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: 1, no: 17 |
NetGPI | no | yes: 0, no: 18 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: A4HNL0
Term | Name | Level | Count |
---|---|---|---|
GO:0010468 | regulation of gene expression | 5 | 1 |
GO:0010608 | post-transcriptional regulation of gene expression | 6 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 19 |
GO:0003723 | RNA binding | 4 | 19 |
GO:0005488 | binding | 1 | 19 |
GO:0097159 | organic cyclic compound binding | 2 | 19 |
GO:1901363 | heterocyclic compound binding | 2 | 19 |
GO:0003729 | mRNA binding | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 13 | 15 | PF00675 | 0.401 |
CLV_NRD_NRD_1 | 441 | 443 | PF00675 | 0.418 |
CLV_NRD_NRD_1 | 448 | 450 | PF00675 | 0.470 |
CLV_PCSK_KEX2_1 | 13 | 15 | PF00082 | 0.407 |
CLV_PCSK_KEX2_1 | 44 | 46 | PF00082 | 0.548 |
CLV_PCSK_KEX2_1 | 441 | 443 | PF00082 | 0.390 |
CLV_PCSK_KEX2_1 | 448 | 450 | PF00082 | 0.445 |
CLV_PCSK_PC1ET2_1 | 44 | 46 | PF00082 | 0.625 |
CLV_PCSK_PC7_1 | 444 | 450 | PF00082 | 0.551 |
CLV_PCSK_SKI1_1 | 104 | 108 | PF00082 | 0.330 |
CLV_PCSK_SKI1_1 | 113 | 117 | PF00082 | 0.380 |
CLV_PCSK_SKI1_1 | 224 | 228 | PF00082 | 0.408 |
CLV_PCSK_SKI1_1 | 342 | 346 | PF00082 | 0.326 |
CLV_PCSK_SKI1_1 | 363 | 367 | PF00082 | 0.246 |
CLV_PCSK_SKI1_1 | 373 | 377 | PF00082 | 0.210 |
CLV_PCSK_SKI1_1 | 388 | 392 | PF00082 | 0.320 |
CLV_PCSK_SKI1_1 | 448 | 452 | PF00082 | 0.608 |
CLV_PCSK_SKI1_1 | 75 | 79 | PF00082 | 0.455 |
DEG_APCC_DBOX_1 | 341 | 349 | PF00400 | 0.320 |
DEG_APCC_DBOX_1 | 74 | 82 | PF00400 | 0.451 |
DOC_PP2B_LxvP_1 | 380 | 383 | PF13499 | 0.307 |
DOC_PP4_FxxP_1 | 508 | 511 | PF00568 | 0.676 |
DOC_USP7_MATH_1 | 122 | 126 | PF00917 | 0.351 |
DOC_USP7_MATH_1 | 182 | 186 | PF00917 | 0.398 |
DOC_USP7_MATH_1 | 239 | 243 | PF00917 | 0.504 |
DOC_USP7_MATH_1 | 421 | 425 | PF00917 | 0.462 |
DOC_USP7_UBL2_3 | 434 | 438 | PF12436 | 0.356 |
DOC_WW_Pin1_4 | 366 | 371 | PF00397 | 0.298 |
DOC_WW_Pin1_4 | 426 | 431 | PF00397 | 0.346 |
DOC_WW_Pin1_4 | 530 | 535 | PF00397 | 0.422 |
LIG_14-3-3_CanoR_1 | 136 | 144 | PF00244 | 0.473 |
LIG_14-3-3_CanoR_1 | 183 | 189 | PF00244 | 0.348 |
LIG_Actin_WH2_2 | 284 | 299 | PF00022 | 0.301 |
LIG_Actin_WH2_2 | 353 | 368 | PF00022 | 0.252 |
LIG_Actin_WH2_2 | 412 | 429 | PF00022 | 0.369 |
LIG_Actin_WH2_2 | 61 | 77 | PF00022 | 0.347 |
LIG_AP2alpha_2 | 301 | 303 | PF02296 | 0.252 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.537 |
LIG_BIR_III_4 | 121 | 125 | PF00653 | 0.418 |
LIG_BIR_III_4 | 70 | 74 | PF00653 | 0.385 |
LIG_BRCT_BRCA1_1 | 227 | 231 | PF00533 | 0.419 |
LIG_CaM_IQ_9 | 84 | 100 | PF13499 | 0.329 |
LIG_FHA_1 | 200 | 206 | PF00498 | 0.429 |
LIG_FHA_1 | 283 | 289 | PF00498 | 0.295 |
LIG_FHA_1 | 335 | 341 | PF00498 | 0.363 |
LIG_FHA_2 | 141 | 147 | PF00498 | 0.523 |
LIG_FHA_2 | 192 | 198 | PF00498 | 0.333 |
LIG_FHA_2 | 201 | 207 | PF00498 | 0.380 |
LIG_FHA_2 | 403 | 409 | PF00498 | 0.291 |
LIG_FHA_2 | 44 | 50 | PF00498 | 0.546 |
LIG_IRF3_LxIS_1 | 161 | 166 | PF10401 | 0.169 |
LIG_LIR_Apic_2 | 507 | 511 | PF02991 | 0.519 |
LIG_LIR_Gen_1 | 199 | 209 | PF02991 | 0.400 |
LIG_LIR_Gen_1 | 228 | 239 | PF02991 | 0.458 |
LIG_LIR_Gen_1 | 249 | 260 | PF02991 | 0.295 |
LIG_LIR_Nem_3 | 196 | 201 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 228 | 234 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 249 | 255 | PF02991 | 0.320 |
LIG_LIR_Nem_3 | 301 | 306 | PF02991 | 0.282 |
LIG_LIR_Nem_3 | 391 | 397 | PF02991 | 0.245 |
LIG_PCNA_yPIPBox_3 | 214 | 226 | PF02747 | 0.318 |
LIG_Pex14_2 | 103 | 107 | PF04695 | 0.329 |
LIG_PTAP_UEV_1 | 330 | 335 | PF05743 | 0.382 |
LIG_PTB_Apo_2 | 425 | 432 | PF02174 | 0.349 |
LIG_PTB_Phospho_1 | 425 | 431 | PF10480 | 0.354 |
LIG_Rb_LxCxE_1 | 23 | 41 | PF01857 | 0.289 |
LIG_SH2_CRK | 201 | 205 | PF00017 | 0.421 |
LIG_SH2_CRK | 474 | 478 | PF00017 | 0.694 |
LIG_SH2_GRB2like | 336 | 339 | PF00017 | 0.331 |
LIG_SH2_NCK_1 | 248 | 252 | PF00017 | 0.332 |
LIG_SH2_STAP1 | 201 | 205 | PF00017 | 0.421 |
LIG_SH2_STAP1 | 248 | 252 | PF00017 | 0.375 |
LIG_SH2_STAP1 | 336 | 340 | PF00017 | 0.359 |
LIG_SH2_STAT3 | 306 | 309 | PF00017 | 0.245 |
LIG_SH2_STAT3 | 336 | 339 | PF00017 | 0.424 |
LIG_SH2_STAT3 | 397 | 400 | PF00017 | 0.245 |
LIG_SH2_STAT5 | 201 | 204 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 306 | 309 | PF00017 | 0.276 |
LIG_SH2_STAT5 | 336 | 339 | PF00017 | 0.331 |
LIG_SH2_STAT5 | 397 | 400 | PF00017 | 0.248 |
LIG_SH2_STAT5 | 86 | 89 | PF00017 | 0.461 |
LIG_SH3_3 | 296 | 302 | PF00018 | 0.277 |
LIG_SH3_3 | 328 | 334 | PF00018 | 0.411 |
LIG_SH3_3 | 461 | 467 | PF00018 | 0.578 |
LIG_SH3_3 | 470 | 476 | PF00018 | 0.517 |
LIG_SUMO_SIM_anti_2 | 159 | 167 | PF11976 | 0.309 |
LIG_SUMO_SIM_par_1 | 159 | 167 | PF11976 | 0.317 |
LIG_SxIP_EBH_1 | 476 | 488 | PF03271 | 0.412 |
LIG_TRAF2_1 | 194 | 197 | PF00917 | 0.267 |
LIG_TRAF2_1 | 2 | 5 | PF00917 | 0.434 |
LIG_TYR_ITIM | 246 | 251 | PF00017 | 0.183 |
LIG_UBA3_1 | 419 | 427 | PF00899 | 0.368 |
LIG_WRC_WIRS_1 | 505 | 510 | PF05994 | 0.524 |
MOD_CDK_SPxxK_3 | 366 | 373 | PF00069 | 0.348 |
MOD_CK1_1 | 137 | 143 | PF00069 | 0.463 |
MOD_CK1_1 | 166 | 172 | PF00069 | 0.306 |
MOD_CK1_1 | 237 | 243 | PF00069 | 0.552 |
MOD_CK1_1 | 404 | 410 | PF00069 | 0.285 |
MOD_CK1_1 | 437 | 443 | PF00069 | 0.509 |
MOD_CK1_1 | 533 | 539 | PF00069 | 0.447 |
MOD_CK2_1 | 191 | 197 | PF00069 | 0.262 |
MOD_CK2_1 | 200 | 206 | PF00069 | 0.322 |
MOD_CK2_1 | 43 | 49 | PF00069 | 0.537 |
MOD_CK2_1 | 543 | 549 | PF00069 | 0.406 |
MOD_GlcNHglycan | 136 | 139 | PF01048 | 0.487 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.502 |
MOD_GlcNHglycan | 167 | 171 | PF01048 | 0.197 |
MOD_GlcNHglycan | 241 | 244 | PF01048 | 0.382 |
MOD_GlcNHglycan | 480 | 483 | PF01048 | 0.692 |
MOD_GlcNHglycan | 51 | 54 | PF01048 | 0.568 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.447 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.496 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.460 |
MOD_GSK3_1 | 220 | 227 | PF00069 | 0.316 |
MOD_GSK3_1 | 283 | 290 | PF00069 | 0.320 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.374 |
MOD_GSK3_1 | 398 | 405 | PF00069 | 0.243 |
MOD_GSK3_1 | 533 | 540 | PF00069 | 0.583 |
MOD_N-GLC_1 | 122 | 127 | PF02516 | 0.339 |
MOD_N-GLC_1 | 218 | 223 | PF02516 | 0.355 |
MOD_N-GLC_1 | 292 | 297 | PF02516 | 0.294 |
MOD_N-GLC_1 | 318 | 323 | PF02516 | 0.508 |
MOD_N-GLC_1 | 334 | 339 | PF02516 | 0.375 |
MOD_N-GLC_1 | 49 | 54 | PF02516 | 0.538 |
MOD_N-GLC_1 | 530 | 535 | PF02516 | 0.718 |
MOD_NEK2_1 | 134 | 139 | PF00069 | 0.466 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.392 |
MOD_NEK2_1 | 292 | 297 | PF00069 | 0.332 |
MOD_NEK2_1 | 365 | 370 | PF00069 | 0.393 |
MOD_NEK2_1 | 390 | 395 | PF00069 | 0.266 |
MOD_NEK2_1 | 537 | 542 | PF00069 | 0.604 |
MOD_PIKK_1 | 182 | 188 | PF00454 | 0.348 |
MOD_PIKK_1 | 318 | 324 | PF00454 | 0.396 |
MOD_PIKK_1 | 410 | 416 | PF00454 | 0.280 |
MOD_PIKK_1 | 458 | 464 | PF00454 | 0.613 |
MOD_PKA_2 | 182 | 188 | PF00069 | 0.348 |
MOD_Plk_1 | 145 | 151 | PF00069 | 0.275 |
MOD_Plk_1 | 218 | 224 | PF00069 | 0.421 |
MOD_Plk_1 | 237 | 243 | PF00069 | 0.284 |
MOD_Plk_1 | 24 | 30 | PF00069 | 0.394 |
MOD_Plk_1 | 292 | 298 | PF00069 | 0.444 |
MOD_Plk_1 | 326 | 332 | PF00069 | 0.554 |
MOD_Plk_1 | 488 | 494 | PF00069 | 0.683 |
MOD_Plk_4 | 200 | 206 | PF00069 | 0.353 |
MOD_Plk_4 | 283 | 289 | PF00069 | 0.256 |
MOD_Plk_4 | 421 | 427 | PF00069 | 0.372 |
MOD_Plk_4 | 504 | 510 | PF00069 | 0.571 |
MOD_Plk_4 | 537 | 543 | PF00069 | 0.429 |
MOD_ProDKin_1 | 366 | 372 | PF00069 | 0.298 |
MOD_ProDKin_1 | 426 | 432 | PF00069 | 0.340 |
MOD_ProDKin_1 | 530 | 536 | PF00069 | 0.422 |
MOD_SUMO_for_1 | 433 | 436 | PF00179 | 0.371 |
MOD_SUMO_rev_2 | 2 | 8 | PF00179 | 0.385 |
MOD_SUMO_rev_2 | 48 | 52 | PF00179 | 0.631 |
TRG_DiLeu_BaEn_1 | 160 | 165 | PF01217 | 0.282 |
TRG_DiLeu_BaLyEn_6 | 130 | 135 | PF01217 | 0.319 |
TRG_ENDOCYTIC_2 | 201 | 204 | PF00928 | 0.425 |
TRG_ENDOCYTIC_2 | 248 | 251 | PF00928 | 0.300 |
TRG_ER_diArg_1 | 441 | 444 | PF00400 | 0.420 |
TRG_ER_diArg_1 | 448 | 450 | PF00400 | 0.476 |
TRG_NES_CRM1_1 | 62 | 76 | PF08389 | 0.215 |
TRG_Pf-PMV_PEXEL_1 | 19 | 23 | PF00026 | 0.380 |
TRG_Pf-PMV_PEXEL_1 | 373 | 378 | PF00026 | 0.245 |
TRG_Pf-PMV_PEXEL_1 | 45 | 49 | PF00026 | 0.624 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P473 | Leptomonas seymouri | 78% | 99% |
A0A0N1PC50 | Leptomonas seymouri | 29% | 95% |
A0A0S4IY52 | Bodo saltans | 29% | 78% |
A0A0S4JMB8 | Bodo saltans | 46% | 79% |
A0A1X0NHM5 | Trypanosomatidae | 29% | 98% |
A0A1X0P8D8 | Trypanosomatidae | 46% | 96% |
A0A3Q8IK20 | Leishmania donovani | 90% | 100% |
A0A3R7NHA6 | Trypanosoma rangeli | 44% | 96% |
A0A422N8V0 | Trypanosoma rangeli | 29% | 100% |
A4HC32 | Leishmania braziliensis | 31% | 96% |
A4ICY3 | Leishmania infantum | 90% | 100% |
D0A0Z9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 94% |
D0A2G7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 96% |
E9AIJ1 | Leishmania braziliensis | 24% | 100% |
E9ASC2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
E9AUS6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
Q4Q274 | Leishmania major | 89% | 100% |
Q4QCQ8 | Leishmania major | 25% | 100% |
Q9LDW3 | Arabidopsis thaliana | 26% | 99% |
Q9LP21 | Arabidopsis thaliana | 28% | 100% |
V5B1W9 | Trypanosoma cruzi | 29% | 98% |
V5BV90 | Trypanosoma cruzi | 45% | 90% |