| 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: 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:0005634 | nucleus | 5 | 1 | 
| GO:0043226 | organelle | 2 | 1 | 
| GO:0043227 | membrane-bounded organelle | 3 | 1 | 
| GO:0043229 | intracellular organelle | 3 | 1 | 
| GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 | 
| GO:0110165 | cellular anatomical entity | 1 | 1 | 
Related structures:
AlphaFold database: A0A2D1QVA3
| Term | Name | Level | Count | 
|---|---|---|---|
| GO:0006355 | regulation of DNA-templated transcription | 6 | 11 | 
| GO:0006357 | regulation of transcription by RNA polymerase II | 7 | 11 | 
| GO:0009889 | regulation of biosynthetic process | 4 | 11 | 
| GO:0010468 | regulation of gene expression | 5 | 11 | 
| GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 11 | 
| GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 11 | 
| GO:0019222 | regulation of metabolic process | 3 | 11 | 
| GO:0031323 | regulation of cellular metabolic process | 4 | 11 | 
| GO:0031326 | regulation of cellular biosynthetic process | 5 | 11 | 
| GO:0050789 | regulation of biological process | 2 | 11 | 
| GO:0050794 | regulation of cellular process | 3 | 11 | 
| GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 11 | 
| GO:0051252 | regulation of RNA metabolic process | 5 | 11 | 
| GO:0060255 | regulation of macromolecule metabolic process | 4 | 11 | 
| GO:0065007 | biological regulation | 1 | 11 | 
| GO:0080090 | regulation of primary metabolic process | 4 | 11 | 
| GO:1903506 | regulation of nucleic acid-templated transcription | 7 | 11 | 
| GO:2001141 | regulation of RNA biosynthetic process | 6 | 11 | 
| GO:0010564 | regulation of cell cycle process | 5 | 1 | 
| GO:0032465 | regulation of cytokinesis | 5 | 1 | 
| GO:0051302 | regulation of cell division | 4 | 1 | 
| GO:0051726 | regulation of cell cycle | 4 | 1 | 
| GO:1902412 | regulation of mitotic cytokinesis | 6 | 1 | 
| Term | Name | Level | Count | 
|---|---|---|---|
| GO:0016538 | cyclin-dependent protein serine/threonine kinase regulator activity | 5 | 11 | 
| GO:0019207 | kinase regulator activity | 3 | 11 | 
| GO:0019887 | protein kinase regulator activity | 4 | 11 | 
| GO:0030234 | enzyme regulator activity | 2 | 11 | 
| GO:0098772 | molecular function regulator activity | 1 | 11 | 
| Leishmania | From | To | Domain/Motif | Score | 
|---|---|---|---|---|
| CLV_NRD_NRD_1 | 174 | 176 | PF00675 | 0.480 | 
| CLV_NRD_NRD_1 | 207 | 209 | PF00675 | 0.521 | 
| CLV_NRD_NRD_1 | 28 | 30 | PF00675 | 0.572 | 
| CLV_NRD_NRD_1 | 45 | 47 | PF00675 | 0.372 | 
| CLV_NRD_NRD_1 | 71 | 73 | PF00675 | 0.379 | 
| CLV_PCSK_FUR_1 | 261 | 265 | PF00082 | 0.470 | 
| CLV_PCSK_KEX2_1 | 174 | 176 | PF00082 | 0.480 | 
| CLV_PCSK_KEX2_1 | 207 | 209 | PF00082 | 0.521 | 
| CLV_PCSK_KEX2_1 | 263 | 265 | PF00082 | 0.498 | 
| CLV_PCSK_KEX2_1 | 28 | 30 | PF00082 | 0.500 | 
| CLV_PCSK_PC1ET2_1 | 263 | 265 | PF00082 | 0.491 | 
| CLV_PCSK_SKI1_1 | 122 | 126 | PF00082 | 0.413 | 
| CLV_PCSK_SKI1_1 | 174 | 178 | PF00082 | 0.372 | 
| DOC_CKS1_1 | 181 | 186 | PF01111 | 0.368 | 
| DOC_CYCLIN_yClb3_PxF_3 | 21 | 29 | PF00134 | 0.621 | 
| DOC_MAPK_gen_1 | 46 | 56 | PF00069 | 0.376 | 
| DOC_MAPK_gen_1 | 72 | 79 | PF00069 | 0.323 | 
| DOC_MAPK_MEF2A_6 | 122 | 131 | PF00069 | 0.403 | 
| DOC_PP4_FxxP_1 | 18 | 21 | PF00568 | 0.671 | 
| DOC_PP4_FxxP_1 | 181 | 184 | PF00568 | 0.334 | 
| DOC_PP4_FxxP_1 | 249 | 252 | PF00568 | 0.504 | 
| DOC_USP7_MATH_1 | 213 | 217 | PF00917 | 0.537 | 
| DOC_USP7_MATH_1 | 8 | 12 | PF00917 | 0.611 | 
| DOC_WW_Pin1_4 | 1 | 6 | PF00397 | 0.635 | 
| DOC_WW_Pin1_4 | 180 | 185 | PF00397 | 0.366 | 
| DOC_WW_Pin1_4 | 285 | 290 | PF00397 | 0.571 | 
| DOC_WW_Pin1_4 | 9 | 14 | PF00397 | 0.580 | 
| LIG_14-3-3_CanoR_1 | 150 | 156 | PF00244 | 0.542 | 
| LIG_14-3-3_CanoR_1 | 193 | 202 | PF00244 | 0.424 | 
| LIG_14-3-3_CanoR_1 | 32 | 40 | PF00244 | 0.488 | 
| LIG_14-3-3_CanoR_1 | 49 | 56 | PF00244 | 0.447 | 
| LIG_Actin_WH2_2 | 135 | 152 | PF00022 | 0.495 | 
| LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.691 | 
| LIG_BRCT_BRCA1_1 | 14 | 18 | PF00533 | 0.693 | 
| LIG_BRCT_BRCA1_1 | 276 | 280 | PF00533 | 0.697 | 
| LIG_BRCT_BRCA1_1 | 283 | 287 | PF00533 | 0.680 | 
| LIG_FHA_1 | 194 | 200 | PF00498 | 0.443 | 
| LIG_FHA_1 | 233 | 239 | PF00498 | 0.457 | 
| LIG_FHA_1 | 49 | 55 | PF00498 | 0.432 | 
| LIG_FHA_1 | 79 | 85 | PF00498 | 0.447 | 
| LIG_FHA_2 | 152 | 158 | PF00498 | 0.552 | 
| LIG_LIR_Apic_2 | 15 | 21 | PF02991 | 0.656 | 
| LIG_LIR_Apic_2 | 180 | 184 | PF02991 | 0.344 | 
| LIG_LIR_Apic_2 | 216 | 221 | PF02991 | 0.506 | 
| LIG_LIR_Gen_1 | 134 | 145 | PF02991 | 0.502 | 
| LIG_LIR_Gen_1 | 197 | 206 | PF02991 | 0.475 | 
| LIG_LIR_Gen_1 | 212 | 221 | PF02991 | 0.531 | 
| LIG_LIR_Gen_1 | 240 | 249 | PF02991 | 0.499 | 
| LIG_LIR_Nem_3 | 134 | 140 | PF02991 | 0.502 | 
| LIG_LIR_Nem_3 | 197 | 203 | PF02991 | 0.464 | 
| LIG_LIR_Nem_3 | 212 | 217 | PF02991 | 0.440 | 
| LIG_LIR_Nem_3 | 240 | 245 | PF02991 | 0.487 | 
| LIG_LIR_Nem_3 | 27 | 33 | PF02991 | 0.499 | 
| LIG_LIR_Nem_3 | 284 | 290 | PF02991 | 0.681 | 
| LIG_OCRL_FandH_1 | 241 | 253 | PF00620 | 0.505 | 
| LIG_Pex14_2 | 139 | 143 | PF04695 | 0.509 | 
| LIG_Pex14_2 | 177 | 181 | PF04695 | 0.331 | 
| LIG_Pex14_2 | 214 | 218 | PF04695 | 0.521 | 
| LIG_SH2_CRK | 200 | 204 | PF00017 | 0.510 | 
| LIG_SH2_SRC | 22 | 25 | PF00017 | 0.644 | 
| LIG_SH2_STAT5 | 22 | 25 | PF00017 | 0.589 | 
| LIG_SH2_STAT5 | 244 | 247 | PF00017 | 0.485 | 
| LIG_SH2_STAT5 | 30 | 33 | PF00017 | 0.397 | 
| LIG_SH2_STAT5 | 43 | 46 | PF00017 | 0.270 | 
| LIG_SH3_3 | 18 | 24 | PF00018 | 0.644 | 
| LIG_SH3_3 | 2 | 8 | PF00018 | 0.635 | 
| LIG_SUMO_SIM_anti_2 | 126 | 131 | PF11976 | 0.496 | 
| LIG_SUMO_SIM_par_1 | 123 | 128 | PF11976 | 0.488 | 
| LIG_TRAF2_1 | 165 | 168 | PF00917 | 0.553 | 
| LIG_TYR_ITIM | 198 | 203 | PF00017 | 0.466 | 
| LIG_WRC_WIRS_1 | 178 | 183 | PF05994 | 0.348 | 
| LIG_WRC_WIRS_1 | 23 | 28 | PF05994 | 0.580 | 
| MOD_CDK_SPxxK_3 | 285 | 292 | PF00069 | 0.687 | 
| MOD_CK1_1 | 12 | 18 | PF00069 | 0.619 | 
| MOD_CK1_1 | 151 | 157 | PF00069 | 0.546 | 
| MOD_CK1_1 | 180 | 186 | PF00069 | 0.368 | 
| MOD_CK1_1 | 216 | 222 | PF00069 | 0.574 | 
| MOD_CK1_1 | 278 | 284 | PF00069 | 0.599 | 
| MOD_CK1_1 | 3 | 9 | PF00069 | 0.678 | 
| MOD_CK2_1 | 151 | 157 | PF00069 | 0.546 | 
| MOD_CK2_1 | 216 | 222 | PF00069 | 0.518 | 
| MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.536 | 
| MOD_GlcNHglycan | 281 | 284 | PF01048 | 0.610 | 
| MOD_GlcNHglycan | 35 | 38 | PF01048 | 0.501 | 
| MOD_GSK3_1 | 209 | 216 | PF00069 | 0.495 | 
| MOD_GSK3_1 | 274 | 281 | PF00069 | 0.612 | 
| MOD_GSK3_1 | 4 | 11 | PF00069 | 0.619 | 
| MOD_GSK3_1 | 50 | 57 | PF00069 | 0.354 | 
| MOD_N-GLC_1 | 109 | 114 | PF02516 | 0.479 | 
| MOD_NEK2_1 | 131 | 136 | PF00069 | 0.398 | 
| MOD_NEK2_1 | 145 | 150 | PF00069 | 0.372 | 
| MOD_NEK2_1 | 177 | 182 | PF00069 | 0.347 | 
| MOD_NEK2_1 | 194 | 199 | PF00069 | 0.346 | 
| MOD_NEK2_1 | 201 | 206 | PF00069 | 0.481 | 
| MOD_NEK2_1 | 31 | 36 | PF00069 | 0.505 | 
| MOD_NEK2_1 | 50 | 55 | PF00069 | 0.150 | 
| MOD_NEK2_1 | 79 | 84 | PF00069 | 0.340 | 
| MOD_PIKK_1 | 264 | 270 | PF00454 | 0.633 | 
| MOD_PIKK_1 | 31 | 37 | PF00454 | 0.488 | 
| MOD_PKA_2 | 31 | 37 | PF00069 | 0.488 | 
| MOD_PKA_2 | 48 | 54 | PF00069 | 0.447 | 
| MOD_Plk_4 | 194 | 200 | PF00069 | 0.439 | 
| MOD_Plk_4 | 213 | 219 | PF00069 | 0.518 | 
| MOD_Plk_4 | 275 | 281 | PF00069 | 0.667 | 
| MOD_Plk_4 | 50 | 56 | PF00069 | 0.352 | 
| MOD_ProDKin_1 | 1 | 7 | PF00069 | 0.633 | 
| MOD_ProDKin_1 | 180 | 186 | PF00069 | 0.368 | 
| MOD_ProDKin_1 | 285 | 291 | PF00069 | 0.570 | 
| MOD_ProDKin_1 | 9 | 15 | PF00069 | 0.579 | 
| MOD_SUMO_for_1 | 88 | 91 | PF00179 | 0.447 | 
| TRG_ENDOCYTIC_2 | 200 | 203 | PF00928 | 0.471 | 
| TRG_ENDOCYTIC_2 | 30 | 33 | PF00928 | 0.440 | 
| TRG_ER_diArg_1 | 173 | 175 | PF00400 | 0.485 | 
| TRG_ER_diArg_1 | 28 | 30 | PF00400 | 0.500 | 
| TRG_NES_CRM1_1 | 133 | 147 | PF08389 | 0.459 | 
| TRG_NES_CRM1_1 | 230 | 240 | PF08389 | 0.497 | 
| TRG_NLS_Bipartite_1 | 247 | 267 | PF00514 | 0.441 | 
| TRG_NLS_Bipartite_1 | 28 | 50 | PF00514 | 0.362 | 
| TRG_NLS_MonoExtN_4 | 261 | 267 | PF00514 | 0.484 | 
| Protein | Taxonomy | Sequence identity | Coverage | 
|---|---|---|---|
| A0A0N1PFK2 | Leptomonas seymouri | 77% | 100% | 
| A0A1X0NWC7 | Trypanosomatidae | 33% | 100% | 
| A0A422N086 | Trypanosoma rangeli | 35% | 100% | 
| A4HK57 | Leishmania braziliensis | 93% | 100% | 
| A4I7P3 | Leishmania infantum | 100% | 100% | 
| D0A9U6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% | 
| E9B2K0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% | 
| Q4Q5K6 | Leishmania major | 95% | 100% | 
| V5BFB1 | Trypanosoma cruzi | 35% | 100% |