11503 / CBS 2605 / JCM 1781 / NBRC 1676 / NRRL YB-4239) | 22% | 76% |
| C9ZQI0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
| D0AAK8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
| E2RDP2 | Canis lupus familiaris | 25% | 84% |
| E9B3G7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 75% | 100% |
| Q1E5M9 | Coccidioides immitis (strain RS) | 25% | 92% |
| Q2HH40 | Chaetomium globosum (strain ATCC 6205 / CBS 148.51 / DSM 1962 / NBRC 6347 / NRRL 1970) | 23% | 89% |
| Q2U5B0 | Aspergillus oryzae (strain ATCC 42149 / RIB 40) | 27% | 98% |
| Q2XPP4 | Oryza sativa subsp. indica | 23% | 83% |
| Q4Q4N3 | Leishmania major | 76% | 100% |
| Q4U3V5 | Cryphonectria parasitica | 24% | 87% |
| Q523C3 | Magnaporthe oryzae (strain 70-15 / ATCC MYA-4617 / FGSC 8958) | 24% | 81% |
| Q5B7L0 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 23% | 99% |
| Q5XH30 | Xenopus laevis | 23% | 88% |
| Q684M2 | Sus scrofa | 26% | 85% |
| Q68EP9 | Xenopus tropicalis | 23% | 88% |
| Q68FJ9 | Xenopus laevis | 23% | 85% |
| Q6CH28 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 24% | 73% |
| Q6FP20 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 24% | 82% |
| Q6PZ02 | Gallus gallus | 23% | 100% |
| Q75E61 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 24% | 76% |
| Q75KP8 | Oryza sativa subsp. japonica | 23% | 84% |
| Q7XPW8 | Oryza sativa subsp. japonica | 23% | 83% |
| Q811C2 | Mus musculus | 24% | 87% |
| Q86TL0 | Homo sapiens | 26% | 84% |
| Q8BGV9 | Mus musculus | 25% | 84% |
| Q8S929 | Arabidopsis thaliana | 26% | 85% |
| Q96DT6 | Homo sapiens | 23% | 87% |
| Q9M1Y0 | Arabidopsis thaliana | 23% | 83% |
| V5AXZ8 | Trypanosoma cruzi | 38% | 100% |
| V5BGZ3 | Trypanosoma cruzi | 25% | 100% |
| W0TGM7 | Kluyveromyces marxianus (strain DMKU3-1042 / BCC 29191 / NBRC 104275) | 23% | 88% |