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: Q4Q5A9
Term | Name | Level | Count |
---|---|---|---|
GO:0008152 | metabolic process | 1 | 1 |
GO:0032259 | methylation | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 1 |
GO:0008168 | methyltransferase activity | 4 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 346 | 350 | PF00656 | 0.644 |
CLV_C14_Caspase3-7 | 358 | 362 | PF00656 | 0.617 |
CLV_C14_Caspase3-7 | 495 | 499 | PF00656 | 0.628 |
CLV_C14_Caspase3-7 | 588 | 592 | PF00656 | 0.501 |
CLV_C14_Caspase3-7 | 632 | 636 | PF00656 | 0.731 |
CLV_NRD_NRD_1 | 2 | 4 | PF00675 | 0.745 |
CLV_NRD_NRD_1 | 214 | 216 | PF00675 | 0.552 |
CLV_NRD_NRD_1 | 31 | 33 | PF00675 | 0.567 |
CLV_NRD_NRD_1 | 320 | 322 | PF00675 | 0.623 |
CLV_NRD_NRD_1 | 464 | 466 | PF00675 | 0.433 |
CLV_NRD_NRD_1 | 568 | 570 | PF00675 | 0.570 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.745 |
CLV_PCSK_KEX2_1 | 214 | 216 | PF00082 | 0.552 |
CLV_PCSK_KEX2_1 | 31 | 33 | PF00082 | 0.575 |
CLV_PCSK_KEX2_1 | 319 | 321 | PF00082 | 0.641 |
CLV_PCSK_KEX2_1 | 464 | 466 | PF00082 | 0.516 |
CLV_PCSK_KEX2_1 | 568 | 570 | PF00082 | 0.570 |
CLV_PCSK_SKI1_1 | 215 | 219 | PF00082 | 0.538 |
CLV_PCSK_SKI1_1 | 395 | 399 | PF00082 | 0.471 |
CLV_PCSK_SKI1_1 | 568 | 572 | PF00082 | 0.586 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.780 |
DEG_SPOP_SBC_1 | 344 | 348 | PF00917 | 0.726 |
DOC_CYCLIN_RxL_1 | 212 | 222 | PF00134 | 0.586 |
DOC_CYCLIN_yClb3_PxF_3 | 374 | 382 | PF00134 | 0.648 |
DOC_MAPK_gen_1 | 232 | 241 | PF00069 | 0.667 |
DOC_MAPK_MEF2A_6 | 198 | 206 | PF00069 | 0.498 |
DOC_PP2B_LxvP_1 | 12 | 15 | PF13499 | 0.711 |
DOC_PP2B_LxvP_1 | 333 | 336 | PF13499 | 0.678 |
DOC_PP2B_LxvP_1 | 522 | 525 | PF13499 | 0.489 |
DOC_PP2B_LxvP_1 | 596 | 599 | PF13499 | 0.387 |
DOC_PP4_FxxP_1 | 296 | 299 | PF00568 | 0.481 |
DOC_USP7_MATH_1 | 122 | 126 | PF00917 | 0.745 |
DOC_USP7_MATH_1 | 344 | 348 | PF00917 | 0.749 |
DOC_USP7_MATH_1 | 350 | 354 | PF00917 | 0.747 |
DOC_USP7_MATH_1 | 355 | 359 | PF00917 | 0.729 |
DOC_USP7_MATH_1 | 407 | 411 | PF00917 | 0.777 |
DOC_USP7_MATH_1 | 416 | 420 | PF00917 | 0.761 |
DOC_USP7_MATH_1 | 472 | 476 | PF00917 | 0.540 |
DOC_USP7_MATH_1 | 494 | 498 | PF00917 | 0.735 |
DOC_USP7_MATH_1 | 556 | 560 | PF00917 | 0.573 |
DOC_USP7_MATH_1 | 59 | 63 | PF00917 | 0.409 |
DOC_WW_Pin1_4 | 133 | 138 | PF00397 | 0.585 |
DOC_WW_Pin1_4 | 148 | 153 | PF00397 | 0.431 |
DOC_WW_Pin1_4 | 242 | 247 | PF00397 | 0.625 |
DOC_WW_Pin1_4 | 301 | 306 | PF00397 | 0.771 |
DOC_WW_Pin1_4 | 364 | 369 | PF00397 | 0.634 |
DOC_WW_Pin1_4 | 419 | 424 | PF00397 | 0.668 |
DOC_WW_Pin1_4 | 476 | 481 | PF00397 | 0.436 |
DOC_WW_Pin1_4 | 487 | 492 | PF00397 | 0.495 |
DOC_WW_Pin1_4 | 557 | 562 | PF00397 | 0.591 |
DOC_WW_Pin1_4 | 70 | 75 | PF00397 | 0.545 |
LIG_14-3-3_CanoR_1 | 16 | 22 | PF00244 | 0.558 |
LIG_14-3-3_CanoR_1 | 2 | 6 | PF00244 | 0.729 |
LIG_14-3-3_CanoR_1 | 214 | 218 | PF00244 | 0.523 |
LIG_14-3-3_CanoR_1 | 232 | 241 | PF00244 | 0.709 |
LIG_14-3-3_CanoR_1 | 659 | 666 | PF00244 | 0.396 |
LIG_Actin_WH2_2 | 384 | 402 | PF00022 | 0.520 |
LIG_APCC_ABBA_1 | 141 | 146 | PF00400 | 0.554 |
LIG_Clathr_ClatBox_1 | 173 | 177 | PF01394 | 0.401 |
LIG_FHA_1 | 233 | 239 | PF00498 | 0.729 |
LIG_FHA_1 | 260 | 266 | PF00498 | 0.565 |
LIG_FHA_1 | 354 | 360 | PF00498 | 0.783 |
LIG_FHA_1 | 365 | 371 | PF00498 | 0.592 |
LIG_FHA_1 | 477 | 483 | PF00498 | 0.462 |
LIG_FHA_1 | 58 | 64 | PF00498 | 0.461 |
LIG_FHA_1 | 612 | 618 | PF00498 | 0.455 |
LIG_FHA_2 | 344 | 350 | PF00498 | 0.721 |
LIG_GBD_Chelix_1 | 267 | 275 | PF00786 | 0.434 |
LIG_HP1_1 | 172 | 176 | PF01393 | 0.424 |
LIG_Integrin_RGD_1 | 630 | 632 | PF01839 | 0.549 |
LIG_LIR_Apic_2 | 146 | 152 | PF02991 | 0.599 |
LIG_LIR_Apic_2 | 295 | 299 | PF02991 | 0.476 |
LIG_LIR_Apic_2 | 475 | 481 | PF02991 | 0.460 |
LIG_LIR_Gen_1 | 324 | 333 | PF02991 | 0.547 |
LIG_LIR_Nem_3 | 136 | 141 | PF02991 | 0.550 |
LIG_LIR_Nem_3 | 324 | 328 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 427 | 431 | PF02991 | 0.512 |
LIG_LIR_Nem_3 | 457 | 461 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 82 | 86 | PF02991 | 0.497 |
LIG_SH2_CRK | 325 | 329 | PF00017 | 0.504 |
LIG_SH2_CRK | 478 | 482 | PF00017 | 0.447 |
LIG_SH2_GRB2like | 435 | 438 | PF00017 | 0.397 |
LIG_SH2_STAP1 | 435 | 439 | PF00017 | 0.445 |
LIG_SH2_STAP1 | 539 | 543 | PF00017 | 0.615 |
LIG_SH2_STAT3 | 255 | 258 | PF00017 | 0.410 |
LIG_SH2_STAT5 | 149 | 152 | PF00017 | 0.551 |
LIG_SH2_STAT5 | 255 | 258 | PF00017 | 0.410 |
LIG_SH2_STAT5 | 277 | 280 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 291 | 294 | PF00017 | 0.535 |
LIG_SH2_STAT5 | 380 | 383 | PF00017 | 0.633 |
LIG_SH2_STAT5 | 428 | 431 | PF00017 | 0.496 |
LIG_SH2_STAT5 | 458 | 461 | PF00017 | 0.365 |
LIG_SH2_STAT5 | 478 | 481 | PF00017 | 0.236 |
LIG_SH2_STAT5 | 68 | 71 | PF00017 | 0.469 |
LIG_SH3_3 | 12 | 18 | PF00018 | 0.743 |
LIG_SH3_3 | 236 | 242 | PF00018 | 0.662 |
LIG_SH3_3 | 251 | 257 | PF00018 | 0.406 |
LIG_SH3_3 | 371 | 377 | PF00018 | 0.499 |
LIG_SH3_3 | 485 | 491 | PF00018 | 0.546 |
LIG_SH3_3 | 660 | 666 | PF00018 | 0.415 |
LIG_SUMO_SIM_par_1 | 17 | 23 | PF11976 | 0.437 |
LIG_SUMO_SIM_par_1 | 172 | 177 | PF11976 | 0.402 |
LIG_TRAF2_1 | 314 | 317 | PF00917 | 0.428 |
LIG_WW_3 | 13 | 17 | PF00397 | 0.627 |
MOD_CDK_SPK_2 | 148 | 153 | PF00069 | 0.387 |
MOD_CDK_SPK_2 | 364 | 369 | PF00069 | 0.669 |
MOD_CK1_1 | 151 | 157 | PF00069 | 0.585 |
MOD_CK1_1 | 343 | 349 | PF00069 | 0.712 |
MOD_CK1_1 | 353 | 359 | PF00069 | 0.785 |
MOD_CK1_1 | 419 | 425 | PF00069 | 0.719 |
MOD_CK1_1 | 492 | 498 | PF00069 | 0.736 |
MOD_CK1_1 | 560 | 566 | PF00069 | 0.566 |
MOD_CK1_1 | 582 | 588 | PF00069 | 0.551 |
MOD_CK1_1 | 62 | 68 | PF00069 | 0.408 |
MOD_CK1_1 | 73 | 79 | PF00069 | 0.407 |
MOD_CK2_1 | 582 | 588 | PF00069 | 0.511 |
MOD_Cter_Amidation | 462 | 465 | PF01082 | 0.389 |
MOD_GlcNHglycan | 124 | 127 | PF01048 | 0.718 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.646 |
MOD_GlcNHglycan | 342 | 345 | PF01048 | 0.785 |
MOD_GlcNHglycan | 352 | 355 | PF01048 | 0.716 |
MOD_GlcNHglycan | 401 | 404 | PF01048 | 0.546 |
MOD_GlcNHglycan | 417 | 421 | PF01048 | 0.725 |
MOD_GlcNHglycan | 449 | 452 | PF01048 | 0.441 |
MOD_GlcNHglycan | 502 | 505 | PF01048 | 0.670 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.453 |
MOD_GlcNHglycan | 652 | 655 | PF01048 | 0.460 |
MOD_GlcNHglycan | 660 | 663 | PF01048 | 0.425 |
MOD_GlcNHglycan | 98 | 102 | PF01048 | 0.776 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.429 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.634 |
MOD_GSK3_1 | 340 | 347 | PF00069 | 0.766 |
MOD_GSK3_1 | 349 | 356 | PF00069 | 0.802 |
MOD_GSK3_1 | 472 | 479 | PF00069 | 0.438 |
MOD_GSK3_1 | 489 | 496 | PF00069 | 0.541 |
MOD_GSK3_1 | 498 | 505 | PF00069 | 0.696 |
MOD_GSK3_1 | 556 | 563 | PF00069 | 0.566 |
MOD_GSK3_1 | 575 | 582 | PF00069 | 0.240 |
MOD_GSK3_1 | 611 | 618 | PF00069 | 0.439 |
MOD_GSK3_1 | 646 | 653 | PF00069 | 0.547 |
MOD_N-GLC_1 | 340 | 345 | PF02516 | 0.549 |
MOD_N-GLC_1 | 364 | 369 | PF02516 | 0.644 |
MOD_N-GLC_1 | 57 | 62 | PF02516 | 0.460 |
MOD_N-GLC_2 | 169 | 171 | PF02516 | 0.451 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.695 |
MOD_NEK2_1 | 292 | 297 | PF00069 | 0.635 |
MOD_NEK2_1 | 399 | 404 | PF00069 | 0.563 |
MOD_NEK2_1 | 429 | 434 | PF00069 | 0.392 |
MOD_NEK2_1 | 447 | 452 | PF00069 | 0.471 |
MOD_NEK2_1 | 500 | 505 | PF00069 | 0.635 |
MOD_NEK2_1 | 57 | 62 | PF00069 | 0.425 |
MOD_NEK2_2 | 59 | 64 | PF00069 | 0.390 |
MOD_PIKK_1 | 193 | 199 | PF00454 | 0.656 |
MOD_PIKK_1 | 646 | 652 | PF00454 | 0.482 |
MOD_PKA_2 | 1 | 7 | PF00069 | 0.785 |
MOD_PKA_2 | 213 | 219 | PF00069 | 0.559 |
MOD_PKA_2 | 27 | 33 | PF00069 | 0.496 |
MOD_PKA_2 | 381 | 387 | PF00069 | 0.568 |
MOD_PKA_2 | 399 | 405 | PF00069 | 0.514 |
MOD_PKA_2 | 658 | 664 | PF00069 | 0.392 |
MOD_PKA_2 | 96 | 102 | PF00069 | 0.693 |
MOD_PKB_1 | 188 | 196 | PF00069 | 0.430 |
MOD_Plk_1 | 539 | 545 | PF00069 | 0.613 |
MOD_Plk_1 | 582 | 588 | PF00069 | 0.473 |
MOD_Plk_4 | 182 | 188 | PF00069 | 0.436 |
MOD_Plk_4 | 424 | 430 | PF00069 | 0.497 |
MOD_Plk_4 | 615 | 621 | PF00069 | 0.401 |
MOD_Plk_4 | 73 | 79 | PF00069 | 0.391 |
MOD_ProDKin_1 | 133 | 139 | PF00069 | 0.580 |
MOD_ProDKin_1 | 148 | 154 | PF00069 | 0.446 |
MOD_ProDKin_1 | 242 | 248 | PF00069 | 0.610 |
MOD_ProDKin_1 | 301 | 307 | PF00069 | 0.771 |
MOD_ProDKin_1 | 364 | 370 | PF00069 | 0.627 |
MOD_ProDKin_1 | 419 | 425 | PF00069 | 0.659 |
MOD_ProDKin_1 | 476 | 482 | PF00069 | 0.436 |
MOD_ProDKin_1 | 487 | 493 | PF00069 | 0.503 |
MOD_ProDKin_1 | 557 | 563 | PF00069 | 0.583 |
MOD_ProDKin_1 | 70 | 76 | PF00069 | 0.542 |
TRG_ENDOCYTIC_2 | 277 | 280 | PF00928 | 0.426 |
TRG_ENDOCYTIC_2 | 325 | 328 | PF00928 | 0.513 |
TRG_ENDOCYTIC_2 | 428 | 431 | PF00928 | 0.519 |
TRG_ER_diArg_1 | 1 | 3 | PF00400 | 0.752 |
TRG_ER_diArg_1 | 187 | 190 | PF00400 | 0.567 |
TRG_ER_diArg_1 | 213 | 215 | PF00400 | 0.534 |
TRG_ER_diArg_1 | 31 | 33 | PF00400 | 0.560 |
TRG_ER_diArg_1 | 318 | 321 | PF00400 | 0.611 |
TRG_ER_diArg_1 | 512 | 515 | PF00400 | 0.334 |
TRG_ER_diArg_1 | 567 | 569 | PF00400 | 0.588 |
TRG_ER_FFAT_2 | 146 | 154 | PF00635 | 0.513 |
TRG_NES_CRM1_1 | 38 | 51 | PF08389 | 0.452 |
TRG_Pf-PMV_PEXEL_1 | 3 | 8 | PF00026 | 0.542 |
TRG_Pf-PMV_PEXEL_1 | 320 | 324 | PF00026 | 0.637 |
TRG_Pf-PMV_PEXEL_1 | 577 | 581 | PF00026 | 0.442 |
TRG_Pf-PMV_PEXEL_1 | 645 | 650 | PF00026 | 0.498 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P977 | Leptomonas seymouri | 48% | 98% |
A0A0S4IV62 | Bodo saltans | 38% | 100% |
A0A1X0NUB8 | Trypanosomatidae | 33% | 100% |
A0A3Q8IFH0 | Leishmania donovani | 90% | 100% |
A0A3R7KBD3 | Trypanosoma rangeli | 37% | 100% |
A4HKF8 | Leishmania braziliensis | 71% | 100% |
A4I7Y6 | Leishmania infantum | 90% | 100% |
D0AA55 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
E9B2U7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
V5BF12 | Trypanosoma cruzi | 37% | 100% |