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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005829 | cytosol | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9APA3
Term | Name | Level | Count |
---|---|---|---|
GO:0002097 | tRNA wobble base modification | 7 | 7 |
GO:0002098 | tRNA wobble uridine modification | 8 | 7 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 7 |
GO:0006396 | RNA processing | 6 | 7 |
GO:0006399 | tRNA metabolic process | 7 | 7 |
GO:0006400 | tRNA modification | 6 | 7 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 7 |
GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
GO:0008033 | tRNA processing | 8 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0009451 | RNA modification | 5 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0016070 | RNA metabolic process | 5 | 7 |
GO:0034227 | tRNA thio-modification | 7 | 7 |
GO:0034470 | ncRNA processing | 7 | 7 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 7 |
GO:0034660 | ncRNA metabolic process | 6 | 7 |
GO:0043170 | macromolecule metabolic process | 3 | 7 |
GO:0043412 | macromolecule modification | 4 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0046483 | heterocycle metabolic process | 3 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:0090304 | nucleic acid metabolic process | 4 | 7 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 7 |
GO:0002143 | tRNA wobble position uridine thiolation | 8 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000049 | tRNA binding | 5 | 7 |
GO:0003676 | nucleic acid binding | 3 | 7 |
GO:0003723 | RNA binding | 4 | 7 |
GO:0005488 | binding | 1 | 7 |
GO:0097159 | organic cyclic compound binding | 2 | 7 |
GO:1901363 | heterocyclic compound binding | 2 | 7 |
GO:0003824 | catalytic activity | 1 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
GO:0016782 | transferase activity, transferring sulphur-containing groups | 3 | 1 |
GO:0016783 | sulfurtransferase activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 170 | 172 | PF00675 | 0.654 |
CLV_NRD_NRD_1 | 322 | 324 | PF00675 | 0.487 |
CLV_NRD_NRD_1 | 523 | 525 | PF00675 | 0.689 |
CLV_NRD_NRD_1 | 82 | 84 | PF00675 | 0.551 |
CLV_PCSK_FUR_1 | 80 | 84 | PF00082 | 0.391 |
CLV_PCSK_KEX2_1 | 82 | 84 | PF00082 | 0.551 |
CLV_PCSK_SKI1_1 | 199 | 203 | PF00082 | 0.566 |
CLV_PCSK_SKI1_1 | 284 | 288 | PF00082 | 0.503 |
CLV_PCSK_SKI1_1 | 297 | 301 | PF00082 | 0.373 |
CLV_PCSK_SKI1_1 | 381 | 385 | PF00082 | 0.383 |
CLV_PCSK_SKI1_1 | 406 | 410 | PF00082 | 0.464 |
CLV_PCSK_SKI1_1 | 419 | 423 | PF00082 | 0.368 |
CLV_PCSK_SKI1_1 | 524 | 528 | PF00082 | 0.750 |
CLV_Separin_Metazoa | 490 | 494 | PF03568 | 0.598 |
DEG_SCF_FBW7_1 | 217 | 223 | PF00400 | 0.837 |
DEG_SCF_FBW7_1 | 604 | 609 | PF00400 | 0.746 |
DEG_SPOP_SBC_1 | 135 | 139 | PF00917 | 0.775 |
DEG_SPOP_SBC_1 | 597 | 601 | PF00917 | 0.627 |
DEG_SPOP_SBC_1 | 611 | 615 | PF00917 | 0.494 |
DOC_CKS1_1 | 217 | 222 | PF01111 | 0.838 |
DOC_CYCLIN_yCln2_LP_2 | 541 | 547 | PF00134 | 0.777 |
DOC_MAPK_gen_1 | 368 | 375 | PF00069 | 0.539 |
DOC_PP2B_LxvP_1 | 130 | 133 | PF13499 | 0.508 |
DOC_PP2B_LxvP_1 | 541 | 544 | PF13499 | 0.784 |
DOC_USP7_MATH_1 | 108 | 112 | PF00917 | 0.717 |
DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.639 |
DOC_USP7_MATH_1 | 135 | 139 | PF00917 | 0.691 |
DOC_USP7_MATH_1 | 141 | 145 | PF00917 | 0.694 |
DOC_USP7_MATH_1 | 220 | 224 | PF00917 | 0.690 |
DOC_USP7_MATH_1 | 247 | 251 | PF00917 | 0.787 |
DOC_USP7_MATH_1 | 348 | 352 | PF00917 | 0.764 |
DOC_USP7_MATH_1 | 448 | 452 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 606 | 610 | PF00917 | 0.819 |
DOC_USP7_MATH_1 | 611 | 615 | PF00917 | 0.695 |
DOC_USP7_MATH_1 | 664 | 668 | PF00917 | 0.641 |
DOC_USP7_UBL2_3 | 192 | 196 | PF12436 | 0.815 |
DOC_USP7_UBL2_3 | 521 | 525 | PF12436 | 0.822 |
DOC_WW_Pin1_4 | 103 | 108 | PF00397 | 0.555 |
DOC_WW_Pin1_4 | 109 | 114 | PF00397 | 0.792 |
DOC_WW_Pin1_4 | 137 | 142 | PF00397 | 0.706 |
DOC_WW_Pin1_4 | 216 | 221 | PF00397 | 0.843 |
DOC_WW_Pin1_4 | 235 | 240 | PF00397 | 0.541 |
DOC_WW_Pin1_4 | 437 | 442 | PF00397 | 0.501 |
DOC_WW_Pin1_4 | 48 | 53 | PF00397 | 0.514 |
DOC_WW_Pin1_4 | 602 | 607 | PF00397 | 0.820 |
LIG_14-3-3_CanoR_1 | 100 | 108 | PF00244 | 0.748 |
LIG_14-3-3_CanoR_1 | 160 | 164 | PF00244 | 0.553 |
LIG_14-3-3_CanoR_1 | 270 | 278 | PF00244 | 0.370 |
LIG_14-3-3_CanoR_1 | 291 | 301 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 305 | 310 | PF00244 | 0.506 |
LIG_14-3-3_CanoR_1 | 381 | 390 | PF00244 | 0.396 |
LIG_14-3-3_CanoR_1 | 406 | 415 | PF00244 | 0.520 |
LIG_14-3-3_CanoR_1 | 416 | 422 | PF00244 | 0.391 |
LIG_14-3-3_CanoR_1 | 673 | 678 | PF00244 | 0.327 |
LIG_14-3-3_CanoR_1 | 74 | 81 | PF00244 | 0.347 |
LIG_APCC_ABBA_1 | 545 | 550 | PF00400 | 0.660 |
LIG_BIR_III_2 | 630 | 634 | PF00653 | 0.567 |
LIG_CSL_BTD_1 | 631 | 634 | PF09270 | 0.574 |
LIG_deltaCOP1_diTrp_1 | 630 | 637 | PF00928 | 0.656 |
LIG_EVH1_2 | 633 | 637 | PF00568 | 0.596 |
LIG_FHA_1 | 200 | 206 | PF00498 | 0.647 |
LIG_FHA_1 | 255 | 261 | PF00498 | 0.553 |
LIG_FHA_1 | 382 | 388 | PF00498 | 0.350 |
LIG_FHA_1 | 407 | 413 | PF00498 | 0.556 |
LIG_FHA_1 | 438 | 444 | PF00498 | 0.505 |
LIG_FHA_1 | 447 | 453 | PF00498 | 0.448 |
LIG_FHA_1 | 572 | 578 | PF00498 | 0.311 |
LIG_FHA_1 | 666 | 672 | PF00498 | 0.646 |
LIG_FHA_2 | 160 | 166 | PF00498 | 0.558 |
LIG_FHA_2 | 555 | 561 | PF00498 | 0.452 |
LIG_FHA_2 | 641 | 647 | PF00498 | 0.741 |
LIG_LIR_Gen_1 | 164 | 174 | PF02991 | 0.551 |
LIG_LIR_Gen_1 | 298 | 309 | PF02991 | 0.590 |
LIG_LIR_Gen_1 | 426 | 436 | PF02991 | 0.465 |
LIG_LIR_Gen_1 | 469 | 478 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 164 | 170 | PF02991 | 0.551 |
LIG_LIR_Nem_3 | 27 | 32 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 298 | 304 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 426 | 432 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 469 | 475 | PF02991 | 0.426 |
LIG_SH2_CRK | 301 | 305 | PF00017 | 0.499 |
LIG_SH2_CRK | 429 | 433 | PF00017 | 0.575 |
LIG_SH2_STAP1 | 271 | 275 | PF00017 | 0.599 |
LIG_SH2_STAP1 | 285 | 289 | PF00017 | 0.393 |
LIG_SH2_STAT3 | 173 | 176 | PF00017 | 0.563 |
LIG_SH2_STAT3 | 581 | 584 | PF00017 | 0.545 |
LIG_SH2_STAT3 | 623 | 626 | PF00017 | 0.541 |
LIG_SH2_STAT3 | 75 | 78 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 173 | 176 | PF00017 | 0.641 |
LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.457 |
LIG_SH2_STAT5 | 279 | 282 | PF00017 | 0.504 |
LIG_SH2_STAT5 | 32 | 35 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 429 | 432 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 439 | 442 | PF00017 | 0.416 |
LIG_SH3_3 | 128 | 134 | PF00018 | 0.490 |
LIG_SH3_3 | 214 | 220 | PF00018 | 0.626 |
LIG_SUMO_SIM_anti_2 | 116 | 122 | PF11976 | 0.508 |
LIG_SUMO_SIM_par_1 | 594 | 602 | PF11976 | 0.721 |
LIG_TRAF2_1 | 162 | 165 | PF00917 | 0.513 |
LIG_TRAF2_1 | 338 | 341 | PF00917 | 0.730 |
LIG_TRAF2_1 | 351 | 354 | PF00917 | 0.556 |
LIG_TRAF2_1 | 487 | 490 | PF00917 | 0.525 |
LIG_TRAF2_2 | 241 | 246 | PF00917 | 0.567 |
LIG_TYR_ITIM | 427 | 432 | PF00017 | 0.585 |
LIG_WW_3 | 177 | 181 | PF00397 | 0.671 |
MOD_CDK_SPK_2 | 602 | 607 | PF00069 | 0.820 |
MOD_CDK_SPxxK_3 | 103 | 110 | PF00069 | 0.735 |
MOD_CK1_1 | 137 | 143 | PF00069 | 0.780 |
MOD_CK1_1 | 231 | 237 | PF00069 | 0.737 |
MOD_CK1_1 | 254 | 260 | PF00069 | 0.521 |
MOD_CK1_1 | 290 | 296 | PF00069 | 0.528 |
MOD_CK1_1 | 466 | 472 | PF00069 | 0.495 |
MOD_CK1_1 | 515 | 521 | PF00069 | 0.704 |
MOD_CK1_1 | 576 | 582 | PF00069 | 0.594 |
MOD_CK1_1 | 599 | 605 | PF00069 | 0.791 |
MOD_CK1_1 | 609 | 615 | PF00069 | 0.648 |
MOD_CK1_1 | 649 | 655 | PF00069 | 0.668 |
MOD_CK1_1 | 99 | 105 | PF00069 | 0.796 |
MOD_CK2_1 | 158 | 164 | PF00069 | 0.549 |
MOD_CK2_1 | 292 | 298 | PF00069 | 0.511 |
MOD_CK2_1 | 348 | 354 | PF00069 | 0.507 |
MOD_CK2_1 | 552 | 558 | PF00069 | 0.679 |
MOD_CK2_1 | 638 | 644 | PF00069 | 0.791 |
MOD_GlcNHglycan | 102 | 105 | PF01048 | 0.703 |
MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.719 |
MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.696 |
MOD_GlcNHglycan | 248 | 252 | PF01048 | 0.530 |
MOD_GlcNHglycan | 253 | 256 | PF01048 | 0.532 |
MOD_GlcNHglycan | 275 | 278 | PF01048 | 0.549 |
MOD_GlcNHglycan | 508 | 512 | PF01048 | 0.713 |
MOD_GlcNHglycan | 514 | 517 | PF01048 | 0.648 |
MOD_GlcNHglycan | 562 | 565 | PF01048 | 0.490 |
MOD_GlcNHglycan | 57 | 60 | PF01048 | 0.491 |
MOD_GlcNHglycan | 601 | 604 | PF01048 | 0.740 |
MOD_GlcNHglycan | 608 | 611 | PF01048 | 0.650 |
MOD_GSK3_1 | 109 | 116 | PF00069 | 0.655 |
MOD_GSK3_1 | 135 | 142 | PF00069 | 0.691 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.762 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.695 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.503 |
MOD_GSK3_1 | 269 | 276 | PF00069 | 0.498 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.623 |
MOD_GSK3_1 | 423 | 430 | PF00069 | 0.432 |
MOD_GSK3_1 | 442 | 449 | PF00069 | 0.648 |
MOD_GSK3_1 | 459 | 466 | PF00069 | 0.439 |
MOD_GSK3_1 | 515 | 522 | PF00069 | 0.755 |
MOD_GSK3_1 | 598 | 605 | PF00069 | 0.739 |
MOD_GSK3_1 | 606 | 613 | PF00069 | 0.678 |
MOD_GSK3_1 | 646 | 653 | PF00069 | 0.643 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.744 |
MOD_N-GLC_1 | 649 | 654 | PF02516 | 0.731 |
MOD_NEK2_1 | 114 | 119 | PF00069 | 0.539 |
MOD_NEK2_1 | 136 | 141 | PF00069 | 0.730 |
MOD_NEK2_1 | 287 | 292 | PF00069 | 0.493 |
MOD_NEK2_1 | 374 | 379 | PF00069 | 0.383 |
MOD_NEK2_1 | 459 | 464 | PF00069 | 0.428 |
MOD_NEK2_1 | 598 | 603 | PF00069 | 0.718 |
MOD_NEK2_2 | 448 | 453 | PF00069 | 0.644 |
MOD_NEK2_2 | 657 | 662 | PF00069 | 0.474 |
MOD_OFUCOSY | 573 | 580 | PF10250 | 0.550 |
MOD_PIKK_1 | 498 | 504 | PF00454 | 0.606 |
MOD_PIKK_1 | 74 | 80 | PF00454 | 0.369 |
MOD_PKA_2 | 159 | 165 | PF00069 | 0.530 |
MOD_PKA_2 | 269 | 275 | PF00069 | 0.517 |
MOD_PKA_2 | 290 | 296 | PF00069 | 0.506 |
MOD_PKA_2 | 492 | 498 | PF00069 | 0.649 |
MOD_PKA_2 | 606 | 612 | PF00069 | 0.814 |
MOD_PKA_2 | 99 | 105 | PF00069 | 0.811 |
MOD_PKB_1 | 303 | 311 | PF00069 | 0.583 |
MOD_Plk_2-3 | 358 | 364 | PF00069 | 0.684 |
MOD_Plk_2-3 | 640 | 646 | PF00069 | 0.732 |
MOD_Plk_4 | 10 | 16 | PF00069 | 0.485 |
MOD_Plk_4 | 114 | 120 | PF00069 | 0.548 |
MOD_Plk_4 | 423 | 429 | PF00069 | 0.433 |
MOD_Plk_4 | 459 | 465 | PF00069 | 0.403 |
MOD_Plk_4 | 60 | 66 | PF00069 | 0.476 |
MOD_Plk_4 | 612 | 618 | PF00069 | 0.587 |
MOD_Plk_4 | 632 | 638 | PF00069 | 0.667 |
MOD_Plk_4 | 673 | 679 | PF00069 | 0.336 |
MOD_ProDKin_1 | 103 | 109 | PF00069 | 0.552 |
MOD_ProDKin_1 | 137 | 143 | PF00069 | 0.705 |
MOD_ProDKin_1 | 216 | 222 | PF00069 | 0.838 |
MOD_ProDKin_1 | 235 | 241 | PF00069 | 0.541 |
MOD_ProDKin_1 | 437 | 443 | PF00069 | 0.499 |
MOD_ProDKin_1 | 48 | 54 | PF00069 | 0.507 |
MOD_ProDKin_1 | 602 | 608 | PF00069 | 0.822 |
TRG_ENDOCYTIC_2 | 271 | 274 | PF00928 | 0.524 |
TRG_ENDOCYTIC_2 | 301 | 304 | PF00928 | 0.499 |
TRG_ENDOCYTIC_2 | 429 | 432 | PF00928 | 0.579 |
TRG_ENDOCYTIC_2 | 467 | 470 | PF00928 | 0.522 |
TRG_ER_diArg_1 | 80 | 83 | PF00400 | 0.534 |
TRG_NLS_MonoExtC_3 | 191 | 196 | PF00514 | 0.734 |
TRG_NLS_MonoExtN_4 | 192 | 199 | PF00514 | 0.720 |
TRG_Pf-PMV_PEXEL_1 | 454 | 458 | PF00026 | 0.503 |
TRG_Pf-PMV_PEXEL_1 | 549 | 553 | PF00026 | 0.476 |
TRG_Pf-PMV_PEXEL_1 | 68 | 72 | PF00026 | 0.462 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDC5 | Leptomonas seymouri | 44% | 100% |
A0A3Q8I9K2 | Leishmania donovani | 84% | 98% |
A4H768 | Leishmania braziliensis | 68% | 97% |
A4HVK7 | Leishmania infantum | 84% | 98% |
Q4QG75 | Leishmania major | 82% | 100% |