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: 36 |
NetGPI | no | yes: 0, no: 36 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HJI7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 232 | 234 | PF00675 | 0.374 |
CLV_NRD_NRD_1 | 341 | 343 | PF00675 | 0.402 |
CLV_NRD_NRD_1 | 372 | 374 | PF00675 | 0.391 |
CLV_NRD_NRD_1 | 482 | 484 | PF00675 | 0.412 |
CLV_PCSK_FUR_1 | 480 | 484 | PF00082 | 0.291 |
CLV_PCSK_KEX2_1 | 232 | 234 | PF00082 | 0.318 |
CLV_PCSK_KEX2_1 | 372 | 374 | PF00082 | 0.385 |
CLV_PCSK_KEX2_1 | 482 | 484 | PF00082 | 0.485 |
CLV_PCSK_KEX2_1 | 489 | 491 | PF00082 | 0.368 |
CLV_PCSK_PC1ET2_1 | 489 | 491 | PF00082 | 0.536 |
CLV_PCSK_SKI1_1 | 272 | 276 | PF00082 | 0.344 |
CLV_PCSK_SKI1_1 | 283 | 287 | PF00082 | 0.330 |
CLV_PCSK_SKI1_1 | 306 | 310 | PF00082 | 0.383 |
CLV_PCSK_SKI1_1 | 448 | 452 | PF00082 | 0.527 |
CLV_Separin_Metazoa | 188 | 192 | PF03568 | 0.219 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.553 |
DEG_SPOP_SBC_1 | 499 | 503 | PF00917 | 0.506 |
DOC_CYCLIN_yCln2_LP_2 | 54 | 57 | PF00134 | 0.320 |
DOC_MAPK_gen_1 | 171 | 181 | PF00069 | 0.326 |
DOC_MAPK_HePTP_8 | 265 | 277 | PF00069 | 0.263 |
DOC_MAPK_MEF2A_6 | 268 | 277 | PF00069 | 0.459 |
DOC_PP1_RVXF_1 | 321 | 327 | PF00149 | 0.315 |
DOC_PP2B_LxvP_1 | 54 | 57 | PF13499 | 0.319 |
DOC_PP2B_PxIxI_1 | 123 | 129 | PF00149 | 0.203 |
DOC_PP4_FxxP_1 | 121 | 124 | PF00568 | 0.198 |
DOC_PP4_FxxP_1 | 430 | 433 | PF00568 | 0.368 |
DOC_USP7_MATH_1 | 231 | 235 | PF00917 | 0.361 |
DOC_USP7_MATH_1 | 454 | 458 | PF00917 | 0.489 |
DOC_USP7_MATH_1 | 461 | 465 | PF00917 | 0.490 |
DOC_USP7_UBL2_3 | 268 | 272 | PF12436 | 0.478 |
DOC_USP7_UBL2_3 | 283 | 287 | PF12436 | 0.392 |
DOC_WW_Pin1_4 | 140 | 145 | PF00397 | 0.342 |
DOC_WW_Pin1_4 | 199 | 204 | PF00397 | 0.340 |
DOC_WW_Pin1_4 | 244 | 249 | PF00397 | 0.438 |
DOC_WW_Pin1_4 | 298 | 303 | PF00397 | 0.260 |
DOC_WW_Pin1_4 | 448 | 453 | PF00397 | 0.541 |
DOC_WW_Pin1_4 | 84 | 89 | PF00397 | 0.488 |
LIG_14-3-3_CanoR_1 | 194 | 200 | PF00244 | 0.382 |
LIG_14-3-3_CanoR_1 | 233 | 242 | PF00244 | 0.160 |
LIG_14-3-3_CanoR_1 | 441 | 447 | PF00244 | 0.484 |
LIG_14-3-3_CanoR_1 | 480 | 486 | PF00244 | 0.385 |
LIG_APCC_ABBA_1 | 275 | 280 | PF00400 | 0.382 |
LIG_BRCT_BRCA1_1 | 463 | 467 | PF00533 | 0.584 |
LIG_deltaCOP1_diTrp_1 | 94 | 101 | PF00928 | 0.477 |
LIG_EH1_1 | 75 | 83 | PF00400 | 0.279 |
LIG_eIF4E_1 | 85 | 91 | PF01652 | 0.437 |
LIG_FHA_1 | 131 | 137 | PF00498 | 0.359 |
LIG_FHA_1 | 157 | 163 | PF00498 | 0.265 |
LIG_FHA_1 | 17 | 23 | PF00498 | 0.571 |
LIG_FHA_1 | 387 | 393 | PF00498 | 0.394 |
LIG_FHA_1 | 424 | 430 | PF00498 | 0.333 |
LIG_FHA_2 | 245 | 251 | PF00498 | 0.194 |
LIG_LIR_Apic_2 | 118 | 124 | PF02991 | 0.260 |
LIG_LIR_Apic_2 | 428 | 433 | PF02991 | 0.398 |
LIG_LIR_Apic_2 | 84 | 88 | PF02991 | 0.227 |
LIG_LIR_Gen_1 | 205 | 215 | PF02991 | 0.407 |
LIG_LIR_Gen_1 | 424 | 433 | PF02991 | 0.413 |
LIG_LIR_Gen_1 | 49 | 59 | PF02991 | 0.325 |
LIG_LIR_Nem_3 | 276 | 281 | PF02991 | 0.348 |
LIG_LIR_Nem_3 | 284 | 289 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 364 | 369 | PF02991 | 0.260 |
LIG_LIR_Nem_3 | 39 | 44 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 424 | 430 | PF02991 | 0.365 |
LIG_LIR_Nem_3 | 49 | 54 | PF02991 | 0.297 |
LIG_Pex14_2 | 427 | 431 | PF04695 | 0.315 |
LIG_REV1ctd_RIR_1 | 283 | 289 | PF16727 | 0.483 |
LIG_SH2_CRK | 224 | 228 | PF00017 | 0.357 |
LIG_SH2_CRK | 366 | 370 | PF00017 | 0.281 |
LIG_SH2_CRK | 41 | 45 | PF00017 | 0.458 |
LIG_SH2_CRK | 85 | 89 | PF00017 | 0.332 |
LIG_SH2_PTP2 | 178 | 181 | PF00017 | 0.223 |
LIG_SH2_SRC | 344 | 347 | PF00017 | 0.387 |
LIG_SH2_STAP1 | 307 | 311 | PF00017 | 0.478 |
LIG_SH2_STAT5 | 178 | 181 | PF00017 | 0.318 |
LIG_SH2_STAT5 | 344 | 347 | PF00017 | 0.365 |
LIG_SH2_STAT5 | 51 | 54 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 85 | 88 | PF00017 | 0.343 |
LIG_SH3_2 | 368 | 373 | PF14604 | 0.513 |
LIG_SH3_3 | 296 | 302 | PF00018 | 0.343 |
LIG_SH3_3 | 365 | 371 | PF00018 | 0.472 |
LIG_SUMO_SIM_anti_2 | 182 | 188 | PF11976 | 0.157 |
LIG_SUMO_SIM_anti_2 | 471 | 478 | PF11976 | 0.385 |
LIG_TRAF2_1 | 63 | 66 | PF00917 | 0.729 |
LIG_TYR_ITIM | 176 | 181 | PF00017 | 0.364 |
LIG_UBA3_1 | 258 | 263 | PF00899 | 0.438 |
LIG_UBA3_1 | 277 | 283 | PF00899 | 0.206 |
LIG_UBA3_1 | 33 | 38 | PF00899 | 0.483 |
MOD_CDK_SPK_2 | 140 | 145 | PF00069 | 0.299 |
MOD_CK1_1 | 234 | 240 | PF00069 | 0.178 |
MOD_CK1_1 | 325 | 331 | PF00069 | 0.381 |
MOD_CK1_1 | 435 | 441 | PF00069 | 0.399 |
MOD_CK1_1 | 60 | 66 | PF00069 | 0.629 |
MOD_CK1_1 | 84 | 90 | PF00069 | 0.324 |
MOD_CK2_1 | 129 | 135 | PF00069 | 0.322 |
MOD_CK2_1 | 140 | 146 | PF00069 | 0.268 |
MOD_CK2_1 | 244 | 250 | PF00069 | 0.194 |
MOD_CK2_1 | 440 | 446 | PF00069 | 0.540 |
MOD_CK2_1 | 60 | 66 | PF00069 | 0.615 |
MOD_GlcNHglycan | 16 | 19 | PF01048 | 0.694 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.409 |
MOD_GlcNHglycan | 363 | 366 | PF01048 | 0.445 |
MOD_GlcNHglycan | 434 | 437 | PF01048 | 0.366 |
MOD_GlcNHglycan | 6 | 11 | PF01048 | 0.724 |
MOD_GlcNHglycan | 62 | 65 | PF01048 | 0.684 |
MOD_GlcNHglycan | 66 | 70 | PF01048 | 0.652 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.459 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.429 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.235 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.402 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.314 |
MOD_GSK3_1 | 240 | 247 | PF00069 | 0.419 |
MOD_GSK3_1 | 322 | 329 | PF00069 | 0.321 |
MOD_GSK3_1 | 386 | 393 | PF00069 | 0.457 |
MOD_GSK3_1 | 394 | 401 | PF00069 | 0.458 |
MOD_NEK2_1 | 394 | 399 | PF00069 | 0.391 |
MOD_NEK2_1 | 500 | 505 | PF00069 | 0.540 |
MOD_NEK2_1 | 81 | 86 | PF00069 | 0.506 |
MOD_NEK2_2 | 124 | 129 | PF00069 | 0.338 |
MOD_PIKK_1 | 156 | 162 | PF00454 | 0.320 |
MOD_PIKK_1 | 249 | 255 | PF00454 | 0.157 |
MOD_PIKK_1 | 394 | 400 | PF00454 | 0.377 |
MOD_PK_1 | 263 | 269 | PF00069 | 0.438 |
MOD_PKA_2 | 144 | 150 | PF00069 | 0.482 |
MOD_PKA_2 | 231 | 237 | PF00069 | 0.305 |
MOD_PKA_2 | 440 | 446 | PF00069 | 0.325 |
MOD_PKA_2 | 481 | 487 | PF00069 | 0.374 |
MOD_Plk_1 | 390 | 396 | PF00069 | 0.445 |
MOD_Plk_1 | 423 | 429 | PF00069 | 0.276 |
MOD_Plk_2-3 | 386 | 392 | PF00069 | 0.342 |
MOD_Plk_4 | 217 | 223 | PF00069 | 0.392 |
MOD_Plk_4 | 254 | 260 | PF00069 | 0.327 |
MOD_Plk_4 | 300 | 306 | PF00069 | 0.283 |
MOD_ProDKin_1 | 140 | 146 | PF00069 | 0.348 |
MOD_ProDKin_1 | 199 | 205 | PF00069 | 0.340 |
MOD_ProDKin_1 | 244 | 250 | PF00069 | 0.438 |
MOD_ProDKin_1 | 298 | 304 | PF00069 | 0.260 |
MOD_ProDKin_1 | 448 | 454 | PF00069 | 0.540 |
MOD_ProDKin_1 | 84 | 90 | PF00069 | 0.486 |
MOD_SUMO_rev_2 | 337 | 345 | PF00179 | 0.259 |
MOD_SUMO_rev_2 | 443 | 450 | PF00179 | 0.347 |
TRG_ENDOCYTIC_2 | 178 | 181 | PF00928 | 0.331 |
TRG_ENDOCYTIC_2 | 224 | 227 | PF00928 | 0.363 |
TRG_ENDOCYTIC_2 | 366 | 369 | PF00928 | 0.261 |
TRG_ENDOCYTIC_2 | 41 | 44 | PF00928 | 0.469 |
TRG_ENDOCYTIC_2 | 51 | 54 | PF00928 | 0.491 |
TRG_ER_diArg_1 | 371 | 373 | PF00400 | 0.357 |
TRG_ER_diArg_1 | 479 | 482 | PF00400 | 0.524 |
TRG_NES_CRM1_1 | 205 | 219 | PF08389 | 0.205 |
TRG_Pf-PMV_PEXEL_1 | 138 | 142 | PF00026 | 0.398 |
TRG_Pf-PMV_PEXEL_1 | 191 | 195 | PF00026 | 0.478 |
TRG_Pf-PMV_PEXEL_1 | 279 | 284 | PF00026 | 0.360 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6D4 | Leptomonas seymouri | 43% | 96% |
A0A0N0P991 | Leptomonas seymouri | 27% | 100% |
A0A0N0P992 | Leptomonas seymouri | 22% | 66% |
A0A0N0P9K9 | Leptomonas seymouri | 27% | 100% |
A0A0N1I2J8 | Leptomonas seymouri | 36% | 100% |
A0A0N1PCS4 | Leptomonas seymouri | 38% | 100% |
A0A0S4J7N0 | Bodo saltans | 25% | 100% |
A0A0S4KJL3 | Bodo saltans | 28% | 100% |
A0A1X0NUH5 | Trypanosomatidae | 23% | 87% |
A0A1X0NUJ5 | Trypanosomatidae | 26% | 100% |
A0A3Q8ICN0 | Leishmania donovani | 40% | 100% |
A0A3Q8IGQ2 | Leishmania donovani | 29% | 100% |
A0A3R7MUL5 | Trypanosoma rangeli | 24% | 92% |
A0A3S5H7R8 | Leishmania donovani | 24% | 66% |
A0A3S7X4P4 | Leishmania donovani | 67% | 97% |
A0A3S7X4R1 | Leishmania donovani | 41% | 100% |
A0A422P1E3 | Trypanosoma rangeli | 27% | 100% |
A4HJI8 | Leishmania braziliensis | 41% | 100% |
A4HJI9 | Leishmania braziliensis | 40% | 100% |
A4HKB3 | Leishmania braziliensis | 29% | 100% |
A4HKB4 | Leishmania braziliensis | 27% | 100% |
A4HKB5 | Leishmania braziliensis | 22% | 67% |
A4I6Y2 | Leishmania infantum | 67% | 97% |
A4I6Y3 | Leishmania infantum | 40% | 100% |
A4I6Y4 | Leishmania infantum | 38% | 100% |
A4I7U3 | Leishmania infantum | 29% | 100% |
A4I7U4 | Leishmania infantum | 24% | 66% |
E9B204 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 64% | 97% |
E9B205 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 41% | 100% |
E9B206 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 39% | 100% |
E9B2Q1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
O43304 | Homo sapiens | 20% | 73% |
O76054 | Homo sapiens | 22% | 100% |
P58875 | Bos taurus | 22% | 100% |
Q03606 | Caenorhabditis elegans | 23% | 70% |
Q0V9N0 | Xenopus tropicalis | 20% | 72% |
Q16KN5 | Aedes aegypti | 22% | 78% |
Q4Q5F6 | Leishmania major | 30% | 100% |
Q4Q655 | Leishmania major | 38% | 100% |
Q4Q656 | Leishmania major | 40% | 99% |
Q4Q657 | Leishmania major | 66% | 100% |
Q92503 | Homo sapiens | 21% | 71% |
Q99J08 | Mus musculus | 23% | 100% |
Q99MS0 | Rattus norvegicus | 23% | 100% |
Q9Z1J8 | Rattus norvegicus | 21% | 100% |
V5BL84 | Trypanosoma cruzi | 26% | 100% |
V5BQT0 | Trypanosoma cruzi | 27% | 91% |