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 |
Related structures:
AlphaFold database: A4H4F3
Term | Name | Level | Count |
---|---|---|---|
GO:0006793 | phosphorus metabolic process | 3 | 1 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016310 | phosphorylation | 5 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 1 |
GO:0016301 | kinase activity | 4 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 203 | 207 | PF00656 | 0.666 |
CLV_C14_Caspase3-7 | 578 | 582 | PF00656 | 0.544 |
CLV_NRD_NRD_1 | 678 | 680 | PF00675 | 0.499 |
CLV_NRD_NRD_1 | 717 | 719 | PF00675 | 0.619 |
CLV_PCSK_FUR_1 | 113 | 117 | PF00082 | 0.351 |
CLV_PCSK_KEX2_1 | 112 | 114 | PF00082 | 0.337 |
CLV_PCSK_KEX2_1 | 115 | 117 | PF00082 | 0.346 |
CLV_PCSK_KEX2_1 | 159 | 161 | PF00082 | 0.534 |
CLV_PCSK_KEX2_1 | 213 | 215 | PF00082 | 0.561 |
CLV_PCSK_KEX2_1 | 300 | 302 | PF00082 | 0.357 |
CLV_PCSK_KEX2_1 | 513 | 515 | PF00082 | 0.414 |
CLV_PCSK_KEX2_1 | 678 | 680 | PF00082 | 0.535 |
CLV_PCSK_KEX2_1 | 717 | 719 | PF00082 | 0.512 |
CLV_PCSK_PC1ET2_1 | 112 | 114 | PF00082 | 0.337 |
CLV_PCSK_PC1ET2_1 | 115 | 117 | PF00082 | 0.346 |
CLV_PCSK_PC1ET2_1 | 159 | 161 | PF00082 | 0.540 |
CLV_PCSK_PC1ET2_1 | 213 | 215 | PF00082 | 0.561 |
CLV_PCSK_PC1ET2_1 | 300 | 302 | PF00082 | 0.409 |
CLV_PCSK_PC1ET2_1 | 513 | 515 | PF00082 | 0.414 |
CLV_PCSK_SKI1_1 | 112 | 116 | PF00082 | 0.356 |
DEG_APCC_DBOX_1 | 704 | 712 | PF00400 | 0.520 |
DEG_APCC_KENBOX_2 | 249 | 253 | PF00400 | 0.409 |
DEG_COP1_1 | 394 | 404 | PF00400 | 0.544 |
DEG_SCF_TRCP1_1 | 27 | 33 | PF00400 | 0.500 |
DEG_SIAH_1 | 684 | 692 | PF03145 | 0.627 |
DEG_SPOP_SBC_1 | 646 | 650 | PF00917 | 0.405 |
DOC_MAPK_gen_1 | 213 | 220 | PF00069 | 0.539 |
DOC_MAPK_HePTP_8 | 407 | 419 | PF00069 | 0.383 |
DOC_MAPK_MEF2A_6 | 132 | 140 | PF00069 | 0.368 |
DOC_MAPK_MEF2A_6 | 213 | 222 | PF00069 | 0.488 |
DOC_MAPK_MEF2A_6 | 410 | 419 | PF00069 | 0.478 |
DOC_PP1_RVXF_1 | 255 | 262 | PF00149 | 0.411 |
DOC_PP1_RVXF_1 | 289 | 296 | PF00149 | 0.219 |
DOC_PP2B_LxvP_1 | 138 | 141 | PF13499 | 0.402 |
DOC_PP2B_LxvP_1 | 417 | 420 | PF13499 | 0.556 |
DOC_PP2B_LxvP_1 | 535 | 538 | PF13499 | 0.545 |
DOC_PP2B_LxvP_1 | 599 | 602 | PF13499 | 0.537 |
DOC_USP7_MATH_1 | 134 | 138 | PF00917 | 0.574 |
DOC_USP7_MATH_1 | 287 | 291 | PF00917 | 0.285 |
DOC_USP7_MATH_1 | 310 | 314 | PF00917 | 0.284 |
DOC_USP7_MATH_1 | 421 | 425 | PF00917 | 0.562 |
DOC_USP7_MATH_1 | 518 | 522 | PF00917 | 0.432 |
DOC_USP7_MATH_1 | 613 | 617 | PF00917 | 0.524 |
DOC_USP7_UBL2_3 | 300 | 304 | PF12436 | 0.325 |
DOC_WW_Pin1_4 | 551 | 556 | PF00397 | 0.628 |
DOC_WW_Pin1_4 | 693 | 698 | PF00397 | 0.580 |
LIG_14-3-3_CanoR_1 | 456 | 462 | PF00244 | 0.416 |
LIG_14-3-3_CanoR_1 | 568 | 575 | PF00244 | 0.647 |
LIG_14-3-3_CanoR_1 | 588 | 597 | PF00244 | 0.368 |
LIG_Actin_WH2_2 | 368 | 385 | PF00022 | 0.187 |
LIG_Actin_WH2_2 | 441 | 458 | PF00022 | 0.506 |
LIG_Actin_WH2_2 | 466 | 483 | PF00022 | 0.452 |
LIG_APCC_ABBA_1 | 411 | 416 | PF00400 | 0.561 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.606 |
LIG_BIR_III_2 | 492 | 496 | PF00653 | 0.379 |
LIG_BIR_III_4 | 581 | 585 | PF00653 | 0.480 |
LIG_BRCT_BRCA1_1 | 592 | 596 | PF00533 | 0.349 |
LIG_CaM_NSCaTE_8 | 457 | 464 | PF13499 | 0.441 |
LIG_CSL_BTD_1 | 399 | 402 | PF09270 | 0.453 |
LIG_CtBP_PxDLS_1 | 189 | 193 | PF00389 | 0.548 |
LIG_FHA_1 | 327 | 333 | PF00498 | 0.325 |
LIG_FHA_1 | 407 | 413 | PF00498 | 0.502 |
LIG_FHA_1 | 584 | 590 | PF00498 | 0.437 |
LIG_FHA_2 | 140 | 146 | PF00498 | 0.551 |
LIG_FHA_2 | 194 | 200 | PF00498 | 0.561 |
LIG_FHA_2 | 31 | 37 | PF00498 | 0.603 |
LIG_FHA_2 | 439 | 445 | PF00498 | 0.429 |
LIG_FHA_2 | 714 | 720 | PF00498 | 0.397 |
LIG_GBD_Chelix_1 | 106 | 114 | PF00786 | 0.396 |
LIG_HP1_1 | 542 | 546 | PF01393 | 0.377 |
LIG_LIR_Gen_1 | 131 | 141 | PF02991 | 0.459 |
LIG_LIR_Gen_1 | 191 | 200 | PF02991 | 0.514 |
LIG_LIR_Gen_1 | 329 | 338 | PF02991 | 0.411 |
LIG_LIR_Gen_1 | 53 | 62 | PF02991 | 0.637 |
LIG_LIR_Gen_1 | 593 | 604 | PF02991 | 0.359 |
LIG_LIR_Gen_1 | 648 | 659 | PF02991 | 0.441 |
LIG_LIR_LC3C_4 | 416 | 419 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 191 | 197 | PF02991 | 0.512 |
LIG_LIR_Nem_3 | 329 | 333 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 53 | 57 | PF02991 | 0.667 |
LIG_LIR_Nem_3 | 593 | 599 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 648 | 654 | PF02991 | 0.457 |
LIG_MYND_1 | 700 | 704 | PF01753 | 0.596 |
LIG_MYND_1 | 706 | 710 | PF01753 | 0.492 |
LIG_NRBOX | 530 | 536 | PF00104 | 0.493 |
LIG_Pex14_2 | 338 | 342 | PF04695 | 0.323 |
LIG_Rb_pABgroove_1 | 706 | 714 | PF01858 | 0.518 |
LIG_SH2_CRK | 451 | 455 | PF00017 | 0.552 |
LIG_SH2_CRK | 651 | 655 | PF00017 | 0.315 |
LIG_SH2_NCK_1 | 23 | 27 | PF00017 | 0.452 |
LIG_SH2_NCK_1 | 490 | 494 | PF00017 | 0.557 |
LIG_SH2_PTP2 | 221 | 224 | PF00017 | 0.447 |
LIG_SH2_PTP2 | 54 | 57 | PF00017 | 0.661 |
LIG_SH2_SRC | 307 | 310 | PF00017 | 0.300 |
LIG_SH2_SRC | 490 | 493 | PF00017 | 0.360 |
LIG_SH2_STAP1 | 130 | 134 | PF00017 | 0.498 |
LIG_SH2_STAP1 | 620 | 624 | PF00017 | 0.614 |
LIG_SH2_STAT3 | 634 | 637 | PF00017 | 0.524 |
LIG_SH2_STAT5 | 109 | 112 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 221 | 224 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 245 | 248 | PF00017 | 0.268 |
LIG_SH2_STAT5 | 269 | 272 | PF00017 | 0.322 |
LIG_SH2_STAT5 | 292 | 295 | PF00017 | 0.292 |
LIG_SH2_STAT5 | 307 | 310 | PF00017 | 0.304 |
LIG_SH2_STAT5 | 361 | 364 | PF00017 | 0.297 |
LIG_SH2_STAT5 | 376 | 379 | PF00017 | 0.435 |
LIG_SH2_STAT5 | 54 | 57 | PF00017 | 0.637 |
LIG_SH3_1 | 221 | 227 | PF00018 | 0.550 |
LIG_SH3_3 | 221 | 227 | PF00018 | 0.550 |
LIG_SH3_3 | 415 | 421 | PF00018 | 0.446 |
LIG_SH3_3 | 512 | 518 | PF00018 | 0.578 |
LIG_SH3_3 | 692 | 698 | PF00018 | 0.575 |
LIG_SH3_3 | 7 | 13 | PF00018 | 0.559 |
LIG_SUMO_SIM_anti_2 | 123 | 129 | PF11976 | 0.553 |
LIG_SUMO_SIM_anti_2 | 499 | 505 | PF11976 | 0.478 |
LIG_SUMO_SIM_anti_2 | 529 | 536 | PF11976 | 0.394 |
LIG_SUMO_SIM_par_1 | 504 | 509 | PF11976 | 0.461 |
LIG_SUMO_SIM_par_1 | 531 | 536 | PF11976 | 0.416 |
LIG_SUMO_SIM_par_1 | 541 | 547 | PF11976 | 0.373 |
LIG_TRAF2_1 | 179 | 182 | PF00917 | 0.708 |
LIG_TYR_ITIM | 192 | 197 | PF00017 | 0.505 |
LIG_TYR_ITSM | 647 | 654 | PF00017 | 0.574 |
MOD_CDK_SPxxK_3 | 551 | 558 | PF00069 | 0.448 |
MOD_CK1_1 | 42 | 48 | PF00069 | 0.505 |
MOD_CK1_1 | 424 | 430 | PF00069 | 0.656 |
MOD_CK1_1 | 460 | 466 | PF00069 | 0.453 |
MOD_CK1_1 | 549 | 555 | PF00069 | 0.698 |
MOD_CK1_1 | 570 | 576 | PF00069 | 0.506 |
MOD_CK1_1 | 640 | 646 | PF00069 | 0.584 |
MOD_CK1_1 | 657 | 663 | PF00069 | 0.538 |
MOD_CK2_1 | 139 | 145 | PF00069 | 0.578 |
MOD_CK2_1 | 176 | 182 | PF00069 | 0.761 |
MOD_CK2_1 | 30 | 36 | PF00069 | 0.746 |
MOD_CK2_1 | 551 | 557 | PF00069 | 0.674 |
MOD_Cter_Amidation | 298 | 301 | PF01082 | 0.409 |
MOD_Cter_Amidation | 511 | 514 | PF01082 | 0.437 |
MOD_DYRK1A_RPxSP_1 | 693 | 697 | PF00069 | 0.584 |
MOD_GlcNHglycan | 240 | 243 | PF01048 | 0.531 |
MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.686 |
MOD_GlcNHglycan | 301 | 304 | PF01048 | 0.378 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.339 |
MOD_GlcNHglycan | 355 | 358 | PF01048 | 0.401 |
MOD_GlcNHglycan | 423 | 426 | PF01048 | 0.509 |
MOD_GlcNHglycan | 462 | 465 | PF01048 | 0.599 |
MOD_GlcNHglycan | 575 | 578 | PF01048 | 0.446 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.593 |
MOD_GlcNHglycan | 639 | 642 | PF01048 | 0.528 |
MOD_GlcNHglycan | 685 | 688 | PF01048 | 0.484 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.519 |
MOD_GSK3_1 | 516 | 523 | PF00069 | 0.525 |
MOD_GSK3_1 | 546 | 553 | PF00069 | 0.502 |
MOD_GSK3_1 | 567 | 574 | PF00069 | 0.558 |
MOD_GSK3_1 | 657 | 664 | PF00069 | 0.515 |
MOD_N-GLC_1 | 42 | 47 | PF02516 | 0.689 |
MOD_NEK2_1 | 234 | 239 | PF00069 | 0.419 |
MOD_NEK2_1 | 333 | 338 | PF00069 | 0.283 |
MOD_NEK2_1 | 405 | 410 | PF00069 | 0.496 |
MOD_NEK2_1 | 546 | 551 | PF00069 | 0.433 |
MOD_NEK2_1 | 57 | 62 | PF00069 | 0.614 |
MOD_NEK2_1 | 589 | 594 | PF00069 | 0.495 |
MOD_NEK2_1 | 647 | 652 | PF00069 | 0.370 |
MOD_NEK2_2 | 355 | 360 | PF00069 | 0.546 |
MOD_PIKK_1 | 87 | 93 | PF00454 | 0.305 |
MOD_PKA_2 | 567 | 573 | PF00069 | 0.516 |
MOD_PKA_2 | 625 | 631 | PF00069 | 0.470 |
MOD_Plk_1 | 134 | 140 | PF00069 | 0.532 |
MOD_Plk_1 | 499 | 505 | PF00069 | 0.438 |
MOD_Plk_1 | 546 | 552 | PF00069 | 0.526 |
MOD_Plk_1 | 570 | 576 | PF00069 | 0.590 |
MOD_Plk_1 | 613 | 619 | PF00069 | 0.570 |
MOD_Plk_1 | 657 | 663 | PF00069 | 0.387 |
MOD_Plk_2-3 | 121 | 127 | PF00069 | 0.548 |
MOD_Plk_2-3 | 176 | 182 | PF00069 | 0.623 |
MOD_Plk_2-3 | 30 | 36 | PF00069 | 0.791 |
MOD_Plk_2-3 | 311 | 317 | PF00069 | 0.279 |
MOD_Plk_4 | 234 | 240 | PF00069 | 0.402 |
MOD_Plk_4 | 334 | 340 | PF00069 | 0.376 |
MOD_Plk_4 | 400 | 406 | PF00069 | 0.616 |
MOD_Plk_4 | 499 | 505 | PF00069 | 0.409 |
MOD_Plk_4 | 613 | 619 | PF00069 | 0.570 |
MOD_Plk_4 | 647 | 653 | PF00069 | 0.519 |
MOD_Plk_4 | 90 | 96 | PF00069 | 0.355 |
MOD_ProDKin_1 | 551 | 557 | PF00069 | 0.633 |
MOD_ProDKin_1 | 693 | 699 | PF00069 | 0.580 |
MOD_SUMO_for_1 | 320 | 323 | PF00179 | 0.409 |
MOD_SUMO_rev_2 | 390 | 399 | PF00179 | 0.435 |
MOD_SUMO_rev_2 | 707 | 716 | PF00179 | 0.628 |
TRG_DiLeu_BaLyEn_6 | 450 | 455 | PF01217 | 0.509 |
TRG_ENDOCYTIC_2 | 194 | 197 | PF00928 | 0.512 |
TRG_ENDOCYTIC_2 | 281 | 284 | PF00928 | 0.391 |
TRG_ENDOCYTIC_2 | 330 | 333 | PF00928 | 0.469 |
TRG_ENDOCYTIC_2 | 451 | 454 | PF00928 | 0.406 |
TRG_ENDOCYTIC_2 | 54 | 57 | PF00928 | 0.661 |
TRG_ENDOCYTIC_2 | 651 | 654 | PF00928 | 0.451 |
TRG_NES_CRM1_1 | 496 | 509 | PF08389 | 0.413 |
TRG_NLS_MonoExtC_3 | 111 | 116 | PF00514 | 0.336 |
TRG_Pf-PMV_PEXEL_1 | 159 | 163 | PF00026 | 0.612 |
TRG_Pf-PMV_PEXEL_1 | 69 | 73 | PF00026 | 0.401 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3V4 | Leptomonas seymouri | 71% | 100% |
A0A0S4IJQ0 | Bodo saltans | 36% | 100% |
A0A1X0NLQ2 | Trypanosomatidae | 42% | 86% |
A0A3S5H5L8 | Leishmania donovani | 87% | 100% |
A0A422NBM9 | Trypanosoma rangeli | 49% | 93% |
A4HSN0 | Leishmania infantum | 87% | 100% |
C9ZU66 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 88% |
E9AKL5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
Q4QJ94 | Leishmania major | 86% | 100% |
V5BBF6 | Trypanosoma cruzi | 50% | 100% |