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: A0A3S5H4W0
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 | 564 | 568 | PF00656 | 0.496 |
CLV_NRD_NRD_1 | 126 | 128 | PF00675 | 0.630 |
CLV_NRD_NRD_1 | 195 | 197 | PF00675 | 0.241 |
CLV_NRD_NRD_1 | 21 | 23 | PF00675 | 0.684 |
CLV_NRD_NRD_1 | 336 | 338 | PF00675 | 0.245 |
CLV_NRD_NRD_1 | 423 | 425 | PF00675 | 0.244 |
CLV_NRD_NRD_1 | 445 | 447 | PF00675 | 0.475 |
CLV_NRD_NRD_1 | 591 | 593 | PF00675 | 0.266 |
CLV_NRD_NRD_1 | 86 | 88 | PF00675 | 0.676 |
CLV_PCSK_KEX2_1 | 125 | 127 | PF00082 | 0.615 |
CLV_PCSK_KEX2_1 | 195 | 197 | PF00082 | 0.227 |
CLV_PCSK_KEX2_1 | 336 | 338 | PF00082 | 0.266 |
CLV_PCSK_KEX2_1 | 423 | 425 | PF00082 | 0.244 |
CLV_PCSK_KEX2_1 | 439 | 441 | PF00082 | 0.427 |
CLV_PCSK_KEX2_1 | 445 | 447 | PF00082 | 0.438 |
CLV_PCSK_KEX2_1 | 550 | 552 | PF00082 | 0.271 |
CLV_PCSK_KEX2_1 | 558 | 560 | PF00082 | 0.361 |
CLV_PCSK_KEX2_1 | 591 | 593 | PF00082 | 0.266 |
CLV_PCSK_KEX2_1 | 86 | 88 | PF00082 | 0.676 |
CLV_PCSK_PC1ET2_1 | 439 | 441 | PF00082 | 0.438 |
CLV_PCSK_PC1ET2_1 | 550 | 552 | PF00082 | 0.271 |
CLV_PCSK_PC1ET2_1 | 558 | 560 | PF00082 | 0.361 |
CLV_PCSK_PC7_1 | 82 | 88 | PF00082 | 0.648 |
CLV_PCSK_SKI1_1 | 128 | 132 | PF00082 | 0.753 |
CLV_PCSK_SKI1_1 | 243 | 247 | PF00082 | 0.337 |
CLV_PCSK_SKI1_1 | 343 | 347 | PF00082 | 0.282 |
CLV_PCSK_SKI1_1 | 446 | 450 | PF00082 | 0.452 |
CLV_PCSK_SKI1_1 | 608 | 612 | PF00082 | 0.420 |
DEG_SPOP_SBC_1 | 17 | 21 | PF00917 | 0.587 |
DOC_CKS1_1 | 149 | 154 | PF01111 | 0.640 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 386 | 395 | PF00134 | 0.441 |
DOC_MAPK_gen_1 | 125 | 131 | PF00069 | 0.712 |
DOC_MAPK_gen_1 | 522 | 531 | PF00069 | 0.538 |
DOC_PP1_RVXF_1 | 125 | 132 | PF00149 | 0.582 |
DOC_PP2B_LxvP_1 | 593 | 596 | PF13499 | 0.571 |
DOC_PP4_MxPP_1 | 1 | 4 | PF00568 | 0.724 |
DOC_USP7_MATH_1 | 11 | 15 | PF00917 | 0.624 |
DOC_USP7_MATH_1 | 115 | 119 | PF00917 | 0.683 |
DOC_USP7_MATH_1 | 17 | 21 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 269 | 273 | PF00917 | 0.412 |
DOC_USP7_MATH_1 | 352 | 356 | PF00917 | 0.536 |
DOC_USP7_MATH_1 | 372 | 376 | PF00917 | 0.517 |
DOC_USP7_MATH_1 | 42 | 46 | PF00917 | 0.724 |
DOC_USP7_MATH_1 | 48 | 52 | PF00917 | 0.694 |
DOC_USP7_MATH_1 | 58 | 62 | PF00917 | 0.678 |
DOC_USP7_MATH_1 | 594 | 598 | PF00917 | 0.579 |
DOC_USP7_MATH_1 | 6 | 10 | PF00917 | 0.656 |
DOC_USP7_UBL2_3 | 23 | 27 | PF12436 | 0.575 |
DOC_USP7_UBL2_3 | 346 | 350 | PF12436 | 0.513 |
DOC_WW_Pin1_4 | 148 | 153 | PF00397 | 0.705 |
DOC_WW_Pin1_4 | 278 | 283 | PF00397 | 0.465 |
DOC_WW_Pin1_4 | 595 | 600 | PF00397 | 0.573 |
LIG_14-3-3_CanoR_1 | 18 | 24 | PF00244 | 0.597 |
LIG_14-3-3_CanoR_1 | 258 | 264 | PF00244 | 0.555 |
LIG_14-3-3_CanoR_1 | 385 | 393 | PF00244 | 0.538 |
LIG_14-3-3_CanoR_1 | 445 | 454 | PF00244 | 0.424 |
LIG_14-3-3_CanoR_1 | 525 | 530 | PF00244 | 0.444 |
LIG_Actin_WH2_2 | 426 | 441 | PF00022 | 0.602 |
LIG_APCC_Cbox_2 | 427 | 433 | PF00515 | 0.501 |
LIG_BRCT_BRCA1_1 | 535 | 539 | PF00533 | 0.501 |
LIG_Clathr_ClatBox_2 | 254 | 259 | PF01394 | 0.444 |
LIG_deltaCOP1_diTrp_1 | 254 | 259 | PF00928 | 0.444 |
LIG_deltaCOP1_diTrp_1 | 507 | 516 | PF00928 | 0.444 |
LIG_FHA_1 | 107 | 113 | PF00498 | 0.517 |
LIG_FHA_1 | 236 | 242 | PF00498 | 0.485 |
LIG_FHA_1 | 282 | 288 | PF00498 | 0.465 |
LIG_FHA_1 | 386 | 392 | PF00498 | 0.538 |
LIG_FHA_1 | 406 | 412 | PF00498 | 0.538 |
LIG_FHA_1 | 519 | 525 | PF00498 | 0.446 |
LIG_FHA_2 | 580 | 586 | PF00498 | 0.571 |
LIG_LIR_Gen_1 | 35 | 43 | PF02991 | 0.511 |
LIG_LIR_Gen_1 | 573 | 583 | PF02991 | 0.457 |
LIG_LIR_Gen_1 | 597 | 606 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 313 | 317 | PF02991 | 0.554 |
LIG_LIR_Nem_3 | 35 | 41 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 597 | 603 | PF02991 | 0.424 |
LIG_Pex14_1 | 607 | 611 | PF04695 | 0.519 |
LIG_PROFILIN_1 | 2 | 8 | PF00235 | 0.629 |
LIG_SH2_CRK | 88 | 92 | PF00017 | 0.684 |
LIG_SH2_STAP1 | 108 | 112 | PF00017 | 0.650 |
LIG_SH2_STAP1 | 308 | 312 | PF00017 | 0.444 |
LIG_SH2_STAT3 | 199 | 202 | PF00017 | 0.500 |
LIG_SH2_STAT5 | 108 | 111 | PF00017 | 0.635 |
LIG_SH2_STAT5 | 199 | 202 | PF00017 | 0.538 |
LIG_SH2_STAT5 | 308 | 311 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 486 | 489 | PF00017 | 0.545 |
LIG_SH3_3 | 146 | 152 | PF00018 | 0.763 |
LIG_SH3_3 | 157 | 163 | PF00018 | 0.611 |
LIG_SH3_3 | 2 | 8 | PF00018 | 0.636 |
LIG_SH3_3 | 276 | 282 | PF00018 | 0.585 |
LIG_SH3_3 | 295 | 301 | PF00018 | 0.387 |
LIG_SH3_3 | 397 | 403 | PF00018 | 0.450 |
LIG_SH3_3 | 593 | 599 | PF00018 | 0.568 |
LIG_SH3_4 | 23 | 30 | PF00018 | 0.613 |
LIG_SUMO_SIM_anti_2 | 491 | 497 | PF11976 | 0.457 |
LIG_SUMO_SIM_anti_2 | 61 | 67 | PF11976 | 0.494 |
LIG_SUMO_SIM_par_1 | 27 | 33 | PF11976 | 0.581 |
LIG_TRAF2_1 | 143 | 146 | PF00917 | 0.599 |
LIG_TRAF2_1 | 582 | 585 | PF00917 | 0.441 |
LIG_WRC_WIRS_1 | 203 | 208 | PF05994 | 0.479 |
LIG_WW_2 | 5 | 8 | PF00397 | 0.634 |
MOD_CK1_1 | 281 | 287 | PF00069 | 0.454 |
MOD_CK1_1 | 376 | 382 | PF00069 | 0.472 |
MOD_CK1_1 | 53 | 59 | PF00069 | 0.660 |
MOD_CK1_1 | 598 | 604 | PF00069 | 0.482 |
MOD_CK1_1 | 9 | 15 | PF00069 | 0.667 |
MOD_CK2_1 | 140 | 146 | PF00069 | 0.593 |
MOD_CK2_1 | 161 | 167 | PF00069 | 0.573 |
MOD_CK2_1 | 579 | 585 | PF00069 | 0.452 |
MOD_CMANNOS | 256 | 259 | PF00535 | 0.244 |
MOD_Cter_Amidation | 556 | 559 | PF01082 | 0.266 |
MOD_Cter_Amidation | 84 | 87 | PF01082 | 0.680 |
MOD_GlcNHglycan | 13 | 16 | PF01048 | 0.622 |
MOD_GlcNHglycan | 142 | 145 | PF01048 | 0.651 |
MOD_GlcNHglycan | 187 | 190 | PF01048 | 0.379 |
MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.326 |
MOD_GlcNHglycan | 267 | 270 | PF01048 | 0.391 |
MOD_GlcNHglycan | 271 | 274 | PF01048 | 0.374 |
MOD_GlcNHglycan | 37 | 41 | PF01048 | 0.545 |
MOD_GlcNHglycan | 375 | 378 | PF01048 | 0.338 |
MOD_GlcNHglycan | 44 | 47 | PF01048 | 0.598 |
MOD_GlcNHglycan | 463 | 466 | PF01048 | 0.334 |
MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.592 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.654 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.739 |
MOD_GSK3_1 | 162 | 169 | PF00069 | 0.582 |
MOD_GSK3_1 | 265 | 272 | PF00069 | 0.464 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.591 |
MOD_GSK3_1 | 360 | 367 | PF00069 | 0.499 |
MOD_GSK3_1 | 368 | 375 | PF00069 | 0.472 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.634 |
MOD_GSK3_1 | 594 | 601 | PF00069 | 0.567 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.661 |
MOD_LATS_1 | 383 | 389 | PF00433 | 0.538 |
MOD_LATS_1 | 549 | 555 | PF00433 | 0.465 |
MOD_NEK2_1 | 166 | 171 | PF00069 | 0.647 |
MOD_NEK2_1 | 283 | 288 | PF00069 | 0.536 |
MOD_NEK2_1 | 360 | 365 | PF00069 | 0.547 |
MOD_NEK2_1 | 373 | 378 | PF00069 | 0.453 |
MOD_NEK2_1 | 395 | 400 | PF00069 | 0.484 |
MOD_NEK2_2 | 535 | 540 | PF00069 | 0.430 |
MOD_PIKK_1 | 166 | 172 | PF00454 | 0.560 |
MOD_PIKK_1 | 306 | 312 | PF00454 | 0.457 |
MOD_PK_1 | 27 | 33 | PF00069 | 0.646 |
MOD_PK_1 | 525 | 531 | PF00069 | 0.501 |
MOD_PKA_2 | 106 | 112 | PF00069 | 0.777 |
MOD_PKA_2 | 17 | 23 | PF00069 | 0.578 |
MOD_PKA_2 | 257 | 263 | PF00069 | 0.525 |
MOD_PKA_2 | 384 | 390 | PF00069 | 0.444 |
MOD_Plk_1 | 32 | 38 | PF00069 | 0.522 |
MOD_Plk_2-3 | 32 | 38 | PF00069 | 0.550 |
MOD_Plk_4 | 237 | 243 | PF00069 | 0.457 |
MOD_Plk_4 | 396 | 402 | PF00069 | 0.444 |
MOD_Plk_4 | 58 | 64 | PF00069 | 0.615 |
MOD_ProDKin_1 | 148 | 154 | PF00069 | 0.706 |
MOD_ProDKin_1 | 278 | 284 | PF00069 | 0.465 |
MOD_ProDKin_1 | 595 | 601 | PF00069 | 0.577 |
TRG_DiLeu_BaEn_3 | 584 | 590 | PF01217 | 0.538 |
TRG_DiLeu_BaLyEn_6 | 377 | 382 | PF01217 | 0.501 |
TRG_DiLeu_BaLyEn_6 | 449 | 454 | PF01217 | 0.471 |
TRG_ENDOCYTIC_2 | 314 | 317 | PF00928 | 0.510 |
TRG_ENDOCYTIC_2 | 457 | 460 | PF00928 | 0.459 |
TRG_ENDOCYTIC_2 | 88 | 91 | PF00928 | 0.689 |
TRG_ER_diArg_1 | 125 | 127 | PF00400 | 0.636 |
TRG_ER_diArg_1 | 590 | 592 | PF00400 | 0.465 |
TRG_ER_diArg_1 | 86 | 88 | PF00400 | 0.742 |
TRG_NLS_MonoExtN_4 | 548 | 554 | PF00514 | 0.471 |
TRG_Pf-PMV_PEXEL_1 | 380 | 384 | PF00026 | 0.301 |
TRG_Pf-PMV_PEXEL_1 | 417 | 422 | PF00026 | 0.257 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HXQ4 | Leptomonas seymouri | 56% | 100% |
A0A1X0P2M3 | Trypanosomatidae | 44% | 100% |
A0A3R7KZ00 | Trypanosoma rangeli | 44% | 100% |
A4H379 | Leishmania braziliensis | 75% | 93% |
A4HRH9 | Leishmania infantum | 99% | 100% |
C9ZXK6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
E9AC47 | Leishmania major | 92% | 100% |
E9AJE3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
V5BLJ6 | Trypanosoma cruzi | 37% | 100% |