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: 18 |
NetGPI | no | yes: 0, no: 18 |
Related structures:
AlphaFold database: A4HKB4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 436 | 440 | PF00656 | 0.689 |
CLV_NRD_NRD_1 | 53 | 55 | PF00675 | 0.343 |
CLV_NRD_NRD_1 | 63 | 65 | PF00675 | 0.276 |
CLV_PCSK_KEX2_1 | 234 | 236 | PF00082 | 0.327 |
CLV_PCSK_KEX2_1 | 300 | 302 | PF00082 | 0.326 |
CLV_PCSK_KEX2_1 | 52 | 54 | PF00082 | 0.370 |
CLV_PCSK_PC1ET2_1 | 234 | 236 | PF00082 | 0.405 |
CLV_PCSK_PC1ET2_1 | 300 | 302 | PF00082 | 0.162 |
CLV_PCSK_SKI1_1 | 205 | 209 | PF00082 | 0.369 |
CLV_PCSK_SKI1_1 | 241 | 245 | PF00082 | 0.301 |
CLV_PCSK_SKI1_1 | 285 | 289 | PF00082 | 0.239 |
CLV_PCSK_SKI1_1 | 325 | 329 | PF00082 | 0.367 |
CLV_PCSK_SKI1_1 | 441 | 445 | PF00082 | 0.528 |
CLV_PCSK_SKI1_1 | 53 | 57 | PF00082 | 0.241 |
CLV_PCSK_SKI1_1 | 59 | 63 | PF00082 | 0.215 |
CLV_Separin_Metazoa | 166 | 170 | PF03568 | 0.342 |
DEG_SCF_TRCP1_1 | 369 | 375 | PF00400 | 0.254 |
DOC_MAPK_gen_1 | 358 | 365 | PF00069 | 0.295 |
DOC_MAPK_gen_1 | 435 | 445 | PF00069 | 0.594 |
DOC_MAPK_MEF2A_6 | 179 | 186 | PF00069 | 0.266 |
DOC_MAPK_RevD_3 | 220 | 235 | PF00069 | 0.162 |
DOC_PP1_RVXF_1 | 478 | 485 | PF00149 | 0.410 |
DOC_PP1_RVXF_1 | 75 | 82 | PF00149 | 0.219 |
DOC_PP2B_LxvP_1 | 261 | 264 | PF13499 | 0.321 |
DOC_USP7_MATH_1 | 135 | 139 | PF00917 | 0.212 |
DOC_USP7_UBL2_3 | 230 | 234 | PF12436 | 0.456 |
DOC_WW_Pin1_4 | 172 | 177 | PF00397 | 0.222 |
DOC_WW_Pin1_4 | 342 | 347 | PF00397 | 0.709 |
DOC_WW_Pin1_4 | 390 | 395 | PF00397 | 0.351 |
LIG_14-3-3_CanoR_1 | 134 | 144 | PF00244 | 0.278 |
LIG_14-3-3_CanoR_1 | 403 | 411 | PF00244 | 0.636 |
LIG_Actin_WH2_2 | 192 | 210 | PF00022 | 0.162 |
LIG_BRCT_BRCA1_1 | 388 | 392 | PF00533 | 0.314 |
LIG_deltaCOP1_diTrp_1 | 88 | 97 | PF00928 | 0.376 |
LIG_FHA_1 | 163 | 169 | PF00498 | 0.406 |
LIG_FHA_1 | 217 | 223 | PF00498 | 0.248 |
LIG_FHA_1 | 335 | 341 | PF00498 | 0.636 |
LIG_FHA_1 | 349 | 355 | PF00498 | 0.436 |
LIG_FHA_1 | 440 | 446 | PF00498 | 0.529 |
LIG_FHA_1 | 463 | 469 | PF00498 | 0.255 |
LIG_FHA_2 | 125 | 131 | PF00498 | 0.384 |
LIG_FHA_2 | 431 | 437 | PF00498 | 0.525 |
LIG_FHA_2 | 8 | 14 | PF00498 | 0.414 |
LIG_LIR_Gen_1 | 138 | 146 | PF02991 | 0.244 |
LIG_LIR_Gen_1 | 375 | 383 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 130 | 136 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 138 | 143 | PF02991 | 0.302 |
LIG_LIR_Nem_3 | 194 | 200 | PF02991 | 0.300 |
LIG_LIR_Nem_3 | 228 | 232 | PF02991 | 0.302 |
LIG_LIR_Nem_3 | 265 | 270 | PF02991 | 0.333 |
LIG_LIR_Nem_3 | 375 | 379 | PF02991 | 0.351 |
LIG_LIR_Nem_3 | 405 | 411 | PF02991 | 0.693 |
LIG_LIR_Nem_3 | 88 | 93 | PF02991 | 0.279 |
LIG_LYPXL_yS_3 | 251 | 254 | PF13949 | 0.208 |
LIG_Pex14_2 | 374 | 378 | PF04695 | 0.458 |
LIG_Pex14_2 | 388 | 392 | PF04695 | 0.298 |
LIG_Pex14_2 | 93 | 97 | PF04695 | 0.331 |
LIG_REV1ctd_RIR_1 | 264 | 272 | PF16727 | 0.333 |
LIG_SH2_CRK | 133 | 137 | PF00017 | 0.400 |
LIG_SH2_CRK | 271 | 275 | PF00017 | 0.339 |
LIG_SH2_CRK | 326 | 330 | PF00017 | 0.433 |
LIG_SH2_CRK | 58 | 62 | PF00017 | 0.315 |
LIG_SH2_GRB2like | 140 | 143 | PF00017 | 0.266 |
LIG_SH2_GRB2like | 191 | 194 | PF00017 | 0.194 |
LIG_SH2_NCK_1 | 326 | 330 | PF00017 | 0.388 |
LIG_SH2_PTP2 | 140 | 143 | PF00017 | 0.337 |
LIG_SH2_SRC | 140 | 143 | PF00017 | 0.262 |
LIG_SH2_STAT5 | 140 | 143 | PF00017 | 0.333 |
LIG_SH2_STAT5 | 198 | 201 | PF00017 | 0.205 |
LIG_SH2_STAT5 | 42 | 45 | PF00017 | 0.489 |
LIG_SH3_3 | 181 | 187 | PF00018 | 0.321 |
LIG_SH3_3 | 408 | 414 | PF00018 | 0.563 |
LIG_SH3_3 | 420 | 426 | PF00018 | 0.683 |
LIG_SUMO_SIM_anti_2 | 180 | 186 | PF11976 | 0.353 |
LIG_SUMO_SIM_anti_2 | 442 | 448 | PF11976 | 0.283 |
LIG_SUMO_SIM_par_1 | 218 | 223 | PF11976 | 0.314 |
LIG_SUMO_SIM_par_1 | 442 | 448 | PF11976 | 0.283 |
LIG_SUMO_SIM_par_1 | 464 | 469 | PF11976 | 0.377 |
LIG_TRAF2_1 | 19 | 22 | PF00917 | 0.272 |
LIG_TRAF2_1 | 24 | 27 | PF00917 | 0.229 |
LIG_TYR_ITIM | 195 | 200 | PF00017 | 0.321 |
MOD_CDK_SPxxK_3 | 172 | 179 | PF00069 | 0.321 |
MOD_CK1_1 | 109 | 115 | PF00069 | 0.434 |
MOD_CK1_1 | 415 | 421 | PF00069 | 0.568 |
MOD_CK1_1 | 430 | 436 | PF00069 | 0.532 |
MOD_CK2_1 | 274 | 280 | PF00069 | 0.262 |
MOD_CK2_1 | 430 | 436 | PF00069 | 0.529 |
MOD_CK2_1 | 7 | 13 | PF00069 | 0.371 |
MOD_GlcNHglycan | 369 | 372 | PF01048 | 0.505 |
MOD_GlcNHglycan | 399 | 402 | PF01048 | 0.587 |
MOD_GlcNHglycan | 404 | 407 | PF01048 | 0.554 |
MOD_GlcNHglycan | 414 | 417 | PF01048 | 0.536 |
MOD_GSK3_1 | 330 | 337 | PF00069 | 0.597 |
MOD_GSK3_1 | 350 | 357 | PF00069 | 0.452 |
MOD_GSK3_1 | 386 | 393 | PF00069 | 0.264 |
MOD_GSK3_1 | 397 | 404 | PF00069 | 0.440 |
MOD_GSK3_1 | 412 | 419 | PF00069 | 0.528 |
MOD_GSK3_1 | 427 | 434 | PF00069 | 0.526 |
MOD_GSK3_1 | 454 | 461 | PF00069 | 0.346 |
MOD_GSK3_1 | 462 | 469 | PF00069 | 0.225 |
MOD_N-GLC_1 | 439 | 444 | PF02516 | 0.346 |
MOD_NEK2_1 | 136 | 141 | PF00069 | 0.236 |
MOD_NEK2_1 | 177 | 182 | PF00069 | 0.358 |
MOD_NEK2_1 | 207 | 212 | PF00069 | 0.414 |
MOD_NEK2_1 | 216 | 221 | PF00069 | 0.296 |
MOD_NEK2_1 | 312 | 317 | PF00069 | 0.279 |
MOD_NEK2_1 | 466 | 471 | PF00069 | 0.278 |
MOD_NEK2_2 | 57 | 62 | PF00069 | 0.207 |
MOD_PKA_2 | 402 | 408 | PF00069 | 0.704 |
MOD_PKA_2 | 430 | 436 | PF00069 | 0.482 |
MOD_Plk_1 | 439 | 445 | PF00069 | 0.336 |
MOD_Plk_1 | 75 | 81 | PF00069 | 0.322 |
MOD_Plk_2-3 | 124 | 130 | PF00069 | 0.456 |
MOD_Plk_2-3 | 372 | 378 | PF00069 | 0.273 |
MOD_Plk_4 | 106 | 112 | PF00069 | 0.314 |
MOD_Plk_4 | 136 | 142 | PF00069 | 0.292 |
MOD_Plk_4 | 177 | 183 | PF00069 | 0.349 |
MOD_Plk_4 | 262 | 268 | PF00069 | 0.296 |
MOD_Plk_4 | 454 | 460 | PF00069 | 0.354 |
MOD_ProDKin_1 | 172 | 178 | PF00069 | 0.222 |
MOD_ProDKin_1 | 342 | 348 | PF00069 | 0.701 |
MOD_ProDKin_1 | 390 | 396 | PF00069 | 0.365 |
MOD_SUMO_rev_2 | 103 | 107 | PF00179 | 0.383 |
MOD_SUMO_rev_2 | 304 | 309 | PF00179 | 0.284 |
TRG_ENDOCYTIC_2 | 133 | 136 | PF00928 | 0.286 |
TRG_ENDOCYTIC_2 | 140 | 143 | PF00928 | 0.297 |
TRG_ENDOCYTIC_2 | 197 | 200 | PF00928 | 0.327 |
TRG_ENDOCYTIC_2 | 251 | 254 | PF00928 | 0.227 |
TRG_ENDOCYTIC_2 | 271 | 274 | PF00928 | 0.343 |
TRG_ENDOCYTIC_2 | 58 | 61 | PF00928 | 0.283 |
TRG_ER_diArg_1 | 52 | 54 | PF00400 | 0.366 |
TRG_NLS_Bipartite_1 | 52 | 68 | PF00514 | 0.225 |
TRG_NLS_MonoExtN_4 | 62 | 68 | PF00514 | 0.232 |
TRG_Pf-PMV_PEXEL_1 | 205 | 209 | PF00026 | 0.335 |
TRG_Pf-PMV_PEXEL_1 | 241 | 245 | PF00026 | 0.336 |
TRG_Pf-PMV_PEXEL_1 | 301 | 305 | PF00026 | 0.216 |
TRG_PTS1 | 490 | 493 | PF00515 | 0.384 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6D4 | Leptomonas seymouri | 23% | 94% |
A0A0N0P991 | Leptomonas seymouri | 28% | 100% |
A0A0N0P9K9 | Leptomonas seymouri | 54% | 100% |
A0A0N1I2J8 | Leptomonas seymouri | 27% | 100% |
A0A0N1PCS4 | Leptomonas seymouri | 25% | 100% |
A0A0S4J7N0 | Bodo saltans | 29% | 100% |
A0A0S4KJL3 | Bodo saltans | 28% | 100% |
A0A1X0NUH5 | Trypanosomatidae | 30% | 85% |
A0A1X0NUJ5 | Trypanosomatidae | 39% | 100% |
A0A3Q8IGQ2 | Leishmania donovani | 24% | 100% |
A0A3R7MUL5 | Trypanosoma rangeli | 27% | 89% |
A0A3S7X4P4 | Leishmania donovani | 27% | 95% |
A0A3S7X4R1 | Leishmania donovani | 24% | 100% |
A0A422P1E3 | Trypanosoma rangeli | 36% | 100% |
A4HJI7 | Leishmania braziliensis | 27% | 100% |
A4HJI8 | Leishmania braziliensis | 24% | 100% |
A4HJI9 | Leishmania braziliensis | 26% | 100% |
A4HKB3 | Leishmania braziliensis | 23% | 100% |
A4I6Y2 | Leishmania infantum | 27% | 95% |
A4I6Y3 | Leishmania infantum | 24% | 100% |
A4I6Y4 | Leishmania infantum | 29% | 100% |
A4I7U3 | Leishmania infantum | 24% | 100% |
B5MCN3 | Homo sapiens | 24% | 100% |
E9B204 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 95% |
E9B205 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
E9B206 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9B2Q1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
O76054 | Homo sapiens | 24% | 100% |
P58875 | Bos taurus | 24% | 100% |
Q16KN5 | Aedes aegypti | 23% | 76% |
Q4Q5F6 | Leishmania major | 25% | 98% |
Q4Q656 | Leishmania major | 25% | 100% |
Q4Q657 | Leishmania major | 26% | 100% |
Q8R0F9 | Mus musculus | 22% | 100% |
Q99J08 | Mus musculus | 25% | 100% |
Q99MS0 | Rattus norvegicus | 25% | 100% |
Q9SCU1 | Arabidopsis thaliana | 23% | 100% |
Q9UDX3 | Homo sapiens | 22% | 100% |
Q9UDX4 | Homo sapiens | 26% | 100% |
Q9Z1J8 | Rattus norvegicus | 27% | 100% |
V5BL84 | Trypanosoma cruzi | 36% | 100% |
V5BQT0 | Trypanosoma cruzi | 28% | 89% |