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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005829 | cytosol | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AZP2
Term | Name | Level | Count |
---|---|---|---|
GO:0006470 | protein dephosphorylation | 5 | 10 |
GO:0006793 | phosphorus metabolic process | 3 | 10 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 10 |
GO:0006807 | nitrogen compound metabolic process | 2 | 10 |
GO:0008152 | metabolic process | 1 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0016311 | dephosphorylation | 5 | 10 |
GO:0019538 | protein metabolic process | 3 | 10 |
GO:0036211 | protein modification process | 4 | 10 |
GO:0043170 | macromolecule metabolic process | 3 | 10 |
GO:0043412 | macromolecule modification | 4 | 10 |
GO:0044237 | cellular metabolic process | 2 | 10 |
GO:0044238 | primary metabolic process | 2 | 10 |
GO:0071704 | organic substance metabolic process | 2 | 10 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 10 |
GO:0007165 | signal transduction | 2 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 10 |
GO:0004721 | phosphoprotein phosphatase activity | 3 | 10 |
GO:0008138 | protein tyrosine/serine/threonine phosphatase activity | 4 | 10 |
GO:0016787 | hydrolase activity | 2 | 10 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 10 |
GO:0016791 | phosphatase activity | 5 | 10 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 10 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 10 |
GO:0004725 | protein tyrosine phosphatase activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 441 | 445 | PF00656 | 0.372 |
CLV_NRD_NRD_1 | 116 | 118 | PF00675 | 0.507 |
CLV_NRD_NRD_1 | 151 | 153 | PF00675 | 0.514 |
CLV_NRD_NRD_1 | 271 | 273 | PF00675 | 0.542 |
CLV_NRD_NRD_1 | 90 | 92 | PF00675 | 0.581 |
CLV_PCSK_KEX2_1 | 271 | 273 | PF00082 | 0.549 |
CLV_PCSK_KEX2_1 | 90 | 92 | PF00082 | 0.564 |
CLV_PCSK_SKI1_1 | 117 | 121 | PF00082 | 0.467 |
CLV_PCSK_SKI1_1 | 352 | 356 | PF00082 | 0.558 |
CLV_PCSK_SKI1_1 | 460 | 464 | PF00082 | 0.550 |
CLV_PCSK_SKI1_1 | 544 | 548 | PF00082 | 0.340 |
CLV_Separin_Metazoa | 320 | 324 | PF03568 | 0.195 |
DEG_APCC_DBOX_1 | 603 | 611 | PF00400 | 0.536 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.355 |
DOC_CKS1_1 | 110 | 115 | PF01111 | 0.325 |
DOC_CYCLIN_RxL_1 | 541 | 551 | PF00134 | 0.353 |
DOC_CYCLIN_yCln2_LP_2 | 411 | 417 | PF00134 | 0.300 |
DOC_MAPK_gen_1 | 114 | 124 | PF00069 | 0.326 |
DOC_MAPK_gen_1 | 245 | 253 | PF00069 | 0.380 |
DOC_MAPK_gen_1 | 53 | 61 | PF00069 | 0.295 |
DOC_MAPK_MEF2A_6 | 55 | 63 | PF00069 | 0.351 |
DOC_PP1_RVXF_1 | 482 | 488 | PF00149 | 0.365 |
DOC_PP2B_LxvP_1 | 15 | 18 | PF13499 | 0.349 |
DOC_PP2B_LxvP_1 | 418 | 421 | PF13499 | 0.342 |
DOC_PP4_FxxP_1 | 625 | 628 | PF00568 | 0.465 |
DOC_USP7_MATH_1 | 225 | 229 | PF00917 | 0.305 |
DOC_USP7_MATH_1 | 387 | 391 | PF00917 | 0.401 |
DOC_USP7_MATH_1 | 473 | 477 | PF00917 | 0.448 |
DOC_USP7_MATH_1 | 478 | 482 | PF00917 | 0.398 |
DOC_USP7_MATH_1 | 499 | 503 | PF00917 | 0.346 |
DOC_USP7_UBL2_3 | 114 | 118 | PF12436 | 0.319 |
DOC_WW_Pin1_4 | 109 | 114 | PF00397 | 0.409 |
LIG_14-3-3_CanoR_1 | 218 | 223 | PF00244 | 0.297 |
LIG_14-3-3_CanoR_1 | 340 | 344 | PF00244 | 0.417 |
LIG_14-3-3_CanoR_1 | 371 | 377 | PF00244 | 0.354 |
LIG_APCC_ABBA_1 | 419 | 424 | PF00400 | 0.347 |
LIG_BRCT_BRCA1_1 | 411 | 415 | PF00533 | 0.274 |
LIG_deltaCOP1_diTrp_1 | 431 | 439 | PF00928 | 0.377 |
LIG_DLG_GKlike_1 | 218 | 226 | PF00625 | 0.263 |
LIG_FHA_1 | 129 | 135 | PF00498 | 0.323 |
LIG_FHA_1 | 204 | 210 | PF00498 | 0.328 |
LIG_FHA_1 | 234 | 240 | PF00498 | 0.299 |
LIG_FHA_1 | 447 | 453 | PF00498 | 0.358 |
LIG_FHA_1 | 611 | 617 | PF00498 | 0.597 |
LIG_FHA_2 | 155 | 161 | PF00498 | 0.426 |
LIG_FHA_2 | 21 | 27 | PF00498 | 0.374 |
LIG_FHA_2 | 282 | 288 | PF00498 | 0.314 |
LIG_FHA_2 | 439 | 445 | PF00498 | 0.415 |
LIG_LIR_Apic_2 | 324 | 330 | PF02991 | 0.371 |
LIG_LIR_Apic_2 | 623 | 628 | PF02991 | 0.451 |
LIG_LIR_Gen_1 | 103 | 113 | PF02991 | 0.308 |
LIG_LIR_Gen_1 | 160 | 171 | PF02991 | 0.348 |
LIG_LIR_Gen_1 | 221 | 231 | PF02991 | 0.368 |
LIG_LIR_Gen_1 | 305 | 315 | PF02991 | 0.333 |
LIG_LIR_Gen_1 | 365 | 373 | PF02991 | 0.342 |
LIG_LIR_Gen_1 | 375 | 385 | PF02991 | 0.267 |
LIG_LIR_Gen_1 | 412 | 423 | PF02991 | 0.280 |
LIG_LIR_Gen_1 | 424 | 434 | PF02991 | 0.337 |
LIG_LIR_Gen_1 | 479 | 488 | PF02991 | 0.401 |
LIG_LIR_Gen_1 | 529 | 537 | PF02991 | 0.355 |
LIG_LIR_Gen_1 | 586 | 596 | PF02991 | 0.523 |
LIG_LIR_Nem_3 | 103 | 108 | PF02991 | 0.296 |
LIG_LIR_Nem_3 | 160 | 166 | PF02991 | 0.375 |
LIG_LIR_Nem_3 | 221 | 226 | PF02991 | 0.305 |
LIG_LIR_Nem_3 | 305 | 311 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 347 | 353 | PF02991 | 0.310 |
LIG_LIR_Nem_3 | 365 | 370 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 375 | 380 | PF02991 | 0.258 |
LIG_LIR_Nem_3 | 412 | 418 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 424 | 429 | PF02991 | 0.373 |
LIG_LIR_Nem_3 | 430 | 435 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 479 | 485 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 496 | 500 | PF02991 | 0.302 |
LIG_LIR_Nem_3 | 529 | 533 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 586 | 592 | PF02991 | 0.527 |
LIG_NRBOX | 606 | 612 | PF00104 | 0.539 |
LIG_PAM2_1 | 404 | 416 | PF00658 | 0.331 |
LIG_Pex14_2 | 373 | 377 | PF04695 | 0.306 |
LIG_Pex14_2 | 413 | 417 | PF04695 | 0.280 |
LIG_Pex14_2 | 462 | 466 | PF04695 | 0.305 |
LIG_PTB_Apo_2 | 210 | 217 | PF02174 | 0.231 |
LIG_PTB_Apo_2 | 343 | 350 | PF02174 | 0.287 |
LIG_REV1ctd_RIR_1 | 600 | 608 | PF16727 | 0.571 |
LIG_SH2_CRK | 163 | 167 | PF00017 | 0.336 |
LIG_SH2_CRK | 327 | 331 | PF00017 | 0.219 |
LIG_SH2_CRK | 351 | 355 | PF00017 | 0.350 |
LIG_SH2_CRK | 482 | 486 | PF00017 | 0.424 |
LIG_SH2_CRK | 589 | 593 | PF00017 | 0.538 |
LIG_SH2_NCK_1 | 155 | 159 | PF00017 | 0.402 |
LIG_SH2_NCK_1 | 163 | 167 | PF00017 | 0.293 |
LIG_SH2_NCK_1 | 308 | 312 | PF00017 | 0.412 |
LIG_SH2_NCK_1 | 327 | 331 | PF00017 | 0.376 |
LIG_SH2_SRC | 422 | 425 | PF00017 | 0.352 |
LIG_SH2_STAP1 | 335 | 339 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 105 | 108 | PF00017 | 0.308 |
LIG_SH2_STAT5 | 163 | 166 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 187 | 190 | PF00017 | 0.332 |
LIG_SH2_STAT5 | 273 | 276 | PF00017 | 0.379 |
LIG_SH2_STAT5 | 308 | 311 | PF00017 | 0.345 |
LIG_SH2_STAT5 | 314 | 317 | PF00017 | 0.276 |
LIG_SH2_STAT5 | 327 | 330 | PF00017 | 0.292 |
LIG_SH2_STAT5 | 381 | 384 | PF00017 | 0.397 |
LIG_SH2_STAT5 | 43 | 46 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 482 | 485 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 589 | 592 | PF00017 | 0.585 |
LIG_SH3_3 | 107 | 113 | PF00018 | 0.308 |
LIG_SH3_3 | 206 | 212 | PF00018 | 0.271 |
LIG_SH3_3 | 612 | 618 | PF00018 | 0.549 |
LIG_Sin3_3 | 329 | 336 | PF02671 | 0.335 |
LIG_Sin3_3 | 543 | 550 | PF02671 | 0.320 |
LIG_SUMO_SIM_anti_2 | 197 | 204 | PF11976 | 0.385 |
LIG_SUMO_SIM_anti_2 | 491 | 496 | PF11976 | 0.418 |
LIG_SUMO_SIM_par_1 | 238 | 243 | PF11976 | 0.395 |
LIG_SUMO_SIM_par_1 | 248 | 256 | PF11976 | 0.275 |
LIG_SUMO_SIM_par_1 | 515 | 521 | PF11976 | 0.377 |
LIG_UBA3_1 | 257 | 266 | PF00899 | 0.377 |
LIG_UBA3_1 | 376 | 383 | PF00899 | 0.360 |
LIG_UBA3_1 | 451 | 455 | PF00899 | 0.214 |
LIG_WRC_WIRS_1 | 494 | 499 | PF05994 | 0.338 |
MOD_CDK_SPK_2 | 109 | 114 | PF00069 | 0.317 |
MOD_CK1_1 | 20 | 26 | PF00069 | 0.381 |
MOD_CK1_1 | 476 | 482 | PF00069 | 0.412 |
MOD_CK1_1 | 510 | 516 | PF00069 | 0.355 |
MOD_CK1_1 | 584 | 590 | PF00069 | 0.566 |
MOD_CK1_1 | 94 | 100 | PF00069 | 0.295 |
MOD_CK2_1 | 281 | 287 | PF00069 | 0.389 |
MOD_CK2_1 | 357 | 363 | PF00069 | 0.337 |
MOD_CK2_1 | 372 | 378 | PF00069 | 0.226 |
MOD_CK2_1 | 606 | 612 | PF00069 | 0.506 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.498 |
MOD_GlcNHglycan | 359 | 362 | PF01048 | 0.534 |
MOD_GlcNHglycan | 389 | 392 | PF01048 | 0.705 |
MOD_GlcNHglycan | 398 | 401 | PF01048 | 0.654 |
MOD_GlcNHglycan | 446 | 449 | PF01048 | 0.517 |
MOD_GlcNHglycan | 474 | 478 | PF01048 | 0.683 |
MOD_GlcNHglycan | 537 | 540 | PF01048 | 0.398 |
MOD_GlcNHglycan | 578 | 581 | PF01048 | 0.327 |
MOD_GlcNHglycan | 586 | 589 | PF01048 | 0.323 |
MOD_GlcNHglycan | 82 | 86 | PF01048 | 0.659 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.325 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.361 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.440 |
MOD_GSK3_1 | 321 | 328 | PF00069 | 0.209 |
MOD_GSK3_1 | 396 | 403 | PF00069 | 0.498 |
MOD_GSK3_1 | 476 | 483 | PF00069 | 0.449 |
MOD_GSK3_1 | 499 | 506 | PF00069 | 0.387 |
MOD_GSK3_1 | 606 | 613 | PF00069 | 0.595 |
MOD_N-GLC_1 | 455 | 460 | PF02516 | 0.541 |
MOD_N-GLC_2 | 66 | 68 | PF02516 | 0.518 |
MOD_NEK2_1 | 120 | 125 | PF00069 | 0.270 |
MOD_NEK2_1 | 339 | 344 | PF00069 | 0.449 |
MOD_NEK2_1 | 42 | 47 | PF00069 | 0.365 |
MOD_NEK2_1 | 466 | 471 | PF00069 | 0.372 |
MOD_NEK2_1 | 554 | 559 | PF00069 | 0.512 |
MOD_NEK2_1 | 562 | 567 | PF00069 | 0.535 |
MOD_NEK2_1 | 610 | 615 | PF00069 | 0.594 |
MOD_NEK2_2 | 372 | 377 | PF00069 | 0.306 |
MOD_NEK2_2 | 620 | 625 | PF00069 | 0.548 |
MOD_PIKK_1 | 192 | 198 | PF00454 | 0.323 |
MOD_PIKK_1 | 518 | 524 | PF00454 | 0.362 |
MOD_PIKK_1 | 552 | 558 | PF00454 | 0.516 |
MOD_PIKK_1 | 91 | 97 | PF00454 | 0.361 |
MOD_PK_1 | 179 | 185 | PF00069 | 0.321 |
MOD_PKA_2 | 203 | 209 | PF00069 | 0.307 |
MOD_PKA_2 | 339 | 345 | PF00069 | 0.335 |
MOD_PKA_2 | 387 | 393 | PF00069 | 0.340 |
MOD_Plk_1 | 100 | 106 | PF00069 | 0.348 |
MOD_Plk_1 | 161 | 167 | PF00069 | 0.361 |
MOD_Plk_1 | 455 | 461 | PF00069 | 0.296 |
MOD_Plk_1 | 605 | 611 | PF00069 | 0.569 |
MOD_Plk_2-3 | 156 | 162 | PF00069 | 0.504 |
MOD_Plk_2-3 | 363 | 369 | PF00069 | 0.394 |
MOD_Plk_2-3 | 564 | 570 | PF00069 | 0.557 |
MOD_Plk_2-3 | 606 | 612 | PF00069 | 0.556 |
MOD_Plk_4 | 120 | 126 | PF00069 | 0.195 |
MOD_Plk_4 | 179 | 185 | PF00069 | 0.314 |
MOD_Plk_4 | 218 | 224 | PF00069 | 0.339 |
MOD_Plk_4 | 253 | 259 | PF00069 | 0.303 |
MOD_Plk_4 | 273 | 279 | PF00069 | 0.380 |
MOD_Plk_4 | 339 | 345 | PF00069 | 0.405 |
MOD_Plk_4 | 372 | 378 | PF00069 | 0.293 |
MOD_Plk_4 | 513 | 519 | PF00069 | 0.399 |
MOD_Plk_4 | 526 | 532 | PF00069 | 0.330 |
MOD_Plk_4 | 606 | 612 | PF00069 | 0.557 |
MOD_Plk_4 | 620 | 626 | PF00069 | 0.482 |
MOD_Plk_4 | 94 | 100 | PF00069 | 0.355 |
MOD_ProDKin_1 | 109 | 115 | PF00069 | 0.411 |
MOD_SUMO_for_1 | 454 | 457 | PF00179 | 0.298 |
MOD_SUMO_rev_2 | 501 | 506 | PF00179 | 0.421 |
TRG_DiLeu_BaEn_1 | 140 | 145 | PF01217 | 0.252 |
TRG_DiLeu_BaEn_1 | 431 | 436 | PF01217 | 0.297 |
TRG_DiLeu_BaEn_1 | 606 | 611 | PF01217 | 0.532 |
TRG_DiLeu_BaLyEn_6 | 541 | 546 | PF01217 | 0.353 |
TRG_ENDOCYTIC_2 | 105 | 108 | PF00928 | 0.342 |
TRG_ENDOCYTIC_2 | 155 | 158 | PF00928 | 0.418 |
TRG_ENDOCYTIC_2 | 163 | 166 | PF00928 | 0.285 |
TRG_ENDOCYTIC_2 | 292 | 295 | PF00928 | 0.320 |
TRG_ENDOCYTIC_2 | 308 | 311 | PF00928 | 0.273 |
TRG_ENDOCYTIC_2 | 350 | 353 | PF00928 | 0.277 |
TRG_ENDOCYTIC_2 | 482 | 485 | PF00928 | 0.460 |
TRG_ENDOCYTIC_2 | 589 | 592 | PF00928 | 0.541 |
TRG_ENDOCYTIC_2 | 76 | 79 | PF00928 | 0.360 |
TRG_ER_diArg_1 | 271 | 273 | PF00400 | 0.346 |
TRG_ER_diArg_1 | 89 | 91 | PF00400 | 0.378 |
TRG_Pf-PMV_PEXEL_1 | 544 | 548 | PF00026 | 0.432 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IM74 | Leptomonas seymouri | 55% | 100% |
A0A1X0NYU6 | Trypanosomatidae | 30% | 100% |
A0A3S7X1C5 | Leishmania donovani | 93% | 100% |
A4HGC1 | Leishmania braziliensis | 78% | 100% |
A4I3F4 | Leishmania infantum | 92% | 100% |
D0A7Y6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
Q4Q8J0 | Leishmania major | 93% | 100% |
V5BQB3 | Trypanosoma cruzi | 28% | 100% |