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: 12 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9B626
Term | Name | Level | Count |
---|---|---|---|
GO:0006793 | phosphorus metabolic process | 3 | 13 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 13 |
GO:0008152 | metabolic process | 1 | 13 |
GO:0009987 | cellular process | 1 | 13 |
GO:0016310 | phosphorylation | 5 | 13 |
GO:0044237 | cellular metabolic process | 2 | 13 |
GO:0006629 | lipid metabolic process | 3 | 1 |
GO:0006644 | phospholipid metabolic process | 4 | 1 |
GO:0006646 | phosphatidylethanolamine biosynthetic process | 6 | 1 |
GO:0006650 | glycerophospholipid metabolic process | 5 | 1 |
GO:0008610 | lipid biosynthetic process | 4 | 1 |
GO:0008654 | phospholipid biosynthetic process | 5 | 1 |
GO:0009058 | biosynthetic process | 2 | 1 |
GO:0019637 | organophosphate metabolic process | 3 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044249 | cellular biosynthetic process | 3 | 1 |
GO:0044255 | cellular lipid metabolic process | 3 | 1 |
GO:0045017 | glycerolipid biosynthetic process | 4 | 1 |
GO:0046337 | phosphatidylethanolamine metabolic process | 6 | 1 |
GO:0046474 | glycerophospholipid biosynthetic process | 5 | 1 |
GO:0046486 | glycerolipid metabolic process | 4 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090407 | organophosphate biosynthetic process | 4 | 1 |
GO:1901576 | organic substance biosynthetic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 13 |
GO:0016301 | kinase activity | 4 | 13 |
GO:0016740 | transferase activity | 2 | 13 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 13 |
GO:0004305 | ethanolamine kinase activity | 5 | 3 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 3 |
GO:0004103 | choline kinase activity | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 53 | 57 | PF00656 | 0.557 |
CLV_C14_Caspase3-7 | 583 | 587 | PF00656 | 0.577 |
CLV_C14_Caspase3-7 | 65 | 69 | PF00656 | 0.663 |
CLV_NRD_NRD_1 | 275 | 277 | PF00675 | 0.238 |
CLV_NRD_NRD_1 | 413 | 415 | PF00675 | 0.304 |
CLV_NRD_NRD_1 | 446 | 448 | PF00675 | 0.302 |
CLV_PCSK_KEX2_1 | 392 | 394 | PF00082 | 0.324 |
CLV_PCSK_PC1ET2_1 | 392 | 394 | PF00082 | 0.362 |
CLV_PCSK_SKI1_1 | 201 | 205 | PF00082 | 0.271 |
CLV_PCSK_SKI1_1 | 27 | 31 | PF00082 | 0.555 |
CLV_PCSK_SKI1_1 | 297 | 301 | PF00082 | 0.344 |
CLV_PCSK_SKI1_1 | 325 | 329 | PF00082 | 0.358 |
CLV_PCSK_SKI1_1 | 35 | 39 | PF00082 | 0.600 |
CLV_PCSK_SKI1_1 | 387 | 391 | PF00082 | 0.348 |
CLV_PCSK_SKI1_1 | 447 | 451 | PF00082 | 0.307 |
CLV_PCSK_SKI1_1 | 585 | 589 | PF00082 | 0.559 |
CLV_Separin_Metazoa | 24 | 28 | PF03568 | 0.594 |
DEG_APCC_DBOX_1 | 296 | 304 | PF00400 | 0.369 |
DEG_APCC_DBOX_1 | 592 | 600 | PF00400 | 0.521 |
DOC_AGCK_PIF_2 | 467 | 472 | PF00069 | 0.480 |
DOC_ANK_TNKS_1 | 494 | 501 | PF00023 | 0.644 |
DOC_CKS1_1 | 309 | 314 | PF01111 | 0.548 |
DOC_CKS1_1 | 43 | 48 | PF01111 | 0.693 |
DOC_CYCLIN_RxL_1 | 153 | 164 | PF00134 | 0.514 |
DOC_CYCLIN_RxL_1 | 354 | 364 | PF00134 | 0.539 |
DOC_CYCLIN_yCln2_LP_2 | 299 | 305 | PF00134 | 0.577 |
DOC_MAPK_gen_1 | 105 | 114 | PF00069 | 0.733 |
DOC_MAPK_gen_1 | 358 | 368 | PF00069 | 0.562 |
DOC_MAPK_gen_1 | 392 | 399 | PF00069 | 0.539 |
DOC_MAPK_JIP1_4 | 156 | 162 | PF00069 | 0.729 |
DOC_MAPK_MEF2A_6 | 392 | 399 | PF00069 | 0.520 |
DOC_MAPK_MEF2A_6 | 463 | 470 | PF00069 | 0.483 |
DOC_PP1_RVXF_1 | 461 | 468 | PF00149 | 0.562 |
DOC_USP7_MATH_1 | 254 | 258 | PF00917 | 0.548 |
DOC_USP7_MATH_1 | 282 | 286 | PF00917 | 0.577 |
DOC_USP7_MATH_1 | 329 | 333 | PF00917 | 0.572 |
DOC_USP7_MATH_1 | 347 | 351 | PF00917 | 0.497 |
DOC_USP7_MATH_1 | 436 | 440 | PF00917 | 0.519 |
DOC_USP7_MATH_1 | 556 | 560 | PF00917 | 0.616 |
DOC_USP7_MATH_1 | 634 | 638 | PF00917 | 0.509 |
DOC_USP7_UBL2_3 | 448 | 452 | PF12436 | 0.511 |
DOC_USP7_UBL2_3 | 96 | 100 | PF12436 | 0.598 |
DOC_WW_Pin1_4 | 143 | 148 | PF00397 | 0.713 |
DOC_WW_Pin1_4 | 231 | 236 | PF00397 | 0.491 |
DOC_WW_Pin1_4 | 261 | 266 | PF00397 | 0.480 |
DOC_WW_Pin1_4 | 308 | 313 | PF00397 | 0.528 |
DOC_WW_Pin1_4 | 42 | 47 | PF00397 | 0.640 |
DOC_WW_Pin1_4 | 586 | 591 | PF00397 | 0.599 |
LIG_14-3-3_CanoR_1 | 108 | 113 | PF00244 | 0.701 |
LIG_14-3-3_CanoR_1 | 156 | 161 | PF00244 | 0.713 |
LIG_14-3-3_CanoR_1 | 276 | 282 | PF00244 | 0.438 |
LIG_14-3-3_CanoR_1 | 361 | 368 | PF00244 | 0.484 |
LIG_14-3-3_CanoR_1 | 372 | 376 | PF00244 | 0.469 |
LIG_APCC_ABBAyCdc20_2 | 463 | 469 | PF00400 | 0.504 |
LIG_BIR_III_2 | 346 | 350 | PF00653 | 0.522 |
LIG_BRCT_BRCA1_1 | 373 | 377 | PF00533 | 0.369 |
LIG_BRCT_BRCA1_1 | 441 | 445 | PF00533 | 0.562 |
LIG_CtBP_PxDLS_1 | 46 | 50 | PF00389 | 0.715 |
LIG_deltaCOP1_diTrp_1 | 127 | 135 | PF00928 | 0.476 |
LIG_FHA_1 | 200 | 206 | PF00498 | 0.405 |
LIG_FHA_1 | 256 | 262 | PF00498 | 0.471 |
LIG_FHA_1 | 361 | 367 | PF00498 | 0.556 |
LIG_FHA_1 | 586 | 592 | PF00498 | 0.460 |
LIG_FHA_1 | 80 | 86 | PF00498 | 0.612 |
LIG_FHA_2 | 150 | 156 | PF00498 | 0.600 |
LIG_FHA_2 | 309 | 315 | PF00498 | 0.531 |
LIG_FHA_2 | 483 | 489 | PF00498 | 0.480 |
LIG_FHA_2 | 534 | 540 | PF00498 | 0.248 |
LIG_FHA_2 | 581 | 587 | PF00498 | 0.619 |
LIG_FHA_2 | 590 | 596 | PF00498 | 0.502 |
LIG_FXI_DFP_1 | 195 | 199 | PF00024 | 0.600 |
LIG_KLC1_Yacidic_2 | 333 | 337 | PF13176 | 0.522 |
LIG_LIR_Gen_1 | 270 | 278 | PF02991 | 0.563 |
LIG_LIR_Gen_1 | 28 | 37 | PF02991 | 0.535 |
LIG_LIR_Gen_1 | 280 | 291 | PF02991 | 0.564 |
LIG_LIR_Gen_1 | 313 | 323 | PF02991 | 0.522 |
LIG_LIR_Gen_1 | 374 | 383 | PF02991 | 0.561 |
LIG_LIR_Gen_1 | 469 | 480 | PF02991 | 0.546 |
LIG_LIR_Gen_1 | 61 | 70 | PF02991 | 0.723 |
LIG_LIR_Gen_1 | 611 | 621 | PF02991 | 0.403 |
LIG_LIR_Gen_1 | 652 | 660 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 127 | 131 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 139 | 143 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 217 | 222 | PF02991 | 0.577 |
LIG_LIR_Nem_3 | 240 | 246 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 270 | 275 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 28 | 34 | PF02991 | 0.527 |
LIG_LIR_Nem_3 | 280 | 286 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 313 | 318 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 355 | 360 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 374 | 378 | PF02991 | 0.555 |
LIG_LIR_Nem_3 | 469 | 475 | PF02991 | 0.493 |
LIG_LIR_Nem_3 | 501 | 507 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 518 | 523 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 6 | 12 | PF02991 | 0.655 |
LIG_LIR_Nem_3 | 611 | 616 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 641 | 645 | PF02991 | 0.361 |
LIG_LIR_Nem_3 | 652 | 656 | PF02991 | 0.348 |
LIG_NRBOX | 385 | 391 | PF00104 | 0.562 |
LIG_PCNA_yPIPBox_3 | 10 | 18 | PF02747 | 0.583 |
LIG_PCNA_yPIPBox_3 | 647 | 661 | PF02747 | 0.479 |
LIG_Pex14_2 | 445 | 449 | PF04695 | 0.562 |
LIG_Rb_pABgroove_1 | 129 | 137 | PF01858 | 0.470 |
LIG_SH2_CRK | 509 | 513 | PF00017 | 0.556 |
LIG_SH2_NCK_1 | 309 | 313 | PF00017 | 0.577 |
LIG_SH2_NCK_1 | 472 | 476 | PF00017 | 0.480 |
LIG_SH2_PTP2 | 653 | 656 | PF00017 | 0.397 |
LIG_SH2_SRC | 31 | 34 | PF00017 | 0.567 |
LIG_SH2_STAP1 | 283 | 287 | PF00017 | 0.562 |
LIG_SH2_STAT3 | 516 | 519 | PF00017 | 0.571 |
LIG_SH2_STAT5 | 315 | 318 | PF00017 | 0.562 |
LIG_SH2_STAT5 | 33 | 36 | PF00017 | 0.571 |
LIG_SH2_STAT5 | 335 | 338 | PF00017 | 0.577 |
LIG_SH2_STAT5 | 472 | 475 | PF00017 | 0.505 |
LIG_SH2_STAT5 | 493 | 496 | PF00017 | 0.480 |
LIG_SH2_STAT5 | 509 | 512 | PF00017 | 0.478 |
LIG_SH2_STAT5 | 535 | 538 | PF00017 | 0.526 |
LIG_SH2_STAT5 | 574 | 577 | PF00017 | 0.386 |
LIG_SH2_STAT5 | 642 | 645 | PF00017 | 0.400 |
LIG_SH2_STAT5 | 653 | 656 | PF00017 | 0.322 |
LIG_SH3_2 | 196 | 201 | PF14604 | 0.607 |
LIG_SH3_3 | 193 | 199 | PF00018 | 0.585 |
LIG_SH3_3 | 550 | 556 | PF00018 | 0.572 |
LIG_SUMO_SIM_anti_2 | 382 | 388 | PF11976 | 0.562 |
LIG_SUMO_SIM_par_1 | 44 | 54 | PF11976 | 0.714 |
LIG_TRAF2_1 | 311 | 314 | PF00917 | 0.536 |
LIG_TRAF2_1 | 512 | 515 | PF00917 | 0.550 |
LIG_UBA3_1 | 173 | 181 | PF00899 | 0.604 |
LIG_UBA3_1 | 385 | 392 | PF00899 | 0.562 |
LIG_WRC_WIRS_1 | 238 | 243 | PF05994 | 0.480 |
LIG_WRC_WIRS_1 | 283 | 288 | PF05994 | 0.573 |
LIG_WRC_WIRS_1 | 612 | 617 | PF05994 | 0.458 |
LIG_WW_3 | 24 | 28 | PF00397 | 0.594 |
MOD_CDK_SPxxK_3 | 586 | 593 | PF00069 | 0.609 |
MOD_CK1_1 | 210 | 216 | PF00069 | 0.562 |
MOD_CK1_1 | 36 | 42 | PF00069 | 0.604 |
MOD_CK1_1 | 439 | 445 | PF00069 | 0.552 |
MOD_CK1_1 | 48 | 54 | PF00069 | 0.552 |
MOD_CK1_1 | 606 | 612 | PF00069 | 0.451 |
MOD_CK2_1 | 149 | 155 | PF00069 | 0.593 |
MOD_CK2_1 | 308 | 314 | PF00069 | 0.505 |
MOD_CK2_1 | 347 | 353 | PF00069 | 0.480 |
MOD_CK2_1 | 482 | 488 | PF00069 | 0.480 |
MOD_CK2_1 | 533 | 539 | PF00069 | 0.235 |
MOD_CK2_1 | 589 | 595 | PF00069 | 0.539 |
MOD_CMANNOS | 610 | 613 | PF00535 | 0.339 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.509 |
MOD_GlcNHglycan | 209 | 212 | PF01048 | 0.354 |
MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.511 |
MOD_GlcNHglycan | 379 | 382 | PF01048 | 0.377 |
MOD_GlcNHglycan | 637 | 640 | PF01048 | 0.413 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.739 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.483 |
MOD_GSK3_1 | 348 | 355 | PF00069 | 0.494 |
MOD_GSK3_1 | 367 | 374 | PF00069 | 0.562 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.694 |
MOD_GSK3_1 | 435 | 442 | PF00069 | 0.514 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.649 |
MOD_GSK3_1 | 534 | 541 | PF00069 | 0.324 |
MOD_GSK3_1 | 585 | 592 | PF00069 | 0.501 |
MOD_GSK3_1 | 622 | 629 | PF00069 | 0.486 |
MOD_LATS_1 | 118 | 124 | PF00433 | 0.661 |
MOD_N-GLC_1 | 120 | 125 | PF02516 | 0.614 |
MOD_N-GLC_1 | 337 | 342 | PF02516 | 0.349 |
MOD_N-GLC_1 | 626 | 631 | PF02516 | 0.373 |
MOD_N-GLC_1 | 68 | 73 | PF02516 | 0.655 |
MOD_NEK2_1 | 318 | 323 | PF00069 | 0.385 |
MOD_NEK2_1 | 336 | 341 | PF00069 | 0.561 |
MOD_NEK2_1 | 352 | 357 | PF00069 | 0.416 |
MOD_NEK2_1 | 360 | 365 | PF00069 | 0.486 |
MOD_NEK2_1 | 397 | 402 | PF00069 | 0.545 |
MOD_NEK2_1 | 482 | 487 | PF00069 | 0.476 |
MOD_NEK2_1 | 533 | 538 | PF00069 | 0.519 |
MOD_NEK2_1 | 55 | 60 | PF00069 | 0.594 |
MOD_NEK2_1 | 600 | 605 | PF00069 | 0.356 |
MOD_NEK2_1 | 608 | 613 | PF00069 | 0.308 |
MOD_NEK2_1 | 62 | 67 | PF00069 | 0.549 |
MOD_NEK2_1 | 89 | 94 | PF00069 | 0.466 |
MOD_NEK2_2 | 33 | 38 | PF00069 | 0.577 |
MOD_PIKK_1 | 167 | 173 | PF00454 | 0.499 |
MOD_PIKK_1 | 337 | 343 | PF00454 | 0.571 |
MOD_PK_1 | 108 | 114 | PF00069 | 0.700 |
MOD_PKA_2 | 360 | 366 | PF00069 | 0.495 |
MOD_PKA_2 | 371 | 377 | PF00069 | 0.444 |
MOD_PKA_2 | 494 | 500 | PF00069 | 0.464 |
MOD_Plk_1 | 120 | 126 | PF00069 | 0.613 |
MOD_Plk_1 | 167 | 173 | PF00069 | 0.531 |
MOD_Plk_1 | 352 | 358 | PF00069 | 0.543 |
MOD_Plk_1 | 4 | 10 | PF00069 | 0.360 |
MOD_Plk_1 | 51 | 57 | PF00069 | 0.722 |
MOD_Plk_4 | 136 | 142 | PF00069 | 0.560 |
MOD_Plk_4 | 199 | 205 | PF00069 | 0.418 |
MOD_Plk_4 | 263 | 269 | PF00069 | 0.520 |
MOD_Plk_4 | 282 | 288 | PF00069 | 0.577 |
MOD_Plk_4 | 371 | 377 | PF00069 | 0.495 |
MOD_Plk_4 | 4 | 10 | PF00069 | 0.553 |
MOD_Plk_4 | 58 | 64 | PF00069 | 0.500 |
MOD_ProDKin_1 | 143 | 149 | PF00069 | 0.716 |
MOD_ProDKin_1 | 231 | 237 | PF00069 | 0.491 |
MOD_ProDKin_1 | 261 | 267 | PF00069 | 0.480 |
MOD_ProDKin_1 | 308 | 314 | PF00069 | 0.528 |
MOD_ProDKin_1 | 42 | 48 | PF00069 | 0.636 |
MOD_ProDKin_1 | 586 | 592 | PF00069 | 0.595 |
MOD_SUMO_for_1 | 37 | 40 | PF00179 | 0.588 |
TRG_DiLeu_BaEn_1 | 168 | 173 | PF01217 | 0.600 |
TRG_DiLeu_BaEn_1 | 270 | 275 | PF01217 | 0.562 |
TRG_DiLeu_BaEn_1 | 314 | 319 | PF01217 | 0.369 |
TRG_DiLeu_BaEn_1 | 81 | 86 | PF01217 | 0.509 |
TRG_DiLeu_BaLyEn_6 | 127 | 132 | PF01217 | 0.562 |
TRG_ENDOCYTIC_2 | 283 | 286 | PF00928 | 0.516 |
TRG_ENDOCYTIC_2 | 31 | 34 | PF00928 | 0.567 |
TRG_ENDOCYTIC_2 | 315 | 318 | PF00928 | 0.522 |
TRG_ENDOCYTIC_2 | 472 | 475 | PF00928 | 0.491 |
TRG_ENDOCYTIC_2 | 477 | 480 | PF00928 | 0.483 |
TRG_ENDOCYTIC_2 | 63 | 66 | PF00928 | 0.739 |
TRG_ENDOCYTIC_2 | 653 | 656 | PF00928 | 0.350 |
TRG_ER_diArg_1 | 230 | 233 | PF00400 | 0.577 |
TRG_NES_CRM1_1 | 214 | 227 | PF08389 | 0.577 |
TRG_Pf-PMV_PEXEL_1 | 457 | 461 | PF00026 | 0.291 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZI3 | Leptomonas seymouri | 69% | 100% |
A0A0S4JCZ4 | Bodo saltans | 23% | 100% |
A0A1X0NH78 | Trypanosomatidae | 42% | 100% |
A0A1X0NIW4 | Trypanosomatidae | 42% | 100% |
A0A3Q8IPA3 | Leishmania donovani | 95% | 100% |
A0A422N9U8 | Trypanosoma rangeli | 43% | 100% |
A4HMG9 | Leishmania braziliensis | 87% | 99% |
A4IB50 | Leishmania infantum | 94% | 100% |
C9ZNP3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
E9AEX0 | Leishmania major | 93% | 100% |
V5BC85 | Trypanosoma cruzi | 45% | 100% |