| Source | Evidence on protein | Close homologs |
|---|---|---|
| Cuervo et al. | no | yes: 0 |
| Hassani et al. | no | yes: 0 |
| Forrest at al. (metacyclic) | no | yes: 2 |
| Forrest at al. (procyclic) | no | yes: 2 |
| Silverman et al. | no | yes: 2 |
| Pissara et al. | yes | yes: 8 |
| 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: 11 |
| NetGPI | no | yes: 0, no: 11 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005737 | cytoplasm | 2 | 1 |
| GO:0110165 | cellular anatomical entity | 1 | 1 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
| GO:0008152 | metabolic process | 1 | 12 |
| GO:0019538 | protein metabolic process | 3 | 12 |
| GO:0036211 | protein modification process | 4 | 12 |
| GO:0043170 | macromolecule metabolic process | 3 | 12 |
| GO:0043412 | macromolecule modification | 4 | 12 |
| GO:0044238 | primary metabolic process | 2 | 12 |
| GO:0071704 | organic substance metabolic process | 2 | 12 |
| GO:1901564 | organonitrogen compound metabolic process | 3 | 12 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0003824 | catalytic activity | 1 | 12 |
| GO:0004077 | biotin-[acetyl-CoA-carboxylase] ligase activity | 4 | 10 |
| GO:0016874 | ligase activity | 2 | 12 |
| GO:0016879 | ligase activity, forming carbon-nitrogen bonds | 3 | 10 |
| GO:0018271 | biotin-protein ligase activity | 3 | 10 |
| GO:0140096 | catalytic activity, acting on a protein | 2 | 10 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_NRD_NRD_1 | 91 | 93 | PF00675 | 0.359 |
| CLV_PCSK_KEX2_1 | 223 | 225 | PF00082 | 0.460 |
| CLV_PCSK_KEX2_1 | 91 | 93 | PF00082 | 0.359 |
| CLV_PCSK_PC1ET2_1 | 223 | 225 | PF00082 | 0.508 |
| CLV_PCSK_SKI1_1 | 163 | 167 | PF00082 | 0.530 |
| CLV_PCSK_SKI1_1 | 217 | 221 | PF00082 | 0.496 |
| CLV_PCSK_SKI1_1 | 23 | 27 | PF00082 | 0.311 |
| CLV_PCSK_SKI1_1 | 92 | 96 | PF00082 | 0.358 |
| DEG_APCC_DBOX_1 | 91 | 99 | PF00400 | 0.558 |
| DEG_SCF_FBW7_1 | 152 | 159 | PF00400 | 0.325 |
| DOC_CYCLIN_yClb5_NLxxxL_5 | 56 | 63 | PF00134 | 0.483 |
| DOC_MAPK_gen_1 | 91 | 97 | PF00069 | 0.558 |
| DOC_MAPK_MEF2A_6 | 56 | 65 | PF00069 | 0.449 |
| DOC_MAPK_RevD_3 | 79 | 92 | PF00069 | 0.558 |
| DOC_PP2B_LxvP_1 | 63 | 66 | PF13499 | 0.411 |
| DOC_USP7_MATH_1 | 105 | 109 | PF00917 | 0.563 |
| DOC_USP7_MATH_1 | 111 | 115 | PF00917 | 0.568 |
| DOC_USP7_UBL2_3 | 213 | 217 | PF12436 | 0.520 |
| DOC_WW_Pin1_4 | 152 | 157 | PF00397 | 0.306 |
| DOC_WW_Pin1_4 | 178 | 183 | PF00397 | 0.443 |
| DOC_WW_Pin1_4 | 196 | 201 | PF00397 | 0.554 |
| DOC_WW_Pin1_4 | 51 | 56 | PF00397 | 0.470 |
| LIG_14-3-3_CanoR_1 | 50 | 55 | PF00244 | 0.491 |
| LIG_CaM_IQ_9 | 37 | 52 | PF13499 | 0.442 |
| LIG_CtBP_PxDLS_1 | 231 | 235 | PF00389 | 0.509 |
| LIG_FHA_1 | 153 | 159 | PF00498 | 0.510 |
| LIG_FHA_1 | 16 | 22 | PF00498 | 0.440 |
| LIG_FHA_1 | 60 | 66 | PF00498 | 0.478 |
| LIG_FHA_2 | 179 | 185 | PF00498 | 0.523 |
| LIG_FHA_2 | 196 | 202 | PF00498 | 0.346 |
| LIG_FHA_2 | 251 | 257 | PF00498 | 0.453 |
| LIG_LIR_Apic_2 | 51 | 55 | PF02991 | 0.508 |
| LIG_LIR_Gen_1 | 209 | 219 | PF02991 | 0.520 |
| LIG_LIR_Nem_3 | 140 | 146 | PF02991 | 0.507 |
| LIG_LIR_Nem_3 | 209 | 214 | PF02991 | 0.531 |
| LIG_LIR_Nem_3 | 241 | 245 | PF02991 | 0.388 |
| LIG_PDZ_Class_2 | 258 | 263 | PF00595 | 0.442 |
| LIG_Pex14_1 | 190 | 194 | PF04695 | 0.338 |
| LIG_SH2_CRK | 60 | 64 | PF00017 | 0.541 |
| LIG_SH2_STAT5 | 143 | 146 | PF00017 | 0.529 |
| LIG_WRC_WIRS_1 | 208 | 213 | PF05994 | 0.476 |
| MOD_CDK_SPK_2 | 51 | 56 | PF00069 | 0.473 |
| MOD_CK1_1 | 238 | 244 | PF00069 | 0.530 |
| MOD_CK2_1 | 132 | 138 | PF00069 | 0.462 |
| MOD_CK2_1 | 195 | 201 | PF00069 | 0.585 |
| MOD_CK2_1 | 203 | 209 | PF00069 | 0.463 |
| MOD_GlcNHglycan | 101 | 106 | PF01048 | 0.292 |
| MOD_GSK3_1 | 101 | 108 | PF00069 | 0.538 |
| MOD_GSK3_1 | 111 | 118 | PF00069 | 0.403 |
| MOD_GSK3_1 | 152 | 159 | PF00069 | 0.511 |
| MOD_GSK3_1 | 196 | 203 | PF00069 | 0.543 |
| MOD_GSK3_1 | 21 | 28 | PF00069 | 0.548 |
| MOD_GSK3_1 | 44 | 51 | PF00069 | 0.524 |
| MOD_NEK2_1 | 215 | 220 | PF00069 | 0.409 |
| MOD_NEK2_1 | 25 | 30 | PF00069 | 0.558 |
| MOD_NEK2_1 | 59 | 64 | PF00069 | 0.462 |
| MOD_PKA_2 | 203 | 209 | PF00069 | 0.470 |
| MOD_PKA_2 | 44 | 50 | PF00069 | 0.465 |
| MOD_Plk_1 | 163 | 169 | PF00069 | 0.537 |
| MOD_Plk_1 | 215 | 221 | PF00069 | 0.415 |
| MOD_Plk_1 | 232 | 238 | PF00069 | 0.466 |
| MOD_Plk_4 | 132 | 138 | PF00069 | 0.480 |
| MOD_Plk_4 | 163 | 169 | PF00069 | 0.554 |
| MOD_Plk_4 | 203 | 209 | PF00069 | 0.486 |
| MOD_ProDKin_1 | 152 | 158 | PF00069 | 0.314 |
| MOD_ProDKin_1 | 178 | 184 | PF00069 | 0.444 |
| MOD_ProDKin_1 | 196 | 202 | PF00069 | 0.550 |
| MOD_ProDKin_1 | 51 | 57 | PF00069 | 0.470 |
| MOD_SUMO_for_1 | 74 | 77 | PF00179 | 0.563 |
| TRG_DiLeu_BaLyEn_6 | 80 | 85 | PF01217 | 0.558 |
| TRG_ENDOCYTIC_2 | 143 | 146 | PF00928 | 0.529 |
| TRG_ENDOCYTIC_2 | 60 | 63 | PF00928 | 0.479 |
| TRG_ER_diArg_1 | 245 | 248 | PF00400 | 0.293 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1HUD5 | Leptomonas seymouri | 71% | 100% |
| A0A0S4JE29 | Bodo saltans | 35% | 85% |
| A0A1X0P3B0 | Trypanosomatidae | 48% | 100% |
| A0A3R7NY08 | Trypanosoma rangeli | 48% | 100% |
| A0A3S7X4E1 | Leishmania donovani | 85% | 100% |
| A4I6N1 | Leishmania infantum | 85% | 100% |
| D0A8L0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
| E9B1Q4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
| Q4Q6F6 | Leishmania major | 83% | 100% |
| Q59014 | Methanocaldococcus jannaschii (strain ATCC 43067 / DSM 2661 / JAL-1 / JCM 10045 / NBRC 100440) | 29% | 100% |
| V5DNJ4 | Trypanosoma cruzi | 50% | 100% |