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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0030532 | small nuclear ribonucleoprotein complex | 3 | 11 |
GO:0032991 | protein-containing complex | 1 | 11 |
GO:0046540 | U4/U6 x U5 tri-snRNP complex | 6 | 11 |
GO:0097525 | spliceosomal snRNP complex | 4 | 11 |
GO:0097526 | spliceosomal tri-snRNP complex | 5 | 11 |
GO:0120114 | Sm-like protein family complex | 2 | 11 |
GO:0140513 | nuclear protein-containing complex | 2 | 11 |
GO:1990904 | ribonucleoprotein complex | 2 | 11 |
Related structures:
AlphaFold database: E9AC47
Term | Name | Level | Count |
---|---|---|---|
GO:0000375 | RNA splicing, via transesterification reactions | 8 | 11 |
GO:0000377 | RNA splicing, via transesterification reactions with bulged adenosine as nucleophile | 9 | 11 |
GO:0000398 | mRNA splicing, via spliceosome | 8 | 11 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 11 |
GO:0006396 | RNA processing | 6 | 11 |
GO:0006397 | mRNA processing | 7 | 11 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0008380 | RNA splicing | 7 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016070 | RNA metabolic process | 5 | 11 |
GO:0016071 | mRNA metabolic process | 6 | 11 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0046483 | heterocycle metabolic process | 3 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:0090304 | nucleic acid metabolic process | 4 | 11 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 560 | 564 | PF00656 | 0.496 |
CLV_NRD_NRD_1 | 127 | 129 | PF00675 | 0.621 |
CLV_NRD_NRD_1 | 191 | 193 | PF00675 | 0.241 |
CLV_NRD_NRD_1 | 26 | 28 | PF00675 | 0.665 |
CLV_NRD_NRD_1 | 332 | 334 | PF00675 | 0.245 |
CLV_NRD_NRD_1 | 419 | 421 | PF00675 | 0.244 |
CLV_NRD_NRD_1 | 441 | 443 | PF00675 | 0.480 |
CLV_NRD_NRD_1 | 587 | 589 | PF00675 | 0.266 |
CLV_NRD_NRD_1 | 87 | 89 | PF00675 | 0.659 |
CLV_PCSK_KEX2_1 | 126 | 128 | PF00082 | 0.602 |
CLV_PCSK_KEX2_1 | 191 | 193 | PF00082 | 0.227 |
CLV_PCSK_KEX2_1 | 332 | 334 | PF00082 | 0.266 |
CLV_PCSK_KEX2_1 | 419 | 421 | PF00082 | 0.244 |
CLV_PCSK_KEX2_1 | 435 | 437 | PF00082 | 0.425 |
CLV_PCSK_KEX2_1 | 441 | 443 | PF00082 | 0.442 |
CLV_PCSK_KEX2_1 | 546 | 548 | PF00082 | 0.271 |
CLV_PCSK_KEX2_1 | 554 | 556 | PF00082 | 0.361 |
CLV_PCSK_KEX2_1 | 587 | 589 | PF00082 | 0.266 |
CLV_PCSK_KEX2_1 | 87 | 89 | PF00082 | 0.659 |
CLV_PCSK_PC1ET2_1 | 435 | 437 | PF00082 | 0.436 |
CLV_PCSK_PC1ET2_1 | 546 | 548 | PF00082 | 0.271 |
CLV_PCSK_PC1ET2_1 | 554 | 556 | PF00082 | 0.361 |
CLV_PCSK_PC7_1 | 83 | 89 | PF00082 | 0.624 |
CLV_PCSK_SKI1_1 | 129 | 133 | PF00082 | 0.747 |
CLV_PCSK_SKI1_1 | 239 | 243 | PF00082 | 0.337 |
CLV_PCSK_SKI1_1 | 442 | 446 | PF00082 | 0.451 |
CLV_PCSK_SKI1_1 | 546 | 550 | PF00082 | 0.281 |
CLV_PCSK_SKI1_1 | 604 | 608 | PF00082 | 0.431 |
DOC_CKS1_1 | 148 | 153 | PF01111 | 0.643 |
DOC_CYCLIN_RxL_1 | 236 | 244 | PF00134 | 0.448 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 382 | 391 | PF00134 | 0.441 |
DOC_MAPK_gen_1 | 126 | 132 | PF00069 | 0.702 |
DOC_MAPK_gen_1 | 24 | 32 | PF00069 | 0.547 |
DOC_MAPK_gen_1 | 518 | 527 | PF00069 | 0.538 |
DOC_PP1_RVXF_1 | 126 | 133 | PF00149 | 0.573 |
DOC_PP2B_LxvP_1 | 589 | 592 | PF13499 | 0.572 |
DOC_PP4_MxPP_1 | 1 | 4 | PF00568 | 0.725 |
DOC_USP7_MATH_1 | 116 | 120 | PF00917 | 0.683 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.627 |
DOC_USP7_MATH_1 | 153 | 157 | PF00917 | 0.659 |
DOC_USP7_MATH_1 | 161 | 165 | PF00917 | 0.531 |
DOC_USP7_MATH_1 | 227 | 231 | PF00917 | 0.534 |
DOC_USP7_MATH_1 | 43 | 47 | PF00917 | 0.730 |
DOC_USP7_MATH_1 | 590 | 594 | PF00917 | 0.581 |
DOC_USP7_MATH_1 | 7 | 11 | PF00917 | 0.661 |
DOC_USP7_UBL2_3 | 24 | 28 | PF12436 | 0.589 |
DOC_WW_Pin1_4 | 147 | 152 | PF00397 | 0.709 |
DOC_WW_Pin1_4 | 15 | 20 | PF00397 | 0.648 |
DOC_WW_Pin1_4 | 274 | 279 | PF00397 | 0.465 |
DOC_WW_Pin1_4 | 591 | 596 | PF00397 | 0.581 |
LIG_14-3-3_CanoR_1 | 254 | 260 | PF00244 | 0.555 |
LIG_14-3-3_CanoR_1 | 381 | 389 | PF00244 | 0.538 |
LIG_14-3-3_CanoR_1 | 441 | 450 | PF00244 | 0.424 |
LIG_14-3-3_CanoR_1 | 521 | 526 | PF00244 | 0.444 |
LIG_Actin_WH2_2 | 422 | 437 | PF00022 | 0.602 |
LIG_Actin_WH2_2 | 595 | 611 | PF00022 | 0.391 |
LIG_APCC_Cbox_2 | 423 | 429 | PF00515 | 0.501 |
LIG_BRCT_BRCA1_1 | 531 | 535 | PF00533 | 0.501 |
LIG_Clathr_ClatBox_2 | 250 | 255 | PF01394 | 0.444 |
LIG_deltaCOP1_diTrp_1 | 250 | 255 | PF00928 | 0.444 |
LIG_deltaCOP1_diTrp_1 | 503 | 512 | PF00928 | 0.444 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.485 |
LIG_FHA_1 | 278 | 284 | PF00498 | 0.465 |
LIG_FHA_1 | 382 | 388 | PF00498 | 0.538 |
LIG_FHA_1 | 402 | 408 | PF00498 | 0.538 |
LIG_FHA_1 | 515 | 521 | PF00498 | 0.446 |
LIG_FHA_2 | 576 | 582 | PF00498 | 0.571 |
LIG_LIR_Apic_2 | 511 | 515 | PF02991 | 0.467 |
LIG_LIR_Gen_1 | 36 | 43 | PF02991 | 0.523 |
LIG_LIR_Gen_1 | 569 | 579 | PF02991 | 0.457 |
LIG_LIR_Gen_1 | 593 | 602 | PF02991 | 0.572 |
LIG_LIR_Nem_3 | 309 | 313 | PF02991 | 0.554 |
LIG_LIR_Nem_3 | 36 | 42 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 593 | 599 | PF02991 | 0.447 |
LIG_Pex14_1 | 603 | 607 | PF04695 | 0.537 |
LIG_PROFILIN_1 | 2 | 8 | PF00235 | 0.628 |
LIG_SH2_CRK | 262 | 266 | PF00017 | 0.412 |
LIG_SH2_CRK | 89 | 93 | PF00017 | 0.660 |
LIG_SH2_STAP1 | 109 | 113 | PF00017 | 0.652 |
LIG_SH2_STAP1 | 304 | 308 | PF00017 | 0.444 |
LIG_SH2_STAT3 | 195 | 198 | PF00017 | 0.500 |
LIG_SH2_STAT5 | 109 | 112 | PF00017 | 0.642 |
LIG_SH2_STAT5 | 195 | 198 | PF00017 | 0.538 |
LIG_SH2_STAT5 | 304 | 307 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 482 | 485 | PF00017 | 0.545 |
LIG_SH3_3 | 1 | 7 | PF00018 | 0.636 |
LIG_SH3_3 | 145 | 151 | PF00018 | 0.763 |
LIG_SH3_3 | 272 | 278 | PF00018 | 0.585 |
LIG_SH3_3 | 291 | 297 | PF00018 | 0.387 |
LIG_SH3_3 | 393 | 399 | PF00018 | 0.450 |
LIG_SH3_3 | 589 | 595 | PF00018 | 0.575 |
LIG_SH3_4 | 24 | 31 | PF00018 | 0.627 |
LIG_SUMO_SIM_anti_2 | 487 | 493 | PF11976 | 0.457 |
LIG_SUMO_SIM_par_1 | 28 | 34 | PF11976 | 0.598 |
LIG_TRAF2_1 | 578 | 581 | PF00917 | 0.441 |
LIG_WW_2 | 6 | 9 | PF00397 | 0.641 |
MOD_CK1_1 | 10 | 16 | PF00069 | 0.669 |
MOD_CK1_1 | 18 | 24 | PF00069 | 0.596 |
MOD_CK1_1 | 277 | 283 | PF00069 | 0.454 |
MOD_CK1_1 | 372 | 378 | PF00069 | 0.472 |
MOD_CK1_1 | 54 | 60 | PF00069 | 0.661 |
MOD_CK1_1 | 594 | 600 | PF00069 | 0.509 |
MOD_CK2_1 | 160 | 166 | PF00069 | 0.561 |
MOD_CK2_1 | 575 | 581 | PF00069 | 0.452 |
MOD_CMANNOS | 252 | 255 | PF00535 | 0.244 |
MOD_Cter_Amidation | 552 | 555 | PF01082 | 0.266 |
MOD_Cter_Amidation | 85 | 88 | PF01082 | 0.658 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.655 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.627 |
MOD_GlcNHglycan | 141 | 144 | PF01048 | 0.646 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.668 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.669 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.326 |
MOD_GlcNHglycan | 267 | 270 | PF01048 | 0.374 |
MOD_GlcNHglycan | 371 | 374 | PF01048 | 0.338 |
MOD_GlcNHglycan | 38 | 42 | PF01048 | 0.564 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.604 |
MOD_GlcNHglycan | 459 | 462 | PF01048 | 0.334 |
MOD_GlcNHglycan | 53 | 56 | PF01048 | 0.593 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.736 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.832 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.572 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.496 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.464 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.607 |
MOD_GSK3_1 | 360 | 367 | PF00069 | 0.500 |
MOD_GSK3_1 | 368 | 375 | PF00069 | 0.468 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.639 |
MOD_GSK3_1 | 590 | 597 | PF00069 | 0.575 |
MOD_GSK3_1 | 7 | 14 | PF00069 | 0.665 |
MOD_LATS_1 | 379 | 385 | PF00433 | 0.538 |
MOD_LATS_1 | 545 | 551 | PF00433 | 0.465 |
MOD_NEK2_1 | 165 | 170 | PF00069 | 0.642 |
MOD_NEK2_1 | 279 | 284 | PF00069 | 0.536 |
MOD_NEK2_1 | 369 | 374 | PF00069 | 0.453 |
MOD_NEK2_1 | 391 | 396 | PF00069 | 0.484 |
MOD_NEK2_2 | 531 | 536 | PF00069 | 0.430 |
MOD_PIKK_1 | 165 | 171 | PF00454 | 0.555 |
MOD_PIKK_1 | 302 | 308 | PF00454 | 0.457 |
MOD_PIKK_1 | 66 | 72 | PF00454 | 0.642 |
MOD_PK_1 | 261 | 267 | PF00069 | 0.394 |
MOD_PK_1 | 28 | 34 | PF00069 | 0.663 |
MOD_PK_1 | 521 | 527 | PF00069 | 0.501 |
MOD_PKA_1 | 546 | 552 | PF00069 | 0.481 |
MOD_PKA_2 | 107 | 113 | PF00069 | 0.782 |
MOD_PKA_2 | 253 | 259 | PF00069 | 0.525 |
MOD_PKA_2 | 380 | 386 | PF00069 | 0.444 |
MOD_PKA_2 | 546 | 552 | PF00069 | 0.436 |
MOD_Plk_1 | 33 | 39 | PF00069 | 0.538 |
MOD_Plk_2-3 | 33 | 39 | PF00069 | 0.567 |
MOD_Plk_4 | 233 | 239 | PF00069 | 0.457 |
MOD_Plk_4 | 364 | 370 | PF00069 | 0.432 |
MOD_Plk_4 | 392 | 398 | PF00069 | 0.444 |
MOD_ProDKin_1 | 147 | 153 | PF00069 | 0.709 |
MOD_ProDKin_1 | 15 | 21 | PF00069 | 0.645 |
MOD_ProDKin_1 | 274 | 280 | PF00069 | 0.465 |
MOD_ProDKin_1 | 591 | 597 | PF00069 | 0.586 |
TRG_DiLeu_BaEn_3 | 580 | 586 | PF01217 | 0.538 |
TRG_DiLeu_BaLyEn_6 | 373 | 378 | PF01217 | 0.501 |
TRG_DiLeu_BaLyEn_6 | 445 | 450 | PF01217 | 0.469 |
TRG_ENDOCYTIC_2 | 262 | 265 | PF00928 | 0.412 |
TRG_ENDOCYTIC_2 | 310 | 313 | PF00928 | 0.510 |
TRG_ENDOCYTIC_2 | 453 | 456 | PF00928 | 0.459 |
TRG_ENDOCYTIC_2 | 89 | 92 | PF00928 | 0.661 |
TRG_ER_diArg_1 | 126 | 128 | PF00400 | 0.623 |
TRG_ER_diArg_1 | 586 | 588 | PF00400 | 0.465 |
TRG_ER_diArg_1 | 87 | 89 | PF00400 | 0.725 |
TRG_Pf-PMV_PEXEL_1 | 239 | 244 | PF00026 | 0.248 |
TRG_Pf-PMV_PEXEL_1 | 376 | 380 | PF00026 | 0.301 |
TRG_Pf-PMV_PEXEL_1 | 413 | 418 | PF00026 | 0.257 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HXQ4 | Leptomonas seymouri | 56% | 100% |
A0A1X0P2M3 | Trypanosomatidae | 44% | 100% |
A0A3R7KZ00 | Trypanosoma rangeli | 40% | 100% |
A0A3S5H4W0 | Leishmania donovani | 92% | 99% |
A4H379 | Leishmania braziliensis | 75% | 100% |
A4HRH9 | Leishmania infantum | 92% | 100% |
C9ZXK6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
E9AJE3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
V5BLJ6 | Trypanosoma cruzi | 37% | 100% |