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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 8 |
GO:0031499 | TRAMP complex | 3 | 8 |
GO:0032991 | protein-containing complex | 1 | 8 |
GO:0110165 | cellular anatomical entity | 1 | 8 |
GO:0140513 | nuclear protein-containing complex | 2 | 8 |
GO:0005730 | nucleolus | 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 |
Related structures:
AlphaFold database: A0A3Q8IDQ5
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 8 |
GO:0006396 | RNA processing | 6 | 8 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 8 |
GO:0006807 | nitrogen compound metabolic process | 2 | 8 |
GO:0008152 | metabolic process | 1 | 8 |
GO:0009987 | cellular process | 1 | 8 |
GO:0016070 | RNA metabolic process | 5 | 8 |
GO:0031123 | RNA 3'-end processing | 7 | 8 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 8 |
GO:0043170 | macromolecule metabolic process | 3 | 8 |
GO:0043631 | RNA polyadenylation | 6 | 8 |
GO:0044237 | cellular metabolic process | 2 | 8 |
GO:0044238 | primary metabolic process | 2 | 8 |
GO:0046483 | heterocycle metabolic process | 3 | 8 |
GO:0071076 | RNA 3' uridylation | 8 | 8 |
GO:0071704 | organic substance metabolic process | 2 | 8 |
GO:0090304 | nucleic acid metabolic process | 4 | 8 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 8 |
GO:0004652 | obsolete polynucleotide adenylyltransferase activity | 6 | 8 |
GO:0005488 | binding | 1 | 7 |
GO:0016740 | transferase activity | 2 | 8 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 8 |
GO:0016779 | nucleotidyltransferase activity | 4 | 8 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043169 | cation binding | 3 | 7 |
GO:0046872 | metal ion binding | 4 | 7 |
GO:0050265 | RNA uridylyltransferase activity | 4 | 8 |
GO:0070566 | adenylyltransferase activity | 5 | 8 |
GO:0070569 | uridylyltransferase activity | 5 | 8 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 8 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 200 | 204 | PF00656 | 0.807 |
CLV_MEL_PAP_1 | 454 | 460 | PF00089 | 0.590 |
CLV_NRD_NRD_1 | 110 | 112 | PF00675 | 0.677 |
CLV_NRD_NRD_1 | 131 | 133 | PF00675 | 0.622 |
CLV_NRD_NRD_1 | 175 | 177 | PF00675 | 0.746 |
CLV_NRD_NRD_1 | 196 | 198 | PF00675 | 0.801 |
CLV_NRD_NRD_1 | 355 | 357 | PF00675 | 0.503 |
CLV_NRD_NRD_1 | 380 | 382 | PF00675 | 0.549 |
CLV_NRD_NRD_1 | 484 | 486 | PF00675 | 0.513 |
CLV_NRD_NRD_1 | 574 | 576 | PF00675 | 0.584 |
CLV_NRD_NRD_1 | 85 | 87 | PF00675 | 0.693 |
CLV_PCSK_FUR_1 | 173 | 177 | PF00082 | 0.774 |
CLV_PCSK_FUR_1 | 378 | 382 | PF00082 | 0.535 |
CLV_PCSK_KEX2_1 | 110 | 112 | PF00082 | 0.651 |
CLV_PCSK_KEX2_1 | 131 | 133 | PF00082 | 0.622 |
CLV_PCSK_KEX2_1 | 173 | 175 | PF00082 | 0.723 |
CLV_PCSK_KEX2_1 | 196 | 198 | PF00082 | 0.801 |
CLV_PCSK_KEX2_1 | 380 | 382 | PF00082 | 0.549 |
CLV_PCSK_KEX2_1 | 484 | 486 | PF00082 | 0.406 |
CLV_PCSK_KEX2_1 | 574 | 576 | PF00082 | 0.602 |
CLV_PCSK_PC7_1 | 570 | 576 | PF00082 | 0.601 |
CLV_PCSK_SKI1_1 | 20 | 24 | PF00082 | 0.620 |
CLV_PCSK_SKI1_1 | 239 | 243 | PF00082 | 0.482 |
CLV_PCSK_SKI1_1 | 338 | 342 | PF00082 | 0.568 |
CLV_PCSK_SKI1_1 | 494 | 498 | PF00082 | 0.462 |
CLV_PCSK_SKI1_1 | 518 | 522 | PF00082 | 0.499 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.588 |
DEG_SPOP_SBC_1 | 216 | 220 | PF00917 | 0.654 |
DOC_CKS1_1 | 89 | 94 | PF01111 | 0.675 |
DOC_CKS1_1 | 98 | 103 | PF01111 | 0.597 |
DOC_CYCLIN_yCln2_LP_2 | 231 | 234 | PF00134 | 0.686 |
DOC_MAPK_gen_1 | 354 | 364 | PF00069 | 0.515 |
DOC_MAPK_gen_1 | 378 | 388 | PF00069 | 0.492 |
DOC_MAPK_MEF2A_6 | 278 | 285 | PF00069 | 0.472 |
DOC_MAPK_MEF2A_6 | 380 | 388 | PF00069 | 0.495 |
DOC_PP2B_LxvP_1 | 231 | 234 | PF13499 | 0.686 |
DOC_PP2B_LxvP_1 | 293 | 296 | PF13499 | 0.400 |
DOC_PP2B_LxvP_1 | 405 | 408 | PF13499 | 0.351 |
DOC_PP4_FxxP_1 | 30 | 33 | PF00568 | 0.661 |
DOC_PP4_FxxP_1 | 496 | 499 | PF00568 | 0.501 |
DOC_USP7_MATH_1 | 331 | 335 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 49 | 53 | PF00917 | 0.673 |
DOC_USP7_MATH_1 | 59 | 63 | PF00917 | 0.582 |
DOC_USP7_UBL2_3 | 494 | 498 | PF12436 | 0.430 |
DOC_WW_Pin1_4 | 105 | 110 | PF00397 | 0.577 |
DOC_WW_Pin1_4 | 123 | 128 | PF00397 | 0.784 |
DOC_WW_Pin1_4 | 142 | 147 | PF00397 | 0.792 |
DOC_WW_Pin1_4 | 211 | 216 | PF00397 | 0.651 |
DOC_WW_Pin1_4 | 253 | 258 | PF00397 | 0.433 |
DOC_WW_Pin1_4 | 544 | 549 | PF00397 | 0.557 |
DOC_WW_Pin1_4 | 88 | 93 | PF00397 | 0.718 |
DOC_WW_Pin1_4 | 97 | 102 | PF00397 | 0.675 |
LIG_14-3-3_CanoR_1 | 196 | 206 | PF00244 | 0.819 |
LIG_14-3-3_CanoR_1 | 273 | 277 | PF00244 | 0.496 |
LIG_14-3-3_CanoR_1 | 34 | 43 | PF00244 | 0.726 |
LIG_14-3-3_CanoR_1 | 354 | 364 | PF00244 | 0.456 |
LIG_14-3-3_CanoR_1 | 533 | 539 | PF00244 | 0.541 |
LIG_BRCT_BRCA1_1 | 26 | 30 | PF00533 | 0.638 |
LIG_BRCT_BRCA1_1 | 357 | 361 | PF00533 | 0.496 |
LIG_BRCT_BRCA1_1 | 534 | 538 | PF00533 | 0.544 |
LIG_CtBP_PxDLS_1 | 8 | 12 | PF00389 | 0.581 |
LIG_EH1_1 | 439 | 447 | PF00400 | 0.390 |
LIG_EVH1_2 | 70 | 74 | PF00568 | 0.614 |
LIG_FHA_1 | 200 | 206 | PF00498 | 0.800 |
LIG_FHA_1 | 21 | 27 | PF00498 | 0.623 |
LIG_FHA_1 | 289 | 295 | PF00498 | 0.429 |
LIG_FHA_1 | 330 | 336 | PF00498 | 0.467 |
LIG_FHA_1 | 561 | 567 | PF00498 | 0.579 |
LIG_FHA_2 | 198 | 204 | PF00498 | 0.579 |
LIG_FHA_2 | 256 | 262 | PF00498 | 0.494 |
LIG_FHA_2 | 477 | 483 | PF00498 | 0.376 |
LIG_Integrin_isoDGR_2 | 148 | 150 | PF01839 | 0.628 |
LIG_IRF3_LxIS_1 | 217 | 224 | PF10401 | 0.653 |
LIG_LIR_Apic_2 | 27 | 33 | PF02991 | 0.649 |
LIG_LIR_Apic_2 | 37 | 43 | PF02991 | 0.598 |
LIG_LIR_Apic_2 | 4 | 8 | PF02991 | 0.533 |
LIG_LIR_Apic_2 | 495 | 499 | PF02991 | 0.501 |
LIG_LIR_Gen_1 | 358 | 368 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 358 | 364 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 480 | 486 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 535 | 541 | PF02991 | 0.503 |
LIG_NRBOX | 247 | 253 | PF00104 | 0.466 |
LIG_NRBOX | 400 | 406 | PF00104 | 0.520 |
LIG_PCNA_yPIPBox_3 | 457 | 470 | PF02747 | 0.485 |
LIG_SH2_CRK | 286 | 290 | PF00017 | 0.404 |
LIG_SH2_NCK_1 | 40 | 44 | PF00017 | 0.687 |
LIG_SH2_NCK_1 | 76 | 80 | PF00017 | 0.621 |
LIG_SH2_SRC | 40 | 43 | PF00017 | 0.687 |
LIG_SH2_STAT3 | 449 | 452 | PF00017 | 0.527 |
LIG_SH2_STAT3 | 490 | 493 | PF00017 | 0.478 |
LIG_SH2_STAT5 | 253 | 256 | PF00017 | 0.549 |
LIG_SH2_STAT5 | 400 | 403 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 449 | 452 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 490 | 493 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 505 | 508 | PF00017 | 0.384 |
LIG_SH2_STAT5 | 558 | 561 | PF00017 | 0.565 |
LIG_SH2_STAT5 | 594 | 597 | PF00017 | 0.550 |
LIG_SH3_1 | 86 | 92 | PF00018 | 0.679 |
LIG_SH3_3 | 140 | 146 | PF00018 | 0.749 |
LIG_SH3_3 | 506 | 512 | PF00018 | 0.445 |
LIG_SH3_3 | 53 | 59 | PF00018 | 0.809 |
LIG_SH3_3 | 86 | 92 | PF00018 | 0.823 |
LIG_SUMO_SIM_anti_2 | 443 | 448 | PF11976 | 0.434 |
LIG_SUMO_SIM_par_1 | 323 | 329 | PF11976 | 0.497 |
LIG_TRFH_1 | 253 | 257 | PF08558 | 0.482 |
LIG_UBA3_1 | 416 | 421 | PF00899 | 0.389 |
MOD_CDK_SPK_2 | 105 | 110 | PF00069 | 0.679 |
MOD_CDK_SPxK_1 | 105 | 111 | PF00069 | 0.681 |
MOD_CK1_1 | 155 | 161 | PF00069 | 0.803 |
MOD_CK1_1 | 177 | 183 | PF00069 | 0.778 |
MOD_CK1_1 | 190 | 196 | PF00069 | 0.723 |
MOD_CK1_1 | 256 | 262 | PF00069 | 0.499 |
MOD_CK1_1 | 288 | 294 | PF00069 | 0.396 |
MOD_CK1_1 | 314 | 320 | PF00069 | 0.569 |
MOD_CK1_1 | 329 | 335 | PF00069 | 0.446 |
MOD_CK1_1 | 547 | 553 | PF00069 | 0.566 |
MOD_CK1_1 | 62 | 68 | PF00069 | 0.749 |
MOD_CK2_1 | 304 | 310 | PF00069 | 0.550 |
MOD_GlcNHglycan | 179 | 183 | PF01048 | 0.791 |
MOD_GlcNHglycan | 192 | 195 | PF01048 | 0.664 |
MOD_GlcNHglycan | 306 | 309 | PF01048 | 0.607 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.448 |
MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.504 |
MOD_GlcNHglycan | 391 | 395 | PF01048 | 0.488 |
MOD_GlcNHglycan | 458 | 461 | PF01048 | 0.509 |
MOD_GlcNHglycan | 534 | 537 | PF01048 | 0.539 |
MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.733 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.815 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.730 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.721 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.682 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.680 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.455 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.666 |
MOD_GSK3_1 | 386 | 393 | PF00069 | 0.479 |
MOD_GSK3_1 | 436 | 443 | PF00069 | 0.397 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.565 |
MOD_GSK3_1 | 518 | 525 | PF00069 | 0.404 |
MOD_N-GLC_1 | 318 | 323 | PF02516 | 0.508 |
MOD_N-GLC_1 | 544 | 549 | PF02516 | 0.522 |
MOD_N-GLC_2 | 425 | 427 | PF02516 | 0.467 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.563 |
MOD_NEK2_1 | 217 | 222 | PF00069 | 0.721 |
MOD_NEK2_1 | 26 | 31 | PF00069 | 0.640 |
MOD_NEK2_1 | 355 | 360 | PF00069 | 0.459 |
MOD_NEK2_1 | 390 | 395 | PF00069 | 0.491 |
MOD_NEK2_1 | 462 | 467 | PF00069 | 0.486 |
MOD_NEK2_1 | 522 | 527 | PF00069 | 0.414 |
MOD_PIKK_1 | 355 | 361 | PF00454 | 0.564 |
MOD_PIKK_1 | 47 | 53 | PF00454 | 0.620 |
MOD_PIKK_1 | 550 | 556 | PF00454 | 0.509 |
MOD_PKA_1 | 174 | 180 | PF00069 | 0.839 |
MOD_PKA_2 | 174 | 180 | PF00069 | 0.839 |
MOD_PKA_2 | 261 | 267 | PF00069 | 0.575 |
MOD_PKA_2 | 272 | 278 | PF00069 | 0.418 |
MOD_PKA_2 | 35 | 41 | PF00069 | 0.736 |
MOD_PKA_2 | 355 | 361 | PF00069 | 0.439 |
MOD_PKA_2 | 456 | 462 | PF00069 | 0.546 |
MOD_PKA_2 | 532 | 538 | PF00069 | 0.474 |
MOD_PKB_1 | 173 | 181 | PF00069 | 0.802 |
MOD_PKB_1 | 197 | 205 | PF00069 | 0.707 |
MOD_PKB_1 | 34 | 42 | PF00069 | 0.686 |
MOD_Plk_1 | 18 | 24 | PF00069 | 0.652 |
MOD_Plk_1 | 386 | 392 | PF00069 | 0.429 |
MOD_Plk_2-3 | 10 | 16 | PF00069 | 0.583 |
MOD_Plk_4 | 201 | 207 | PF00069 | 0.704 |
MOD_Plk_4 | 227 | 233 | PF00069 | 0.642 |
MOD_Plk_4 | 357 | 363 | PF00069 | 0.360 |
MOD_Plk_4 | 518 | 524 | PF00069 | 0.422 |
MOD_Plk_4 | 534 | 540 | PF00069 | 0.401 |
MOD_ProDKin_1 | 105 | 111 | PF00069 | 0.579 |
MOD_ProDKin_1 | 123 | 129 | PF00069 | 0.779 |
MOD_ProDKin_1 | 142 | 148 | PF00069 | 0.795 |
MOD_ProDKin_1 | 211 | 217 | PF00069 | 0.652 |
MOD_ProDKin_1 | 253 | 259 | PF00069 | 0.444 |
MOD_ProDKin_1 | 544 | 550 | PF00069 | 0.553 |
MOD_ProDKin_1 | 88 | 94 | PF00069 | 0.720 |
MOD_ProDKin_1 | 97 | 103 | PF00069 | 0.676 |
MOD_SUMO_rev_2 | 133 | 138 | PF00179 | 0.623 |
MOD_SUMO_rev_2 | 259 | 266 | PF00179 | 0.501 |
MOD_SUMO_rev_2 | 382 | 386 | PF00179 | 0.563 |
TRG_DiLeu_BaLyEn_6 | 412 | 417 | PF01217 | 0.445 |
TRG_ENDOCYTIC_2 | 286 | 289 | PF00928 | 0.408 |
TRG_ER_diArg_1 | 109 | 111 | PF00400 | 0.734 |
TRG_ER_diArg_1 | 173 | 176 | PF00400 | 0.753 |
TRG_ER_diArg_1 | 196 | 199 | PF00400 | 0.712 |
TRG_ER_diArg_1 | 33 | 36 | PF00400 | 0.681 |
TRG_ER_diArg_1 | 378 | 381 | PF00400 | 0.538 |
TRG_ER_diArg_1 | 454 | 457 | PF00400 | 0.544 |
TRG_ER_diArg_1 | 483 | 485 | PF00400 | 0.424 |
TRG_NES_CRM1_1 | 284 | 299 | PF08389 | 0.463 |
TRG_Pf-PMV_PEXEL_1 | 267 | 271 | PF00026 | 0.506 |
TRG_Pf-PMV_PEXEL_1 | 484 | 489 | PF00026 | 0.501 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PD64 | Leptomonas seymouri | 57% | 100% |
A4HEQ5 | Leishmania braziliensis | 70% | 100% |
A4I1Y4 | Leishmania infantum | 99% | 100% |
C9ZS34 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
E9AY31 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q4Q9E2 | Leishmania major | 92% | 100% |