Carries a conserved CRAL-TRIO domain. Its didtant homologs are cytoplasmic and are involved in antiviral response.
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: 29 |
NetGPI | no | yes: 0, no: 29 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4Q5F6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 433 | 437 | PF00656 | 0.507 |
CLV_NRD_NRD_1 | 149 | 151 | PF00675 | 0.388 |
CLV_NRD_NRD_1 | 168 | 170 | PF00675 | 0.388 |
CLV_NRD_NRD_1 | 221 | 223 | PF00675 | 0.258 |
CLV_PCSK_KEX2_1 | 149 | 151 | PF00082 | 0.388 |
CLV_PCSK_KEX2_1 | 221 | 223 | PF00082 | 0.266 |
CLV_PCSK_KEX2_1 | 417 | 419 | PF00082 | 0.552 |
CLV_PCSK_PC1ET2_1 | 417 | 419 | PF00082 | 0.587 |
CLV_PCSK_SKI1_1 | 165 | 169 | PF00082 | 0.295 |
CLV_PCSK_SKI1_1 | 241 | 245 | PF00082 | 0.326 |
CLV_PCSK_SKI1_1 | 279 | 283 | PF00082 | 0.381 |
CLV_PCSK_SKI1_1 | 35 | 39 | PF00082 | 0.447 |
CLV_PCSK_SKI1_1 | 77 | 81 | PF00082 | 0.418 |
DEG_APCC_DBOX_1 | 148 | 156 | PF00400 | 0.420 |
DEG_APCC_DBOX_1 | 164 | 172 | PF00400 | 0.239 |
DOC_CKS1_1 | 53 | 58 | PF01111 | 0.415 |
DOC_CYCLIN_yCln2_LP_2 | 11 | 17 | PF00134 | 0.325 |
DOC_MAPK_gen_1 | 169 | 177 | PF00069 | 0.388 |
DOC_MAPK_gen_1 | 221 | 229 | PF00069 | 0.281 |
DOC_MAPK_gen_1 | 404 | 412 | PF00069 | 0.559 |
DOC_MAPK_gen_1 | 80 | 89 | PF00069 | 0.271 |
DOC_MAPK_MEF2A_6 | 169 | 177 | PF00069 | 0.233 |
DOC_MAPK_MEF2A_6 | 404 | 412 | PF00069 | 0.559 |
DOC_PP1_RVXF_1 | 290 | 296 | PF00149 | 0.292 |
DOC_PP4_FxxP_1 | 295 | 298 | PF00568 | 0.345 |
DOC_SPAK_OSR1_1 | 387 | 391 | PF12202 | 0.443 |
DOC_USP7_MATH_1 | 304 | 308 | PF00917 | 0.373 |
DOC_WW_Pin1_4 | 124 | 129 | PF00397 | 0.550 |
DOC_WW_Pin1_4 | 134 | 139 | PF00397 | 0.399 |
DOC_WW_Pin1_4 | 294 | 299 | PF00397 | 0.422 |
DOC_WW_Pin1_4 | 472 | 477 | PF00397 | 0.482 |
DOC_WW_Pin1_4 | 52 | 57 | PF00397 | 0.469 |
LIG_14-3-3_CanoR_1 | 131 | 137 | PF00244 | 0.437 |
LIG_14-3-3_CanoR_1 | 22 | 30 | PF00244 | 0.465 |
LIG_14-3-3_CanoR_1 | 222 | 228 | PF00244 | 0.367 |
LIG_14-3-3_CanoR_1 | 279 | 289 | PF00244 | 0.378 |
LIG_14-3-3_CanoR_1 | 387 | 391 | PF00244 | 0.383 |
LIG_14-3-3_CanoR_1 | 418 | 426 | PF00244 | 0.503 |
LIG_14-3-3_CanoR_1 | 465 | 473 | PF00244 | 0.466 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.491 |
LIG_BRCT_BRCA1_1 | 388 | 392 | PF00533 | 0.406 |
LIG_deltaCOP1_diTrp_1 | 372 | 378 | PF00928 | 0.316 |
LIG_deltaCOP1_diTrp_1 | 97 | 104 | PF00928 | 0.426 |
LIG_FHA_1 | 1 | 7 | PF00498 | 0.519 |
LIG_FHA_1 | 135 | 141 | PF00498 | 0.362 |
LIG_FHA_1 | 162 | 168 | PF00498 | 0.282 |
LIG_FHA_1 | 22 | 28 | PF00498 | 0.421 |
LIG_FHA_1 | 224 | 230 | PF00498 | 0.308 |
LIG_FHA_1 | 300 | 306 | PF00498 | 0.382 |
LIG_FHA_1 | 338 | 344 | PF00498 | 0.627 |
LIG_FHA_1 | 349 | 355 | PF00498 | 0.418 |
LIG_FHA_1 | 48 | 54 | PF00498 | 0.501 |
LIG_FHA_2 | 177 | 183 | PF00498 | 0.299 |
LIG_FHA_2 | 337 | 343 | PF00498 | 0.698 |
LIG_FHA_2 | 417 | 423 | PF00498 | 0.582 |
LIG_GBD_Chelix_1 | 154 | 162 | PF00786 | 0.203 |
LIG_LIR_Apic_2 | 294 | 298 | PF02991 | 0.360 |
LIG_LIR_Apic_2 | 436 | 441 | PF02991 | 0.500 |
LIG_LIR_Apic_2 | 97 | 101 | PF02991 | 0.287 |
LIG_LIR_Gen_1 | 182 | 193 | PF02991 | 0.388 |
LIG_LIR_Gen_1 | 385 | 394 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 182 | 188 | PF02991 | 0.290 |
LIG_LIR_Nem_3 | 235 | 239 | PF02991 | 0.354 |
LIG_LIR_Nem_3 | 36 | 41 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 385 | 391 | PF02991 | 0.379 |
LIG_Pex14_2 | 184 | 188 | PF04695 | 0.233 |
LIG_Pex14_2 | 38 | 42 | PF04695 | 0.272 |
LIG_Pex14_2 | 388 | 392 | PF04695 | 0.340 |
LIG_Pex14_2 | 88 | 92 | PF04695 | 0.367 |
LIG_REV1ctd_RIR_1 | 86 | 95 | PF16727 | 0.260 |
LIG_SH2_CRK | 278 | 282 | PF00017 | 0.344 |
LIG_SH2_CRK | 65 | 69 | PF00017 | 0.319 |
LIG_SH2_NCK_1 | 109 | 113 | PF00017 | 0.297 |
LIG_SH2_SRC | 202 | 205 | PF00017 | 0.258 |
LIG_SH2_STAP1 | 65 | 69 | PF00017 | 0.412 |
LIG_SH2_STAT3 | 393 | 396 | PF00017 | 0.458 |
LIG_SH3_1 | 170 | 176 | PF00018 | 0.213 |
LIG_SH3_3 | 170 | 176 | PF00018 | 0.442 |
LIG_SH3_3 | 265 | 271 | PF00018 | 0.377 |
LIG_SUMO_SIM_par_1 | 225 | 230 | PF11976 | 0.359 |
LIG_TRAF2_1 | 180 | 183 | PF00917 | 0.213 |
LIG_TRAF2_1 | 339 | 342 | PF00917 | 0.609 |
LIG_TRFH_1 | 4 | 8 | PF08558 | 0.309 |
LIG_TYR_ITIM | 154 | 159 | PF00017 | 0.405 |
LIG_TYR_ITIM | 234 | 239 | PF00017 | 0.386 |
LIG_TYR_ITIM | 63 | 68 | PF00017 | 0.225 |
LIG_WRC_WIRS_1 | 1 | 6 | PF05994 | 0.352 |
MOD_CDK_SPxxK_3 | 124 | 131 | PF00069 | 0.334 |
MOD_CK1_1 | 102 | 108 | PF00069 | 0.459 |
MOD_CK1_1 | 455 | 461 | PF00069 | 0.476 |
MOD_CK2_1 | 176 | 182 | PF00069 | 0.353 |
MOD_CK2_1 | 336 | 342 | PF00069 | 0.526 |
MOD_CK2_1 | 416 | 422 | PF00069 | 0.563 |
MOD_CK2_1 | 472 | 478 | PF00069 | 0.513 |
MOD_Cter_Amidation | 358 | 361 | PF01082 | 0.463 |
MOD_GlcNHglycan | 101 | 104 | PF01048 | 0.457 |
MOD_GlcNHglycan | 282 | 285 | PF01048 | 0.361 |
MOD_GlcNHglycan | 35 | 38 | PF01048 | 0.323 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.352 |
MOD_GSK3_1 | 348 | 355 | PF00069 | 0.455 |
MOD_GSK3_1 | 377 | 384 | PF00069 | 0.397 |
MOD_GSK3_1 | 412 | 419 | PF00069 | 0.537 |
MOD_N-GLC_1 | 299 | 304 | PF02516 | 0.372 |
MOD_N-GLC_1 | 352 | 357 | PF02516 | 0.306 |
MOD_N-GLC_2 | 223 | 225 | PF02516 | 0.388 |
MOD_NEK2_1 | 122 | 127 | PF00069 | 0.440 |
MOD_NEK2_1 | 244 | 249 | PF00069 | 0.339 |
MOD_NEK2_1 | 280 | 285 | PF00069 | 0.318 |
MOD_NEK2_1 | 378 | 383 | PF00069 | 0.337 |
MOD_PIKK_1 | 21 | 27 | PF00454 | 0.437 |
MOD_PKA_1 | 417 | 423 | PF00069 | 0.548 |
MOD_PKA_2 | 21 | 27 | PF00069 | 0.471 |
MOD_PKA_2 | 386 | 392 | PF00069 | 0.423 |
MOD_PKA_2 | 417 | 423 | PF00069 | 0.514 |
MOD_PKA_2 | 47 | 53 | PF00069 | 0.410 |
MOD_PKB_1 | 409 | 417 | PF00069 | 0.338 |
MOD_Plk_1 | 352 | 358 | PF00069 | 0.465 |
MOD_Plk_1 | 412 | 418 | PF00069 | 0.388 |
MOD_Plk_4 | 223 | 229 | PF00069 | 0.366 |
MOD_Plk_4 | 304 | 310 | PF00069 | 0.384 |
MOD_Plk_4 | 434 | 440 | PF00069 | 0.412 |
MOD_Plk_4 | 452 | 458 | PF00069 | 0.342 |
MOD_ProDKin_1 | 124 | 130 | PF00069 | 0.546 |
MOD_ProDKin_1 | 134 | 140 | PF00069 | 0.396 |
MOD_ProDKin_1 | 294 | 300 | PF00069 | 0.422 |
MOD_ProDKin_1 | 472 | 478 | PF00069 | 0.489 |
MOD_ProDKin_1 | 52 | 58 | PF00069 | 0.458 |
MOD_SUMO_for_1 | 426 | 429 | PF00179 | 0.420 |
TRG_DiLeu_BaLyEn_6 | 276 | 281 | PF01217 | 0.417 |
TRG_DiLeu_BaLyEn_6 | 36 | 41 | PF01217 | 0.503 |
TRG_DiLeu_BaLyEn_6 | 58 | 63 | PF01217 | 0.314 |
TRG_ENDOCYTIC_2 | 130 | 133 | PF00928 | 0.415 |
TRG_ENDOCYTIC_2 | 156 | 159 | PF00928 | 0.374 |
TRG_ENDOCYTIC_2 | 236 | 239 | PF00928 | 0.355 |
TRG_ENDOCYTIC_2 | 278 | 281 | PF00928 | 0.360 |
TRG_ENDOCYTIC_2 | 65 | 68 | PF00928 | 0.324 |
TRG_ER_diArg_1 | 220 | 222 | PF00400 | 0.254 |
TRG_ER_diArg_1 | 408 | 411 | PF00400 | 0.548 |
TRG_NLS_MonoExtC_3 | 168 | 173 | PF00514 | 0.233 |
TRG_Pf-PMV_PEXEL_1 | 241 | 245 | PF00026 | 0.392 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6D4 | Leptomonas seymouri | 27% | 91% |
A0A0N0P991 | Leptomonas seymouri | 66% | 100% |
A0A0N0P9K9 | Leptomonas seymouri | 29% | 100% |
A0A0N1I2J8 | Leptomonas seymouri | 32% | 100% |
A0A0N1PCS4 | Leptomonas seymouri | 31% | 100% |
A0A0S4J7N0 | Bodo saltans | 25% | 100% |
A0A0S4KJL3 | Bodo saltans | 33% | 100% |
A0A1X0NUH5 | Trypanosomatidae | 25% | 82% |
A0A1X0NUJ5 | Trypanosomatidae | 30% | 100% |
A0A3Q8ICN0 | Leishmania donovani | 30% | 96% |
A0A3Q8IGQ2 | Leishmania donovani | 94% | 100% |
A0A3R7MUL5 | Trypanosoma rangeli | 24% | 87% |
A0A3S7X4P4 | Leishmania donovani | 28% | 92% |
A0A3S7X4R1 | Leishmania donovani | 33% | 97% |
A0A422P1E3 | Trypanosoma rangeli | 28% | 100% |
A4HJI7 | Leishmania braziliensis | 30% | 94% |
A4HJI8 | Leishmania braziliensis | 32% | 100% |
A4HJI9 | Leishmania braziliensis | 30% | 100% |
A4HKB3 | Leishmania braziliensis | 82% | 100% |
A4HKB4 | Leishmania braziliensis | 25% | 97% |
A4I6Y2 | Leishmania infantum | 28% | 92% |
A4I6Y3 | Leishmania infantum | 33% | 97% |
A4I6Y4 | Leishmania infantum | 31% | 100% |
A4I7U3 | Leishmania infantum | 94% | 100% |
A8Y5H7 | Mus musculus | 23% | 67% |
E9B204 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 92% |
E9B205 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 97% |
E9B206 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E9B2Q1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
O43304 | Homo sapiens | 26% | 69% |
Q0V9N0 | Xenopus tropicalis | 25% | 68% |
Q16KN5 | Aedes aegypti | 22% | 74% |
Q29JQ0 | Drosophila pseudoobscura pseudoobscura | 22% | 71% |
Q4Q655 | Leishmania major | 30% | 99% |
Q4Q656 | Leishmania major | 33% | 97% |
Q4Q657 | Leishmania major | 27% | 92% |
Q7PWB1 | Anopheles gambiae | 22% | 70% |
Q92503 | Homo sapiens | 23% | 67% |
Q99J08 | Mus musculus | 22% | 100% |
Q99MS0 | Rattus norvegicus | 22% | 100% |
Q9VMD6 | Drosophila melanogaster | 23% | 73% |
V5BL84 | Trypanosoma cruzi | 26% | 100% |
V5BQT0 | Trypanosoma cruzi | 25% | 86% |