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: A0A451EJ97
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 | 108 | 112 | PF00656 | 0.522 |
CLV_NRD_NRD_1 | 160 | 162 | PF00675 | 0.647 |
CLV_NRD_NRD_1 | 196 | 198 | PF00675 | 0.414 |
CLV_NRD_NRD_1 | 273 | 275 | PF00675 | 0.576 |
CLV_NRD_NRD_1 | 287 | 289 | PF00675 | 0.553 |
CLV_NRD_NRD_1 | 351 | 353 | PF00675 | 0.581 |
CLV_NRD_NRD_1 | 356 | 358 | PF00675 | 0.479 |
CLV_NRD_NRD_1 | 375 | 377 | PF00675 | 0.265 |
CLV_NRD_NRD_1 | 403 | 405 | PF00675 | 0.606 |
CLV_NRD_NRD_1 | 433 | 435 | PF00675 | 0.441 |
CLV_NRD_NRD_1 | 529 | 531 | PF00675 | 0.585 |
CLV_PCSK_FUR_1 | 373 | 377 | PF00082 | 0.436 |
CLV_PCSK_KEX2_1 | 160 | 162 | PF00082 | 0.647 |
CLV_PCSK_KEX2_1 | 196 | 198 | PF00082 | 0.414 |
CLV_PCSK_KEX2_1 | 273 | 275 | PF00082 | 0.603 |
CLV_PCSK_KEX2_1 | 287 | 289 | PF00082 | 0.580 |
CLV_PCSK_KEX2_1 | 350 | 352 | PF00082 | 0.563 |
CLV_PCSK_KEX2_1 | 356 | 358 | PF00082 | 0.489 |
CLV_PCSK_KEX2_1 | 375 | 377 | PF00082 | 0.367 |
CLV_PCSK_KEX2_1 | 433 | 435 | PF00082 | 0.448 |
CLV_PCSK_KEX2_1 | 528 | 530 | PF00082 | 0.587 |
CLV_PCSK_PC7_1 | 156 | 162 | PF00082 | 0.521 |
CLV_PCSK_PC7_1 | 352 | 358 | PF00082 | 0.531 |
CLV_PCSK_SKI1_1 | 295 | 299 | PF00082 | 0.711 |
CLV_PCSK_SKI1_1 | 357 | 361 | PF00082 | 0.583 |
CLV_PCSK_SKI1_1 | 375 | 379 | PF00082 | 0.319 |
CLV_PCSK_SKI1_1 | 439 | 443 | PF00082 | 0.440 |
CLV_PCSK_SKI1_1 | 453 | 457 | PF00082 | 0.349 |
DEG_APCC_DBOX_1 | 374 | 382 | PF00400 | 0.422 |
DEG_APCC_DBOX_1 | 433 | 441 | PF00400 | 0.370 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.560 |
DEG_SPOP_SBC_1 | 88 | 92 | PF00917 | 0.599 |
DEG_SPOP_SBC_1 | 94 | 98 | PF00917 | 0.602 |
DOC_CYCLIN_RxL_1 | 448 | 461 | PF00134 | 0.433 |
DOC_CYCLIN_yCln2_LP_2 | 116 | 119 | PF00134 | 0.567 |
DOC_CYCLIN_yCln2_LP_2 | 181 | 187 | PF00134 | 0.383 |
DOC_CYCLIN_yCln2_LP_2 | 77 | 83 | PF00134 | 0.615 |
DOC_PP1_RVXF_1 | 133 | 140 | PF00149 | 0.605 |
DOC_PP2B_LxvP_1 | 116 | 119 | PF13499 | 0.567 |
DOC_PP2B_LxvP_1 | 148 | 151 | PF13499 | 0.431 |
DOC_PP2B_LxvP_1 | 181 | 184 | PF13499 | 0.465 |
DOC_PP2B_LxvP_1 | 300 | 303 | PF13499 | 0.633 |
DOC_PP2B_LxvP_1 | 77 | 80 | PF13499 | 0.635 |
DOC_PP4_FxxP_1 | 139 | 142 | PF00568 | 0.483 |
DOC_USP7_MATH_1 | 23 | 27 | PF00917 | 0.550 |
DOC_USP7_MATH_1 | 249 | 253 | PF00917 | 0.746 |
DOC_USP7_MATH_1 | 272 | 276 | PF00917 | 0.658 |
DOC_USP7_MATH_1 | 306 | 310 | PF00917 | 0.636 |
DOC_USP7_MATH_1 | 313 | 317 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 359 | 363 | PF00917 | 0.601 |
DOC_USP7_MATH_1 | 368 | 372 | PF00917 | 0.509 |
DOC_USP7_MATH_1 | 377 | 381 | PF00917 | 0.301 |
DOC_USP7_MATH_1 | 396 | 400 | PF00917 | 0.442 |
DOC_USP7_MATH_1 | 84 | 88 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 93 | 97 | PF00917 | 0.682 |
DOC_WW_Pin1_4 | 364 | 369 | PF00397 | 0.431 |
DOC_WW_Pin1_4 | 67 | 72 | PF00397 | 0.592 |
LIG_14-3-3_CanoR_1 | 357 | 366 | PF00244 | 0.525 |
LIG_14-3-3_CanoR_1 | 424 | 429 | PF00244 | 0.559 |
LIG_14-3-3_CanoR_1 | 63 | 68 | PF00244 | 0.577 |
LIG_BIR_III_4 | 248 | 252 | PF00653 | 0.617 |
LIG_eIF4E_1 | 149 | 155 | PF01652 | 0.446 |
LIG_FHA_1 | 100 | 106 | PF00498 | 0.571 |
LIG_FHA_1 | 214 | 220 | PF00498 | 0.488 |
LIG_FHA_1 | 462 | 468 | PF00498 | 0.388 |
LIG_FHA_1 | 500 | 506 | PF00498 | 0.579 |
LIG_FHA_1 | 64 | 70 | PF00498 | 0.520 |
LIG_FHA_2 | 456 | 462 | PF00498 | 0.335 |
LIG_LIR_Apic_2 | 114 | 118 | PF02991 | 0.526 |
LIG_LIR_Nem_3 | 70 | 76 | PF02991 | 0.546 |
LIG_NRBOX | 177 | 183 | PF00104 | 0.374 |
LIG_PCNA_yPIPBox_3 | 156 | 166 | PF02747 | 0.398 |
LIG_SH2_CRK | 149 | 153 | PF00017 | 0.502 |
LIG_SH2_NCK_1 | 42 | 46 | PF00017 | 0.539 |
LIG_SH2_SRC | 149 | 152 | PF00017 | 0.536 |
LIG_SH2_SRC | 413 | 416 | PF00017 | 0.448 |
LIG_SH2_STAP1 | 168 | 172 | PF00017 | 0.387 |
LIG_SH2_STAT5 | 207 | 210 | PF00017 | 0.336 |
LIG_SH2_STAT5 | 386 | 389 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 408 | 411 | PF00017 | 0.440 |
LIG_SH2_STAT5 | 562 | 565 | PF00017 | 0.489 |
LIG_SH3_1 | 412 | 418 | PF00018 | 0.496 |
LIG_SH3_3 | 107 | 113 | PF00018 | 0.568 |
LIG_SH3_3 | 261 | 267 | PF00018 | 0.653 |
LIG_SH3_3 | 300 | 306 | PF00018 | 0.631 |
LIG_SH3_3 | 390 | 396 | PF00018 | 0.459 |
LIG_SH3_3 | 412 | 418 | PF00018 | 0.499 |
LIG_TRAF2_1 | 318 | 321 | PF00917 | 0.631 |
LIG_UBA3_1 | 557 | 565 | PF00899 | 0.359 |
LIG_WW_3 | 421 | 425 | PF00397 | 0.499 |
MOD_CK1_1 | 25 | 31 | PF00069 | 0.582 |
MOD_CK1_1 | 252 | 258 | PF00069 | 0.766 |
MOD_CK1_1 | 304 | 310 | PF00069 | 0.619 |
MOD_CK1_1 | 358 | 364 | PF00069 | 0.446 |
MOD_CK1_1 | 87 | 93 | PF00069 | 0.543 |
MOD_CK2_1 | 118 | 124 | PF00069 | 0.607 |
MOD_CK2_1 | 315 | 321 | PF00069 | 0.613 |
MOD_CK2_1 | 396 | 402 | PF00069 | 0.457 |
MOD_CK2_1 | 455 | 461 | PF00069 | 0.325 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.598 |
MOD_GlcNHglycan | 247 | 252 | PF01048 | 0.626 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.665 |
MOD_GlcNHglycan | 306 | 309 | PF01048 | 0.686 |
MOD_GlcNHglycan | 325 | 328 | PF01048 | 0.672 |
MOD_GlcNHglycan | 357 | 360 | PF01048 | 0.436 |
MOD_GlcNHglycan | 361 | 364 | PF01048 | 0.398 |
MOD_GlcNHglycan | 388 | 391 | PF01048 | 0.474 |
MOD_GlcNHglycan | 492 | 495 | PF01048 | 0.555 |
MOD_GlcNHglycan | 502 | 505 | PF01048 | 0.587 |
MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.652 |
MOD_GSK3_1 | 118 | 125 | PF00069 | 0.617 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.412 |
MOD_GSK3_1 | 252 | 259 | PF00069 | 0.736 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.580 |
MOD_GSK3_1 | 355 | 362 | PF00069 | 0.515 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.405 |
MOD_GSK3_1 | 461 | 468 | PF00069 | 0.373 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.632 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.626 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.609 |
MOD_LATS_1 | 522 | 528 | PF00433 | 0.594 |
MOD_LATS_1 | 61 | 67 | PF00433 | 0.508 |
MOD_N-GLC_1 | 499 | 504 | PF02516 | 0.598 |
MOD_NEK2_1 | 123 | 128 | PF00069 | 0.528 |
MOD_NEK2_1 | 345 | 350 | PF00069 | 0.580 |
MOD_NEK2_1 | 407 | 412 | PF00069 | 0.391 |
MOD_NEK2_1 | 455 | 460 | PF00069 | 0.368 |
MOD_OFUCOSY | 210 | 217 | PF10250 | 0.376 |
MOD_PIKK_1 | 123 | 129 | PF00454 | 0.540 |
MOD_PIKK_1 | 394 | 400 | PF00454 | 0.508 |
MOD_PIKK_1 | 416 | 422 | PF00454 | 0.417 |
MOD_PKA_2 | 272 | 278 | PF00069 | 0.624 |
MOD_PKA_2 | 280 | 286 | PF00069 | 0.520 |
MOD_PKA_2 | 355 | 361 | PF00069 | 0.473 |
MOD_Plk_2-3 | 164 | 170 | PF00069 | 0.396 |
MOD_Plk_4 | 111 | 117 | PF00069 | 0.587 |
MOD_Plk_4 | 173 | 179 | PF00069 | 0.450 |
MOD_Plk_4 | 377 | 383 | PF00069 | 0.488 |
MOD_ProDKin_1 | 364 | 370 | PF00069 | 0.426 |
MOD_ProDKin_1 | 67 | 73 | PF00069 | 0.587 |
TRG_DiLeu_BaLyEn_6 | 141 | 146 | PF01217 | 0.467 |
TRG_ER_diArg_1 | 160 | 162 | PF00400 | 0.593 |
TRG_ER_diArg_1 | 287 | 290 | PF00400 | 0.601 |
TRG_ER_diArg_1 | 341 | 344 | PF00400 | 0.583 |
TRG_ER_diArg_1 | 349 | 352 | PF00400 | 0.525 |
TRG_ER_diArg_1 | 372 | 375 | PF00400 | 0.452 |
TRG_ER_diArg_1 | 432 | 434 | PF00400 | 0.455 |
TRG_ER_diArg_1 | 51 | 54 | PF00400 | 0.664 |
TRG_ER_diArg_1 | 528 | 530 | PF00400 | 0.590 |
TRG_Pf-PMV_PEXEL_1 | 160 | 164 | PF00026 | 0.460 |
TRG_Pf-PMV_PEXEL_1 | 559 | 564 | PF00026 | 0.483 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IL81 | Leptomonas seymouri | 37% | 96% |
A4H366 | Leishmania braziliensis | 69% | 100% |
A4HRG3 | Leishmania infantum | 99% | 100% |
E9AC31 | Leishmania major | 88% | 98% |
E9AJC8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 97% |