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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
Related structures:
AlphaFold database: A4H5S3
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006399 | tRNA metabolic process | 7 | 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:0009058 | biosynthetic process | 2 | 12 |
GO:0009059 | macromolecule biosynthetic process | 4 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016070 | RNA metabolic process | 5 | 12 |
GO:0018130 | heterocycle biosynthetic process | 4 | 12 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 12 |
GO:0032774 | RNA biosynthetic process | 5 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 12 |
GO:0034660 | ncRNA metabolic process | 6 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044249 | cellular biosynthetic process | 3 | 12 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 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:0097056 | obsolete selenocysteinyl-tRNA(Sec) biosynthetic process | 6 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 12 |
GO:1901576 | organic substance biosynthetic process | 3 | 12 |
GO:0001514 | selenocysteine incorporation | 7 | 1 |
GO:0006414 | translational elongation | 5 | 1 |
GO:0006417 | regulation of translation | 6 | 1 |
GO:0006451 | translational readthrough | 6 | 1 |
GO:0009889 | regulation of biosynthetic process | 4 | 1 |
GO:0010468 | regulation of gene expression | 5 | 1 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 1 |
GO:0010608 | post-transcriptional regulation of gene expression | 6 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 1 |
GO:0034248 | regulation of amide metabolic process | 5 | 1 |
GO:0034645 | obsolete cellular macromolecule biosynthetic process | 4 | 9 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 9 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
GO:0051246 | regulation of protein metabolic process | 5 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:2000112 | obsolete regulation of cellular macromolecule biosynthetic process | 6 | 1 |
GO:0006412 | translation | 4 | 8 |
GO:0006518 | peptide metabolic process | 4 | 8 |
GO:0019538 | protein metabolic process | 3 | 8 |
GO:0043043 | peptide biosynthetic process | 5 | 8 |
GO:0043603 | amide metabolic process | 3 | 8 |
GO:0043604 | amide biosynthetic process | 4 | 8 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 8 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000049 | tRNA binding | 5 | 12 |
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003723 | RNA binding | 4 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016785 | selenotransferase activity | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0098621 | phosphoseryl-selenocysteinyl-tRNA selenium transferase activity | 4 | 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:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 406 | 410 | PF00656 | 0.446 |
CLV_NRD_NRD_1 | 402 | 404 | PF00675 | 0.289 |
CLV_NRD_NRD_1 | 473 | 475 | PF00675 | 0.294 |
CLV_PCSK_KEX2_1 | 402 | 404 | PF00082 | 0.259 |
CLV_PCSK_KEX2_1 | 473 | 475 | PF00082 | 0.292 |
CLV_PCSK_SKI1_1 | 229 | 233 | PF00082 | 0.722 |
CLV_PCSK_SKI1_1 | 279 | 283 | PF00082 | 0.309 |
CLV_PCSK_SKI1_1 | 298 | 302 | PF00082 | 0.377 |
CLV_PCSK_SKI1_1 | 34 | 38 | PF00082 | 0.466 |
CLV_PCSK_SKI1_1 | 403 | 407 | PF00082 | 0.246 |
CLV_PCSK_SKI1_1 | 426 | 430 | PF00082 | 0.203 |
CLV_PCSK_SKI1_1 | 589 | 593 | PF00082 | 0.270 |
CLV_PCSK_SKI1_1 | 59 | 63 | PF00082 | 0.522 |
CLV_PCSK_SKI1_1 | 88 | 92 | PF00082 | 0.401 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.474 |
DEG_SCF_FBW7_1 | 590 | 596 | PF00400 | 0.446 |
DEG_SCF_TRCP1_1 | 314 | 319 | PF00400 | 0.441 |
DEG_SPOP_SBC_1 | 328 | 332 | PF00917 | 0.621 |
DEG_SPOP_SBC_1 | 362 | 366 | PF00917 | 0.410 |
DOC_CKS1_1 | 590 | 595 | PF01111 | 0.446 |
DOC_CYCLIN_RxL_1 | 108 | 118 | PF00134 | 0.442 |
DOC_MAPK_DCC_7 | 16 | 26 | PF00069 | 0.464 |
DOC_MAPK_gen_1 | 487 | 496 | PF00069 | 0.508 |
DOC_MAPK_gen_1 | 499 | 507 | PF00069 | 0.417 |
DOC_MAPK_HePTP_8 | 168 | 180 | PF00069 | 0.442 |
DOC_MAPK_MEF2A_6 | 171 | 180 | PF00069 | 0.442 |
DOC_MAPK_MEF2A_6 | 455 | 464 | PF00069 | 0.424 |
DOC_MAPK_MEF2A_6 | 533 | 542 | PF00069 | 0.470 |
DOC_MAPK_RevD_3 | 387 | 403 | PF00069 | 0.446 |
DOC_PP1_RVXF_1 | 267 | 274 | PF00149 | 0.309 |
DOC_PP1_RVXF_1 | 414 | 420 | PF00149 | 0.446 |
DOC_PP2B_PxIxI_1 | 21 | 27 | PF00149 | 0.458 |
DOC_PP4_FxxP_1 | 428 | 431 | PF00568 | 0.400 |
DOC_USP7_MATH_1 | 163 | 167 | PF00917 | 0.400 |
DOC_USP7_MATH_1 | 328 | 332 | PF00917 | 0.662 |
DOC_USP7_MATH_1 | 52 | 56 | PF00917 | 0.428 |
DOC_USP7_MATH_1 | 550 | 554 | PF00917 | 0.446 |
DOC_USP7_MATH_1 | 593 | 597 | PF00917 | 0.499 |
DOC_USP7_UBL2_3 | 279 | 283 | PF12436 | 0.302 |
DOC_WW_Pin1_4 | 324 | 329 | PF00397 | 0.742 |
DOC_WW_Pin1_4 | 456 | 461 | PF00397 | 0.410 |
DOC_WW_Pin1_4 | 47 | 52 | PF00397 | 0.754 |
DOC_WW_Pin1_4 | 589 | 594 | PF00397 | 0.446 |
LIG_14-3-3_CanoR_1 | 2 | 12 | PF00244 | 0.471 |
LIG_14-3-3_CanoR_1 | 259 | 265 | PF00244 | 0.541 |
LIG_14-3-3_CanoR_1 | 455 | 459 | PF00244 | 0.430 |
LIG_14-3-3_CanoR_1 | 474 | 480 | PF00244 | 0.542 |
LIG_14-3-3_CanoR_1 | 582 | 586 | PF00244 | 0.469 |
LIG_Actin_WH2_2 | 194 | 210 | PF00022 | 0.442 |
LIG_BIR_III_4 | 286 | 290 | PF00653 | 0.451 |
LIG_BRCT_BRCA1_1 | 334 | 338 | PF00533 | 0.489 |
LIG_FAT_LD_1 | 635 | 643 | PF03623 | 0.434 |
LIG_FHA_1 | 103 | 109 | PF00498 | 0.271 |
LIG_FHA_1 | 145 | 151 | PF00498 | 0.496 |
LIG_FHA_1 | 171 | 177 | PF00498 | 0.479 |
LIG_FHA_1 | 200 | 206 | PF00498 | 0.418 |
LIG_FHA_1 | 213 | 219 | PF00498 | 0.323 |
LIG_FHA_1 | 328 | 334 | PF00498 | 0.439 |
LIG_FHA_1 | 375 | 381 | PF00498 | 0.514 |
LIG_FHA_1 | 81 | 87 | PF00498 | 0.496 |
LIG_FHA_2 | 211 | 217 | PF00498 | 0.538 |
LIG_FHA_2 | 253 | 259 | PF00498 | 0.619 |
LIG_FHA_2 | 404 | 410 | PF00498 | 0.446 |
LIG_FHA_2 | 517 | 523 | PF00498 | 0.366 |
LIG_LIR_Apic_2 | 425 | 431 | PF02991 | 0.400 |
LIG_LIR_Apic_2 | 544 | 548 | PF02991 | 0.344 |
LIG_LIR_Apic_2 | 644 | 649 | PF02991 | 0.429 |
LIG_LIR_Gen_1 | 69 | 80 | PF02991 | 0.278 |
LIG_LIR_Nem_3 | 605 | 609 | PF02991 | 0.416 |
LIG_PCNA_PIPBox_1 | 458 | 467 | PF02747 | 0.446 |
LIG_PCNA_yPIPBox_3 | 171 | 181 | PF02747 | 0.445 |
LIG_PDZ_Class_2 | 645 | 650 | PF00595 | 0.347 |
LIG_Pex14_1 | 480 | 484 | PF04695 | 0.410 |
LIG_PTB_Apo_2 | 391 | 398 | PF02174 | 0.403 |
LIG_PTB_Apo_2 | 478 | 485 | PF02174 | 0.344 |
LIG_PTB_Phospho_1 | 391 | 397 | PF10480 | 0.403 |
LIG_PTB_Phospho_1 | 478 | 484 | PF10480 | 0.344 |
LIG_SH2_CRK | 545 | 549 | PF00017 | 0.446 |
LIG_SH2_STAP1 | 516 | 520 | PF00017 | 0.430 |
LIG_SH2_STAT3 | 397 | 400 | PF00017 | 0.400 |
LIG_SH2_STAT5 | 270 | 273 | PF00017 | 0.295 |
LIG_SH2_STAT5 | 383 | 386 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 391 | 394 | PF00017 | 0.400 |
LIG_SH2_STAT5 | 72 | 75 | PF00017 | 0.398 |
LIG_SH3_3 | 190 | 196 | PF00018 | 0.424 |
LIG_SH3_3 | 259 | 265 | PF00018 | 0.597 |
LIG_SH3_3 | 268 | 274 | PF00018 | 0.359 |
LIG_SH3_3 | 288 | 294 | PF00018 | 0.379 |
LIG_SH3_3 | 296 | 302 | PF00018 | 0.502 |
LIG_SH3_3 | 350 | 356 | PF00018 | 0.424 |
LIG_SH3_3 | 368 | 374 | PF00018 | 0.400 |
LIG_SH3_3 | 384 | 390 | PF00018 | 0.402 |
LIG_SH3_3 | 517 | 523 | PF00018 | 0.476 |
LIG_SH3_3 | 582 | 588 | PF00018 | 0.412 |
LIG_SH3_3 | 592 | 598 | PF00018 | 0.435 |
LIG_SH3_3 | 614 | 620 | PF00018 | 0.442 |
LIG_Sin3_3 | 190 | 197 | PF02671 | 0.446 |
LIG_SUMO_SIM_anti_2 | 105 | 110 | PF11976 | 0.219 |
LIG_SUMO_SIM_anti_2 | 202 | 207 | PF11976 | 0.410 |
LIG_SUMO_SIM_anti_2 | 503 | 512 | PF11976 | 0.503 |
LIG_SUMO_SIM_par_1 | 173 | 179 | PF11976 | 0.503 |
LIG_SUMO_SIM_par_1 | 503 | 512 | PF11976 | 0.503 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.556 |
MOD_CK1_1 | 324 | 330 | PF00069 | 0.669 |
MOD_CK1_1 | 331 | 337 | PF00069 | 0.546 |
MOD_CK1_1 | 364 | 370 | PF00069 | 0.424 |
MOD_CK1_1 | 50 | 56 | PF00069 | 0.658 |
MOD_CK1_1 | 583 | 589 | PF00069 | 0.442 |
MOD_CK1_1 | 596 | 602 | PF00069 | 0.442 |
MOD_CK1_1 | 79 | 85 | PF00069 | 0.542 |
MOD_CK2_1 | 210 | 216 | PF00069 | 0.479 |
MOD_CK2_1 | 260 | 266 | PF00069 | 0.389 |
MOD_CK2_1 | 437 | 443 | PF00069 | 0.481 |
MOD_CK2_1 | 516 | 522 | PF00069 | 0.344 |
MOD_CK2_1 | 628 | 634 | PF00069 | 0.443 |
MOD_Cter_Amidation | 471 | 474 | PF01082 | 0.325 |
MOD_DYRK1A_RPxSP_1 | 589 | 593 | PF00069 | 0.446 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.335 |
MOD_GlcNHglycan | 152 | 155 | PF01048 | 0.138 |
MOD_GlcNHglycan | 239 | 242 | PF01048 | 0.573 |
MOD_GlcNHglycan | 262 | 265 | PF01048 | 0.498 |
MOD_GlcNHglycan | 305 | 308 | PF01048 | 0.666 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.691 |
MOD_GlcNHglycan | 422 | 425 | PF01048 | 0.224 |
MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.645 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.432 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.528 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.552 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.624 |
MOD_GSK3_1 | 310 | 317 | PF00069 | 0.724 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.686 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.471 |
MOD_GSK3_1 | 345 | 352 | PF00069 | 0.395 |
MOD_GSK3_1 | 432 | 439 | PF00069 | 0.506 |
MOD_GSK3_1 | 534 | 541 | PF00069 | 0.410 |
MOD_GSK3_1 | 589 | 596 | PF00069 | 0.458 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.430 |
MOD_LATS_1 | 14 | 20 | PF00433 | 0.469 |
MOD_N-GLC_1 | 236 | 241 | PF02516 | 0.453 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.474 |
MOD_NEK2_1 | 115 | 120 | PF00069 | 0.258 |
MOD_NEK2_1 | 138 | 143 | PF00069 | 0.474 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.461 |
MOD_NEK2_1 | 227 | 232 | PF00069 | 0.622 |
MOD_NEK2_1 | 236 | 241 | PF00069 | 0.613 |
MOD_NEK2_1 | 303 | 308 | PF00069 | 0.542 |
MOD_NEK2_1 | 333 | 338 | PF00069 | 0.384 |
MOD_NEK2_1 | 363 | 368 | PF00069 | 0.400 |
MOD_NEK2_1 | 464 | 469 | PF00069 | 0.454 |
MOD_NEK2_1 | 580 | 585 | PF00069 | 0.442 |
MOD_NEK2_1 | 80 | 85 | PF00069 | 0.442 |
MOD_OFUCOSY | 361 | 368 | PF10250 | 0.200 |
MOD_PIKK_1 | 28 | 34 | PF00454 | 0.444 |
MOD_PIKK_1 | 354 | 360 | PF00454 | 0.446 |
MOD_PKA_2 | 1 | 7 | PF00069 | 0.472 |
MOD_PKA_2 | 454 | 460 | PF00069 | 0.404 |
MOD_PKA_2 | 581 | 587 | PF00069 | 0.354 |
MOD_PKA_2 | 76 | 82 | PF00069 | 0.507 |
MOD_Plk_1 | 102 | 108 | PF00069 | 0.535 |
MOD_Plk_1 | 257 | 263 | PF00069 | 0.592 |
MOD_Plk_1 | 374 | 380 | PF00069 | 0.503 |
MOD_Plk_1 | 516 | 522 | PF00069 | 0.533 |
MOD_Plk_1 | 534 | 540 | PF00069 | 0.402 |
MOD_Plk_1 | 57 | 63 | PF00069 | 0.475 |
MOD_Plk_4 | 164 | 170 | PF00069 | 0.400 |
MOD_Plk_4 | 333 | 339 | PF00069 | 0.521 |
MOD_Plk_4 | 432 | 438 | PF00069 | 0.470 |
MOD_Plk_4 | 596 | 602 | PF00069 | 0.395 |
MOD_ProDKin_1 | 324 | 330 | PF00069 | 0.739 |
MOD_ProDKin_1 | 456 | 462 | PF00069 | 0.410 |
MOD_ProDKin_1 | 47 | 53 | PF00069 | 0.752 |
MOD_ProDKin_1 | 589 | 595 | PF00069 | 0.446 |
TRG_DiLeu_BaEn_1 | 634 | 639 | PF01217 | 0.467 |
TRG_DiLeu_BaLyEn_6 | 486 | 491 | PF01217 | 0.446 |
TRG_DiLeu_BaLyEn_6 | 617 | 622 | PF01217 | 0.442 |
TRG_ENDOCYTIC_2 | 72 | 75 | PF00928 | 0.415 |
TRG_ER_diArg_1 | 139 | 142 | PF00400 | 0.503 |
TRG_ER_diArg_1 | 402 | 404 | PF00400 | 0.494 |
TRG_ER_diArg_1 | 484 | 487 | PF00400 | 0.407 |
TRG_Pf-PMV_PEXEL_1 | 477 | 482 | PF00026 | 0.277 |
TRG_Pf-PMV_PEXEL_1 | 489 | 493 | PF00026 | 0.261 |
TRG_Pf-PMV_PEXEL_1 | 574 | 579 | PF00026 | 0.297 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IGI4 | Leptomonas seymouri | 64% | 100% |
A0A0S4KH93 | Bodo saltans | 40% | 100% |
A0A1X0NN47 | Trypanosomatidae | 46% | 96% |
A0A3R7N0G5 | Trypanosoma rangeli | 52% | 100% |
A0A3S7WQS5 | Leishmania donovani | 84% | 100% |
A4HU16 | Leishmania infantum | 84% | 100% |
D0A9I4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 52% | 100% |
E9AMU7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
Q18953 | Caenorhabditis elegans | 32% | 100% |
Q28EN2 | Xenopus tropicalis | 35% | 100% |
Q4QHS9 | Leishmania major | 83% | 100% |
Q54VQ6 | Dictyostelium discoideum | 34% | 100% |
Q5RAK7 | Pongo abelii | 35% | 100% |
Q61JN8 | Caenorhabditis briggsae | 32% | 100% |
Q6P6M7 | Mus musculus | 34% | 100% |
Q803A7 | Danio rerio | 35% | 100% |
Q9HD40 | Homo sapiens | 35% | 100% |
V5BBE8 | Trypanosoma cruzi | 52% | 100% |