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 | 2 |
GO:0005654 | nucleoplasm | 2 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: E9ADM0
Term | Name | Level | Count |
---|---|---|---|
GO:0000375 | RNA splicing, via transesterification reactions | 8 | 2 |
GO:0000377 | RNA splicing, via transesterification reactions with bulged adenosine as nucleophile | 9 | 2 |
GO:0000398 | mRNA splicing, via spliceosome | 8 | 2 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 2 |
GO:0006396 | RNA processing | 6 | 2 |
GO:0006397 | mRNA processing | 7 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0008380 | RNA splicing | 7 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016070 | RNA metabolic process | 5 | 2 |
GO:0016071 | mRNA metabolic process | 6 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0090304 | nucleic acid metabolic process | 4 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 4 |
GO:0003723 | RNA binding | 4 | 2 |
GO:0005488 | binding | 1 | 9 |
GO:0043167 | ion binding | 2 | 9 |
GO:0043169 | cation binding | 3 | 9 |
GO:0046872 | metal ion binding | 4 | 9 |
GO:0097159 | organic cyclic compound binding | 2 | 4 |
GO:1901363 | heterocyclic compound binding | 2 | 4 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 195 | 197 | PF00675 | 0.540 |
CLV_NRD_NRD_1 | 264 | 266 | PF00675 | 0.683 |
CLV_NRD_NRD_1 | 414 | 416 | PF00675 | 0.578 |
CLV_NRD_NRD_1 | 61 | 63 | PF00675 | 0.694 |
CLV_PCSK_KEX2_1 | 195 | 197 | PF00082 | 0.540 |
CLV_PCSK_KEX2_1 | 333 | 335 | PF00082 | 0.423 |
CLV_PCSK_KEX2_1 | 410 | 412 | PF00082 | 0.538 |
CLV_PCSK_KEX2_1 | 61 | 63 | PF00082 | 0.693 |
CLV_PCSK_PC1ET2_1 | 333 | 335 | PF00082 | 0.509 |
CLV_PCSK_PC1ET2_1 | 410 | 412 | PF00082 | 0.538 |
CLV_PCSK_SKI1_1 | 315 | 319 | PF00082 | 0.560 |
CLV_PCSK_SKI1_1 | 341 | 345 | PF00082 | 0.501 |
DEG_SCF_TRCP1_1 | 19 | 25 | PF00400 | 0.686 |
DEG_SPOP_SBC_1 | 102 | 106 | PF00917 | 0.719 |
DEG_SPOP_SBC_1 | 384 | 388 | PF00917 | 0.755 |
DEG_SPOP_SBC_1 | 47 | 51 | PF00917 | 0.727 |
DOC_CKS1_1 | 134 | 139 | PF01111 | 0.572 |
DOC_CKS1_1 | 389 | 394 | PF01111 | 0.720 |
DOC_CKS1_1 | 475 | 480 | PF01111 | 0.703 |
DOC_CYCLIN_RxL_1 | 339 | 347 | PF00134 | 0.636 |
DOC_CYCLIN_yCln2_LP_2 | 389 | 395 | PF00134 | 0.745 |
DOC_CYCLIN_yCln2_LP_2 | 520 | 523 | PF00134 | 0.590 |
DOC_MAPK_DCC_7 | 505 | 514 | PF00069 | 0.679 |
DOC_MAPK_MEF2A_6 | 212 | 219 | PF00069 | 0.501 |
DOC_MAPK_MEF2A_6 | 505 | 514 | PF00069 | 0.669 |
DOC_PP1_RVXF_1 | 250 | 256 | PF00149 | 0.548 |
DOC_PP2B_LxvP_1 | 131 | 134 | PF13499 | 0.693 |
DOC_PP2B_LxvP_1 | 169 | 172 | PF13499 | 0.565 |
DOC_PP2B_LxvP_1 | 520 | 523 | PF13499 | 0.590 |
DOC_PP4_FxxP_1 | 296 | 299 | PF00568 | 0.527 |
DOC_PP4_FxxP_1 | 491 | 494 | PF00568 | 0.568 |
DOC_USP7_MATH_1 | 102 | 106 | PF00917 | 0.719 |
DOC_USP7_MATH_1 | 199 | 203 | PF00917 | 0.601 |
DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.705 |
DOC_USP7_MATH_1 | 384 | 388 | PF00917 | 0.727 |
DOC_USP7_MATH_1 | 476 | 480 | PF00917 | 0.711 |
DOC_USP7_UBL2_3 | 396 | 400 | PF12436 | 0.731 |
DOC_USP7_UBL2_3 | 416 | 420 | PF12436 | 0.586 |
DOC_WW_Pin1_4 | 133 | 138 | PF00397 | 0.647 |
DOC_WW_Pin1_4 | 33 | 38 | PF00397 | 0.725 |
DOC_WW_Pin1_4 | 361 | 366 | PF00397 | 0.715 |
DOC_WW_Pin1_4 | 380 | 385 | PF00397 | 0.760 |
DOC_WW_Pin1_4 | 388 | 393 | PF00397 | 0.728 |
DOC_WW_Pin1_4 | 474 | 479 | PF00397 | 0.678 |
DOC_WW_Pin1_4 | 64 | 69 | PF00397 | 0.718 |
LIG_14-3-3_CanoR_1 | 250 | 256 | PF00244 | 0.553 |
LIG_14-3-3_CanoR_1 | 39 | 44 | PF00244 | 0.734 |
LIG_14-3-3_CanoR_1 | 415 | 422 | PF00244 | 0.680 |
LIG_14-3-3_CanoR_1 | 511 | 517 | PF00244 | 0.640 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.758 |
LIG_BRCT_BRCA1_1 | 13 | 17 | PF00533 | 0.703 |
LIG_BRCT_BRCA1_1 | 470 | 474 | PF00533 | 0.715 |
LIG_DLG_GKlike_1 | 39 | 47 | PF00625 | 0.783 |
LIG_FHA_1 | 224 | 230 | PF00498 | 0.414 |
LIG_FHA_1 | 373 | 379 | PF00498 | 0.654 |
LIG_FHA_2 | 134 | 140 | PF00498 | 0.622 |
LIG_FHA_2 | 206 | 212 | PF00498 | 0.551 |
LIG_FHA_2 | 389 | 395 | PF00498 | 0.539 |
LIG_LIR_Apic_2 | 301 | 305 | PF02991 | 0.540 |
LIG_LIR_Apic_2 | 489 | 494 | PF02991 | 0.713 |
LIG_LIR_Gen_1 | 22 | 31 | PF02991 | 0.726 |
LIG_LIR_Gen_1 | 322 | 331 | PF02991 | 0.496 |
LIG_LIR_Nem_3 | 22 | 27 | PF02991 | 0.718 |
LIG_LIR_Nem_3 | 322 | 328 | PF02991 | 0.457 |
LIG_MYND_1 | 108 | 112 | PF01753 | 0.756 |
LIG_NRP_CendR_1 | 534 | 537 | PF00754 | 0.692 |
LIG_SH2_CRK | 497 | 501 | PF00017 | 0.650 |
LIG_SH2_SRC | 164 | 167 | PF00017 | 0.532 |
LIG_SH2_STAP1 | 164 | 168 | PF00017 | 0.529 |
LIG_SH2_STAP1 | 174 | 178 | PF00017 | 0.467 |
LIG_SH2_STAP1 | 336 | 340 | PF00017 | 0.556 |
LIG_SH2_STAP1 | 43 | 47 | PF00017 | 0.725 |
LIG_SH2_STAT5 | 205 | 208 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 216 | 219 | PF00017 | 0.374 |
LIG_SH2_STAT5 | 497 | 500 | PF00017 | 0.531 |
LIG_SH3_1 | 303 | 309 | PF00018 | 0.551 |
LIG_SH3_3 | 10 | 16 | PF00018 | 0.765 |
LIG_SH3_3 | 105 | 111 | PF00018 | 0.729 |
LIG_SH3_3 | 131 | 137 | PF00018 | 0.607 |
LIG_SH3_3 | 303 | 309 | PF00018 | 0.517 |
LIG_SH3_3 | 371 | 377 | PF00018 | 0.678 |
LIG_SH3_3 | 419 | 425 | PF00018 | 0.753 |
LIG_SH3_3 | 472 | 478 | PF00018 | 0.704 |
LIG_SH3_3 | 507 | 513 | PF00018 | 0.678 |
LIG_TRAF2_1 | 221 | 224 | PF00917 | 0.559 |
LIG_TRFH_1 | 255 | 259 | PF08558 | 0.606 |
LIG_TYR_ITIM | 495 | 500 | PF00017 | 0.646 |
LIG_WW_1 | 96 | 99 | PF00397 | 0.748 |
MOD_CDC14_SPxK_1 | 36 | 39 | PF00782 | 0.753 |
MOD_CDC14_SPxK_1 | 364 | 367 | PF00782 | 0.721 |
MOD_CDK_SPxK_1 | 33 | 39 | PF00069 | 0.750 |
MOD_CDK_SPxK_1 | 361 | 367 | PF00069 | 0.722 |
MOD_CK1_1 | 103 | 109 | PF00069 | 0.565 |
MOD_CK1_1 | 184 | 190 | PF00069 | 0.471 |
MOD_CK1_1 | 20 | 26 | PF00069 | 0.648 |
MOD_CK1_1 | 248 | 254 | PF00069 | 0.478 |
MOD_CK1_1 | 30 | 36 | PF00069 | 0.594 |
MOD_CK1_1 | 307 | 313 | PF00069 | 0.501 |
MOD_CK1_1 | 319 | 325 | PF00069 | 0.568 |
MOD_CK1_1 | 350 | 356 | PF00069 | 0.625 |
MOD_CK1_1 | 379 | 385 | PF00069 | 0.740 |
MOD_CK1_1 | 388 | 394 | PF00069 | 0.726 |
MOD_CK1_1 | 42 | 48 | PF00069 | 0.744 |
MOD_CK1_1 | 454 | 460 | PF00069 | 0.711 |
MOD_CK1_1 | 49 | 55 | PF00069 | 0.700 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.471 |
MOD_CK1_1 | 91 | 97 | PF00069 | 0.744 |
MOD_CK2_1 | 133 | 139 | PF00069 | 0.630 |
MOD_CK2_1 | 205 | 211 | PF00069 | 0.561 |
MOD_CK2_1 | 217 | 223 | PF00069 | 0.419 |
MOD_CK2_1 | 229 | 235 | PF00069 | 0.425 |
MOD_CK2_1 | 388 | 394 | PF00069 | 0.598 |
MOD_CK2_1 | 48 | 54 | PF00069 | 0.788 |
MOD_CK2_1 | 512 | 518 | PF00069 | 0.617 |
MOD_CK2_1 | 64 | 70 | PF00069 | 0.532 |
MOD_DYRK1A_RPxSP_1 | 64 | 68 | PF00069 | 0.753 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.508 |
MOD_GlcNHglycan | 18 | 22 | PF01048 | 0.707 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.434 |
MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.637 |
MOD_GlcNHglycan | 321 | 324 | PF01048 | 0.585 |
MOD_GlcNHglycan | 378 | 381 | PF01048 | 0.734 |
MOD_GlcNHglycan | 416 | 419 | PF01048 | 0.733 |
MOD_GlcNHglycan | 453 | 456 | PF01048 | 0.706 |
MOD_GlcNHglycan | 470 | 473 | PF01048 | 0.519 |
MOD_GlcNHglycan | 70 | 74 | PF01048 | 0.583 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.733 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.405 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.613 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.603 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.622 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.691 |
MOD_GSK3_1 | 372 | 379 | PF00069 | 0.729 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.676 |
MOD_GSK3_1 | 395 | 402 | PF00069 | 0.558 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.688 |
MOD_GSK3_1 | 450 | 457 | PF00069 | 0.676 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.525 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.664 |
MOD_LATS_1 | 263 | 269 | PF00433 | 0.739 |
MOD_LATS_1 | 448 | 454 | PF00433 | 0.800 |
MOD_LATS_1 | 60 | 66 | PF00433 | 0.755 |
MOD_LATS_1 | 9 | 15 | PF00433 | 0.713 |
MOD_N-GLC_1 | 199 | 204 | PF02516 | 0.606 |
MOD_NEK2_1 | 17 | 22 | PF00069 | 0.705 |
MOD_NEK2_1 | 229 | 234 | PF00069 | 0.488 |
MOD_NEK2_1 | 253 | 258 | PF00069 | 0.489 |
MOD_NEK2_1 | 317 | 322 | PF00069 | 0.537 |
MOD_NEK2_1 | 344 | 349 | PF00069 | 0.677 |
MOD_NEK2_1 | 463 | 468 | PF00069 | 0.588 |
MOD_NEK2_1 | 495 | 500 | PF00069 | 0.556 |
MOD_NEK2_1 | 87 | 92 | PF00069 | 0.687 |
MOD_NEK2_2 | 199 | 204 | PF00069 | 0.589 |
MOD_PIKK_1 | 436 | 442 | PF00454 | 0.760 |
MOD_PIKK_1 | 476 | 482 | PF00454 | 0.731 |
MOD_PK_1 | 78 | 84 | PF00069 | 0.711 |
MOD_PKA_1 | 265 | 271 | PF00069 | 0.692 |
MOD_PKA_2 | 153 | 159 | PF00069 | 0.566 |
MOD_PKA_2 | 251 | 257 | PF00069 | 0.589 |
MOD_PKA_2 | 273 | 279 | PF00069 | 0.638 |
MOD_PKA_2 | 414 | 420 | PF00069 | 0.644 |
MOD_PKB_1 | 64 | 72 | PF00069 | 0.707 |
MOD_Plk_1 | 174 | 180 | PF00069 | 0.564 |
MOD_Plk_1 | 199 | 205 | PF00069 | 0.588 |
MOD_Plk_2-3 | 326 | 332 | PF00069 | 0.563 |
MOD_Plk_4 | 126 | 132 | PF00069 | 0.706 |
MOD_Plk_4 | 164 | 170 | PF00069 | 0.505 |
MOD_Plk_4 | 78 | 84 | PF00069 | 0.699 |
MOD_ProDKin_1 | 133 | 139 | PF00069 | 0.646 |
MOD_ProDKin_1 | 33 | 39 | PF00069 | 0.728 |
MOD_ProDKin_1 | 361 | 367 | PF00069 | 0.718 |
MOD_ProDKin_1 | 380 | 386 | PF00069 | 0.763 |
MOD_ProDKin_1 | 388 | 394 | PF00069 | 0.730 |
MOD_ProDKin_1 | 474 | 480 | PF00069 | 0.679 |
MOD_ProDKin_1 | 64 | 70 | PF00069 | 0.720 |
MOD_SUMO_rev_2 | 337 | 343 | PF00179 | 0.574 |
MOD_SUMO_rev_2 | 388 | 398 | PF00179 | 0.534 |
TRG_DiLeu_BaLyEn_6 | 516 | 521 | PF01217 | 0.583 |
TRG_ENDOCYTIC_2 | 216 | 219 | PF00928 | 0.427 |
TRG_ENDOCYTIC_2 | 497 | 500 | PF00928 | 0.644 |
TRG_ER_diArg_1 | 194 | 196 | PF00400 | 0.525 |
TRG_ER_diArg_1 | 249 | 252 | PF00400 | 0.541 |
TRG_ER_diArg_1 | 61 | 64 | PF00400 | 0.671 |
TRG_NLS_MonoExtC_3 | 408 | 414 | PF00514 | 0.583 |
TRG_Pf-PMV_PEXEL_1 | 410 | 414 | PF00026 | 0.552 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3Y5 | Leptomonas seymouri | 46% | 100% |
A0A3Q8IE82 | Leishmania donovani | 93% | 100% |
A0A422NUU8 | Trypanosoma rangeli | 31% | 100% |
A4HH26 | Leishmania braziliensis | 80% | 100% |
A4I471 | Leishmania infantum | 93% | 100% |
C9ZKQ7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
E9AM61 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
V5DLD2 | Trypanosoma cruzi | 27% | 100% |