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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4I8P1
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 10 |
GO:0006396 | RNA processing | 6 | 10 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 10 |
GO:0006807 | nitrogen compound metabolic process | 2 | 10 |
GO:0008152 | metabolic process | 1 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0016070 | RNA metabolic process | 5 | 10 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 10 |
GO:0043170 | macromolecule metabolic process | 3 | 10 |
GO:0044237 | cellular metabolic process | 2 | 10 |
GO:0044238 | primary metabolic process | 2 | 10 |
GO:0046483 | heterocycle metabolic process | 3 | 10 |
GO:0071704 | organic substance metabolic process | 2 | 10 |
GO:0090304 | nucleic acid metabolic process | 4 | 10 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 10 |
GO:0006399 | tRNA metabolic process | 7 | 1 |
GO:0008033 | tRNA processing | 8 | 1 |
GO:0034470 | ncRNA processing | 7 | 1 |
GO:0034660 | ncRNA metabolic process | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 10 |
GO:0003723 | RNA binding | 4 | 10 |
GO:0003824 | catalytic activity | 1 | 10 |
GO:0004000 | adenosine deaminase activity | 4 | 10 |
GO:0005488 | binding | 1 | 10 |
GO:0016787 | hydrolase activity | 2 | 10 |
GO:0016810 | hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds | 3 | 10 |
GO:0016814 | hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in cyclic amidines | 4 | 10 |
GO:0019239 | deaminase activity | 3 | 10 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
GO:0008251 | tRNA-specific adenosine deaminase activity | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 147 | 151 | PF00656 | 0.537 |
CLV_C14_Caspase3-7 | 582 | 586 | PF00656 | 0.572 |
CLV_NRD_NRD_1 | 114 | 116 | PF00675 | 0.491 |
CLV_NRD_NRD_1 | 143 | 145 | PF00675 | 0.340 |
CLV_NRD_NRD_1 | 158 | 160 | PF00675 | 0.232 |
CLV_NRD_NRD_1 | 187 | 189 | PF00675 | 0.347 |
CLV_NRD_NRD_1 | 325 | 327 | PF00675 | 0.255 |
CLV_NRD_NRD_1 | 368 | 370 | PF00675 | 0.552 |
CLV_NRD_NRD_1 | 430 | 432 | PF00675 | 0.610 |
CLV_NRD_NRD_1 | 483 | 485 | PF00675 | 0.638 |
CLV_PCSK_FUR_1 | 141 | 145 | PF00082 | 0.218 |
CLV_PCSK_FUR_1 | 366 | 370 | PF00082 | 0.507 |
CLV_PCSK_KEX2_1 | 114 | 116 | PF00082 | 0.485 |
CLV_PCSK_KEX2_1 | 143 | 145 | PF00082 | 0.326 |
CLV_PCSK_KEX2_1 | 158 | 160 | PF00082 | 0.232 |
CLV_PCSK_KEX2_1 | 186 | 188 | PF00082 | 0.322 |
CLV_PCSK_KEX2_1 | 324 | 326 | PF00082 | 0.255 |
CLV_PCSK_KEX2_1 | 368 | 370 | PF00082 | 0.594 |
CLV_PCSK_KEX2_1 | 432 | 434 | PF00082 | 0.575 |
CLV_PCSK_KEX2_1 | 483 | 485 | PF00082 | 0.638 |
CLV_PCSK_PC1ET2_1 | 432 | 434 | PF00082 | 0.575 |
CLV_PCSK_PC7_1 | 479 | 485 | PF00082 | 0.572 |
CLV_PCSK_SKI1_1 | 143 | 147 | PF00082 | 0.352 |
CLV_PCSK_SKI1_1 | 274 | 278 | PF00082 | 0.249 |
CLV_PCSK_SKI1_1 | 385 | 389 | PF00082 | 0.483 |
DEG_APCC_DBOX_1 | 560 | 568 | PF00400 | 0.534 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.691 |
DOC_ANK_TNKS_1 | 49 | 56 | PF00023 | 0.432 |
DOC_CKS1_1 | 381 | 386 | PF01111 | 0.405 |
DOC_CYCLIN_RxL_1 | 140 | 150 | PF00134 | 0.564 |
DOC_CYCLIN_yCln2_LP_2 | 498 | 504 | PF00134 | 0.467 |
DOC_MAPK_DCC_7 | 324 | 334 | PF00069 | 0.501 |
DOC_MAPK_gen_1 | 114 | 121 | PF00069 | 0.400 |
DOC_MAPK_gen_1 | 141 | 148 | PF00069 | 0.546 |
DOC_MAPK_gen_1 | 158 | 164 | PF00069 | 0.409 |
DOC_MAPK_gen_1 | 312 | 321 | PF00069 | 0.455 |
DOC_MAPK_gen_1 | 76 | 84 | PF00069 | 0.508 |
DOC_MAPK_MEF2A_6 | 114 | 121 | PF00069 | 0.357 |
DOC_PP1_RVXF_1 | 573 | 579 | PF00149 | 0.653 |
DOC_PP2B_LxvP_1 | 342 | 345 | PF13499 | 0.490 |
DOC_PP2B_LxvP_1 | 89 | 92 | PF13499 | 0.376 |
DOC_PP4_FxxP_1 | 330 | 333 | PF00568 | 0.473 |
DOC_USP7_MATH_1 | 104 | 108 | PF00917 | 0.505 |
DOC_USP7_MATH_1 | 169 | 173 | PF00917 | 0.547 |
DOC_USP7_MATH_1 | 230 | 234 | PF00917 | 0.545 |
DOC_USP7_MATH_1 | 408 | 412 | PF00917 | 0.582 |
DOC_USP7_MATH_1 | 443 | 447 | PF00917 | 0.593 |
DOC_USP7_MATH_1 | 579 | 583 | PF00917 | 0.733 |
DOC_USP7_MATH_1 | 59 | 63 | PF00917 | 0.673 |
DOC_USP7_MATH_1 | 66 | 70 | PF00917 | 0.681 |
DOC_USP7_UBL2_3 | 106 | 110 | PF12436 | 0.537 |
DOC_WW_Pin1_4 | 200 | 205 | PF00397 | 0.594 |
DOC_WW_Pin1_4 | 24 | 29 | PF00397 | 0.461 |
DOC_WW_Pin1_4 | 263 | 268 | PF00397 | 0.418 |
DOC_WW_Pin1_4 | 279 | 284 | PF00397 | 0.511 |
DOC_WW_Pin1_4 | 380 | 385 | PF00397 | 0.384 |
DOC_WW_Pin1_4 | 395 | 400 | PF00397 | 0.473 |
DOC_WW_Pin1_4 | 485 | 490 | PF00397 | 0.571 |
DOC_WW_Pin1_4 | 5 | 10 | PF00397 | 0.591 |
LIG_14-3-3_CanoR_1 | 174 | 180 | PF00244 | 0.533 |
LIG_14-3-3_CanoR_1 | 302 | 308 | PF00244 | 0.485 |
LIG_14-3-3_CanoR_1 | 335 | 342 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 483 | 489 | PF00244 | 0.587 |
LIG_APCC_ABBAyCdc20_2 | 369 | 375 | PF00400 | 0.428 |
LIG_BIR_III_2 | 132 | 136 | PF00653 | 0.490 |
LIG_BRCT_BRCA1_1 | 390 | 394 | PF00533 | 0.583 |
LIG_CaM_IQ_9 | 360 | 376 | PF13499 | 0.382 |
LIG_deltaCOP1_diTrp_1 | 311 | 316 | PF00928 | 0.537 |
LIG_FHA_1 | 209 | 215 | PF00498 | 0.542 |
LIG_FHA_1 | 308 | 314 | PF00498 | 0.537 |
LIG_FHA_1 | 395 | 401 | PF00498 | 0.493 |
LIG_FHA_1 | 475 | 481 | PF00498 | 0.444 |
LIG_FHA_2 | 268 | 274 | PF00498 | 0.586 |
LIG_FHA_2 | 485 | 491 | PF00498 | 0.566 |
LIG_FHA_2 | 567 | 573 | PF00498 | 0.650 |
LIG_FHA_2 | 6 | 12 | PF00498 | 0.651 |
LIG_LIR_Gen_1 | 177 | 185 | PF02991 | 0.575 |
LIG_LIR_Gen_1 | 383 | 394 | PF02991 | 0.499 |
LIG_LIR_Gen_1 | 419 | 429 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 177 | 183 | PF02991 | 0.581 |
LIG_LIR_Nem_3 | 383 | 389 | PF02991 | 0.341 |
LIG_LIR_Nem_3 | 419 | 424 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 448 | 454 | PF02991 | 0.508 |
LIG_SH2_CRK | 281 | 285 | PF00017 | 0.522 |
LIG_SH2_NCK_1 | 533 | 537 | PF00017 | 0.678 |
LIG_SH2_PTP2 | 116 | 119 | PF00017 | 0.416 |
LIG_SH2_STAP1 | 180 | 184 | PF00017 | 0.522 |
LIG_SH2_STAP1 | 533 | 537 | PF00017 | 0.605 |
LIG_SH2_STAT5 | 116 | 119 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 271 | 274 | PF00017 | 0.397 |
LIG_SH2_STAT5 | 93 | 96 | PF00017 | 0.347 |
LIG_SH3_1 | 325 | 331 | PF00018 | 0.470 |
LIG_SH3_3 | 325 | 331 | PF00018 | 0.482 |
LIG_SH3_3 | 338 | 344 | PF00018 | 0.433 |
LIG_SH3_3 | 378 | 384 | PF00018 | 0.535 |
LIG_SH3_3 | 486 | 492 | PF00018 | 0.527 |
LIG_SUMO_SIM_anti_2 | 515 | 521 | PF11976 | 0.515 |
LIG_SUMO_SIM_par_1 | 144 | 150 | PF11976 | 0.490 |
LIG_TRAF2_1 | 8 | 11 | PF00917 | 0.609 |
MOD_CDK_SPK_2 | 380 | 385 | PF00069 | 0.418 |
MOD_CDK_SPxxK_3 | 5 | 12 | PF00069 | 0.583 |
MOD_CK1_1 | 120 | 126 | PF00069 | 0.476 |
MOD_CK1_1 | 233 | 239 | PF00069 | 0.532 |
MOD_CK1_1 | 255 | 261 | PF00069 | 0.558 |
MOD_CK1_1 | 376 | 382 | PF00069 | 0.461 |
MOD_CK1_1 | 411 | 417 | PF00069 | 0.487 |
MOD_CK2_1 | 255 | 261 | PF00069 | 0.514 |
MOD_CK2_1 | 4 | 10 | PF00069 | 0.657 |
MOD_CK2_1 | 484 | 490 | PF00069 | 0.608 |
MOD_CK2_1 | 510 | 516 | PF00069 | 0.481 |
MOD_Cter_Amidation | 322 | 325 | PF01082 | 0.255 |
MOD_GlcNHglycan | 106 | 109 | PF01048 | 0.514 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.226 |
MOD_GlcNHglycan | 170 | 174 | PF01048 | 0.322 |
MOD_GlcNHglycan | 188 | 191 | PF01048 | 0.155 |
MOD_GlcNHglycan | 200 | 203 | PF01048 | 0.290 |
MOD_GlcNHglycan | 232 | 235 | PF01048 | 0.309 |
MOD_GlcNHglycan | 256 | 260 | PF01048 | 0.351 |
MOD_GlcNHglycan | 390 | 393 | PF01048 | 0.518 |
MOD_GlcNHglycan | 445 | 448 | PF01048 | 0.573 |
MOD_GlcNHglycan | 455 | 458 | PF01048 | 0.737 |
MOD_GlcNHglycan | 520 | 523 | PF01048 | 0.640 |
MOD_GlcNHglycan | 526 | 529 | PF01048 | 0.678 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.607 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.522 |
MOD_GSK3_1 | 263 | 270 | PF00069 | 0.531 |
MOD_GSK3_1 | 303 | 310 | PF00069 | 0.501 |
MOD_GSK3_1 | 376 | 383 | PF00069 | 0.559 |
MOD_GSK3_1 | 423 | 430 | PF00069 | 0.543 |
MOD_GSK3_1 | 443 | 450 | PF00069 | 0.601 |
MOD_GSK3_1 | 520 | 527 | PF00069 | 0.641 |
MOD_GSK3_1 | 566 | 573 | PF00069 | 0.652 |
MOD_N-GLC_1 | 303 | 308 | PF02516 | 0.298 |
MOD_N-GLC_1 | 414 | 419 | PF02516 | 0.414 |
MOD_N-GLC_1 | 551 | 556 | PF02516 | 0.572 |
MOD_NEK2_1 | 208 | 213 | PF00069 | 0.562 |
MOD_NEK2_1 | 216 | 221 | PF00069 | 0.584 |
MOD_NEK2_1 | 222 | 227 | PF00069 | 0.488 |
MOD_NEK2_1 | 305 | 310 | PF00069 | 0.462 |
MOD_NEK2_1 | 334 | 339 | PF00069 | 0.540 |
MOD_NEK2_1 | 394 | 399 | PF00069 | 0.517 |
MOD_NEK2_1 | 510 | 515 | PF00069 | 0.470 |
MOD_NEK2_1 | 524 | 529 | PF00069 | 0.462 |
MOD_NEK2_1 | 553 | 558 | PF00069 | 0.668 |
MOD_NEK2_1 | 577 | 582 | PF00069 | 0.679 |
MOD_NEK2_1 | 87 | 92 | PF00069 | 0.365 |
MOD_NEK2_2 | 570 | 575 | PF00069 | 0.605 |
MOD_PIKK_1 | 553 | 559 | PF00454 | 0.621 |
MOD_PK_1 | 335 | 341 | PF00069 | 0.457 |
MOD_PKA_1 | 186 | 192 | PF00069 | 0.544 |
MOD_PKA_1 | 483 | 489 | PF00069 | 0.587 |
MOD_PKA_2 | 173 | 179 | PF00069 | 0.537 |
MOD_PKA_2 | 186 | 192 | PF00069 | 0.537 |
MOD_PKA_2 | 208 | 214 | PF00069 | 0.522 |
MOD_PKA_2 | 334 | 340 | PF00069 | 0.511 |
MOD_PKA_2 | 483 | 489 | PF00069 | 0.587 |
MOD_PKA_2 | 591 | 597 | PF00069 | 0.543 |
MOD_Plk_1 | 303 | 309 | PF00069 | 0.498 |
MOD_Plk_1 | 376 | 382 | PF00069 | 0.512 |
MOD_Plk_1 | 460 | 466 | PF00069 | 0.540 |
MOD_Plk_1 | 551 | 557 | PF00069 | 0.566 |
MOD_Plk_1 | 570 | 576 | PF00069 | 0.624 |
MOD_Plk_4 | 267 | 273 | PF00069 | 0.483 |
MOD_Plk_4 | 460 | 466 | PF00069 | 0.605 |
MOD_Plk_4 | 542 | 548 | PF00069 | 0.583 |
MOD_ProDKin_1 | 200 | 206 | PF00069 | 0.594 |
MOD_ProDKin_1 | 24 | 30 | PF00069 | 0.461 |
MOD_ProDKin_1 | 263 | 269 | PF00069 | 0.418 |
MOD_ProDKin_1 | 279 | 285 | PF00069 | 0.511 |
MOD_ProDKin_1 | 380 | 386 | PF00069 | 0.378 |
MOD_ProDKin_1 | 395 | 401 | PF00069 | 0.478 |
MOD_ProDKin_1 | 485 | 491 | PF00069 | 0.569 |
MOD_ProDKin_1 | 5 | 11 | PF00069 | 0.589 |
TRG_DiLeu_BaLyEn_6 | 141 | 146 | PF01217 | 0.491 |
TRG_DiLeu_BaLyEn_6 | 286 | 291 | PF01217 | 0.490 |
TRG_DiLeu_BaLyEn_6 | 572 | 577 | PF01217 | 0.582 |
TRG_ENDOCYTIC_2 | 116 | 119 | PF00928 | 0.418 |
TRG_ENDOCYTIC_2 | 180 | 183 | PF00928 | 0.522 |
TRG_ENDOCYTIC_2 | 281 | 284 | PF00928 | 0.517 |
TRG_ER_diArg_1 | 113 | 115 | PF00400 | 0.502 |
TRG_ER_diArg_1 | 141 | 144 | PF00400 | 0.527 |
TRG_ER_diArg_1 | 185 | 188 | PF00400 | 0.522 |
TRG_ER_diArg_1 | 324 | 326 | PF00400 | 0.455 |
TRG_ER_diArg_1 | 365 | 368 | PF00400 | 0.513 |
TRG_ER_diArg_1 | 418 | 421 | PF00400 | 0.461 |
TRG_ER_diArg_1 | 589 | 592 | PF00400 | 0.575 |
TRG_NLS_MonoExtC_3 | 430 | 435 | PF00514 | 0.616 |
TRG_Pf-PMV_PEXEL_1 | 143 | 147 | PF00026 | 0.359 |
TRG_Pf-PMV_PEXEL_1 | 17 | 21 | PF00026 | 0.492 |
TRG_Pf-PMV_PEXEL_1 | 50 | 54 | PF00026 | 0.515 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P680 | Leptomonas seymouri | 39% | 100% |
A0A1X0P1S5 | Trypanosomatidae | 29% | 88% |
A0A3Q8IGD9 | Leishmania donovani | 100% | 100% |
A0A422NGA7 | Trypanosoma rangeli | 30% | 98% |
A4HJ19 | Leishmania braziliensis | 71% | 100% |
D0A4L8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 97% |
E9B3K2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
Q4Q4J9 | Leishmania major | 90% | 100% |