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: A4HKV3
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0016925 | protein sumoylation | 7 | 1 |
GO:0018193 | peptidyl-amino acid modification | 5 | 1 |
GO:0018205 | peptidyl-lysine modification | 6 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0032446 | protein modification by small protein conjugation | 6 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 11 |
GO:0008270 | zinc ion binding | 6 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043169 | cation binding | 3 | 11 |
GO:0046872 | metal ion binding | 4 | 11 |
GO:0046914 | transition metal ion binding | 5 | 11 |
GO:0003824 | catalytic activity | 1 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
GO:0019787 | ubiquitin-like protein transferase activity | 3 | 1 |
GO:0019789 | SUMO transferase activity | 4 | 1 |
GO:0061659 | ubiquitin-like protein ligase activity | 4 | 1 |
GO:0061665 | SUMO ligase activity | 5 | 1 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 335 | 339 | PF00656 | 0.530 |
CLV_C14_Caspase3-7 | 350 | 354 | PF00656 | 0.602 |
CLV_C14_Caspase3-7 | 596 | 600 | PF00656 | 0.440 |
CLV_NRD_NRD_1 | 145 | 147 | PF00675 | 0.407 |
CLV_NRD_NRD_1 | 185 | 187 | PF00675 | 0.646 |
CLV_NRD_NRD_1 | 206 | 208 | PF00675 | 0.639 |
CLV_NRD_NRD_1 | 284 | 286 | PF00675 | 0.495 |
CLV_NRD_NRD_1 | 328 | 330 | PF00675 | 0.569 |
CLV_NRD_NRD_1 | 384 | 386 | PF00675 | 0.622 |
CLV_NRD_NRD_1 | 407 | 409 | PF00675 | 0.506 |
CLV_NRD_NRD_1 | 508 | 510 | PF00675 | 0.385 |
CLV_NRD_NRD_1 | 559 | 561 | PF00675 | 0.566 |
CLV_NRD_NRD_1 | 616 | 618 | PF00675 | 0.534 |
CLV_PCSK_FUR_1 | 326 | 330 | PF00082 | 0.619 |
CLV_PCSK_FUR_1 | 614 | 618 | PF00082 | 0.605 |
CLV_PCSK_KEX2_1 | 144 | 146 | PF00082 | 0.423 |
CLV_PCSK_KEX2_1 | 184 | 186 | PF00082 | 0.596 |
CLV_PCSK_KEX2_1 | 206 | 208 | PF00082 | 0.639 |
CLV_PCSK_KEX2_1 | 284 | 286 | PF00082 | 0.396 |
CLV_PCSK_KEX2_1 | 328 | 330 | PF00082 | 0.535 |
CLV_PCSK_KEX2_1 | 384 | 386 | PF00082 | 0.622 |
CLV_PCSK_KEX2_1 | 407 | 409 | PF00082 | 0.577 |
CLV_PCSK_KEX2_1 | 508 | 510 | PF00082 | 0.385 |
CLV_PCSK_KEX2_1 | 559 | 561 | PF00082 | 0.446 |
CLV_PCSK_KEX2_1 | 614 | 616 | PF00082 | 0.520 |
CLV_PCSK_PC7_1 | 611 | 617 | PF00082 | 0.497 |
CLV_PCSK_SKI1_1 | 174 | 178 | PF00082 | 0.418 |
CLV_PCSK_SKI1_1 | 192 | 196 | PF00082 | 0.488 |
CLV_PCSK_SKI1_1 | 545 | 549 | PF00082 | 0.442 |
CLV_PCSK_SKI1_1 | 624 | 628 | PF00082 | 0.482 |
DEG_APCC_DBOX_1 | 407 | 415 | PF00400 | 0.678 |
DEG_SCF_FBW7_1 | 364 | 371 | PF00400 | 0.500 |
DEG_SPOP_SBC_1 | 286 | 290 | PF00917 | 0.386 |
DOC_ANK_TNKS_1 | 614 | 621 | PF00023 | 0.458 |
DOC_CKS1_1 | 211 | 216 | PF01111 | 0.613 |
DOC_CYCLIN_RxL_1 | 540 | 552 | PF00134 | 0.535 |
DOC_CYCLIN_yCln2_LP_2 | 533 | 539 | PF00134 | 0.260 |
DOC_MAPK_gen_1 | 326 | 336 | PF00069 | 0.613 |
DOC_PP1_RVXF_1 | 172 | 178 | PF00149 | 0.392 |
DOC_PP2B_LxvP_1 | 533 | 536 | PF13499 | 0.423 |
DOC_PP2B_LxvP_1 | 604 | 607 | PF13499 | 0.380 |
DOC_PP4_FxxP_1 | 610 | 613 | PF00568 | 0.411 |
DOC_SPAK_OSR1_1 | 579 | 583 | PF12202 | 0.461 |
DOC_USP7_MATH_1 | 245 | 249 | PF00917 | 0.444 |
DOC_USP7_MATH_1 | 27 | 31 | PF00917 | 0.681 |
DOC_USP7_MATH_1 | 368 | 372 | PF00917 | 0.622 |
DOC_USP7_MATH_1 | 376 | 380 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 437 | 441 | PF00917 | 0.603 |
DOC_USP7_MATH_1 | 463 | 467 | PF00917 | 0.539 |
DOC_USP7_MATH_1 | 47 | 51 | PF00917 | 0.436 |
DOC_USP7_MATH_1 | 512 | 516 | PF00917 | 0.411 |
DOC_USP7_MATH_1 | 618 | 622 | PF00917 | 0.614 |
DOC_USP7_MATH_1 | 642 | 646 | PF00917 | 0.698 |
DOC_USP7_MATH_1 | 656 | 660 | PF00917 | 0.735 |
DOC_WW_Pin1_4 | 198 | 203 | PF00397 | 0.771 |
DOC_WW_Pin1_4 | 210 | 215 | PF00397 | 0.649 |
DOC_WW_Pin1_4 | 364 | 369 | PF00397 | 0.533 |
DOC_WW_Pin1_4 | 387 | 392 | PF00397 | 0.724 |
DOC_WW_Pin1_4 | 432 | 437 | PF00397 | 0.648 |
DOC_WW_Pin1_4 | 64 | 69 | PF00397 | 0.620 |
LIG_14-3-3_CanoR_1 | 189 | 198 | PF00244 | 0.610 |
LIG_14-3-3_CanoR_1 | 206 | 214 | PF00244 | 0.799 |
LIG_14-3-3_CanoR_1 | 284 | 293 | PF00244 | 0.357 |
LIG_14-3-3_CanoR_1 | 649 | 654 | PF00244 | 0.492 |
LIG_14-3-3_CterR_2 | 660 | 663 | PF00244 | 0.468 |
LIG_Actin_WH2_2 | 306 | 322 | PF00022 | 0.331 |
LIG_BRCT_BRCA1_1 | 227 | 231 | PF00533 | 0.500 |
LIG_CtBP_PxDLS_1 | 14 | 18 | PF00389 | 0.501 |
LIG_deltaCOP1_diTrp_1 | 569 | 575 | PF00928 | 0.402 |
LIG_FHA_1 | 306 | 312 | PF00498 | 0.430 |
LIG_FHA_1 | 523 | 529 | PF00498 | 0.381 |
LIG_FHA_1 | 648 | 654 | PF00498 | 0.492 |
LIG_FHA_2 | 130 | 136 | PF00498 | 0.493 |
LIG_FHA_2 | 137 | 143 | PF00498 | 0.331 |
LIG_FHA_2 | 322 | 328 | PF00498 | 0.665 |
LIG_FHA_2 | 330 | 336 | PF00498 | 0.612 |
LIG_FHA_2 | 338 | 344 | PF00498 | 0.441 |
LIG_FHA_2 | 401 | 407 | PF00498 | 0.545 |
LIG_FHA_2 | 652 | 658 | PF00498 | 0.481 |
LIG_LIR_Gen_1 | 228 | 237 | PF02991 | 0.341 |
LIG_LIR_Gen_1 | 260 | 266 | PF02991 | 0.431 |
LIG_LIR_Gen_1 | 345 | 352 | PF02991 | 0.448 |
LIG_LIR_Gen_1 | 373 | 381 | PF02991 | 0.639 |
LIG_LIR_Gen_1 | 546 | 556 | PF02991 | 0.600 |
LIG_LIR_Nem_3 | 228 | 234 | PF02991 | 0.376 |
LIG_LIR_Nem_3 | 343 | 347 | PF02991 | 0.627 |
LIG_LIR_Nem_3 | 373 | 378 | PF02991 | 0.673 |
LIG_LIR_Nem_3 | 552 | 556 | PF02991 | 0.614 |
LIG_LIR_Nem_3 | 633 | 639 | PF02991 | 0.612 |
LIG_Pex14_1 | 571 | 575 | PF04695 | 0.412 |
LIG_Pex14_2 | 177 | 181 | PF04695 | 0.351 |
LIG_Pex14_2 | 580 | 584 | PF04695 | 0.446 |
LIG_SH2_CRK | 237 | 241 | PF00017 | 0.467 |
LIG_SH2_CRK | 375 | 379 | PF00017 | 0.506 |
LIG_SH2_CRK | 544 | 548 | PF00017 | 0.572 |
LIG_SH2_CRK | 553 | 557 | PF00017 | 0.568 |
LIG_SH2_CRK | 564 | 568 | PF00017 | 0.362 |
LIG_SH2_NCK_1 | 375 | 379 | PF00017 | 0.506 |
LIG_SH2_NCK_1 | 553 | 557 | PF00017 | 0.609 |
LIG_SH2_SRC | 564 | 567 | PF00017 | 0.587 |
LIG_SH2_STAP1 | 344 | 348 | PF00017 | 0.634 |
LIG_SH2_STAP1 | 553 | 557 | PF00017 | 0.537 |
LIG_SH2_STAT3 | 123 | 126 | PF00017 | 0.538 |
LIG_SH2_STAT3 | 90 | 93 | PF00017 | 0.518 |
LIG_SH2_STAT5 | 347 | 350 | PF00017 | 0.651 |
LIG_SH2_STAT5 | 537 | 540 | PF00017 | 0.429 |
LIG_SH3_3 | 110 | 116 | PF00018 | 0.523 |
LIG_SH3_3 | 272 | 278 | PF00018 | 0.444 |
LIG_SH3_3 | 388 | 394 | PF00018 | 0.735 |
LIG_SH3_3 | 9 | 15 | PF00018 | 0.506 |
LIG_SUMO_SIM_par_1 | 260 | 267 | PF11976 | 0.384 |
LIG_SUMO_SIM_par_1 | 308 | 314 | PF11976 | 0.437 |
LIG_SxIP_EBH_1 | 65 | 74 | PF03271 | 0.505 |
LIG_TRAF2_1 | 139 | 142 | PF00917 | 0.419 |
LIG_TRAF2_1 | 403 | 406 | PF00917 | 0.524 |
LIG_Vh1_VBS_1 | 286 | 304 | PF01044 | 0.364 |
LIG_WRC_WIRS_1 | 38 | 43 | PF05994 | 0.534 |
LIG_WRC_WIRS_1 | 58 | 63 | PF05994 | 0.459 |
MOD_CK1_1 | 105 | 111 | PF00069 | 0.639 |
MOD_CK1_1 | 158 | 164 | PF00069 | 0.399 |
MOD_CK1_1 | 16 | 22 | PF00069 | 0.484 |
MOD_CK1_1 | 188 | 194 | PF00069 | 0.572 |
MOD_CK1_1 | 210 | 216 | PF00069 | 0.613 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.522 |
MOD_CK1_1 | 37 | 43 | PF00069 | 0.532 |
MOD_CK1_1 | 371 | 377 | PF00069 | 0.595 |
MOD_CK1_1 | 380 | 386 | PF00069 | 0.692 |
MOD_CK1_1 | 398 | 404 | PF00069 | 0.482 |
MOD_CK1_1 | 514 | 520 | PF00069 | 0.394 |
MOD_CK1_1 | 600 | 606 | PF00069 | 0.433 |
MOD_CK2_1 | 136 | 142 | PF00069 | 0.441 |
MOD_CK2_1 | 146 | 152 | PF00069 | 0.410 |
MOD_CK2_1 | 286 | 292 | PF00069 | 0.283 |
MOD_CK2_1 | 321 | 327 | PF00069 | 0.573 |
MOD_CK2_1 | 329 | 335 | PF00069 | 0.605 |
MOD_CK2_1 | 343 | 349 | PF00069 | 0.401 |
MOD_CK2_1 | 399 | 405 | PF00069 | 0.526 |
MOD_CK2_1 | 543 | 549 | PF00069 | 0.530 |
MOD_CK2_1 | 552 | 558 | PF00069 | 0.619 |
MOD_CK2_1 | 575 | 581 | PF00069 | 0.296 |
MOD_CK2_1 | 651 | 657 | PF00069 | 0.484 |
MOD_DYRK1A_RPxSP_1 | 387 | 391 | PF00069 | 0.609 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.484 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.544 |
MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.469 |
MOD_GlcNHglycan | 23 | 26 | PF01048 | 0.644 |
MOD_GlcNHglycan | 439 | 442 | PF01048 | 0.575 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.576 |
MOD_GlcNHglycan | 50 | 53 | PF01048 | 0.575 |
MOD_GlcNHglycan | 619 | 623 | PF01048 | 0.640 |
MOD_GlcNHglycan | 632 | 635 | PF01048 | 0.433 |
MOD_GlcNHglycan | 640 | 643 | PF01048 | 0.588 |
MOD_GlcNHglycan | 81 | 84 | PF01048 | 0.556 |
MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.563 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.573 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.506 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.348 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.552 |
MOD_GSK3_1 | 198 | 205 | PF00069 | 0.607 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.383 |
MOD_GSK3_1 | 264 | 271 | PF00069 | 0.384 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.618 |
MOD_GSK3_1 | 376 | 383 | PF00069 | 0.565 |
MOD_GSK3_1 | 395 | 402 | PF00069 | 0.727 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.561 |
MOD_GSK3_1 | 435 | 442 | PF00069 | 0.629 |
MOD_GSK3_1 | 510 | 517 | PF00069 | 0.405 |
MOD_GSK3_1 | 571 | 578 | PF00069 | 0.284 |
MOD_GSK3_1 | 638 | 645 | PF00069 | 0.747 |
MOD_GSK3_1 | 647 | 654 | PF00069 | 0.496 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.594 |
MOD_N-GLC_1 | 371 | 376 | PF02516 | 0.700 |
MOD_NEK2_1 | 17 | 22 | PF00069 | 0.655 |
MOD_NEK2_1 | 473 | 478 | PF00069 | 0.467 |
MOD_NEK2_1 | 510 | 515 | PF00069 | 0.477 |
MOD_NEK2_1 | 543 | 548 | PF00069 | 0.532 |
MOD_PIKK_1 | 207 | 213 | PF00454 | 0.640 |
MOD_PIKK_1 | 337 | 343 | PF00454 | 0.456 |
MOD_PIKK_1 | 439 | 445 | PF00454 | 0.670 |
MOD_PIKK_1 | 463 | 469 | PF00454 | 0.378 |
MOD_PIKK_1 | 473 | 479 | PF00454 | 0.354 |
MOD_PIKK_1 | 624 | 630 | PF00454 | 0.598 |
MOD_PIKK_1 | 642 | 648 | PF00454 | 0.684 |
MOD_PK_1 | 385 | 391 | PF00069 | 0.498 |
MOD_PKA_1 | 185 | 191 | PF00069 | 0.422 |
MOD_PKA_1 | 329 | 335 | PF00069 | 0.411 |
MOD_PKA_2 | 185 | 191 | PF00069 | 0.577 |
MOD_PKA_2 | 205 | 211 | PF00069 | 0.795 |
MOD_PKA_2 | 48 | 54 | PF00069 | 0.498 |
MOD_PKA_2 | 648 | 654 | PF00069 | 0.492 |
MOD_PKB_1 | 144 | 152 | PF00069 | 0.319 |
MOD_Plk_1 | 229 | 235 | PF00069 | 0.281 |
MOD_Plk_1 | 371 | 377 | PF00069 | 0.499 |
MOD_Plk_2-3 | 343 | 349 | PF00069 | 0.621 |
MOD_Plk_2-3 | 552 | 558 | PF00069 | 0.540 |
MOD_Plk_4 | 258 | 264 | PF00069 | 0.431 |
MOD_Plk_4 | 296 | 302 | PF00069 | 0.278 |
MOD_Plk_4 | 329 | 335 | PF00069 | 0.411 |
MOD_Plk_4 | 343 | 349 | PF00069 | 0.401 |
MOD_Plk_4 | 37 | 43 | PF00069 | 0.532 |
MOD_Plk_4 | 420 | 426 | PF00069 | 0.487 |
MOD_Plk_4 | 522 | 528 | PF00069 | 0.354 |
MOD_Plk_4 | 600 | 606 | PF00069 | 0.512 |
MOD_ProDKin_1 | 198 | 204 | PF00069 | 0.771 |
MOD_ProDKin_1 | 210 | 216 | PF00069 | 0.644 |
MOD_ProDKin_1 | 364 | 370 | PF00069 | 0.532 |
MOD_ProDKin_1 | 387 | 393 | PF00069 | 0.725 |
MOD_ProDKin_1 | 432 | 438 | PF00069 | 0.648 |
MOD_ProDKin_1 | 64 | 70 | PF00069 | 0.621 |
MOD_SUMO_for_1 | 417 | 420 | PF00179 | 0.531 |
MOD_SUMO_for_1 | 483 | 486 | PF00179 | 0.511 |
TRG_DiLeu_BaEn_1 | 220 | 225 | PF01217 | 0.575 |
TRG_ENDOCYTIC_2 | 237 | 240 | PF00928 | 0.434 |
TRG_ENDOCYTIC_2 | 375 | 378 | PF00928 | 0.508 |
TRG_ENDOCYTIC_2 | 544 | 547 | PF00928 | 0.554 |
TRG_ENDOCYTIC_2 | 553 | 556 | PF00928 | 0.560 |
TRG_ENDOCYTIC_2 | 636 | 639 | PF00928 | 0.519 |
TRG_ER_diArg_1 | 143 | 146 | PF00400 | 0.321 |
TRG_ER_diArg_1 | 184 | 186 | PF00400 | 0.609 |
TRG_ER_diArg_1 | 284 | 286 | PF00400 | 0.502 |
TRG_ER_diArg_1 | 384 | 387 | PF00400 | 0.626 |
TRG_ER_diArg_1 | 507 | 509 | PF00400 | 0.388 |
TRG_ER_diArg_1 | 613 | 616 | PF00400 | 0.522 |
TRG_Pf-PMV_PEXEL_1 | 146 | 150 | PF00026 | 0.310 |
TRG_Pf-PMV_PEXEL_1 | 545 | 549 | PF00026 | 0.558 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P907 | Leptomonas seymouri | 59% | 100% |
A0A1X0NSE9 | Trypanosomatidae | 35% | 100% |
A0A3R7NRN3 | Trypanosoma rangeli | 38% | 100% |
A0A3S7X626 | Leishmania donovani | 84% | 100% |
A4I8D2 | Leishmania infantum | 84% | 100% |
D0AAU1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
E9B391 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
Q4Q4W4 | Leishmania major | 84% | 100% |
V5B5L3 | Trypanosoma cruzi | 39% | 100% |