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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AJC8
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006396 | RNA processing | 6 | 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:0009987 | cellular process | 1 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0031123 | RNA 3'-end processing | 7 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0071076 | RNA 3' uridylation | 8 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 1 |
GO:0016779 | nucleotidyltransferase activity | 4 | 1 |
GO:0050265 | RNA uridylyltransferase activity | 4 | 1 |
GO:0070569 | uridylyltransferase activity | 5 | 1 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 1 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 239 | 243 | PF00656 | 0.509 |
CLV_NRD_NRD_1 | 155 | 157 | PF00675 | 0.684 |
CLV_NRD_NRD_1 | 191 | 193 | PF00675 | 0.403 |
CLV_NRD_NRD_1 | 279 | 281 | PF00675 | 0.589 |
CLV_NRD_NRD_1 | 336 | 338 | PF00675 | 0.586 |
CLV_NRD_NRD_1 | 418 | 420 | PF00675 | 0.456 |
CLV_NRD_NRD_1 | 514 | 516 | PF00675 | 0.599 |
CLV_PCSK_KEX2_1 | 155 | 157 | PF00082 | 0.684 |
CLV_PCSK_KEX2_1 | 191 | 193 | PF00082 | 0.403 |
CLV_PCSK_KEX2_1 | 279 | 281 | PF00082 | 0.616 |
CLV_PCSK_KEX2_1 | 335 | 337 | PF00082 | 0.570 |
CLV_PCSK_KEX2_1 | 418 | 420 | PF00082 | 0.462 |
CLV_PCSK_KEX2_1 | 514 | 516 | PF00082 | 0.596 |
CLV_PCSK_PC7_1 | 151 | 157 | PF00082 | 0.604 |
CLV_PCSK_PC7_1 | 331 | 337 | PF00082 | 0.527 |
CLV_PCSK_SKI1_1 | 273 | 277 | PF00082 | 0.536 |
CLV_PCSK_SKI1_1 | 287 | 291 | PF00082 | 0.712 |
CLV_PCSK_SKI1_1 | 438 | 442 | PF00082 | 0.352 |
DEG_APCC_DBOX_1 | 418 | 426 | PF00400 | 0.380 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.529 |
DEG_SPOP_SBC_1 | 483 | 487 | PF00917 | 0.477 |
DEG_SPOP_SBC_1 | 94 | 98 | PF00917 | 0.592 |
DOC_CYCLIN_RxL_1 | 433 | 443 | PF00134 | 0.426 |
DOC_CYCLIN_yCln2_LP_2 | 176 | 182 | PF00134 | 0.385 |
DOC_CYCLIN_yCln2_LP_2 | 442 | 448 | PF00134 | 0.389 |
DOC_PP1_RVXF_1 | 128 | 135 | PF00149 | 0.642 |
DOC_PP2B_LxvP_1 | 143 | 146 | PF13499 | 0.539 |
DOC_PP2B_LxvP_1 | 176 | 179 | PF13499 | 0.468 |
DOC_PP2B_LxvP_1 | 292 | 295 | PF13499 | 0.632 |
DOC_PP2B_LxvP_1 | 77 | 80 | PF13499 | 0.653 |
DOC_PP4_FxxP_1 | 134 | 137 | PF00568 | 0.533 |
DOC_USP7_MATH_1 | 23 | 27 | PF00917 | 0.548 |
DOC_USP7_MATH_1 | 244 | 248 | PF00917 | 0.743 |
DOC_USP7_MATH_1 | 344 | 348 | PF00917 | 0.601 |
DOC_USP7_MATH_1 | 353 | 357 | PF00917 | 0.509 |
DOC_USP7_MATH_1 | 362 | 366 | PF00917 | 0.303 |
DOC_USP7_MATH_1 | 381 | 385 | PF00917 | 0.435 |
DOC_USP7_MATH_1 | 84 | 88 | PF00917 | 0.645 |
DOC_WW_Pin1_4 | 349 | 354 | PF00397 | 0.427 |
DOC_WW_Pin1_4 | 484 | 489 | PF00397 | 0.599 |
LIG_14-3-3_CanoR_1 | 343 | 349 | PF00244 | 0.510 |
LIG_14-3-3_CanoR_1 | 361 | 367 | PF00244 | 0.249 |
LIG_14-3-3_CanoR_1 | 393 | 400 | PF00244 | 0.296 |
LIG_14-3-3_CanoR_1 | 409 | 414 | PF00244 | 0.559 |
LIG_14-3-3_CanoR_1 | 514 | 522 | PF00244 | 0.437 |
LIG_14-3-3_CanoR_1 | 68 | 76 | PF00244 | 0.546 |
LIG_APCC_ABBA_1 | 468 | 473 | PF00400 | 0.369 |
LIG_eIF4E_1 | 144 | 150 | PF01652 | 0.494 |
LIG_FHA_1 | 209 | 215 | PF00498 | 0.516 |
LIG_FHA_1 | 447 | 453 | PF00498 | 0.386 |
LIG_FHA_1 | 484 | 490 | PF00498 | 0.571 |
LIG_FHA_2 | 205 | 211 | PF00498 | 0.310 |
LIG_LIR_Nem_3 | 70 | 76 | PF02991 | 0.549 |
LIG_NRBOX | 172 | 178 | PF00104 | 0.381 |
LIG_PCNA_yPIPBox_3 | 151 | 161 | PF02747 | 0.418 |
LIG_PCNA_yPIPBox_3 | 273 | 285 | PF02747 | 0.507 |
LIG_PCNA_yPIPBox_3 | 358 | 367 | PF02747 | 0.268 |
LIG_Pex14_1 | 57 | 61 | PF04695 | 0.442 |
LIG_SH2_CRK | 144 | 148 | PF00017 | 0.557 |
LIG_SH2_NCK_1 | 42 | 46 | PF00017 | 0.517 |
LIG_SH2_SRC | 144 | 147 | PF00017 | 0.598 |
LIG_SH2_SRC | 398 | 401 | PF00017 | 0.459 |
LIG_SH2_STAP1 | 163 | 167 | PF00017 | 0.392 |
LIG_SH2_STAP1 | 448 | 452 | PF00017 | 0.274 |
LIG_SH2_STAT3 | 357 | 360 | PF00017 | 0.295 |
LIG_SH2_STAT3 | 547 | 550 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 202 | 205 | PF00017 | 0.351 |
LIG_SH2_STAT5 | 371 | 374 | PF00017 | 0.368 |
LIG_SH2_STAT5 | 448 | 451 | PF00017 | 0.277 |
LIG_SH2_STAT5 | 547 | 550 | PF00017 | 0.490 |
LIG_SH3_1 | 397 | 403 | PF00018 | 0.506 |
LIG_SH3_3 | 107 | 113 | PF00018 | 0.613 |
LIG_SH3_3 | 256 | 262 | PF00018 | 0.646 |
LIG_SH3_3 | 292 | 298 | PF00018 | 0.633 |
LIG_SH3_3 | 375 | 381 | PF00018 | 0.449 |
LIG_SH3_3 | 397 | 403 | PF00018 | 0.509 |
LIG_TRAF2_1 | 310 | 313 | PF00917 | 0.664 |
LIG_WW_3 | 406 | 410 | PF00397 | 0.502 |
MOD_CK1_1 | 247 | 253 | PF00069 | 0.765 |
MOD_CK1_1 | 25 | 31 | PF00069 | 0.579 |
MOD_CK1_1 | 296 | 302 | PF00069 | 0.626 |
MOD_CK1_1 | 502 | 508 | PF00069 | 0.529 |
MOD_CK2_1 | 112 | 118 | PF00069 | 0.614 |
MOD_CK2_1 | 204 | 210 | PF00069 | 0.290 |
MOD_CK2_1 | 381 | 387 | PF00069 | 0.450 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.580 |
MOD_GlcNHglycan | 244 | 247 | PF01048 | 0.607 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.664 |
MOD_GlcNHglycan | 29 | 32 | PF01048 | 0.495 |
MOD_GlcNHglycan | 298 | 301 | PF01048 | 0.693 |
MOD_GlcNHglycan | 373 | 376 | PF01048 | 0.467 |
MOD_GlcNHglycan | 477 | 480 | PF01048 | 0.550 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.703 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.434 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.446 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.735 |
MOD_GSK3_1 | 349 | 356 | PF00069 | 0.402 |
MOD_GSK3_1 | 446 | 453 | PF00069 | 0.371 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.573 |
MOD_GSK3_1 | 89 | 96 | PF00069 | 0.685 |
MOD_NEK2_1 | 117 | 122 | PF00069 | 0.587 |
MOD_NEK2_1 | 132 | 137 | PF00069 | 0.478 |
MOD_NEK2_1 | 330 | 335 | PF00069 | 0.605 |
MOD_NEK2_1 | 44 | 49 | PF00069 | 0.356 |
MOD_NEK2_1 | 440 | 445 | PF00069 | 0.370 |
MOD_NEK2_2 | 268 | 273 | PF00069 | 0.514 |
MOD_PIKK_1 | 117 | 123 | PF00454 | 0.579 |
MOD_PIKK_1 | 379 | 385 | PF00454 | 0.501 |
MOD_PIKK_1 | 401 | 407 | PF00454 | 0.416 |
MOD_PKA_2 | 330 | 336 | PF00069 | 0.543 |
MOD_PKA_2 | 392 | 398 | PF00069 | 0.286 |
MOD_PKA_2 | 513 | 519 | PF00069 | 0.439 |
MOD_PKA_2 | 67 | 73 | PF00069 | 0.581 |
MOD_PKB_1 | 341 | 349 | PF00069 | 0.390 |
MOD_Plk_2-3 | 159 | 165 | PF00069 | 0.401 |
MOD_Plk_4 | 168 | 174 | PF00069 | 0.455 |
MOD_Plk_4 | 362 | 368 | PF00069 | 0.490 |
MOD_ProDKin_1 | 349 | 355 | PF00069 | 0.422 |
MOD_ProDKin_1 | 484 | 490 | PF00069 | 0.601 |
TRG_DiLeu_BaLyEn_6 | 136 | 141 | PF01217 | 0.573 |
TRG_ER_diArg_1 | 155 | 157 | PF00400 | 0.629 |
TRG_ER_diArg_1 | 279 | 282 | PF00400 | 0.630 |
TRG_ER_diArg_1 | 326 | 329 | PF00400 | 0.600 |
TRG_ER_diArg_1 | 334 | 337 | PF00400 | 0.536 |
TRG_ER_diArg_1 | 417 | 419 | PF00400 | 0.479 |
TRG_ER_diArg_1 | 51 | 54 | PF00400 | 0.587 |
TRG_Pf-PMV_PEXEL_1 | 155 | 159 | PF00026 | 0.488 |
TRG_Pf-PMV_PEXEL_1 | 544 | 549 | PF00026 | 0.482 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IL81 | Leptomonas seymouri | 38% | 94% |
A0A451EJ97 | Leishmania donovani | 81% | 97% |
A4H366 | Leishmania braziliensis | 67% | 100% |
A4HRG3 | Leishmania infantum | 82% | 87% |
E9AC31 | Leishmania major | 79% | 99% |