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: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: E9B388
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 1 |
GO:0006886 | intracellular protein transport | 4 | 1 |
GO:0008104 | protein localization | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0015031 | protein transport | 4 | 1 |
GO:0033036 | macromolecule localization | 2 | 1 |
GO:0045184 | establishment of protein localization | 3 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
GO:0070727 | cellular macromolecule localization | 3 | 1 |
GO:0071702 | organic substance transport | 4 | 1 |
GO:0071705 | nitrogen compound transport | 4 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 7 |
GO:0005488 | binding | 1 | 7 |
GO:0036094 | small molecule binding | 2 | 7 |
GO:0097159 | organic cyclic compound binding | 2 | 7 |
GO:1901265 | nucleoside phosphate binding | 3 | 7 |
GO:1901363 | heterocyclic compound binding | 2 | 7 |
GO:0003824 | catalytic activity | 1 | 1 |
GO:0003924 | GTPase activity | 7 | 1 |
GO:0016462 | pyrophosphatase activity | 5 | 1 |
GO:0016787 | hydrolase activity | 2 | 1 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 1 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 1 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 267 | 269 | PF00675 | 0.565 |
CLV_NRD_NRD_1 | 340 | 342 | PF00675 | 0.541 |
CLV_NRD_NRD_1 | 444 | 446 | PF00675 | 0.514 |
CLV_NRD_NRD_1 | 467 | 469 | PF00675 | 0.565 |
CLV_NRD_NRD_1 | 63 | 65 | PF00675 | 0.376 |
CLV_NRD_NRD_1 | 668 | 670 | PF00675 | 0.503 |
CLV_NRD_NRD_1 | 79 | 81 | PF00675 | 0.343 |
CLV_NRD_NRD_1 | 813 | 815 | PF00675 | 0.532 |
CLV_PCSK_FUR_1 | 811 | 815 | PF00082 | 0.555 |
CLV_PCSK_KEX2_1 | 267 | 269 | PF00082 | 0.565 |
CLV_PCSK_KEX2_1 | 339 | 341 | PF00082 | 0.487 |
CLV_PCSK_KEX2_1 | 467 | 469 | PF00082 | 0.535 |
CLV_PCSK_KEX2_1 | 63 | 65 | PF00082 | 0.397 |
CLV_PCSK_KEX2_1 | 668 | 670 | PF00082 | 0.503 |
CLV_PCSK_KEX2_1 | 811 | 813 | PF00082 | 0.531 |
CLV_PCSK_PC1ET2_1 | 339 | 341 | PF00082 | 0.487 |
CLV_PCSK_SKI1_1 | 13 | 17 | PF00082 | 0.565 |
CLV_PCSK_SKI1_1 | 139 | 143 | PF00082 | 0.342 |
CLV_PCSK_SKI1_1 | 183 | 187 | PF00082 | 0.343 |
CLV_PCSK_SKI1_1 | 455 | 459 | PF00082 | 0.432 |
CLV_PCSK_SKI1_1 | 573 | 577 | PF00082 | 0.499 |
CLV_PCSK_SKI1_1 | 65 | 69 | PF00082 | 0.364 |
CLV_PCSK_SKI1_1 | 813 | 817 | PF00082 | 0.558 |
DEG_APCC_DBOX_1 | 449 | 457 | PF00400 | 0.367 |
DEG_APCC_DBOX_1 | 610 | 618 | PF00400 | 0.467 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.772 |
DEG_ODPH_VHL_1 | 541 | 554 | PF01847 | 0.412 |
DEG_SPOP_SBC_1 | 239 | 243 | PF00917 | 0.756 |
DEG_SPOP_SBC_1 | 24 | 28 | PF00917 | 0.737 |
DEG_SPOP_SBC_1 | 248 | 252 | PF00917 | 0.537 |
DEG_SPOP_SBC_1 | 96 | 100 | PF00917 | 0.343 |
DOC_CKS1_1 | 416 | 421 | PF01111 | 0.453 |
DOC_CKS1_1 | 532 | 537 | PF01111 | 0.518 |
DOC_CYCLIN_yCln2_LP_2 | 233 | 239 | PF00134 | 0.630 |
DOC_CYCLIN_yCln2_LP_2 | 416 | 422 | PF00134 | 0.479 |
DOC_CYCLIN_yCln2_LP_2 | 487 | 493 | PF00134 | 0.377 |
DOC_MAPK_DCC_7 | 46 | 56 | PF00069 | 0.647 |
DOC_MAPK_DCC_7 | 570 | 580 | PF00069 | 0.311 |
DOC_MAPK_gen_1 | 167 | 175 | PF00069 | 0.245 |
DOC_MAPK_gen_1 | 339 | 346 | PF00069 | 0.483 |
DOC_MAPK_gen_1 | 539 | 546 | PF00069 | 0.398 |
DOC_MAPK_gen_1 | 548 | 556 | PF00069 | 0.391 |
DOC_MAPK_gen_1 | 570 | 580 | PF00069 | 0.499 |
DOC_MAPK_gen_1 | 609 | 616 | PF00069 | 0.447 |
DOC_MAPK_gen_1 | 63 | 69 | PF00069 | 0.345 |
DOC_MAPK_MEF2A_6 | 339 | 348 | PF00069 | 0.475 |
DOC_MAPK_MEF2A_6 | 548 | 556 | PF00069 | 0.489 |
DOC_PP1_RVXF_1 | 453 | 459 | PF00149 | 0.375 |
DOC_PP1_RVXF_1 | 51 | 57 | PF00149 | 0.613 |
DOC_PP1_RVXF_1 | 551 | 557 | PF00149 | 0.389 |
DOC_PP2B_LxvP_1 | 233 | 236 | PF13499 | 0.622 |
DOC_PP2B_LxvP_1 | 716 | 719 | PF13499 | 0.622 |
DOC_PP2B_LxvP_1 | 749 | 752 | PF13499 | 0.481 |
DOC_PP4_FxxP_1 | 458 | 461 | PF00568 | 0.392 |
DOC_PP4_FxxP_1 | 574 | 577 | PF00568 | 0.310 |
DOC_USP7_MATH_1 | 237 | 241 | PF00917 | 0.763 |
DOC_USP7_MATH_1 | 24 | 28 | PF00917 | 0.673 |
DOC_USP7_MATH_1 | 249 | 253 | PF00917 | 0.498 |
DOC_USP7_MATH_1 | 642 | 646 | PF00917 | 0.453 |
DOC_USP7_MATH_2 | 490 | 496 | PF00917 | 0.488 |
DOC_USP7_UBL2_3 | 208 | 212 | PF12436 | 0.431 |
DOC_WW_Pin1_4 | 415 | 420 | PF00397 | 0.437 |
DOC_WW_Pin1_4 | 531 | 536 | PF00397 | 0.432 |
DOC_WW_Pin1_4 | 638 | 643 | PF00397 | 0.515 |
DOC_WW_Pin1_4 | 754 | 759 | PF00397 | 0.597 |
DOC_WW_Pin1_4 | 818 | 823 | PF00397 | 0.724 |
LIG_14-3-3_CanoR_1 | 253 | 263 | PF00244 | 0.491 |
LIG_14-3-3_CanoR_1 | 349 | 356 | PF00244 | 0.462 |
LIG_14-3-3_CanoR_1 | 404 | 410 | PF00244 | 0.465 |
LIG_14-3-3_CanoR_1 | 668 | 672 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 720 | 726 | PF00244 | 0.553 |
LIG_14-3-3_CanoR_1 | 97 | 104 | PF00244 | 0.426 |
LIG_APCC_ABBA_1 | 623 | 628 | PF00400 | 0.374 |
LIG_APCC_ABBAyCdc20_2 | 622 | 628 | PF00400 | 0.374 |
LIG_BRCT_BRCA1_1 | 25 | 29 | PF00533 | 0.539 |
LIG_BRCT_BRCA1_1 | 494 | 498 | PF00533 | 0.517 |
LIG_BRCT_BRCA1_1 | 820 | 824 | PF00533 | 0.557 |
LIG_BRCT_BRCA1_1 | 84 | 88 | PF00533 | 0.443 |
LIG_deltaCOP1_diTrp_1 | 561 | 567 | PF00928 | 0.393 |
LIG_EH1_1 | 341 | 349 | PF00400 | 0.477 |
LIG_FHA_1 | 131 | 137 | PF00498 | 0.365 |
LIG_FHA_1 | 722 | 728 | PF00498 | 0.573 |
LIG_FHA_1 | 775 | 781 | PF00498 | 0.688 |
LIG_FHA_1 | 97 | 103 | PF00498 | 0.343 |
LIG_FHA_2 | 187 | 193 | PF00498 | 0.343 |
LIG_FHA_2 | 780 | 786 | PF00498 | 0.571 |
LIG_LIR_Apic_2 | 522 | 527 | PF02991 | 0.393 |
LIG_LIR_Gen_1 | 112 | 123 | PF02991 | 0.258 |
LIG_LIR_Gen_1 | 140 | 150 | PF02991 | 0.338 |
LIG_LIR_Gen_1 | 351 | 360 | PF02991 | 0.495 |
LIG_LIR_Gen_1 | 411 | 420 | PF02991 | 0.475 |
LIG_LIR_Gen_1 | 495 | 506 | PF02991 | 0.491 |
LIG_LIR_Gen_1 | 555 | 563 | PF02991 | 0.397 |
LIG_LIR_Nem_3 | 112 | 118 | PF02991 | 0.289 |
LIG_LIR_Nem_3 | 140 | 145 | PF02991 | 0.338 |
LIG_LIR_Nem_3 | 174 | 179 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 411 | 415 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 495 | 501 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 555 | 559 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 561 | 567 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 662 | 666 | PF02991 | 0.383 |
LIG_MYND_1 | 527 | 531 | PF01753 | 0.403 |
LIG_PCNA_yPIPBox_3 | 566 | 575 | PF02747 | 0.436 |
LIG_Pex14_1 | 378 | 382 | PF04695 | 0.361 |
LIG_Pex14_2 | 142 | 146 | PF04695 | 0.343 |
LIG_REV1ctd_RIR_1 | 86 | 93 | PF16727 | 0.401 |
LIG_SH2_CRK | 572 | 576 | PF00017 | 0.426 |
LIG_SH2_CRK | 663 | 667 | PF00017 | 0.397 |
LIG_SH2_CRK | 753 | 757 | PF00017 | 0.596 |
LIG_SH2_SRC | 525 | 528 | PF00017 | 0.518 |
LIG_SH2_SRC | 581 | 584 | PF00017 | 0.651 |
LIG_SH2_SRC | 71 | 74 | PF00017 | 0.399 |
LIG_SH2_STAP1 | 265 | 269 | PF00017 | 0.572 |
LIG_SH2_STAP1 | 387 | 391 | PF00017 | 0.469 |
LIG_SH2_STAP1 | 412 | 416 | PF00017 | 0.396 |
LIG_SH2_STAT3 | 14 | 17 | PF00017 | 0.607 |
LIG_SH2_STAT5 | 134 | 137 | PF00017 | 0.435 |
LIG_SH2_STAT5 | 14 | 17 | PF00017 | 0.507 |
LIG_SH2_STAT5 | 304 | 307 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 382 | 385 | PF00017 | 0.371 |
LIG_SH2_STAT5 | 431 | 434 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 448 | 451 | PF00017 | 0.363 |
LIG_SH2_STAT5 | 525 | 528 | PF00017 | 0.385 |
LIG_SH2_STAT5 | 748 | 751 | PF00017 | 0.433 |
LIG_SH2_STAT5 | 786 | 789 | PF00017 | 0.520 |
LIG_SH3_3 | 393 | 399 | PF00018 | 0.477 |
LIG_SH3_3 | 503 | 509 | PF00018 | 0.509 |
LIG_SH3_3 | 577 | 583 | PF00018 | 0.548 |
LIG_SH3_3 | 669 | 675 | PF00018 | 0.436 |
LIG_SUMO_SIM_anti_2 | 393 | 398 | PF11976 | 0.409 |
LIG_SUMO_SIM_par_1 | 183 | 189 | PF11976 | 0.443 |
LIG_SUMO_SIM_par_1 | 489 | 497 | PF11976 | 0.451 |
LIG_SUMO_SIM_par_1 | 722 | 728 | PF11976 | 0.573 |
LIG_TRAF2_1 | 124 | 127 | PF00917 | 0.368 |
LIG_TRAF2_1 | 364 | 367 | PF00917 | 0.498 |
LIG_TRAF2_1 | 603 | 606 | PF00917 | 0.523 |
LIG_TRAF2_1 | 759 | 762 | PF00917 | 0.699 |
LIG_TRFH_1 | 556 | 560 | PF08558 | 0.364 |
LIG_TYR_ITIM | 69 | 74 | PF00017 | 0.399 |
LIG_UBA3_1 | 141 | 147 | PF00899 | 0.328 |
LIG_UBA3_1 | 301 | 310 | PF00899 | 0.475 |
LIG_UBA3_1 | 331 | 339 | PF00899 | 0.466 |
LIG_WRC_WIRS_1 | 213 | 218 | PF05994 | 0.437 |
MOD_CDC14_SPxK_1 | 757 | 760 | PF00782 | 0.692 |
MOD_CDK_SPK_2 | 638 | 643 | PF00069 | 0.515 |
MOD_CDK_SPxK_1 | 754 | 760 | PF00069 | 0.649 |
MOD_CK1_1 | 128 | 134 | PF00069 | 0.372 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.564 |
MOD_CK1_1 | 240 | 246 | PF00069 | 0.731 |
MOD_CK1_1 | 27 | 33 | PF00069 | 0.719 |
MOD_CK1_1 | 277 | 283 | PF00069 | 0.427 |
MOD_CK1_1 | 408 | 414 | PF00069 | 0.473 |
MOD_CK1_1 | 634 | 640 | PF00069 | 0.429 |
MOD_CK1_1 | 690 | 696 | PF00069 | 0.538 |
MOD_CK1_1 | 738 | 744 | PF00069 | 0.523 |
MOD_CK1_1 | 774 | 780 | PF00069 | 0.742 |
MOD_CK2_1 | 146 | 152 | PF00069 | 0.357 |
MOD_CK2_1 | 361 | 367 | PF00069 | 0.413 |
MOD_CK2_1 | 431 | 437 | PF00069 | 0.423 |
MOD_CK2_1 | 779 | 785 | PF00069 | 0.581 |
MOD_CK2_1 | 89 | 95 | PF00069 | 0.376 |
MOD_CK2_1 | 97 | 103 | PF00069 | 0.279 |
MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.365 |
MOD_GlcNHglycan | 157 | 160 | PF01048 | 0.313 |
MOD_GlcNHglycan | 293 | 296 | PF01048 | 0.410 |
MOD_GlcNHglycan | 298 | 301 | PF01048 | 0.356 |
MOD_GlcNHglycan | 636 | 639 | PF01048 | 0.517 |
MOD_GlcNHglycan | 710 | 713 | PF01048 | 0.553 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.405 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.343 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.720 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.527 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.639 |
MOD_GSK3_1 | 515 | 522 | PF00069 | 0.541 |
MOD_GSK3_1 | 634 | 641 | PF00069 | 0.489 |
MOD_GSK3_1 | 688 | 695 | PF00069 | 0.518 |
MOD_GSK3_1 | 767 | 774 | PF00069 | 0.756 |
MOD_N-GLC_1 | 224 | 229 | PF02516 | 0.551 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.343 |
MOD_NEK2_1 | 186 | 191 | PF00069 | 0.343 |
MOD_NEK2_1 | 238 | 243 | PF00069 | 0.764 |
MOD_NEK2_1 | 274 | 279 | PF00069 | 0.377 |
MOD_NEK2_1 | 29 | 34 | PF00069 | 0.668 |
MOD_NEK2_1 | 405 | 410 | PF00069 | 0.384 |
MOD_NEK2_1 | 515 | 520 | PF00069 | 0.317 |
MOD_NEK2_1 | 721 | 726 | PF00069 | 0.479 |
MOD_NEK2_1 | 735 | 740 | PF00069 | 0.368 |
MOD_NEK2_1 | 798 | 803 | PF00069 | 0.536 |
MOD_NEK2_1 | 89 | 94 | PF00069 | 0.405 |
MOD_NEK2_2 | 75 | 80 | PF00069 | 0.343 |
MOD_OFUCOSY | 736 | 742 | PF10250 | 0.518 |
MOD_PIKK_1 | 515 | 521 | PF00454 | 0.582 |
MOD_PIKK_1 | 719 | 725 | PF00454 | 0.571 |
MOD_PK_1 | 760 | 766 | PF00069 | 0.794 |
MOD_PKA_2 | 326 | 332 | PF00069 | 0.495 |
MOD_PKA_2 | 348 | 354 | PF00069 | 0.532 |
MOD_PKA_2 | 610 | 616 | PF00069 | 0.483 |
MOD_PKA_2 | 642 | 648 | PF00069 | 0.563 |
MOD_PKA_2 | 667 | 673 | PF00069 | 0.508 |
MOD_PKA_2 | 719 | 725 | PF00069 | 0.498 |
MOD_PKA_2 | 96 | 102 | PF00069 | 0.399 |
MOD_Plk_1 | 105 | 111 | PF00069 | 0.480 |
MOD_Plk_1 | 137 | 143 | PF00069 | 0.343 |
MOD_Plk_1 | 760 | 766 | PF00069 | 0.736 |
MOD_Plk_2-3 | 492 | 498 | PF00069 | 0.510 |
MOD_Plk_4 | 130 | 136 | PF00069 | 0.344 |
MOD_Plk_4 | 390 | 396 | PF00069 | 0.369 |
MOD_Plk_4 | 405 | 411 | PF00069 | 0.493 |
MOD_Plk_4 | 576 | 582 | PF00069 | 0.497 |
MOD_Plk_4 | 610 | 616 | PF00069 | 0.483 |
MOD_Plk_4 | 631 | 637 | PF00069 | 0.485 |
MOD_Plk_4 | 721 | 727 | PF00069 | 0.497 |
MOD_ProDKin_1 | 415 | 421 | PF00069 | 0.444 |
MOD_ProDKin_1 | 531 | 537 | PF00069 | 0.434 |
MOD_ProDKin_1 | 638 | 644 | PF00069 | 0.512 |
MOD_ProDKin_1 | 754 | 760 | PF00069 | 0.612 |
MOD_ProDKin_1 | 818 | 824 | PF00069 | 0.727 |
TRG_DiLeu_BaEn_1 | 390 | 395 | PF01217 | 0.441 |
TRG_DiLeu_BaEn_1 | 483 | 488 | PF01217 | 0.477 |
TRG_DiLeu_BaEn_1 | 728 | 733 | PF01217 | 0.414 |
TRG_DiLeu_BaEn_2 | 137 | 143 | PF01217 | 0.443 |
TRG_DiLeu_BaLyEn_6 | 511 | 516 | PF01217 | 0.328 |
TRG_ENDOCYTIC_2 | 412 | 415 | PF00928 | 0.393 |
TRG_ENDOCYTIC_2 | 572 | 575 | PF00928 | 0.365 |
TRG_ENDOCYTIC_2 | 663 | 666 | PF00928 | 0.390 |
TRG_ENDOCYTIC_2 | 71 | 74 | PF00928 | 0.399 |
TRG_ENDOCYTIC_2 | 748 | 751 | PF00928 | 0.433 |
TRG_ER_diArg_1 | 267 | 269 | PF00400 | 0.581 |
TRG_ER_diArg_1 | 466 | 468 | PF00400 | 0.516 |
TRG_ER_diArg_1 | 52 | 55 | PF00400 | 0.549 |
TRG_ER_diArg_1 | 550 | 553 | PF00400 | 0.454 |
TRG_ER_diArg_1 | 598 | 601 | PF00400 | 0.567 |
TRG_ER_diArg_1 | 811 | 814 | PF00400 | 0.555 |
TRG_NLS_MonoExtC_3 | 338 | 343 | PF00514 | 0.480 |
TRG_Pf-PMV_PEXEL_1 | 170 | 174 | PF00026 | 0.443 |
TRG_Pf-PMV_PEXEL_1 | 814 | 818 | PF00026 | 0.581 |
TRG_Pf-PMV_PEXEL_1 | 91 | 95 | PF00026 | 0.373 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I9V2 | Leptomonas seymouri | 78% | 82% |
A0A1X0NT83 | Trypanosomatidae | 49% | 82% |
A0A3S5H7S9 | Leishmania donovani | 95% | 100% |
A0A422NYM8 | Trypanosoma rangeli | 46% | 84% |
A4HKV0 | Leishmania braziliensis | 88% | 100% |
A4I8C9 | Leishmania infantum | 95% | 100% |
Q4Q4W7 | Leishmania major | 95% | 100% |
V5DM76 | Trypanosoma cruzi | 46% | 94% |