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:0032991 | protein-containing complex | 1 | 1 |
GO:1990904 | ribonucleoprotein complex | 2 | 1 |
GO:0005840 | ribosome | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4I6F5
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 | 0.714 |
CLV_C14_Caspase3-7 | 312 | 316 | PF00656 | 0.555 |
CLV_NRD_NRD_1 | 158 | 160 | PF00675 | 0.665 |
CLV_NRD_NRD_1 | 189 | 191 | PF00675 | 0.518 |
CLV_NRD_NRD_1 | 199 | 201 | PF00675 | 0.524 |
CLV_NRD_NRD_1 | 209 | 211 | PF00675 | 0.462 |
CLV_NRD_NRD_1 | 454 | 456 | PF00675 | 0.548 |
CLV_PCSK_FUR_1 | 196 | 200 | PF00082 | 0.516 |
CLV_PCSK_FUR_1 | 207 | 211 | PF00082 | 0.528 |
CLV_PCSK_KEX2_1 | 158 | 160 | PF00082 | 0.655 |
CLV_PCSK_KEX2_1 | 189 | 191 | PF00082 | 0.502 |
CLV_PCSK_KEX2_1 | 198 | 200 | PF00082 | 0.466 |
CLV_PCSK_KEX2_1 | 209 | 211 | PF00082 | 0.378 |
CLV_PCSK_KEX2_1 | 93 | 95 | PF00082 | 0.460 |
CLV_PCSK_PC1ET2_1 | 198 | 200 | PF00082 | 0.475 |
CLV_PCSK_PC1ET2_1 | 93 | 95 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 210 | 214 | PF00082 | 0.487 |
CLV_PCSK_SKI1_1 | 22 | 26 | PF00082 | 0.760 |
CLV_PCSK_SKI1_1 | 338 | 342 | PF00082 | 0.564 |
CLV_PCSK_SKI1_1 | 374 | 378 | PF00082 | 0.372 |
CLV_PCSK_SKI1_1 | 399 | 403 | PF00082 | 0.352 |
CLV_PCSK_SKI1_1 | 407 | 411 | PF00082 | 0.349 |
CLV_PCSK_SKI1_1 | 456 | 460 | PF00082 | 0.577 |
CLV_PCSK_SKI1_1 | 530 | 534 | PF00082 | 0.477 |
CLV_PCSK_SKI1_1 | 541 | 545 | PF00082 | 0.418 |
DEG_APCC_DBOX_1 | 404 | 412 | PF00400 | 0.495 |
DEG_APCC_DBOX_1 | 529 | 537 | PF00400 | 0.419 |
DEG_SPOP_SBC_1 | 130 | 134 | PF00917 | 0.510 |
DEG_SPOP_SBC_1 | 28 | 32 | PF00917 | 0.591 |
DEG_SPOP_SBC_1 | 323 | 327 | PF00917 | 0.550 |
DOC_MAPK_gen_1 | 374 | 384 | PF00069 | 0.276 |
DOC_MAPK_gen_1 | 385 | 394 | PF00069 | 0.446 |
DOC_MAPK_gen_1 | 399 | 408 | PF00069 | 0.536 |
DOC_MAPK_gen_1 | 514 | 523 | PF00069 | 0.486 |
DOC_MAPK_MEF2A_6 | 402 | 410 | PF00069 | 0.536 |
DOC_PP4_FxxP_1 | 261 | 264 | PF00568 | 0.554 |
DOC_USP7_MATH_1 | 174 | 178 | PF00917 | 0.469 |
DOC_USP7_MATH_1 | 220 | 224 | PF00917 | 0.702 |
DOC_USP7_MATH_1 | 28 | 32 | PF00917 | 0.715 |
DOC_USP7_MATH_1 | 322 | 326 | PF00917 | 0.655 |
DOC_USP7_MATH_1 | 339 | 343 | PF00917 | 0.559 |
DOC_USP7_MATH_1 | 430 | 434 | PF00917 | 0.705 |
DOC_USP7_MATH_1 | 443 | 447 | PF00917 | 0.615 |
DOC_USP7_MATH_1 | 450 | 454 | PF00917 | 0.449 |
DOC_USP7_MATH_1 | 49 | 53 | PF00917 | 0.646 |
DOC_USP7_MATH_1 | 513 | 517 | PF00917 | 0.525 |
DOC_USP7_MATH_1 | 535 | 539 | PF00917 | 0.351 |
DOC_USP7_MATH_1 | 58 | 62 | PF00917 | 0.634 |
DOC_USP7_UBL2_3 | 21 | 25 | PF12436 | 0.726 |
DOC_USP7_UBL2_3 | 452 | 456 | PF12436 | 0.645 |
DOC_WW_Pin1_4 | 125 | 130 | PF00397 | 0.612 |
DOC_WW_Pin1_4 | 29 | 34 | PF00397 | 0.558 |
DOC_WW_Pin1_4 | 324 | 329 | PF00397 | 0.699 |
DOC_WW_Pin1_4 | 441 | 446 | PF00397 | 0.751 |
DOC_WW_Pin1_4 | 78 | 83 | PF00397 | 0.607 |
LIG_14-3-3_CanoR_1 | 244 | 254 | PF00244 | 0.571 |
LIG_14-3-3_CanoR_1 | 504 | 510 | PF00244 | 0.535 |
LIG_14-3-3_CanoR_1 | 541 | 551 | PF00244 | 0.392 |
LIG_BRCT_BRCA1_1 | 341 | 345 | PF00533 | 0.519 |
LIG_CaM_IQ_9 | 201 | 217 | PF13499 | 0.412 |
LIG_CaM_IQ_9 | 391 | 407 | PF13499 | 0.536 |
LIG_FHA_1 | 349 | 355 | PF00498 | 0.316 |
LIG_FHA_1 | 551 | 557 | PF00498 | 0.543 |
LIG_FHA_2 | 155 | 161 | PF00498 | 0.535 |
LIG_FHA_2 | 234 | 240 | PF00498 | 0.667 |
LIG_FHA_2 | 310 | 316 | PF00498 | 0.571 |
LIG_FHA_2 | 411 | 417 | PF00498 | 0.496 |
LIG_FHA_2 | 459 | 465 | PF00498 | 0.418 |
LIG_FHA_2 | 552 | 558 | PF00498 | 0.519 |
LIG_LIR_Apic_2 | 260 | 264 | PF02991 | 0.558 |
LIG_LIR_Gen_1 | 177 | 186 | PF02991 | 0.401 |
LIG_LIR_Gen_1 | 360 | 370 | PF02991 | 0.327 |
LIG_LIR_Nem_3 | 177 | 182 | PF02991 | 0.372 |
LIG_LIR_Nem_3 | 257 | 261 | PF02991 | 0.506 |
LIG_LIR_Nem_3 | 265 | 270 | PF02991 | 0.484 |
LIG_LIR_Nem_3 | 283 | 289 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 360 | 366 | PF02991 | 0.342 |
LIG_LIR_Nem_3 | 508 | 512 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 538 | 542 | PF02991 | 0.359 |
LIG_LYPXL_yS_3 | 286 | 289 | PF13949 | 0.473 |
LIG_MYND_3 | 119 | 123 | PF01753 | 0.500 |
LIG_PCNA_yPIPBox_3 | 290 | 303 | PF02747 | 0.346 |
LIG_SH2_NCK_1 | 163 | 167 | PF00017 | 0.405 |
LIG_SH2_STAP1 | 163 | 167 | PF00017 | 0.405 |
LIG_SH2_STAP1 | 509 | 513 | PF00017 | 0.341 |
LIG_SH2_STAP1 | 539 | 543 | PF00017 | 0.336 |
LIG_SH2_STAP1 | 547 | 551 | PF00017 | 0.370 |
LIG_SH2_STAT3 | 370 | 373 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 256 | 259 | PF00017 | 0.650 |
LIG_SH2_STAT5 | 349 | 352 | PF00017 | 0.331 |
LIG_SH2_STAT5 | 390 | 393 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 542 | 545 | PF00017 | 0.498 |
LIG_SH2_STAT5 | 547 | 550 | PF00017 | 0.486 |
LIG_SH3_3 | 419 | 425 | PF00018 | 0.663 |
LIG_SH3_3 | 426 | 432 | PF00018 | 0.580 |
LIG_SH3_3 | 472 | 478 | PF00018 | 0.585 |
LIG_SUMO_SIM_par_1 | 407 | 414 | PF11976 | 0.518 |
LIG_SxIP_EBH_1 | 318 | 327 | PF03271 | 0.421 |
LIG_UBA3_1 | 365 | 371 | PF00899 | 0.456 |
LIG_WRC_WIRS_1 | 258 | 263 | PF05994 | 0.627 |
MOD_CDK_SPxxK_3 | 441 | 448 | PF00069 | 0.573 |
MOD_CK1_1 | 132 | 138 | PF00069 | 0.720 |
MOD_CK1_1 | 233 | 239 | PF00069 | 0.690 |
MOD_CK1_1 | 327 | 333 | PF00069 | 0.627 |
MOD_CK1_1 | 451 | 457 | PF00069 | 0.581 |
MOD_CK1_1 | 500 | 506 | PF00069 | 0.420 |
MOD_CK2_1 | 134 | 140 | PF00069 | 0.726 |
MOD_CK2_1 | 154 | 160 | PF00069 | 0.597 |
MOD_CK2_1 | 410 | 416 | PF00069 | 0.317 |
MOD_CK2_1 | 458 | 464 | PF00069 | 0.434 |
MOD_CK2_1 | 551 | 557 | PF00069 | 0.506 |
MOD_Cter_Amidation | 187 | 190 | PF01082 | 0.363 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.551 |
MOD_GlcNHglycan | 248 | 251 | PF01048 | 0.743 |
MOD_GlcNHglycan | 275 | 278 | PF01048 | 0.502 |
MOD_GlcNHglycan | 422 | 425 | PF01048 | 0.696 |
MOD_GlcNHglycan | 445 | 448 | PF01048 | 0.651 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.664 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.583 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.693 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.432 |
MOD_GSK3_1 | 226 | 233 | PF00069 | 0.666 |
MOD_GSK3_1 | 242 | 249 | PF00069 | 0.753 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.741 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.653 |
MOD_GSK3_1 | 348 | 355 | PF00069 | 0.363 |
MOD_GSK3_1 | 439 | 446 | PF00069 | 0.659 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.656 |
MOD_GSK3_1 | 54 | 61 | PF00069 | 0.577 |
MOD_GSK3_1 | 541 | 548 | PF00069 | 0.402 |
MOD_NEK2_1 | 131 | 136 | PF00069 | 0.443 |
MOD_NEK2_1 | 232 | 237 | PF00069 | 0.574 |
MOD_NEK2_1 | 333 | 338 | PF00069 | 0.662 |
MOD_NEK2_1 | 340 | 345 | PF00069 | 0.509 |
MOD_NEK2_1 | 361 | 366 | PF00069 | 0.371 |
MOD_NEK2_1 | 497 | 502 | PF00069 | 0.488 |
MOD_NEK2_1 | 551 | 556 | PF00069 | 0.503 |
MOD_NEK2_1 | 9 | 14 | PF00069 | 0.688 |
MOD_NEK2_2 | 174 | 179 | PF00069 | 0.317 |
MOD_NEK2_2 | 458 | 463 | PF00069 | 0.533 |
MOD_PIKK_1 | 161 | 167 | PF00454 | 0.548 |
MOD_PIKK_1 | 333 | 339 | PF00454 | 0.579 |
MOD_PIKK_1 | 49 | 55 | PF00454 | 0.748 |
MOD_PKA_2 | 144 | 150 | PF00069 | 0.493 |
MOD_PKA_2 | 226 | 232 | PF00069 | 0.679 |
MOD_PKA_2 | 243 | 249 | PF00069 | 0.593 |
MOD_PKA_2 | 480 | 486 | PF00069 | 0.686 |
MOD_PKA_2 | 505 | 511 | PF00069 | 0.533 |
MOD_PKA_2 | 54 | 60 | PF00069 | 0.637 |
MOD_PKA_2 | 87 | 93 | PF00069 | 0.529 |
MOD_Plk_1 | 551 | 557 | PF00069 | 0.461 |
MOD_Plk_2-3 | 140 | 146 | PF00069 | 0.687 |
MOD_Plk_2-3 | 309 | 315 | PF00069 | 0.496 |
MOD_Plk_4 | 174 | 180 | PF00069 | 0.421 |
MOD_Plk_4 | 263 | 269 | PF00069 | 0.532 |
MOD_Plk_4 | 316 | 322 | PF00069 | 0.616 |
MOD_Plk_4 | 340 | 346 | PF00069 | 0.567 |
MOD_Plk_4 | 41 | 47 | PF00069 | 0.743 |
MOD_Plk_4 | 551 | 557 | PF00069 | 0.413 |
MOD_ProDKin_1 | 125 | 131 | PF00069 | 0.612 |
MOD_ProDKin_1 | 29 | 35 | PF00069 | 0.558 |
MOD_ProDKin_1 | 324 | 330 | PF00069 | 0.703 |
MOD_ProDKin_1 | 441 | 447 | PF00069 | 0.750 |
MOD_ProDKin_1 | 78 | 84 | PF00069 | 0.600 |
TRG_DiLeu_BaEn_1 | 464 | 469 | PF01217 | 0.419 |
TRG_ENDOCYTIC_2 | 179 | 182 | PF00928 | 0.370 |
TRG_ENDOCYTIC_2 | 258 | 261 | PF00928 | 0.506 |
TRG_ENDOCYTIC_2 | 286 | 289 | PF00928 | 0.593 |
TRG_ER_diArg_1 | 189 | 191 | PF00400 | 0.506 |
TRG_ER_diArg_1 | 199 | 201 | PF00400 | 0.474 |
TRG_ER_diArg_1 | 206 | 209 | PF00400 | 0.469 |
TRG_ER_diArg_1 | 387 | 390 | PF00400 | 0.357 |
TRG_ER_diArg_1 | 405 | 408 | PF00400 | 0.355 |
TRG_ER_diArg_1 | 504 | 507 | PF00400 | 0.405 |
TRG_ER_diArg_1 | 86 | 89 | PF00400 | 0.599 |
TRG_NLS_MonoExtN_4 | 196 | 202 | PF00514 | 0.470 |
TRG_NLS_MonoExtN_4 | 452 | 459 | PF00514 | 0.530 |
TRG_Pf-PMV_PEXEL_1 | 230 | 234 | PF00026 | 0.559 |
TRG_Pf-PMV_PEXEL_1 | 374 | 378 | PF00026 | 0.448 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IMN8 | Leptomonas seymouri | 50% | 100% |
A0A1X0NJ63 | Trypanosomatidae | 27% | 87% |
A0A3R7LBH7 | Trypanosoma rangeli | 32% | 99% |
A0A3S7X464 | Leishmania donovani | 98% | 100% |
A4HJ40 | Leishmania braziliensis | 69% | 100% |
C9ZN70 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
E9B1L2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
Q9BHF1 | Leishmania major | 92% | 100% |
V5BDV6 | Trypanosoma cruzi | 28% | 93% |