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: 24 |
NetGPI | no | yes: 0, no: 24 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 4 |
GO:0005737 | cytoplasm | 2 | 3 |
Related structures:
AlphaFold database: E9AUS6
Term | Name | Level | Count |
---|---|---|---|
GO:0010468 | regulation of gene expression | 5 | 3 |
GO:0010608 | post-transcriptional regulation of gene expression | 6 | 3 |
GO:0019222 | regulation of metabolic process | 3 | 3 |
GO:0050789 | regulation of biological process | 2 | 3 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 3 |
GO:0065007 | biological regulation | 1 | 3 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 25 |
GO:0003723 | RNA binding | 4 | 25 |
GO:0005488 | binding | 1 | 25 |
GO:0097159 | organic cyclic compound binding | 2 | 25 |
GO:1901363 | heterocyclic compound binding | 2 | 25 |
GO:0003729 | mRNA binding | 5 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 64 | 68 | PF00656 | 0.338 |
CLV_NRD_NRD_1 | 125 | 127 | PF00675 | 0.360 |
CLV_NRD_NRD_1 | 134 | 136 | PF00675 | 0.402 |
CLV_NRD_NRD_1 | 19 | 21 | PF00675 | 0.602 |
CLV_NRD_NRD_1 | 250 | 252 | PF00675 | 0.285 |
CLV_NRD_NRD_1 | 419 | 421 | PF00675 | 0.701 |
CLV_PCSK_KEX2_1 | 125 | 127 | PF00082 | 0.360 |
CLV_PCSK_KEX2_1 | 134 | 136 | PF00082 | 0.402 |
CLV_PCSK_KEX2_1 | 19 | 21 | PF00082 | 0.434 |
CLV_PCSK_KEX2_1 | 250 | 252 | PF00082 | 0.300 |
CLV_PCSK_KEX2_1 | 291 | 293 | PF00082 | 0.470 |
CLV_PCSK_KEX2_1 | 317 | 319 | PF00082 | 0.569 |
CLV_PCSK_KEX2_1 | 419 | 421 | PF00082 | 0.547 |
CLV_PCSK_PC1ET2_1 | 291 | 293 | PF00082 | 0.470 |
CLV_PCSK_PC1ET2_1 | 317 | 319 | PF00082 | 0.472 |
CLV_PCSK_SKI1_1 | 180 | 184 | PF00082 | 0.300 |
CLV_PCSK_SKI1_1 | 250 | 254 | PF00082 | 0.388 |
CLV_PCSK_SKI1_1 | 298 | 302 | PF00082 | 0.360 |
CLV_PCSK_SKI1_1 | 394 | 398 | PF00082 | 0.481 |
CLV_PCSK_SKI1_1 | 51 | 55 | PF00082 | 0.388 |
CLV_Separin_Metazoa | 177 | 181 | PF03568 | 0.439 |
CLV_Separin_Metazoa | 391 | 395 | PF03568 | 0.475 |
DEG_APCC_DBOX_1 | 124 | 132 | PF00400 | 0.403 |
DEG_APCC_DBOX_1 | 179 | 187 | PF00400 | 0.300 |
DEG_APCC_DBOX_1 | 250 | 258 | PF00400 | 0.457 |
DEG_Kelch_Keap1_1 | 370 | 375 | PF01344 | 0.471 |
DOC_CYCLIN_RxL_1 | 247 | 256 | PF00134 | 0.406 |
DOC_MAPK_gen_1 | 76 | 84 | PF00069 | 0.278 |
DOC_MAPK_MEF2A_6 | 76 | 84 | PF00069 | 0.406 |
DOC_USP7_MATH_1 | 316 | 320 | PF00917 | 0.428 |
DOC_USP7_MATH_1 | 362 | 366 | PF00917 | 0.539 |
DOC_USP7_MATH_1 | 376 | 380 | PF00917 | 0.569 |
DOC_USP7_MATH_1 | 399 | 403 | PF00917 | 0.484 |
DOC_USP7_UBL2_3 | 309 | 313 | PF12436 | 0.474 |
DOC_WW_Pin1_4 | 44 | 49 | PF00397 | 0.370 |
LIG_14-3-3_CanoR_1 | 125 | 129 | PF00244 | 0.370 |
LIG_14-3-3_CanoR_1 | 208 | 216 | PF00244 | 0.487 |
LIG_14-3-3_CanoR_1 | 34 | 41 | PF00244 | 0.440 |
LIG_14-3-3_CanoR_1 | 394 | 399 | PF00244 | 0.482 |
LIG_14-3-3_CanoR_1 | 59 | 69 | PF00244 | 0.486 |
LIG_14-3-3_CterR_2 | 428 | 433 | PF00244 | 0.504 |
LIG_Actin_WH2_1 | 250 | 267 | PF00022 | 0.346 |
LIG_Actin_WH2_1 | 62 | 80 | PF00022 | 0.364 |
LIG_Actin_WH2_2 | 63 | 80 | PF00022 | 0.362 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.440 |
LIG_BIR_III_2 | 353 | 357 | PF00653 | 0.434 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.440 |
LIG_EH1_1 | 274 | 282 | PF00400 | 0.408 |
LIG_FHA_1 | 100 | 106 | PF00498 | 0.331 |
LIG_FHA_1 | 16 | 22 | PF00498 | 0.519 |
LIG_FHA_1 | 218 | 224 | PF00498 | 0.486 |
LIG_FHA_2 | 90 | 96 | PF00498 | 0.421 |
LIG_LIR_Gen_1 | 397 | 407 | PF02991 | 0.738 |
LIG_LIR_Nem_3 | 192 | 197 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 270 | 275 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 289 | 293 | PF02991 | 0.404 |
LIG_SH2_SRC | 351 | 354 | PF00017 | 0.450 |
LIG_SH2_STAT3 | 197 | 200 | PF00017 | 0.324 |
LIG_SH2_STAT3 | 421 | 424 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 123 | 126 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 152 | 155 | PF00017 | 0.421 |
LIG_SH2_STAT5 | 214 | 217 | PF00017 | 0.422 |
LIG_SH2_STAT5 | 351 | 354 | PF00017 | 0.407 |
LIG_SH2_STAT5 | 384 | 387 | PF00017 | 0.516 |
LIG_SH3_3 | 255 | 261 | PF00018 | 0.474 |
LIG_SH3_3 | 281 | 287 | PF00018 | 0.524 |
LIG_SH3_3 | 393 | 399 | PF00018 | 0.469 |
LIG_SH3_3 | 4 | 10 | PF00018 | 0.674 |
LIG_SUMO_SIM_par_1 | 279 | 285 | PF11976 | 0.210 |
LIG_UBA3_1 | 223 | 230 | PF00899 | 0.378 |
MOD_CDK_SPxxK_3 | 44 | 51 | PF00069 | 0.365 |
MOD_CK1_1 | 121 | 127 | PF00069 | 0.347 |
MOD_CK1_1 | 206 | 212 | PF00069 | 0.334 |
MOD_CK1_1 | 282 | 288 | PF00069 | 0.395 |
MOD_CK1_1 | 365 | 371 | PF00069 | 0.483 |
MOD_CK1_1 | 377 | 383 | PF00069 | 0.478 |
MOD_CK1_1 | 402 | 408 | PF00069 | 0.446 |
MOD_CK1_1 | 68 | 74 | PF00069 | 0.347 |
MOD_CK2_1 | 127 | 133 | PF00069 | 0.341 |
MOD_CK2_1 | 369 | 375 | PF00069 | 0.579 |
MOD_CK2_1 | 89 | 95 | PF00069 | 0.400 |
MOD_GlcNHglycan | 138 | 142 | PF01048 | 0.529 |
MOD_GlcNHglycan | 21 | 24 | PF01048 | 0.485 |
MOD_GlcNHglycan | 318 | 321 | PF01048 | 0.545 |
MOD_GlcNHglycan | 364 | 367 | PF01048 | 0.548 |
MOD_GlcNHglycan | 375 | 379 | PF01048 | 0.503 |
MOD_GlcNHglycan | 405 | 408 | PF01048 | 0.603 |
MOD_GlcNHglycan | 415 | 418 | PF01048 | 0.499 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.402 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.491 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.425 |
MOD_GSK3_1 | 362 | 369 | PF00069 | 0.689 |
MOD_GSK3_1 | 370 | 377 | PF00069 | 0.719 |
MOD_GSK3_1 | 399 | 406 | PF00069 | 0.491 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.416 |
MOD_N-GLC_1 | 369 | 374 | PF02516 | 0.463 |
MOD_N-GLC_2 | 116 | 118 | PF02516 | 0.418 |
MOD_NEK2_1 | 109 | 114 | PF00069 | 0.371 |
MOD_NEK2_1 | 117 | 122 | PF00069 | 0.373 |
MOD_NEK2_1 | 153 | 158 | PF00069 | 0.385 |
MOD_NEK2_1 | 224 | 229 | PF00069 | 0.339 |
MOD_NEK2_1 | 403 | 408 | PF00069 | 0.442 |
MOD_PIKK_1 | 118 | 124 | PF00454 | 0.401 |
MOD_PIKK_1 | 153 | 159 | PF00454 | 0.355 |
MOD_PIKK_1 | 57 | 63 | PF00454 | 0.420 |
MOD_PKA_1 | 19 | 25 | PF00069 | 0.398 |
MOD_PKA_2 | 124 | 130 | PF00069 | 0.328 |
MOD_PKA_2 | 19 | 25 | PF00069 | 0.408 |
MOD_PKA_2 | 207 | 213 | PF00069 | 0.498 |
MOD_PKA_2 | 33 | 39 | PF00069 | 0.469 |
MOD_PKA_2 | 366 | 372 | PF00069 | 0.714 |
MOD_Plk_1 | 137 | 143 | PF00069 | 0.372 |
MOD_Plk_4 | 109 | 115 | PF00069 | 0.392 |
MOD_Plk_4 | 127 | 133 | PF00069 | 0.341 |
MOD_Plk_4 | 49 | 55 | PF00069 | 0.260 |
MOD_Plk_4 | 65 | 71 | PF00069 | 0.445 |
MOD_ProDKin_1 | 44 | 50 | PF00069 | 0.365 |
MOD_SUMO_for_1 | 308 | 311 | PF00179 | 0.498 |
MOD_SUMO_rev_2 | 375 | 385 | PF00179 | 0.457 |
TRG_DiLeu_BaEn_2 | 390 | 396 | PF01217 | 0.482 |
TRG_ENDOCYTIC_2 | 272 | 275 | PF00928 | 0.345 |
TRG_ER_diArg_1 | 19 | 21 | PF00400 | 0.431 |
TRG_ER_diArg_1 | 249 | 251 | PF00400 | 0.400 |
TRG_ER_diArg_1 | 296 | 299 | PF00400 | 0.395 |
TRG_ER_diArg_1 | 419 | 421 | PF00400 | 0.486 |
TRG_ER_diArg_1 | 75 | 78 | PF00400 | 0.374 |
TRG_NES_CRM1_1 | 181 | 192 | PF08389 | 0.304 |
TRG_NES_CRM1_1 | 72 | 83 | PF08389 | 0.374 |
TRG_Pf-PMV_PEXEL_1 | 250 | 255 | PF00026 | 0.364 |
TRG_Pf-PMV_PEXEL_1 | 91 | 95 | PF00026 | 0.306 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4J9I9 | Bodo saltans | 33% | 88% |
A0A1X0NJM4 | Trypanosomatidae | 39% | 99% |
A0A1X0NW83 | Trypanosomatidae | 55% | 75% |
A0A1X0P8D8 | Trypanosomatidae | 21% | 75% |
A0A3Q8IA47 | Leishmania donovani | 85% | 74% |
A0A3Q8IK20 | Leishmania donovani | 25% | 78% |
A0A3R7NFN9 | Trypanosoma rangeli | 52% | 80% |
A0A3R7NHA6 | Trypanosoma rangeli | 25% | 76% |
A0A3S5IQY1 | Trypanosoma rangeli | 35% | 100% |
A0A3S7WW64 | Leishmania donovani | 93% | 79% |
A4H4H3 | Leishmania braziliensis | 34% | 90% |
A4HNL0 | Leishmania braziliensis | 25% | 79% |
A4HYX9 | Leishmania infantum | 85% | 74% |
A4HYY0 | Leishmania infantum | 93% | 79% |
A4ICY3 | Leishmania infantum | 25% | 78% |
C9ZT94 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
E8NHJ3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 98% | 100% |
E9AIJ1 | Leishmania braziliensis | 71% | 100% |
E9AKN3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 92% |
E9ASC2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 78% |
Q10238 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 22% | 75% |
Q4Q274 | Leishmania major | 24% | 78% |
Q4QCQ8 | Leishmania major | 91% | 99% |
Q4QCQ9 | Leishmania major | 73% | 98% |
Q9LDW3 | Arabidopsis thaliana | 24% | 78% |
V5B968 | Trypanosoma cruzi | 35% | 93% |