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:0005840 | ribosome | 5 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043228 | non-membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:1990904 | ribonucleoprotein complex | 2 | 1 |
Related structures:
AlphaFold database: A0A3S7X464
Term | Name | Level | Count |
---|---|---|---|
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:0008152 | metabolic process | 1 | 1 |
GO:0009058 | biosynthetic process | 2 | 1 |
GO:0009059 | macromolecule biosynthetic process | 4 | 1 |
GO:0009889 | regulation of biosynthetic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 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 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044249 | cellular biosynthetic process | 3 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
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:0071704 | organic substance metabolic process | 2 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:1901576 | organic substance biosynthetic process | 3 | 1 |
GO:2000112 | obsolete regulation of cellular macromolecule biosynthetic process | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 11 |
GO:0003723 | RNA binding | 4 | 11 |
GO:0003729 | mRNA binding | 5 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0035368 | selenocysteine insertion sequence binding | 6 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
GO:0003730 | mRNA 3'-UTR binding | 6 | 1 |
GO:0043021 | ribonucleoprotein complex binding | 3 | 1 |
GO:0044877 | protein-containing complex binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 248 | 252 | PF00656 | 0.743 |
CLV_C14_Caspase3-7 | 312 | 316 | PF00656 | 0.449 |
CLV_NRD_NRD_1 | 158 | 160 | PF00675 | 0.665 |
CLV_NRD_NRD_1 | 199 | 201 | PF00675 | 0.489 |
CLV_NRD_NRD_1 | 209 | 211 | PF00675 | 0.418 |
CLV_NRD_NRD_1 | 455 | 457 | PF00675 | 0.558 |
CLV_PCSK_FUR_1 | 196 | 200 | PF00082 | 0.507 |
CLV_PCSK_FUR_1 | 207 | 211 | PF00082 | 0.523 |
CLV_PCSK_KEX2_1 | 158 | 160 | PF00082 | 0.654 |
CLV_PCSK_KEX2_1 | 198 | 200 | PF00082 | 0.443 |
CLV_PCSK_KEX2_1 | 209 | 211 | PF00082 | 0.341 |
CLV_PCSK_KEX2_1 | 93 | 95 | PF00082 | 0.481 |
CLV_PCSK_PC1ET2_1 | 198 | 200 | PF00082 | 0.458 |
CLV_PCSK_PC1ET2_1 | 93 | 95 | PF00082 | 0.505 |
CLV_PCSK_SKI1_1 | 210 | 214 | PF00082 | 0.459 |
CLV_PCSK_SKI1_1 | 22 | 26 | PF00082 | 0.797 |
CLV_PCSK_SKI1_1 | 338 | 342 | PF00082 | 0.547 |
CLV_PCSK_SKI1_1 | 374 | 378 | PF00082 | 0.365 |
CLV_PCSK_SKI1_1 | 399 | 403 | PF00082 | 0.482 |
CLV_PCSK_SKI1_1 | 407 | 411 | PF00082 | 0.442 |
CLV_PCSK_SKI1_1 | 457 | 461 | PF00082 | 0.577 |
CLV_PCSK_SKI1_1 | 531 | 535 | PF00082 | 0.474 |
CLV_PCSK_SKI1_1 | 542 | 546 | PF00082 | 0.417 |
DEG_APCC_DBOX_1 | 404 | 412 | PF00400 | 0.376 |
DEG_APCC_DBOX_1 | 530 | 538 | PF00400 | 0.412 |
DEG_SPOP_SBC_1 | 134 | 138 | PF00917 | 0.551 |
DEG_SPOP_SBC_1 | 28 | 32 | PF00917 | 0.609 |
DEG_SPOP_SBC_1 | 323 | 327 | PF00917 | 0.550 |
DOC_MAPK_gen_1 | 374 | 384 | PF00069 | 0.397 |
DOC_MAPK_gen_1 | 385 | 394 | PF00069 | 0.405 |
DOC_MAPK_gen_1 | 399 | 408 | PF00069 | 0.421 |
DOC_MAPK_gen_1 | 515 | 524 | PF00069 | 0.483 |
DOC_MAPK_MEF2A_6 | 402 | 410 | PF00069 | 0.467 |
DOC_PP4_FxxP_1 | 261 | 264 | PF00568 | 0.548 |
DOC_USP7_MATH_1 | 109 | 113 | PF00917 | 0.590 |
DOC_USP7_MATH_1 | 134 | 138 | PF00917 | 0.747 |
DOC_USP7_MATH_1 | 174 | 178 | PF00917 | 0.441 |
DOC_USP7_MATH_1 | 220 | 224 | PF00917 | 0.710 |
DOC_USP7_MATH_1 | 28 | 32 | PF00917 | 0.738 |
DOC_USP7_MATH_1 | 322 | 326 | PF00917 | 0.611 |
DOC_USP7_MATH_1 | 339 | 343 | PF00917 | 0.540 |
DOC_USP7_MATH_1 | 431 | 435 | PF00917 | 0.741 |
DOC_USP7_MATH_1 | 444 | 448 | PF00917 | 0.681 |
DOC_USP7_MATH_1 | 451 | 455 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 49 | 53 | PF00917 | 0.666 |
DOC_USP7_MATH_1 | 514 | 518 | PF00917 | 0.522 |
DOC_USP7_MATH_1 | 536 | 540 | PF00917 | 0.349 |
DOC_USP7_MATH_1 | 58 | 62 | PF00917 | 0.536 |
DOC_USP7_UBL2_3 | 21 | 25 | PF12436 | 0.759 |
DOC_USP7_UBL2_3 | 453 | 457 | PF12436 | 0.663 |
DOC_WW_Pin1_4 | 125 | 130 | PF00397 | 0.669 |
DOC_WW_Pin1_4 | 29 | 34 | PF00397 | 0.581 |
DOC_WW_Pin1_4 | 324 | 329 | PF00397 | 0.700 |
DOC_WW_Pin1_4 | 442 | 447 | PF00397 | 0.777 |
DOC_WW_Pin1_4 | 78 | 83 | PF00397 | 0.624 |
LIG_14-3-3_CanoR_1 | 244 | 254 | PF00244 | 0.583 |
LIG_14-3-3_CanoR_1 | 505 | 511 | PF00244 | 0.534 |
LIG_14-3-3_CanoR_1 | 542 | 552 | PF00244 | 0.413 |
LIG_BRCT_BRCA1_1 | 341 | 345 | PF00533 | 0.498 |
LIG_CaM_IQ_9 | 201 | 217 | PF13499 | 0.407 |
LIG_CaM_IQ_9 | 391 | 407 | PF13499 | 0.470 |
LIG_FHA_1 | 349 | 355 | PF00498 | 0.330 |
LIG_FHA_1 | 552 | 558 | PF00498 | 0.550 |
LIG_FHA_2 | 155 | 161 | PF00498 | 0.540 |
LIG_FHA_2 | 234 | 240 | PF00498 | 0.701 |
LIG_FHA_2 | 310 | 316 | PF00498 | 0.563 |
LIG_FHA_2 | 411 | 417 | PF00498 | 0.521 |
LIG_FHA_2 | 460 | 466 | PF00498 | 0.410 |
LIG_FHA_2 | 553 | 559 | PF00498 | 0.518 |
LIG_LIR_Apic_2 | 260 | 264 | PF02991 | 0.553 |
LIG_LIR_Gen_1 | 177 | 186 | PF02991 | 0.400 |
LIG_LIR_Gen_1 | 360 | 370 | PF02991 | 0.324 |
LIG_LIR_Nem_3 | 177 | 182 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 257 | 261 | PF02991 | 0.540 |
LIG_LIR_Nem_3 | 265 | 270 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 283 | 289 | PF02991 | 0.329 |
LIG_LIR_Nem_3 | 360 | 366 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 509 | 513 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 539 | 543 | PF02991 | 0.387 |
LIG_LYPXL_yS_3 | 286 | 289 | PF13949 | 0.464 |
LIG_MYND_3 | 119 | 123 | PF01753 | 0.515 |
LIG_PCNA_yPIPBox_3 | 290 | 303 | PF02747 | 0.344 |
LIG_PROFILIN_1 | 425 | 431 | PF00235 | 0.470 |
LIG_SH2_NCK_1 | 163 | 167 | PF00017 | 0.404 |
LIG_SH2_STAP1 | 163 | 167 | PF00017 | 0.404 |
LIG_SH2_STAP1 | 510 | 514 | PF00017 | 0.340 |
LIG_SH2_STAP1 | 540 | 544 | PF00017 | 0.342 |
LIG_SH2_STAP1 | 548 | 552 | PF00017 | 0.379 |
LIG_SH2_STAT3 | 370 | 373 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 256 | 259 | PF00017 | 0.575 |
LIG_SH2_STAT5 | 349 | 352 | PF00017 | 0.330 |
LIG_SH2_STAT5 | 390 | 393 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 543 | 546 | PF00017 | 0.521 |
LIG_SH2_STAT5 | 548 | 551 | PF00017 | 0.510 |
LIG_SH3_3 | 415 | 421 | PF00018 | 0.592 |
LIG_SH3_3 | 422 | 428 | PF00018 | 0.690 |
LIG_SH3_3 | 432 | 438 | PF00018 | 0.519 |
LIG_SH3_3 | 473 | 479 | PF00018 | 0.572 |
LIG_SUMO_SIM_par_1 | 407 | 414 | PF11976 | 0.393 |
LIG_SxIP_EBH_1 | 318 | 327 | PF03271 | 0.423 |
LIG_UBA3_1 | 365 | 371 | PF00899 | 0.454 |
LIG_WRC_WIRS_1 | 258 | 263 | PF05994 | 0.631 |
MOD_CDK_SPxxK_3 | 442 | 449 | PF00069 | 0.586 |
MOD_CK1_1 | 112 | 118 | PF00069 | 0.630 |
MOD_CK1_1 | 132 | 138 | PF00069 | 0.740 |
MOD_CK1_1 | 233 | 239 | PF00069 | 0.706 |
MOD_CK1_1 | 327 | 333 | PF00069 | 0.635 |
MOD_CK1_1 | 452 | 458 | PF00069 | 0.572 |
MOD_CK1_1 | 501 | 507 | PF00069 | 0.370 |
MOD_CK2_1 | 134 | 140 | PF00069 | 0.736 |
MOD_CK2_1 | 154 | 160 | PF00069 | 0.596 |
MOD_CK2_1 | 410 | 416 | PF00069 | 0.363 |
MOD_CK2_1 | 459 | 465 | PF00069 | 0.422 |
MOD_CK2_1 | 552 | 558 | PF00069 | 0.519 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.562 |
MOD_GlcNHglycan | 248 | 251 | PF01048 | 0.553 |
MOD_GlcNHglycan | 275 | 278 | PF01048 | 0.527 |
MOD_GlcNHglycan | 422 | 425 | PF01048 | 0.711 |
MOD_GlcNHglycan | 446 | 449 | PF01048 | 0.608 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.541 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.625 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.698 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.358 |
MOD_GSK3_1 | 226 | 233 | PF00069 | 0.686 |
MOD_GSK3_1 | 242 | 249 | PF00069 | 0.724 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.762 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.751 |
MOD_GSK3_1 | 348 | 355 | PF00069 | 0.362 |
MOD_GSK3_1 | 440 | 447 | PF00069 | 0.665 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.671 |
MOD_GSK3_1 | 54 | 61 | PF00069 | 0.607 |
MOD_GSK3_1 | 542 | 549 | PF00069 | 0.420 |
MOD_NEK2_1 | 232 | 237 | PF00069 | 0.581 |
MOD_NEK2_1 | 333 | 338 | PF00069 | 0.674 |
MOD_NEK2_1 | 340 | 345 | PF00069 | 0.526 |
MOD_NEK2_1 | 361 | 366 | PF00069 | 0.346 |
MOD_NEK2_1 | 498 | 503 | PF00069 | 0.489 |
MOD_NEK2_1 | 552 | 557 | PF00069 | 0.519 |
MOD_NEK2_1 | 9 | 14 | PF00069 | 0.696 |
MOD_NEK2_2 | 174 | 179 | PF00069 | 0.317 |
MOD_NEK2_2 | 459 | 464 | PF00069 | 0.532 |
MOD_PIKK_1 | 161 | 167 | PF00454 | 0.566 |
MOD_PIKK_1 | 333 | 339 | PF00454 | 0.574 |
MOD_PIKK_1 | 49 | 55 | PF00454 | 0.618 |
MOD_PKA_2 | 226 | 232 | PF00069 | 0.687 |
MOD_PKA_2 | 243 | 249 | PF00069 | 0.568 |
MOD_PKA_2 | 481 | 487 | PF00069 | 0.691 |
MOD_PKA_2 | 506 | 512 | PF00069 | 0.534 |
MOD_PKA_2 | 54 | 60 | PF00069 | 0.725 |
MOD_PKA_2 | 87 | 93 | PF00069 | 0.553 |
MOD_Plk_1 | 552 | 558 | PF00069 | 0.485 |
MOD_Plk_2-3 | 140 | 146 | PF00069 | 0.696 |
MOD_Plk_2-3 | 309 | 315 | PF00069 | 0.496 |
MOD_Plk_4 | 174 | 180 | PF00069 | 0.419 |
MOD_Plk_4 | 263 | 269 | PF00069 | 0.501 |
MOD_Plk_4 | 316 | 322 | PF00069 | 0.585 |
MOD_Plk_4 | 340 | 346 | PF00069 | 0.579 |
MOD_Plk_4 | 41 | 47 | PF00069 | 0.764 |
MOD_Plk_4 | 552 | 558 | PF00069 | 0.414 |
MOD_ProDKin_1 | 125 | 131 | PF00069 | 0.669 |
MOD_ProDKin_1 | 29 | 35 | PF00069 | 0.580 |
MOD_ProDKin_1 | 324 | 330 | PF00069 | 0.706 |
MOD_ProDKin_1 | 442 | 448 | PF00069 | 0.775 |
MOD_ProDKin_1 | 78 | 84 | PF00069 | 0.620 |
TRG_DiLeu_BaEn_1 | 465 | 470 | PF01217 | 0.411 |
TRG_ENDOCYTIC_2 | 179 | 182 | PF00928 | 0.370 |
TRG_ENDOCYTIC_2 | 258 | 261 | PF00928 | 0.544 |
TRG_ENDOCYTIC_2 | 286 | 289 | PF00928 | 0.464 |
TRG_ER_diArg_1 | 199 | 201 | PF00400 | 0.477 |
TRG_ER_diArg_1 | 206 | 209 | PF00400 | 0.479 |
TRG_ER_diArg_1 | 387 | 390 | PF00400 | 0.356 |
TRG_ER_diArg_1 | 405 | 408 | PF00400 | 0.205 |
TRG_ER_diArg_1 | 505 | 508 | PF00400 | 0.402 |
TRG_ER_diArg_1 | 86 | 89 | PF00400 | 0.593 |
TRG_NLS_MonoExtN_4 | 196 | 202 | PF00514 | 0.463 |
TRG_NLS_MonoExtN_4 | 453 | 460 | PF00514 | 0.539 |
TRG_Pf-PMV_PEXEL_1 | 230 | 234 | PF00026 | 0.570 |
TRG_Pf-PMV_PEXEL_1 | 374 | 378 | PF00026 | 0.441 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IMN8 | Leptomonas seymouri | 51% | 100% |
A0A1X0NJ63 | Trypanosomatidae | 27% | 88% |
A0A3R7LBH7 | Trypanosoma rangeli | 31% | 99% |
A4HJ40 | Leishmania braziliensis | 68% | 100% |
A4I6F5 | Leishmania infantum | 98% | 100% |
C9ZN70 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
E9B1L2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
Q9BHF1 | Leishmania major | 91% | 100% |
V5BDV6 | Trypanosoma cruzi | 28% | 94% |