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: E9AC31
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_NRD_NRD_1 | 160 | 162 | PF00675 | 0.713 |
CLV_NRD_NRD_1 | 196 | 198 | PF00675 | 0.408 |
CLV_NRD_NRD_1 | 342 | 344 | PF00675 | 0.551 |
CLV_NRD_NRD_1 | 347 | 349 | PF00675 | 0.447 |
CLV_NRD_NRD_1 | 366 | 368 | PF00675 | 0.251 |
CLV_NRD_NRD_1 | 394 | 396 | PF00675 | 0.601 |
CLV_NRD_NRD_1 | 424 | 426 | PF00675 | 0.452 |
CLV_NRD_NRD_1 | 520 | 522 | PF00675 | 0.585 |
CLV_NRD_NRD_1 | 63 | 65 | PF00675 | 0.564 |
CLV_PCSK_FUR_1 | 278 | 282 | PF00082 | 0.534 |
CLV_PCSK_FUR_1 | 364 | 368 | PF00082 | 0.424 |
CLV_PCSK_KEX2_1 | 160 | 162 | PF00082 | 0.713 |
CLV_PCSK_KEX2_1 | 196 | 198 | PF00082 | 0.408 |
CLV_PCSK_KEX2_1 | 280 | 282 | PF00082 | 0.581 |
CLV_PCSK_KEX2_1 | 341 | 343 | PF00082 | 0.535 |
CLV_PCSK_KEX2_1 | 347 | 349 | PF00082 | 0.457 |
CLV_PCSK_KEX2_1 | 366 | 368 | PF00082 | 0.354 |
CLV_PCSK_KEX2_1 | 424 | 426 | PF00082 | 0.459 |
CLV_PCSK_KEX2_1 | 519 | 521 | PF00082 | 0.593 |
CLV_PCSK_KEX2_1 | 63 | 65 | PF00082 | 0.564 |
CLV_PCSK_PC1ET2_1 | 280 | 282 | PF00082 | 0.534 |
CLV_PCSK_PC7_1 | 156 | 162 | PF00082 | 0.637 |
CLV_PCSK_PC7_1 | 343 | 349 | PF00082 | 0.499 |
CLV_PCSK_SKI1_1 | 179 | 183 | PF00082 | 0.325 |
CLV_PCSK_SKI1_1 | 286 | 290 | PF00082 | 0.715 |
CLV_PCSK_SKI1_1 | 348 | 352 | PF00082 | 0.553 |
CLV_PCSK_SKI1_1 | 366 | 370 | PF00082 | 0.306 |
CLV_PCSK_SKI1_1 | 430 | 434 | PF00082 | 0.447 |
CLV_PCSK_SKI1_1 | 444 | 448 | PF00082 | 0.343 |
DEG_APCC_DBOX_1 | 365 | 373 | PF00400 | 0.412 |
DEG_APCC_DBOX_1 | 424 | 432 | PF00400 | 0.380 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.570 |
DEG_SPOP_SBC_1 | 94 | 98 | PF00917 | 0.598 |
DOC_CYCLIN_RxL_1 | 439 | 449 | PF00134 | 0.420 |
DOC_CYCLIN_yCln2_LP_2 | 181 | 187 | PF00134 | 0.381 |
DOC_CYCLIN_yCln2_LP_2 | 448 | 454 | PF00134 | 0.380 |
DOC_CYCLIN_yCln2_LP_2 | 77 | 83 | PF00134 | 0.616 |
DOC_MAPK_gen_1 | 63 | 69 | PF00069 | 0.564 |
DOC_MAPK_MEF2A_6 | 327 | 336 | PF00069 | 0.455 |
DOC_PP1_RVXF_1 | 133 | 140 | PF00149 | 0.634 |
DOC_PP2B_LxvP_1 | 148 | 151 | PF13499 | 0.537 |
DOC_PP2B_LxvP_1 | 181 | 184 | PF13499 | 0.459 |
DOC_PP2B_LxvP_1 | 291 | 294 | PF13499 | 0.630 |
DOC_PP2B_LxvP_1 | 77 | 80 | PF13499 | 0.636 |
DOC_PP4_FxxP_1 | 139 | 142 | PF00568 | 0.532 |
DOC_USP7_MATH_1 | 23 | 27 | PF00917 | 0.565 |
DOC_USP7_MATH_1 | 249 | 253 | PF00917 | 0.740 |
DOC_USP7_MATH_1 | 272 | 276 | PF00917 | 0.669 |
DOC_USP7_MATH_1 | 297 | 301 | PF00917 | 0.625 |
DOC_USP7_MATH_1 | 304 | 308 | PF00917 | 0.629 |
DOC_USP7_MATH_1 | 350 | 354 | PF00917 | 0.574 |
DOC_USP7_MATH_1 | 359 | 363 | PF00917 | 0.497 |
DOC_USP7_MATH_1 | 368 | 372 | PF00917 | 0.296 |
DOC_USP7_MATH_1 | 387 | 391 | PF00917 | 0.430 |
DOC_USP7_MATH_1 | 84 | 88 | PF00917 | 0.636 |
DOC_USP7_MATH_1 | 93 | 97 | PF00917 | 0.776 |
DOC_USP7_UBL2_3 | 276 | 280 | PF12436 | 0.538 |
DOC_WW_Pin1_4 | 112 | 117 | PF00397 | 0.722 |
DOC_WW_Pin1_4 | 355 | 360 | PF00397 | 0.416 |
DOC_WW_Pin1_4 | 490 | 495 | PF00397 | 0.610 |
LIG_14-3-3_CanoR_1 | 348 | 357 | PF00244 | 0.499 |
LIG_14-3-3_CanoR_1 | 415 | 420 | PF00244 | 0.550 |
LIG_14-3-3_CanoR_1 | 68 | 76 | PF00244 | 0.553 |
LIG_BIR_III_4 | 226 | 230 | PF00653 | 0.524 |
LIG_BIR_III_4 | 248 | 252 | PF00653 | 0.608 |
LIG_eIF4E_1 | 149 | 155 | PF01652 | 0.505 |
LIG_FHA_1 | 214 | 220 | PF00498 | 0.485 |
LIG_FHA_1 | 257 | 263 | PF00498 | 0.561 |
LIG_FHA_1 | 453 | 459 | PF00498 | 0.383 |
LIG_FHA_1 | 491 | 497 | PF00498 | 0.589 |
LIG_FHA_2 | 31 | 37 | PF00498 | 0.514 |
LIG_FHA_2 | 498 | 504 | PF00498 | 0.538 |
LIG_LIR_Nem_3 | 70 | 76 | PF02991 | 0.549 |
LIG_NRBOX | 177 | 183 | PF00104 | 0.380 |
LIG_SH2_CRK | 149 | 153 | PF00017 | 0.556 |
LIG_SH2_NCK_1 | 42 | 46 | PF00017 | 0.572 |
LIG_SH2_SRC | 149 | 152 | PF00017 | 0.603 |
LIG_SH2_SRC | 404 | 407 | PF00017 | 0.441 |
LIG_SH2_STAP1 | 168 | 172 | PF00017 | 0.400 |
LIG_SH2_STAT3 | 553 | 556 | PF00017 | 0.378 |
LIG_SH2_STAT5 | 207 | 210 | PF00017 | 0.334 |
LIG_SH2_STAT5 | 344 | 347 | PF00017 | 0.404 |
LIG_SH2_STAT5 | 377 | 380 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 399 | 402 | PF00017 | 0.433 |
LIG_SH2_STAT5 | 553 | 556 | PF00017 | 0.499 |
LIG_SH3_1 | 403 | 409 | PF00018 | 0.495 |
LIG_SH3_3 | 110 | 116 | PF00018 | 0.584 |
LIG_SH3_3 | 261 | 267 | PF00018 | 0.624 |
LIG_SH3_3 | 291 | 297 | PF00018 | 0.625 |
LIG_SH3_3 | 353 | 359 | PF00018 | 0.354 |
LIG_SH3_3 | 381 | 387 | PF00018 | 0.451 |
LIG_SH3_3 | 403 | 409 | PF00018 | 0.497 |
LIG_SH3_3 | 96 | 102 | PF00018 | 0.580 |
LIG_TRAF2_1 | 309 | 312 | PF00917 | 0.619 |
LIG_WW_3 | 412 | 416 | PF00397 | 0.495 |
MOD_CK1_1 | 25 | 31 | PF00069 | 0.605 |
MOD_CK1_1 | 252 | 258 | PF00069 | 0.751 |
MOD_CK1_1 | 295 | 301 | PF00069 | 0.608 |
MOD_CK1_1 | 349 | 355 | PF00069 | 0.418 |
MOD_CK2_1 | 118 | 124 | PF00069 | 0.654 |
MOD_CK2_1 | 306 | 312 | PF00069 | 0.600 |
MOD_CK2_1 | 387 | 393 | PF00069 | 0.446 |
MOD_CK2_1 | 497 | 503 | PF00069 | 0.618 |
MOD_Cter_Amidation | 61 | 64 | PF01082 | 0.565 |
MOD_GlcNHglycan | 247 | 252 | PF01048 | 0.618 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.641 |
MOD_GlcNHglycan | 29 | 32 | PF01048 | 0.523 |
MOD_GlcNHglycan | 297 | 300 | PF01048 | 0.674 |
MOD_GlcNHglycan | 316 | 319 | PF01048 | 0.662 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.406 |
MOD_GlcNHglycan | 352 | 355 | PF01048 | 0.372 |
MOD_GlcNHglycan | 379 | 382 | PF01048 | 0.476 |
MOD_GlcNHglycan | 483 | 486 | PF01048 | 0.556 |
MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.662 |
MOD_GSK3_1 | 118 | 125 | PF00069 | 0.665 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.409 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.468 |
MOD_GSK3_1 | 252 | 259 | PF00069 | 0.721 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.525 |
MOD_GSK3_1 | 346 | 353 | PF00069 | 0.485 |
MOD_GSK3_1 | 355 | 362 | PF00069 | 0.390 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.628 |
MOD_LATS_1 | 513 | 519 | PF00433 | 0.591 |
MOD_N-GLC_1 | 490 | 495 | PF02516 | 0.607 |
MOD_NEK2_1 | 336 | 341 | PF00069 | 0.568 |
MOD_NEK2_1 | 398 | 403 | PF00069 | 0.388 |
MOD_NEK2_1 | 446 | 451 | PF00069 | 0.363 |
MOD_PIKK_1 | 385 | 391 | PF00454 | 0.494 |
MOD_PKA_2 | 252 | 258 | PF00069 | 0.537 |
MOD_PKA_2 | 272 | 278 | PF00069 | 0.636 |
MOD_PKA_2 | 346 | 352 | PF00069 | 0.444 |
MOD_PKA_2 | 67 | 73 | PF00069 | 0.605 |
MOD_Plk_2-3 | 164 | 170 | PF00069 | 0.413 |
MOD_Plk_2-3 | 213 | 219 | PF00069 | 0.429 |
MOD_Plk_4 | 118 | 124 | PF00069 | 0.647 |
MOD_Plk_4 | 173 | 179 | PF00069 | 0.459 |
MOD_Plk_4 | 368 | 374 | PF00069 | 0.480 |
MOD_ProDKin_1 | 112 | 118 | PF00069 | 0.719 |
MOD_ProDKin_1 | 355 | 361 | PF00069 | 0.411 |
MOD_ProDKin_1 | 490 | 496 | PF00069 | 0.612 |
TRG_DiLeu_BaLyEn_6 | 141 | 146 | PF01217 | 0.566 |
TRG_ER_diArg_1 | 160 | 162 | PF00400 | 0.659 |
TRG_ER_diArg_1 | 267 | 270 | PF00400 | 0.523 |
TRG_ER_diArg_1 | 331 | 334 | PF00400 | 0.553 |
TRG_ER_diArg_1 | 340 | 343 | PF00400 | 0.502 |
TRG_ER_diArg_1 | 363 | 366 | PF00400 | 0.443 |
TRG_ER_diArg_1 | 423 | 425 | PF00400 | 0.475 |
TRG_ER_diArg_1 | 51 | 54 | PF00400 | 0.677 |
TRG_ER_diArg_1 | 519 | 521 | PF00400 | 0.596 |
TRG_Pf-PMV_PEXEL_1 | 160 | 164 | PF00026 | 0.513 |
TRG_Pf-PMV_PEXEL_1 | 550 | 555 | PF00026 | 0.484 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IL81 | Leptomonas seymouri | 35% | 95% |
A0A451EJ97 | Leishmania donovani | 88% | 98% |
A4H366 | Leishmania braziliensis | 67% | 97% |
A4HRG3 | Leishmania infantum | 88% | 88% |
E9AJC8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 100% |