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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: Q4Q9U1
Term | Name | Level | Count |
---|---|---|---|
GO:0001510 | RNA methylation | 4 | 8 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 8 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 8 |
GO:0006807 | nitrogen compound metabolic process | 2 | 8 |
GO:0008152 | metabolic process | 1 | 8 |
GO:0009451 | RNA modification | 5 | 8 |
GO:0009987 | cellular process | 1 | 8 |
GO:0016070 | RNA metabolic process | 5 | 8 |
GO:0032259 | methylation | 2 | 8 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 8 |
GO:0043170 | macromolecule metabolic process | 3 | 8 |
GO:0043412 | macromolecule modification | 4 | 8 |
GO:0043414 | macromolecule methylation | 3 | 8 |
GO:0044237 | cellular metabolic process | 2 | 8 |
GO:0044238 | primary metabolic process | 2 | 8 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 8 |
GO:0046483 | heterocycle metabolic process | 3 | 8 |
GO:0071704 | organic substance metabolic process | 2 | 8 |
GO:0090304 | nucleic acid metabolic process | 4 | 8 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 8 |
GO:0003723 | RNA binding | 4 | 8 |
GO:0003824 | catalytic activity | 1 | 8 |
GO:0005488 | binding | 1 | 8 |
GO:0008168 | methyltransferase activity | 4 | 8 |
GO:0016740 | transferase activity | 2 | 8 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 8 |
GO:0097159 | organic cyclic compound binding | 2 | 8 |
GO:1901363 | heterocyclic compound binding | 2 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 391 | 395 | PF00656 | 0.434 |
CLV_C14_Caspase3-7 | 76 | 80 | PF00656 | 0.492 |
CLV_NRD_NRD_1 | 156 | 158 | PF00675 | 0.698 |
CLV_NRD_NRD_1 | 372 | 374 | PF00675 | 0.511 |
CLV_NRD_NRD_1 | 501 | 503 | PF00675 | 0.502 |
CLV_NRD_NRD_1 | 557 | 559 | PF00675 | 0.264 |
CLV_PCSK_KEX2_1 | 372 | 374 | PF00082 | 0.511 |
CLV_PCSK_KEX2_1 | 501 | 503 | PF00082 | 0.510 |
CLV_PCSK_PC1ET2_1 | 501 | 503 | PF00082 | 0.510 |
CLV_PCSK_SKI1_1 | 115 | 119 | PF00082 | 0.480 |
CLV_PCSK_SKI1_1 | 309 | 313 | PF00082 | 0.452 |
CLV_PCSK_SKI1_1 | 498 | 502 | PF00082 | 0.458 |
CLV_PCSK_SKI1_1 | 558 | 562 | PF00082 | 0.264 |
DEG_APCC_DBOX_1 | 304 | 312 | PF00400 | 0.453 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.352 |
DEG_SPOP_SBC_1 | 323 | 327 | PF00917 | 0.665 |
DOC_CKS1_1 | 98 | 103 | PF01111 | 0.576 |
DOC_CYCLIN_RxL_1 | 157 | 170 | PF00134 | 0.486 |
DOC_CYCLIN_RxL_1 | 305 | 315 | PF00134 | 0.434 |
DOC_CYCLIN_RxL_1 | 552 | 563 | PF00134 | 0.469 |
DOC_CYCLIN_yClb1_LxF_4 | 592 | 598 | PF00134 | 0.505 |
DOC_MAPK_DCC_7 | 676 | 684 | PF00069 | 0.450 |
DOC_MAPK_gen_1 | 112 | 121 | PF00069 | 0.449 |
DOC_MAPK_gen_1 | 447 | 456 | PF00069 | 0.481 |
DOC_MAPK_JIP1_4 | 162 | 168 | PF00069 | 0.423 |
DOC_MAPK_MEF2A_6 | 115 | 123 | PF00069 | 0.432 |
DOC_MAPK_MEF2A_6 | 158 | 167 | PF00069 | 0.553 |
DOC_MAPK_MEF2A_6 | 402 | 409 | PF00069 | 0.342 |
DOC_MAPK_NFAT4_5 | 402 | 410 | PF00069 | 0.343 |
DOC_PP2B_LxvP_1 | 182 | 185 | PF13499 | 0.505 |
DOC_PP2B_LxvP_1 | 465 | 468 | PF13499 | 0.585 |
DOC_PP2B_LxvP_1 | 527 | 530 | PF13499 | 0.437 |
DOC_PP4_FxxP_1 | 110 | 113 | PF00568 | 0.541 |
DOC_USP7_MATH_1 | 111 | 115 | PF00917 | 0.534 |
DOC_USP7_MATH_1 | 262 | 266 | PF00917 | 0.519 |
DOC_USP7_MATH_1 | 323 | 327 | PF00917 | 0.665 |
DOC_USP7_MATH_1 | 427 | 431 | PF00917 | 0.513 |
DOC_USP7_MATH_1 | 466 | 470 | PF00917 | 0.697 |
DOC_USP7_MATH_1 | 507 | 511 | PF00917 | 0.573 |
DOC_USP7_MATH_1 | 54 | 58 | PF00917 | 0.515 |
DOC_WW_Pin1_4 | 13 | 18 | PF00397 | 0.493 |
DOC_WW_Pin1_4 | 132 | 137 | PF00397 | 0.595 |
DOC_WW_Pin1_4 | 143 | 148 | PF00397 | 0.736 |
DOC_WW_Pin1_4 | 295 | 300 | PF00397 | 0.420 |
DOC_WW_Pin1_4 | 324 | 329 | PF00397 | 0.744 |
DOC_WW_Pin1_4 | 364 | 369 | PF00397 | 0.443 |
DOC_WW_Pin1_4 | 37 | 42 | PF00397 | 0.590 |
DOC_WW_Pin1_4 | 383 | 388 | PF00397 | 0.609 |
DOC_WW_Pin1_4 | 468 | 473 | PF00397 | 0.601 |
DOC_WW_Pin1_4 | 474 | 479 | PF00397 | 0.536 |
DOC_WW_Pin1_4 | 568 | 573 | PF00397 | 0.505 |
DOC_WW_Pin1_4 | 90 | 95 | PF00397 | 0.601 |
DOC_WW_Pin1_4 | 97 | 102 | PF00397 | 0.546 |
LIG_14-3-3_CanoR_1 | 24 | 28 | PF00244 | 0.465 |
LIG_14-3-3_CanoR_1 | 264 | 268 | PF00244 | 0.528 |
LIG_14-3-3_CanoR_1 | 305 | 309 | PF00244 | 0.405 |
LIG_14-3-3_CanoR_1 | 324 | 328 | PF00244 | 0.541 |
LIG_14-3-3_CanoR_1 | 459 | 468 | PF00244 | 0.533 |
LIG_14-3-3_CanoR_1 | 608 | 617 | PF00244 | 0.464 |
LIG_Actin_WH2_2 | 356 | 374 | PF00022 | 0.460 |
LIG_APCC_ABBA_1 | 682 | 687 | PF00400 | 0.507 |
LIG_BRCT_BRCA1_1 | 190 | 194 | PF00533 | 0.484 |
LIG_DCNL_PONY_1 | 1 | 4 | PF03556 | 0.351 |
LIG_EVH1_1 | 329 | 333 | PF00568 | 0.654 |
LIG_FHA_1 | 116 | 122 | PF00498 | 0.525 |
LIG_FHA_1 | 129 | 135 | PF00498 | 0.482 |
LIG_FHA_1 | 18 | 24 | PF00498 | 0.473 |
LIG_FHA_1 | 264 | 270 | PF00498 | 0.437 |
LIG_FHA_1 | 401 | 407 | PF00498 | 0.353 |
LIG_FHA_1 | 475 | 481 | PF00498 | 0.575 |
LIG_FHA_1 | 484 | 490 | PF00498 | 0.493 |
LIG_FHA_1 | 582 | 588 | PF00498 | 0.454 |
LIG_FHA_1 | 66 | 72 | PF00498 | 0.399 |
LIG_FHA_1 | 667 | 673 | PF00498 | 0.380 |
LIG_FHA_1 | 81 | 87 | PF00498 | 0.520 |
LIG_FHA_2 | 16 | 22 | PF00498 | 0.458 |
LIG_FHA_2 | 210 | 216 | PF00498 | 0.582 |
LIG_FHA_2 | 274 | 280 | PF00498 | 0.279 |
LIG_FHA_2 | 374 | 380 | PF00498 | 0.555 |
LIG_FHA_2 | 389 | 395 | PF00498 | 0.337 |
LIG_FHA_2 | 583 | 589 | PF00498 | 0.441 |
LIG_GSK3_LRP6_1 | 97 | 102 | PF00069 | 0.477 |
LIG_LIR_Apic_2 | 108 | 113 | PF02991 | 0.538 |
LIG_LIR_Apic_2 | 59 | 65 | PF02991 | 0.407 |
LIG_LIR_Gen_1 | 519 | 530 | PF02991 | 0.465 |
LIG_LIR_Gen_1 | 683 | 693 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 135 | 140 | PF02991 | 0.619 |
LIG_LIR_Nem_3 | 240 | 245 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 26 | 31 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 279 | 283 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 435 | 441 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 5 | 10 | PF02991 | 0.496 |
LIG_LIR_Nem_3 | 519 | 525 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 600 | 604 | PF02991 | 0.519 |
LIG_LIR_Nem_3 | 683 | 688 | PF02991 | 0.498 |
LIG_LYPXL_yS_3 | 601 | 604 | PF13949 | 0.464 |
LIG_MYND_1 | 538 | 542 | PF01753 | 0.439 |
LIG_NRBOX | 307 | 313 | PF00104 | 0.467 |
LIG_NRBOX | 405 | 411 | PF00104 | 0.391 |
LIG_NRBOX | 452 | 458 | PF00104 | 0.401 |
LIG_NRBOX | 81 | 87 | PF00104 | 0.454 |
LIG_PCNA_PIPBox_1 | 454 | 463 | PF02747 | 0.480 |
LIG_PCNA_yPIPBox_3 | 445 | 457 | PF02747 | 0.419 |
LIG_PDZ_Class_1 | 703 | 708 | PF00595 | 0.525 |
LIG_Pex14_2 | 696 | 700 | PF04695 | 0.290 |
LIG_RPA_C_Fungi | 605 | 617 | PF08784 | 0.324 |
LIG_SH2_CRK | 14 | 18 | PF00017 | 0.493 |
LIG_SH2_CRK | 62 | 66 | PF00017 | 0.425 |
LIG_SH2_NCK_1 | 14 | 18 | PF00017 | 0.477 |
LIG_SH2_NCK_1 | 62 | 66 | PF00017 | 0.482 |
LIG_SH2_NCK_1 | 685 | 689 | PF00017 | 0.500 |
LIG_SH2_SRC | 12 | 15 | PF00017 | 0.475 |
LIG_SH2_SRC | 183 | 186 | PF00017 | 0.374 |
LIG_SH2_SRC | 685 | 688 | PF00017 | 0.486 |
LIG_SH2_STAP1 | 353 | 357 | PF00017 | 0.353 |
LIG_SH2_STAT3 | 10 | 13 | PF00017 | 0.479 |
LIG_SH2_STAT3 | 626 | 629 | PF00017 | 0.394 |
LIG_SH2_STAT5 | 205 | 208 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 484 | 487 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 7 | 10 | PF00017 | 0.529 |
LIG_SH2_STAT5 | 705 | 708 | PF00017 | 0.523 |
LIG_SH3_1 | 157 | 163 | PF00018 | 0.575 |
LIG_SH3_1 | 569 | 575 | PF00018 | 0.374 |
LIG_SH3_3 | 157 | 163 | PF00018 | 0.645 |
LIG_SH3_3 | 24 | 30 | PF00018 | 0.427 |
LIG_SH3_3 | 327 | 333 | PF00018 | 0.739 |
LIG_SH3_3 | 477 | 483 | PF00018 | 0.492 |
LIG_SH3_3 | 569 | 575 | PF00018 | 0.374 |
LIG_SH3_3 | 91 | 97 | PF00018 | 0.506 |
LIG_SUMO_SIM_anti_2 | 667 | 676 | PF11976 | 0.468 |
LIG_SUMO_SIM_par_1 | 163 | 170 | PF11976 | 0.317 |
LIG_SUMO_SIM_par_1 | 680 | 687 | PF11976 | 0.402 |
LIG_TRAF2_1 | 414 | 417 | PF00917 | 0.504 |
LIG_TRAF2_1 | 448 | 451 | PF00917 | 0.476 |
LIG_TRAF2_1 | 586 | 589 | PF00917 | 0.317 |
LIG_UBA3_1 | 311 | 316 | PF00899 | 0.638 |
MOD_CDK_SPK_2 | 37 | 42 | PF00069 | 0.587 |
MOD_CK1_1 | 143 | 149 | PF00069 | 0.658 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.457 |
MOD_CK1_1 | 273 | 279 | PF00069 | 0.318 |
MOD_CK1_1 | 304 | 310 | PF00069 | 0.473 |
MOD_CK1_1 | 35 | 41 | PF00069 | 0.378 |
MOD_CK1_1 | 473 | 479 | PF00069 | 0.637 |
MOD_CK1_1 | 511 | 517 | PF00069 | 0.525 |
MOD_CK1_1 | 546 | 552 | PF00069 | 0.385 |
MOD_CK1_1 | 571 | 577 | PF00069 | 0.338 |
MOD_CK1_1 | 581 | 587 | PF00069 | 0.244 |
MOD_CK1_1 | 635 | 641 | PF00069 | 0.677 |
MOD_CK1_1 | 92 | 98 | PF00069 | 0.633 |
MOD_CK2_1 | 148 | 154 | PF00069 | 0.774 |
MOD_CK2_1 | 15 | 21 | PF00069 | 0.450 |
MOD_CK2_1 | 209 | 215 | PF00069 | 0.562 |
MOD_CK2_1 | 273 | 279 | PF00069 | 0.276 |
MOD_CK2_1 | 332 | 338 | PF00069 | 0.649 |
MOD_CK2_1 | 582 | 588 | PF00069 | 0.292 |
MOD_DYRK1A_RPxSP_1 | 324 | 328 | PF00069 | 0.559 |
MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.588 |
MOD_GlcNHglycan | 237 | 240 | PF01048 | 0.442 |
MOD_GlcNHglycan | 272 | 275 | PF01048 | 0.438 |
MOD_GlcNHglycan | 334 | 337 | PF01048 | 0.702 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.685 |
MOD_GlcNHglycan | 429 | 432 | PF01048 | 0.508 |
MOD_GlcNHglycan | 44 | 47 | PF01048 | 0.538 |
MOD_GlcNHglycan | 468 | 471 | PF01048 | 0.649 |
MOD_GlcNHglycan | 512 | 516 | PF01048 | 0.659 |
MOD_GlcNHglycan | 552 | 555 | PF01048 | 0.292 |
MOD_GlcNHglycan | 702 | 705 | PF01048 | 0.442 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.548 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.430 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.589 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.599 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.515 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.652 |
MOD_GSK3_1 | 401 | 408 | PF00069 | 0.368 |
MOD_GSK3_1 | 466 | 473 | PF00069 | 0.673 |
MOD_GSK3_1 | 507 | 514 | PF00069 | 0.524 |
MOD_GSK3_1 | 546 | 553 | PF00069 | 0.350 |
MOD_GSK3_1 | 578 | 585 | PF00069 | 0.317 |
MOD_GSK3_1 | 618 | 625 | PF00069 | 0.336 |
MOD_GSK3_1 | 632 | 639 | PF00069 | 0.543 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.648 |
MOD_N-GLC_1 | 217 | 222 | PF02516 | 0.589 |
MOD_N-GLC_1 | 351 | 356 | PF02516 | 0.331 |
MOD_N-GLC_1 | 474 | 479 | PF02516 | 0.594 |
MOD_NEK2_1 | 139 | 144 | PF00069 | 0.595 |
MOD_NEK2_1 | 23 | 28 | PF00069 | 0.476 |
MOD_NEK2_1 | 284 | 289 | PF00069 | 0.540 |
MOD_NEK2_1 | 312 | 317 | PF00069 | 0.479 |
MOD_NEK2_1 | 405 | 410 | PF00069 | 0.356 |
MOD_NEK2_1 | 560 | 565 | PF00069 | 0.312 |
MOD_NEK2_1 | 597 | 602 | PF00069 | 0.459 |
MOD_NEK2_1 | 700 | 705 | PF00069 | 0.372 |
MOD_NEK2_2 | 619 | 624 | PF00069 | 0.219 |
MOD_OFUCOSY | 270 | 277 | PF10250 | 0.263 |
MOD_PK_1 | 52 | 58 | PF00069 | 0.605 |
MOD_PKA_1 | 502 | 508 | PF00069 | 0.509 |
MOD_PKA_2 | 111 | 117 | PF00069 | 0.469 |
MOD_PKA_2 | 177 | 183 | PF00069 | 0.321 |
MOD_PKA_2 | 23 | 29 | PF00069 | 0.461 |
MOD_PKA_2 | 263 | 269 | PF00069 | 0.476 |
MOD_PKA_2 | 304 | 310 | PF00069 | 0.596 |
MOD_PKA_2 | 323 | 329 | PF00069 | 0.714 |
MOD_Plk_1 | 351 | 357 | PF00069 | 0.329 |
MOD_Plk_1 | 416 | 422 | PF00069 | 0.562 |
MOD_Plk_1 | 52 | 58 | PF00069 | 0.605 |
MOD_Plk_2-3 | 686 | 692 | PF00069 | 0.496 |
MOD_Plk_4 | 23 | 29 | PF00069 | 0.454 |
MOD_Plk_4 | 263 | 269 | PF00069 | 0.440 |
MOD_Plk_4 | 279 | 285 | PF00069 | 0.365 |
MOD_Plk_4 | 352 | 358 | PF00069 | 0.338 |
MOD_Plk_4 | 388 | 394 | PF00069 | 0.475 |
MOD_Plk_4 | 401 | 407 | PF00069 | 0.256 |
MOD_Plk_4 | 452 | 458 | PF00069 | 0.479 |
MOD_ProDKin_1 | 13 | 19 | PF00069 | 0.486 |
MOD_ProDKin_1 | 132 | 138 | PF00069 | 0.598 |
MOD_ProDKin_1 | 143 | 149 | PF00069 | 0.740 |
MOD_ProDKin_1 | 295 | 301 | PF00069 | 0.420 |
MOD_ProDKin_1 | 324 | 330 | PF00069 | 0.745 |
MOD_ProDKin_1 | 364 | 370 | PF00069 | 0.440 |
MOD_ProDKin_1 | 37 | 43 | PF00069 | 0.590 |
MOD_ProDKin_1 | 383 | 389 | PF00069 | 0.594 |
MOD_ProDKin_1 | 468 | 474 | PF00069 | 0.600 |
MOD_ProDKin_1 | 568 | 574 | PF00069 | 0.375 |
MOD_ProDKin_1 | 90 | 96 | PF00069 | 0.601 |
MOD_ProDKin_1 | 97 | 103 | PF00069 | 0.541 |
MOD_SUMO_rev_2 | 273 | 283 | PF00179 | 0.462 |
TRG_DiLeu_BaLyEn_6 | 668 | 673 | PF01217 | 0.467 |
TRG_ENDOCYTIC_2 | 353 | 356 | PF00928 | 0.355 |
TRG_ENDOCYTIC_2 | 601 | 604 | PF00928 | 0.317 |
TRG_ENDOCYTIC_2 | 685 | 688 | PF00928 | 0.486 |
TRG_ER_diArg_1 | 371 | 373 | PF00400 | 0.498 |
TRG_ER_diArg_1 | 445 | 448 | PF00400 | 0.486 |
TRG_NLS_MonoExtC_3 | 500 | 506 | PF00514 | 0.508 |
TRG_NLS_MonoExtN_4 | 498 | 505 | PF00514 | 0.426 |
TRG_Pf-PMV_PEXEL_1 | 502 | 506 | PF00026 | 0.517 |
TRG_Pf-PMV_PEXEL_1 | 558 | 562 | PF00026 | 0.317 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PA86 | Leptomonas seymouri | 49% | 99% |
A0A0S4JUU1 | Bodo saltans | 30% | 100% |
A0A1X0NZU0 | Trypanosomatidae | 35% | 100% |
A0A3Q8IGM4 | Leishmania donovani | 92% | 100% |
A4HEK2 | Leishmania braziliensis | 78% | 84% |
A4I1J6 | Leishmania infantum | 92% | 100% |
Q84MA1 | Arabidopsis thaliana | 25% | 100% |