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: 19 |
NetGPI | no | yes: 0, no: 20 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
GO:0005737 | cytoplasm | 2 | 2 |
Related structures:
AlphaFold database: E9ASC2
Term | Name | Level | Count |
---|---|---|---|
GO:0010468 | regulation of gene expression | 5 | 2 |
GO:0010608 | post-transcriptional regulation of gene expression | 6 | 2 |
GO:0019222 | regulation of metabolic process | 3 | 2 |
GO:0050789 | regulation of biological process | 2 | 2 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 21 |
GO:0003723 | RNA binding | 4 | 21 |
GO:0005488 | binding | 1 | 21 |
GO:0097159 | organic cyclic compound binding | 2 | 21 |
GO:1901363 | heterocyclic compound binding | 2 | 21 |
GO:0003729 | mRNA binding | 5 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 13 | 15 | PF00675 | 0.449 |
CLV_NRD_NRD_1 | 442 | 444 | PF00675 | 0.420 |
CLV_NRD_NRD_1 | 449 | 451 | PF00675 | 0.458 |
CLV_PCSK_KEX2_1 | 13 | 15 | PF00082 | 0.448 |
CLV_PCSK_KEX2_1 | 44 | 46 | PF00082 | 0.539 |
CLV_PCSK_KEX2_1 | 442 | 444 | PF00082 | 0.460 |
CLV_PCSK_KEX2_1 | 449 | 451 | PF00082 | 0.508 |
CLV_PCSK_PC1ET2_1 | 44 | 46 | PF00082 | 0.617 |
CLV_PCSK_PC7_1 | 445 | 451 | PF00082 | 0.584 |
CLV_PCSK_SKI1_1 | 104 | 108 | PF00082 | 0.398 |
CLV_PCSK_SKI1_1 | 113 | 117 | PF00082 | 0.463 |
CLV_PCSK_SKI1_1 | 140 | 144 | PF00082 | 0.582 |
CLV_PCSK_SKI1_1 | 224 | 228 | PF00082 | 0.445 |
CLV_PCSK_SKI1_1 | 343 | 347 | PF00082 | 0.360 |
CLV_PCSK_SKI1_1 | 364 | 368 | PF00082 | 0.310 |
CLV_PCSK_SKI1_1 | 374 | 378 | PF00082 | 0.311 |
CLV_PCSK_SKI1_1 | 389 | 393 | PF00082 | 0.387 |
CLV_PCSK_SKI1_1 | 449 | 453 | PF00082 | 0.605 |
CLV_PCSK_SKI1_1 | 69 | 73 | PF00082 | 0.505 |
CLV_PCSK_SKI1_1 | 75 | 79 | PF00082 | 0.465 |
DEG_APCC_DBOX_1 | 342 | 350 | PF00400 | 0.354 |
DEG_APCC_DBOX_1 | 74 | 82 | PF00400 | 0.492 |
DOC_CYCLIN_RxL_1 | 443 | 456 | PF00134 | 0.411 |
DOC_CYCLIN_yCln2_LP_2 | 472 | 475 | PF00134 | 0.554 |
DOC_PP2B_LxvP_1 | 381 | 384 | PF13499 | 0.351 |
DOC_PP2B_LxvP_1 | 472 | 475 | PF13499 | 0.716 |
DOC_PP4_FxxP_1 | 148 | 151 | PF00568 | 0.354 |
DOC_PP4_FxxP_1 | 510 | 513 | PF00568 | 0.712 |
DOC_USP7_MATH_1 | 122 | 126 | PF00917 | 0.377 |
DOC_USP7_MATH_1 | 182 | 186 | PF00917 | 0.411 |
DOC_USP7_MATH_1 | 422 | 426 | PF00917 | 0.526 |
DOC_USP7_MATH_1 | 490 | 494 | PF00917 | 0.649 |
DOC_USP7_UBL2_3 | 435 | 439 | PF12436 | 0.407 |
DOC_WW_Pin1_4 | 225 | 230 | PF00397 | 0.348 |
DOC_WW_Pin1_4 | 367 | 372 | PF00397 | 0.365 |
DOC_WW_Pin1_4 | 427 | 432 | PF00397 | 0.384 |
DOC_WW_Pin1_4 | 456 | 461 | PF00397 | 0.672 |
LIG_14-3-3_CanoR_1 | 183 | 191 | PF00244 | 0.354 |
LIG_Actin_WH2_2 | 284 | 299 | PF00022 | 0.335 |
LIG_Actin_WH2_2 | 354 | 369 | PF00022 | 0.249 |
LIG_Actin_WH2_2 | 413 | 430 | PF00022 | 0.398 |
LIG_Actin_WH2_2 | 61 | 77 | PF00022 | 0.385 |
LIG_AP2alpha_2 | 301 | 303 | PF02296 | 0.258 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.542 |
LIG_BIR_III_4 | 121 | 125 | PF00653 | 0.452 |
LIG_BIR_III_4 | 70 | 74 | PF00653 | 0.425 |
LIG_BRCT_BRCA1_1 | 227 | 231 | PF00533 | 0.462 |
LIG_BRCT_BRCA1_1 | 26 | 30 | PF00533 | 0.374 |
LIG_CaM_IQ_9 | 84 | 100 | PF13499 | 0.376 |
LIG_EVH1_2 | 535 | 539 | PF00568 | 0.546 |
LIG_FHA_1 | 137 | 143 | PF00498 | 0.449 |
LIG_FHA_1 | 200 | 206 | PF00498 | 0.459 |
LIG_FHA_1 | 283 | 289 | PF00498 | 0.329 |
LIG_FHA_1 | 336 | 342 | PF00498 | 0.403 |
LIG_FHA_2 | 141 | 147 | PF00498 | 0.539 |
LIG_FHA_2 | 150 | 156 | PF00498 | 0.451 |
LIG_FHA_2 | 192 | 198 | PF00498 | 0.372 |
LIG_FHA_2 | 319 | 325 | PF00498 | 0.506 |
LIG_FHA_2 | 404 | 410 | PF00498 | 0.325 |
LIG_FHA_2 | 44 | 50 | PF00498 | 0.548 |
LIG_LIR_Apic_2 | 146 | 151 | PF02991 | 0.359 |
LIG_LIR_Apic_2 | 509 | 513 | PF02991 | 0.556 |
LIG_LIR_Gen_1 | 199 | 209 | PF02991 | 0.438 |
LIG_LIR_Gen_1 | 228 | 238 | PF02991 | 0.501 |
LIG_LIR_Gen_1 | 249 | 260 | PF02991 | 0.346 |
LIG_LIR_Gen_1 | 499 | 508 | PF02991 | 0.667 |
LIG_LIR_Nem_3 | 196 | 201 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 228 | 234 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 249 | 255 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 301 | 306 | PF02991 | 0.324 |
LIG_LIR_Nem_3 | 392 | 398 | PF02991 | 0.284 |
LIG_LIR_Nem_3 | 499 | 503 | PF02991 | 0.638 |
LIG_MYND_1 | 471 | 475 | PF01753 | 0.730 |
LIG_PCNA_yPIPBox_3 | 214 | 226 | PF02747 | 0.329 |
LIG_PCNA_yPIPBox_3 | 504 | 515 | PF02747 | 0.528 |
LIG_Pex14_2 | 103 | 107 | PF04695 | 0.361 |
LIG_PTB_Apo_2 | 426 | 433 | PF02174 | 0.350 |
LIG_PTB_Phospho_1 | 426 | 432 | PF10480 | 0.355 |
LIG_SH2_CRK | 201 | 205 | PF00017 | 0.471 |
LIG_SH2_CRK | 476 | 480 | PF00017 | 0.566 |
LIG_SH2_GRB2like | 337 | 340 | PF00017 | 0.359 |
LIG_SH2_NCK_1 | 248 | 252 | PF00017 | 0.386 |
LIG_SH2_STAP1 | 201 | 205 | PF00017 | 0.471 |
LIG_SH2_STAP1 | 248 | 252 | PF00017 | 0.441 |
LIG_SH2_STAP1 | 337 | 341 | PF00017 | 0.387 |
LIG_SH2_STAT3 | 306 | 309 | PF00017 | 0.283 |
LIG_SH2_STAT3 | 337 | 340 | PF00017 | 0.452 |
LIG_SH2_STAT3 | 398 | 401 | PF00017 | 0.249 |
LIG_SH2_STAT5 | 201 | 204 | PF00017 | 0.433 |
LIG_SH2_STAT5 | 306 | 309 | PF00017 | 0.291 |
LIG_SH2_STAT5 | 337 | 340 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 398 | 401 | PF00017 | 0.252 |
LIG_SH2_STAT5 | 86 | 89 | PF00017 | 0.479 |
LIG_SH3_3 | 201 | 207 | PF00018 | 0.462 |
LIG_SH3_3 | 296 | 302 | PF00018 | 0.271 |
LIG_SH3_3 | 468 | 474 | PF00018 | 0.684 |
LIG_SH3_3 | 529 | 535 | PF00018 | 0.687 |
LIG_SUMO_SIM_anti_2 | 159 | 167 | PF11976 | 0.344 |
LIG_SUMO_SIM_par_1 | 159 | 167 | PF11976 | 0.344 |
LIG_TRAF2_1 | 194 | 197 | PF00917 | 0.294 |
LIG_TRAF2_1 | 2 | 5 | PF00917 | 0.454 |
LIG_TRAF2_1 | 467 | 470 | PF00917 | 0.716 |
LIG_UBA3_1 | 420 | 428 | PF00899 | 0.405 |
LIG_WRC_WIRS_1 | 507 | 512 | PF05994 | 0.561 |
MOD_CDK_SPK_2 | 225 | 230 | PF00069 | 0.229 |
MOD_CDK_SPxxK_3 | 367 | 374 | PF00069 | 0.383 |
MOD_CK1_1 | 237 | 243 | PF00069 | 0.613 |
MOD_CK1_1 | 405 | 411 | PF00069 | 0.332 |
MOD_CK1_1 | 438 | 444 | PF00069 | 0.531 |
MOD_CK2_1 | 149 | 155 | PF00069 | 0.519 |
MOD_CK2_1 | 191 | 197 | PF00069 | 0.299 |
MOD_CK2_1 | 200 | 206 | PF00069 | 0.355 |
MOD_CK2_1 | 318 | 324 | PF00069 | 0.497 |
MOD_CK2_1 | 43 | 49 | PF00069 | 0.538 |
MOD_GlcNHglycan | 136 | 139 | PF01048 | 0.496 |
MOD_GlcNHglycan | 238 | 242 | PF01048 | 0.517 |
MOD_GlcNHglycan | 482 | 485 | PF01048 | 0.763 |
MOD_GlcNHglycan | 51 | 54 | PF01048 | 0.630 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.483 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.436 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.447 |
MOD_GSK3_1 | 220 | 227 | PF00069 | 0.385 |
MOD_GSK3_1 | 283 | 290 | PF00069 | 0.354 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.474 |
MOD_GSK3_1 | 399 | 406 | PF00069 | 0.267 |
MOD_N-GLC_1 | 122 | 127 | PF02516 | 0.372 |
MOD_N-GLC_1 | 218 | 223 | PF02516 | 0.394 |
MOD_N-GLC_1 | 292 | 297 | PF02516 | 0.339 |
MOD_N-GLC_1 | 318 | 323 | PF02516 | 0.536 |
MOD_N-GLC_1 | 335 | 340 | PF02516 | 0.332 |
MOD_N-GLC_1 | 49 | 54 | PF02516 | 0.628 |
MOD_N-GLC_1 | 544 | 549 | PF02516 | 0.711 |
MOD_NEK2_1 | 134 | 139 | PF00069 | 0.422 |
MOD_NEK2_1 | 292 | 297 | PF00069 | 0.368 |
MOD_NEK2_1 | 366 | 371 | PF00069 | 0.425 |
MOD_NEK2_1 | 391 | 396 | PF00069 | 0.294 |
MOD_PIKK_1 | 182 | 188 | PF00454 | 0.383 |
MOD_PIKK_1 | 411 | 417 | PF00454 | 0.313 |
MOD_PIKK_1 | 459 | 465 | PF00454 | 0.682 |
MOD_PKA_2 | 182 | 188 | PF00069 | 0.383 |
MOD_Plk_1 | 218 | 224 | PF00069 | 0.459 |
MOD_Plk_1 | 24 | 30 | PF00069 | 0.404 |
MOD_Plk_1 | 292 | 298 | PF00069 | 0.481 |
MOD_Plk_1 | 490 | 496 | PF00069 | 0.734 |
MOD_Plk_4 | 200 | 206 | PF00069 | 0.408 |
MOD_Plk_4 | 283 | 289 | PF00069 | 0.301 |
MOD_Plk_4 | 422 | 428 | PF00069 | 0.417 |
MOD_Plk_4 | 506 | 512 | PF00069 | 0.605 |
MOD_ProDKin_1 | 225 | 231 | PF00069 | 0.344 |
MOD_ProDKin_1 | 367 | 373 | PF00069 | 0.365 |
MOD_ProDKin_1 | 427 | 433 | PF00069 | 0.378 |
MOD_ProDKin_1 | 456 | 462 | PF00069 | 0.679 |
MOD_SUMO_for_1 | 434 | 437 | PF00179 | 0.455 |
MOD_SUMO_rev_2 | 2 | 8 | PF00179 | 0.422 |
MOD_SUMO_rev_2 | 48 | 52 | PF00179 | 0.653 |
TRG_DiLeu_BaEn_1 | 160 | 165 | PF01217 | 0.317 |
TRG_DiLeu_BaLyEn_6 | 130 | 135 | PF01217 | 0.351 |
TRG_DiLeu_BaLyEn_6 | 447 | 452 | PF01217 | 0.411 |
TRG_DiLeu_BaLyEn_6 | 468 | 473 | PF01217 | 0.557 |
TRG_ENDOCYTIC_2 | 201 | 204 | PF00928 | 0.474 |
TRG_ENDOCYTIC_2 | 248 | 251 | PF00928 | 0.314 |
TRG_ER_diArg_1 | 442 | 445 | PF00400 | 0.454 |
TRG_ER_diArg_1 | 449 | 451 | PF00400 | 0.506 |
TRG_Pf-PMV_PEXEL_1 | 166 | 171 | PF00026 | 0.479 |
TRG_Pf-PMV_PEXEL_1 | 19 | 23 | PF00026 | 0.398 |
TRG_Pf-PMV_PEXEL_1 | 374 | 379 | PF00026 | 0.321 |
TRG_Pf-PMV_PEXEL_1 | 45 | 49 | PF00026 | 0.627 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P473 | Leptomonas seymouri | 80% | 99% |
A0A0S4IY52 | Bodo saltans | 28% | 78% |
A0A0S4JMB8 | Bodo saltans | 46% | 79% |
A0A1X0NHM5 | Trypanosomatidae | 29% | 98% |
A0A1X0P8D8 | Trypanosomatidae | 46% | 96% |
A0A3Q8IK20 | Leishmania donovani | 98% | 100% |
A0A3R7NHA6 | Trypanosoma rangeli | 45% | 97% |
A0A422N8V0 | Trypanosoma rangeli | 28% | 100% |
A4HNL0 | Leishmania braziliensis | 89% | 100% |
A4ICY3 | Leishmania infantum | 98% | 100% |
C9ZII7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 82% |
D0A2G7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 97% |
E8NHJ3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 100% |
E9AIJ1 | Leishmania braziliensis | 23% | 100% |
E9AUS6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
Q4Q274 | Leishmania major | 98% | 100% |
Q4QCQ8 | Leishmania major | 24% | 100% |
V5B1W9 | Trypanosoma cruzi | 29% | 99% |
V5BV90 | Trypanosoma cruzi | 46% | 91% |