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:0005681 | spliceosomal complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
GO:1990904 | ribonucleoprotein complex | 2 | 1 |
Related structures:
AlphaFold database: E9AWS0
Term | Name | Level | Count |
---|---|---|---|
GO:0000375 | RNA splicing, via transesterification reactions | 8 | 7 |
GO:0000377 | RNA splicing, via transesterification reactions with bulged adenosine as nucleophile | 9 | 7 |
GO:0000398 | mRNA splicing, via spliceosome | 8 | 7 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 7 |
GO:0006396 | RNA processing | 6 | 7 |
GO:0006397 | mRNA processing | 7 | 7 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 7 |
GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0008380 | RNA splicing | 7 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0016070 | RNA metabolic process | 5 | 7 |
GO:0016071 | mRNA metabolic process | 6 | 7 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 7 |
GO:0043170 | macromolecule metabolic process | 3 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0046483 | heterocycle metabolic process | 3 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:0090304 | nucleic acid metabolic process | 4 | 7 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 155 | 159 | PF00656 | 0.575 |
CLV_C14_Caspase3-7 | 21 | 25 | PF00656 | 0.657 |
CLV_NRD_NRD_1 | 188 | 190 | PF00675 | 0.691 |
CLV_NRD_NRD_1 | 258 | 260 | PF00675 | 0.530 |
CLV_NRD_NRD_1 | 326 | 328 | PF00675 | 0.573 |
CLV_NRD_NRD_1 | 374 | 376 | PF00675 | 0.577 |
CLV_NRD_NRD_1 | 528 | 530 | PF00675 | 0.574 |
CLV_NRD_NRD_1 | 87 | 89 | PF00675 | 0.654 |
CLV_PCSK_KEX2_1 | 14 | 16 | PF00082 | 0.713 |
CLV_PCSK_KEX2_1 | 188 | 190 | PF00082 | 0.691 |
CLV_PCSK_KEX2_1 | 22 | 24 | PF00082 | 0.719 |
CLV_PCSK_KEX2_1 | 528 | 530 | PF00082 | 0.487 |
CLV_PCSK_KEX2_1 | 87 | 89 | PF00082 | 0.654 |
CLV_PCSK_PC1ET2_1 | 14 | 16 | PF00082 | 0.713 |
CLV_PCSK_PC1ET2_1 | 22 | 24 | PF00082 | 0.719 |
CLV_PCSK_SKI1_1 | 335 | 339 | PF00082 | 0.447 |
CLV_PCSK_SKI1_1 | 361 | 365 | PF00082 | 0.294 |
DEG_APCC_DBOX_1 | 169 | 177 | PF00400 | 0.526 |
DEG_SCF_FBW7_1 | 212 | 217 | PF00400 | 0.542 |
DEG_SCF_FBW7_1 | 273 | 280 | PF00400 | 0.616 |
DEG_SCF_TRCP1_1 | 158 | 164 | PF00400 | 0.504 |
DEG_SPOP_SBC_1 | 106 | 110 | PF00917 | 0.610 |
DEG_SPOP_SBC_1 | 267 | 271 | PF00917 | 0.788 |
DEG_SPOP_SBC_1 | 281 | 285 | PF00917 | 0.701 |
DOC_CDC14_PxL_1 | 35 | 43 | PF14671 | 0.584 |
DOC_CYCLIN_RxL_1 | 332 | 341 | PF00134 | 0.469 |
DOC_MAPK_gen_1 | 516 | 525 | PF00069 | 0.510 |
DOC_MAPK_gen_1 | 555 | 562 | PF00069 | 0.496 |
DOC_PP1_RVXF_1 | 333 | 339 | PF00149 | 0.357 |
DOC_PP1_RVXF_1 | 359 | 365 | PF00149 | 0.464 |
DOC_PP2B_LxvP_1 | 420 | 423 | PF13499 | 0.644 |
DOC_PP4_FxxP_1 | 139 | 142 | PF00568 | 0.467 |
DOC_USP7_MATH_1 | 100 | 104 | PF00917 | 0.631 |
DOC_USP7_MATH_1 | 106 | 110 | PF00917 | 0.621 |
DOC_USP7_MATH_1 | 166 | 170 | PF00917 | 0.762 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.603 |
DOC_USP7_MATH_1 | 208 | 212 | PF00917 | 0.708 |
DOC_USP7_MATH_1 | 214 | 218 | PF00917 | 0.462 |
DOC_USP7_MATH_1 | 268 | 272 | PF00917 | 0.707 |
DOC_USP7_MATH_1 | 281 | 285 | PF00917 | 0.741 |
DOC_USP7_MATH_1 | 286 | 290 | PF00917 | 0.752 |
DOC_USP7_MATH_1 | 400 | 404 | PF00917 | 0.669 |
DOC_USP7_MATH_1 | 92 | 96 | PF00917 | 0.736 |
DOC_USP7_UBL2_3 | 203 | 207 | PF12436 | 0.507 |
DOC_USP7_UBL2_3 | 324 | 328 | PF12436 | 0.565 |
DOC_USP7_UBL2_3 | 454 | 458 | PF12436 | 0.374 |
DOC_WW_Pin1_4 | 138 | 143 | PF00397 | 0.470 |
DOC_WW_Pin1_4 | 210 | 215 | PF00397 | 0.622 |
DOC_WW_Pin1_4 | 273 | 278 | PF00397 | 0.651 |
DOC_WW_Pin1_4 | 284 | 289 | PF00397 | 0.675 |
DOC_WW_Pin1_4 | 327 | 332 | PF00397 | 0.614 |
DOC_WW_Pin1_4 | 396 | 401 | PF00397 | 0.604 |
DOC_WW_Pin1_4 | 414 | 419 | PF00397 | 0.630 |
LIG_14-3-3_CanoR_1 | 188 | 196 | PF00244 | 0.781 |
LIG_14-3-3_CanoR_1 | 259 | 268 | PF00244 | 0.561 |
LIG_14-3-3_CanoR_1 | 441 | 450 | PF00244 | 0.455 |
LIG_14-3-3_CanoR_1 | 53 | 61 | PF00244 | 0.705 |
LIG_14-3-3_CanoR_1 | 87 | 93 | PF00244 | 0.703 |
LIG_BIR_III_2 | 9 | 13 | PF00653 | 0.666 |
LIG_BIR_III_4 | 127 | 131 | PF00653 | 0.537 |
LIG_BRCT_BRCA1_1 | 108 | 112 | PF00533 | 0.608 |
LIG_BRCT_BRCA1_1 | 135 | 139 | PF00533 | 0.503 |
LIG_BRCT_BRCA1_1 | 216 | 220 | PF00533 | 0.656 |
LIG_Clathr_ClatBox_1 | 504 | 508 | PF01394 | 0.494 |
LIG_deltaCOP1_diTrp_1 | 131 | 139 | PF00928 | 0.473 |
LIG_EVH1_1 | 420 | 424 | PF00568 | 0.591 |
LIG_FHA_1 | 295 | 301 | PF00498 | 0.484 |
LIG_FHA_1 | 399 | 405 | PF00498 | 0.588 |
LIG_FHA_1 | 43 | 49 | PF00498 | 0.400 |
LIG_FHA_1 | 499 | 505 | PF00498 | 0.443 |
LIG_FHA_1 | 554 | 560 | PF00498 | 0.497 |
LIG_FHA_2 | 182 | 188 | PF00498 | 0.664 |
LIG_FHA_2 | 317 | 323 | PF00498 | 0.531 |
LIG_FHA_2 | 339 | 345 | PF00498 | 0.477 |
LIG_FHA_2 | 545 | 551 | PF00498 | 0.349 |
LIG_LIR_Apic_2 | 136 | 142 | PF02991 | 0.468 |
LIG_LIR_Gen_1 | 217 | 228 | PF02991 | 0.649 |
LIG_LIR_Nem_3 | 217 | 223 | PF02991 | 0.582 |
LIG_MLH1_MIPbox_1 | 109 | 113 | PF16413 | 0.607 |
LIG_MYND_1 | 418 | 422 | PF01753 | 0.657 |
LIG_PAM2_1 | 423 | 435 | PF00658 | 0.541 |
LIG_PCNA_yPIPBox_3 | 249 | 260 | PF02747 | 0.504 |
LIG_Pex14_1 | 135 | 139 | PF04695 | 0.471 |
LIG_REV1ctd_RIR_1 | 362 | 368 | PF16727 | 0.453 |
LIG_SH2_PTP2 | 226 | 229 | PF00017 | 0.545 |
LIG_SH2_STAT5 | 226 | 229 | PF00017 | 0.547 |
LIG_SH2_STAT5 | 372 | 375 | PF00017 | 0.632 |
LIG_SH3_3 | 275 | 281 | PF00018 | 0.563 |
LIG_SH3_3 | 415 | 421 | PF00018 | 0.709 |
LIG_SUMO_SIM_par_1 | 521 | 527 | PF11976 | 0.514 |
LIG_TRAF2_1 | 319 | 322 | PF00917 | 0.528 |
MOD_CDK_SPxxK_3 | 138 | 145 | PF00069 | 0.473 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.679 |
MOD_CK1_1 | 18 | 24 | PF00069 | 0.569 |
MOD_CK1_1 | 279 | 285 | PF00069 | 0.700 |
MOD_CK1_1 | 293 | 299 | PF00069 | 0.561 |
MOD_CK1_1 | 314 | 320 | PF00069 | 0.688 |
MOD_CK1_1 | 395 | 401 | PF00069 | 0.600 |
MOD_CK1_1 | 414 | 420 | PF00069 | 0.535 |
MOD_CK1_1 | 42 | 48 | PF00069 | 0.440 |
MOD_CK2_1 | 296 | 302 | PF00069 | 0.496 |
MOD_CK2_1 | 316 | 322 | PF00069 | 0.533 |
MOD_CK2_1 | 544 | 550 | PF00069 | 0.359 |
MOD_Cter_Amidation | 325 | 328 | PF01082 | 0.548 |
MOD_Cter_Amidation | 451 | 454 | PF01082 | 0.404 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.631 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.604 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.758 |
MOD_GlcNHglycan | 190 | 193 | PF01048 | 0.714 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.693 |
MOD_GlcNHglycan | 216 | 219 | PF01048 | 0.502 |
MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.593 |
MOD_GlcNHglycan | 270 | 273 | PF01048 | 0.777 |
MOD_GlcNHglycan | 292 | 295 | PF01048 | 0.776 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.552 |
MOD_GlcNHglycan | 41 | 44 | PF01048 | 0.508 |
MOD_GlcNHglycan | 413 | 416 | PF01048 | 0.650 |
MOD_GlcNHglycan | 477 | 480 | PF01048 | 0.672 |
MOD_GlcNHglycan | 482 | 485 | PF01048 | 0.660 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.774 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.650 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.588 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.693 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.797 |
MOD_GSK3_1 | 203 | 210 | PF00069 | 0.758 |
MOD_GSK3_1 | 268 | 275 | PF00069 | 0.702 |
MOD_GSK3_1 | 276 | 283 | PF00069 | 0.615 |
MOD_GSK3_1 | 286 | 293 | PF00069 | 0.637 |
MOD_GSK3_1 | 392 | 399 | PF00069 | 0.561 |
MOD_GSK3_1 | 410 | 417 | PF00069 | 0.600 |
MOD_GSK3_1 | 456 | 463 | PF00069 | 0.413 |
MOD_GSK3_1 | 480 | 487 | PF00069 | 0.748 |
MOD_GSK3_1 | 492 | 499 | PF00069 | 0.568 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.555 |
MOD_LATS_1 | 13 | 19 | PF00433 | 0.697 |
MOD_N-GLC_1 | 182 | 187 | PF02516 | 0.725 |
MOD_N-GLC_1 | 395 | 400 | PF02516 | 0.634 |
MOD_N-GLC_1 | 553 | 558 | PF02516 | 0.371 |
MOD_NEK2_1 | 134 | 139 | PF00069 | 0.604 |
MOD_NEK2_1 | 143 | 148 | PF00069 | 0.703 |
MOD_NEK2_1 | 234 | 239 | PF00069 | 0.555 |
MOD_NEK2_1 | 338 | 343 | PF00069 | 0.395 |
MOD_NEK2_1 | 355 | 360 | PF00069 | 0.382 |
MOD_NEK2_1 | 377 | 382 | PF00069 | 0.432 |
MOD_NEK2_1 | 75 | 80 | PF00069 | 0.774 |
MOD_NEK2_2 | 484 | 489 | PF00069 | 0.725 |
MOD_NEK2_2 | 71 | 76 | PF00069 | 0.511 |
MOD_PKA_1 | 188 | 194 | PF00069 | 0.643 |
MOD_PKA_1 | 22 | 28 | PF00069 | 0.648 |
MOD_PKA_2 | 187 | 193 | PF00069 | 0.713 |
MOD_PKA_2 | 22 | 28 | PF00069 | 0.796 |
MOD_PKA_2 | 440 | 446 | PF00069 | 0.447 |
MOD_PKA_2 | 75 | 81 | PF00069 | 0.579 |
MOD_PKA_2 | 86 | 92 | PF00069 | 0.622 |
MOD_Plk_1 | 338 | 344 | PF00069 | 0.409 |
MOD_Plk_1 | 544 | 550 | PF00069 | 0.463 |
MOD_Plk_4 | 296 | 302 | PF00069 | 0.556 |
MOD_Plk_4 | 509 | 515 | PF00069 | 0.376 |
MOD_ProDKin_1 | 138 | 144 | PF00069 | 0.471 |
MOD_ProDKin_1 | 210 | 216 | PF00069 | 0.617 |
MOD_ProDKin_1 | 273 | 279 | PF00069 | 0.651 |
MOD_ProDKin_1 | 284 | 290 | PF00069 | 0.677 |
MOD_ProDKin_1 | 327 | 333 | PF00069 | 0.600 |
MOD_ProDKin_1 | 396 | 402 | PF00069 | 0.607 |
MOD_ProDKin_1 | 414 | 420 | PF00069 | 0.629 |
TRG_DiLeu_BaEn_1 | 500 | 505 | PF01217 | 0.462 |
TRG_DiLeu_BaLyEn_6 | 332 | 337 | PF01217 | 0.387 |
TRG_DiLeu_BaLyEn_6 | 434 | 439 | PF01217 | 0.369 |
TRG_ENDOCYTIC_2 | 226 | 229 | PF00928 | 0.547 |
TRG_ER_diArg_1 | 44 | 47 | PF00400 | 0.566 |
TRG_ER_diArg_1 | 466 | 469 | PF00400 | 0.528 |
TRG_ER_diArg_1 | 535 | 538 | PF00400 | 0.506 |
TRG_Pf-PMV_PEXEL_1 | 327 | 332 | PF00026 | 0.595 |
TRG_Pf-PMV_PEXEL_1 | 335 | 339 | PF00026 | 0.435 |
TRG_Pf-PMV_PEXEL_1 | 46 | 50 | PF00026 | 0.598 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PD00 | Leptomonas seymouri | 46% | 100% |
A0A3S7WYC4 | Leishmania donovani | 83% | 98% |
A4HDD7 | Leishmania braziliensis | 69% | 98% |
A4I0R8 | Leishmania infantum | 82% | 98% |
D0A749 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
Q4QAQ4 | Leishmania major | 81% | 100% |
V5BR63 | Trypanosoma cruzi | 32% | 100% |