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: E9B6K0
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 | 328 | 332 | PF00656 | 0.462 |
CLV_C14_Caspase3-7 | 567 | 571 | PF00656 | 0.550 |
CLV_NRD_NRD_1 | 358 | 360 | PF00675 | 0.297 |
CLV_NRD_NRD_1 | 596 | 598 | PF00675 | 0.603 |
CLV_PCSK_KEX2_1 | 267 | 269 | PF00082 | 0.571 |
CLV_PCSK_KEX2_1 | 358 | 360 | PF00082 | 0.297 |
CLV_PCSK_KEX2_1 | 495 | 497 | PF00082 | 0.313 |
CLV_PCSK_PC1ET2_1 | 267 | 269 | PF00082 | 0.591 |
CLV_PCSK_PC1ET2_1 | 495 | 497 | PF00082 | 0.313 |
CLV_PCSK_SKI1_1 | 254 | 258 | PF00082 | 0.552 |
CLV_PCSK_SKI1_1 | 308 | 312 | PF00082 | 0.365 |
CLV_PCSK_SKI1_1 | 317 | 321 | PF00082 | 0.298 |
CLV_PCSK_SKI1_1 | 34 | 38 | PF00082 | 0.592 |
CLV_PCSK_SKI1_1 | 39 | 43 | PF00082 | 0.577 |
CLV_PCSK_SKI1_1 | 472 | 476 | PF00082 | 0.417 |
CLV_PCSK_SKI1_1 | 624 | 628 | PF00082 | 0.378 |
DEG_APCC_DBOX_1 | 33 | 41 | PF00400 | 0.620 |
DOC_CKS1_1 | 165 | 170 | PF01111 | 0.738 |
DOC_CYCLIN_RxL_1 | 34 | 47 | PF00134 | 0.523 |
DOC_CYCLIN_RxL_1 | 561 | 571 | PF00134 | 0.479 |
DOC_CYCLIN_RxL_1 | 621 | 632 | PF00134 | 0.517 |
DOC_CYCLIN_yCln2_LP_2 | 217 | 223 | PF00134 | 0.737 |
DOC_MAPK_gen_1 | 369 | 375 | PF00069 | 0.522 |
DOC_MAPK_gen_1 | 595 | 603 | PF00069 | 0.515 |
DOC_PP1_RVXF_1 | 421 | 427 | PF00149 | 0.470 |
DOC_PP1_RVXF_1 | 562 | 569 | PF00149 | 0.468 |
DOC_PP1_RVXF_1 | 622 | 629 | PF00149 | 0.480 |
DOC_PP4_FxxP_1 | 310 | 313 | PF00568 | 0.322 |
DOC_USP7_MATH_1 | 116 | 120 | PF00917 | 0.689 |
DOC_USP7_MATH_1 | 231 | 235 | PF00917 | 0.739 |
DOC_USP7_MATH_1 | 325 | 329 | PF00917 | 0.394 |
DOC_USP7_MATH_1 | 504 | 508 | PF00917 | 0.313 |
DOC_USP7_MATH_1 | 85 | 89 | PF00917 | 0.751 |
DOC_WW_Pin1_4 | 107 | 112 | PF00397 | 0.645 |
DOC_WW_Pin1_4 | 129 | 134 | PF00397 | 0.657 |
DOC_WW_Pin1_4 | 138 | 143 | PF00397 | 0.567 |
DOC_WW_Pin1_4 | 160 | 165 | PF00397 | 0.612 |
DOC_WW_Pin1_4 | 167 | 172 | PF00397 | 0.603 |
DOC_WW_Pin1_4 | 189 | 194 | PF00397 | 0.670 |
DOC_WW_Pin1_4 | 198 | 203 | PF00397 | 0.658 |
DOC_WW_Pin1_4 | 216 | 221 | PF00397 | 0.547 |
DOC_WW_Pin1_4 | 245 | 250 | PF00397 | 0.588 |
DOC_WW_Pin1_4 | 568 | 573 | PF00397 | 0.533 |
DOC_WW_Pin1_4 | 608 | 613 | PF00397 | 0.382 |
LIG_14-3-3_CanoR_1 | 237 | 247 | PF00244 | 0.566 |
LIG_14-3-3_CanoR_1 | 39 | 44 | PF00244 | 0.652 |
LIG_14-3-3_CanoR_1 | 503 | 510 | PF00244 | 0.332 |
LIG_14-3-3_CanoR_1 | 86 | 90 | PF00244 | 0.727 |
LIG_AP2alpha_2 | 632 | 634 | PF02296 | 0.433 |
LIG_APCC_ABBA_1 | 299 | 304 | PF00400 | 0.520 |
LIG_APCC_ABBAyCdc20_2 | 317 | 323 | PF00400 | 0.459 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.652 |
LIG_BRCT_BRCA1_1 | 241 | 245 | PF00533 | 0.550 |
LIG_BRCT_BRCA1_1 | 306 | 310 | PF00533 | 0.450 |
LIG_Clathr_ClatBox_1 | 475 | 479 | PF01394 | 0.332 |
LIG_deltaCOP1_diTrp_1 | 647 | 651 | PF00928 | 0.361 |
LIG_FHA_1 | 19 | 25 | PF00498 | 0.612 |
LIG_FHA_1 | 216 | 222 | PF00498 | 0.669 |
LIG_FHA_1 | 224 | 230 | PF00498 | 0.678 |
LIG_FHA_1 | 234 | 240 | PF00498 | 0.610 |
LIG_FHA_1 | 296 | 302 | PF00498 | 0.465 |
LIG_FHA_1 | 405 | 411 | PF00498 | 0.445 |
LIG_FHA_1 | 489 | 495 | PF00498 | 0.384 |
LIG_FHA_2 | 255 | 261 | PF00498 | 0.479 |
LIG_FHA_2 | 372 | 378 | PF00498 | 0.469 |
LIG_FHA_2 | 468 | 474 | PF00498 | 0.313 |
LIG_FHA_2 | 541 | 547 | PF00498 | 0.417 |
LIG_FHA_2 | 600 | 606 | PF00498 | 0.373 |
LIG_FHA_2 | 644 | 650 | PF00498 | 0.383 |
LIG_FXI_DFP_1 | 426 | 430 | PF00024 | 0.285 |
LIG_GBD_Chelix_1 | 408 | 416 | PF00786 | 0.245 |
LIG_HCF-1_HBM_1 | 456 | 459 | PF13415 | 0.311 |
LIG_LIR_Apic_2 | 307 | 313 | PF02991 | 0.334 |
LIG_LIR_Apic_2 | 499 | 504 | PF02991 | 0.417 |
LIG_LIR_Gen_1 | 371 | 378 | PF02991 | 0.471 |
LIG_LIR_Gen_1 | 402 | 413 | PF02991 | 0.531 |
LIG_LIR_Gen_1 | 454 | 462 | PF02991 | 0.297 |
LIG_LIR_Gen_1 | 514 | 523 | PF02991 | 0.297 |
LIG_LIR_Gen_1 | 550 | 558 | PF02991 | 0.349 |
LIG_LIR_Gen_1 | 623 | 633 | PF02991 | 0.431 |
LIG_LIR_Gen_1 | 646 | 656 | PF02991 | 0.367 |
LIG_LIR_Nem_3 | 318 | 324 | PF02991 | 0.336 |
LIG_LIR_Nem_3 | 349 | 354 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 371 | 375 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 399 | 403 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 451 | 455 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 456 | 462 | PF02991 | 0.283 |
LIG_LIR_Nem_3 | 514 | 518 | PF02991 | 0.297 |
LIG_LIR_Nem_3 | 623 | 628 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 646 | 651 | PF02991 | 0.365 |
LIG_MAD2 | 496 | 504 | PF02301 | 0.313 |
LIG_NRBOX | 284 | 290 | PF00104 | 0.539 |
LIG_PALB2_WD40_1 | 533 | 541 | PF16756 | 0.297 |
LIG_Pex14_2 | 616 | 620 | PF04695 | 0.305 |
LIG_PTAP_UEV_1 | 178 | 183 | PF05743 | 0.622 |
LIG_PTB_Apo_2 | 345 | 352 | PF02174 | 0.428 |
LIG_PTB_Apo_2 | 614 | 621 | PF02174 | 0.326 |
LIG_PTB_Phospho_1 | 345 | 351 | PF10480 | 0.431 |
LIG_SH2_CRK | 351 | 355 | PF00017 | 0.430 |
LIG_SH2_CRK | 501 | 505 | PF00017 | 0.417 |
LIG_SH2_GRB2like | 20 | 23 | PF00017 | 0.557 |
LIG_SH2_NCK_1 | 347 | 351 | PF00017 | 0.405 |
LIG_SH2_STAP1 | 20 | 24 | PF00017 | 0.578 |
LIG_SH2_STAP1 | 455 | 459 | PF00017 | 0.310 |
LIG_SH2_STAP1 | 578 | 582 | PF00017 | 0.445 |
LIG_SH2_STAP1 | 656 | 660 | PF00017 | 0.373 |
LIG_SH2_STAT5 | 125 | 128 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 20 | 23 | PF00017 | 0.545 |
LIG_SH2_STAT5 | 384 | 387 | PF00017 | 0.458 |
LIG_SH2_STAT5 | 452 | 455 | PF00017 | 0.307 |
LIG_SH2_STAT5 | 459 | 462 | PF00017 | 0.297 |
LIG_SH2_STAT5 | 520 | 523 | PF00017 | 0.297 |
LIG_SH3_2 | 113 | 118 | PF14604 | 0.710 |
LIG_SH3_3 | 110 | 116 | PF00018 | 0.644 |
LIG_SH3_3 | 132 | 138 | PF00018 | 0.699 |
LIG_SH3_3 | 162 | 168 | PF00018 | 0.651 |
LIG_SH3_3 | 176 | 182 | PF00018 | 0.521 |
LIG_SH3_3 | 208 | 214 | PF00018 | 0.591 |
LIG_SH3_3 | 244 | 250 | PF00018 | 0.628 |
LIG_SH3_3 | 347 | 353 | PF00018 | 0.396 |
LIG_SUMO_SIM_par_1 | 352 | 357 | PF11976 | 0.457 |
LIG_SUMO_SIM_par_1 | 39 | 44 | PF11976 | 0.615 |
LIG_TYR_ITAM | 348 | 364 | PF00017 | 0.414 |
LIG_UBA3_1 | 438 | 444 | PF00899 | 0.531 |
MOD_CDK_SPK_2 | 198 | 203 | PF00069 | 0.738 |
MOD_CDK_SPxxK_3 | 111 | 118 | PF00069 | 0.699 |
MOD_CDK_SPxxK_3 | 167 | 174 | PF00069 | 0.735 |
MOD_CK1_1 | 119 | 125 | PF00069 | 0.745 |
MOD_CK1_1 | 198 | 204 | PF00069 | 0.675 |
MOD_CK1_1 | 488 | 494 | PF00069 | 0.387 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.689 |
MOD_CK1_1 | 608 | 614 | PF00069 | 0.476 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.722 |
MOD_CK2_1 | 22 | 28 | PF00069 | 0.548 |
MOD_CK2_1 | 227 | 233 | PF00069 | 0.694 |
MOD_CK2_1 | 263 | 269 | PF00069 | 0.477 |
MOD_CK2_1 | 274 | 280 | PF00069 | 0.404 |
MOD_CK2_1 | 373 | 379 | PF00069 | 0.501 |
MOD_CK2_1 | 547 | 553 | PF00069 | 0.297 |
MOD_CK2_1 | 94 | 100 | PF00069 | 0.487 |
MOD_DYRK1A_RPxSP_1 | 107 | 111 | PF00069 | 0.644 |
MOD_DYRK1A_RPxSP_1 | 160 | 164 | PF00069 | 0.640 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.683 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.725 |
MOD_GlcNHglycan | 178 | 182 | PF01048 | 0.590 |
MOD_GlcNHglycan | 187 | 190 | PF01048 | 0.614 |
MOD_GlcNHglycan | 229 | 232 | PF01048 | 0.574 |
MOD_GlcNHglycan | 241 | 244 | PF01048 | 0.468 |
MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.410 |
MOD_GlcNHglycan | 43 | 46 | PF01048 | 0.574 |
MOD_GlcNHglycan | 506 | 509 | PF01048 | 0.309 |
MOD_GlcNHglycan | 549 | 552 | PF01048 | 0.311 |
MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.731 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.658 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.656 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.644 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.512 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.656 |
MOD_GSK3_1 | 223 | 230 | PF00069 | 0.596 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.620 |
MOD_GSK3_1 | 263 | 270 | PF00069 | 0.510 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.642 |
MOD_N-GLC_1 | 223 | 228 | PF02516 | 0.489 |
MOD_N-GLC_1 | 620 | 625 | PF02516 | 0.410 |
MOD_NEK2_1 | 204 | 209 | PF00069 | 0.662 |
MOD_NEK2_1 | 227 | 232 | PF00069 | 0.630 |
MOD_NEK2_1 | 238 | 243 | PF00069 | 0.480 |
MOD_NEK2_1 | 354 | 359 | PF00069 | 0.439 |
MOD_NEK2_1 | 363 | 368 | PF00069 | 0.512 |
MOD_NEK2_1 | 41 | 46 | PF00069 | 0.603 |
MOD_NEK2_1 | 620 | 625 | PF00069 | 0.393 |
MOD_NEK2_1 | 94 | 99 | PF00069 | 0.716 |
MOD_PKA_1 | 267 | 273 | PF00069 | 0.526 |
MOD_PKA_2 | 231 | 237 | PF00069 | 0.662 |
MOD_PKA_2 | 267 | 273 | PF00069 | 0.522 |
MOD_PKA_2 | 85 | 91 | PF00069 | 0.768 |
MOD_Plk_1 | 204 | 210 | PF00069 | 0.640 |
MOD_Plk_1 | 223 | 229 | PF00069 | 0.414 |
MOD_Plk_1 | 578 | 584 | PF00069 | 0.425 |
MOD_Plk_2-3 | 371 | 377 | PF00069 | 0.485 |
MOD_Plk_2-3 | 451 | 457 | PF00069 | 0.408 |
MOD_Plk_2-3 | 467 | 473 | PF00069 | 0.197 |
MOD_Plk_4 | 140 | 146 | PF00069 | 0.689 |
MOD_Plk_4 | 295 | 301 | PF00069 | 0.562 |
MOD_Plk_4 | 485 | 491 | PF00069 | 0.327 |
MOD_ProDKin_1 | 107 | 113 | PF00069 | 0.644 |
MOD_ProDKin_1 | 129 | 135 | PF00069 | 0.655 |
MOD_ProDKin_1 | 138 | 144 | PF00069 | 0.568 |
MOD_ProDKin_1 | 160 | 166 | PF00069 | 0.611 |
MOD_ProDKin_1 | 167 | 173 | PF00069 | 0.602 |
MOD_ProDKin_1 | 189 | 195 | PF00069 | 0.668 |
MOD_ProDKin_1 | 198 | 204 | PF00069 | 0.658 |
MOD_ProDKin_1 | 216 | 222 | PF00069 | 0.549 |
MOD_ProDKin_1 | 245 | 251 | PF00069 | 0.590 |
MOD_ProDKin_1 | 568 | 574 | PF00069 | 0.531 |
MOD_ProDKin_1 | 608 | 614 | PF00069 | 0.377 |
MOD_SUMO_for_1 | 368 | 371 | PF00179 | 0.493 |
MOD_SUMO_rev_2 | 436 | 446 | PF00179 | 0.456 |
MOD_SUMO_rev_2 | 524 | 530 | PF00179 | 0.354 |
TRG_DiLeu_BaEn_1 | 284 | 289 | PF01217 | 0.530 |
TRG_DiLeu_BaEn_4 | 280 | 286 | PF01217 | 0.545 |
TRG_DiLeu_LyEn_5 | 284 | 289 | PF01217 | 0.530 |
TRG_ENDOCYTIC_2 | 347 | 350 | PF00928 | 0.401 |
TRG_ENDOCYTIC_2 | 351 | 354 | PF00928 | 0.379 |
TRG_ENDOCYTIC_2 | 361 | 364 | PF00928 | 0.456 |
TRG_ENDOCYTIC_2 | 455 | 458 | PF00928 | 0.310 |
TRG_ENDOCYTIC_2 | 462 | 465 | PF00928 | 0.297 |
TRG_ENDOCYTIC_2 | 520 | 523 | PF00928 | 0.297 |
TRG_ENDOCYTIC_2 | 552 | 555 | PF00928 | 0.390 |
TRG_ENDOCYTIC_2 | 656 | 659 | PF00928 | 0.371 |
TRG_ER_diArg_1 | 358 | 360 | PF00400 | 0.297 |
TRG_ER_diArg_1 | 639 | 642 | PF00400 | 0.576 |
TRG_NES_CRM1_1 | 304 | 318 | PF08389 | 0.482 |
TRG_NES_CRM1_1 | 31 | 47 | PF08389 | 0.602 |
TRG_Pf-PMV_PEXEL_1 | 271 | 276 | PF00026 | 0.500 |
TRG_Pf-PMV_PEXEL_1 | 358 | 362 | PF00026 | 0.297 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2Z7 | Leptomonas seymouri | 77% | 100% |
A0A0S4JHD9 | Bodo saltans | 40% | 90% |
A0A1X0P683 | Trypanosomatidae | 50% | 100% |
A0A3R7MAB5 | Trypanosoma rangeli | 52% | 99% |
A0A3S7X9I6 | Leishmania donovani | 95% | 100% |
A4HMY8 | Leishmania braziliensis | 84% | 98% |
A4IBL2 | Leishmania infantum | 95% | 100% |
C9ZZ28 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 98% |
E9AFE5 | Leishmania major | 95% | 100% |
Q5QIT3 | Arabidopsis thaliana | 34% | 100% |
Q8VZQ4 | Arabidopsis thaliana | 34% | 100% |
Q9SLI8 | Arabidopsis thaliana | 34% | 100% |
Q9XGR4 | Arabidopsis thaliana | 35% | 100% |
Q9Y5P8 | Homo sapiens | 31% | 100% |
V5BY37 | Trypanosoma cruzi | 51% | 99% |