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: A4HGC1
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 | 344 | 348 | PF00656 | 0.211 |
CLV_C14_Caspase3-7 | 441 | 445 | PF00656 | 0.375 |
CLV_NRD_NRD_1 | 117 | 119 | PF00675 | 0.510 |
CLV_NRD_NRD_1 | 151 | 153 | PF00675 | 0.510 |
CLV_NRD_NRD_1 | 271 | 273 | PF00675 | 0.539 |
CLV_NRD_NRD_1 | 90 | 92 | PF00675 | 0.586 |
CLV_PCSK_KEX2_1 | 117 | 119 | PF00082 | 0.492 |
CLV_PCSK_KEX2_1 | 271 | 273 | PF00082 | 0.546 |
CLV_PCSK_KEX2_1 | 90 | 92 | PF00082 | 0.569 |
CLV_PCSK_SKI1_1 | 117 | 121 | PF00082 | 0.487 |
CLV_PCSK_SKI1_1 | 352 | 356 | PF00082 | 0.560 |
CLV_PCSK_SKI1_1 | 452 | 456 | PF00082 | 0.585 |
CLV_PCSK_SKI1_1 | 460 | 464 | PF00082 | 0.559 |
CLV_PCSK_SKI1_1 | 544 | 548 | PF00082 | 0.340 |
CLV_PCSK_SKI1_1 | 600 | 604 | PF00082 | 0.228 |
DEG_APCC_DBOX_1 | 603 | 611 | PF00400 | 0.531 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.365 |
DEG_SPOP_SBC_1 | 109 | 113 | PF00917 | 0.252 |
DOC_CYCLIN_RxL_1 | 215 | 225 | PF00134 | 0.242 |
DOC_CYCLIN_RxL_1 | 541 | 551 | PF00134 | 0.353 |
DOC_CYCLIN_yCln2_LP_2 | 411 | 417 | PF00134 | 0.298 |
DOC_MAPK_gen_1 | 117 | 124 | PF00069 | 0.317 |
DOC_MAPK_gen_1 | 245 | 253 | PF00069 | 0.383 |
DOC_MAPK_gen_1 | 452 | 461 | PF00069 | 0.228 |
DOC_MAPK_MEF2A_6 | 207 | 216 | PF00069 | 0.207 |
DOC_MAPK_MEF2A_6 | 455 | 463 | PF00069 | 0.222 |
DOC_PP1_RVXF_1 | 216 | 223 | PF00149 | 0.188 |
DOC_PP1_RVXF_1 | 482 | 488 | PF00149 | 0.369 |
DOC_PP2B_LxvP_1 | 418 | 421 | PF13499 | 0.342 |
DOC_USP7_MATH_1 | 110 | 114 | PF00917 | 0.331 |
DOC_USP7_MATH_1 | 404 | 408 | PF00917 | 0.256 |
DOC_USP7_MATH_1 | 478 | 482 | PF00917 | 0.385 |
DOC_USP7_MATH_1 | 499 | 503 | PF00917 | 0.350 |
DOC_USP7_MATH_1 | 523 | 527 | PF00917 | 0.263 |
DOC_USP7_MATH_1 | 581 | 585 | PF00917 | 0.478 |
DOC_WW_Pin1_4 | 126 | 131 | PF00397 | 0.266 |
DOC_WW_Pin1_4 | 339 | 344 | PF00397 | 0.264 |
LIG_14-3-3_CanoR_1 | 218 | 223 | PF00244 | 0.297 |
LIG_14-3-3_CanoR_1 | 371 | 377 | PF00244 | 0.350 |
LIG_APCC_ABBA_1 | 419 | 424 | PF00400 | 0.349 |
LIG_BRCT_BRCA1_1 | 411 | 415 | PF00533 | 0.272 |
LIG_BRCT_BRCA1_1 | 468 | 472 | PF00533 | 0.334 |
LIG_deltaCOP1_diTrp_1 | 431 | 439 | PF00928 | 0.379 |
LIG_FHA_1 | 129 | 135 | PF00498 | 0.337 |
LIG_FHA_1 | 204 | 210 | PF00498 | 0.328 |
LIG_FHA_1 | 456 | 462 | PF00498 | 0.320 |
LIG_FHA_1 | 504 | 510 | PF00498 | 0.297 |
LIG_FHA_1 | 52 | 58 | PF00498 | 0.227 |
LIG_FHA_1 | 617 | 623 | PF00498 | 0.564 |
LIG_FHA_2 | 282 | 288 | PF00498 | 0.314 |
LIG_FHA_2 | 439 | 445 | PF00498 | 0.419 |
LIG_LIR_Gen_1 | 160 | 171 | PF02991 | 0.344 |
LIG_LIR_Gen_1 | 221 | 231 | PF02991 | 0.356 |
LIG_LIR_Gen_1 | 305 | 315 | PF02991 | 0.325 |
LIG_LIR_Gen_1 | 364 | 373 | PF02991 | 0.348 |
LIG_LIR_Gen_1 | 375 | 385 | PF02991 | 0.262 |
LIG_LIR_Gen_1 | 412 | 423 | PF02991 | 0.279 |
LIG_LIR_Gen_1 | 424 | 431 | PF02991 | 0.339 |
LIG_LIR_Gen_1 | 480 | 488 | PF02991 | 0.393 |
LIG_LIR_Gen_1 | 96 | 105 | PF02991 | 0.272 |
LIG_LIR_Nem_3 | 160 | 166 | PF02991 | 0.367 |
LIG_LIR_Nem_3 | 221 | 226 | PF02991 | 0.256 |
LIG_LIR_Nem_3 | 228 | 232 | PF02991 | 0.249 |
LIG_LIR_Nem_3 | 290 | 295 | PF02991 | 0.286 |
LIG_LIR_Nem_3 | 305 | 311 | PF02991 | 0.322 |
LIG_LIR_Nem_3 | 347 | 353 | PF02991 | 0.312 |
LIG_LIR_Nem_3 | 364 | 370 | PF02991 | 0.370 |
LIG_LIR_Nem_3 | 375 | 380 | PF02991 | 0.254 |
LIG_LIR_Nem_3 | 412 | 418 | PF02991 | 0.303 |
LIG_LIR_Nem_3 | 424 | 429 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 430 | 435 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 480 | 485 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 496 | 500 | PF02991 | 0.302 |
LIG_LIR_Nem_3 | 570 | 575 | PF02991 | 0.524 |
LIG_LIR_Nem_3 | 74 | 79 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 86 | 92 | PF02991 | 0.313 |
LIG_LIR_Nem_3 | 96 | 102 | PF02991 | 0.260 |
LIG_NRBOX | 606 | 612 | PF00104 | 0.536 |
LIG_PAM2_1 | 404 | 416 | PF00658 | 0.328 |
LIG_Pex14_2 | 373 | 377 | PF04695 | 0.303 |
LIG_Pex14_2 | 413 | 417 | PF04695 | 0.279 |
LIG_Pex14_2 | 462 | 466 | PF04695 | 0.311 |
LIG_REV1ctd_RIR_1 | 600 | 608 | PF16727 | 0.566 |
LIG_RPA_C_Fungi | 174 | 186 | PF08784 | 0.208 |
LIG_SH2_CRK | 163 | 167 | PF00017 | 0.412 |
LIG_SH2_CRK | 351 | 355 | PF00017 | 0.430 |
LIG_SH2_CRK | 482 | 486 | PF00017 | 0.539 |
LIG_SH2_NCK_1 | 163 | 167 | PF00017 | 0.352 |
LIG_SH2_NCK_1 | 308 | 312 | PF00017 | 0.496 |
LIG_SH2_SRC | 422 | 425 | PF00017 | 0.435 |
LIG_SH2_STAP1 | 335 | 339 | PF00017 | 0.571 |
LIG_SH2_STAP1 | 558 | 562 | PF00017 | 0.347 |
LIG_SH2_STAT5 | 105 | 108 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 163 | 166 | PF00017 | 0.379 |
LIG_SH2_STAT5 | 187 | 190 | PF00017 | 0.403 |
LIG_SH2_STAT5 | 273 | 276 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 308 | 311 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 314 | 317 | PF00017 | 0.318 |
LIG_SH2_STAT5 | 381 | 384 | PF00017 | 0.481 |
LIG_SH2_STAT5 | 43 | 46 | PF00017 | 0.463 |
LIG_SH2_STAT5 | 482 | 485 | PF00017 | 0.543 |
LIG_SH2_STAT5 | 589 | 592 | PF00017 | 0.490 |
LIG_SH3_3 | 119 | 125 | PF00018 | 0.394 |
LIG_SH3_3 | 12 | 18 | PF00018 | 0.331 |
LIG_SH3_3 | 517 | 523 | PF00018 | 0.348 |
LIG_SH3_3 | 612 | 618 | PF00018 | 0.418 |
LIG_Sin3_3 | 329 | 336 | PF02671 | 0.404 |
LIG_Sin3_3 | 543 | 550 | PF02671 | 0.322 |
LIG_SUMO_SIM_par_1 | 258 | 264 | PF11976 | 0.309 |
LIG_SUMO_SIM_par_1 | 515 | 521 | PF11976 | 0.499 |
LIG_SUMO_SIM_par_1 | 573 | 580 | PF11976 | 0.357 |
LIG_SUMO_SIM_par_1 | 581 | 587 | PF11976 | 0.313 |
LIG_UBA3_1 | 257 | 266 | PF00899 | 0.454 |
LIG_UBA3_1 | 376 | 383 | PF00899 | 0.434 |
LIG_WRC_WIRS_1 | 494 | 499 | PF05994 | 0.410 |
MOD_CK1_1 | 20 | 26 | PF00069 | 0.487 |
MOD_CK1_1 | 397 | 403 | PF00069 | 0.376 |
MOD_CK1_1 | 510 | 516 | PF00069 | 0.489 |
MOD_CK1_1 | 576 | 582 | PF00069 | 0.423 |
MOD_CK1_1 | 584 | 590 | PF00069 | 0.461 |
MOD_CK2_1 | 218 | 224 | PF00069 | 0.229 |
MOD_CK2_1 | 281 | 287 | PF00069 | 0.481 |
MOD_CK2_1 | 357 | 363 | PF00069 | 0.417 |
MOD_CK2_1 | 372 | 378 | PF00069 | 0.251 |
MOD_CK2_1 | 467 | 473 | PF00069 | 0.520 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.355 |
MOD_GlcNHglycan | 233 | 238 | PF01048 | 0.323 |
MOD_GlcNHglycan | 329 | 332 | PF01048 | 0.249 |
MOD_GlcNHglycan | 359 | 362 | PF01048 | 0.416 |
MOD_GlcNHglycan | 389 | 392 | PF01048 | 0.614 |
MOD_GlcNHglycan | 406 | 409 | PF01048 | 0.357 |
MOD_GlcNHglycan | 473 | 478 | PF01048 | 0.604 |
MOD_GlcNHglycan | 537 | 540 | PF01048 | 0.398 |
MOD_GlcNHglycan | 558 | 561 | PF01048 | 0.272 |
MOD_GlcNHglycan | 579 | 582 | PF01048 | 0.407 |
MOD_GlcNHglycan | 586 | 589 | PF01048 | 0.401 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.350 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.392 |
MOD_GSK3_1 | 218 | 225 | PF00069 | 0.295 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.562 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.554 |
MOD_GSK3_1 | 357 | 364 | PF00069 | 0.321 |
MOD_GSK3_1 | 499 | 506 | PF00069 | 0.498 |
MOD_GSK3_1 | 552 | 559 | PF00069 | 0.394 |
MOD_GSK3_1 | 573 | 580 | PF00069 | 0.390 |
MOD_N-GLC_1 | 245 | 250 | PF02516 | 0.286 |
MOD_N-GLC_1 | 71 | 76 | PF02516 | 0.393 |
MOD_N-GLC_2 | 66 | 68 | PF02516 | 0.392 |
MOD_NEK2_1 | 120 | 125 | PF00069 | 0.331 |
MOD_NEK2_1 | 222 | 227 | PF00069 | 0.355 |
MOD_NEK2_1 | 4 | 9 | PF00069 | 0.343 |
MOD_NEK2_1 | 42 | 47 | PF00069 | 0.458 |
MOD_NEK2_1 | 466 | 471 | PF00069 | 0.467 |
MOD_NEK2_1 | 533 | 538 | PF00069 | 0.346 |
MOD_NEK2_1 | 554 | 559 | PF00069 | 0.376 |
MOD_NEK2_1 | 562 | 567 | PF00069 | 0.402 |
MOD_NEK2_1 | 59 | 64 | PF00069 | 0.229 |
MOD_NEK2_1 | 624 | 629 | PF00069 | 0.501 |
MOD_NEK2_2 | 372 | 377 | PF00069 | 0.363 |
MOD_PIKK_1 | 499 | 505 | PF00454 | 0.300 |
MOD_PIKK_1 | 518 | 524 | PF00454 | 0.458 |
MOD_PIKK_1 | 91 | 97 | PF00454 | 0.448 |
MOD_PK_1 | 179 | 185 | PF00069 | 0.387 |
MOD_PKA_2 | 203 | 209 | PF00069 | 0.368 |
MOD_PKA_2 | 387 | 393 | PF00069 | 0.384 |
MOD_Plk_1 | 161 | 167 | PF00069 | 0.436 |
MOD_Plk_1 | 605 | 611 | PF00069 | 0.448 |
MOD_Plk_4 | 179 | 185 | PF00069 | 0.377 |
MOD_Plk_4 | 218 | 224 | PF00069 | 0.412 |
MOD_Plk_4 | 253 | 259 | PF00069 | 0.359 |
MOD_Plk_4 | 273 | 279 | PF00069 | 0.464 |
MOD_Plk_4 | 287 | 293 | PF00069 | 0.352 |
MOD_Plk_4 | 372 | 378 | PF00069 | 0.345 |
MOD_Plk_4 | 513 | 519 | PF00069 | 0.546 |
MOD_Plk_4 | 573 | 579 | PF00069 | 0.403 |
MOD_Plk_4 | 59 | 65 | PF00069 | 0.221 |
MOD_Plk_4 | 606 | 612 | PF00069 | 0.433 |
MOD_ProDKin_1 | 126 | 132 | PF00069 | 0.306 |
MOD_ProDKin_1 | 339 | 345 | PF00069 | 0.297 |
TRG_DiLeu_BaEn_1 | 140 | 145 | PF01217 | 0.292 |
TRG_DiLeu_BaEn_1 | 431 | 436 | PF01217 | 0.363 |
TRG_DiLeu_BaEn_1 | 606 | 611 | PF01217 | 0.398 |
TRG_DiLeu_BaLyEn_6 | 198 | 203 | PF01217 | 0.202 |
TRG_DiLeu_BaLyEn_6 | 541 | 546 | PF01217 | 0.353 |
TRG_ENDOCYTIC_2 | 155 | 158 | PF00928 | 0.511 |
TRG_ENDOCYTIC_2 | 163 | 166 | PF00928 | 0.341 |
TRG_ENDOCYTIC_2 | 229 | 232 | PF00928 | 0.233 |
TRG_ENDOCYTIC_2 | 292 | 295 | PF00928 | 0.383 |
TRG_ENDOCYTIC_2 | 308 | 311 | PF00928 | 0.309 |
TRG_ENDOCYTIC_2 | 350 | 353 | PF00928 | 0.331 |
TRG_ENDOCYTIC_2 | 482 | 485 | PF00928 | 0.583 |
TRG_ENDOCYTIC_2 | 76 | 79 | PF00928 | 0.452 |
TRG_ER_diArg_1 | 117 | 119 | PF00400 | 0.267 |
TRG_ER_diArg_1 | 271 | 273 | PF00400 | 0.417 |
TRG_ER_diArg_1 | 89 | 91 | PF00400 | 0.478 |
TRG_Pf-PMV_PEXEL_1 | 207 | 211 | PF00026 | 0.221 |
TRG_Pf-PMV_PEXEL_1 | 544 | 548 | PF00026 | 0.432 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IM74 | Leptomonas seymouri | 54% | 100% |
A0A1X0NYU6 | Trypanosomatidae | 28% | 100% |
A0A3S7X1C5 | Leishmania donovani | 79% | 100% |
A4I3F4 | Leishmania infantum | 78% | 100% |
D0A7Y6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
E9AZP2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 100% |
Q4Q8J0 | Leishmania major | 78% | 100% |
V5BQB3 | Trypanosoma cruzi | 27% | 100% |