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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000159 | protein phosphatase type 2A complex | 5 | 1 |
GO:0008287 | protein serine/threonine phosphatase complex | 4 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1903293 | phosphatase complex | 3 | 1 |
Related structures:
AlphaFold database: A4HMY8
Term | Name | Level | Count |
---|---|---|---|
GO:0006470 | protein dephosphorylation | 5 | 1 |
GO:0006793 | phosphorus metabolic process | 3 | 1 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016311 | dephosphorylation | 5 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 12 |
GO:0005509 | calcium ion binding | 5 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043169 | cation binding | 3 | 12 |
GO:0046872 | metal ion binding | 4 | 12 |
GO:0019208 | phosphatase regulator activity | 3 | 1 |
GO:0019888 | protein phosphatase regulator activity | 4 | 1 |
GO:0030234 | enzyme regulator activity | 2 | 1 |
GO:0098772 | molecular function regulator activity | 1 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 274 | 278 | PF00656 | 0.535 |
CLV_C14_Caspase3-7 | 551 | 555 | PF00656 | 0.558 |
CLV_NRD_NRD_1 | 342 | 344 | PF00675 | 0.246 |
CLV_NRD_NRD_1 | 580 | 582 | PF00675 | 0.606 |
CLV_PCSK_KEX2_1 | 342 | 344 | PF00082 | 0.246 |
CLV_PCSK_KEX2_1 | 479 | 481 | PF00082 | 0.314 |
CLV_PCSK_PC1ET2_1 | 479 | 481 | PF00082 | 0.314 |
CLV_PCSK_SKI1_1 | 238 | 242 | PF00082 | 0.543 |
CLV_PCSK_SKI1_1 | 292 | 296 | PF00082 | 0.365 |
CLV_PCSK_SKI1_1 | 301 | 305 | PF00082 | 0.292 |
CLV_PCSK_SKI1_1 | 34 | 38 | PF00082 | 0.599 |
CLV_PCSK_SKI1_1 | 456 | 460 | PF00082 | 0.418 |
CLV_PCSK_SKI1_1 | 608 | 612 | PF00082 | 0.383 |
DEG_APCC_DBOX_1 | 33 | 41 | PF00400 | 0.625 |
DOC_CKS1_1 | 149 | 154 | PF01111 | 0.748 |
DOC_CYCLIN_RxL_1 | 34 | 44 | PF00134 | 0.512 |
DOC_CYCLIN_RxL_1 | 545 | 555 | PF00134 | 0.483 |
DOC_CYCLIN_RxL_1 | 605 | 616 | PF00134 | 0.523 |
DOC_CYCLIN_yCln2_LP_2 | 201 | 207 | PF00134 | 0.731 |
DOC_MAPK_gen_1 | 251 | 259 | PF00069 | 0.536 |
DOC_MAPK_gen_1 | 579 | 587 | PF00069 | 0.516 |
DOC_PP1_RVXF_1 | 405 | 411 | PF00149 | 0.471 |
DOC_PP1_RVXF_1 | 546 | 553 | PF00149 | 0.471 |
DOC_PP1_RVXF_1 | 606 | 613 | PF00149 | 0.485 |
DOC_PP2B_LxvP_1 | 201 | 204 | PF13499 | 0.689 |
DOC_PP4_FxxP_1 | 294 | 297 | PF00568 | 0.322 |
DOC_USP7_MATH_1 | 108 | 112 | PF00917 | 0.730 |
DOC_USP7_MATH_1 | 168 | 172 | PF00917 | 0.622 |
DOC_USP7_MATH_1 | 207 | 211 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 215 | 219 | PF00917 | 0.745 |
DOC_USP7_MATH_1 | 488 | 492 | PF00917 | 0.314 |
DOC_USP7_MATH_1 | 69 | 73 | PF00917 | 0.728 |
DOC_WW_Pin1_4 | 113 | 118 | PF00397 | 0.653 |
DOC_WW_Pin1_4 | 122 | 127 | PF00397 | 0.548 |
DOC_WW_Pin1_4 | 144 | 149 | PF00397 | 0.616 |
DOC_WW_Pin1_4 | 151 | 156 | PF00397 | 0.614 |
DOC_WW_Pin1_4 | 173 | 178 | PF00397 | 0.655 |
DOC_WW_Pin1_4 | 182 | 187 | PF00397 | 0.659 |
DOC_WW_Pin1_4 | 229 | 234 | PF00397 | 0.585 |
DOC_WW_Pin1_4 | 552 | 557 | PF00397 | 0.542 |
DOC_WW_Pin1_4 | 592 | 597 | PF00397 | 0.386 |
DOC_WW_Pin1_4 | 91 | 96 | PF00397 | 0.631 |
LIG_14-3-3_CanoR_1 | 179 | 184 | PF00244 | 0.655 |
LIG_14-3-3_CanoR_1 | 221 | 231 | PF00244 | 0.580 |
LIG_14-3-3_CanoR_1 | 328 | 338 | PF00244 | 0.250 |
LIG_14-3-3_CanoR_1 | 487 | 494 | PF00244 | 0.333 |
LIG_AP2alpha_2 | 616 | 618 | PF02296 | 0.449 |
LIG_APCC_ABBA_1 | 283 | 288 | PF00400 | 0.506 |
LIG_APCC_ABBAyCdc20_2 | 301 | 307 | PF00400 | 0.457 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.663 |
LIG_BIR_III_2 | 88 | 92 | PF00653 | 0.523 |
LIG_BRCT_BRCA1_1 | 290 | 294 | PF00533 | 0.451 |
LIG_Clathr_ClatBox_1 | 459 | 463 | PF01394 | 0.333 |
LIG_deltaCOP1_diTrp_1 | 631 | 635 | PF00928 | 0.366 |
LIG_FHA_1 | 19 | 25 | PF00498 | 0.612 |
LIG_FHA_1 | 218 | 224 | PF00498 | 0.627 |
LIG_FHA_1 | 280 | 286 | PF00498 | 0.448 |
LIG_FHA_1 | 317 | 323 | PF00498 | 0.394 |
LIG_FHA_1 | 389 | 395 | PF00498 | 0.446 |
LIG_FHA_1 | 425 | 431 | PF00498 | 0.413 |
LIG_FHA_1 | 473 | 479 | PF00498 | 0.385 |
LIG_FHA_1 | 60 | 66 | PF00498 | 0.492 |
LIG_FHA_2 | 212 | 218 | PF00498 | 0.651 |
LIG_FHA_2 | 239 | 245 | PF00498 | 0.470 |
LIG_FHA_2 | 356 | 362 | PF00498 | 0.470 |
LIG_FHA_2 | 452 | 458 | PF00498 | 0.314 |
LIG_FHA_2 | 525 | 531 | PF00498 | 0.418 |
LIG_FHA_2 | 584 | 590 | PF00498 | 0.378 |
LIG_FHA_2 | 628 | 634 | PF00498 | 0.387 |
LIG_FHA_2 | 81 | 87 | PF00498 | 0.511 |
LIG_FXI_DFP_1 | 410 | 414 | PF00024 | 0.286 |
LIG_GBD_Chelix_1 | 392 | 400 | PF00786 | 0.246 |
LIG_HCF-1_HBM_1 | 440 | 443 | PF13415 | 0.309 |
LIG_LIR_Apic_2 | 291 | 297 | PF02991 | 0.334 |
LIG_LIR_Apic_2 | 483 | 488 | PF02991 | 0.418 |
LIG_LIR_Gen_1 | 302 | 309 | PF02991 | 0.228 |
LIG_LIR_Gen_1 | 329 | 338 | PF02991 | 0.407 |
LIG_LIR_Gen_1 | 355 | 362 | PF02991 | 0.472 |
LIG_LIR_Gen_1 | 386 | 397 | PF02991 | 0.532 |
LIG_LIR_Gen_1 | 438 | 446 | PF02991 | 0.298 |
LIG_LIR_Gen_1 | 498 | 507 | PF02991 | 0.298 |
LIG_LIR_Gen_1 | 534 | 542 | PF02991 | 0.350 |
LIG_LIR_Gen_1 | 607 | 617 | PF02991 | 0.439 |
LIG_LIR_Gen_1 | 630 | 640 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 302 | 308 | PF02991 | 0.334 |
LIG_LIR_Nem_3 | 329 | 334 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 355 | 359 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 383 | 387 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 435 | 439 | PF02991 | 0.327 |
LIG_LIR_Nem_3 | 440 | 446 | PF02991 | 0.284 |
LIG_LIR_Nem_3 | 498 | 502 | PF02991 | 0.298 |
LIG_LIR_Nem_3 | 607 | 612 | PF02991 | 0.410 |
LIG_LIR_Nem_3 | 630 | 635 | PF02991 | 0.370 |
LIG_MAD2 | 480 | 488 | PF02301 | 0.314 |
LIG_NRBOX | 268 | 274 | PF00104 | 0.531 |
LIG_PALB2_WD40_1 | 517 | 525 | PF16756 | 0.298 |
LIG_PTAP_UEV_1 | 162 | 167 | PF05743 | 0.641 |
LIG_SH2_CRK | 335 | 339 | PF00017 | 0.425 |
LIG_SH2_CRK | 345 | 349 | PF00017 | 0.532 |
LIG_SH2_CRK | 485 | 489 | PF00017 | 0.418 |
LIG_SH2_NCK_1 | 331 | 335 | PF00017 | 0.403 |
LIG_SH2_STAP1 | 20 | 24 | PF00017 | 0.576 |
LIG_SH2_STAP1 | 331 | 335 | PF00017 | 0.390 |
LIG_SH2_STAP1 | 439 | 443 | PF00017 | 0.309 |
LIG_SH2_STAP1 | 562 | 566 | PF00017 | 0.446 |
LIG_SH2_STAP1 | 640 | 644 | PF00017 | 0.372 |
LIG_SH2_STAT5 | 169 | 172 | PF00017 | 0.495 |
LIG_SH2_STAT5 | 20 | 23 | PF00017 | 0.543 |
LIG_SH2_STAT5 | 368 | 371 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 436 | 439 | PF00017 | 0.308 |
LIG_SH2_STAT5 | 443 | 446 | PF00017 | 0.298 |
LIG_SH2_STAT5 | 504 | 507 | PF00017 | 0.298 |
LIG_SH3_2 | 97 | 102 | PF14604 | 0.698 |
LIG_SH3_3 | 116 | 122 | PF00018 | 0.689 |
LIG_SH3_3 | 146 | 152 | PF00018 | 0.659 |
LIG_SH3_3 | 160 | 166 | PF00018 | 0.519 |
LIG_SH3_3 | 201 | 207 | PF00018 | 0.606 |
LIG_SH3_3 | 228 | 234 | PF00018 | 0.628 |
LIG_SH3_3 | 94 | 100 | PF00018 | 0.632 |
LIG_SUMO_SIM_par_1 | 38 | 44 | PF11976 | 0.605 |
LIG_TYR_ITSM | 327 | 334 | PF00017 | 0.440 |
LIG_UBA3_1 | 422 | 428 | PF00899 | 0.532 |
MOD_CDC14_SPxK_1 | 176 | 179 | PF00782 | 0.513 |
MOD_CDK_SPK_2 | 182 | 187 | PF00069 | 0.739 |
MOD_CDK_SPK_2 | 91 | 96 | PF00069 | 0.636 |
MOD_CDK_SPxK_1 | 173 | 179 | PF00069 | 0.507 |
MOD_CDK_SPxxK_3 | 151 | 158 | PF00069 | 0.735 |
MOD_CDK_SPxxK_3 | 95 | 102 | PF00069 | 0.687 |
MOD_CK1_1 | 171 | 177 | PF00069 | 0.507 |
MOD_CK1_1 | 182 | 188 | PF00069 | 0.675 |
MOD_CK1_1 | 472 | 478 | PF00069 | 0.388 |
MOD_CK1_1 | 592 | 598 | PF00069 | 0.480 |
MOD_CK1_1 | 79 | 85 | PF00069 | 0.696 |
MOD_CK2_1 | 211 | 217 | PF00069 | 0.695 |
MOD_CK2_1 | 22 | 28 | PF00069 | 0.547 |
MOD_CK2_1 | 247 | 253 | PF00069 | 0.461 |
MOD_CK2_1 | 357 | 363 | PF00069 | 0.502 |
MOD_CK2_1 | 531 | 537 | PF00069 | 0.298 |
MOD_DYRK1A_RPxSP_1 | 144 | 148 | PF00069 | 0.645 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.694 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.722 |
MOD_GlcNHglycan | 110 | 113 | PF01048 | 0.718 |
MOD_GlcNHglycan | 162 | 166 | PF01048 | 0.607 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.592 |
MOD_GlcNHglycan | 197 | 200 | PF01048 | 0.603 |
MOD_GlcNHglycan | 338 | 341 | PF01048 | 0.240 |
MOD_GlcNHglycan | 43 | 46 | PF01048 | 0.546 |
MOD_GlcNHglycan | 490 | 493 | PF01048 | 0.310 |
MOD_GlcNHglycan | 533 | 536 | PF01048 | 0.312 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.647 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.642 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.513 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.625 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.628 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.493 |
MOD_GSK3_1 | 275 | 282 | PF00069 | 0.493 |
MOD_GSK3_1 | 303 | 310 | PF00069 | 0.302 |
MOD_GSK3_1 | 334 | 341 | PF00069 | 0.480 |
MOD_GSK3_1 | 357 | 364 | PF00069 | 0.427 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.565 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.586 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.644 |
MOD_N-GLC_1 | 103 | 108 | PF02516 | 0.712 |
MOD_N-GLC_1 | 260 | 265 | PF02516 | 0.344 |
MOD_N-GLC_1 | 275 | 280 | PF02516 | 0.295 |
MOD_N-GLC_1 | 604 | 609 | PF02516 | 0.414 |
MOD_NEK2_1 | 188 | 193 | PF00069 | 0.656 |
MOD_NEK2_1 | 19 | 24 | PF00069 | 0.396 |
MOD_NEK2_1 | 211 | 216 | PF00069 | 0.630 |
MOD_NEK2_1 | 222 | 227 | PF00069 | 0.498 |
MOD_NEK2_1 | 338 | 343 | PF00069 | 0.439 |
MOD_NEK2_1 | 347 | 352 | PF00069 | 0.513 |
MOD_NEK2_1 | 41 | 46 | PF00069 | 0.578 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.687 |
MOD_PIKK_1 | 6 | 12 | PF00454 | 0.540 |
MOD_PK_1 | 275 | 281 | PF00069 | 0.340 |
MOD_PKA_1 | 251 | 257 | PF00069 | 0.507 |
MOD_PKA_2 | 215 | 221 | PF00069 | 0.671 |
MOD_Plk_1 | 188 | 194 | PF00069 | 0.632 |
MOD_Plk_1 | 275 | 281 | PF00069 | 0.469 |
MOD_Plk_1 | 562 | 568 | PF00069 | 0.426 |
MOD_Plk_2-3 | 260 | 266 | PF00069 | 0.474 |
MOD_Plk_2-3 | 355 | 361 | PF00069 | 0.486 |
MOD_Plk_2-3 | 435 | 441 | PF00069 | 0.406 |
MOD_Plk_2-3 | 451 | 457 | PF00069 | 0.198 |
MOD_Plk_4 | 19 | 25 | PF00069 | 0.451 |
MOD_Plk_4 | 279 | 285 | PF00069 | 0.546 |
MOD_Plk_4 | 469 | 475 | PF00069 | 0.329 |
MOD_ProDKin_1 | 113 | 119 | PF00069 | 0.648 |
MOD_ProDKin_1 | 122 | 128 | PF00069 | 0.546 |
MOD_ProDKin_1 | 144 | 150 | PF00069 | 0.616 |
MOD_ProDKin_1 | 151 | 157 | PF00069 | 0.611 |
MOD_ProDKin_1 | 173 | 179 | PF00069 | 0.657 |
MOD_ProDKin_1 | 182 | 188 | PF00069 | 0.658 |
MOD_ProDKin_1 | 229 | 235 | PF00069 | 0.586 |
MOD_ProDKin_1 | 552 | 558 | PF00069 | 0.541 |
MOD_ProDKin_1 | 592 | 598 | PF00069 | 0.381 |
MOD_ProDKin_1 | 91 | 97 | PF00069 | 0.627 |
MOD_SUMO_rev_2 | 420 | 430 | PF00179 | 0.457 |
MOD_SUMO_rev_2 | 508 | 514 | PF00179 | 0.355 |
TRG_DiLeu_BaEn_1 | 268 | 273 | PF01217 | 0.525 |
TRG_DiLeu_BaEn_4 | 264 | 270 | PF01217 | 0.537 |
TRG_DiLeu_LyEn_5 | 268 | 273 | PF01217 | 0.525 |
TRG_ENDOCYTIC_2 | 331 | 334 | PF00928 | 0.399 |
TRG_ENDOCYTIC_2 | 335 | 338 | PF00928 | 0.374 |
TRG_ENDOCYTIC_2 | 345 | 348 | PF00928 | 0.457 |
TRG_ENDOCYTIC_2 | 439 | 442 | PF00928 | 0.309 |
TRG_ENDOCYTIC_2 | 446 | 449 | PF00928 | 0.298 |
TRG_ENDOCYTIC_2 | 504 | 507 | PF00928 | 0.298 |
TRG_ENDOCYTIC_2 | 536 | 539 | PF00928 | 0.391 |
TRG_ENDOCYTIC_2 | 640 | 643 | PF00928 | 0.373 |
TRG_ER_diArg_1 | 342 | 344 | PF00400 | 0.446 |
TRG_ER_diArg_1 | 623 | 626 | PF00400 | 0.591 |
TRG_NES_CRM1_1 | 288 | 302 | PF08389 | 0.480 |
TRG_Pf-PMV_PEXEL_1 | 342 | 346 | PF00026 | 0.246 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2Z7 | Leptomonas seymouri | 74% | 98% |
A0A0S4JHD9 | Bodo saltans | 40% | 88% |
A0A1X0P683 | Trypanosomatidae | 49% | 98% |
A0A3R7MAB5 | Trypanosoma rangeli | 50% | 97% |
A0A3S7X9I6 | Leishmania donovani | 84% | 98% |
A4IBL2 | Leishmania infantum | 84% | 98% |
C9ZZ28 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 95% |
E9AFE5 | Leishmania major | 85% | 100% |
E9B6K0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 98% |
Q5QIT3 | Arabidopsis thaliana | 33% | 100% |
Q8VZQ4 | Arabidopsis thaliana | 33% | 100% |
Q9SLI8 | Arabidopsis thaliana | 33% | 100% |
Q9Y5P8 | Homo sapiens | 30% | 100% |
V5BY37 | Trypanosoma cruzi | 50% | 97% |