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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 8 |
GO:0110165 | cellular anatomical entity | 1 | 8 |
Related structures:
AlphaFold database: E8NHC2
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 8 |
GO:0006644 | phospholipid metabolic process | 4 | 8 |
GO:0006793 | phosphorus metabolic process | 3 | 8 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 8 |
GO:0008152 | metabolic process | 1 | 8 |
GO:0008610 | lipid biosynthetic process | 4 | 8 |
GO:0008654 | phospholipid biosynthetic process | 5 | 8 |
GO:0009058 | biosynthetic process | 2 | 8 |
GO:0009987 | cellular process | 1 | 8 |
GO:0019637 | organophosphate metabolic process | 3 | 8 |
GO:0044237 | cellular metabolic process | 2 | 8 |
GO:0044238 | primary metabolic process | 2 | 8 |
GO:0044255 | cellular lipid metabolic process | 3 | 8 |
GO:0071704 | organic substance metabolic process | 2 | 8 |
GO:0090407 | organophosphate biosynthetic process | 4 | 8 |
GO:1901576 | organic substance biosynthetic process | 3 | 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 8 |
GO:0016740 | transferase activity | 2 | 8 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 8 |
GO:0016780 | phosphotransferase activity, for other substituted phosphate groups | 4 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 121 | 125 | PF00656 | 0.474 |
CLV_C14_Caspase3-7 | 268 | 272 | PF00656 | 0.693 |
CLV_C14_Caspase3-7 | 519 | 523 | PF00656 | 0.723 |
CLV_NRD_NRD_1 | 129 | 131 | PF00675 | 0.272 |
CLV_NRD_NRD_1 | 35 | 37 | PF00675 | 0.371 |
CLV_NRD_NRD_1 | 371 | 373 | PF00675 | 0.611 |
CLV_NRD_NRD_1 | 384 | 386 | PF00675 | 0.638 |
CLV_NRD_NRD_1 | 422 | 424 | PF00675 | 0.354 |
CLV_NRD_NRD_1 | 457 | 459 | PF00675 | 0.489 |
CLV_NRD_NRD_1 | 482 | 484 | PF00675 | 0.442 |
CLV_NRD_NRD_1 | 615 | 617 | PF00675 | 0.548 |
CLV_PCSK_KEX2_1 | 129 | 131 | PF00082 | 0.272 |
CLV_PCSK_KEX2_1 | 371 | 373 | PF00082 | 0.611 |
CLV_PCSK_KEX2_1 | 384 | 386 | PF00082 | 0.638 |
CLV_PCSK_KEX2_1 | 422 | 424 | PF00082 | 0.354 |
CLV_PCSK_KEX2_1 | 457 | 459 | PF00082 | 0.489 |
CLV_PCSK_KEX2_1 | 482 | 484 | PF00082 | 0.442 |
CLV_PCSK_SKI1_1 | 12 | 16 | PF00082 | 0.374 |
CLV_PCSK_SKI1_1 | 190 | 194 | PF00082 | 0.547 |
CLV_PCSK_SKI1_1 | 297 | 301 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 326 | 330 | PF00082 | 0.341 |
CLV_PCSK_SKI1_1 | 336 | 340 | PF00082 | 0.279 |
CLV_PCSK_SKI1_1 | 600 | 604 | PF00082 | 0.499 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.658 |
DEG_ODPH_VHL_1 | 46 | 58 | PF01847 | 0.381 |
DEG_ODPH_VHL_1 | 460 | 472 | PF01847 | 0.442 |
DEG_SCF_FBW7_2 | 370 | 377 | PF00400 | 0.413 |
DOC_CDC14_PxL_1 | 273 | 281 | PF14671 | 0.612 |
DOC_CYCLIN_yClb3_PxF_3 | 99 | 105 | PF00134 | 0.351 |
DOC_MAPK_gen_1 | 10 | 17 | PF00069 | 0.621 |
DOC_MAPK_gen_1 | 36 | 44 | PF00069 | 0.569 |
DOC_MAPK_gen_1 | 384 | 390 | PF00069 | 0.431 |
DOC_MAPK_HePTP_8 | 34 | 46 | PF00069 | 0.502 |
DOC_MAPK_MEF2A_6 | 10 | 17 | PF00069 | 0.621 |
DOC_MAPK_MEF2A_6 | 190 | 197 | PF00069 | 0.351 |
DOC_MAPK_MEF2A_6 | 342 | 350 | PF00069 | 0.489 |
DOC_MAPK_MEF2A_6 | 37 | 46 | PF00069 | 0.503 |
DOC_MAPK_MEF2A_6 | 398 | 407 | PF00069 | 0.323 |
DOC_MAPK_MEF2A_6 | 438 | 445 | PF00069 | 0.323 |
DOC_MAPK_MEF2A_6 | 457 | 466 | PF00069 | 0.272 |
DOC_MAPK_NFAT4_5 | 10 | 18 | PF00069 | 0.621 |
DOC_MAPK_NFAT4_5 | 190 | 198 | PF00069 | 0.355 |
DOC_MAPK_NFAT4_5 | 438 | 446 | PF00069 | 0.323 |
DOC_MAPK_RevD_3 | 443 | 458 | PF00069 | 0.497 |
DOC_PP2B_LxvP_1 | 193 | 196 | PF13499 | 0.301 |
DOC_PP2B_LxvP_1 | 577 | 580 | PF13499 | 0.564 |
DOC_PP4_FxxP_1 | 582 | 585 | PF00568 | 0.554 |
DOC_SPAK_OSR1_1 | 385 | 389 | PF12202 | 0.429 |
DOC_USP7_MATH_1 | 163 | 167 | PF00917 | 0.516 |
DOC_USP7_MATH_1 | 356 | 360 | PF00917 | 0.347 |
DOC_USP7_MATH_1 | 493 | 497 | PF00917 | 0.687 |
DOC_USP7_MATH_1 | 518 | 522 | PF00917 | 0.752 |
DOC_USP7_MATH_1 | 523 | 527 | PF00917 | 0.764 |
DOC_USP7_MATH_1 | 532 | 536 | PF00917 | 0.587 |
DOC_WW_Pin1_4 | 132 | 137 | PF00397 | 0.472 |
DOC_WW_Pin1_4 | 370 | 375 | PF00397 | 0.407 |
DOC_WW_Pin1_4 | 608 | 613 | PF00397 | 0.654 |
DOC_WW_Pin1_4 | 86 | 91 | PF00397 | 0.546 |
LIG_14-3-3_CanoR_1 | 130 | 136 | PF00244 | 0.490 |
LIG_14-3-3_CanoR_1 | 342 | 347 | PF00244 | 0.492 |
LIG_14-3-3_CanoR_1 | 457 | 461 | PF00244 | 0.289 |
LIG_Actin_WH2_2 | 577 | 595 | PF00022 | 0.637 |
LIG_BIR_III_2 | 522 | 526 | PF00653 | 0.661 |
LIG_BIR_III_4 | 269 | 273 | PF00653 | 0.616 |
LIG_BRCT_BRCA1_1 | 386 | 390 | PF00533 | 0.447 |
LIG_BRCT_BRCA1_1 | 449 | 453 | PF00533 | 0.381 |
LIG_eIF4E_1 | 188 | 194 | PF01652 | 0.272 |
LIG_EVH1_2 | 101 | 105 | PF00568 | 0.309 |
LIG_FHA_1 | 167 | 173 | PF00498 | 0.478 |
LIG_FHA_1 | 177 | 183 | PF00498 | 0.313 |
LIG_FHA_1 | 213 | 219 | PF00498 | 0.381 |
LIG_FHA_1 | 294 | 300 | PF00498 | 0.620 |
LIG_FHA_1 | 343 | 349 | PF00498 | 0.469 |
LIG_FHA_1 | 429 | 435 | PF00498 | 0.309 |
LIG_FHA_1 | 571 | 577 | PF00498 | 0.608 |
LIG_FHA_1 | 60 | 66 | PF00498 | 0.373 |
LIG_FHA_1 | 603 | 609 | PF00498 | 0.705 |
LIG_FHA_1 | 86 | 92 | PF00498 | 0.530 |
LIG_FHA_2 | 182 | 188 | PF00498 | 0.348 |
LIG_FHA_2 | 262 | 268 | PF00498 | 0.646 |
LIG_FHA_2 | 413 | 419 | PF00498 | 0.478 |
LIG_FHA_2 | 517 | 523 | PF00498 | 0.761 |
LIG_FHA_2 | 535 | 541 | PF00498 | 0.664 |
LIG_FHA_2 | 80 | 86 | PF00498 | 0.499 |
LIG_GBD_Chelix_1 | 112 | 120 | PF00786 | 0.442 |
LIG_LIR_Gen_1 | 169 | 178 | PF02991 | 0.305 |
LIG_LIR_Gen_1 | 24 | 34 | PF02991 | 0.622 |
LIG_LIR_Gen_1 | 271 | 280 | PF02991 | 0.589 |
LIG_LIR_Gen_1 | 340 | 351 | PF02991 | 0.538 |
LIG_LIR_Gen_1 | 506 | 514 | PF02991 | 0.718 |
LIG_LIR_Gen_1 | 559 | 570 | PF02991 | 0.555 |
LIG_LIR_Nem_3 | 169 | 173 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 184 | 188 | PF02991 | 0.305 |
LIG_LIR_Nem_3 | 271 | 276 | PF02991 | 0.599 |
LIG_LIR_Nem_3 | 340 | 346 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 387 | 393 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 40 | 44 | PF02991 | 0.563 |
LIG_LIR_Nem_3 | 450 | 456 | PF02991 | 0.347 |
LIG_LIR_Nem_3 | 506 | 510 | PF02991 | 0.720 |
LIG_LIR_Nem_3 | 559 | 565 | PF02991 | 0.562 |
LIG_NRBOX | 115 | 121 | PF00104 | 0.395 |
LIG_PCNA_PIPBox_1 | 325 | 334 | PF02747 | 0.586 |
LIG_PCNA_yPIPBox_3 | 325 | 336 | PF02747 | 0.640 |
LIG_Pex14_1 | 185 | 189 | PF04695 | 0.272 |
LIG_Pex14_2 | 181 | 185 | PF04695 | 0.348 |
LIG_Pex14_2 | 386 | 390 | PF04695 | 0.420 |
LIG_PROFILIN_1 | 97 | 103 | PF00235 | 0.308 |
LIG_Rb_LxCxE_1 | 76 | 95 | PF01857 | 0.402 |
LIG_SH2_CRK | 189 | 193 | PF00017 | 0.357 |
LIG_SH2_CRK | 343 | 347 | PF00017 | 0.489 |
LIG_SH2_CRK | 367 | 371 | PF00017 | 0.318 |
LIG_SH2_CRK | 436 | 440 | PF00017 | 0.381 |
LIG_SH2_SRC | 4 | 7 | PF00017 | 0.596 |
LIG_SH2_SRC | 41 | 44 | PF00017 | 0.551 |
LIG_SH2_STAP1 | 436 | 440 | PF00017 | 0.426 |
LIG_SH2_STAP1 | 541 | 545 | PF00017 | 0.664 |
LIG_SH2_STAP1 | 552 | 556 | PF00017 | 0.601 |
LIG_SH2_STAT5 | 16 | 19 | PF00017 | 0.529 |
LIG_SH2_STAT5 | 212 | 215 | PF00017 | 0.304 |
LIG_SH2_STAT5 | 25 | 28 | PF00017 | 0.510 |
LIG_SH2_STAT5 | 262 | 265 | PF00017 | 0.599 |
LIG_SH2_STAT5 | 4 | 7 | PF00017 | 0.522 |
LIG_SH2_STAT5 | 41 | 44 | PF00017 | 0.471 |
LIG_SH2_STAT5 | 436 | 439 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 474 | 477 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 512 | 515 | PF00017 | 0.756 |
LIG_SH2_STAT5 | 80 | 83 | PF00017 | 0.463 |
LIG_SH3_1 | 289 | 295 | PF00018 | 0.631 |
LIG_SH3_2 | 292 | 297 | PF14604 | 0.624 |
LIG_SH3_3 | 215 | 221 | PF00018 | 0.361 |
LIG_SH3_3 | 289 | 295 | PF00018 | 0.587 |
LIG_SH3_3 | 91 | 97 | PF00018 | 0.510 |
LIG_SUMO_SIM_anti_2 | 169 | 176 | PF11976 | 0.442 |
LIG_SUMO_SIM_par_1 | 169 | 176 | PF11976 | 0.381 |
LIG_SUMO_SIM_par_1 | 400 | 406 | PF11976 | 0.383 |
LIG_TRAF2_1 | 184 | 187 | PF00917 | 0.348 |
LIG_TYR_ITIM | 341 | 346 | PF00017 | 0.522 |
LIG_TYR_ITIM | 39 | 44 | PF00017 | 0.598 |
LIG_TYR_ITIM | 434 | 439 | PF00017 | 0.381 |
LIG_UBA3_1 | 1 | 10 | PF00899 | 0.625 |
LIG_WRC_WIRS_1 | 177 | 182 | PF05994 | 0.442 |
LIG_WRC_WIRS_1 | 404 | 409 | PF05994 | 0.442 |
MOD_CDC14_SPxK_1 | 611 | 614 | PF00782 | 0.665 |
MOD_CDK_SPxK_1 | 608 | 614 | PF00069 | 0.658 |
MOD_CK1_1 | 156 | 162 | PF00069 | 0.487 |
MOD_CK1_1 | 166 | 172 | PF00069 | 0.530 |
MOD_CK1_1 | 319 | 325 | PF00069 | 0.610 |
MOD_CK1_1 | 531 | 537 | PF00069 | 0.723 |
MOD_CK1_1 | 558 | 564 | PF00069 | 0.530 |
MOD_CK2_1 | 181 | 187 | PF00069 | 0.348 |
MOD_CK2_1 | 261 | 267 | PF00069 | 0.674 |
MOD_CK2_1 | 79 | 85 | PF00069 | 0.497 |
MOD_CMANNOS | 167 | 170 | PF00535 | 0.272 |
MOD_CMANNOS | 214 | 217 | PF00535 | 0.426 |
MOD_Cter_Amidation | 382 | 385 | PF01082 | 0.644 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.323 |
MOD_GlcNHglycan | 318 | 321 | PF01048 | 0.439 |
MOD_GlcNHglycan | 333 | 336 | PF01048 | 0.378 |
MOD_GlcNHglycan | 358 | 361 | PF01048 | 0.385 |
MOD_GlcNHglycan | 409 | 412 | PF01048 | 0.488 |
MOD_GlcNHglycan | 449 | 452 | PF01048 | 0.621 |
MOD_GlcNHglycan | 489 | 492 | PF01048 | 0.464 |
MOD_GlcNHglycan | 495 | 498 | PF01048 | 0.547 |
MOD_GlcNHglycan | 514 | 517 | PF01048 | 0.347 |
MOD_GlcNHglycan | 530 | 533 | PF01048 | 0.537 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.638 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.463 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.532 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.629 |
MOD_GSK3_1 | 403 | 410 | PF00069 | 0.426 |
MOD_GSK3_1 | 510 | 517 | PF00069 | 0.785 |
MOD_GSK3_1 | 528 | 535 | PF00069 | 0.742 |
MOD_GSK3_1 | 604 | 611 | PF00069 | 0.640 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.484 |
MOD_N-GLC_1 | 282 | 287 | PF02516 | 0.354 |
MOD_N-GLC_1 | 476 | 481 | PF02516 | 0.453 |
MOD_NEK2_1 | 282 | 287 | PF00069 | 0.636 |
MOD_NEK2_1 | 331 | 336 | PF00069 | 0.595 |
MOD_NEK2_1 | 407 | 412 | PF00069 | 0.352 |
MOD_NEK2_1 | 428 | 433 | PF00069 | 0.315 |
MOD_NEK2_1 | 434 | 439 | PF00069 | 0.320 |
MOD_NEK2_1 | 456 | 461 | PF00069 | 0.283 |
MOD_NEK2_1 | 555 | 560 | PF00069 | 0.523 |
MOD_NEK2_1 | 565 | 570 | PF00069 | 0.498 |
MOD_NEK2_1 | 58 | 63 | PF00069 | 0.401 |
MOD_NEK2_1 | 596 | 601 | PF00069 | 0.599 |
MOD_NEK2_2 | 337 | 342 | PF00069 | 0.644 |
MOD_PIKK_1 | 476 | 482 | PF00454 | 0.566 |
MOD_PK_1 | 384 | 390 | PF00069 | 0.431 |
MOD_PKA_1 | 384 | 390 | PF00069 | 0.431 |
MOD_PKA_2 | 128 | 134 | PF00069 | 0.472 |
MOD_PKA_2 | 384 | 390 | PF00069 | 0.419 |
MOD_PKA_2 | 456 | 462 | PF00069 | 0.289 |
MOD_PKA_2 | 570 | 576 | PF00069 | 0.533 |
MOD_Plk_1 | 21 | 27 | PF00069 | 0.511 |
MOD_Plk_1 | 476 | 482 | PF00069 | 0.625 |
MOD_Plk_4 | 166 | 172 | PF00069 | 0.501 |
MOD_Plk_4 | 173 | 179 | PF00069 | 0.375 |
MOD_Plk_4 | 319 | 325 | PF00069 | 0.553 |
MOD_Plk_4 | 470 | 476 | PF00069 | 0.358 |
MOD_ProDKin_1 | 132 | 138 | PF00069 | 0.472 |
MOD_ProDKin_1 | 370 | 376 | PF00069 | 0.411 |
MOD_ProDKin_1 | 608 | 614 | PF00069 | 0.658 |
MOD_ProDKin_1 | 86 | 92 | PF00069 | 0.549 |
TRG_DiLeu_BaEn_1 | 572 | 577 | PF01217 | 0.601 |
TRG_ENDOCYTIC_2 | 117 | 120 | PF00928 | 0.323 |
TRG_ENDOCYTIC_2 | 189 | 192 | PF00928 | 0.345 |
TRG_ENDOCYTIC_2 | 27 | 30 | PF00928 | 0.508 |
TRG_ENDOCYTIC_2 | 343 | 346 | PF00928 | 0.491 |
TRG_ENDOCYTIC_2 | 367 | 370 | PF00928 | 0.309 |
TRG_ENDOCYTIC_2 | 41 | 44 | PF00928 | 0.488 |
TRG_ENDOCYTIC_2 | 436 | 439 | PF00928 | 0.381 |
TRG_ENDOCYTIC_2 | 552 | 555 | PF00928 | 0.556 |
TRG_ER_diArg_1 | 370 | 372 | PF00400 | 0.404 |
TRG_ER_diArg_1 | 384 | 386 | PF00400 | 0.438 |
TRG_ER_diArg_1 | 421 | 423 | PF00400 | 0.553 |
TRG_ER_diArg_1 | 456 | 458 | PF00400 | 0.370 |
TRG_ER_diArg_1 | 481 | 483 | PF00400 | 0.636 |
TRG_Pf-PMV_PEXEL_1 | 234 | 238 | PF00026 | 0.441 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2Y1 | Leptomonas seymouri | 64% | 100% |
A0A0S4J7L0 | Bodo saltans | 45% | 100% |
A0A1X0P8W0 | Trypanosomatidae | 43% | 100% |
A0A3S5H562 | Leishmania donovani | 100% | 100% |
E9AJW6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 97% |
V5BXC7 | Trypanosoma cruzi | 45% | 100% |