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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 16 |
NetGPI | no | yes: 0, no: 16 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
Related structures:
AlphaFold database: E9B3V4
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 17 |
GO:0003824 | catalytic activity | 1 | 17 |
GO:0005488 | binding | 1 | 17 |
GO:0005524 | ATP binding | 5 | 17 |
GO:0016462 | pyrophosphatase activity | 5 | 17 |
GO:0016787 | hydrolase activity | 2 | 17 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 17 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 17 |
GO:0016887 | ATP hydrolysis activity | 7 | 17 |
GO:0017076 | purine nucleotide binding | 4 | 17 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 17 |
GO:0030554 | adenyl nucleotide binding | 5 | 17 |
GO:0032553 | ribonucleotide binding | 3 | 17 |
GO:0032555 | purine ribonucleotide binding | 4 | 17 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 17 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 17 |
GO:0036094 | small molecule binding | 2 | 17 |
GO:0043167 | ion binding | 2 | 17 |
GO:0043168 | anion binding | 3 | 17 |
GO:0097159 | organic cyclic compound binding | 2 | 17 |
GO:0097367 | carbohydrate derivative binding | 2 | 17 |
GO:1901265 | nucleoside phosphate binding | 3 | 17 |
GO:1901363 | heterocyclic compound binding | 2 | 17 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 204 | 208 | PF00656 | 0.597 |
CLV_C14_Caspase3-7 | 381 | 385 | PF00656 | 0.737 |
CLV_C14_Caspase3-7 | 410 | 414 | PF00656 | 0.535 |
CLV_C14_Caspase3-7 | 429 | 433 | PF00656 | 0.742 |
CLV_C14_Caspase3-7 | 450 | 454 | PF00656 | 0.780 |
CLV_C14_Caspase3-7 | 58 | 62 | PF00656 | 0.682 |
CLV_C14_Caspase3-7 | 613 | 617 | PF00656 | 0.748 |
CLV_NRD_NRD_1 | 439 | 441 | PF00675 | 0.543 |
CLV_PCSK_FUR_1 | 437 | 441 | PF00082 | 0.571 |
CLV_PCSK_KEX2_1 | 351 | 353 | PF00082 | 0.316 |
CLV_PCSK_KEX2_1 | 439 | 441 | PF00082 | 0.547 |
CLV_PCSK_KEX2_1 | 507 | 509 | PF00082 | 0.552 |
CLV_PCSK_PC1ET2_1 | 351 | 353 | PF00082 | 0.343 |
CLV_PCSK_PC1ET2_1 | 507 | 509 | PF00082 | 0.510 |
CLV_PCSK_SKI1_1 | 326 | 330 | PF00082 | 0.369 |
CLV_PCSK_SKI1_1 | 352 | 356 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 370 | 374 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 485 | 489 | PF00082 | 0.600 |
CLV_PCSK_SKI1_1 | 591 | 595 | PF00082 | 0.437 |
CLV_PCSK_SKI1_1 | 83 | 87 | PF00082 | 0.435 |
CLV_PCSK_SKI1_1 | 92 | 96 | PF00082 | 0.466 |
CLV_Separin_Metazoa | 645 | 649 | PF03568 | 0.649 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.453 |
DEG_SPOP_SBC_1 | 448 | 452 | PF00917 | 0.587 |
DEG_SPOP_SBC_1 | 60 | 64 | PF00917 | 0.667 |
DOC_CYCLIN_RxL_1 | 192 | 203 | PF00134 | 0.730 |
DOC_CYCLIN_yCln2_LP_2 | 296 | 302 | PF00134 | 0.623 |
DOC_CYCLIN_yCln2_LP_2 | 399 | 405 | PF00134 | 0.588 |
DOC_MAPK_gen_1 | 351 | 359 | PF00069 | 0.516 |
DOC_PP2B_LxvP_1 | 106 | 109 | PF13499 | 0.741 |
DOC_SPAK_OSR1_1 | 376 | 380 | PF12202 | 0.660 |
DOC_SPAK_OSR1_1 | 97 | 101 | PF12202 | 0.738 |
DOC_USP7_MATH_1 | 176 | 180 | PF00917 | 0.791 |
DOC_USP7_MATH_1 | 200 | 204 | PF00917 | 0.680 |
DOC_USP7_MATH_1 | 227 | 231 | PF00917 | 0.725 |
DOC_USP7_MATH_1 | 286 | 290 | PF00917 | 0.667 |
DOC_USP7_MATH_1 | 32 | 36 | PF00917 | 0.425 |
DOC_USP7_MATH_1 | 449 | 453 | PF00917 | 0.689 |
DOC_USP7_MATH_1 | 614 | 618 | PF00917 | 0.763 |
DOC_USP7_UBL2_3 | 206 | 210 | PF12436 | 0.667 |
DOC_USP7_UBL2_3 | 313 | 317 | PF12436 | 0.642 |
DOC_USP7_UBL2_3 | 378 | 382 | PF12436 | 0.683 |
DOC_USP7_UBL2_3 | 383 | 387 | PF12436 | 0.734 |
DOC_USP7_UBL2_3 | 503 | 507 | PF12436 | 0.768 |
DOC_WW_Pin1_4 | 129 | 134 | PF00397 | 0.709 |
DOC_WW_Pin1_4 | 623 | 628 | PF00397 | 0.557 |
LIG_14-3-3_CanoR_1 | 140 | 147 | PF00244 | 0.777 |
LIG_14-3-3_CanoR_1 | 148 | 152 | PF00244 | 0.680 |
LIG_14-3-3_CanoR_1 | 361 | 369 | PF00244 | 0.516 |
LIG_14-3-3_CanoR_1 | 52 | 57 | PF00244 | 0.665 |
LIG_14-3-3_CanoR_1 | 574 | 584 | PF00244 | 0.655 |
LIG_14-3-3_CanoR_1 | 83 | 93 | PF00244 | 0.649 |
LIG_Actin_WH2_2 | 1 | 19 | PF00022 | 0.478 |
LIG_Actin_WH2_2 | 134 | 150 | PF00022 | 0.767 |
LIG_Actin_WH2_2 | 538 | 553 | PF00022 | 0.650 |
LIG_BRCT_BRCA1_1 | 294 | 298 | PF00533 | 0.554 |
LIG_BRCT_BRCA1_1 | 373 | 377 | PF00533 | 0.644 |
LIG_BRCT_BRCA1_1 | 63 | 67 | PF00533 | 0.724 |
LIG_CSL_BTD_1 | 44 | 47 | PF09270 | 0.682 |
LIG_eIF4E_1 | 253 | 259 | PF01652 | 0.638 |
LIG_eIF4E_1 | 349 | 355 | PF01652 | 0.527 |
LIG_FHA_1 | 118 | 124 | PF00498 | 0.728 |
LIG_FHA_1 | 140 | 146 | PF00498 | 0.738 |
LIG_FHA_1 | 16 | 22 | PF00498 | 0.411 |
LIG_FHA_1 | 413 | 419 | PF00498 | 0.625 |
LIG_FHA_1 | 486 | 492 | PF00498 | 0.794 |
LIG_FHA_1 | 519 | 525 | PF00498 | 0.589 |
LIG_FHA_1 | 537 | 543 | PF00498 | 0.565 |
LIG_FHA_1 | 554 | 560 | PF00498 | 0.554 |
LIG_FHA_1 | 578 | 584 | PF00498 | 0.642 |
LIG_FHA_1 | 605 | 611 | PF00498 | 0.761 |
LIG_FHA_1 | 79 | 85 | PF00498 | 0.689 |
LIG_FHA_1 | 89 | 95 | PF00498 | 0.687 |
LIG_FHA_2 | 150 | 156 | PF00498 | 0.770 |
LIG_FHA_2 | 202 | 208 | PF00498 | 0.754 |
LIG_FHA_2 | 246 | 252 | PF00498 | 0.634 |
LIG_FHA_2 | 348 | 354 | PF00498 | 0.546 |
LIG_FHA_2 | 427 | 433 | PF00498 | 0.738 |
LIG_FHA_2 | 448 | 454 | PF00498 | 0.798 |
LIG_FHA_2 | 495 | 501 | PF00498 | 0.738 |
LIG_FHA_2 | 637 | 643 | PF00498 | 0.576 |
LIG_LIR_Apic_2 | 315 | 321 | PF02991 | 0.591 |
LIG_LIR_Gen_1 | 102 | 113 | PF02991 | 0.694 |
LIG_LIR_Gen_1 | 2 | 12 | PF02991 | 0.417 |
LIG_LIR_Gen_1 | 292 | 300 | PF02991 | 0.531 |
LIG_LIR_Nem_3 | 102 | 108 | PF02991 | 0.701 |
LIG_LIR_Nem_3 | 189 | 193 | PF02991 | 0.730 |
LIG_LIR_Nem_3 | 2 | 7 | PF02991 | 0.425 |
LIG_LIR_Nem_3 | 292 | 296 | PF02991 | 0.527 |
LIG_LIR_Nem_3 | 44 | 49 | PF02991 | 0.614 |
LIG_MLH1_MIPbox_1 | 294 | 298 | PF16413 | 0.553 |
LIG_NRBOX | 326 | 332 | PF00104 | 0.457 |
LIG_NRBOX | 589 | 595 | PF00104 | 0.648 |
LIG_PCNA_PIPBox_1 | 570 | 579 | PF02747 | 0.548 |
LIG_Pex14_2 | 293 | 297 | PF04695 | 0.517 |
LIG_Pex14_2 | 373 | 377 | PF04695 | 0.627 |
LIG_PTB_Apo_2 | 122 | 129 | PF02174 | 0.734 |
LIG_PTB_Apo_2 | 6 | 13 | PF02174 | 0.439 |
LIG_SH2_CRK | 126 | 130 | PF00017 | 0.743 |
LIG_SH2_CRK | 255 | 259 | PF00017 | 0.592 |
LIG_SH2_CRK | 318 | 322 | PF00017 | 0.644 |
LIG_SH2_NCK_1 | 318 | 322 | PF00017 | 0.644 |
LIG_SH2_PTP2 | 4 | 7 | PF00017 | 0.331 |
LIG_SH2_SRC | 318 | 321 | PF00017 | 0.637 |
LIG_SH2_STAP1 | 119 | 123 | PF00017 | 0.715 |
LIG_SH2_STAT3 | 253 | 256 | PF00017 | 0.567 |
LIG_SH2_STAT5 | 105 | 108 | PF00017 | 0.735 |
LIG_SH2_STAT5 | 119 | 122 | PF00017 | 0.696 |
LIG_SH2_STAT5 | 126 | 129 | PF00017 | 0.666 |
LIG_SH2_STAT5 | 196 | 199 | PF00017 | 0.676 |
LIG_SH2_STAT5 | 253 | 256 | PF00017 | 0.573 |
LIG_SH2_STAT5 | 349 | 352 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 4 | 7 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 40 | 43 | PF00017 | 0.582 |
LIG_SH2_STAT5 | 407 | 410 | PF00017 | 0.533 |
LIG_SH2_STAT5 | 56 | 59 | PF00017 | 0.593 |
LIG_SH2_STAT5 | 576 | 579 | PF00017 | 0.634 |
LIG_SH2_STAT5 | 89 | 92 | PF00017 | 0.587 |
LIG_SH3_1 | 318 | 324 | PF00018 | 0.642 |
LIG_SH3_2 | 321 | 326 | PF14604 | 0.596 |
LIG_SH3_3 | 296 | 302 | PF00018 | 0.613 |
LIG_SH3_3 | 318 | 324 | PF00018 | 0.586 |
LIG_SH3_3 | 90 | 96 | PF00018 | 0.704 |
LIG_SUMO_SIM_anti_2 | 2 | 9 | PF11976 | 0.473 |
LIG_SUMO_SIM_anti_2 | 641 | 648 | PF11976 | 0.589 |
LIG_TRAF2_1 | 175 | 178 | PF00917 | 0.792 |
LIG_TRAF2_1 | 364 | 367 | PF00917 | 0.470 |
LIG_TRAF2_1 | 639 | 642 | PF00917 | 0.620 |
LIG_TYR_ITIM | 103 | 108 | PF00017 | 0.729 |
LIG_UBA3_1 | 304 | 313 | PF00899 | 0.594 |
MOD_CDC14_SPxK_1 | 132 | 135 | PF00782 | 0.708 |
MOD_CDK_SPxK_1 | 129 | 135 | PF00069 | 0.710 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.411 |
MOD_CK1_1 | 170 | 176 | PF00069 | 0.783 |
MOD_CK1_1 | 179 | 185 | PF00069 | 0.769 |
MOD_CK1_1 | 208 | 214 | PF00069 | 0.678 |
MOD_CK1_1 | 289 | 295 | PF00069 | 0.562 |
MOD_CK1_1 | 394 | 400 | PF00069 | 0.666 |
MOD_CK1_1 | 451 | 457 | PF00069 | 0.775 |
MOD_CK1_1 | 55 | 61 | PF00069 | 0.690 |
MOD_CK1_1 | 578 | 584 | PF00069 | 0.650 |
MOD_CK2_1 | 227 | 233 | PF00069 | 0.727 |
MOD_CK2_1 | 361 | 367 | PF00069 | 0.469 |
MOD_CK2_1 | 454 | 460 | PF00069 | 0.772 |
MOD_CK2_1 | 494 | 500 | PF00069 | 0.738 |
MOD_CK2_1 | 589 | 595 | PF00069 | 0.633 |
MOD_CK2_1 | 623 | 629 | PF00069 | 0.561 |
MOD_CK2_1 | 636 | 642 | PF00069 | 0.553 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.567 |
MOD_GlcNHglycan | 288 | 291 | PF01048 | 0.268 |
MOD_GlcNHglycan | 35 | 38 | PF01048 | 0.452 |
MOD_GlcNHglycan | 373 | 376 | PF01048 | 0.418 |
MOD_GlcNHglycan | 456 | 459 | PF01048 | 0.524 |
MOD_GlcNHglycan | 471 | 474 | PF01048 | 0.578 |
MOD_GlcNHglycan | 616 | 620 | PF01048 | 0.546 |
MOD_GlcNHglycan | 63 | 66 | PF01048 | 0.523 |
MOD_GlcNHglycan | 71 | 76 | PF01048 | 0.511 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.714 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.592 |
MOD_GSK3_1 | 334 | 341 | PF00069 | 0.452 |
MOD_GSK3_1 | 357 | 364 | PF00069 | 0.492 |
MOD_GSK3_1 | 447 | 454 | PF00069 | 0.768 |
MOD_GSK3_1 | 458 | 465 | PF00069 | 0.797 |
MOD_GSK3_1 | 485 | 492 | PF00069 | 0.753 |
MOD_GSK3_1 | 503 | 510 | PF00069 | 0.723 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.684 |
MOD_GSK3_1 | 595 | 602 | PF00069 | 0.637 |
MOD_GSK3_1 | 604 | 611 | PF00069 | 0.751 |
MOD_GSK3_1 | 615 | 622 | PF00069 | 0.616 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.662 |
MOD_N-GLC_1 | 117 | 122 | PF02516 | 0.518 |
MOD_N-GLC_1 | 129 | 134 | PF02516 | 0.355 |
MOD_N-GLC_1 | 469 | 474 | PF02516 | 0.582 |
MOD_N-GLC_1 | 599 | 604 | PF02516 | 0.346 |
MOD_N-GLC_2 | 125 | 127 | PF02516 | 0.330 |
MOD_NEK2_1 | 12 | 17 | PF00069 | 0.441 |
MOD_NEK2_1 | 147 | 152 | PF00069 | 0.742 |
MOD_NEK2_1 | 181 | 186 | PF00069 | 0.780 |
MOD_NEK2_1 | 259 | 264 | PF00069 | 0.550 |
MOD_NEK2_1 | 33 | 38 | PF00069 | 0.401 |
MOD_NEK2_1 | 355 | 360 | PF00069 | 0.502 |
MOD_NEK2_1 | 41 | 46 | PF00069 | 0.526 |
MOD_NEK2_1 | 577 | 582 | PF00069 | 0.658 |
MOD_NEK2_2 | 553 | 558 | PF00069 | 0.579 |
MOD_NEK2_2 | 78 | 83 | PF00069 | 0.699 |
MOD_OFUCOSY | 390 | 395 | PF10250 | 0.334 |
MOD_PIKK_1 | 170 | 176 | PF00454 | 0.742 |
MOD_PIKK_1 | 181 | 187 | PF00454 | 0.773 |
MOD_PIKK_1 | 494 | 500 | PF00454 | 0.789 |
MOD_PK_1 | 104 | 110 | PF00069 | 0.753 |
MOD_PKA_1 | 507 | 513 | PF00069 | 0.742 |
MOD_PKA_2 | 139 | 145 | PF00069 | 0.770 |
MOD_PKA_2 | 147 | 153 | PF00069 | 0.739 |
MOD_PKA_2 | 458 | 464 | PF00069 | 0.657 |
MOD_PKA_2 | 507 | 513 | PF00069 | 0.741 |
MOD_Plk_1 | 232 | 238 | PF00069 | 0.705 |
MOD_Plk_1 | 442 | 448 | PF00069 | 0.761 |
MOD_Plk_1 | 615 | 621 | PF00069 | 0.715 |
MOD_Plk_2-3 | 589 | 595 | PF00069 | 0.619 |
MOD_Plk_2-3 | 636 | 642 | PF00069 | 0.619 |
MOD_Plk_4 | 227 | 233 | PF00069 | 0.737 |
MOD_Plk_4 | 292 | 298 | PF00069 | 0.516 |
MOD_Plk_4 | 52 | 58 | PF00069 | 0.693 |
MOD_Plk_4 | 545 | 551 | PF00069 | 0.621 |
MOD_Plk_4 | 578 | 584 | PF00069 | 0.686 |
MOD_Plk_4 | 85 | 91 | PF00069 | 0.639 |
MOD_ProDKin_1 | 129 | 135 | PF00069 | 0.710 |
MOD_ProDKin_1 | 623 | 629 | PF00069 | 0.555 |
MOD_SUMO_for_1 | 420 | 423 | PF00179 | 0.712 |
MOD_SUMO_rev_2 | 237 | 246 | PF00179 | 0.707 |
MOD_SUMO_rev_2 | 309 | 315 | PF00179 | 0.580 |
MOD_SUMO_rev_2 | 451 | 457 | PF00179 | 0.760 |
MOD_SUMO_rev_2 | 460 | 465 | PF00179 | 0.751 |
MOD_SUMO_rev_2 | 99 | 106 | PF00179 | 0.726 |
TRG_DiLeu_BaEn_1 | 589 | 594 | PF01217 | 0.643 |
TRG_DiLeu_BaLyEn_6 | 254 | 259 | PF01217 | 0.636 |
TRG_DiLeu_BaLyEn_6 | 300 | 305 | PF01217 | 0.614 |
TRG_ENDOCYTIC_2 | 105 | 108 | PF00928 | 0.703 |
TRG_ENDOCYTIC_2 | 126 | 129 | PF00928 | 0.701 |
TRG_ENDOCYTIC_2 | 196 | 199 | PF00928 | 0.653 |
TRG_ENDOCYTIC_2 | 255 | 258 | PF00928 | 0.563 |
TRG_ENDOCYTIC_2 | 4 | 7 | PF00928 | 0.420 |
TRG_NES_CRM1_1 | 136 | 149 | PF08389 | 0.775 |
TRG_NES_CRM1_1 | 367 | 381 | PF08389 | 0.629 |
TRG_Pf-PMV_PEXEL_1 | 252 | 256 | PF00026 | 0.367 |
TRG_Pf-PMV_PEXEL_1 | 591 | 595 | PF00026 | 0.431 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4V2 | Leptomonas seymouri | 59% | 98% |
A0A0S4JAD3 | Bodo saltans | 30% | 100% |
A0A0S4JHU3 | Bodo saltans | 33% | 100% |
A0A1X0NTT2 | Trypanosomatidae | 28% | 97% |
A0A1X0P9I4 | Trypanosomatidae | 29% | 81% |
A0A3S7X6K2 | Leishmania donovani | 91% | 100% |
A0A422NUH1 | Trypanosoma rangeli | 30% | 97% |
A0A422P3P3 | Trypanosoma rangeli | 33% | 100% |
A4HLH5 | Leishmania braziliensis | 72% | 97% |
A4I8Y5 | Leishmania infantum | 91% | 100% |
C9ZQW4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
C9ZSJ9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 98% |
D0A1W6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 91% |
Q4Q470 | Leishmania major | 90% | 100% |
V5DQN5 | Trypanosoma cruzi | 33% | 100% |