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: A0A3Q8I9K2
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 | 617 | 621 | PF00656 | 0.710 |
CLV_NRD_NRD_1 | 172 | 174 | PF00675 | 0.677 |
CLV_NRD_NRD_1 | 324 | 326 | PF00675 | 0.473 |
CLV_NRD_NRD_1 | 525 | 527 | PF00675 | 0.752 |
CLV_NRD_NRD_1 | 82 | 84 | PF00675 | 0.618 |
CLV_PCSK_KEX2_1 | 194 | 196 | PF00082 | 0.676 |
CLV_PCSK_KEX2_1 | 82 | 84 | PF00082 | 0.618 |
CLV_PCSK_PC1ET2_1 | 194 | 196 | PF00082 | 0.676 |
CLV_PCSK_PC7_1 | 78 | 84 | PF00082 | 0.571 |
CLV_PCSK_SKI1_1 | 286 | 290 | PF00082 | 0.590 |
CLV_PCSK_SKI1_1 | 299 | 303 | PF00082 | 0.426 |
CLV_PCSK_SKI1_1 | 408 | 412 | PF00082 | 0.506 |
CLV_PCSK_SKI1_1 | 421 | 425 | PF00082 | 0.445 |
CLV_PCSK_SKI1_1 | 526 | 530 | PF00082 | 0.832 |
CLV_Separin_Metazoa | 492 | 496 | PF03568 | 0.664 |
DEG_SCF_FBW7_1 | 219 | 225 | PF00400 | 0.839 |
DEG_SCF_FBW7_1 | 606 | 611 | PF00400 | 0.743 |
DEG_SPOP_SBC_1 | 137 | 141 | PF00917 | 0.819 |
DEG_SPOP_SBC_1 | 599 | 603 | PF00917 | 0.606 |
DOC_CKS1_1 | 219 | 224 | PF01111 | 0.837 |
DOC_CYCLIN_yCln2_LP_2 | 543 | 549 | PF00134 | 0.775 |
DOC_MAPK_gen_1 | 370 | 377 | PF00069 | 0.549 |
DOC_PP2B_LxvP_1 | 130 | 133 | PF13499 | 0.539 |
DOC_PP2B_LxvP_1 | 543 | 546 | PF13499 | 0.758 |
DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.633 |
DOC_USP7_MATH_1 | 137 | 141 | PF00917 | 0.735 |
DOC_USP7_MATH_1 | 143 | 147 | PF00917 | 0.752 |
DOC_USP7_MATH_1 | 222 | 226 | PF00917 | 0.695 |
DOC_USP7_MATH_1 | 249 | 253 | PF00917 | 0.796 |
DOC_USP7_MATH_1 | 349 | 353 | PF00917 | 0.659 |
DOC_USP7_MATH_1 | 450 | 454 | PF00917 | 0.656 |
DOC_USP7_MATH_1 | 608 | 612 | PF00917 | 0.822 |
DOC_USP7_MATH_1 | 613 | 617 | PF00917 | 0.737 |
DOC_USP7_MATH_1 | 622 | 626 | PF00917 | 0.752 |
DOC_USP7_MATH_1 | 680 | 684 | PF00917 | 0.707 |
DOC_USP7_UBL2_3 | 194 | 198 | PF12436 | 0.819 |
DOC_USP7_UBL2_3 | 523 | 527 | PF12436 | 0.836 |
DOC_WW_Pin1_4 | 103 | 108 | PF00397 | 0.564 |
DOC_WW_Pin1_4 | 109 | 114 | PF00397 | 0.623 |
DOC_WW_Pin1_4 | 139 | 144 | PF00397 | 0.721 |
DOC_WW_Pin1_4 | 218 | 223 | PF00397 | 0.842 |
DOC_WW_Pin1_4 | 237 | 242 | PF00397 | 0.544 |
DOC_WW_Pin1_4 | 439 | 444 | PF00397 | 0.537 |
DOC_WW_Pin1_4 | 48 | 53 | PF00397 | 0.509 |
DOC_WW_Pin1_4 | 500 | 505 | PF00397 | 0.609 |
DOC_WW_Pin1_4 | 604 | 609 | PF00397 | 0.816 |
DOC_WW_Pin1_4 | 611 | 616 | PF00397 | 0.705 |
DOC_WW_Pin1_4 | 625 | 630 | PF00397 | 0.508 |
DOC_WW_Pin1_4 | 84 | 89 | PF00397 | 0.702 |
LIG_14-3-3_CanoR_1 | 100 | 107 | PF00244 | 0.671 |
LIG_14-3-3_CanoR_1 | 160 | 166 | PF00244 | 0.574 |
LIG_14-3-3_CanoR_1 | 293 | 303 | PF00244 | 0.516 |
LIG_14-3-3_CanoR_1 | 307 | 312 | PF00244 | 0.521 |
LIG_14-3-3_CanoR_1 | 408 | 417 | PF00244 | 0.544 |
LIG_14-3-3_CanoR_1 | 418 | 424 | PF00244 | 0.397 |
LIG_14-3-3_CanoR_1 | 554 | 563 | PF00244 | 0.589 |
LIG_APCC_ABBA_1 | 547 | 552 | PF00400 | 0.687 |
LIG_BIR_III_2 | 645 | 649 | PF00653 | 0.621 |
LIG_CSL_BTD_1 | 646 | 649 | PF09270 | 0.616 |
LIG_deltaCOP1_diTrp_1 | 645 | 652 | PF00928 | 0.708 |
LIG_EH1_1 | 459 | 467 | PF00400 | 0.388 |
LIG_EVH1_1 | 132 | 136 | PF00568 | 0.678 |
LIG_EVH1_2 | 648 | 652 | PF00568 | 0.643 |
LIG_FHA_1 | 202 | 208 | PF00498 | 0.687 |
LIG_FHA_1 | 257 | 263 | PF00498 | 0.603 |
LIG_FHA_1 | 409 | 415 | PF00498 | 0.592 |
LIG_FHA_1 | 440 | 446 | PF00498 | 0.542 |
LIG_FHA_1 | 449 | 455 | PF00498 | 0.551 |
LIG_FHA_1 | 682 | 688 | PF00498 | 0.700 |
LIG_FHA_2 | 162 | 168 | PF00498 | 0.575 |
LIG_FHA_2 | 249 | 255 | PF00498 | 0.609 |
LIG_FHA_2 | 615 | 621 | PF00498 | 0.704 |
LIG_FHA_2 | 656 | 662 | PF00498 | 0.745 |
LIG_LIR_Gen_1 | 166 | 176 | PF02991 | 0.572 |
LIG_LIR_Gen_1 | 300 | 311 | PF02991 | 0.607 |
LIG_LIR_Gen_1 | 471 | 480 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 166 | 172 | PF02991 | 0.567 |
LIG_LIR_Nem_3 | 27 | 32 | PF02991 | 0.466 |
LIG_LIR_Nem_3 | 300 | 306 | PF02991 | 0.516 |
LIG_LIR_Nem_3 | 471 | 477 | PF02991 | 0.471 |
LIG_SH2_CRK | 303 | 307 | PF00017 | 0.501 |
LIG_SH2_CRK | 431 | 435 | PF00017 | 0.580 |
LIG_SH2_STAP1 | 273 | 277 | PF00017 | 0.605 |
LIG_SH2_STAP1 | 287 | 291 | PF00017 | 0.408 |
LIG_SH2_STAT3 | 175 | 178 | PF00017 | 0.552 |
LIG_SH2_STAT3 | 638 | 641 | PF00017 | 0.608 |
LIG_SH2_STAT5 | 175 | 178 | PF00017 | 0.676 |
LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 281 | 284 | PF00017 | 0.512 |
LIG_SH2_STAT5 | 32 | 35 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 431 | 434 | PF00017 | 0.529 |
LIG_SH2_STAT5 | 441 | 444 | PF00017 | 0.484 |
LIG_SH3_3 | 128 | 134 | PF00018 | 0.464 |
LIG_SUMO_SIM_anti_2 | 116 | 122 | PF11976 | 0.599 |
LIG_SUMO_SIM_par_1 | 596 | 604 | PF11976 | 0.703 |
LIG_TRAF2_1 | 164 | 167 | PF00917 | 0.560 |
LIG_TRAF2_1 | 339 | 342 | PF00917 | 0.733 |
LIG_TRAF2_1 | 489 | 492 | PF00917 | 0.628 |
LIG_TYR_ITIM | 429 | 434 | PF00017 | 0.588 |
LIG_WW_3 | 179 | 183 | PF00397 | 0.691 |
MOD_CDK_SPK_2 | 604 | 609 | PF00069 | 0.816 |
MOD_CDK_SPxK_1 | 84 | 90 | PF00069 | 0.660 |
MOD_CDK_SPxxK_3 | 103 | 110 | PF00069 | 0.743 |
MOD_CK1_1 | 108 | 114 | PF00069 | 0.665 |
MOD_CK1_1 | 139 | 145 | PF00069 | 0.822 |
MOD_CK1_1 | 218 | 224 | PF00069 | 0.681 |
MOD_CK1_1 | 233 | 239 | PF00069 | 0.716 |
MOD_CK1_1 | 252 | 258 | PF00069 | 0.505 |
MOD_CK1_1 | 292 | 298 | PF00069 | 0.541 |
MOD_CK1_1 | 468 | 474 | PF00069 | 0.596 |
MOD_CK1_1 | 517 | 523 | PF00069 | 0.709 |
MOD_CK1_1 | 578 | 584 | PF00069 | 0.656 |
MOD_CK1_1 | 601 | 607 | PF00069 | 0.776 |
MOD_CK1_1 | 611 | 617 | PF00069 | 0.682 |
MOD_CK1_1 | 625 | 631 | PF00069 | 0.543 |
MOD_CK1_1 | 665 | 671 | PF00069 | 0.683 |
MOD_CK1_1 | 99 | 105 | PF00069 | 0.767 |
MOD_CK2_1 | 160 | 166 | PF00069 | 0.565 |
MOD_CK2_1 | 248 | 254 | PF00069 | 0.618 |
MOD_CK2_1 | 294 | 300 | PF00069 | 0.501 |
MOD_CK2_1 | 554 | 560 | PF00069 | 0.685 |
MOD_CK2_1 | 620 | 626 | PF00069 | 0.696 |
MOD_CK2_1 | 653 | 659 | PF00069 | 0.814 |
MOD_GlcNHglycan | 107 | 110 | PF01048 | 0.610 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.746 |
MOD_GlcNHglycan | 232 | 235 | PF01048 | 0.751 |
MOD_GlcNHglycan | 236 | 239 | PF01048 | 0.772 |
MOD_GlcNHglycan | 251 | 254 | PF01048 | 0.520 |
MOD_GlcNHglycan | 277 | 280 | PF01048 | 0.565 |
MOD_GlcNHglycan | 500 | 503 | PF01048 | 0.778 |
MOD_GlcNHglycan | 519 | 522 | PF01048 | 0.676 |
MOD_GlcNHglycan | 57 | 60 | PF01048 | 0.499 |
MOD_GlcNHglycan | 603 | 606 | PF01048 | 0.728 |
MOD_GlcNHglycan | 610 | 613 | PF01048 | 0.661 |
MOD_GlcNHglycan | 622 | 625 | PF01048 | 0.492 |
MOD_GlcNHglycan | 655 | 658 | PF01048 | 0.683 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.716 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.672 |
MOD_GSK3_1 | 218 | 225 | PF00069 | 0.778 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.665 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.535 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.478 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.658 |
MOD_GSK3_1 | 444 | 451 | PF00069 | 0.673 |
MOD_GSK3_1 | 517 | 524 | PF00069 | 0.762 |
MOD_GSK3_1 | 600 | 607 | PF00069 | 0.726 |
MOD_GSK3_1 | 662 | 669 | PF00069 | 0.653 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.743 |
MOD_N-GLC_1 | 498 | 503 | PF02516 | 0.562 |
MOD_N-GLC_1 | 586 | 591 | PF02516 | 0.573 |
MOD_N-GLC_1 | 665 | 670 | PF02516 | 0.746 |
MOD_NEK2_1 | 114 | 119 | PF00069 | 0.553 |
MOD_NEK2_1 | 138 | 143 | PF00069 | 0.772 |
MOD_NEK2_1 | 277 | 282 | PF00069 | 0.574 |
MOD_NEK2_1 | 289 | 294 | PF00069 | 0.510 |
MOD_NEK2_1 | 364 | 369 | PF00069 | 0.774 |
MOD_NEK2_1 | 376 | 381 | PF00069 | 0.387 |
MOD_NEK2_1 | 465 | 470 | PF00069 | 0.515 |
MOD_NEK2_1 | 598 | 603 | PF00069 | 0.689 |
MOD_NEK2_2 | 450 | 455 | PF00069 | 0.651 |
MOD_OFUCOSY | 575 | 582 | PF10250 | 0.630 |
MOD_PIKK_1 | 515 | 521 | PF00454 | 0.800 |
MOD_PKA_2 | 161 | 167 | PF00069 | 0.546 |
MOD_PKA_2 | 271 | 277 | PF00069 | 0.523 |
MOD_PKA_2 | 292 | 298 | PF00069 | 0.519 |
MOD_PKA_2 | 608 | 614 | PF00069 | 0.824 |
MOD_PKA_2 | 653 | 659 | PF00069 | 0.689 |
MOD_PKA_2 | 99 | 105 | PF00069 | 0.817 |
MOD_PKB_1 | 305 | 313 | PF00069 | 0.601 |
MOD_Plk_2-3 | 655 | 661 | PF00069 | 0.741 |
MOD_Plk_4 | 10 | 16 | PF00069 | 0.483 |
MOD_Plk_4 | 114 | 120 | PF00069 | 0.633 |
MOD_Plk_4 | 277 | 283 | PF00069 | 0.511 |
MOD_Plk_4 | 562 | 568 | PF00069 | 0.597 |
MOD_Plk_4 | 60 | 66 | PF00069 | 0.486 |
MOD_Plk_4 | 614 | 620 | PF00069 | 0.677 |
MOD_Plk_4 | 647 | 653 | PF00069 | 0.717 |
MOD_ProDKin_1 | 103 | 109 | PF00069 | 0.561 |
MOD_ProDKin_1 | 139 | 145 | PF00069 | 0.720 |
MOD_ProDKin_1 | 218 | 224 | PF00069 | 0.836 |
MOD_ProDKin_1 | 237 | 243 | PF00069 | 0.544 |
MOD_ProDKin_1 | 439 | 445 | PF00069 | 0.537 |
MOD_ProDKin_1 | 48 | 54 | PF00069 | 0.503 |
MOD_ProDKin_1 | 500 | 506 | PF00069 | 0.613 |
MOD_ProDKin_1 | 604 | 610 | PF00069 | 0.817 |
MOD_ProDKin_1 | 611 | 617 | PF00069 | 0.705 |
MOD_ProDKin_1 | 625 | 631 | PF00069 | 0.508 |
MOD_ProDKin_1 | 84 | 90 | PF00069 | 0.710 |
TRG_ENDOCYTIC_2 | 273 | 276 | PF00928 | 0.608 |
TRG_ENDOCYTIC_2 | 303 | 306 | PF00928 | 0.503 |
TRG_ENDOCYTIC_2 | 431 | 434 | PF00928 | 0.583 |
TRG_ENDOCYTIC_2 | 469 | 472 | PF00928 | 0.527 |
TRG_ER_diArg_1 | 81 | 83 | PF00400 | 0.601 |
TRG_NLS_MonoExtC_3 | 193 | 198 | PF00514 | 0.728 |
TRG_NLS_MonoExtN_4 | 194 | 201 | PF00514 | 0.728 |
TRG_Pf-PMV_PEXEL_1 | 68 | 72 | PF00026 | 0.469 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDC5 | Leptomonas seymouri | 42% | 100% |
A4H768 | Leishmania braziliensis | 68% | 97% |
A4HVK7 | Leishmania infantum | 99% | 100% |
E9APA3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 98% |
Q4QG75 | Leishmania major | 88% | 99% |