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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0005654 | nucleoplasm | 2 | 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: A4HH26
Term | Name | Level | Count |
---|---|---|---|
GO:0000375 | RNA splicing, via transesterification reactions | 8 | 1 |
GO:0000377 | RNA splicing, via transesterification reactions with bulged adenosine as nucleophile | 9 | 1 |
GO:0000398 | mRNA splicing, via spliceosome | 8 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006396 | RNA processing | 6 | 1 |
GO:0006397 | mRNA processing | 7 | 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:0008380 | RNA splicing | 7 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0016071 | mRNA metabolic process | 6 | 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: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:0005488 | binding | 1 | 8 |
GO:0043167 | ion binding | 2 | 8 |
GO:0043169 | cation binding | 3 | 8 |
GO:0046872 | metal ion binding | 4 | 8 |
GO:0003676 | nucleic acid binding | 3 | 3 |
GO:0003723 | RNA binding | 4 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 3 |
GO:1901363 | heterocyclic compound binding | 2 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 121 | 125 | PF00656 | 0.609 |
CLV_C14_Caspase3-7 | 423 | 427 | PF00656 | 0.519 |
CLV_NRD_NRD_1 | 265 | 267 | PF00675 | 0.687 |
CLV_NRD_NRD_1 | 414 | 416 | PF00675 | 0.581 |
CLV_NRD_NRD_1 | 467 | 469 | PF00675 | 0.569 |
CLV_NRD_NRD_1 | 57 | 59 | PF00675 | 0.696 |
CLV_NRD_NRD_1 | 61 | 63 | PF00675 | 0.709 |
CLV_PCSK_FUR_1 | 55 | 59 | PF00082 | 0.591 |
CLV_PCSK_KEX2_1 | 265 | 267 | PF00082 | 0.562 |
CLV_PCSK_KEX2_1 | 333 | 335 | PF00082 | 0.392 |
CLV_PCSK_KEX2_1 | 410 | 412 | PF00082 | 0.526 |
CLV_PCSK_KEX2_1 | 467 | 469 | PF00082 | 0.569 |
CLV_PCSK_KEX2_1 | 57 | 59 | PF00082 | 0.693 |
CLV_PCSK_KEX2_1 | 61 | 63 | PF00082 | 0.705 |
CLV_PCSK_PC1ET2_1 | 333 | 335 | PF00082 | 0.490 |
CLV_PCSK_PC1ET2_1 | 410 | 412 | PF00082 | 0.526 |
CLV_PCSK_PC7_1 | 57 | 63 | PF00082 | 0.581 |
CLV_PCSK_SKI1_1 | 212 | 216 | PF00082 | 0.471 |
CLV_PCSK_SKI1_1 | 315 | 319 | PF00082 | 0.557 |
CLV_PCSK_SKI1_1 | 341 | 345 | PF00082 | 0.499 |
CLV_PCSK_SKI1_1 | 429 | 433 | PF00082 | 0.672 |
DEG_SPOP_SBC_1 | 474 | 478 | PF00917 | 0.726 |
DOC_CKS1_1 | 120 | 125 | PF01111 | 0.525 |
DOC_CKS1_1 | 134 | 139 | PF01111 | 0.573 |
DOC_CKS1_1 | 374 | 379 | PF01111 | 0.566 |
DOC_CYCLIN_RxL_1 | 339 | 347 | PF00134 | 0.651 |
DOC_CYCLIN_yCln2_LP_2 | 519 | 522 | PF00134 | 0.566 |
DOC_MAPK_DCC_7 | 504 | 513 | PF00069 | 0.686 |
DOC_MAPK_MEF2A_6 | 504 | 513 | PF00069 | 0.686 |
DOC_PP1_RVXF_1 | 250 | 256 | PF00149 | 0.539 |
DOC_PP2B_LxvP_1 | 131 | 134 | PF13499 | 0.691 |
DOC_PP2B_LxvP_1 | 169 | 172 | PF13499 | 0.594 |
DOC_PP2B_LxvP_1 | 519 | 522 | PF13499 | 0.566 |
DOC_PP4_FxxP_1 | 105 | 108 | PF00568 | 0.499 |
DOC_PP4_FxxP_1 | 296 | 299 | PF00568 | 0.525 |
DOC_PP4_FxxP_1 | 490 | 493 | PF00568 | 0.555 |
DOC_PP4_MxPP_1 | 109 | 112 | PF00568 | 0.498 |
DOC_USP7_MATH_1 | 199 | 203 | PF00917 | 0.610 |
DOC_USP7_MATH_1 | 307 | 311 | PF00917 | 0.483 |
DOC_USP7_MATH_1 | 350 | 354 | PF00917 | 0.787 |
DOC_USP7_MATH_1 | 389 | 393 | PF00917 | 0.771 |
DOC_USP7_MATH_1 | 474 | 478 | PF00917 | 0.713 |
DOC_USP7_UBL2_3 | 416 | 420 | PF12436 | 0.454 |
DOC_WW_Pin1_4 | 119 | 124 | PF00397 | 0.624 |
DOC_WW_Pin1_4 | 133 | 138 | PF00397 | 0.645 |
DOC_WW_Pin1_4 | 183 | 188 | PF00397 | 0.558 |
DOC_WW_Pin1_4 | 373 | 378 | PF00397 | 0.649 |
DOC_WW_Pin1_4 | 385 | 390 | PF00397 | 0.695 |
DOC_WW_Pin1_4 | 64 | 69 | PF00397 | 0.707 |
DOC_WW_Pin1_4 | 99 | 104 | PF00397 | 0.764 |
LIG_14-3-3_CanoR_1 | 250 | 256 | PF00244 | 0.545 |
LIG_14-3-3_CanoR_1 | 39 | 44 | PF00244 | 0.729 |
LIG_14-3-3_CanoR_1 | 415 | 422 | PF00244 | 0.603 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.789 |
LIG_BRCT_BRCA1_1 | 101 | 105 | PF00533 | 0.495 |
LIG_BRCT_BRCA1_1 | 469 | 473 | PF00533 | 0.770 |
LIG_DLG_GKlike_1 | 39 | 47 | PF00625 | 0.779 |
LIG_FHA_1 | 224 | 230 | PF00498 | 0.418 |
LIG_FHA_1 | 426 | 432 | PF00498 | 0.527 |
LIG_FHA_2 | 134 | 140 | PF00498 | 0.624 |
LIG_FHA_2 | 206 | 212 | PF00498 | 0.568 |
LIG_FHA_2 | 368 | 374 | PF00498 | 0.654 |
LIG_LIR_Apic_2 | 102 | 108 | PF02991 | 0.527 |
LIG_LIR_Apic_2 | 301 | 305 | PF02991 | 0.544 |
LIG_LIR_Apic_2 | 488 | 493 | PF02991 | 0.696 |
LIG_LIR_Gen_1 | 215 | 222 | PF02991 | 0.329 |
LIG_LIR_Gen_1 | 22 | 31 | PF02991 | 0.772 |
LIG_LIR_Gen_1 | 322 | 331 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 215 | 219 | PF02991 | 0.317 |
LIG_LIR_Nem_3 | 22 | 27 | PF02991 | 0.771 |
LIG_LIR_Nem_3 | 322 | 328 | PF02991 | 0.484 |
LIG_MYND_1 | 108 | 112 | PF01753 | 0.765 |
LIG_NRP_CendR_1 | 533 | 536 | PF00754 | 0.716 |
LIG_SH2_CRK | 496 | 500 | PF00017 | 0.632 |
LIG_SH2_SRC | 164 | 167 | PF00017 | 0.543 |
LIG_SH2_STAP1 | 164 | 168 | PF00017 | 0.533 |
LIG_SH2_STAP1 | 174 | 178 | PF00017 | 0.461 |
LIG_SH2_STAP1 | 336 | 340 | PF00017 | 0.547 |
LIG_SH2_STAT5 | 205 | 208 | PF00017 | 0.490 |
LIG_SH2_STAT5 | 216 | 219 | PF00017 | 0.403 |
LIG_SH2_STAT5 | 327 | 330 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 496 | 499 | PF00017 | 0.553 |
LIG_SH3_1 | 303 | 309 | PF00018 | 0.572 |
LIG_SH3_3 | 10 | 16 | PF00018 | 0.782 |
LIG_SH3_3 | 105 | 111 | PF00018 | 0.716 |
LIG_SH3_3 | 117 | 123 | PF00018 | 0.703 |
LIG_SH3_3 | 131 | 137 | PF00018 | 0.605 |
LIG_SH3_3 | 303 | 309 | PF00018 | 0.537 |
LIG_SH3_3 | 371 | 377 | PF00018 | 0.636 |
LIG_SH3_3 | 506 | 512 | PF00018 | 0.680 |
LIG_SUMO_SIM_par_1 | 511 | 517 | PF11976 | 0.375 |
LIG_TRAF2_1 | 221 | 224 | PF00917 | 0.574 |
LIG_TRFH_1 | 255 | 259 | PF08558 | 0.597 |
LIG_TYR_ITIM | 494 | 499 | PF00017 | 0.639 |
LIG_WW_1 | 96 | 99 | PF00397 | 0.749 |
MOD_CK1_1 | 20 | 26 | PF00069 | 0.678 |
MOD_CK1_1 | 248 | 254 | PF00069 | 0.487 |
MOD_CK1_1 | 30 | 36 | PF00069 | 0.516 |
MOD_CK1_1 | 319 | 325 | PF00069 | 0.509 |
MOD_CK1_1 | 383 | 389 | PF00069 | 0.745 |
MOD_CK1_1 | 42 | 48 | PF00069 | 0.723 |
MOD_CK1_1 | 451 | 457 | PF00069 | 0.695 |
MOD_CK1_1 | 49 | 55 | PF00069 | 0.658 |
MOD_CK1_1 | 88 | 94 | PF00069 | 0.764 |
MOD_CK2_1 | 133 | 139 | PF00069 | 0.629 |
MOD_CK2_1 | 205 | 211 | PF00069 | 0.590 |
MOD_CK2_1 | 217 | 223 | PF00069 | 0.468 |
MOD_CK2_1 | 229 | 235 | PF00069 | 0.510 |
MOD_CK2_1 | 367 | 373 | PF00069 | 0.572 |
MOD_CK2_1 | 48 | 54 | PF00069 | 0.811 |
MOD_CK2_1 | 511 | 517 | PF00069 | 0.643 |
MOD_CK2_1 | 64 | 70 | PF00069 | 0.542 |
MOD_DYRK1A_RPxSP_1 | 64 | 68 | PF00069 | 0.754 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.525 |
MOD_GlcNHglycan | 18 | 22 | PF01048 | 0.757 |
MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.651 |
MOD_GlcNHglycan | 321 | 324 | PF01048 | 0.414 |
MOD_GlcNHglycan | 352 | 355 | PF01048 | 0.629 |
MOD_GlcNHglycan | 378 | 381 | PF01048 | 0.734 |
MOD_GlcNHglycan | 383 | 386 | PF01048 | 0.713 |
MOD_GlcNHglycan | 391 | 394 | PF01048 | 0.661 |
MOD_GlcNHglycan | 416 | 419 | PF01048 | 0.714 |
MOD_GlcNHglycan | 453 | 456 | PF01048 | 0.692 |
MOD_GlcNHglycan | 469 | 472 | PF01048 | 0.525 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.763 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.441 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.659 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.580 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.655 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.693 |
MOD_GSK3_1 | 376 | 383 | PF00069 | 0.716 |
MOD_GSK3_1 | 384 | 391 | PF00069 | 0.659 |
MOD_GSK3_1 | 425 | 432 | PF00069 | 0.565 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.602 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.521 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.697 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.671 |
MOD_LATS_1 | 263 | 269 | PF00433 | 0.728 |
MOD_LATS_1 | 447 | 453 | PF00433 | 0.795 |
MOD_N-GLC_1 | 199 | 204 | PF02516 | 0.611 |
MOD_N-GLC_1 | 357 | 362 | PF02516 | 0.572 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.521 |
MOD_NEK2_1 | 114 | 119 | PF00069 | 0.504 |
MOD_NEK2_1 | 229 | 234 | PF00069 | 0.488 |
MOD_NEK2_1 | 253 | 258 | PF00069 | 0.504 |
MOD_NEK2_1 | 317 | 322 | PF00069 | 0.537 |
MOD_NEK2_1 | 344 | 349 | PF00069 | 0.702 |
MOD_NEK2_1 | 37 | 42 | PF00069 | 0.709 |
MOD_NEK2_1 | 494 | 499 | PF00069 | 0.576 |
MOD_PIKK_1 | 475 | 481 | PF00454 | 0.731 |
MOD_PKA_1 | 265 | 271 | PF00069 | 0.720 |
MOD_PKA_1 | 467 | 473 | PF00069 | 0.572 |
MOD_PKA_2 | 153 | 159 | PF00069 | 0.555 |
MOD_PKA_2 | 251 | 257 | PF00069 | 0.594 |
MOD_PKA_2 | 265 | 271 | PF00069 | 0.489 |
MOD_PKA_2 | 414 | 420 | PF00069 | 0.661 |
MOD_PKA_2 | 448 | 454 | PF00069 | 0.525 |
MOD_PKA_2 | 467 | 473 | PF00069 | 0.569 |
MOD_PKB_1 | 64 | 72 | PF00069 | 0.725 |
MOD_Plk_1 | 174 | 180 | PF00069 | 0.582 |
MOD_Plk_1 | 199 | 205 | PF00069 | 0.608 |
MOD_Plk_1 | 85 | 91 | PF00069 | 0.746 |
MOD_Plk_2-3 | 135 | 141 | PF00069 | 0.342 |
MOD_Plk_2-3 | 326 | 332 | PF00069 | 0.551 |
MOD_Plk_4 | 101 | 107 | PF00069 | 0.668 |
MOD_Plk_4 | 114 | 120 | PF00069 | 0.567 |
MOD_Plk_4 | 126 | 132 | PF00069 | 0.702 |
MOD_Plk_4 | 164 | 170 | PF00069 | 0.506 |
MOD_ProDKin_1 | 119 | 125 | PF00069 | 0.624 |
MOD_ProDKin_1 | 133 | 139 | PF00069 | 0.644 |
MOD_ProDKin_1 | 183 | 189 | PF00069 | 0.548 |
MOD_ProDKin_1 | 373 | 379 | PF00069 | 0.649 |
MOD_ProDKin_1 | 385 | 391 | PF00069 | 0.697 |
MOD_ProDKin_1 | 64 | 70 | PF00069 | 0.707 |
MOD_ProDKin_1 | 99 | 105 | PF00069 | 0.766 |
MOD_SUMO_rev_2 | 337 | 343 | PF00179 | 0.560 |
TRG_DiLeu_BaLyEn_6 | 515 | 520 | PF01217 | 0.556 |
TRG_ENDOCYTIC_2 | 216 | 219 | PF00928 | 0.449 |
TRG_ENDOCYTIC_2 | 496 | 499 | PF00928 | 0.627 |
TRG_ER_diArg_1 | 249 | 252 | PF00400 | 0.563 |
TRG_ER_diArg_1 | 466 | 468 | PF00400 | 0.574 |
TRG_ER_diArg_1 | 55 | 58 | PF00400 | 0.672 |
TRG_ER_diArg_1 | 61 | 64 | PF00400 | 0.681 |
TRG_NLS_MonoExtC_3 | 408 | 414 | PF00514 | 0.590 |
TRG_Pf-PMV_PEXEL_1 | 410 | 414 | PF00026 | 0.524 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3Y5 | Leptomonas seymouri | 44% | 100% |
A0A3Q8IE82 | Leishmania donovani | 79% | 100% |
A4I471 | Leishmania infantum | 78% | 100% |
C9ZKQ7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
E9ADM0 | Leishmania major | 80% | 100% |
E9AM61 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 100% |
V5DLD2 | Trypanosoma cruzi | 26% | 100% |