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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: A0A3Q8IEK7
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006396 | RNA processing | 6 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 3 |
GO:0008270 | zinc ion binding | 6 | 1 |
GO:0043167 | ion binding | 2 | 3 |
GO:0043169 | cation binding | 3 | 3 |
GO:0046872 | metal ion binding | 4 | 3 |
GO:0046914 | transition metal ion binding | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 128 | 132 | PF00656 | 0.599 |
CLV_C14_Caspase3-7 | 324 | 328 | PF00656 | 0.776 |
CLV_C14_Caspase3-7 | 417 | 421 | PF00656 | 0.468 |
CLV_C14_Caspase3-7 | 585 | 589 | PF00656 | 0.665 |
CLV_C14_Caspase3-7 | 78 | 82 | PF00656 | 0.577 |
CLV_C14_Caspase3-7 | 97 | 101 | PF00656 | 0.682 |
CLV_NRD_NRD_1 | 220 | 222 | PF00675 | 0.612 |
CLV_NRD_NRD_1 | 265 | 267 | PF00675 | 0.690 |
CLV_NRD_NRD_1 | 363 | 365 | PF00675 | 0.588 |
CLV_NRD_NRD_1 | 624 | 626 | PF00675 | 0.650 |
CLV_NRD_NRD_1 | 629 | 631 | PF00675 | 0.661 |
CLV_PCSK_KEX2_1 | 220 | 222 | PF00082 | 0.612 |
CLV_PCSK_KEX2_1 | 265 | 267 | PF00082 | 0.757 |
CLV_PCSK_KEX2_1 | 512 | 514 | PF00082 | 0.519 |
CLV_PCSK_KEX2_1 | 629 | 631 | PF00082 | 0.661 |
CLV_PCSK_PC1ET2_1 | 512 | 514 | PF00082 | 0.519 |
CLV_PCSK_PC7_1 | 625 | 631 | PF00082 | 0.663 |
CLV_PCSK_SKI1_1 | 103 | 107 | PF00082 | 0.541 |
CLV_PCSK_SKI1_1 | 130 | 134 | PF00082 | 0.458 |
CLV_PCSK_SKI1_1 | 226 | 230 | PF00082 | 0.679 |
CLV_PCSK_SKI1_1 | 365 | 369 | PF00082 | 0.620 |
CLV_PCSK_SKI1_1 | 46 | 50 | PF00082 | 0.479 |
CLV_PCSK_SKI1_1 | 550 | 554 | PF00082 | 0.489 |
CLV_PCSK_SKI1_1 | 575 | 579 | PF00082 | 0.660 |
CLV_PCSK_SKI1_1 | 625 | 629 | PF00082 | 0.708 |
CLV_PCSK_SKI1_1 | 636 | 640 | PF00082 | 0.698 |
DEG_APCC_DBOX_1 | 102 | 110 | PF00400 | 0.552 |
DOC_ANK_TNKS_1 | 331 | 338 | PF00023 | 0.693 |
DOC_CDC14_PxL_1 | 515 | 523 | PF14671 | 0.526 |
DOC_CKS1_1 | 577 | 582 | PF01111 | 0.757 |
DOC_CKS1_1 | 92 | 97 | PF01111 | 0.685 |
DOC_CYCLIN_RxL_1 | 524 | 536 | PF00134 | 0.645 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 303 | 312 | PF00134 | 0.586 |
DOC_CYCLIN_yCln2_LP_2 | 92 | 98 | PF00134 | 0.586 |
DOC_MAPK_DCC_7 | 513 | 523 | PF00069 | 0.435 |
DOC_MAPK_gen_1 | 226 | 236 | PF00069 | 0.604 |
DOC_MAPK_gen_1 | 512 | 523 | PF00069 | 0.626 |
DOC_MAPK_MEF2A_6 | 139 | 146 | PF00069 | 0.636 |
DOC_MAPK_MEF2A_6 | 516 | 525 | PF00069 | 0.503 |
DOC_MAPK_RevD_3 | 616 | 631 | PF00069 | 0.796 |
DOC_PP1_RVXF_1 | 121 | 128 | PF00149 | 0.565 |
DOC_PP1_RVXF_1 | 141 | 147 | PF00149 | 0.391 |
DOC_PP4_FxxP_1 | 380 | 383 | PF00568 | 0.511 |
DOC_PP4_FxxP_1 | 577 | 580 | PF00568 | 0.658 |
DOC_USP7_MATH_1 | 107 | 111 | PF00917 | 0.656 |
DOC_USP7_MATH_1 | 126 | 130 | PF00917 | 0.281 |
DOC_USP7_MATH_1 | 178 | 182 | PF00917 | 0.790 |
DOC_USP7_MATH_1 | 281 | 285 | PF00917 | 0.592 |
DOC_USP7_MATH_1 | 321 | 325 | PF00917 | 0.661 |
DOC_USP7_MATH_1 | 339 | 343 | PF00917 | 0.737 |
DOC_USP7_MATH_1 | 347 | 351 | PF00917 | 0.704 |
DOC_USP7_MATH_1 | 433 | 437 | PF00917 | 0.712 |
DOC_USP7_MATH_1 | 450 | 454 | PF00917 | 0.719 |
DOC_USP7_MATH_1 | 459 | 463 | PF00917 | 0.750 |
DOC_USP7_MATH_1 | 486 | 490 | PF00917 | 0.561 |
DOC_USP7_MATH_1 | 573 | 577 | PF00917 | 0.661 |
DOC_USP7_MATH_1 | 581 | 585 | PF00917 | 0.589 |
DOC_USP7_MATH_1 | 602 | 606 | PF00917 | 0.705 |
DOC_USP7_MATH_1 | 608 | 612 | PF00917 | 0.719 |
DOC_USP7_MATH_1 | 79 | 83 | PF00917 | 0.784 |
DOC_USP7_UBL2_3 | 139 | 143 | PF12436 | 0.636 |
DOC_USP7_UBL2_3 | 632 | 636 | PF12436 | 0.648 |
DOC_WW_Pin1_4 | 168 | 173 | PF00397 | 0.764 |
DOC_WW_Pin1_4 | 345 | 350 | PF00397 | 0.743 |
DOC_WW_Pin1_4 | 576 | 581 | PF00397 | 0.650 |
DOC_WW_Pin1_4 | 610 | 615 | PF00397 | 0.682 |
DOC_WW_Pin1_4 | 91 | 96 | PF00397 | 0.690 |
LIG_14-3-3_CanoR_1 | 300 | 309 | PF00244 | 0.562 |
LIG_14-3-3_CanoR_1 | 360 | 368 | PF00244 | 0.571 |
LIG_14-3-3_CanoR_1 | 369 | 378 | PF00244 | 0.499 |
LIG_14-3-3_CanoR_1 | 407 | 412 | PF00244 | 0.581 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.590 |
LIG_BIR_III_4 | 425 | 429 | PF00653 | 0.570 |
LIG_BIR_III_4 | 607 | 611 | PF00653 | 0.788 |
LIG_BRCT_BRCA1_1 | 123 | 127 | PF00533 | 0.629 |
LIG_BRCT_BRCA1_1 | 371 | 375 | PF00533 | 0.453 |
LIG_BRCT_BRCA1_1 | 400 | 404 | PF00533 | 0.638 |
LIG_FHA_1 | 13 | 19 | PF00498 | 0.571 |
LIG_FHA_1 | 229 | 235 | PF00498 | 0.708 |
LIG_FHA_1 | 611 | 617 | PF00498 | 0.705 |
LIG_FHA_1 | 71 | 77 | PF00498 | 0.706 |
LIG_FHA_2 | 106 | 112 | PF00498 | 0.667 |
LIG_FHA_2 | 225 | 231 | PF00498 | 0.758 |
LIG_FHA_2 | 28 | 34 | PF00498 | 0.630 |
LIG_FHA_2 | 415 | 421 | PF00498 | 0.449 |
LIG_FHA_2 | 583 | 589 | PF00498 | 0.756 |
LIG_LIR_Apic_2 | 410 | 414 | PF02991 | 0.497 |
LIG_LIR_Apic_2 | 504 | 509 | PF02991 | 0.588 |
LIG_LIR_Apic_2 | 576 | 580 | PF02991 | 0.726 |
LIG_LIR_Gen_1 | 116 | 127 | PF02991 | 0.549 |
LIG_LIR_Gen_1 | 145 | 154 | PF02991 | 0.619 |
LIG_LIR_Gen_1 | 210 | 219 | PF02991 | 0.566 |
LIG_LIR_Gen_1 | 372 | 383 | PF02991 | 0.460 |
LIG_LIR_Gen_1 | 462 | 472 | PF02991 | 0.707 |
LIG_LIR_Gen_1 | 474 | 485 | PF02991 | 0.278 |
LIG_LIR_Nem_3 | 116 | 122 | PF02991 | 0.622 |
LIG_LIR_Nem_3 | 145 | 149 | PF02991 | 0.619 |
LIG_LIR_Nem_3 | 210 | 215 | PF02991 | 0.565 |
LIG_LIR_Nem_3 | 296 | 302 | PF02991 | 0.586 |
LIG_LIR_Nem_3 | 372 | 378 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 462 | 467 | PF02991 | 0.735 |
LIG_LIR_Nem_3 | 474 | 480 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 514 | 518 | PF02991 | 0.615 |
LIG_MYND_3 | 518 | 522 | PF01753 | 0.518 |
LIG_SH2_NCK_1 | 50 | 54 | PF00017 | 0.583 |
LIG_SH2_STAP1 | 115 | 119 | PF00017 | 0.557 |
LIG_SH2_STAT5 | 115 | 118 | PF00017 | 0.472 |
LIG_SH3_2 | 621 | 626 | PF14604 | 0.659 |
LIG_SH3_3 | 101 | 107 | PF00018 | 0.722 |
LIG_SH3_3 | 150 | 156 | PF00018 | 0.524 |
LIG_SH3_3 | 171 | 177 | PF00018 | 0.763 |
LIG_SH3_3 | 212 | 218 | PF00018 | 0.736 |
LIG_SH3_3 | 540 | 546 | PF00018 | 0.638 |
LIG_SH3_3 | 596 | 602 | PF00018 | 0.620 |
LIG_SH3_3 | 615 | 621 | PF00018 | 0.615 |
LIG_SUMO_SIM_par_1 | 468 | 474 | PF11976 | 0.552 |
LIG_SUMO_SIM_par_1 | 611 | 619 | PF11976 | 0.614 |
LIG_TYR_ITIM | 553 | 558 | PF00017 | 0.533 |
LIG_UBA3_1 | 23 | 32 | PF00899 | 0.567 |
LIG_UBA3_1 | 308 | 315 | PF00899 | 0.562 |
LIG_WRC_WIRS_1 | 574 | 579 | PF05994 | 0.724 |
MOD_CDK_SPxxK_3 | 168 | 175 | PF00069 | 0.728 |
MOD_CK1_1 | 275 | 281 | PF00069 | 0.687 |
MOD_CK1_1 | 348 | 354 | PF00069 | 0.666 |
MOD_CK1_1 | 462 | 468 | PF00069 | 0.717 |
MOD_CK1_1 | 497 | 503 | PF00069 | 0.684 |
MOD_CK1_1 | 576 | 582 | PF00069 | 0.706 |
MOD_CK1_1 | 609 | 615 | PF00069 | 0.684 |
MOD_CK1_1 | 91 | 97 | PF00069 | 0.724 |
MOD_CK2_1 | 105 | 111 | PF00069 | 0.672 |
MOD_CK2_1 | 27 | 33 | PF00069 | 0.612 |
MOD_CK2_1 | 347 | 353 | PF00069 | 0.706 |
MOD_CK2_1 | 538 | 544 | PF00069 | 0.638 |
MOD_Cter_Amidation | 263 | 266 | PF01082 | 0.693 |
MOD_GlcNHglycan | 277 | 280 | PF01048 | 0.697 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.640 |
MOD_GlcNHglycan | 323 | 326 | PF01048 | 0.659 |
MOD_GlcNHglycan | 371 | 374 | PF01048 | 0.453 |
MOD_GlcNHglycan | 452 | 455 | PF01048 | 0.754 |
MOD_GlcNHglycan | 464 | 467 | PF01048 | 0.448 |
MOD_GlcNHglycan | 488 | 491 | PF01048 | 0.319 |
MOD_GlcNHglycan | 568 | 571 | PF01048 | 0.704 |
MOD_GlcNHglycan | 581 | 584 | PF01048 | 0.639 |
MOD_GlcNHglycan | 604 | 607 | PF01048 | 0.797 |
MOD_GlcNHglycan | 608 | 611 | PF01048 | 0.785 |
MOD_GlcNHglycan | 618 | 621 | PF01048 | 0.697 |
MOD_GlcNHglycan | 96 | 99 | PF01048 | 0.701 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.462 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.468 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.698 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.716 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.738 |
MOD_GSK3_1 | 317 | 324 | PF00069 | 0.640 |
MOD_GSK3_1 | 335 | 342 | PF00069 | 0.711 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.489 |
MOD_GSK3_1 | 455 | 462 | PF00069 | 0.759 |
MOD_GSK3_1 | 494 | 501 | PF00069 | 0.566 |
MOD_GSK3_1 | 602 | 609 | PF00069 | 0.736 |
MOD_GSK3_1 | 632 | 639 | PF00069 | 0.730 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.724 |
MOD_N-GLC_1 | 486 | 491 | PF02516 | 0.386 |
MOD_N-GLC_1 | 530 | 535 | PF02516 | 0.596 |
MOD_N-GLC_2 | 118 | 120 | PF02516 | 0.464 |
MOD_N-GLC_2 | 479 | 481 | PF02516 | 0.303 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.644 |
MOD_NEK2_1 | 185 | 190 | PF00069 | 0.675 |
MOD_NEK2_1 | 243 | 248 | PF00069 | 0.677 |
MOD_NEK2_1 | 272 | 277 | PF00069 | 0.763 |
MOD_NEK2_1 | 340 | 345 | PF00069 | 0.699 |
MOD_NEK2_1 | 368 | 373 | PF00069 | 0.597 |
MOD_NEK2_1 | 616 | 621 | PF00069 | 0.732 |
MOD_NEK2_1 | 90 | 95 | PF00069 | 0.778 |
MOD_NEK2_2 | 224 | 229 | PF00069 | 0.554 |
MOD_NEK2_2 | 60 | 65 | PF00069 | 0.612 |
MOD_PKA_1 | 625 | 631 | PF00069 | 0.682 |
MOD_PKA_2 | 264 | 270 | PF00069 | 0.733 |
MOD_PKA_2 | 359 | 365 | PF00069 | 0.581 |
MOD_PKA_2 | 368 | 374 | PF00069 | 0.506 |
MOD_PKA_2 | 51 | 57 | PF00069 | 0.647 |
MOD_Plk_1 | 414 | 420 | PF00069 | 0.623 |
MOD_Plk_1 | 433 | 439 | PF00069 | 0.585 |
MOD_Plk_1 | 486 | 492 | PF00069 | 0.586 |
MOD_Plk_1 | 530 | 536 | PF00069 | 0.689 |
MOD_Plk_2-3 | 517 | 523 | PF00069 | 0.459 |
MOD_Plk_4 | 148 | 154 | PF00069 | 0.612 |
MOD_Plk_4 | 155 | 161 | PF00069 | 0.722 |
MOD_Plk_4 | 459 | 465 | PF00069 | 0.744 |
MOD_Plk_4 | 501 | 507 | PF00069 | 0.577 |
MOD_ProDKin_1 | 168 | 174 | PF00069 | 0.760 |
MOD_ProDKin_1 | 345 | 351 | PF00069 | 0.739 |
MOD_ProDKin_1 | 576 | 582 | PF00069 | 0.650 |
MOD_ProDKin_1 | 610 | 616 | PF00069 | 0.686 |
MOD_ProDKin_1 | 91 | 97 | PF00069 | 0.686 |
MOD_SUMO_for_1 | 236 | 239 | PF00179 | 0.771 |
MOD_SUMO_rev_2 | 359 | 367 | PF00179 | 0.630 |
MOD_SUMO_rev_2 | 392 | 401 | PF00179 | 0.564 |
MOD_SUMO_rev_2 | 453 | 459 | PF00179 | 0.681 |
TRG_ENDOCYTIC_2 | 50 | 53 | PF00928 | 0.469 |
TRG_ENDOCYTIC_2 | 555 | 558 | PF00928 | 0.525 |
TRG_ER_diArg_1 | 219 | 221 | PF00400 | 0.613 |
TRG_ER_diArg_1 | 265 | 268 | PF00400 | 0.653 |
TRG_ER_diArg_1 | 472 | 475 | PF00400 | 0.643 |
TRG_Pf-PMV_PEXEL_1 | 393 | 397 | PF00026 | 0.590 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I7W2 | Leptomonas seymouri | 37% | 88% |
A0A1X0P2C9 | Trypanosomatidae | 34% | 100% |
A0A3R7MIW1 | Trypanosoma rangeli | 34% | 100% |
A4HHX0 | Leishmania braziliensis | 72% | 100% |
A4I520 | Leishmania infantum | 100% | 100% |
C9ZQH9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
E9B0F0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4Q7T3 | Leishmania major | 90% | 99% |
Q585P3 | Trypanosoma brucei brucei (strain 927/4 GUTat10.1) | 35% | 100% |
V5DD36 | Trypanosoma cruzi | 33% | 100% |