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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005654 | nucleoplasm | 2 | 1 |
GO:0005681 | spliceosomal complex | 3 | 1 |
GO:0005684 | U2-type spliceosomal complex | 4 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0071006 | U2-type catalytic step 1 spliceosome | 4 | 1 |
GO:0071012 | catalytic step 1 spliceosome | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1990904 | ribonucleoprotein complex | 2 | 1 |
Related structures:
AlphaFold database: E9ALV1
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 | 210 | 214 | PF00656 | 0.327 |
CLV_C14_Caspase3-7 | 261 | 265 | PF00656 | 0.222 |
CLV_C14_Caspase3-7 | 348 | 352 | PF00656 | 0.527 |
CLV_C14_Caspase3-7 | 396 | 400 | PF00656 | 0.816 |
CLV_NRD_NRD_1 | 20 | 22 | PF00675 | 0.411 |
CLV_NRD_NRD_1 | 203 | 205 | PF00675 | 0.389 |
CLV_NRD_NRD_1 | 288 | 290 | PF00675 | 0.404 |
CLV_NRD_NRD_1 | 323 | 325 | PF00675 | 0.426 |
CLV_NRD_NRD_1 | 333 | 335 | PF00675 | 0.596 |
CLV_NRD_NRD_1 | 34 | 36 | PF00675 | 0.414 |
CLV_NRD_NRD_1 | 374 | 376 | PF00675 | 0.521 |
CLV_NRD_NRD_1 | 66 | 68 | PF00675 | 0.357 |
CLV_NRD_NRD_1 | 78 | 80 | PF00675 | 0.355 |
CLV_PCSK_FUR_1 | 201 | 205 | PF00082 | 0.389 |
CLV_PCSK_FUR_1 | 32 | 36 | PF00082 | 0.411 |
CLV_PCSK_KEX2_1 | 127 | 129 | PF00082 | 0.411 |
CLV_PCSK_KEX2_1 | 203 | 205 | PF00082 | 0.389 |
CLV_PCSK_KEX2_1 | 288 | 290 | PF00082 | 0.381 |
CLV_PCSK_KEX2_1 | 323 | 325 | PF00082 | 0.503 |
CLV_PCSK_KEX2_1 | 333 | 335 | PF00082 | 0.635 |
CLV_PCSK_KEX2_1 | 34 | 36 | PF00082 | 0.411 |
CLV_PCSK_KEX2_1 | 49 | 51 | PF00082 | 0.183 |
CLV_PCSK_KEX2_1 | 66 | 68 | PF00082 | 0.411 |
CLV_PCSK_KEX2_1 | 78 | 80 | PF00082 | 0.411 |
CLV_PCSK_KEX2_1 | 83 | 85 | PF00082 | 0.411 |
CLV_PCSK_PC1ET2_1 | 127 | 129 | PF00082 | 0.389 |
CLV_PCSK_PC1ET2_1 | 34 | 36 | PF00082 | 0.411 |
CLV_PCSK_PC1ET2_1 | 49 | 51 | PF00082 | 0.183 |
CLV_PCSK_PC1ET2_1 | 83 | 85 | PF00082 | 0.513 |
CLV_PCSK_PC7_1 | 199 | 205 | PF00082 | 0.389 |
CLV_PCSK_PC7_1 | 79 | 85 | PF00082 | 0.513 |
CLV_PCSK_SKI1_1 | 253 | 257 | PF00082 | 0.416 |
CLV_PCSK_SKI1_1 | 323 | 327 | PF00082 | 0.513 |
CLV_PCSK_SKI1_1 | 333 | 337 | PF00082 | 0.630 |
CLV_PCSK_SKI1_1 | 415 | 419 | PF00082 | 0.730 |
DEG_SCF_FBW7_1 | 111 | 117 | PF00400 | 0.411 |
DEG_SCF_FBW7_1 | 370 | 377 | PF00400 | 0.644 |
DEG_SPOP_SBC_1 | 229 | 233 | PF00917 | 0.513 |
DEG_SPOP_SBC_1 | 241 | 245 | PF00917 | 0.298 |
DEG_SPOP_SBC_1 | 339 | 343 | PF00917 | 0.648 |
DEG_SPOP_SBC_1 | 364 | 368 | PF00917 | 0.730 |
DOC_CKS1_1 | 111 | 116 | PF01111 | 0.411 |
DOC_CYCLIN_yClb3_PxF_3 | 412 | 418 | PF00134 | 0.625 |
DOC_MAPK_gen_1 | 223 | 230 | PF00069 | 0.222 |
DOC_MAPK_gen_1 | 49 | 57 | PF00069 | 0.411 |
DOC_MAPK_gen_1 | 83 | 91 | PF00069 | 0.513 |
DOC_PP4_FxxP_1 | 249 | 252 | PF00568 | 0.513 |
DOC_PP4_FxxP_1 | 444 | 447 | PF00568 | 0.816 |
DOC_PP4_FxxP_1 | 53 | 56 | PF00568 | 0.411 |
DOC_USP7_MATH_1 | 229 | 233 | PF00917 | 0.382 |
DOC_USP7_MATH_1 | 242 | 246 | PF00917 | 0.432 |
DOC_USP7_MATH_1 | 374 | 378 | PF00917 | 0.723 |
DOC_USP7_MATH_1 | 400 | 404 | PF00917 | 0.721 |
DOC_USP7_MATH_1 | 417 | 421 | PF00917 | 0.635 |
DOC_USP7_MATH_1 | 445 | 449 | PF00917 | 0.749 |
DOC_USP7_MATH_1 | 69 | 73 | PF00917 | 0.411 |
DOC_USP7_UBL2_3 | 376 | 380 | PF12436 | 0.711 |
DOC_WW_Pin1_4 | 110 | 115 | PF00397 | 0.411 |
DOC_WW_Pin1_4 | 237 | 242 | PF00397 | 0.471 |
DOC_WW_Pin1_4 | 370 | 375 | PF00397 | 0.599 |
LIG_14-3-3_CanoR_1 | 333 | 340 | PF00244 | 0.708 |
LIG_14-3-3_CanoR_1 | 423 | 429 | PF00244 | 0.722 |
LIG_14-3-3_CanoR_1 | 50 | 54 | PF00244 | 0.411 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.629 |
LIG_BRCT_BRCA1_1 | 245 | 249 | PF00533 | 0.513 |
LIG_FHA_1 | 252 | 258 | PF00498 | 0.272 |
LIG_FHA_1 | 425 | 431 | PF00498 | 0.748 |
LIG_FHA_1 | 50 | 56 | PF00498 | 0.411 |
LIG_FHA_2 | 107 | 113 | PF00498 | 0.411 |
LIG_FHA_2 | 185 | 191 | PF00498 | 0.222 |
LIG_FHA_2 | 231 | 237 | PF00498 | 0.513 |
LIG_FHA_2 | 307 | 313 | PF00498 | 0.319 |
LIG_FHA_2 | 339 | 345 | PF00498 | 0.536 |
LIG_LIR_Apic_2 | 10 | 16 | PF02991 | 0.411 |
LIG_LIR_Apic_2 | 246 | 252 | PF02991 | 0.513 |
LIG_LIR_Apic_2 | 358 | 364 | PF02991 | 0.524 |
LIG_LIR_Apic_2 | 442 | 447 | PF02991 | 0.821 |
LIG_LIR_Apic_2 | 52 | 56 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 130 | 136 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 17 | 23 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 276 | 282 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 287 | 293 | PF02991 | 0.411 |
LIG_NRBOX | 463 | 469 | PF00104 | 0.521 |
LIG_Pex14_2 | 53 | 57 | PF04695 | 0.411 |
LIG_SH2_GRB2like | 387 | 390 | PF00017 | 0.492 |
LIG_SH2_GRB2like | 75 | 78 | PF00017 | 0.411 |
LIG_SH2_PTP2 | 13 | 16 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 106 | 109 | PF00017 | 0.416 |
LIG_SH2_STAT5 | 120 | 123 | PF00017 | 0.425 |
LIG_SH2_STAT5 | 13 | 16 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 85 | 88 | PF00017 | 0.411 |
LIG_SH3_1 | 108 | 114 | PF00018 | 0.411 |
LIG_SH3_3 | 108 | 114 | PF00018 | 0.411 |
LIG_SH3_3 | 410 | 416 | PF00018 | 0.759 |
LIG_SUMO_SIM_anti_2 | 93 | 98 | PF11976 | 0.411 |
LIG_SUMO_SIM_par_1 | 426 | 432 | PF11976 | 0.514 |
LIG_TRAF2_1 | 143 | 146 | PF00917 | 0.407 |
LIG_TRAF2_1 | 182 | 185 | PF00917 | 0.513 |
LIG_TRAF2_1 | 342 | 345 | PF00917 | 0.540 |
MOD_CDK_SPK_2 | 110 | 115 | PF00069 | 0.411 |
MOD_CDK_SPK_2 | 370 | 375 | PF00069 | 0.520 |
MOD_CDK_SPxK_1 | 370 | 376 | PF00069 | 0.520 |
MOD_CK1_1 | 231 | 237 | PF00069 | 0.491 |
MOD_CK1_1 | 240 | 246 | PF00069 | 0.278 |
MOD_CK1_1 | 403 | 409 | PF00069 | 0.662 |
MOD_CK1_1 | 426 | 432 | PF00069 | 0.759 |
MOD_CK1_1 | 448 | 454 | PF00069 | 0.545 |
MOD_CK2_1 | 106 | 112 | PF00069 | 0.411 |
MOD_CK2_1 | 230 | 236 | PF00069 | 0.513 |
MOD_CK2_1 | 263 | 269 | PF00069 | 0.449 |
MOD_CK2_1 | 306 | 312 | PF00069 | 0.397 |
MOD_CK2_1 | 338 | 344 | PF00069 | 0.568 |
MOD_Cter_Amidation | 32 | 35 | PF01082 | 0.411 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.376 |
MOD_GlcNHglycan | 264 | 268 | PF01048 | 0.489 |
MOD_GlcNHglycan | 357 | 360 | PF01048 | 0.727 |
MOD_GlcNHglycan | 367 | 370 | PF01048 | 0.681 |
MOD_GlcNHglycan | 431 | 434 | PF01048 | 0.718 |
MOD_GlcNHglycan | 436 | 439 | PF01048 | 0.633 |
MOD_GlcNHglycan | 447 | 450 | PF01048 | 0.528 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.506 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.393 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.411 |
MOD_GSK3_1 | 236 | 243 | PF00069 | 0.416 |
MOD_GSK3_1 | 306 | 313 | PF00069 | 0.397 |
MOD_GSK3_1 | 370 | 377 | PF00069 | 0.604 |
MOD_GSK3_1 | 424 | 431 | PF00069 | 0.773 |
MOD_N-GLC_1 | 4 | 9 | PF02516 | 0.586 |
MOD_NEK2_1 | 197 | 202 | PF00069 | 0.411 |
MOD_NEK2_1 | 228 | 233 | PF00069 | 0.299 |
MOD_NEK2_1 | 310 | 315 | PF00069 | 0.222 |
MOD_NEK2_1 | 365 | 370 | PF00069 | 0.810 |
MOD_NEK2_1 | 418 | 423 | PF00069 | 0.543 |
MOD_PIKK_1 | 448 | 454 | PF00454 | 0.836 |
MOD_PK_1 | 375 | 381 | PF00069 | 0.714 |
MOD_PKA_1 | 333 | 339 | PF00069 | 0.629 |
MOD_PKA_1 | 375 | 381 | PF00069 | 0.714 |
MOD_PKA_1 | 49 | 55 | PF00069 | 0.411 |
MOD_PKA_2 | 202 | 208 | PF00069 | 0.436 |
MOD_PKA_2 | 333 | 339 | PF00069 | 0.629 |
MOD_PKA_2 | 374 | 380 | PF00069 | 0.503 |
MOD_PKA_2 | 49 | 55 | PF00069 | 0.411 |
MOD_PKA_2 | 69 | 75 | PF00069 | 0.411 |
MOD_Plk_1 | 311 | 317 | PF00069 | 0.393 |
MOD_Plk_1 | 4 | 10 | PF00069 | 0.586 |
MOD_Plk_1 | 400 | 406 | PF00069 | 0.741 |
MOD_Plk_4 | 193 | 199 | PF00069 | 0.362 |
MOD_Plk_4 | 400 | 406 | PF00069 | 0.764 |
MOD_Plk_4 | 460 | 466 | PF00069 | 0.811 |
MOD_ProDKin_1 | 110 | 116 | PF00069 | 0.411 |
MOD_ProDKin_1 | 237 | 243 | PF00069 | 0.471 |
MOD_ProDKin_1 | 370 | 376 | PF00069 | 0.599 |
MOD_SUMO_for_1 | 150 | 153 | PF00179 | 0.411 |
TRG_DiLeu_BaLyEn_6 | 463 | 468 | PF01217 | 0.523 |
TRG_ER_diArg_1 | 198 | 201 | PF00400 | 0.400 |
TRG_ER_diArg_1 | 202 | 204 | PF00400 | 0.411 |
TRG_ER_diArg_1 | 288 | 290 | PF00400 | 0.411 |
TRG_ER_diArg_1 | 322 | 324 | PF00400 | 0.425 |
TRG_ER_diArg_1 | 333 | 335 | PF00400 | 0.584 |
TRG_ER_diArg_1 | 66 | 68 | PF00400 | 0.411 |
TRG_ER_diArg_1 | 88 | 91 | PF00400 | 0.222 |
TRG_NLS_Bipartite_1 | 21 | 38 | PF00514 | 0.411 |
TRG_NLS_MonoExtN_4 | 32 | 38 | PF00514 | 0.411 |
TRG_Pf-PMV_PEXEL_1 | 170 | 174 | PF00026 | 0.411 |
TRG_Pf-PMV_PEXEL_1 | 177 | 181 | PF00026 | 0.411 |
TRG_Pf-PMV_PEXEL_1 | 21 | 25 | PF00026 | 0.411 |
TRG_Pf-PMV_PEXEL_1 | 291 | 296 | PF00026 | 0.390 |
TRG_Pf-PMV_PEXEL_1 | 466 | 470 | PF00026 | 0.709 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HY11 | Leptomonas seymouri | 56% | 100% |
A0A3Q8IF48 | Leishmania donovani | 86% | 100% |
A4HHD4 | Leishmania braziliensis | 74% | 99% |
A4I4H9 | Leishmania infantum | 86% | 100% |
E9ADY0 | Leishmania major | 85% | 100% |