| 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: 6 |
| NetGPI | no | yes: 0, no: 6 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005737 | cytoplasm | 2 | 1 |
| GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HTG0
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006470 | protein dephosphorylation | 5 | 7 |
| GO:0006793 | phosphorus metabolic process | 3 | 7 |
| GO:0006796 | phosphate-containing compound metabolic process | 4 | 7 |
| GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
| GO:0008152 | metabolic process | 1 | 7 |
| GO:0009987 | cellular process | 1 | 7 |
| GO:0016311 | dephosphorylation | 5 | 7 |
| GO:0019538 | protein metabolic process | 3 | 7 |
| GO:0036211 | protein modification process | 4 | 7 |
| GO:0043170 | macromolecule metabolic process | 3 | 7 |
| GO:0043412 | macromolecule modification | 4 | 7 |
| GO:0044237 | cellular metabolic process | 2 | 7 |
| GO:0044238 | primary metabolic process | 2 | 7 |
| GO:0071704 | organic substance metabolic process | 2 | 7 |
| GO:1901564 | organonitrogen compound metabolic process | 3 | 7 |
| GO:0009966 | regulation of signal transduction | 4 | 1 |
| GO:0009968 | negative regulation of signal transduction | 5 | 1 |
| GO:0010646 | regulation of cell communication | 4 | 1 |
| GO:0010648 | negative regulation of cell communication | 5 | 1 |
| GO:0023051 | regulation of signaling | 3 | 1 |
| GO:0023057 | negative regulation of signaling | 4 | 1 |
| GO:0043408 | regulation of MAPK cascade | 6 | 1 |
| GO:0043409 | negative regulation of MAPK cascade | 7 | 1 |
| GO:0048519 | negative regulation of biological process | 3 | 1 |
| GO:0048523 | negative regulation of cellular process | 4 | 1 |
| GO:0048583 | regulation of response to stimulus | 3 | 1 |
| GO:0048585 | negative regulation of response to stimulus | 4 | 1 |
| GO:0050789 | regulation of biological process | 2 | 1 |
| GO:0050794 | regulation of cellular process | 3 | 1 |
| GO:0065007 | biological regulation | 1 | 1 |
| GO:1902531 | regulation of intracellular signal transduction | 5 | 1 |
| GO:1902532 | negative regulation of intracellular signal transduction | 6 | 1 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0003824 | catalytic activity | 1 | 7 |
| GO:0004721 | phosphoprotein phosphatase activity | 3 | 7 |
| GO:0004722 | protein serine/threonine phosphatase activity | 4 | 6 |
| GO:0004725 | protein tyrosine phosphatase activity | 4 | 5 |
| GO:0008138 | protein tyrosine/serine/threonine phosphatase activity | 4 | 7 |
| GO:0016787 | hydrolase activity | 2 | 7 |
| GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 7 |
| GO:0016791 | phosphatase activity | 5 | 7 |
| GO:0017018 | myosin phosphatase activity | 5 | 6 |
| GO:0042578 | phosphoric ester hydrolase activity | 4 | 7 |
| GO:0140096 | catalytic activity, acting on a protein | 2 | 7 |
| GO:0008330 | protein tyrosine/threonine phosphatase activity | 4 | 1 |
| GO:0017017 | MAP kinase tyrosine/serine/threonine phosphatase activity | 5 | 1 |
| GO:0033549 | MAP kinase phosphatase activity | 4 | 1 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 287 | 291 | PF00656 | 0.607 |
| CLV_C14_Caspase3-7 | 292 | 296 | PF00656 | 0.553 |
| CLV_C14_Caspase3-7 | 62 | 66 | PF00656 | 0.303 |
| CLV_NRD_NRD_1 | 179 | 181 | PF00675 | 0.332 |
| CLV_NRD_NRD_1 | 193 | 195 | PF00675 | 0.303 |
| CLV_NRD_NRD_1 | 207 | 209 | PF00675 | 0.381 |
| CLV_PCSK_FUR_1 | 205 | 209 | PF00082 | 0.378 |
| CLV_PCSK_KEX2_1 | 179 | 181 | PF00082 | 0.303 |
| CLV_PCSK_KEX2_1 | 207 | 209 | PF00082 | 0.381 |
| CLV_PCSK_KEX2_1 | 234 | 236 | PF00082 | 0.395 |
| CLV_PCSK_PC1ET2_1 | 234 | 236 | PF00082 | 0.442 |
| CLV_PCSK_SKI1_1 | 152 | 156 | PF00082 | 0.303 |
| CLV_PCSK_SKI1_1 | 229 | 233 | PF00082 | 0.465 |
| CLV_PCSK_SKI1_1 | 317 | 321 | PF00082 | 0.658 |
| CLV_PCSK_SKI1_1 | 344 | 348 | PF00082 | 0.512 |
| CLV_PCSK_SKI1_1 | 380 | 384 | PF00082 | 0.588 |
| CLV_PCSK_SKI1_1 | 392 | 396 | PF00082 | 0.508 |
| DOC_CYCLIN_RxL_1 | 226 | 233 | PF00134 | 0.465 |
| DOC_MAPK_gen_1 | 150 | 158 | PF00069 | 0.420 |
| DOC_MAPK_gen_1 | 194 | 202 | PF00069 | 0.464 |
| DOC_MAPK_MEF2A_6 | 180 | 189 | PF00069 | 0.303 |
| DOC_PP2B_LxvP_1 | 372 | 375 | PF13499 | 0.403 |
| DOC_USP7_MATH_1 | 221 | 225 | PF00917 | 0.444 |
| DOC_USP7_MATH_1 | 24 | 28 | PF00917 | 0.634 |
| DOC_USP7_MATH_1 | 284 | 288 | PF00917 | 0.794 |
| DOC_USP7_MATH_1 | 293 | 297 | PF00917 | 0.608 |
| DOC_USP7_MATH_1 | 319 | 323 | PF00917 | 0.606 |
| DOC_USP7_MATH_1 | 33 | 37 | PF00917 | 0.634 |
| DOC_USP7_MATH_1 | 332 | 336 | PF00917 | 0.653 |
| DOC_WW_Pin1_4 | 20 | 25 | PF00397 | 0.653 |
| DOC_WW_Pin1_4 | 29 | 34 | PF00397 | 0.581 |
| DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.595 |
| LIG_14-3-3_CanoR_1 | 150 | 158 | PF00244 | 0.303 |
| LIG_14-3-3_CanoR_1 | 207 | 216 | PF00244 | 0.427 |
| LIG_14-3-3_CanoR_1 | 240 | 246 | PF00244 | 0.439 |
| LIG_14-3-3_CanoR_1 | 269 | 273 | PF00244 | 0.570 |
| LIG_14-3-3_CanoR_1 | 277 | 283 | PF00244 | 0.606 |
| LIG_14-3-3_CanoR_1 | 338 | 347 | PF00244 | 0.463 |
| LIG_Actin_RPEL_3 | 143 | 162 | PF02755 | 0.303 |
| LIG_BIR_III_4 | 427 | 431 | PF00653 | 0.632 |
| LIG_BRCT_BRCA1_1 | 198 | 202 | PF00533 | 0.431 |
| LIG_BRCT_BRCA1_1 | 363 | 367 | PF00533 | 0.599 |
| LIG_BRCT_BRCA1_1 | 400 | 404 | PF00533 | 0.519 |
| LIG_Clathr_ClatBox_1 | 297 | 301 | PF01394 | 0.558 |
| LIG_FHA_1 | 105 | 111 | PF00498 | 0.307 |
| LIG_FHA_1 | 115 | 121 | PF00498 | 0.358 |
| LIG_FHA_1 | 153 | 159 | PF00498 | 0.324 |
| LIG_FHA_1 | 242 | 248 | PF00498 | 0.444 |
| LIG_FHA_1 | 432 | 438 | PF00498 | 0.631 |
| LIG_FHA_1 | 50 | 56 | PF00498 | 0.450 |
| LIG_FHA_1 | 97 | 103 | PF00498 | 0.327 |
| LIG_FHA_2 | 351 | 357 | PF00498 | 0.353 |
| LIG_FHA_2 | 417 | 423 | PF00498 | 0.698 |
| LIG_GBD_Chelix_1 | 298 | 306 | PF00786 | 0.546 |
| LIG_LIR_Gen_1 | 206 | 216 | PF02991 | 0.429 |
| LIG_LIR_Gen_1 | 364 | 375 | PF02991 | 0.590 |
| LIG_LIR_Gen_1 | 56 | 63 | PF02991 | 0.365 |
| LIG_LIR_Nem_3 | 206 | 212 | PF02991 | 0.375 |
| LIG_LIR_Nem_3 | 364 | 370 | PF02991 | 0.595 |
| LIG_LIR_Nem_3 | 56 | 60 | PF02991 | 0.365 |
| LIG_LIR_Nem_3 | 86 | 91 | PF02991 | 0.303 |
| LIG_Pex14_2 | 278 | 282 | PF04695 | 0.609 |
| LIG_REV1ctd_RIR_1 | 349 | 359 | PF16727 | 0.416 |
| LIG_SH2_GRB2like | 163 | 166 | PF00017 | 0.303 |
| LIG_SH2_STAT5 | 160 | 163 | PF00017 | 0.303 |
| LIG_SH2_STAT5 | 175 | 178 | PF00017 | 0.303 |
| LIG_SH2_STAT5 | 245 | 248 | PF00017 | 0.460 |
| LIG_SH2_STAT5 | 59 | 62 | PF00017 | 0.365 |
| LIG_SH2_STAT5 | 79 | 82 | PF00017 | 0.183 |
| LIG_SH3_3 | 280 | 286 | PF00018 | 0.670 |
| LIG_SH3_3 | 434 | 440 | PF00018 | 0.623 |
| LIG_SH3_3 | 444 | 450 | PF00018 | 0.528 |
| LIG_TRAF2_1 | 201 | 204 | PF00917 | 0.420 |
| LIG_TRAF2_1 | 84 | 87 | PF00917 | 0.347 |
| LIG_WRC_WIRS_1 | 97 | 102 | PF05994 | 0.303 |
| MOD_CDC14_SPxK_1 | 32 | 35 | PF00782 | 0.661 |
| MOD_CDK_SPxK_1 | 29 | 35 | PF00069 | 0.664 |
| MOD_CK1_1 | 268 | 274 | PF00069 | 0.723 |
| MOD_CK1_1 | 27 | 33 | PF00069 | 0.609 |
| MOD_CK1_1 | 399 | 405 | PF00069 | 0.492 |
| MOD_CK2_1 | 165 | 171 | PF00069 | 0.303 |
| MOD_CK2_1 | 198 | 204 | PF00069 | 0.602 |
| MOD_CK2_1 | 350 | 356 | PF00069 | 0.351 |
| MOD_CK2_1 | 41 | 47 | PF00069 | 0.513 |
| MOD_CK2_1 | 416 | 422 | PF00069 | 0.641 |
| MOD_CK2_1 | 81 | 87 | PF00069 | 0.347 |
| MOD_GlcNHglycan | 103 | 107 | PF01048 | 0.320 |
| MOD_GlcNHglycan | 152 | 155 | PF01048 | 0.283 |
| MOD_GlcNHglycan | 278 | 281 | PF01048 | 0.648 |
| MOD_GlcNHglycan | 329 | 333 | PF01048 | 0.573 |
| MOD_GlcNHglycan | 363 | 366 | PF01048 | 0.471 |
| MOD_GlcNHglycan | 375 | 378 | PF01048 | 0.302 |
| MOD_GlcNHglycan | 422 | 425 | PF01048 | 0.641 |
| MOD_GSK3_1 | 148 | 155 | PF00069 | 0.285 |
| MOD_GSK3_1 | 161 | 168 | PF00069 | 0.335 |
| MOD_GSK3_1 | 20 | 27 | PF00069 | 0.594 |
| MOD_GSK3_1 | 203 | 210 | PF00069 | 0.414 |
| MOD_GSK3_1 | 284 | 291 | PF00069 | 0.674 |
| MOD_GSK3_1 | 29 | 36 | PF00069 | 0.592 |
| MOD_GSK3_1 | 3 | 10 | PF00069 | 0.602 |
| MOD_GSK3_1 | 328 | 335 | PF00069 | 0.625 |
| MOD_GSK3_1 | 338 | 345 | PF00069 | 0.473 |
| MOD_GSK3_1 | 392 | 399 | PF00069 | 0.541 |
| MOD_GSK3_1 | 409 | 416 | PF00069 | 0.657 |
| MOD_N-GLC_1 | 81 | 86 | PF02516 | 0.303 |
| MOD_NEK2_1 | 161 | 166 | PF00069 | 0.303 |
| MOD_NEK2_1 | 196 | 201 | PF00069 | 0.392 |
| MOD_NEK2_1 | 278 | 283 | PF00069 | 0.640 |
| MOD_NEK2_1 | 400 | 405 | PF00069 | 0.488 |
| MOD_NEK2_2 | 33 | 38 | PF00069 | 0.644 |
| MOD_NEK2_2 | 59 | 64 | PF00069 | 0.365 |
| MOD_OFUCOSY | 348 | 354 | PF10250 | 0.345 |
| MOD_PIKK_1 | 221 | 227 | PF00454 | 0.415 |
| MOD_PIKK_1 | 431 | 437 | PF00454 | 0.626 |
| MOD_PIKK_1 | 49 | 55 | PF00454 | 0.363 |
| MOD_PIKK_1 | 81 | 87 | PF00454 | 0.303 |
| MOD_PIKK_1 | 9 | 15 | PF00454 | 0.655 |
| MOD_PKA_1 | 207 | 213 | PF00069 | 0.370 |
| MOD_PKA_2 | 207 | 213 | PF00069 | 0.370 |
| MOD_PKA_2 | 268 | 274 | PF00069 | 0.596 |
| MOD_PKA_2 | 27 | 33 | PF00069 | 0.747 |
| MOD_PKA_2 | 276 | 282 | PF00069 | 0.600 |
| MOD_PKA_2 | 41 | 47 | PF00069 | 0.527 |
| MOD_PKB_1 | 150 | 158 | PF00069 | 0.303 |
| MOD_PKB_1 | 205 | 213 | PF00069 | 0.434 |
| MOD_Plk_1 | 342 | 348 | PF00069 | 0.419 |
| MOD_Plk_2-3 | 198 | 204 | PF00069 | 0.434 |
| MOD_Plk_2-3 | 87 | 93 | PF00069 | 0.303 |
| MOD_Plk_4 | 152 | 158 | PF00069 | 0.303 |
| MOD_Plk_4 | 241 | 247 | PF00069 | 0.443 |
| MOD_Plk_4 | 293 | 299 | PF00069 | 0.641 |
| MOD_Plk_4 | 332 | 338 | PF00069 | 0.642 |
| MOD_Plk_4 | 342 | 348 | PF00069 | 0.461 |
| MOD_Plk_4 | 400 | 406 | PF00069 | 0.590 |
| MOD_ProDKin_1 | 20 | 26 | PF00069 | 0.653 |
| MOD_ProDKin_1 | 29 | 35 | PF00069 | 0.581 |
| MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.595 |
| MOD_SUMO_rev_2 | 86 | 95 | PF00179 | 0.379 |
| TRG_DiLeu_BaEn_2 | 210 | 216 | PF01217 | 0.420 |
| TRG_DiLeu_BaEn_4 | 191 | 197 | PF01217 | 0.303 |
| TRG_ENDOCYTIC_2 | 209 | 212 | PF00928 | 0.369 |
| TRG_ENDOCYTIC_2 | 88 | 91 | PF00928 | 0.303 |
| TRG_ER_diArg_1 | 124 | 127 | PF00400 | 0.365 |
| TRG_ER_diArg_1 | 179 | 181 | PF00400 | 0.303 |
| TRG_ER_diArg_1 | 205 | 208 | PF00400 | 0.441 |
| TRG_Pf-PMV_PEXEL_1 | 194 | 198 | PF00026 | 0.303 |
| TRG_Pf-PMV_PEXEL_1 | 217 | 222 | PF00026 | 0.384 |
| TRG_Pf-PMV_PEXEL_1 | 229 | 233 | PF00026 | 0.402 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N0P9F6 | Leptomonas seymouri | 56% | 85% |
| A0A3S5H628 | Leishmania donovani | 99% | 100% |
| A4H577 | Leishmania braziliensis | 75% | 100% |
| E9AM88 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
| Q4QIF9 | Leishmania major | 91% | 100% |