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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009892 | negative regulation of metabolic process | 4 | 1 |
GO:0009893 | positive regulation of metabolic process | 4 | 1 |
GO:0009894 | regulation of catabolic process | 4 | 1 |
GO:0009895 | negative regulation of catabolic process | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010468 | regulation of gene expression | 5 | 1 |
GO:0010604 | positive regulation of macromolecule metabolic process | 5 | 1 |
GO:0010605 | negative regulation of macromolecule metabolic process | 5 | 1 |
GO:0010608 | post-transcriptional regulation of gene expression | 6 | 1 |
GO:0010628 | positive regulation of gene expression | 6 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031324 | negative regulation of cellular metabolic process | 5 | 1 |
GO:0031329 | regulation of cellular catabolic process | 5 | 1 |
GO:0031330 | negative regulation of cellular catabolic process | 6 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043487 | regulation of RNA stability | 3 | 1 |
GO:0043488 | regulation of mRNA stability | 4 | 1 |
GO:0043489 | RNA stabilization | 4 | 1 |
GO:0043631 | RNA polyadenylation | 6 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0045934 | negative regulation of nucleobase-containing compound metabolic process | 6 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0048255 | mRNA stabilization | 5 | 1 |
GO:0048518 | positive regulation of biological process | 3 | 1 |
GO:0048519 | negative regulation of biological process | 3 | 1 |
GO:0048523 | negative regulation of cellular process | 4 | 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:0051172 | negative regulation of nitrogen compound metabolic process | 5 | 1 |
GO:0051252 | regulation of RNA metabolic process | 5 | 1 |
GO:0051253 | negative regulation of RNA metabolic process | 6 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0061013 | regulation of mRNA catabolic process | 6 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0065008 | regulation of biological quality | 2 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
GO:1902369 | negative regulation of RNA catabolic process | 7 | 1 |
GO:1902373 | negative regulation of mRNA catabolic process | 7 | 1 |
GO:1903311 | regulation of mRNA metabolic process | 6 | 1 |
GO:1903312 | negative regulation of mRNA metabolic process | 7 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003723 | RNA binding | 4 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 373 | 377 | PF00656 | 0.642 |
CLV_C14_Caspase3-7 | 484 | 488 | PF00656 | 0.518 |
CLV_NRD_NRD_1 | 228 | 230 | PF00675 | 0.444 |
CLV_NRD_NRD_1 | 33 | 35 | PF00675 | 0.485 |
CLV_NRD_NRD_1 | 389 | 391 | PF00675 | 0.736 |
CLV_NRD_NRD_1 | 436 | 438 | PF00675 | 0.455 |
CLV_NRD_NRD_1 | 602 | 604 | PF00675 | 0.346 |
CLV_NRD_NRD_1 | 78 | 80 | PF00675 | 0.404 |
CLV_NRD_NRD_1 | 85 | 87 | PF00675 | 0.388 |
CLV_PCSK_KEX2_1 | 228 | 230 | PF00082 | 0.444 |
CLV_PCSK_KEX2_1 | 389 | 391 | PF00082 | 0.736 |
CLV_PCSK_KEX2_1 | 412 | 414 | PF00082 | 0.397 |
CLV_PCSK_KEX2_1 | 436 | 438 | PF00082 | 0.455 |
CLV_PCSK_KEX2_1 | 602 | 604 | PF00082 | 0.346 |
CLV_PCSK_KEX2_1 | 78 | 80 | PF00082 | 0.404 |
CLV_PCSK_KEX2_1 | 85 | 87 | PF00082 | 0.388 |
CLV_PCSK_PC1ET2_1 | 412 | 414 | PF00082 | 0.416 |
CLV_PCSK_PC7_1 | 74 | 80 | PF00082 | 0.472 |
CLV_PCSK_SKI1_1 | 146 | 150 | PF00082 | 0.309 |
CLV_PCSK_SKI1_1 | 151 | 155 | PF00082 | 0.313 |
CLV_PCSK_SKI1_1 | 166 | 170 | PF00082 | 0.215 |
CLV_PCSK_SKI1_1 | 197 | 201 | PF00082 | 0.481 |
CLV_PCSK_SKI1_1 | 486 | 490 | PF00082 | 0.510 |
CLV_PCSK_SKI1_1 | 591 | 595 | PF00082 | 0.473 |
CLV_Separin_Metazoa | 265 | 269 | PF03568 | 0.574 |
DEG_APCC_DBOX_1 | 165 | 173 | PF00400 | 0.280 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.449 |
DEG_ODPH_VHL_1 | 417 | 428 | PF01847 | 0.526 |
DEG_SPOP_SBC_1 | 361 | 365 | PF00917 | 0.422 |
DOC_CYCLIN_RxL_1 | 329 | 338 | PF00134 | 0.348 |
DOC_MAPK_gen_1 | 119 | 128 | PF00069 | 0.355 |
DOC_MAPK_gen_1 | 545 | 552 | PF00069 | 0.339 |
DOC_MAPK_gen_1 | 602 | 611 | PF00069 | 0.375 |
DOC_MAPK_HePTP_8 | 105 | 117 | PF00069 | 0.365 |
DOC_MAPK_MEF2A_6 | 108 | 117 | PF00069 | 0.346 |
DOC_MAPK_MEF2A_6 | 545 | 552 | PF00069 | 0.358 |
DOC_PP1_RVXF_1 | 330 | 337 | PF00149 | 0.307 |
DOC_PP1_RVXF_1 | 507 | 513 | PF00149 | 0.515 |
DOC_PP2B_LxvP_1 | 212 | 215 | PF13499 | 0.426 |
DOC_PP2B_LxvP_1 | 416 | 419 | PF13499 | 0.544 |
DOC_PP2B_PxIxI_1 | 112 | 118 | PF00149 | 0.342 |
DOC_PP4_FxxP_1 | 255 | 258 | PF00568 | 0.405 |
DOC_USP7_MATH_1 | 179 | 183 | PF00917 | 0.585 |
DOC_USP7_MATH_1 | 248 | 252 | PF00917 | 0.492 |
DOC_USP7_MATH_1 | 278 | 282 | PF00917 | 0.494 |
DOC_USP7_MATH_1 | 293 | 297 | PF00917 | 0.682 |
DOC_USP7_MATH_1 | 361 | 365 | PF00917 | 0.548 |
DOC_USP7_MATH_1 | 370 | 374 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 548 | 552 | PF00917 | 0.460 |
DOC_USP7_MATH_1 | 630 | 634 | PF00917 | 0.453 |
DOC_USP7_MATH_1 | 674 | 678 | PF00917 | 0.467 |
DOC_USP7_MATH_1 | 73 | 77 | PF00917 | 0.539 |
DOC_USP7_MATH_2 | 179 | 185 | PF00917 | 0.517 |
DOC_USP7_MATH_2 | 559 | 565 | PF00917 | 0.388 |
DOC_WW_Pin1_4 | 10 | 15 | PF00397 | 0.368 |
DOC_WW_Pin1_4 | 269 | 274 | PF00397 | 0.546 |
LIG_14-3-3_CanoR_1 | 157 | 162 | PF00244 | 0.392 |
LIG_14-3-3_CanoR_1 | 197 | 205 | PF00244 | 0.689 |
LIG_14-3-3_CanoR_1 | 277 | 284 | PF00244 | 0.483 |
LIG_14-3-3_CanoR_1 | 310 | 316 | PF00244 | 0.544 |
LIG_14-3-3_CanoR_1 | 360 | 368 | PF00244 | 0.553 |
LIG_14-3-3_CanoR_1 | 491 | 495 | PF00244 | 0.575 |
LIG_14-3-3_CanoR_1 | 643 | 650 | PF00244 | 0.424 |
LIG_14-3-3_CanoR_1 | 72 | 78 | PF00244 | 0.453 |
LIG_14-3-3_CanoR_1 | 9 | 13 | PF00244 | 0.317 |
LIG_Actin_RPEL_3 | 115 | 134 | PF02755 | 0.343 |
LIG_Actin_WH2_2 | 13 | 31 | PF00022 | 0.548 |
LIG_APCC_ABBA_1 | 126 | 131 | PF00400 | 0.384 |
LIG_APCC_ABBA_1 | 333 | 338 | PF00400 | 0.292 |
LIG_APCC_ABBAyCdc20_2 | 332 | 338 | PF00400 | 0.311 |
LIG_APCC_Cbox_1 | 617 | 623 | PF00515 | 0.238 |
LIG_APCC_Cbox_2 | 617 | 623 | PF00515 | 0.238 |
LIG_deltaCOP1_diTrp_1 | 135 | 144 | PF00928 | 0.495 |
LIG_deltaCOP1_diTrp_1 | 472 | 476 | PF00928 | 0.375 |
LIG_EH_1 | 345 | 349 | PF12763 | 0.367 |
LIG_FHA_1 | 209 | 215 | PF00498 | 0.480 |
LIG_FHA_2 | 204 | 210 | PF00498 | 0.445 |
LIG_FHA_2 | 590 | 596 | PF00498 | 0.308 |
LIG_GBD_Chelix_1 | 581 | 589 | PF00786 | 0.455 |
LIG_LIR_Apic_2 | 252 | 258 | PF02991 | 0.410 |
LIG_LIR_Apic_2 | 472 | 478 | PF02991 | 0.355 |
LIG_LIR_Gen_1 | 217 | 227 | PF02991 | 0.452 |
LIG_LIR_Gen_1 | 345 | 356 | PF02991 | 0.384 |
LIG_LIR_Gen_1 | 471 | 481 | PF02991 | 0.367 |
LIG_LIR_LC3C_4 | 579 | 583 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 164 | 168 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 18 | 24 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 217 | 223 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 313 | 318 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 345 | 351 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 38 | 44 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 465 | 470 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 471 | 476 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 622 | 627 | PF02991 | 0.370 |
LIG_LIR_Nem_3 | 645 | 650 | PF02991 | 0.427 |
LIG_LYPXL_yS_3 | 315 | 318 | PF13949 | 0.364 |
LIG_MAD2 | 653 | 661 | PF02301 | 0.494 |
LIG_PCNA_PIPBox_1 | 264 | 273 | PF02747 | 0.438 |
LIG_PCNA_PIPBox_1 | 99 | 108 | PF02747 | 0.415 |
LIG_PCNA_yPIPBox_3 | 261 | 271 | PF02747 | 0.531 |
LIG_PCNA_yPIPBox_3 | 323 | 334 | PF02747 | 0.413 |
LIG_PCNA_yPIPBox_3 | 92 | 106 | PF02747 | 0.426 |
LIG_SH2_CRK | 150 | 154 | PF00017 | 0.294 |
LIG_SH2_CRK | 165 | 169 | PF00017 | 0.327 |
LIG_SH2_GRB2like | 475 | 478 | PF00017 | 0.335 |
LIG_SH2_NCK_1 | 500 | 504 | PF00017 | 0.360 |
LIG_SH2_NCK_1 | 562 | 566 | PF00017 | 0.547 |
LIG_SH2_STAP1 | 669 | 673 | PF00017 | 0.348 |
LIG_SH2_STAT3 | 381 | 384 | PF00017 | 0.510 |
LIG_SH2_STAT5 | 16 | 19 | PF00017 | 0.347 |
LIG_SH2_STAT5 | 167 | 170 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 220 | 223 | PF00017 | 0.300 |
LIG_SH2_STAT5 | 225 | 228 | PF00017 | 0.289 |
LIG_SH2_STAT5 | 231 | 234 | PF00017 | 0.304 |
LIG_SH2_STAT5 | 357 | 360 | PF00017 | 0.547 |
LIG_SH2_STAT5 | 475 | 478 | PF00017 | 0.339 |
LIG_SH2_STAT5 | 533 | 536 | PF00017 | 0.386 |
LIG_SH2_STAT5 | 627 | 630 | PF00017 | 0.273 |
LIG_SH2_STAT5 | 647 | 650 | PF00017 | 0.433 |
LIG_SH3_3 | 107 | 113 | PF00018 | 0.340 |
LIG_SH3_3 | 306 | 312 | PF00018 | 0.528 |
LIG_SH3_3 | 346 | 352 | PF00018 | 0.366 |
LIG_SH3_3 | 532 | 538 | PF00018 | 0.387 |
LIG_SH3_3 | 553 | 559 | PF00018 | 0.381 |
LIG_SH3_3 | 59 | 65 | PF00018 | 0.502 |
LIG_SH3_3 | 626 | 632 | PF00018 | 0.503 |
LIG_SUMO_SIM_par_1 | 101 | 107 | PF11976 | 0.359 |
LIG_TYR_ITIM | 148 | 153 | PF00017 | 0.293 |
MOD_CDK_SPK_2 | 269 | 274 | PF00069 | 0.379 |
MOD_CK1_1 | 184 | 190 | PF00069 | 0.661 |
MOD_CK1_1 | 203 | 209 | PF00069 | 0.572 |
MOD_CK1_1 | 272 | 278 | PF00069 | 0.532 |
MOD_CK1_1 | 285 | 291 | PF00069 | 0.480 |
MOD_CK1_1 | 362 | 368 | PF00069 | 0.527 |
MOD_CK1_1 | 404 | 410 | PF00069 | 0.470 |
MOD_CK1_1 | 465 | 471 | PF00069 | 0.453 |
MOD_CK1_1 | 490 | 496 | PF00069 | 0.553 |
MOD_CK2_1 | 195 | 201 | PF00069 | 0.769 |
MOD_CK2_1 | 203 | 209 | PF00069 | 0.744 |
MOD_CK2_1 | 589 | 595 | PF00069 | 0.321 |
MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.722 |
MOD_GlcNHglycan | 284 | 287 | PF01048 | 0.614 |
MOD_GlcNHglycan | 467 | 470 | PF01048 | 0.466 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.585 |
MOD_GlcNHglycan | 563 | 566 | PF01048 | 0.486 |
MOD_GlcNHglycan | 644 | 647 | PF01048 | 0.479 |
MOD_GlcNHglycan | 656 | 660 | PF01048 | 0.445 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.363 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.720 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.680 |
MOD_GSK3_1 | 203 | 210 | PF00069 | 0.702 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.557 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.663 |
MOD_GSK3_1 | 356 | 363 | PF00069 | 0.454 |
MOD_GSK3_1 | 529 | 536 | PF00069 | 0.478 |
MOD_GSK3_1 | 563 | 570 | PF00069 | 0.513 |
MOD_GSK3_1 | 655 | 662 | PF00069 | 0.424 |
MOD_N-GLC_1 | 184 | 189 | PF02516 | 0.567 |
MOD_N-GLC_1 | 248 | 253 | PF02516 | 0.453 |
MOD_NEK2_1 | 199 | 204 | PF00069 | 0.741 |
MOD_NEK2_1 | 253 | 258 | PF00069 | 0.397 |
MOD_NEK2_1 | 427 | 432 | PF00069 | 0.443 |
MOD_NEK2_1 | 44 | 49 | PF00069 | 0.589 |
MOD_NEK2_1 | 589 | 594 | PF00069 | 0.302 |
MOD_NEK2_1 | 655 | 660 | PF00069 | 0.397 |
MOD_NEK2_1 | 8 | 13 | PF00069 | 0.365 |
MOD_NEK2_2 | 67 | 72 | PF00069 | 0.564 |
MOD_NEK2_2 | 73 | 78 | PF00069 | 0.507 |
MOD_PIKK_1 | 276 | 282 | PF00454 | 0.619 |
MOD_PIKK_1 | 45 | 51 | PF00454 | 0.590 |
MOD_PKA_2 | 179 | 185 | PF00069 | 0.654 |
MOD_PKA_2 | 203 | 209 | PF00069 | 0.661 |
MOD_PKA_2 | 276 | 282 | PF00069 | 0.472 |
MOD_PKA_2 | 359 | 365 | PF00069 | 0.574 |
MOD_PKA_2 | 490 | 496 | PF00069 | 0.449 |
MOD_PKA_2 | 642 | 648 | PF00069 | 0.404 |
MOD_PKA_2 | 73 | 79 | PF00069 | 0.516 |
MOD_PKA_2 | 8 | 14 | PF00069 | 0.366 |
MOD_PKB_1 | 308 | 316 | PF00069 | 0.468 |
MOD_Plk_1 | 200 | 206 | PF00069 | 0.510 |
MOD_Plk_1 | 208 | 214 | PF00069 | 0.627 |
MOD_Plk_1 | 471 | 477 | PF00069 | 0.371 |
MOD_Plk_4 | 404 | 410 | PF00069 | 0.481 |
MOD_Plk_4 | 462 | 468 | PF00069 | 0.411 |
MOD_Plk_4 | 529 | 535 | PF00069 | 0.459 |
MOD_Plk_4 | 548 | 554 | PF00069 | 0.407 |
MOD_Plk_4 | 611 | 617 | PF00069 | 0.344 |
MOD_ProDKin_1 | 10 | 16 | PF00069 | 0.364 |
MOD_ProDKin_1 | 269 | 275 | PF00069 | 0.551 |
MOD_SUMO_for_1 | 260 | 263 | PF00179 | 0.483 |
MOD_SUMO_rev_2 | 32 | 37 | PF00179 | 0.421 |
TRG_DiLeu_BaEn_1 | 326 | 331 | PF01217 | 0.406 |
TRG_DiLeu_BaEn_1 | 338 | 343 | PF01217 | 0.422 |
TRG_DiLeu_BaEn_4 | 461 | 467 | PF01217 | 0.598 |
TRG_DiLeu_BaEn_4 | 484 | 490 | PF01217 | 0.400 |
TRG_ENDOCYTIC_2 | 150 | 153 | PF00928 | 0.308 |
TRG_ENDOCYTIC_2 | 165 | 168 | PF00928 | 0.444 |
TRG_ENDOCYTIC_2 | 220 | 223 | PF00928 | 0.304 |
TRG_ENDOCYTIC_2 | 315 | 318 | PF00928 | 0.364 |
TRG_ENDOCYTIC_2 | 647 | 650 | PF00928 | 0.374 |
TRG_ER_diArg_1 | 227 | 229 | PF00400 | 0.443 |
TRG_ER_diArg_1 | 308 | 311 | PF00400 | 0.587 |
TRG_ER_diArg_1 | 388 | 390 | PF00400 | 0.504 |
TRG_ER_diArg_1 | 435 | 437 | PF00400 | 0.450 |
TRG_ER_diArg_1 | 601 | 603 | PF00400 | 0.344 |
TRG_ER_diArg_1 | 71 | 74 | PF00400 | 0.471 |
TRG_ER_diArg_1 | 77 | 79 | PF00400 | 0.390 |
TRG_Pf-PMV_PEXEL_1 | 166 | 170 | PF00026 | 0.483 |
TRG_Pf-PMV_PEXEL_1 | 197 | 201 | PF00026 | 0.481 |
TRG_Pf-PMV_PEXEL_1 | 436 | 440 | PF00026 | 0.426 |
TRG_Pf-PMV_PEXEL_1 | 653 | 657 | PF00026 | 0.361 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I7Z6 | Leptomonas seymouri | 69% | 92% |
A0A0S4IW89 | Bodo saltans | 35% | 100% |
A0A1X0P3U7 | Trypanosomatidae | 51% | 93% |
A0A3S7X701 | Leishmania donovani | 87% | 100% |
A0A422P030 | Trypanosoma rangeli | 53% | 96% |
D0A659 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 91% |
E9AHR9 | Leishmania infantum | 87% | 100% |
E9B490 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
Q4Q3T6 | Leishmania major | 87% | 100% |
V5BP67 | Trypanosoma cruzi | 51% | 98% |