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:0030532 | small nuclear ribonucleoprotein complex | 3 | 10 |
GO:0032991 | protein-containing complex | 1 | 10 |
GO:0046540 | U4/U6 x U5 tri-snRNP complex | 6 | 10 |
GO:0097525 | spliceosomal snRNP complex | 4 | 10 |
GO:0097526 | spliceosomal tri-snRNP complex | 5 | 10 |
GO:0120114 | Sm-like protein family complex | 2 | 10 |
GO:0140513 | nuclear protein-containing complex | 2 | 10 |
GO:1990904 | ribonucleoprotein complex | 2 | 10 |
Related structures:
AlphaFold database: E9AJE3
Term | Name | Level | Count |
---|---|---|---|
GO:0000375 | RNA splicing, via transesterification reactions | 8 | 10 |
GO:0000377 | RNA splicing, via transesterification reactions with bulged adenosine as nucleophile | 9 | 10 |
GO:0000398 | mRNA splicing, via spliceosome | 8 | 10 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 10 |
GO:0006396 | RNA processing | 6 | 10 |
GO:0006397 | mRNA processing | 7 | 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:0008380 | RNA splicing | 7 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0016070 | RNA metabolic process | 5 | 10 |
GO:0016071 | mRNA metabolic process | 6 | 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 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 561 | 565 | PF00656 | 0.583 |
CLV_NRD_NRD_1 | 108 | 110 | PF00675 | 0.672 |
CLV_NRD_NRD_1 | 124 | 126 | PF00675 | 0.667 |
CLV_NRD_NRD_1 | 206 | 208 | PF00675 | 0.311 |
CLV_NRD_NRD_1 | 26 | 28 | PF00675 | 0.710 |
CLV_NRD_NRD_1 | 329 | 331 | PF00675 | 0.296 |
CLV_NRD_NRD_1 | 333 | 335 | PF00675 | 0.292 |
CLV_NRD_NRD_1 | 420 | 422 | PF00675 | 0.290 |
CLV_NRD_NRD_1 | 442 | 444 | PF00675 | 0.542 |
CLV_NRD_NRD_1 | 588 | 590 | PF00675 | 0.336 |
CLV_NRD_NRD_1 | 84 | 86 | PF00675 | 0.799 |
CLV_PCSK_FUR_1 | 204 | 208 | PF00082 | 0.183 |
CLV_PCSK_KEX2_1 | 108 | 110 | PF00082 | 0.649 |
CLV_PCSK_KEX2_1 | 123 | 125 | PF00082 | 0.638 |
CLV_PCSK_KEX2_1 | 206 | 208 | PF00082 | 0.311 |
CLV_PCSK_KEX2_1 | 329 | 331 | PF00082 | 0.310 |
CLV_PCSK_KEX2_1 | 333 | 335 | PF00082 | 0.306 |
CLV_PCSK_KEX2_1 | 420 | 422 | PF00082 | 0.290 |
CLV_PCSK_KEX2_1 | 436 | 438 | PF00082 | 0.489 |
CLV_PCSK_KEX2_1 | 442 | 444 | PF00082 | 0.506 |
CLV_PCSK_KEX2_1 | 547 | 549 | PF00082 | 0.321 |
CLV_PCSK_KEX2_1 | 555 | 557 | PF00082 | 0.379 |
CLV_PCSK_KEX2_1 | 588 | 590 | PF00082 | 0.336 |
CLV_PCSK_KEX2_1 | 84 | 86 | PF00082 | 0.784 |
CLV_PCSK_PC1ET2_1 | 436 | 438 | PF00082 | 0.503 |
CLV_PCSK_PC1ET2_1 | 547 | 549 | PF00082 | 0.321 |
CLV_PCSK_PC1ET2_1 | 555 | 557 | PF00082 | 0.379 |
CLV_PCSK_PC7_1 | 329 | 335 | PF00082 | 0.327 |
CLV_PCSK_PC7_1 | 80 | 86 | PF00082 | 0.744 |
CLV_PCSK_SKI1_1 | 126 | 130 | PF00082 | 0.775 |
CLV_PCSK_SKI1_1 | 238 | 242 | PF00082 | 0.361 |
CLV_PCSK_SKI1_1 | 340 | 344 | PF00082 | 0.311 |
CLV_PCSK_SKI1_1 | 443 | 447 | PF00082 | 0.464 |
CLV_PCSK_SKI1_1 | 605 | 609 | PF00082 | 0.484 |
DEG_APCC_DBOX_1 | 609 | 617 | PF00400 | 0.415 |
DEG_SPOP_SBC_1 | 18 | 22 | PF00917 | 0.662 |
DEG_SPOP_SBC_1 | 360 | 364 | PF00917 | 0.433 |
DOC_CKS1_1 | 146 | 151 | PF01111 | 0.742 |
DOC_CYCLIN_RxL_1 | 235 | 243 | PF00134 | 0.508 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 383 | 392 | PF00134 | 0.492 |
DOC_MAPK_gen_1 | 24 | 32 | PF00069 | 0.613 |
DOC_MAPK_gen_1 | 519 | 528 | PF00069 | 0.561 |
DOC_PP2B_LxvP_1 | 590 | 593 | PF13499 | 0.561 |
DOC_PP4_MxPP_1 | 1 | 4 | PF00568 | 0.755 |
DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.810 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.705 |
DOC_USP7_MATH_1 | 151 | 155 | PF00917 | 0.734 |
DOC_USP7_MATH_1 | 18 | 22 | PF00917 | 0.620 |
DOC_USP7_MATH_1 | 360 | 364 | PF00917 | 0.503 |
DOC_USP7_MATH_1 | 369 | 373 | PF00917 | 0.416 |
DOC_USP7_MATH_1 | 43 | 47 | PF00917 | 0.732 |
DOC_USP7_MATH_1 | 56 | 60 | PF00917 | 0.517 |
DOC_USP7_MATH_1 | 591 | 595 | PF00917 | 0.561 |
DOC_USP7_MATH_1 | 7 | 11 | PF00917 | 0.761 |
DOC_USP7_UBL2_3 | 24 | 28 | PF12436 | 0.659 |
DOC_USP7_UBL2_3 | 343 | 347 | PF12436 | 0.542 |
DOC_WW_Pin1_4 | 145 | 150 | PF00397 | 0.763 |
DOC_WW_Pin1_4 | 275 | 280 | PF00397 | 0.536 |
DOC_WW_Pin1_4 | 592 | 597 | PF00397 | 0.561 |
LIG_14-3-3_CanoR_1 | 19 | 25 | PF00244 | 0.647 |
LIG_14-3-3_CanoR_1 | 253 | 259 | PF00244 | 0.575 |
LIG_14-3-3_CanoR_1 | 382 | 390 | PF00244 | 0.561 |
LIG_14-3-3_CanoR_1 | 442 | 451 | PF00244 | 0.466 |
LIG_14-3-3_CanoR_1 | 522 | 527 | PF00244 | 0.490 |
LIG_Actin_WH2_2 | 423 | 438 | PF00022 | 0.692 |
LIG_Actin_WH2_2 | 596 | 612 | PF00022 | 0.452 |
LIG_APCC_Cbox_2 | 424 | 430 | PF00515 | 0.591 |
LIG_BIR_III_4 | 112 | 116 | PF00653 | 0.717 |
LIG_BRCT_BRCA1_1 | 532 | 536 | PF00533 | 0.591 |
LIG_Clathr_ClatBox_2 | 249 | 254 | PF01394 | 0.490 |
LIG_deltaCOP1_diTrp_1 | 249 | 254 | PF00928 | 0.490 |
LIG_deltaCOP1_diTrp_1 | 504 | 513 | PF00928 | 0.490 |
LIG_FHA_1 | 231 | 237 | PF00498 | 0.543 |
LIG_FHA_1 | 279 | 285 | PF00498 | 0.536 |
LIG_FHA_1 | 383 | 389 | PF00498 | 0.561 |
LIG_FHA_1 | 403 | 409 | PF00498 | 0.355 |
LIG_FHA_1 | 516 | 522 | PF00498 | 0.493 |
LIG_FHA_1 | 567 | 573 | PF00498 | 0.444 |
LIG_FHA_2 | 206 | 212 | PF00498 | 0.517 |
LIG_FHA_2 | 214 | 220 | PF00498 | 0.477 |
LIG_FHA_2 | 323 | 329 | PF00498 | 0.429 |
LIG_FHA_2 | 577 | 583 | PF00498 | 0.586 |
LIG_LIR_Gen_1 | 36 | 44 | PF02991 | 0.590 |
LIG_LIR_Gen_1 | 570 | 580 | PF02991 | 0.508 |
LIG_LIR_Gen_1 | 594 | 603 | PF02991 | 0.561 |
LIG_LIR_Nem_3 | 302 | 308 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 310 | 314 | PF02991 | 0.573 |
LIG_LIR_Nem_3 | 36 | 42 | PF02991 | 0.588 |
LIG_LIR_Nem_3 | 594 | 600 | PF02991 | 0.490 |
LIG_Pex14_1 | 604 | 608 | PF04695 | 0.554 |
LIG_PROFILIN_1 | 2 | 8 | PF00235 | 0.718 |
LIG_SH2_CRK | 261 | 265 | PF00017 | 0.452 |
LIG_SH2_CRK | 86 | 90 | PF00017 | 0.797 |
LIG_SH2_STAP1 | 106 | 110 | PF00017 | 0.710 |
LIG_SH2_STAP1 | 305 | 309 | PF00017 | 0.490 |
LIG_SH2_STAT3 | 194 | 197 | PF00017 | 0.561 |
LIG_SH2_STAT5 | 106 | 109 | PF00017 | 0.686 |
LIG_SH2_STAT5 | 194 | 197 | PF00017 | 0.540 |
LIG_SH2_STAT5 | 305 | 308 | PF00017 | 0.536 |
LIG_SH2_STAT5 | 483 | 486 | PF00017 | 0.561 |
LIG_SH3_3 | 1 | 7 | PF00018 | 0.732 |
LIG_SH3_3 | 154 | 160 | PF00018 | 0.590 |
LIG_SH3_3 | 273 | 279 | PF00018 | 0.598 |
LIG_SH3_3 | 292 | 298 | PF00018 | 0.420 |
LIG_SH3_3 | 394 | 400 | PF00018 | 0.490 |
LIG_SH3_3 | 590 | 596 | PF00018 | 0.561 |
LIG_SH3_4 | 24 | 31 | PF00018 | 0.727 |
LIG_SUMO_SIM_anti_2 | 488 | 494 | PF11976 | 0.508 |
LIG_SUMO_SIM_par_1 | 28 | 34 | PF11976 | 0.683 |
LIG_TRAF2_1 | 140 | 143 | PF00917 | 0.653 |
LIG_TRAF2_1 | 325 | 328 | PF00917 | 0.440 |
LIG_TRAF2_1 | 579 | 582 | PF00917 | 0.474 |
LIG_WW_2 | 6 | 9 | PF00397 | 0.734 |
MOD_CK1_1 | 10 | 16 | PF00069 | 0.783 |
MOD_CK1_1 | 265 | 271 | PF00069 | 0.436 |
MOD_CK1_1 | 278 | 284 | PF00069 | 0.517 |
MOD_CK1_1 | 362 | 368 | PF00069 | 0.513 |
MOD_CK1_1 | 373 | 379 | PF00069 | 0.505 |
MOD_CK1_1 | 595 | 601 | PF00069 | 0.548 |
MOD_CK2_1 | 137 | 143 | PF00069 | 0.651 |
MOD_CK2_1 | 158 | 164 | PF00069 | 0.691 |
MOD_CK2_1 | 205 | 211 | PF00069 | 0.490 |
MOD_CK2_1 | 213 | 219 | PF00069 | 0.449 |
MOD_CK2_1 | 322 | 328 | PF00069 | 0.429 |
MOD_CK2_1 | 576 | 582 | PF00069 | 0.486 |
MOD_CMANNOS | 251 | 254 | PF00535 | 0.290 |
MOD_Cter_Amidation | 204 | 207 | PF01082 | 0.183 |
MOD_Cter_Amidation | 553 | 556 | PF01082 | 0.336 |
MOD_Cter_Amidation | 82 | 85 | PF01082 | 0.781 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.751 |
MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.708 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.701 |
MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.613 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.392 |
MOD_GlcNHglycan | 211 | 214 | PF01048 | 0.325 |
MOD_GlcNHglycan | 267 | 270 | PF01048 | 0.380 |
MOD_GlcNHglycan | 364 | 367 | PF01048 | 0.355 |
MOD_GlcNHglycan | 372 | 375 | PF01048 | 0.349 |
MOD_GlcNHglycan | 38 | 42 | PF01048 | 0.596 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.596 |
MOD_GlcNHglycan | 50 | 53 | PF01048 | 0.594 |
MOD_GlcNHglycan | 74 | 78 | PF01048 | 0.550 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.735 |
MOD_GSK3_1 | 158 | 165 | PF00069 | 0.672 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.450 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.685 |
MOD_GSK3_1 | 358 | 365 | PF00069 | 0.523 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.481 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.669 |
MOD_GSK3_1 | 591 | 598 | PF00069 | 0.558 |
MOD_GSK3_1 | 7 | 14 | PF00069 | 0.791 |
MOD_LATS_1 | 380 | 386 | PF00433 | 0.561 |
MOD_LATS_1 | 546 | 552 | PF00433 | 0.536 |
MOD_N-GLC_1 | 262 | 267 | PF02516 | 0.183 |
MOD_N-GLC_1 | 556 | 561 | PF02516 | 0.183 |
MOD_NEK2_1 | 163 | 168 | PF00069 | 0.712 |
MOD_NEK2_1 | 280 | 285 | PF00069 | 0.551 |
MOD_NEK2_1 | 370 | 375 | PF00069 | 0.503 |
MOD_NEK2_1 | 392 | 397 | PF00069 | 0.524 |
MOD_PIKK_1 | 163 | 169 | PF00454 | 0.727 |
MOD_PIKK_1 | 193 | 199 | PF00454 | 0.514 |
MOD_PIKK_1 | 303 | 309 | PF00454 | 0.508 |
MOD_PK_1 | 28 | 34 | PF00069 | 0.709 |
MOD_PK_1 | 522 | 528 | PF00069 | 0.591 |
MOD_PKA_2 | 104 | 110 | PF00069 | 0.753 |
MOD_PKA_2 | 18 | 24 | PF00069 | 0.650 |
MOD_PKA_2 | 205 | 211 | PF00069 | 0.432 |
MOD_PKA_2 | 252 | 258 | PF00069 | 0.551 |
MOD_PKA_2 | 381 | 387 | PF00069 | 0.490 |
MOD_Plk_1 | 33 | 39 | PF00069 | 0.594 |
MOD_Plk_2-3 | 33 | 39 | PF00069 | 0.693 |
MOD_Plk_4 | 232 | 238 | PF00069 | 0.508 |
MOD_Plk_4 | 393 | 399 | PF00069 | 0.490 |
MOD_Plk_4 | 56 | 62 | PF00069 | 0.658 |
MOD_Plk_4 | 582 | 588 | PF00069 | 0.394 |
MOD_ProDKin_1 | 145 | 151 | PF00069 | 0.763 |
MOD_ProDKin_1 | 275 | 281 | PF00069 | 0.536 |
MOD_ProDKin_1 | 592 | 598 | PF00069 | 0.561 |
TRG_DiLeu_BaEn_3 | 581 | 587 | PF01217 | 0.561 |
TRG_DiLeu_BaLyEn_6 | 374 | 379 | PF01217 | 0.591 |
TRG_DiLeu_BaLyEn_6 | 446 | 451 | PF01217 | 0.592 |
TRG_ENDOCYTIC_2 | 261 | 264 | PF00928 | 0.452 |
TRG_ENDOCYTIC_2 | 311 | 314 | PF00928 | 0.539 |
TRG_ENDOCYTIC_2 | 454 | 457 | PF00928 | 0.511 |
TRG_ENDOCYTIC_2 | 86 | 89 | PF00928 | 0.800 |
TRG_ER_diArg_1 | 123 | 125 | PF00400 | 0.671 |
TRG_ER_diArg_1 | 187 | 190 | PF00400 | 0.511 |
TRG_ER_diArg_1 | 204 | 207 | PF00400 | 0.511 |
TRG_ER_diArg_1 | 587 | 589 | PF00400 | 0.536 |
TRG_ER_diArg_1 | 84 | 86 | PF00400 | 0.779 |
TRG_NLS_MonoExtN_4 | 545 | 551 | PF00514 | 0.542 |
TRG_Pf-PMV_PEXEL_1 | 238 | 243 | PF00026 | 0.308 |
TRG_Pf-PMV_PEXEL_1 | 377 | 381 | PF00026 | 0.391 |
TRG_Pf-PMV_PEXEL_1 | 414 | 419 | PF00026 | 0.308 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HXQ4 | Leptomonas seymouri | 56% | 100% |
A0A3R7KZ00 | Trypanosoma rangeli | 41% | 100% |
A0A3S5H4W0 | Leishmania donovani | 88% | 100% |
A4H379 | Leishmania braziliensis | 76% | 93% |
A4HRH9 | Leishmania infantum | 88% | 100% |
C9ZXK6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
E9AC47 | Leishmania major | 86% | 100% |
V5BLJ6 | Trypanosoma cruzi | 40% | 100% |