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:0005634 | nucleus | 5 | 12 |
GO:0005737 | cytoplasm | 2 | 12 |
GO:0043226 | organelle | 2 | 12 |
GO:0043227 | membrane-bounded organelle | 3 | 12 |
GO:0043229 | intracellular organelle | 3 | 12 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
Related structures:
AlphaFold database: E9APW5
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006396 | RNA processing | 6 | 12 |
GO:0006397 | mRNA processing | 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:0009987 | cellular process | 1 | 12 |
GO:0016070 | RNA metabolic process | 5 | 12 |
GO:0016071 | mRNA metabolic process | 6 | 12 |
GO:0031123 | RNA 3'-end processing | 7 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0043631 | RNA polyadenylation | 6 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0071076 | RNA 3' uridylation | 8 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0090304 | nucleic acid metabolic process | 4 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
GO:0006378 | mRNA polyadenylation | 7 | 1 |
GO:0031124 | mRNA 3'-end processing | 8 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003723 | RNA binding | 4 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004652 | obsolete polynucleotide adenylyltransferase activity | 6 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 12 |
GO:0016779 | nucleotidyltransferase activity | 4 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0030554 | adenyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0043169 | cation binding | 3 | 12 |
GO:0046872 | metal ion binding | 4 | 12 |
GO:0050265 | RNA uridylyltransferase activity | 4 | 12 |
GO:0070566 | adenylyltransferase activity | 5 | 12 |
GO:0070569 | uridylyltransferase activity | 5 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 12 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 302 | 306 | PF00656 | 0.317 |
CLV_C14_Caspase3-7 | 388 | 392 | PF00656 | 0.296 |
CLV_C14_Caspase3-7 | 622 | 626 | PF00656 | 0.768 |
CLV_C14_Caspase3-7 | 646 | 650 | PF00656 | 0.772 |
CLV_NRD_NRD_1 | 50 | 52 | PF00675 | 0.308 |
CLV_NRD_NRD_1 | 652 | 654 | PF00675 | 0.679 |
CLV_PCSK_KEX2_1 | 49 | 51 | PF00082 | 0.308 |
CLV_PCSK_KEX2_1 | 654 | 656 | PF00082 | 0.730 |
CLV_PCSK_PC1ET2_1 | 654 | 656 | PF00082 | 0.730 |
CLV_PCSK_SKI1_1 | 204 | 208 | PF00082 | 0.313 |
CLV_PCSK_SKI1_1 | 212 | 216 | PF00082 | 0.283 |
CLV_PCSK_SKI1_1 | 51 | 55 | PF00082 | 0.301 |
CLV_PCSK_SKI1_1 | 9 | 13 | PF00082 | 0.470 |
DEG_APCC_DBOX_1 | 207 | 215 | PF00400 | 0.301 |
DEG_APCC_DBOX_1 | 50 | 58 | PF00400 | 0.301 |
DEG_SPOP_SBC_1 | 602 | 606 | PF00917 | 0.754 |
DOC_CKS1_1 | 312 | 317 | PF01111 | 0.301 |
DOC_MAPK_DCC_7 | 140 | 149 | PF00069 | 0.317 |
DOC_MAPK_FxFP_2 | 228 | 231 | PF00069 | 0.317 |
DOC_MAPK_gen_1 | 300 | 309 | PF00069 | 0.317 |
DOC_MAPK_HePTP_8 | 53 | 65 | PF00069 | 0.421 |
DOC_MAPK_MEF2A_6 | 140 | 149 | PF00069 | 0.317 |
DOC_MAPK_MEF2A_6 | 378 | 387 | PF00069 | 0.324 |
DOC_MAPK_MEF2A_6 | 56 | 65 | PF00069 | 0.404 |
DOC_PP1_RVXF_1 | 405 | 411 | PF00149 | 0.324 |
DOC_PP2B_LxvP_1 | 108 | 111 | PF13499 | 0.448 |
DOC_PP2B_PxIxI_1 | 541 | 547 | PF00149 | 0.317 |
DOC_PP4_FxxP_1 | 228 | 231 | PF00568 | 0.317 |
DOC_PP4_FxxP_1 | 436 | 439 | PF00568 | 0.386 |
DOC_PP4_FxxP_1 | 73 | 76 | PF00568 | 0.317 |
DOC_USP7_MATH_1 | 299 | 303 | PF00917 | 0.317 |
DOC_USP7_MATH_1 | 613 | 617 | PF00917 | 0.776 |
DOC_USP7_MATH_1 | 624 | 628 | PF00917 | 0.785 |
DOC_USP7_MATH_1 | 644 | 648 | PF00917 | 0.652 |
DOC_USP7_MATH_1 | 678 | 682 | PF00917 | 0.734 |
DOC_USP7_MATH_1 | 685 | 689 | PF00917 | 0.678 |
DOC_USP7_MATH_1 | 89 | 93 | PF00917 | 0.460 |
DOC_USP7_MATH_2 | 299 | 305 | PF00917 | 0.317 |
DOC_USP7_UBL2_3 | 215 | 219 | PF12436 | 0.301 |
DOC_WW_Pin1_4 | 311 | 316 | PF00397 | 0.301 |
LIG_14-3-3_CanoR_1 | 208 | 212 | PF00244 | 0.412 |
LIG_14-3-3_CanoR_1 | 258 | 264 | PF00244 | 0.345 |
LIG_14-3-3_CanoR_1 | 288 | 297 | PF00244 | 0.421 |
LIG_14-3-3_CanoR_1 | 417 | 422 | PF00244 | 0.358 |
LIG_14-3-3_CanoR_1 | 460 | 464 | PF00244 | 0.156 |
LIG_14-3-3_CanoR_1 | 49 | 54 | PF00244 | 0.315 |
LIG_14-3-3_CanoR_1 | 522 | 528 | PF00244 | 0.409 |
LIG_14-3-3_CanoR_1 | 66 | 70 | PF00244 | 0.242 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.571 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.487 |
LIG_BRCT_BRCA1_1 | 224 | 228 | PF00533 | 0.317 |
LIG_EH1_1 | 194 | 202 | PF00400 | 0.335 |
LIG_FHA_1 | 171 | 177 | PF00498 | 0.301 |
LIG_FHA_1 | 238 | 244 | PF00498 | 0.421 |
LIG_FHA_1 | 312 | 318 | PF00498 | 0.312 |
LIG_FHA_1 | 674 | 680 | PF00498 | 0.615 |
LIG_FHA_2 | 272 | 278 | PF00498 | 0.386 |
LIG_FHA_2 | 3 | 9 | PF00498 | 0.647 |
LIG_FHA_2 | 37 | 43 | PF00498 | 0.397 |
LIG_FHA_2 | 418 | 424 | PF00498 | 0.396 |
LIG_FHA_2 | 543 | 549 | PF00498 | 0.302 |
LIG_LIR_Apic_2 | 225 | 231 | PF02991 | 0.317 |
LIG_LIR_Apic_2 | 265 | 269 | PF02991 | 0.336 |
LIG_LIR_Apic_2 | 71 | 76 | PF02991 | 0.316 |
LIG_LIR_Gen_1 | 117 | 127 | PF02991 | 0.448 |
LIG_LIR_Gen_1 | 523 | 531 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 117 | 123 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 157 | 163 | PF02991 | 0.301 |
LIG_LIR_Nem_3 | 257 | 263 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 393 | 398 | PF02991 | 0.341 |
LIG_LIR_Nem_3 | 422 | 427 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 523 | 527 | PF02991 | 0.386 |
LIG_MYND_1 | 311 | 315 | PF01753 | 0.317 |
LIG_PDZ_Class_2 | 701 | 706 | PF00595 | 0.540 |
LIG_Pex14_2 | 213 | 217 | PF04695 | 0.301 |
LIG_Pex14_2 | 375 | 379 | PF04695 | 0.448 |
LIG_PTB_Apo_2 | 318 | 325 | PF02174 | 0.301 |
LIG_PTB_Phospho_1 | 318 | 324 | PF10480 | 0.335 |
LIG_REV1ctd_RIR_1 | 257 | 265 | PF16727 | 0.296 |
LIG_REV1ctd_RIR_1 | 373 | 382 | PF16727 | 0.421 |
LIG_SH2_CRK | 424 | 428 | PF00017 | 0.421 |
LIG_SH2_GRB2like | 224 | 227 | PF00017 | 0.317 |
LIG_SH2_SRC | 398 | 401 | PF00017 | 0.412 |
LIG_SH2_STAP1 | 224 | 228 | PF00017 | 0.317 |
LIG_SH2_STAT3 | 247 | 250 | PF00017 | 0.421 |
LIG_SH2_STAT5 | 282 | 285 | PF00017 | 0.317 |
LIG_SH2_STAT5 | 382 | 385 | PF00017 | 0.301 |
LIG_SH2_STAT5 | 500 | 503 | PF00017 | 0.304 |
LIG_SH2_STAT5 | 562 | 565 | PF00017 | 0.535 |
LIG_SH3_3 | 309 | 315 | PF00018 | 0.301 |
LIG_SH3_3 | 366 | 372 | PF00018 | 0.475 |
LIG_SUMO_SIM_par_1 | 542 | 548 | PF11976 | 0.286 |
LIG_TRAF2_1 | 43 | 46 | PF00917 | 0.380 |
LIG_TRAF2_1 | 568 | 571 | PF00917 | 0.629 |
LIG_UBA3_1 | 197 | 204 | PF00899 | 0.317 |
LIG_WRC_WIRS_1 | 521 | 526 | PF05994 | 0.386 |
LIG_WRC_WIRS_1 | 552 | 557 | PF05994 | 0.421 |
MOD_CK1_1 | 112 | 118 | PF00069 | 0.534 |
MOD_CK1_1 | 159 | 165 | PF00069 | 0.295 |
MOD_CK1_1 | 184 | 190 | PF00069 | 0.301 |
MOD_CK1_1 | 222 | 228 | PF00069 | 0.448 |
MOD_CK1_1 | 450 | 456 | PF00069 | 0.343 |
MOD_CK1_1 | 462 | 468 | PF00069 | 0.242 |
MOD_CK1_1 | 487 | 493 | PF00069 | 0.376 |
MOD_CK1_1 | 585 | 591 | PF00069 | 0.761 |
MOD_CK1_1 | 607 | 613 | PF00069 | 0.746 |
MOD_CK1_1 | 616 | 622 | PF00069 | 0.732 |
MOD_CK1_1 | 629 | 635 | PF00069 | 0.688 |
MOD_CK1_1 | 647 | 653 | PF00069 | 0.692 |
MOD_CK2_1 | 271 | 277 | PF00069 | 0.335 |
MOD_CK2_1 | 29 | 35 | PF00069 | 0.405 |
MOD_CK2_1 | 349 | 355 | PF00069 | 0.447 |
MOD_CK2_1 | 36 | 42 | PF00069 | 0.347 |
MOD_CK2_1 | 387 | 393 | PF00069 | 0.301 |
MOD_CK2_1 | 49 | 55 | PF00069 | 0.117 |
MOD_CK2_1 | 571 | 577 | PF00069 | 0.712 |
MOD_CK2_1 | 624 | 630 | PF00069 | 0.748 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.419 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.568 |
MOD_GlcNHglycan | 231 | 234 | PF01048 | 0.301 |
MOD_GlcNHglycan | 351 | 354 | PF01048 | 0.500 |
MOD_GlcNHglycan | 467 | 470 | PF01048 | 0.367 |
MOD_GlcNHglycan | 486 | 490 | PF01048 | 0.344 |
MOD_GlcNHglycan | 511 | 514 | PF01048 | 0.337 |
MOD_GlcNHglycan | 589 | 592 | PF01048 | 0.674 |
MOD_GlcNHglycan | 621 | 624 | PF01048 | 0.667 |
MOD_GlcNHglycan | 625 | 629 | PF01048 | 0.634 |
MOD_GlcNHglycan | 680 | 683 | PF01048 | 0.710 |
MOD_GlcNHglycan | 687 | 690 | PF01048 | 0.640 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.248 |
MOD_GSK3_1 | 413 | 420 | PF00069 | 0.343 |
MOD_GSK3_1 | 443 | 450 | PF00069 | 0.368 |
MOD_GSK3_1 | 454 | 461 | PF00069 | 0.276 |
MOD_GSK3_1 | 474 | 481 | PF00069 | 0.362 |
MOD_GSK3_1 | 484 | 491 | PF00069 | 0.418 |
MOD_GSK3_1 | 505 | 512 | PF00069 | 0.404 |
MOD_GSK3_1 | 597 | 604 | PF00069 | 0.684 |
MOD_GSK3_1 | 613 | 620 | PF00069 | 0.788 |
MOD_GSK3_1 | 624 | 631 | PF00069 | 0.733 |
MOD_GSK3_1 | 643 | 650 | PF00069 | 0.683 |
MOD_GSK3_1 | 674 | 681 | PF00069 | 0.685 |
MOD_LATS_1 | 651 | 657 | PF00433 | 0.601 |
MOD_N-GLC_1 | 324 | 329 | PF02516 | 0.301 |
MOD_N-GLC_1 | 412 | 417 | PF02516 | 0.421 |
MOD_N-GLC_1 | 582 | 587 | PF02516 | 0.778 |
MOD_N-GLC_2 | 321 | 323 | PF02516 | 0.301 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.448 |
MOD_NEK2_1 | 207 | 212 | PF00069 | 0.425 |
MOD_NEK2_1 | 259 | 264 | PF00069 | 0.421 |
MOD_NEK2_1 | 283 | 288 | PF00069 | 0.301 |
MOD_NEK2_1 | 349 | 354 | PF00069 | 0.556 |
MOD_NEK2_2 | 319 | 324 | PF00069 | 0.448 |
MOD_NEK2_2 | 520 | 525 | PF00069 | 0.448 |
MOD_PK_1 | 219 | 225 | PF00069 | 0.448 |
MOD_PK_1 | 49 | 55 | PF00069 | 0.320 |
MOD_PKA_1 | 49 | 55 | PF00069 | 0.335 |
MOD_PKA_1 | 653 | 659 | PF00069 | 0.753 |
MOD_PKA_2 | 112 | 118 | PF00069 | 0.448 |
MOD_PKA_2 | 139 | 145 | PF00069 | 0.358 |
MOD_PKA_2 | 207 | 213 | PF00069 | 0.370 |
MOD_PKA_2 | 299 | 305 | PF00069 | 0.317 |
MOD_PKA_2 | 446 | 452 | PF00069 | 0.362 |
MOD_PKA_2 | 459 | 465 | PF00069 | 0.349 |
MOD_PKA_2 | 49 | 55 | PF00069 | 0.302 |
MOD_PKA_2 | 65 | 71 | PF00069 | 0.256 |
MOD_PKB_1 | 445 | 453 | PF00069 | 0.421 |
MOD_Plk_1 | 156 | 162 | PF00069 | 0.301 |
MOD_Plk_1 | 181 | 187 | PF00069 | 0.302 |
MOD_Plk_1 | 29 | 35 | PF00069 | 0.450 |
MOD_Plk_1 | 324 | 330 | PF00069 | 0.317 |
MOD_Plk_2-3 | 170 | 176 | PF00069 | 0.301 |
MOD_Plk_4 | 181 | 187 | PF00069 | 0.312 |
MOD_Plk_4 | 262 | 268 | PF00069 | 0.335 |
MOD_Plk_4 | 491 | 497 | PF00069 | 0.421 |
MOD_Plk_4 | 523 | 529 | PF00069 | 0.368 |
MOD_Plk_4 | 551 | 557 | PF00069 | 0.408 |
MOD_Plk_4 | 65 | 71 | PF00069 | 0.301 |
MOD_ProDKin_1 | 311 | 317 | PF00069 | 0.301 |
MOD_SUMO_for_1 | 127 | 130 | PF00179 | 0.534 |
MOD_SUMO_for_1 | 670 | 673 | PF00179 | 0.751 |
MOD_SUMO_rev_2 | 298 | 304 | PF00179 | 0.318 |
MOD_SUMO_rev_2 | 352 | 358 | PF00179 | 0.420 |
TRG_ENDOCYTIC_2 | 382 | 385 | PF00928 | 0.307 |
TRG_ENDOCYTIC_2 | 424 | 427 | PF00928 | 0.421 |
TRG_ER_diArg_1 | 287 | 290 | PF00400 | 0.448 |
TRG_ER_diArg_1 | 405 | 408 | PF00400 | 0.421 |
TRG_ER_diArg_1 | 444 | 447 | PF00400 | 0.296 |
TRG_ER_diArg_1 | 49 | 51 | PF00400 | 0.317 |
TRG_NLS_MonoExtC_3 | 652 | 657 | PF00514 | 0.737 |
TRG_Pf-PMV_PEXEL_1 | 332 | 336 | PF00026 | 0.295 |
TRG_Pf-PMV_PEXEL_1 | 529 | 533 | PF00026 | 0.317 |
TRG_Pf-PMV_PEXEL_1 | 633 | 637 | PF00026 | 0.699 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2K1 | Leptomonas seymouri | 73% | 96% |
A0A0S4JIG5 | Bodo saltans | 47% | 100% |
A0A1X0NP17 | Trypanosomatidae | 61% | 100% |
A0A3Q8ID77 | Leishmania donovani | 94% | 100% |
A0A3R7KE83 | Trypanosoma rangeli | 66% | 100% |
A4H7T8 | Leishmania braziliensis | 87% | 100% |
A4HW64 | Leishmania infantum | 94% | 100% |
A4I4T6 | Leishmania infantum | 26% | 100% |
C9ZSW0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 59% | 100% |
E9AEC2 | Leishmania major | 27% | 100% |
E9ALG4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
P29468 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 28% | 100% |
Q4QFL6 | Leishmania major | 94% | 99% |
V5BKK6 | Trypanosoma cruzi | 59% | 86% |