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: 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: A4H839
Term | Name | Level | Count |
---|---|---|---|
GO:0006450 | regulation of translational fidelity | 3 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0065008 | regulation of biological quality | 2 | 1 |
GO:0006082 | organic acid metabolic process | 3 | 4 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 4 |
GO:0006399 | tRNA metabolic process | 7 | 4 |
GO:0006520 | amino acid metabolic process | 3 | 4 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 4 |
GO:0006807 | nitrogen compound metabolic process | 2 | 4 |
GO:0008152 | metabolic process | 1 | 4 |
GO:0009987 | cellular process | 1 | 4 |
GO:0016070 | RNA metabolic process | 5 | 4 |
GO:0019752 | carboxylic acid metabolic process | 5 | 4 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 4 |
GO:0034660 | ncRNA metabolic process | 6 | 4 |
GO:0043038 | amino acid activation | 4 | 4 |
GO:0043039 | tRNA aminoacylation | 5 | 4 |
GO:0043170 | macromolecule metabolic process | 3 | 4 |
GO:0043436 | oxoacid metabolic process | 4 | 4 |
GO:0044237 | cellular metabolic process | 2 | 4 |
GO:0044238 | primary metabolic process | 2 | 4 |
GO:0044281 | small molecule metabolic process | 2 | 4 |
GO:0046483 | heterocycle metabolic process | 3 | 4 |
GO:0071704 | organic substance metabolic process | 2 | 4 |
GO:0090304 | nucleic acid metabolic process | 4 | 4 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 4 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 4 |
GO:0006418 | tRNA aminoacylation for protein translation | 6 | 3 |
GO:0006419 | alanyl-tRNA aminoacylation | 7 | 3 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0036094 | small molecule binding | 2 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
GO:0002161 | aminoacyl-tRNA editing activity | 5 | 1 |
GO:0002196 | Ser-tRNA(Ala) hydrolase activity | 6 | 1 |
GO:0003824 | catalytic activity | 1 | 5 |
GO:0016787 | hydrolase activity | 2 | 1 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 1 |
GO:0052689 | carboxylic ester hydrolase activity | 4 | 1 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 5 |
GO:0140101 | catalytic activity, acting on a tRNA | 4 | 5 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 5 |
GO:0004812 | aminoacyl-tRNA ligase activity | 4 | 4 |
GO:0005524 | ATP binding | 5 | 4 |
GO:0016874 | ligase activity | 2 | 4 |
GO:0016875 | ligase activity, forming carbon-oxygen bonds | 3 | 4 |
GO:0017076 | purine nucleotide binding | 4 | 4 |
GO:0030554 | adenyl nucleotide binding | 5 | 4 |
GO:0032553 | ribonucleotide binding | 3 | 4 |
GO:0032555 | purine ribonucleotide binding | 4 | 4 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 4 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 4 |
GO:0043167 | ion binding | 2 | 4 |
GO:0043168 | anion binding | 3 | 4 |
GO:0097367 | carbohydrate derivative binding | 2 | 4 |
GO:0004813 | alanine-tRNA ligase activity | 5 | 3 |
GO:0003676 | nucleic acid binding | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 48 | 52 | PF00656 | 0.462 |
CLV_NRD_NRD_1 | 10 | 12 | PF00675 | 0.307 |
CLV_NRD_NRD_1 | 107 | 109 | PF00675 | 0.402 |
CLV_NRD_NRD_1 | 135 | 137 | PF00675 | 0.381 |
CLV_NRD_NRD_1 | 239 | 241 | PF00675 | 0.583 |
CLV_NRD_NRD_1 | 349 | 351 | PF00675 | 0.420 |
CLV_NRD_NRD_1 | 393 | 395 | PF00675 | 0.413 |
CLV_PCSK_KEX2_1 | 10 | 12 | PF00082 | 0.307 |
CLV_PCSK_KEX2_1 | 107 | 109 | PF00082 | 0.402 |
CLV_PCSK_KEX2_1 | 135 | 137 | PF00082 | 0.381 |
CLV_PCSK_KEX2_1 | 239 | 241 | PF00082 | 0.592 |
CLV_PCSK_KEX2_1 | 349 | 351 | PF00082 | 0.459 |
CLV_PCSK_KEX2_1 | 362 | 364 | PF00082 | 0.398 |
CLV_PCSK_KEX2_1 | 393 | 395 | PF00082 | 0.413 |
CLV_PCSK_PC1ET2_1 | 362 | 364 | PF00082 | 0.477 |
CLV_PCSK_SKI1_1 | 24 | 28 | PF00082 | 0.434 |
CLV_PCSK_SKI1_1 | 359 | 363 | PF00082 | 0.405 |
CLV_PCSK_SKI1_1 | 44 | 48 | PF00082 | 0.405 |
CLV_PCSK_SKI1_1 | 466 | 470 | PF00082 | 0.334 |
DOC_CYCLIN_yCln2_LP_2 | 115 | 121 | PF00134 | 0.493 |
DOC_CYCLIN_yCln2_LP_2 | 168 | 174 | PF00134 | 0.435 |
DOC_MAPK_gen_1 | 359 | 368 | PF00069 | 0.442 |
DOC_MAPK_gen_1 | 393 | 401 | PF00069 | 0.468 |
DOC_MAPK_HePTP_8 | 380 | 392 | PF00069 | 0.341 |
DOC_MAPK_MEF2A_6 | 303 | 311 | PF00069 | 0.386 |
DOC_MAPK_MEF2A_6 | 383 | 392 | PF00069 | 0.563 |
DOC_MAPK_MEF2A_6 | 393 | 401 | PF00069 | 0.501 |
DOC_PP1_RVXF_1 | 306 | 312 | PF00149 | 0.351 |
DOC_PP1_RVXF_1 | 472 | 478 | PF00149 | 0.552 |
DOC_PP2B_LxvP_1 | 159 | 162 | PF13499 | 0.497 |
DOC_USP7_MATH_1 | 162 | 166 | PF00917 | 0.412 |
DOC_USP7_MATH_1 | 181 | 185 | PF00917 | 0.417 |
DOC_USP7_MATH_1 | 244 | 248 | PF00917 | 0.652 |
DOC_USP7_MATH_1 | 275 | 279 | PF00917 | 0.529 |
DOC_USP7_MATH_1 | 378 | 382 | PF00917 | 0.432 |
DOC_USP7_MATH_2 | 340 | 346 | PF00917 | 0.312 |
DOC_USP7_UBL2_3 | 462 | 466 | PF12436 | 0.553 |
DOC_USP7_UBL2_3 | 480 | 484 | PF12436 | 0.446 |
DOC_WW_Pin1_4 | 114 | 119 | PF00397 | 0.448 |
DOC_WW_Pin1_4 | 185 | 190 | PF00397 | 0.490 |
DOC_WW_Pin1_4 | 217 | 222 | PF00397 | 0.399 |
DOC_WW_Pin1_4 | 447 | 452 | PF00397 | 0.556 |
LIG_14-3-3_CanoR_1 | 269 | 274 | PF00244 | 0.422 |
LIG_14-3-3_CanoR_1 | 319 | 325 | PF00244 | 0.315 |
LIG_14-3-3_CanoR_1 | 350 | 360 | PF00244 | 0.510 |
LIG_14-3-3_CanoR_1 | 363 | 367 | PF00244 | 0.471 |
LIG_14-3-3_CanoR_1 | 427 | 434 | PF00244 | 0.657 |
LIG_Actin_WH2_2 | 402 | 417 | PF00022 | 0.531 |
LIG_BIR_III_4 | 410 | 414 | PF00653 | 0.502 |
LIG_BRCT_BRCA1_1 | 62 | 66 | PF00533 | 0.366 |
LIG_CaM_NSCaTE_8 | 364 | 371 | PF13499 | 0.281 |
LIG_FHA_1 | 148 | 154 | PF00498 | 0.421 |
LIG_FHA_1 | 156 | 162 | PF00498 | 0.413 |
LIG_FHA_1 | 25 | 31 | PF00498 | 0.426 |
LIG_FHA_1 | 263 | 269 | PF00498 | 0.460 |
LIG_FHA_1 | 352 | 358 | PF00498 | 0.445 |
LIG_FHA_1 | 363 | 369 | PF00498 | 0.411 |
LIG_FHA_1 | 385 | 391 | PF00498 | 0.546 |
LIG_FHA_1 | 428 | 434 | PF00498 | 0.515 |
LIG_FHA_1 | 76 | 82 | PF00498 | 0.523 |
LIG_FHA_1 | 95 | 101 | PF00498 | 0.420 |
LIG_FHA_2 | 286 | 292 | PF00498 | 0.425 |
LIG_FHA_2 | 444 | 450 | PF00498 | 0.512 |
LIG_FHA_2 | 480 | 486 | PF00498 | 0.533 |
LIG_LIR_Gen_1 | 169 | 179 | PF02991 | 0.399 |
LIG_LIR_Gen_1 | 225 | 233 | PF02991 | 0.471 |
LIG_LIR_Gen_1 | 341 | 347 | PF02991 | 0.487 |
LIG_LIR_Gen_1 | 400 | 409 | PF02991 | 0.395 |
LIG_LIR_Gen_1 | 485 | 493 | PF02991 | 0.508 |
LIG_LIR_Nem_3 | 169 | 175 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 188 | 193 | PF02991 | 0.354 |
LIG_LIR_Nem_3 | 225 | 230 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 341 | 346 | PF02991 | 0.515 |
LIG_LIR_Nem_3 | 400 | 405 | PF02991 | 0.376 |
LIG_LIR_Nem_3 | 485 | 489 | PF02991 | 0.508 |
LIG_LIR_Nem_3 | 75 | 79 | PF02991 | 0.374 |
LIG_LIR_Nem_3 | 8 | 12 | PF02991 | 0.515 |
LIG_PCNA_yPIPBox_3 | 146 | 155 | PF02747 | 0.415 |
LIG_SH2_CRK | 172 | 176 | PF00017 | 0.467 |
LIG_SH2_CRK | 56 | 60 | PF00017 | 0.431 |
LIG_SH2_STAP1 | 56 | 60 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 172 | 175 | PF00017 | 0.401 |
LIG_SH2_STAT5 | 193 | 196 | PF00017 | 0.487 |
LIG_SH2_STAT5 | 296 | 299 | PF00017 | 0.477 |
LIG_SH2_STAT5 | 310 | 313 | PF00017 | 0.329 |
LIG_SH3_3 | 128 | 134 | PF00018 | 0.437 |
LIG_SH3_3 | 183 | 189 | PF00018 | 0.509 |
LIG_SH3_3 | 261 | 267 | PF00018 | 0.506 |
LIG_SH3_3 | 385 | 391 | PF00018 | 0.544 |
LIG_SUMO_SIM_anti_2 | 341 | 348 | PF11976 | 0.536 |
LIG_SUMO_SIM_par_1 | 364 | 370 | PF11976 | 0.532 |
LIG_SUMO_SIM_par_1 | 416 | 421 | PF11976 | 0.467 |
LIG_SUMO_SIM_par_1 | 99 | 104 | PF11976 | 0.551 |
LIG_Vh1_VBS_1 | 418 | 436 | PF01044 | 0.350 |
MOD_CK1_1 | 117 | 123 | PF00069 | 0.418 |
MOD_CK1_1 | 338 | 344 | PF00069 | 0.553 |
MOD_CK1_1 | 351 | 357 | PF00069 | 0.360 |
MOD_CK1_1 | 382 | 388 | PF00069 | 0.466 |
MOD_CK1_1 | 91 | 97 | PF00069 | 0.456 |
MOD_CK2_1 | 285 | 291 | PF00069 | 0.428 |
MOD_CK2_1 | 443 | 449 | PF00069 | 0.475 |
MOD_CK2_1 | 479 | 485 | PF00069 | 0.498 |
MOD_GlcNHglycan | 334 | 338 | PF01048 | 0.488 |
MOD_GlcNHglycan | 369 | 372 | PF01048 | 0.377 |
MOD_GlcNHglycan | 384 | 387 | PF01048 | 0.513 |
MOD_GlcNHglycan | 420 | 423 | PF01048 | 0.428 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.685 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.397 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.406 |
MOD_GSK3_1 | 181 | 188 | PF00069 | 0.476 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.354 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.401 |
MOD_GSK3_1 | 338 | 345 | PF00069 | 0.545 |
MOD_GSK3_1 | 378 | 385 | PF00069 | 0.610 |
MOD_GSK3_1 | 418 | 425 | PF00069 | 0.337 |
MOD_GSK3_1 | 429 | 436 | PF00069 | 0.524 |
MOD_GSK3_1 | 443 | 450 | PF00069 | 0.516 |
MOD_GSK3_1 | 89 | 96 | PF00069 | 0.713 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.523 |
MOD_NEK2_1 | 26 | 31 | PF00069 | 0.440 |
MOD_NEK2_1 | 335 | 340 | PF00069 | 0.490 |
MOD_NEK2_1 | 409 | 414 | PF00069 | 0.288 |
MOD_NEK2_1 | 60 | 65 | PF00069 | 0.351 |
MOD_NEK2_2 | 461 | 466 | PF00069 | 0.563 |
MOD_NEK2_2 | 479 | 484 | PF00069 | 0.487 |
MOD_PK_1 | 45 | 51 | PF00069 | 0.475 |
MOD_PKA_1 | 198 | 204 | PF00069 | 0.493 |
MOD_PKA_1 | 362 | 368 | PF00069 | 0.520 |
MOD_PKA_2 | 18 | 24 | PF00069 | 0.339 |
MOD_PKA_2 | 338 | 344 | PF00069 | 0.545 |
MOD_PKA_2 | 348 | 354 | PF00069 | 0.532 |
MOD_PKA_2 | 362 | 368 | PF00069 | 0.520 |
MOD_PKA_2 | 382 | 388 | PF00069 | 0.379 |
MOD_PKA_2 | 426 | 432 | PF00069 | 0.648 |
MOD_Plk_4 | 18 | 24 | PF00069 | 0.404 |
MOD_Plk_4 | 26 | 32 | PF00069 | 0.401 |
MOD_Plk_4 | 302 | 308 | PF00069 | 0.522 |
MOD_Plk_4 | 320 | 326 | PF00069 | 0.270 |
MOD_Plk_4 | 342 | 348 | PF00069 | 0.565 |
MOD_Plk_4 | 384 | 390 | PF00069 | 0.590 |
MOD_Plk_4 | 429 | 435 | PF00069 | 0.435 |
MOD_Plk_4 | 60 | 66 | PF00069 | 0.350 |
MOD_ProDKin_1 | 114 | 120 | PF00069 | 0.454 |
MOD_ProDKin_1 | 185 | 191 | PF00069 | 0.489 |
MOD_ProDKin_1 | 217 | 223 | PF00069 | 0.403 |
MOD_ProDKin_1 | 447 | 453 | PF00069 | 0.553 |
MOD_SUMO_for_1 | 206 | 209 | PF00179 | 0.482 |
MOD_SUMO_rev_2 | 85 | 89 | PF00179 | 0.481 |
TRG_DiLeu_BaEn_1 | 485 | 490 | PF01217 | 0.505 |
TRG_DiLeu_BaLyEn_6 | 96 | 101 | PF01217 | 0.369 |
TRG_ENDOCYTIC_2 | 172 | 175 | PF00928 | 0.385 |
TRG_ENDOCYTIC_2 | 56 | 59 | PF00928 | 0.404 |
TRG_ER_diArg_1 | 106 | 108 | PF00400 | 0.446 |
TRG_ER_diArg_1 | 134 | 136 | PF00400 | 0.411 |
TRG_ER_diArg_1 | 255 | 258 | PF00400 | 0.616 |
TRG_ER_diArg_1 | 392 | 394 | PF00400 | 0.405 |
TRG_ER_diArg_1 | 405 | 408 | PF00400 | 0.396 |
TRG_ER_diArg_1 | 9 | 11 | PF00400 | 0.550 |
TRG_Pf-PMV_PEXEL_1 | 258 | 262 | PF00026 | 0.575 |
TRG_Pf-PMV_PEXEL_1 | 329 | 334 | PF00026 | 0.484 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1V1 | Leptomonas seymouri | 70% | 100% |
A0A0S4J566 | Bodo saltans | 40% | 100% |
A0A1X0NTW0 | Trypanosomatidae | 42% | 100% |
A0A3S7WTE7 | Leishmania donovani | 82% | 100% |
A0A422NRG2 | Trypanosoma rangeli | 42% | 100% |
A4HWG6 | Leishmania infantum | 82% | 100% |
C9ZXY1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
E9AQ67 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
O57734 | Pyrococcus horikoshii (strain ATCC 700860 / DSM 12428 / JCM 9974 / NBRC 100139 / OT-3) | 23% | 100% |
P53960 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 32% | 100% |
Q08B09 | Xenopus laevis | 29% | 100% |
Q4QFB6 | Leishmania major | 83% | 100% |
Q6DEJ5 | Danio rerio | 30% | 100% |
Q7ZYJ9 | Xenopus laevis | 29% | 100% |
Q9BTE6 | Homo sapiens | 29% | 100% |