Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 2 |
Forrest at al. (procyclic) | no | yes: 2 |
Silverman et al. | no | yes: 2 |
Pissara et al. | yes | yes: 8 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 4 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 4 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9ANV2
Term | Name | Level | Count |
---|---|---|---|
GO:0006082 | organic acid metabolic process | 3 | 11 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 11 |
GO:0006399 | tRNA metabolic process | 7 | 11 |
GO:0006418 | tRNA aminoacylation for protein translation | 6 | 11 |
GO:0006423 | cysteinyl-tRNA aminoacylation | 7 | 11 |
GO:0006520 | amino acid metabolic process | 3 | 11 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016070 | RNA metabolic process | 5 | 11 |
GO:0019752 | carboxylic acid metabolic process | 5 | 11 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 11 |
GO:0034660 | ncRNA metabolic process | 6 | 11 |
GO:0043038 | amino acid activation | 4 | 11 |
GO:0043039 | tRNA aminoacylation | 5 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0043436 | oxoacid metabolic process | 4 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0044281 | small molecule metabolic process | 2 | 11 |
GO:0046483 | heterocycle metabolic process | 3 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:0090304 | nucleic acid metabolic process | 4 | 11 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 11 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004812 | aminoacyl-tRNA ligase activity | 4 | 11 |
GO:0004817 | cysteine-tRNA ligase activity | 5 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0005524 | ATP binding | 5 | 11 |
GO:0016874 | ligase activity | 2 | 11 |
GO:0016875 | ligase activity, forming carbon-oxygen bonds | 3 | 11 |
GO:0017076 | purine nucleotide binding | 4 | 11 |
GO:0030554 | adenyl nucleotide binding | 5 | 11 |
GO:0032553 | ribonucleotide binding | 3 | 11 |
GO:0032555 | purine ribonucleotide binding | 4 | 11 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 11 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 11 |
GO:0036094 | small molecule binding | 2 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043168 | anion binding | 3 | 11 |
GO:0043169 | cation binding | 3 | 11 |
GO:0046872 | metal ion binding | 4 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:0097367 | carbohydrate derivative binding | 2 | 11 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 11 |
GO:0140101 | catalytic activity, acting on a tRNA | 4 | 11 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 11 |
GO:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 609 | 613 | PF00656 | 0.539 |
CLV_NRD_NRD_1 | 154 | 156 | PF00675 | 0.316 |
CLV_NRD_NRD_1 | 236 | 238 | PF00675 | 0.300 |
CLV_NRD_NRD_1 | 559 | 561 | PF00675 | 0.420 |
CLV_NRD_NRD_1 | 667 | 669 | PF00675 | 0.460 |
CLV_NRD_NRD_1 | 676 | 678 | PF00675 | 0.512 |
CLV_NRD_NRD_1 | 686 | 688 | PF00675 | 0.429 |
CLV_NRD_NRD_1 | 705 | 707 | PF00675 | 0.477 |
CLV_NRD_NRD_1 | 87 | 89 | PF00675 | 0.257 |
CLV_PCSK_KEX2_1 | 113 | 115 | PF00082 | 0.257 |
CLV_PCSK_KEX2_1 | 154 | 156 | PF00082 | 0.316 |
CLV_PCSK_KEX2_1 | 20 | 22 | PF00082 | 0.463 |
CLV_PCSK_KEX2_1 | 333 | 335 | PF00082 | 0.270 |
CLV_PCSK_KEX2_1 | 667 | 669 | PF00082 | 0.668 |
CLV_PCSK_KEX2_1 | 686 | 688 | PF00082 | 0.424 |
CLV_PCSK_KEX2_1 | 705 | 707 | PF00082 | 0.458 |
CLV_PCSK_KEX2_1 | 87 | 89 | PF00082 | 0.257 |
CLV_PCSK_PC1ET2_1 | 113 | 115 | PF00082 | 0.257 |
CLV_PCSK_PC1ET2_1 | 154 | 156 | PF00082 | 0.350 |
CLV_PCSK_PC1ET2_1 | 20 | 22 | PF00082 | 0.488 |
CLV_PCSK_PC1ET2_1 | 333 | 335 | PF00082 | 0.270 |
CLV_PCSK_PC1ET2_1 | 686 | 688 | PF00082 | 0.432 |
CLV_PCSK_SKI1_1 | 110 | 114 | PF00082 | 0.257 |
CLV_PCSK_SKI1_1 | 156 | 160 | PF00082 | 0.382 |
CLV_PCSK_SKI1_1 | 241 | 245 | PF00082 | 0.253 |
CLV_PCSK_SKI1_1 | 422 | 426 | PF00082 | 0.257 |
CLV_PCSK_SKI1_1 | 428 | 432 | PF00082 | 0.257 |
CLV_PCSK_SKI1_1 | 437 | 441 | PF00082 | 0.257 |
CLV_PCSK_SKI1_1 | 451 | 455 | PF00082 | 0.257 |
CLV_PCSK_SKI1_1 | 481 | 485 | PF00082 | 0.342 |
CLV_PCSK_SKI1_1 | 507 | 511 | PF00082 | 0.466 |
CLV_PCSK_SKI1_1 | 694 | 698 | PF00082 | 0.552 |
CLV_PCSK_SKI1_1 | 738 | 742 | PF00082 | 0.503 |
CLV_PCSK_SKI1_1 | 749 | 753 | PF00082 | 0.418 |
DEG_APCC_DBOX_1 | 436 | 444 | PF00400 | 0.470 |
DOC_MAPK_gen_1 | 172 | 182 | PF00069 | 0.472 |
DOC_MAPK_gen_1 | 428 | 436 | PF00069 | 0.457 |
DOC_MAPK_MEF2A_6 | 175 | 184 | PF00069 | 0.472 |
DOC_PP1_RVXF_1 | 449 | 455 | PF00149 | 0.457 |
DOC_PP1_RVXF_1 | 55 | 62 | PF00149 | 0.453 |
DOC_PP4_FxxP_1 | 344 | 347 | PF00568 | 0.457 |
DOC_USP7_MATH_1 | 147 | 151 | PF00917 | 0.501 |
DOC_USP7_MATH_1 | 208 | 212 | PF00917 | 0.516 |
DOC_USP7_UBL2_3 | 688 | 692 | PF12436 | 0.394 |
DOC_USP7_UBL2_3 | 738 | 742 | PF12436 | 0.469 |
DOC_USP7_UBL2_3 | 745 | 749 | PF12436 | 0.426 |
DOC_WW_Pin1_4 | 332 | 337 | PF00397 | 0.493 |
DOC_WW_Pin1_4 | 351 | 356 | PF00397 | 0.415 |
LIG_14-3-3_CanoR_1 | 130 | 138 | PF00244 | 0.577 |
LIG_14-3-3_CanoR_1 | 221 | 227 | PF00244 | 0.481 |
LIG_14-3-3_CanoR_1 | 260 | 268 | PF00244 | 0.457 |
LIG_14-3-3_CanoR_1 | 311 | 318 | PF00244 | 0.513 |
LIG_14-3-3_CanoR_1 | 351 | 355 | PF00244 | 0.379 |
LIG_14-3-3_CanoR_1 | 553 | 559 | PF00244 | 0.386 |
LIG_14-3-3_CanoR_1 | 60 | 69 | PF00244 | 0.485 |
LIG_14-3-3_CanoR_1 | 694 | 699 | PF00244 | 0.516 |
LIG_14-3-3_CanoR_1 | 78 | 84 | PF00244 | 0.390 |
LIG_ActinCP_TwfCPI_2 | 344 | 351 | PF01115 | 0.488 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.570 |
LIG_BRCT_BRCA1_1 | 286 | 290 | PF00533 | 0.464 |
LIG_BRCT_BRCA1_1 | 700 | 704 | PF00533 | 0.492 |
LIG_deltaCOP1_diTrp_1 | 349 | 356 | PF00928 | 0.457 |
LIG_FHA_1 | 140 | 146 | PF00498 | 0.413 |
LIG_FHA_1 | 260 | 266 | PF00498 | 0.457 |
LIG_FHA_1 | 43 | 49 | PF00498 | 0.422 |
LIG_FHA_1 | 447 | 453 | PF00498 | 0.513 |
LIG_FHA_1 | 497 | 503 | PF00498 | 0.476 |
LIG_FHA_1 | 80 | 86 | PF00498 | 0.457 |
LIG_FHA_2 | 103 | 109 | PF00498 | 0.457 |
LIG_FHA_2 | 311 | 317 | PF00498 | 0.459 |
LIG_FHA_2 | 65 | 71 | PF00498 | 0.377 |
LIG_LIR_Apic_2 | 26 | 30 | PF02991 | 0.338 |
LIG_LIR_Apic_2 | 349 | 355 | PF02991 | 0.457 |
LIG_LIR_Gen_1 | 201 | 210 | PF02991 | 0.473 |
LIG_LIR_Gen_1 | 277 | 288 | PF02991 | 0.564 |
LIG_LIR_Gen_1 | 526 | 534 | PF02991 | 0.463 |
LIG_LIR_Gen_1 | 593 | 604 | PF02991 | 0.563 |
LIG_LIR_Gen_1 | 753 | 758 | PF02991 | 0.483 |
LIG_LIR_Gen_1 | 82 | 90 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 201 | 206 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 26 | 31 | PF02991 | 0.311 |
LIG_LIR_Nem_3 | 277 | 283 | PF02991 | 0.564 |
LIG_LIR_Nem_3 | 301 | 305 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 407 | 412 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 526 | 531 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 567 | 573 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 593 | 599 | PF02991 | 0.584 |
LIG_LIR_Nem_3 | 691 | 696 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 713 | 719 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 753 | 757 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 82 | 86 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 91 | 96 | PF02991 | 0.457 |
LIG_LYPXL_yS_3 | 28 | 31 | PF13949 | 0.474 |
LIG_LYPXL_yS_3 | 302 | 305 | PF13949 | 0.470 |
LIG_MLH1_MIPbox_1 | 286 | 290 | PF16413 | 0.457 |
LIG_MLH1_MIPbox_1 | 700 | 704 | PF16413 | 0.492 |
LIG_MYND_1 | 303 | 307 | PF01753 | 0.470 |
LIG_PCNA_PIPBox_1 | 617 | 626 | PF02747 | 0.363 |
LIG_PCNA_TLS_4 | 87 | 94 | PF02747 | 0.457 |
LIG_PCNA_yPIPBox_3 | 611 | 624 | PF02747 | 0.357 |
LIG_Pex14_1 | 386 | 390 | PF04695 | 0.470 |
LIG_Pex14_1 | 409 | 413 | PF04695 | 0.457 |
LIG_Pex14_2 | 203 | 207 | PF04695 | 0.457 |
LIG_SH2_CRK | 96 | 100 | PF00017 | 0.470 |
LIG_SH2_NCK_1 | 239 | 243 | PF00017 | 0.550 |
LIG_SH2_NCK_1 | 719 | 723 | PF00017 | 0.541 |
LIG_SH2_NCK_1 | 96 | 100 | PF00017 | 0.537 |
LIG_SH2_SRC | 719 | 722 | PF00017 | 0.543 |
LIG_SH2_STAP1 | 239 | 243 | PF00017 | 0.470 |
LIG_SH2_STAP1 | 750 | 754 | PF00017 | 0.478 |
LIG_SH2_STAP1 | 96 | 100 | PF00017 | 0.513 |
LIG_SH2_STAT3 | 264 | 267 | PF00017 | 0.488 |
LIG_SH2_STAT5 | 264 | 267 | PF00017 | 0.457 |
LIG_SH2_STAT5 | 282 | 285 | PF00017 | 0.457 |
LIG_SH2_STAT5 | 295 | 298 | PF00017 | 0.518 |
LIG_SH2_STAT5 | 412 | 415 | PF00017 | 0.457 |
LIG_SH2_STAT5 | 547 | 550 | PF00017 | 0.385 |
LIG_SH2_STAT5 | 565 | 568 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 62 | 65 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 703 | 706 | PF00017 | 0.441 |
LIG_SH2_STAT5 | 80 | 83 | PF00017 | 0.406 |
LIG_SH2_STAT5 | 93 | 96 | PF00017 | 0.457 |
LIG_SH3_3 | 344 | 350 | PF00018 | 0.457 |
LIG_SH3_3 | 643 | 649 | PF00018 | 0.511 |
LIG_SUMO_SIM_anti_2 | 486 | 491 | PF11976 | 0.390 |
LIG_TRAF2_1 | 669 | 672 | PF00917 | 0.567 |
LIG_TRAF2_1 | 731 | 734 | PF00917 | 0.572 |
LIG_TYR_ITSM | 24 | 31 | PF00017 | 0.282 |
LIG_WRC_WIRS_1 | 80 | 85 | PF05994 | 0.295 |
MOD_CK1_1 | 222 | 228 | PF00069 | 0.329 |
MOD_CK1_1 | 466 | 472 | PF00069 | 0.314 |
MOD_CK2_1 | 147 | 153 | PF00069 | 0.251 |
MOD_CK2_1 | 311 | 317 | PF00069 | 0.302 |
MOD_CK2_1 | 40 | 46 | PF00069 | 0.362 |
MOD_CK2_1 | 466 | 472 | PF00069 | 0.295 |
MOD_CK2_1 | 750 | 756 | PF00069 | 0.426 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.570 |
MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.384 |
MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.376 |
MOD_GlcNHglycan | 219 | 224 | PF01048 | 0.374 |
MOD_GlcNHglycan | 382 | 385 | PF01048 | 0.314 |
MOD_GlcNHglycan | 549 | 552 | PF01048 | 0.477 |
MOD_GlcNHglycan | 554 | 557 | PF01048 | 0.381 |
MOD_GlcNHglycan | 588 | 591 | PF01048 | 0.660 |
MOD_GSK3_1 | 365 | 372 | PF00069 | 0.295 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.407 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.160 |
MOD_GSK3_1 | 694 | 701 | PF00069 | 0.458 |
MOD_GSK3_1 | 720 | 727 | PF00069 | 0.495 |
MOD_N-GLC_1 | 102 | 107 | PF02516 | 0.295 |
MOD_N-GLC_1 | 311 | 316 | PF02516 | 0.295 |
MOD_N-GLC_1 | 463 | 468 | PF02516 | 0.322 |
MOD_N-GLC_2 | 395 | 397 | PF02516 | 0.295 |
MOD_NEK2_1 | 184 | 189 | PF00069 | 0.320 |
MOD_NEK2_1 | 424 | 429 | PF00069 | 0.306 |
MOD_NEK2_1 | 443 | 448 | PF00069 | 0.220 |
MOD_NEK2_1 | 94 | 99 | PF00069 | 0.426 |
MOD_NEK2_2 | 284 | 289 | PF00069 | 0.295 |
MOD_PIKK_1 | 184 | 190 | PF00454 | 0.339 |
MOD_PIKK_1 | 404 | 410 | PF00454 | 0.407 |
MOD_PIKK_1 | 496 | 502 | PF00454 | 0.492 |
MOD_PKA_1 | 741 | 747 | PF00069 | 0.484 |
MOD_PKA_2 | 129 | 135 | PF00069 | 0.444 |
MOD_PKA_2 | 259 | 265 | PF00069 | 0.295 |
MOD_PKA_2 | 310 | 316 | PF00069 | 0.426 |
MOD_PKA_2 | 350 | 356 | PF00069 | 0.194 |
MOD_PKA_2 | 552 | 558 | PF00069 | 0.380 |
MOD_PKB_1 | 21 | 29 | PF00069 | 0.366 |
MOD_Plk_1 | 284 | 290 | PF00069 | 0.339 |
MOD_Plk_1 | 365 | 371 | PF00069 | 0.295 |
MOD_Plk_1 | 466 | 472 | PF00069 | 0.325 |
MOD_Plk_1 | 69 | 75 | PF00069 | 0.314 |
MOD_Plk_2-3 | 733 | 739 | PF00069 | 0.557 |
MOD_Plk_4 | 23 | 29 | PF00069 | 0.330 |
MOD_Plk_4 | 284 | 290 | PF00069 | 0.311 |
MOD_Plk_4 | 365 | 371 | PF00069 | 0.295 |
MOD_Plk_4 | 5 | 11 | PF00069 | 0.640 |
MOD_Plk_4 | 527 | 533 | PF00069 | 0.458 |
MOD_Plk_4 | 536 | 542 | PF00069 | 0.403 |
MOD_Plk_4 | 554 | 560 | PF00069 | 0.253 |
MOD_Plk_4 | 599 | 605 | PF00069 | 0.452 |
MOD_Plk_4 | 64 | 70 | PF00069 | 0.295 |
MOD_Plk_4 | 761 | 767 | PF00069 | 0.585 |
MOD_Plk_4 | 772 | 778 | PF00069 | 0.531 |
MOD_Plk_4 | 94 | 100 | PF00069 | 0.380 |
MOD_ProDKin_1 | 332 | 338 | PF00069 | 0.346 |
MOD_ProDKin_1 | 351 | 357 | PF00069 | 0.236 |
MOD_SUMO_for_1 | 19 | 22 | PF00179 | 0.466 |
MOD_SUMO_rev_2 | 106 | 112 | PF00179 | 0.295 |
MOD_SUMO_rev_2 | 174 | 180 | PF00179 | 0.296 |
MOD_SUMO_rev_2 | 186 | 194 | PF00179 | 0.297 |
MOD_SUMO_rev_2 | 383 | 391 | PF00179 | 0.314 |
MOD_SUMO_rev_2 | 612 | 620 | PF00179 | 0.475 |
MOD_SUMO_rev_2 | 708 | 717 | PF00179 | 0.538 |
MOD_SUMO_rev_2 | 733 | 743 | PF00179 | 0.484 |
TRG_DiLeu_BaLyEn_6 | 448 | 453 | PF01217 | 0.295 |
TRG_ENDOCYTIC_2 | 28 | 31 | PF00928 | 0.486 |
TRG_ENDOCYTIC_2 | 302 | 305 | PF00928 | 0.295 |
TRG_ENDOCYTIC_2 | 719 | 722 | PF00928 | 0.456 |
TRG_ENDOCYTIC_2 | 754 | 757 | PF00928 | 0.446 |
TRG_ENDOCYTIC_2 | 80 | 83 | PF00928 | 0.295 |
TRG_ENDOCYTIC_2 | 96 | 99 | PF00928 | 0.295 |
TRG_ER_diArg_1 | 114 | 117 | PF00400 | 0.295 |
TRG_ER_diArg_1 | 704 | 706 | PF00400 | 0.495 |
TRG_ER_diArg_1 | 86 | 88 | PF00400 | 0.295 |
TRG_NLS_MonoExtC_3 | 685 | 691 | PF00514 | 0.432 |
TRG_NLS_MonoExtN_4 | 110 | 117 | PF00514 | 0.295 |
TRG_Pf-PMV_PEXEL_1 | 662 | 666 | PF00026 | 0.529 |
TRG_Pf-PMV_PEXEL_1 | 677 | 682 | PF00026 | 0.516 |
TRG_Pf-PMV_PEXEL_1 | 687 | 691 | PF00026 | 0.429 |
TRG_Pf-PMV_PEXEL_1 | 87 | 91 | PF00026 | 0.261 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2U0 | Leptomonas seymouri | 83% | 99% |
A0A0S4JIJ5 | Bodo saltans | 64% | 100% |
A0A1X0NM71 | Trypanosomatidae | 69% | 98% |
A0A3S7WRW6 | Leishmania donovani | 96% | 100% |
A0A422N5J6 | Trypanosoma rangeli | 67% | 100% |
A4H6U0 | Leishmania braziliensis | 89% | 99% |
C9ZQB2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 65% | 100% |
E9AGB4 | Leishmania infantum | 96% | 100% |
P49589 | Homo sapiens | 41% | 100% |
P53852 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 40% | 100% |
Q09860 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 39% | 100% |
Q291L4 | Drosophila pseudoobscura pseudoobscura | 41% | 100% |
Q4QGR8 | Leishmania major | 96% | 100% |
Q4R550 | Macaca fascicularis | 42% | 100% |
Q54KR1 | Dictyostelium discoideum | 44% | 100% |
Q5F408 | Gallus gallus | 40% | 100% |
Q5M7N8 | Xenopus tropicalis | 41% | 100% |
Q7KN90 | Drosophila melanogaster | 40% | 100% |
Q7ZWR2 | Xenopus laevis | 41% | 100% |
Q9ER72 | Mus musculus | 40% | 94% |