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 | 2 |
GO:1990904 | ribonucleoprotein complex | 2 | 2 |
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: Q9BHF1
Term | Name | Level | Count |
---|---|---|---|
GO:0001514 | selenocysteine incorporation | 7 | 2 |
GO:0006414 | translational elongation | 5 | 2 |
GO:0006417 | regulation of translation | 6 | 2 |
GO:0006451 | translational readthrough | 6 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009058 | biosynthetic process | 2 | 2 |
GO:0009059 | macromolecule biosynthetic process | 4 | 2 |
GO:0009889 | regulation of biosynthetic process | 4 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0010468 | regulation of gene expression | 5 | 2 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 2 |
GO:0010608 | post-transcriptional regulation of gene expression | 6 | 2 |
GO:0019222 | regulation of metabolic process | 3 | 2 |
GO:0031323 | regulation of cellular metabolic process | 4 | 2 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 2 |
GO:0034248 | regulation of amide metabolic process | 5 | 2 |
GO:0034645 | obsolete cellular macromolecule biosynthetic process | 4 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044249 | cellular biosynthetic process | 3 | 2 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 2 |
GO:0050789 | regulation of biological process | 2 | 2 |
GO:0050794 | regulation of cellular process | 3 | 2 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 2 |
GO:0051246 | regulation of protein metabolic process | 5 | 2 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0080090 | regulation of primary metabolic process | 4 | 2 |
GO:1901576 | organic substance biosynthetic process | 3 | 2 |
GO:2000112 | obsolete regulation of cellular macromolecule biosynthetic process | 6 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 11 |
GO:0003723 | RNA binding | 4 | 11 |
GO:0003729 | mRNA binding | 5 | 11 |
GO:0003730 | mRNA 3'-UTR binding | 6 | 2 |
GO:0005488 | binding | 1 | 11 |
GO:0035368 | selenocysteine insertion sequence binding | 6 | 11 |
GO:0043021 | ribonucleoprotein complex binding | 3 | 2 |
GO:0044877 | protein-containing complex binding | 2 | 2 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 247 | 251 | PF00656 | 0.705 |
CLV_C14_Caspase3-7 | 311 | 315 | PF00656 | 0.530 |
CLV_NRD_NRD_1 | 157 | 159 | PF00675 | 0.683 |
CLV_NRD_NRD_1 | 198 | 200 | PF00675 | 0.543 |
CLV_NRD_NRD_1 | 208 | 210 | PF00675 | 0.483 |
CLV_NRD_NRD_1 | 442 | 444 | PF00675 | 0.686 |
CLV_NRD_NRD_1 | 456 | 458 | PF00675 | 0.601 |
CLV_PCSK_FUR_1 | 206 | 210 | PF00082 | 0.560 |
CLV_PCSK_KEX2_1 | 157 | 159 | PF00082 | 0.674 |
CLV_PCSK_KEX2_1 | 168 | 170 | PF00082 | 0.490 |
CLV_PCSK_KEX2_1 | 197 | 199 | PF00082 | 0.469 |
CLV_PCSK_KEX2_1 | 208 | 210 | PF00082 | 0.369 |
CLV_PCSK_KEX2_1 | 442 | 444 | PF00082 | 0.662 |
CLV_PCSK_KEX2_1 | 93 | 95 | PF00082 | 0.516 |
CLV_PCSK_PC1ET2_1 | 168 | 170 | PF00082 | 0.393 |
CLV_PCSK_PC1ET2_1 | 197 | 199 | PF00082 | 0.493 |
CLV_PCSK_PC1ET2_1 | 93 | 95 | PF00082 | 0.559 |
CLV_PCSK_SKI1_1 | 209 | 213 | PF00082 | 0.510 |
CLV_PCSK_SKI1_1 | 22 | 26 | PF00082 | 0.811 |
CLV_PCSK_SKI1_1 | 337 | 341 | PF00082 | 0.685 |
CLV_PCSK_SKI1_1 | 373 | 377 | PF00082 | 0.412 |
CLV_PCSK_SKI1_1 | 398 | 402 | PF00082 | 0.519 |
CLV_PCSK_SKI1_1 | 406 | 410 | PF00082 | 0.480 |
CLV_PCSK_SKI1_1 | 458 | 462 | PF00082 | 0.617 |
CLV_PCSK_SKI1_1 | 532 | 536 | PF00082 | 0.515 |
CLV_PCSK_SKI1_1 | 543 | 547 | PF00082 | 0.471 |
DEG_APCC_DBOX_1 | 403 | 411 | PF00400 | 0.439 |
DEG_APCC_DBOX_1 | 531 | 539 | PF00400 | 0.543 |
DEG_SPOP_SBC_1 | 134 | 138 | PF00917 | 0.639 |
DEG_SPOP_SBC_1 | 28 | 32 | PF00917 | 0.713 |
DEG_SPOP_SBC_1 | 322 | 326 | PF00917 | 0.691 |
DOC_MAPK_gen_1 | 373 | 383 | PF00069 | 0.441 |
DOC_MAPK_gen_1 | 384 | 393 | PF00069 | 0.409 |
DOC_MAPK_gen_1 | 398 | 407 | PF00069 | 0.474 |
DOC_MAPK_gen_1 | 516 | 525 | PF00069 | 0.521 |
DOC_MAPK_MEF2A_6 | 401 | 409 | PF00069 | 0.505 |
DOC_PP2B_LxvP_1 | 424 | 427 | PF13499 | 0.536 |
DOC_PP4_FxxP_1 | 260 | 263 | PF00568 | 0.700 |
DOC_USP7_MATH_1 | 122 | 126 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 134 | 138 | PF00917 | 0.768 |
DOC_USP7_MATH_1 | 184 | 188 | PF00917 | 0.587 |
DOC_USP7_MATH_1 | 245 | 249 | PF00917 | 0.730 |
DOC_USP7_MATH_1 | 252 | 256 | PF00917 | 0.753 |
DOC_USP7_MATH_1 | 28 | 32 | PF00917 | 0.767 |
DOC_USP7_MATH_1 | 321 | 325 | PF00917 | 0.666 |
DOC_USP7_MATH_1 | 338 | 342 | PF00917 | 0.679 |
DOC_USP7_MATH_1 | 432 | 436 | PF00917 | 0.757 |
DOC_USP7_MATH_1 | 445 | 449 | PF00917 | 0.663 |
DOC_USP7_MATH_1 | 452 | 456 | PF00917 | 0.635 |
DOC_USP7_MATH_1 | 515 | 519 | PF00917 | 0.560 |
DOC_USP7_MATH_1 | 537 | 541 | PF00917 | 0.445 |
DOC_USP7_UBL2_3 | 21 | 25 | PF12436 | 0.792 |
DOC_USP7_UBL2_3 | 454 | 458 | PF12436 | 0.693 |
DOC_WW_Pin1_4 | 125 | 130 | PF00397 | 0.774 |
DOC_WW_Pin1_4 | 29 | 34 | PF00397 | 0.668 |
DOC_WW_Pin1_4 | 323 | 328 | PF00397 | 0.714 |
DOC_WW_Pin1_4 | 443 | 448 | PF00397 | 0.776 |
DOC_WW_Pin1_4 | 78 | 83 | PF00397 | 0.683 |
LIG_14-3-3_CanoR_1 | 161 | 167 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 243 | 253 | PF00244 | 0.685 |
LIG_14-3-3_CanoR_1 | 506 | 512 | PF00244 | 0.545 |
LIG_14-3-3_CanoR_1 | 543 | 553 | PF00244 | 0.486 |
LIG_14-3-3_CanoR_1 | 6 | 10 | PF00244 | 0.717 |
LIG_BRCT_BRCA1_1 | 340 | 344 | PF00533 | 0.616 |
LIG_CaM_IQ_9 | 200 | 216 | PF13499 | 0.500 |
LIG_CaM_IQ_9 | 390 | 406 | PF13499 | 0.508 |
LIG_EVH1_1 | 424 | 428 | PF00568 | 0.533 |
LIG_FHA_1 | 125 | 131 | PF00498 | 0.541 |
LIG_FHA_1 | 348 | 354 | PF00498 | 0.376 |
LIG_FHA_1 | 553 | 559 | PF00498 | 0.573 |
LIG_FHA_2 | 154 | 160 | PF00498 | 0.596 |
LIG_FHA_2 | 233 | 239 | PF00498 | 0.725 |
LIG_FHA_2 | 309 | 315 | PF00498 | 0.603 |
LIG_FHA_2 | 410 | 416 | PF00498 | 0.546 |
LIG_FHA_2 | 461 | 467 | PF00498 | 0.470 |
LIG_LIR_Apic_2 | 259 | 263 | PF02991 | 0.703 |
LIG_LIR_Gen_1 | 175 | 185 | PF02991 | 0.470 |
LIG_LIR_Gen_1 | 359 | 369 | PF02991 | 0.385 |
LIG_LIR_Gen_1 | 41 | 49 | PF02991 | 0.528 |
LIG_LIR_Nem_3 | 175 | 181 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 255 | 260 | PF02991 | 0.562 |
LIG_LIR_Nem_3 | 282 | 288 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 359 | 365 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 41 | 45 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 510 | 514 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 540 | 544 | PF02991 | 0.412 |
LIG_LYPXL_yS_3 | 285 | 288 | PF13949 | 0.590 |
LIG_PROFILIN_1 | 425 | 431 | PF00235 | 0.504 |
LIG_SH2_CRK | 42 | 46 | PF00017 | 0.526 |
LIG_SH2_NCK_1 | 162 | 166 | PF00017 | 0.493 |
LIG_SH2_STAP1 | 162 | 166 | PF00017 | 0.493 |
LIG_SH2_STAP1 | 511 | 515 | PF00017 | 0.401 |
LIG_SH2_STAP1 | 541 | 545 | PF00017 | 0.394 |
LIG_SH2_STAP1 | 549 | 553 | PF00017 | 0.422 |
LIG_SH2_STAT3 | 369 | 372 | PF00017 | 0.403 |
LIG_SH2_STAT5 | 348 | 351 | PF00017 | 0.394 |
LIG_SH2_STAT5 | 389 | 392 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 42 | 45 | PF00017 | 0.528 |
LIG_SH2_STAT5 | 544 | 547 | PF00017 | 0.518 |
LIG_SH2_STAT5 | 549 | 552 | PF00017 | 0.522 |
LIG_SH3_3 | 116 | 122 | PF00018 | 0.682 |
LIG_SH3_3 | 414 | 420 | PF00018 | 0.650 |
LIG_SH3_3 | 422 | 428 | PF00018 | 0.692 |
LIG_SH3_3 | 433 | 439 | PF00018 | 0.639 |
LIG_SH3_3 | 474 | 480 | PF00018 | 0.623 |
LIG_SUMO_SIM_par_1 | 406 | 413 | PF11976 | 0.442 |
LIG_UBA3_1 | 364 | 370 | PF00899 | 0.492 |
LIG_WRC_WIRS_1 | 257 | 262 | PF05994 | 0.677 |
MOD_CDK_SPxxK_3 | 443 | 450 | PF00069 | 0.682 |
MOD_CK1_1 | 125 | 131 | PF00069 | 0.690 |
MOD_CK1_1 | 132 | 138 | PF00069 | 0.769 |
MOD_CK1_1 | 219 | 225 | PF00069 | 0.547 |
MOD_CK1_1 | 232 | 238 | PF00069 | 0.742 |
MOD_CK1_1 | 326 | 332 | PF00069 | 0.678 |
MOD_CK1_1 | 453 | 459 | PF00069 | 0.681 |
MOD_CK1_1 | 502 | 508 | PF00069 | 0.488 |
MOD_CK2_1 | 134 | 140 | PF00069 | 0.763 |
MOD_CK2_1 | 153 | 159 | PF00069 | 0.642 |
MOD_CK2_1 | 409 | 415 | PF00069 | 0.418 |
MOD_CK2_1 | 460 | 466 | PF00069 | 0.483 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.674 |
MOD_GlcNHglycan | 149 | 153 | PF01048 | 0.633 |
MOD_GlcNHglycan | 247 | 250 | PF01048 | 0.737 |
MOD_GlcNHglycan | 274 | 277 | PF01048 | 0.559 |
MOD_GlcNHglycan | 421 | 424 | PF01048 | 0.692 |
MOD_GlcNHglycan | 447 | 450 | PF01048 | 0.713 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.678 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.648 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.784 |
MOD_GSK3_1 | 252 | 259 | PF00069 | 0.576 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.778 |
MOD_GSK3_1 | 322 | 329 | PF00069 | 0.702 |
MOD_GSK3_1 | 347 | 354 | PF00069 | 0.416 |
MOD_GSK3_1 | 441 | 448 | PF00069 | 0.694 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.734 |
MOD_GSK3_1 | 543 | 550 | PF00069 | 0.456 |
MOD_NEK2_1 | 216 | 221 | PF00069 | 0.574 |
MOD_NEK2_1 | 231 | 236 | PF00069 | 0.671 |
MOD_NEK2_1 | 256 | 261 | PF00069 | 0.589 |
MOD_NEK2_1 | 332 | 337 | PF00069 | 0.646 |
MOD_NEK2_1 | 339 | 344 | PF00069 | 0.520 |
MOD_NEK2_1 | 360 | 365 | PF00069 | 0.403 |
MOD_NEK2_1 | 499 | 504 | PF00069 | 0.522 |
MOD_NEK2_1 | 553 | 558 | PF00069 | 0.544 |
MOD_NEK2_1 | 9 | 14 | PF00069 | 0.756 |
MOD_NEK2_2 | 460 | 465 | PF00069 | 0.573 |
MOD_PIKK_1 | 160 | 166 | PF00454 | 0.590 |
MOD_PIKK_1 | 332 | 338 | PF00454 | 0.710 |
MOD_PIKK_1 | 49 | 55 | PF00454 | 0.772 |
MOD_PKA_2 | 160 | 166 | PF00069 | 0.467 |
MOD_PKA_2 | 225 | 231 | PF00069 | 0.692 |
MOD_PKA_2 | 441 | 447 | PF00069 | 0.715 |
MOD_PKA_2 | 482 | 488 | PF00069 | 0.712 |
MOD_PKA_2 | 5 | 11 | PF00069 | 0.708 |
MOD_PKA_2 | 507 | 513 | PF00069 | 0.544 |
MOD_PKA_2 | 54 | 60 | PF00069 | 0.762 |
MOD_PKA_2 | 87 | 93 | PF00069 | 0.598 |
MOD_Plk_1 | 553 | 559 | PF00069 | 0.566 |
MOD_Plk_2-3 | 140 | 146 | PF00069 | 0.749 |
MOD_Plk_2-3 | 308 | 314 | PF00069 | 0.606 |
MOD_Plk_2-3 | 5 | 11 | PF00069 | 0.612 |
MOD_Plk_4 | 252 | 258 | PF00069 | 0.660 |
MOD_Plk_4 | 262 | 268 | PF00069 | 0.588 |
MOD_Plk_4 | 339 | 345 | PF00069 | 0.577 |
MOD_Plk_4 | 41 | 47 | PF00069 | 0.764 |
MOD_Plk_4 | 553 | 559 | PF00069 | 0.488 |
MOD_ProDKin_1 | 125 | 131 | PF00069 | 0.774 |
MOD_ProDKin_1 | 29 | 35 | PF00069 | 0.666 |
MOD_ProDKin_1 | 323 | 329 | PF00069 | 0.720 |
MOD_ProDKin_1 | 443 | 449 | PF00069 | 0.775 |
MOD_ProDKin_1 | 78 | 84 | PF00069 | 0.676 |
TRG_DiLeu_BaEn_1 | 466 | 471 | PF01217 | 0.544 |
TRG_ENDOCYTIC_2 | 178 | 181 | PF00928 | 0.444 |
TRG_ENDOCYTIC_2 | 257 | 260 | PF00928 | 0.572 |
TRG_ENDOCYTIC_2 | 285 | 288 | PF00928 | 0.590 |
TRG_ENDOCYTIC_2 | 42 | 45 | PF00928 | 0.528 |
TRG_ER_diArg_1 | 198 | 200 | PF00400 | 0.500 |
TRG_ER_diArg_1 | 205 | 208 | PF00400 | 0.495 |
TRG_ER_diArg_1 | 386 | 389 | PF00400 | 0.445 |
TRG_ER_diArg_1 | 404 | 407 | PF00400 | 0.533 |
TRG_ER_diArg_1 | 441 | 443 | PF00400 | 0.708 |
TRG_ER_diArg_1 | 506 | 509 | PF00400 | 0.457 |
TRG_ER_diArg_1 | 86 | 89 | PF00400 | 0.623 |
TRG_NLS_Bipartite_1 | 442 | 461 | PF00514 | 0.677 |
TRG_NLS_MonoExtN_4 | 195 | 201 | PF00514 | 0.527 |
TRG_NLS_MonoExtN_4 | 454 | 461 | PF00514 | 0.592 |
TRG_Pf-PMV_PEXEL_1 | 229 | 233 | PF00026 | 0.656 |
TRG_Pf-PMV_PEXEL_1 | 373 | 377 | PF00026 | 0.481 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IMN8 | Leptomonas seymouri | 50% | 100% |
A0A1X0NJ63 | Trypanosomatidae | 27% | 88% |
A0A3R7LBH7 | Trypanosoma rangeli | 31% | 99% |
A0A3S7X464 | Leishmania donovani | 91% | 100% |
A4HJ40 | Leishmania braziliensis | 70% | 99% |
A4I6F5 | Leishmania infantum | 92% | 100% |
C9ZN70 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
E9B1L2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
V5BDV6 | Trypanosoma cruzi | 28% | 94% |