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: A4H768
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_C14_Caspase3-7 | 643 | 647 | PF00656 | 0.613 |
CLV_NRD_NRD_1 | 173 | 175 | PF00675 | 0.655 |
CLV_NRD_NRD_1 | 341 | 343 | PF00675 | 0.546 |
CLV_NRD_NRD_1 | 508 | 510 | PF00675 | 0.678 |
CLV_NRD_NRD_1 | 537 | 539 | PF00675 | 0.572 |
CLV_NRD_NRD_1 | 82 | 84 | PF00675 | 0.522 |
CLV_PCSK_KEX2_1 | 341 | 343 | PF00082 | 0.546 |
CLV_PCSK_KEX2_1 | 537 | 539 | PF00082 | 0.572 |
CLV_PCSK_KEX2_1 | 82 | 84 | PF00082 | 0.522 |
CLV_PCSK_SKI1_1 | 195 | 199 | PF00082 | 0.513 |
CLV_PCSK_SKI1_1 | 282 | 286 | PF00082 | 0.522 |
CLV_PCSK_SKI1_1 | 295 | 299 | PF00082 | 0.374 |
CLV_PCSK_SKI1_1 | 404 | 408 | PF00082 | 0.462 |
CLV_PCSK_SKI1_1 | 417 | 421 | PF00082 | 0.366 |
CLV_PCSK_SKI1_1 | 509 | 513 | PF00082 | 0.739 |
DEG_SCF_FBW7_1 | 220 | 226 | PF00400 | 0.807 |
DEG_SPOP_SBC_1 | 104 | 108 | PF00917 | 0.536 |
DEG_SPOP_SBC_1 | 109 | 113 | PF00917 | 0.533 |
DEG_SPOP_SBC_1 | 138 | 142 | PF00917 | 0.799 |
DEG_SPOP_SBC_1 | 143 | 147 | PF00917 | 0.706 |
DEG_SPOP_SBC_1 | 660 | 664 | PF00917 | 0.467 |
DOC_CKS1_1 | 220 | 225 | PF01111 | 0.808 |
DOC_CYCLIN_yCln2_LP_2 | 526 | 532 | PF00134 | 0.742 |
DOC_PP2B_LxvP_1 | 130 | 133 | PF13499 | 0.522 |
DOC_PP2B_LxvP_1 | 135 | 138 | PF13499 | 0.662 |
DOC_PP2B_LxvP_1 | 526 | 529 | PF13499 | 0.762 |
DOC_USP7_MATH_1 | 104 | 108 | PF00917 | 0.702 |
DOC_USP7_MATH_1 | 138 | 142 | PF00917 | 0.714 |
DOC_USP7_MATH_1 | 144 | 148 | PF00917 | 0.701 |
DOC_USP7_MATH_1 | 236 | 240 | PF00917 | 0.765 |
DOC_USP7_MATH_1 | 446 | 450 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 498 | 502 | PF00917 | 0.583 |
DOC_USP7_MATH_1 | 591 | 595 | PF00917 | 0.795 |
DOC_USP7_MATH_1 | 604 | 608 | PF00917 | 0.754 |
DOC_USP7_MATH_1 | 665 | 669 | PF00917 | 0.562 |
DOC_USP7_UBL2_3 | 195 | 199 | PF12436 | 0.766 |
DOC_USP7_UBL2_3 | 506 | 510 | PF12436 | 0.809 |
DOC_WW_Pin1_4 | 139 | 144 | PF00397 | 0.703 |
DOC_WW_Pin1_4 | 219 | 224 | PF00397 | 0.805 |
DOC_WW_Pin1_4 | 232 | 237 | PF00397 | 0.629 |
DOC_WW_Pin1_4 | 435 | 440 | PF00397 | 0.541 |
DOC_WW_Pin1_4 | 48 | 53 | PF00397 | 0.509 |
DOC_WW_Pin1_4 | 587 | 592 | PF00397 | 0.780 |
DOC_WW_Pin1_4 | 626 | 631 | PF00397 | 0.405 |
LIG_14-3-3_CanoR_1 | 163 | 167 | PF00244 | 0.562 |
LIG_14-3-3_CanoR_1 | 276 | 285 | PF00244 | 0.547 |
LIG_14-3-3_CanoR_1 | 303 | 308 | PF00244 | 0.504 |
LIG_14-3-3_CanoR_1 | 404 | 413 | PF00244 | 0.518 |
LIG_14-3-3_CanoR_1 | 414 | 420 | PF00244 | 0.388 |
LIG_14-3-3_CanoR_1 | 525 | 529 | PF00244 | 0.634 |
LIG_14-3-3_CanoR_1 | 537 | 542 | PF00244 | 0.579 |
LIG_14-3-3_CanoR_1 | 592 | 599 | PF00244 | 0.551 |
LIG_APCC_ABBA_1 | 530 | 535 | PF00400 | 0.605 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.380 |
LIG_BRCT_BRCA1_1 | 1 | 5 | PF00533 | 0.380 |
LIG_BRCT_BRCA1_1 | 25 | 29 | PF00533 | 0.299 |
LIG_deltaCOP1_diTrp_1 | 626 | 633 | PF00928 | 0.661 |
LIG_EVH1_1 | 132 | 136 | PF00568 | 0.662 |
LIG_FHA_1 | 110 | 116 | PF00498 | 0.513 |
LIG_FHA_1 | 186 | 192 | PF00498 | 0.531 |
LIG_FHA_1 | 220 | 226 | PF00498 | 0.652 |
LIG_FHA_1 | 405 | 411 | PF00498 | 0.552 |
LIG_FHA_1 | 436 | 442 | PF00498 | 0.554 |
LIG_FHA_1 | 445 | 451 | PF00498 | 0.440 |
LIG_FHA_1 | 525 | 531 | PF00498 | 0.549 |
LIG_FHA_1 | 662 | 668 | PF00498 | 0.650 |
LIG_FHA_2 | 163 | 169 | PF00498 | 0.567 |
LIG_LIR_Gen_1 | 168 | 177 | PF02991 | 0.550 |
LIG_LIR_Gen_1 | 296 | 307 | PF02991 | 0.590 |
LIG_LIR_Gen_1 | 424 | 434 | PF02991 | 0.468 |
LIG_LIR_Gen_1 | 467 | 476 | PF02991 | 0.479 |
LIG_LIR_Gen_1 | 545 | 555 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 168 | 173 | PF02991 | 0.552 |
LIG_LIR_Nem_3 | 26 | 32 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 296 | 302 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 424 | 430 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 467 | 473 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 545 | 550 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 614 | 619 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 69 | 73 | PF02991 | 0.333 |
LIG_PDZ_Class_2 | 670 | 675 | PF00595 | 0.363 |
LIG_SH2_CRK | 299 | 303 | PF00017 | 0.500 |
LIG_SH2_CRK | 427 | 431 | PF00017 | 0.580 |
LIG_SH2_CRK | 547 | 551 | PF00017 | 0.373 |
LIG_SH2_NCK_1 | 547 | 551 | PF00017 | 0.373 |
LIG_SH2_STAP1 | 269 | 273 | PF00017 | 0.590 |
LIG_SH2_STAT5 | 176 | 179 | PF00017 | 0.653 |
LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 277 | 280 | PF00017 | 0.504 |
LIG_SH2_STAT5 | 32 | 35 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 427 | 430 | PF00017 | 0.445 |
LIG_SH2_STAT5 | 437 | 440 | PF00017 | 0.470 |
LIG_SH3_3 | 116 | 122 | PF00018 | 0.539 |
LIG_SH3_3 | 128 | 134 | PF00018 | 0.510 |
LIG_SH3_3 | 217 | 223 | PF00018 | 0.595 |
LIG_SUMO_SIM_anti_2 | 116 | 122 | PF11976 | 0.500 |
LIG_TRAF2_1 | 158 | 161 | PF00917 | 0.524 |
LIG_TRAF2_1 | 41 | 44 | PF00917 | 0.348 |
LIG_TRAF2_1 | 485 | 488 | PF00917 | 0.517 |
LIG_TRFH_1 | 581 | 585 | PF08558 | 0.494 |
LIG_TYR_ITIM | 425 | 430 | PF00017 | 0.585 |
LIG_WW_2 | 133 | 136 | PF00397 | 0.466 |
LIG_WW_3 | 180 | 184 | PF00397 | 0.700 |
MOD_CDK_SPK_2 | 587 | 592 | PF00069 | 0.780 |
MOD_CK1_1 | 105 | 111 | PF00069 | 0.758 |
MOD_CK1_1 | 113 | 119 | PF00069 | 0.504 |
MOD_CK1_1 | 142 | 148 | PF00069 | 0.759 |
MOD_CK1_1 | 226 | 232 | PF00069 | 0.704 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.782 |
MOD_CK1_1 | 248 | 254 | PF00069 | 0.536 |
MOD_CK1_1 | 288 | 294 | PF00069 | 0.531 |
MOD_CK1_1 | 464 | 470 | PF00069 | 0.492 |
MOD_CK1_1 | 587 | 593 | PF00069 | 0.758 |
MOD_CK1_1 | 594 | 600 | PF00069 | 0.668 |
MOD_CK1_1 | 606 | 612 | PF00069 | 0.489 |
MOD_CK1_1 | 635 | 641 | PF00069 | 0.616 |
MOD_CK1_1 | 649 | 655 | PF00069 | 0.621 |
MOD_CK1_1 | 663 | 669 | PF00069 | 0.352 |
MOD_CK2_1 | 145 | 151 | PF00069 | 0.587 |
MOD_CK2_1 | 162 | 168 | PF00069 | 0.544 |
MOD_CK2_1 | 290 | 296 | PF00069 | 0.515 |
MOD_CK2_1 | 537 | 543 | PF00069 | 0.624 |
MOD_GlcNHglycan | 107 | 110 | PF01048 | 0.605 |
MOD_GlcNHglycan | 151 | 155 | PF01048 | 0.756 |
MOD_GlcNHglycan | 195 | 198 | PF01048 | 0.579 |
MOD_GlcNHglycan | 228 | 231 | PF01048 | 0.645 |
MOD_GlcNHglycan | 232 | 235 | PF01048 | 0.675 |
MOD_GlcNHglycan | 246 | 250 | PF01048 | 0.550 |
MOD_GlcNHglycan | 392 | 395 | PF01048 | 0.378 |
MOD_GlcNHglycan | 490 | 493 | PF01048 | 0.608 |
MOD_GlcNHglycan | 494 | 497 | PF01048 | 0.636 |
MOD_GlcNHglycan | 57 | 60 | PF01048 | 0.495 |
MOD_GlcNHglycan | 643 | 646 | PF01048 | 0.743 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.650 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.709 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.501 |
MOD_GSK3_1 | 219 | 226 | PF00069 | 0.732 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.698 |
MOD_GSK3_1 | 267 | 274 | PF00069 | 0.491 |
MOD_GSK3_1 | 356 | 363 | PF00069 | 0.661 |
MOD_GSK3_1 | 421 | 428 | PF00069 | 0.433 |
MOD_GSK3_1 | 440 | 447 | PF00069 | 0.673 |
MOD_GSK3_1 | 457 | 464 | PF00069 | 0.434 |
MOD_GSK3_1 | 488 | 495 | PF00069 | 0.599 |
MOD_GSK3_1 | 587 | 594 | PF00069 | 0.681 |
MOD_GSK3_1 | 603 | 610 | PF00069 | 0.515 |
MOD_GSK3_1 | 624 | 631 | PF00069 | 0.402 |
MOD_GSK3_1 | 632 | 639 | PF00069 | 0.546 |
MOD_GSK3_1 | 641 | 648 | PF00069 | 0.643 |
MOD_GSK3_1 | 649 | 656 | PF00069 | 0.583 |
MOD_GSK3_1 | 659 | 666 | PF00069 | 0.404 |
MOD_NEK2_1 | 114 | 119 | PF00069 | 0.520 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.567 |
MOD_NEK2_1 | 23 | 28 | PF00069 | 0.301 |
MOD_NEK2_1 | 285 | 290 | PF00069 | 0.510 |
MOD_NEK2_1 | 360 | 365 | PF00069 | 0.733 |
MOD_NEK2_1 | 457 | 462 | PF00069 | 0.424 |
MOD_NEK2_1 | 624 | 629 | PF00069 | 0.357 |
MOD_NEK2_1 | 633 | 638 | PF00069 | 0.479 |
MOD_NEK2_2 | 446 | 451 | PF00069 | 0.631 |
MOD_OFUCOSY | 93 | 100 | PF10250 | 0.464 |
MOD_PIKK_1 | 236 | 242 | PF00454 | 0.597 |
MOD_PIKK_1 | 498 | 504 | PF00454 | 0.780 |
MOD_PIKK_1 | 665 | 671 | PF00454 | 0.361 |
MOD_PKA_1 | 537 | 543 | PF00069 | 0.521 |
MOD_PKA_2 | 162 | 168 | PF00069 | 0.538 |
MOD_PKA_2 | 524 | 530 | PF00069 | 0.682 |
MOD_PKA_2 | 537 | 543 | PF00069 | 0.451 |
MOD_PKA_2 | 591 | 597 | PF00069 | 0.797 |
MOD_PKB_1 | 301 | 309 | PF00069 | 0.581 |
MOD_Plk_1 | 361 | 367 | PF00069 | 0.650 |
MOD_Plk_1 | 594 | 600 | PF00069 | 0.554 |
MOD_Plk_1 | 607 | 613 | PF00069 | 0.422 |
MOD_Plk_2-3 | 356 | 362 | PF00069 | 0.656 |
MOD_Plk_4 | 10 | 16 | PF00069 | 0.474 |
MOD_Plk_4 | 110 | 116 | PF00069 | 0.623 |
MOD_Plk_4 | 421 | 427 | PF00069 | 0.433 |
MOD_Plk_4 | 457 | 463 | PF00069 | 0.398 |
MOD_Plk_4 | 60 | 66 | PF00069 | 0.473 |
MOD_Plk_4 | 607 | 613 | PF00069 | 0.543 |
MOD_Plk_4 | 628 | 634 | PF00069 | 0.681 |
MOD_ProDKin_1 | 139 | 145 | PF00069 | 0.701 |
MOD_ProDKin_1 | 219 | 225 | PF00069 | 0.807 |
MOD_ProDKin_1 | 232 | 238 | PF00069 | 0.630 |
MOD_ProDKin_1 | 435 | 441 | PF00069 | 0.542 |
MOD_ProDKin_1 | 48 | 54 | PF00069 | 0.501 |
MOD_ProDKin_1 | 587 | 593 | PF00069 | 0.781 |
MOD_ProDKin_1 | 626 | 632 | PF00069 | 0.405 |
MOD_SUMO_for_1 | 334 | 337 | PF00179 | 0.533 |
MOD_SUMO_rev_2 | 189 | 197 | PF00179 | 0.511 |
TRG_ENDOCYTIC_2 | 269 | 272 | PF00928 | 0.514 |
TRG_ENDOCYTIC_2 | 299 | 302 | PF00928 | 0.499 |
TRG_ENDOCYTIC_2 | 427 | 430 | PF00928 | 0.581 |
TRG_ENDOCYTIC_2 | 465 | 468 | PF00928 | 0.520 |
TRG_ENDOCYTIC_2 | 547 | 550 | PF00928 | 0.387 |
TRG_ER_diArg_1 | 340 | 342 | PF00400 | 0.544 |
TRG_ER_diArg_1 | 536 | 538 | PF00400 | 0.567 |
TRG_ER_diArg_1 | 81 | 83 | PF00400 | 0.515 |
TRG_NLS_MonoExtN_4 | 195 | 202 | PF00514 | 0.675 |
TRG_Pf-PMV_PEXEL_1 | 452 | 456 | PF00026 | 0.479 |
TRG_Pf-PMV_PEXEL_1 | 622 | 626 | PF00026 | 0.349 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDC5 | Leptomonas seymouri | 43% | 100% |
A0A3Q8I9K2 | Leishmania donovani | 68% | 97% |
A4HVK7 | Leishmania infantum | 68% | 97% |
E9APA3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 68% | 99% |
Q4QG75 | Leishmania major | 66% | 100% |