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: 3 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 20 |
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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 1 |
GO:0097014 | ciliary plasm | 5 | 1 |
GO:0099568 | cytoplasmic region | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0006082 | organic acid metabolic process | 3 | 12 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006399 | tRNA metabolic process | 7 | 12 |
GO:0006418 | tRNA aminoacylation for protein translation | 6 | 12 |
GO:0006520 | amino acid metabolic process | 3 | 12 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016070 | RNA metabolic process | 5 | 12 |
GO:0019752 | carboxylic acid metabolic process | 5 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0034660 | ncRNA metabolic process | 6 | 12 |
GO:0043038 | amino acid activation | 4 | 12 |
GO:0043039 | tRNA aminoacylation | 5 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0043436 | oxoacid metabolic process | 4 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044281 | small molecule metabolic process | 2 | 12 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0090304 | nucleic acid metabolic process | 4 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004812 | aminoacyl-tRNA ligase activity | 4 | 12 |
GO:0004831 | tyrosine-tRNA ligase activity | 5 | 6 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0016874 | ligase activity | 2 | 12 |
GO:0016875 | ligase activity, forming carbon-oxygen bonds | 3 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0030554 | adenyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 12 |
GO:0140101 | catalytic activity, acting on a tRNA | 4 | 12 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 226 | 230 | PF00656 | 0.503 |
CLV_C14_Caspase3-7 | 519 | 523 | PF00656 | 0.539 |
CLV_NRD_NRD_1 | 185 | 187 | PF00675 | 0.303 |
CLV_NRD_NRD_1 | 200 | 202 | PF00675 | 0.303 |
CLV_NRD_NRD_1 | 217 | 219 | PF00675 | 0.257 |
CLV_NRD_NRD_1 | 242 | 244 | PF00675 | 0.309 |
CLV_NRD_NRD_1 | 353 | 355 | PF00675 | 0.510 |
CLV_NRD_NRD_1 | 476 | 478 | PF00675 | 0.374 |
CLV_NRD_NRD_1 | 576 | 578 | PF00675 | 0.425 |
CLV_PCSK_KEX2_1 | 217 | 219 | PF00082 | 0.257 |
CLV_PCSK_KEX2_1 | 576 | 578 | PF00082 | 0.428 |
CLV_PCSK_SKI1_1 | 109 | 113 | PF00082 | 0.327 |
CLV_PCSK_SKI1_1 | 128 | 132 | PF00082 | 0.228 |
CLV_PCSK_SKI1_1 | 201 | 205 | PF00082 | 0.314 |
CLV_PCSK_SKI1_1 | 453 | 457 | PF00082 | 0.521 |
CLV_PCSK_SKI1_1 | 478 | 482 | PF00082 | 0.444 |
CLV_PCSK_SKI1_1 | 504 | 508 | PF00082 | 0.434 |
CLV_PCSK_SKI1_1 | 577 | 581 | PF00082 | 0.443 |
CLV_PCSK_SKI1_1 | 657 | 661 | PF00082 | 0.511 |
CLV_PCSK_SKI1_1 | 666 | 670 | PF00082 | 0.609 |
CLV_PCSK_SKI1_1 | 677 | 681 | PF00082 | 0.612 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.571 |
DEG_SPOP_SBC_1 | 516 | 520 | PF00917 | 0.466 |
DOC_CKS1_1 | 621 | 626 | PF01111 | 0.532 |
DOC_CYCLIN_RxL_1 | 475 | 485 | PF00134 | 0.439 |
DOC_CYCLIN_RxL_1 | 652 | 663 | PF00134 | 0.495 |
DOC_CYCLIN_yCln2_LP_2 | 384 | 390 | PF00134 | 0.504 |
DOC_MAPK_gen_1 | 201 | 208 | PF00069 | 0.503 |
DOC_MAPK_gen_1 | 354 | 362 | PF00069 | 0.682 |
DOC_MAPK_MEF2A_6 | 504 | 513 | PF00069 | 0.573 |
DOC_MAPK_MEF2A_6 | 642 | 650 | PF00069 | 0.439 |
DOC_PP1_RVXF_1 | 107 | 113 | PF00149 | 0.504 |
DOC_PP2B_LxvP_1 | 329 | 332 | PF13499 | 0.643 |
DOC_PP2B_LxvP_1 | 384 | 387 | PF13499 | 0.510 |
DOC_PP2B_PxIxI_1 | 591 | 597 | PF00149 | 0.541 |
DOC_USP7_MATH_1 | 221 | 225 | PF00917 | 0.503 |
DOC_USP7_MATH_1 | 307 | 311 | PF00917 | 0.561 |
DOC_USP7_MATH_1 | 317 | 321 | PF00917 | 0.485 |
DOC_USP7_MATH_1 | 349 | 353 | PF00917 | 0.534 |
DOC_USP7_MATH_1 | 419 | 423 | PF00917 | 0.564 |
DOC_USP7_UBL2_3 | 351 | 355 | PF12436 | 0.511 |
DOC_USP7_UBL2_3 | 676 | 680 | PF12436 | 0.508 |
DOC_WW_Pin1_4 | 620 | 625 | PF00397 | 0.536 |
LIG_14-3-3_CanoR_1 | 252 | 260 | PF00244 | 0.605 |
LIG_14-3-3_CanoR_1 | 504 | 513 | PF00244 | 0.510 |
LIG_Actin_WH2_1 | 477 | 495 | PF00022 | 0.382 |
LIG_Actin_WH2_2 | 480 | 495 | PF00022 | 0.513 |
LIG_BRCT_BRCA1_1 | 229 | 233 | PF00533 | 0.503 |
LIG_CSL_BTD_1 | 378 | 381 | PF09270 | 0.370 |
LIG_FHA_1 | 357 | 363 | PF00498 | 0.662 |
LIG_FHA_1 | 407 | 413 | PF00498 | 0.538 |
LIG_FHA_2 | 235 | 241 | PF00498 | 0.514 |
LIG_FHA_2 | 298 | 304 | PF00498 | 0.510 |
LIG_FHA_2 | 424 | 430 | PF00498 | 0.437 |
LIG_FHA_2 | 454 | 460 | PF00498 | 0.431 |
LIG_FHA_2 | 517 | 523 | PF00498 | 0.446 |
LIG_KLC1_Yacidic_2 | 564 | 569 | PF13176 | 0.529 |
LIG_LIR_Apic_2 | 620 | 624 | PF02991 | 0.591 |
LIG_LIR_Gen_1 | 194 | 203 | PF02991 | 0.503 |
LIG_LIR_Gen_1 | 277 | 287 | PF02991 | 0.528 |
LIG_LIR_Gen_1 | 300 | 309 | PF02991 | 0.514 |
LIG_LIR_Gen_1 | 416 | 425 | PF02991 | 0.388 |
LIG_LIR_Gen_1 | 467 | 476 | PF02991 | 0.442 |
LIG_LIR_Gen_1 | 73 | 82 | PF02991 | 0.503 |
LIG_LIR_Nem_3 | 124 | 130 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 194 | 198 | PF02991 | 0.503 |
LIG_LIR_Nem_3 | 277 | 282 | PF02991 | 0.514 |
LIG_LIR_Nem_3 | 296 | 301 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 4 | 10 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 416 | 420 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 467 | 472 | PF02991 | 0.514 |
LIG_LIR_Nem_3 | 73 | 77 | PF02991 | 0.503 |
LIG_LYPXL_S_1 | 162 | 166 | PF13949 | 0.303 |
LIG_LYPXL_yS_3 | 163 | 166 | PF13949 | 0.503 |
LIG_NRBOX | 645 | 651 | PF00104 | 0.439 |
LIG_NRP_CendR_1 | 680 | 682 | PF00754 | 0.641 |
LIG_REV1ctd_RIR_1 | 170 | 179 | PF16727 | 0.503 |
LIG_SH2_CRK | 284 | 288 | PF00017 | 0.532 |
LIG_SH2_CRK | 446 | 450 | PF00017 | 0.432 |
LIG_SH2_CRK | 583 | 587 | PF00017 | 0.444 |
LIG_SH2_CRK | 7 | 11 | PF00017 | 0.415 |
LIG_SH2_NCK_1 | 284 | 288 | PF00017 | 0.528 |
LIG_SH2_NCK_1 | 583 | 587 | PF00017 | 0.586 |
LIG_SH2_NCK_1 | 621 | 625 | PF00017 | 0.593 |
LIG_SH2_STAT5 | 195 | 198 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 249 | 252 | PF00017 | 0.514 |
LIG_SH2_STAT5 | 278 | 281 | PF00017 | 0.528 |
LIG_SH2_STAT5 | 532 | 535 | PF00017 | 0.560 |
LIG_SH2_STAT5 | 567 | 570 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 95 | 98 | PF00017 | 0.503 |
LIG_SH3_2 | 368 | 373 | PF14604 | 0.608 |
LIG_SH3_3 | 158 | 164 | PF00018 | 0.570 |
LIG_SH3_3 | 365 | 371 | PF00018 | 0.539 |
LIG_SH3_3 | 409 | 415 | PF00018 | 0.366 |
LIG_SH3_5 | 274 | 278 | PF00018 | 0.503 |
LIG_SUMO_SIM_anti_2 | 409 | 414 | PF11976 | 0.380 |
LIG_SUMO_SIM_par_1 | 204 | 209 | PF11976 | 0.503 |
LIG_SUMO_SIM_par_1 | 386 | 392 | PF11976 | 0.510 |
LIG_SUMO_SIM_par_1 | 409 | 416 | PF11976 | 0.406 |
LIG_SUMO_SIM_par_1 | 509 | 514 | PF11976 | 0.458 |
LIG_TRAF2_1 | 115 | 118 | PF00917 | 0.561 |
LIG_TRAF2_1 | 339 | 342 | PF00917 | 0.469 |
LIG_TRAF2_1 | 586 | 589 | PF00917 | 0.539 |
LIG_UBA3_1 | 171 | 175 | PF00899 | 0.503 |
MOD_CK1_1 | 258 | 264 | PF00069 | 0.525 |
MOD_CK1_1 | 620 | 626 | PF00069 | 0.580 |
MOD_CK2_1 | 112 | 118 | PF00069 | 0.503 |
MOD_CK2_1 | 336 | 342 | PF00069 | 0.536 |
MOD_CK2_1 | 423 | 429 | PF00069 | 0.457 |
MOD_CK2_1 | 453 | 459 | PF00069 | 0.439 |
MOD_CK2_1 | 479 | 485 | PF00069 | 0.546 |
MOD_CK2_1 | 9 | 15 | PF00069 | 0.418 |
MOD_Cter_Amidation | 199 | 202 | PF01082 | 0.303 |
MOD_GlcNHglycan | 229 | 232 | PF01048 | 0.303 |
MOD_GlcNHglycan | 255 | 258 | PF01048 | 0.412 |
MOD_GlcNHglycan | 40 | 44 | PF01048 | 0.303 |
MOD_GlcNHglycan | 416 | 420 | PF01048 | 0.461 |
MOD_GlcNHglycan | 431 | 435 | PF01048 | 0.379 |
MOD_GlcNHglycan | 583 | 586 | PF01048 | 0.580 |
MOD_GlcNHglycan | 632 | 635 | PF01048 | 0.451 |
MOD_GlcNHglycan | 651 | 655 | PF01048 | 0.417 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.504 |
MOD_GSK3_1 | 223 | 230 | PF00069 | 0.503 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.544 |
MOD_GSK3_1 | 307 | 314 | PF00069 | 0.571 |
MOD_GSK3_1 | 415 | 422 | PF00069 | 0.477 |
MOD_GSK3_1 | 511 | 518 | PF00069 | 0.381 |
MOD_N-GLC_1 | 617 | 622 | PF02516 | 0.468 |
MOD_N-GLC_1 | 666 | 671 | PF02516 | 0.492 |
MOD_N-GLC_2 | 58 | 60 | PF02516 | 0.303 |
MOD_NEK2_1 | 362 | 367 | PF00069 | 0.585 |
MOD_NEK2_1 | 468 | 473 | PF00069 | 0.543 |
MOD_NEK2_1 | 509 | 514 | PF00069 | 0.393 |
MOD_NEK2_1 | 650 | 655 | PF00069 | 0.504 |
MOD_NEK2_1 | 9 | 14 | PF00069 | 0.404 |
MOD_Plk_1 | 415 | 421 | PF00069 | 0.374 |
MOD_Plk_1 | 617 | 623 | PF00069 | 0.469 |
MOD_Plk_1 | 666 | 672 | PF00069 | 0.544 |
MOD_Plk_2-3 | 311 | 317 | PF00069 | 0.581 |
MOD_Plk_4 | 122 | 128 | PF00069 | 0.546 |
MOD_Plk_4 | 144 | 150 | PF00069 | 0.516 |
MOD_Plk_4 | 408 | 414 | PF00069 | 0.521 |
MOD_Plk_4 | 468 | 474 | PF00069 | 0.514 |
MOD_ProDKin_1 | 620 | 626 | PF00069 | 0.534 |
MOD_SUMO_rev_2 | 22 | 32 | PF00179 | 0.476 |
TRG_DiLeu_BaEn_1 | 194 | 199 | PF01217 | 0.490 |
TRG_DiLeu_BaEn_1 | 22 | 27 | PF01217 | 0.419 |
TRG_DiLeu_BaEn_1 | 325 | 330 | PF01217 | 0.546 |
TRG_DiLeu_BaEn_1 | 342 | 347 | PF01217 | 0.518 |
TRG_DiLeu_LyEn_5 | 28 | 33 | PF01217 | 0.453 |
TRG_ENDOCYTIC_2 | 126 | 129 | PF00928 | 0.531 |
TRG_ENDOCYTIC_2 | 163 | 166 | PF00928 | 0.503 |
TRG_ENDOCYTIC_2 | 195 | 198 | PF00928 | 0.503 |
TRG_ENDOCYTIC_2 | 301 | 304 | PF00928 | 0.503 |
TRG_ENDOCYTIC_2 | 36 | 39 | PF00928 | 0.503 |
TRG_ENDOCYTIC_2 | 7 | 10 | PF00928 | 0.434 |
TRG_ER_diArg_1 | 216 | 218 | PF00400 | 0.457 |
TRG_ER_diArg_1 | 575 | 577 | PF00400 | 0.480 |
TRG_NES_CRM1_1 | 640 | 651 | PF08389 | 0.478 |
TRG_NLS_Bipartite_1 | 186 | 205 | PF00514 | 0.503 |
TRG_NLS_MonoExtC_3 | 200 | 205 | PF00514 | 0.503 |
TRG_NLS_MonoExtC_3 | 576 | 581 | PF00514 | 0.443 |
TRG_NLS_MonoExtN_4 | 576 | 581 | PF00514 | 0.458 |
TRG_Pf-PMV_PEXEL_1 | 24 | 28 | PF00026 | 0.519 |
TRG_Pf-PMV_PEXEL_1 | 243 | 247 | PF00026 | 0.405 |
TRG_Pf-PMV_PEXEL_1 | 94 | 98 | PF00026 | 0.370 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3B3 | Leptomonas seymouri | 82% | 100% |
A0A0S4JQB1 | Bodo saltans | 61% | 76% |
A0A1X0NNR8 | Trypanosomatidae | 63% | 98% |
A0A422NFL4 | Trypanosoma rangeli | 61% | 99% |
A4H7V7 | Leishmania braziliensis | 89% | 100% |
A4HW83 | Leishmania infantum | 100% | 100% |
C9ZST4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 60% | 98% |
E9APY5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
F4HWL4 | Arabidopsis thaliana | 37% | 91% |
Q4QFJ7 | Leishmania major | 97% | 100% |
V5AW05 | Trypanosoma cruzi | 61% | 99% |