| 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: 12 |
| NetGPI | no | yes: 0, no: 12 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005737 | cytoplasm | 2 | 2 |
| GO:0110165 | cellular anatomical entity | 1 | 3 |
| GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: Q4Q9N3
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0003824 | catalytic activity | 1 | 13 |
| GO:0004721 | phosphoprotein phosphatase activity | 3 | 13 |
| GO:0004722 | protein serine/threonine phosphatase activity | 4 | 13 |
| GO:0005488 | binding | 1 | 13 |
| GO:0016787 | hydrolase activity | 2 | 13 |
| GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 13 |
| GO:0016791 | phosphatase activity | 5 | 13 |
| GO:0017018 | myosin phosphatase activity | 5 | 13 |
| GO:0042578 | phosphoric ester hydrolase activity | 4 | 13 |
| GO:0043167 | ion binding | 2 | 13 |
| GO:0043169 | cation binding | 3 | 13 |
| GO:0046872 | metal ion binding | 4 | 13 |
| GO:0140096 | catalytic activity, acting on a protein | 2 | 13 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_MEL_PAP_1 | 352 | 358 | PF00089 | 0.292 |
| CLV_NRD_NRD_1 | 174 | 176 | PF00675 | 0.277 |
| CLV_NRD_NRD_1 | 71 | 73 | PF00675 | 0.456 |
| CLV_NRD_NRD_1 | 74 | 76 | PF00675 | 0.430 |
| CLV_NRD_NRD_1 | 80 | 82 | PF00675 | 0.378 |
| CLV_PCSK_FUR_1 | 72 | 76 | PF00082 | 0.459 |
| CLV_PCSK_KEX2_1 | 73 | 75 | PF00082 | 0.439 |
| CLV_PCSK_KEX2_1 | 82 | 84 | PF00082 | 0.421 |
| CLV_PCSK_PC1ET2_1 | 73 | 75 | PF00082 | 0.475 |
| CLV_PCSK_PC1ET2_1 | 82 | 84 | PF00082 | 0.394 |
| CLV_PCSK_SKI1_1 | 155 | 159 | PF00082 | 0.286 |
| CLV_PCSK_SKI1_1 | 311 | 315 | PF00082 | 0.349 |
| DEG_SPOP_SBC_1 | 164 | 168 | PF00917 | 0.464 |
| DOC_CKS1_1 | 30 | 35 | PF01111 | 0.611 |
| DOC_MAPK_gen_1 | 155 | 164 | PF00069 | 0.534 |
| DOC_MAPK_gen_1 | 342 | 351 | PF00069 | 0.464 |
| DOC_MAPK_gen_1 | 81 | 89 | PF00069 | 0.415 |
| DOC_MAPK_MEF2A_6 | 345 | 353 | PF00069 | 0.464 |
| DOC_PP4_FxxP_1 | 213 | 216 | PF00568 | 0.443 |
| DOC_USP7_MATH_1 | 3 | 7 | PF00917 | 0.749 |
| DOC_USP7_MATH_1 | 328 | 332 | PF00917 | 0.439 |
| DOC_WW_Pin1_4 | 277 | 282 | PF00397 | 0.558 |
| DOC_WW_Pin1_4 | 29 | 34 | PF00397 | 0.607 |
| DOC_WW_Pin1_4 | 324 | 329 | PF00397 | 0.437 |
| DOC_WW_Pin1_4 | 57 | 62 | PF00397 | 0.449 |
| LIG_14-3-3_CanoR_1 | 198 | 203 | PF00244 | 0.543 |
| LIG_14-3-3_CanoR_1 | 355 | 362 | PF00244 | 0.367 |
| LIG_14-3-3_CanoR_1 | 4 | 8 | PF00244 | 0.718 |
| LIG_14-3-3_CanoR_1 | 74 | 79 | PF00244 | 0.435 |
| LIG_14-3-3_CanoR_1 | 81 | 87 | PF00244 | 0.410 |
| LIG_BIR_III_4 | 340 | 344 | PF00653 | 0.443 |
| LIG_BRCT_BRCA1_1 | 200 | 204 | PF00533 | 0.503 |
| LIG_BRCT_BRCA1_1 | 50 | 54 | PF00533 | 0.432 |
| LIG_BRCT_BRCA1_2 | 50 | 56 | PF00533 | 0.436 |
| LIG_FHA_1 | 152 | 158 | PF00498 | 0.549 |
| LIG_FHA_1 | 166 | 172 | PF00498 | 0.313 |
| LIG_FHA_1 | 253 | 259 | PF00498 | 0.464 |
| LIG_FHA_1 | 348 | 354 | PF00498 | 0.466 |
| LIG_FHA_1 | 43 | 49 | PF00498 | 0.527 |
| LIG_FHA_2 | 30 | 36 | PF00498 | 0.600 |
| LIG_FHA_2 | 356 | 362 | PF00498 | 0.369 |
| LIG_LIR_Apic_2 | 29 | 33 | PF02991 | 0.498 |
| LIG_LIR_Apic_2 | 301 | 305 | PF02991 | 0.492 |
| LIG_LIR_Gen_1 | 150 | 161 | PF02991 | 0.466 |
| LIG_LIR_Gen_1 | 327 | 336 | PF02991 | 0.444 |
| LIG_LIR_Gen_1 | 85 | 93 | PF02991 | 0.384 |
| LIG_LIR_Nem_3 | 150 | 156 | PF02991 | 0.466 |
| LIG_LIR_Nem_3 | 85 | 89 | PF02991 | 0.414 |
| LIG_MLH1_MIPbox_1 | 200 | 204 | PF16413 | 0.383 |
| LIG_Pex14_2 | 213 | 217 | PF04695 | 0.443 |
| LIG_Pex14_2 | 259 | 263 | PF04695 | 0.464 |
| LIG_RPA_C_Fungi | 257 | 269 | PF08784 | 0.364 |
| LIG_SH2_CRK | 102 | 106 | PF00017 | 0.295 |
| LIG_SH2_CRK | 153 | 157 | PF00017 | 0.422 |
| LIG_SH2_PTP2 | 302 | 305 | PF00017 | 0.324 |
| LIG_SH2_SRC | 302 | 305 | PF00017 | 0.324 |
| LIG_SH2_STAP1 | 153 | 157 | PF00017 | 0.444 |
| LIG_SH2_STAT5 | 153 | 156 | PF00017 | 0.444 |
| LIG_SH2_STAT5 | 203 | 206 | PF00017 | 0.404 |
| LIG_SH2_STAT5 | 302 | 305 | PF00017 | 0.295 |
| LIG_SH3_3 | 5 | 11 | PF00018 | 0.720 |
| LIG_SH3_4 | 58 | 65 | PF00018 | 0.639 |
| LIG_SUMO_SIM_anti_2 | 191 | 198 | PF11976 | 0.324 |
| LIG_SUMO_SIM_anti_2 | 249 | 256 | PF11976 | 0.364 |
| LIG_SUMO_SIM_anti_2 | 347 | 354 | PF11976 | 0.325 |
| LIG_SUMO_SIM_par_1 | 347 | 354 | PF11976 | 0.325 |
| LIG_TRAF2_1 | 244 | 247 | PF00917 | 0.366 |
| LIG_TRAF2_1 | 358 | 361 | PF00917 | 0.408 |
| LIG_TRAF2_2 | 244 | 249 | PF00917 | 0.412 |
| MOD_CDK_SPxK_1 | 57 | 63 | PF00069 | 0.547 |
| MOD_CDK_SPxxK_3 | 277 | 284 | PF00069 | 0.444 |
| MOD_CK1_1 | 29 | 35 | PF00069 | 0.615 |
| MOD_CK1_1 | 354 | 360 | PF00069 | 0.391 |
| MOD_CK2_1 | 354 | 360 | PF00069 | 0.391 |
| MOD_CK2_1 | 82 | 88 | PF00069 | 0.419 |
| MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.641 |
| MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.295 |
| MOD_GlcNHglycan | 292 | 295 | PF01048 | 0.355 |
| MOD_GSK3_1 | 324 | 331 | PF00069 | 0.314 |
| MOD_GSK3_1 | 347 | 354 | PF00069 | 0.327 |
| MOD_GSK3_1 | 360 | 367 | PF00069 | 0.359 |
| MOD_N-GLC_1 | 198 | 203 | PF02516 | 0.210 |
| MOD_N-GLC_1 | 363 | 368 | PF02516 | 0.532 |
| MOD_NEK2_1 | 135 | 140 | PF00069 | 0.378 |
| MOD_NEK2_1 | 189 | 194 | PF00069 | 0.357 |
| MOD_NEK2_1 | 290 | 295 | PF00069 | 0.324 |
| MOD_NEK2_1 | 362 | 367 | PF00069 | 0.402 |
| MOD_NEK2_2 | 170 | 175 | PF00069 | 0.422 |
| MOD_NEK2_2 | 92 | 97 | PF00069 | 0.325 |
| MOD_NMyristoyl | 1 | 7 | PF02799 | 0.617 |
| MOD_PIKK_1 | 262 | 268 | PF00454 | 0.298 |
| MOD_PK_1 | 74 | 80 | PF00069 | 0.522 |
| MOD_PKA_1 | 74 | 80 | PF00069 | 0.434 |
| MOD_PKA_1 | 82 | 88 | PF00069 | 0.405 |
| MOD_PKA_2 | 239 | 245 | PF00069 | 0.340 |
| MOD_PKA_2 | 3 | 9 | PF00069 | 0.715 |
| MOD_PKA_2 | 354 | 360 | PF00069 | 0.362 |
| MOD_PKA_2 | 74 | 80 | PF00069 | 0.434 |
| MOD_PKA_2 | 82 | 88 | PF00069 | 0.405 |
| MOD_PKB_1 | 72 | 80 | PF00069 | 0.439 |
| MOD_Plk_1 | 198 | 204 | PF00069 | 0.410 |
| MOD_Plk_1 | 347 | 353 | PF00069 | 0.295 |
| MOD_Plk_1 | 92 | 98 | PF00069 | 0.324 |
| MOD_Plk_4 | 119 | 125 | PF00069 | 0.365 |
| MOD_Plk_4 | 328 | 334 | PF00069 | 0.295 |
| MOD_Plk_4 | 82 | 88 | PF00069 | 0.426 |
| MOD_Plk_4 | 92 | 98 | PF00069 | 0.324 |
| MOD_ProDKin_1 | 277 | 283 | PF00069 | 0.456 |
| MOD_ProDKin_1 | 29 | 35 | PF00069 | 0.615 |
| MOD_ProDKin_1 | 324 | 330 | PF00069 | 0.287 |
| MOD_ProDKin_1 | 57 | 63 | PF00069 | 0.467 |
| MOD_SUMO_rev_2 | 293 | 300 | PF00179 | 0.310 |
| MOD_SUMO_rev_2 | 35 | 44 | PF00179 | 0.512 |
| TRG_DiLeu_BaEn_2 | 92 | 98 | PF01217 | 0.324 |
| TRG_ENDOCYTIC_2 | 102 | 105 | PF00928 | 0.335 |
| TRG_ENDOCYTIC_2 | 153 | 156 | PF00928 | 0.422 |
| TRG_ER_diArg_1 | 197 | 200 | PF00400 | 0.308 |
| TRG_ER_diArg_1 | 72 | 75 | PF00400 | 0.448 |
| TRG_ER_diArg_1 | 80 | 83 | PF00400 | 0.384 |
| TRG_NLS_MonoExtN_4 | 72 | 77 | PF00514 | 0.504 |
| TRG_Pf-PMV_PEXEL_1 | 311 | 315 | PF00026 | 0.444 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1I2Z6 | Leptomonas seymouri | 80% | 100% |
| A0A0N1IH92 | Leptomonas seymouri | 27% | 100% |
| A0A0S4IN49 | Bodo saltans | 37% | 100% |
| A0A0S4JK95 | Bodo saltans | 62% | 100% |
| A0A0S4JS91 | Bodo saltans | 62% | 100% |
| A0A1X0NY52 | Trypanosomatidae | 61% | 96% |
| A0A1X0P4F0 | Trypanosomatidae | 26% | 100% |
| A0A1X0P973 | Trypanosomatidae | 28% | 100% |
| A0A3Q8IBW1 | Leishmania donovani | 96% | 100% |
| A0A3R7N5R3 | Trypanosoma rangeli | 28% | 100% |
| A0A3R7RFR7 | Trypanosoma rangeli | 28% | 100% |
| A0A422P4L0 | Trypanosoma rangeli | 66% | 100% |
| A4HEA8 | Leishmania braziliensis | 92% | 99% |
| A4I1Q4 | Leishmania infantum | 96% | 100% |
| B3MTI8 | Drosophila ananassae | 33% | 100% |
| B3P5D3 | Drosophila erecta | 37% | 100% |
| B4G653 | Drosophila persimilis | 34% | 100% |
| B4HZE7 | Drosophila sechellia | 37% | 100% |
| B4JYN1 | Drosophila grimshawi | 35% | 100% |
| B4K616 | Drosophila mojavensis | 38% | 100% |
| B4M5T5 | Drosophila virilis | 37% | 100% |
| B4NBL6 | Drosophila willistoni | 39% | 100% |
| B4PPK3 | Drosophila yakuba | 37% | 100% |
| B4R089 | Drosophila simulans | 37% | 100% |
| C9ZKA8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 65% | 100% |
| C9ZN10 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
| D0A5X5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
| E9AXT8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
| O64730 | Arabidopsis thaliana | 30% | 100% |
| P38797 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 32% | 100% |
| Q09189 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 32% | 100% |
| Q29AP0 | Drosophila pseudoobscura pseudoobscura | 36% | 100% |
| Q339D2 | Oryza sativa subsp. japonica | 31% | 79% |
| Q5U3N5 | Danio rerio | 37% | 100% |
| Q6GR25 | Xenopus laevis | 37% | 100% |
| Q6H7J3 | Oryza sativa subsp. japonica | 32% | 100% |
| Q6H7J4 | Oryza sativa subsp. japonica | 28% | 100% |
| Q6NVE9 | Mus musculus | 38% | 100% |
| Q8NI37 | Homo sapiens | 38% | 100% |
| Q942P9 | Oryza sativa subsp. japonica | 29% | 100% |
| Q9LVQ8 | Arabidopsis thaliana | 34% | 89% |
| Q9SUK9 | Arabidopsis thaliana | 32% | 79% |
| Q9VAH4 | Drosophila melanogaster | 37% | 100% |
| V5AT69 | Trypanosoma cruzi | 27% | 100% |
| V5AUW7 | Trypanosoma cruzi | 31% | 100% |
| V5BMI3 | Trypanosoma cruzi | 64% | 85% |