Uncharacterized Protein, Uncharacterized
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: 17 |
NetGPI | no | yes: 0, no: 17 |
Related structures:
AlphaFold database: E9AHS5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 182 | 184 | PF00675 | 0.427 |
CLV_NRD_NRD_1 | 34 | 36 | PF00675 | 0.450 |
CLV_NRD_NRD_1 | 460 | 462 | PF00675 | 0.543 |
CLV_PCSK_FUR_1 | 34 | 38 | PF00082 | 0.433 |
CLV_PCSK_KEX2_1 | 184 | 186 | PF00082 | 0.430 |
CLV_PCSK_KEX2_1 | 34 | 36 | PF00082 | 0.465 |
CLV_PCSK_KEX2_1 | 462 | 464 | PF00082 | 0.588 |
CLV_PCSK_PC1ET2_1 | 184 | 186 | PF00082 | 0.513 |
CLV_PCSK_PC1ET2_1 | 36 | 38 | PF00082 | 0.469 |
CLV_PCSK_PC1ET2_1 | 462 | 464 | PF00082 | 0.588 |
CLV_PCSK_SKI1_1 | 129 | 133 | PF00082 | 0.381 |
CLV_PCSK_SKI1_1 | 252 | 256 | PF00082 | 0.336 |
CLV_PCSK_SKI1_1 | 338 | 342 | PF00082 | 0.396 |
CLV_PCSK_SKI1_1 | 345 | 349 | PF00082 | 0.393 |
CLV_PCSK_SKI1_1 | 36 | 40 | PF00082 | 0.447 |
CLV_PCSK_SKI1_1 | 438 | 442 | PF00082 | 0.478 |
DEG_APCC_DBOX_1 | 337 | 345 | PF00400 | 0.430 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.445 |
DOC_CYCLIN_RxL_1 | 247 | 259 | PF00134 | 0.356 |
DOC_CYCLIN_yCln2_LP_2 | 318 | 324 | PF00134 | 0.367 |
DOC_CYCLIN_yCln2_LP_2 | 44 | 50 | PF00134 | 0.406 |
DOC_MAPK_FxFP_2 | 74 | 77 | PF00069 | 0.405 |
DOC_MAPK_gen_1 | 183 | 192 | PF00069 | 0.422 |
DOC_PP1_RVXF_1 | 396 | 402 | PF00149 | 0.398 |
DOC_PP1_SILK_1 | 51 | 56 | PF00149 | 0.490 |
DOC_PP2B_LxvP_1 | 282 | 285 | PF13499 | 0.405 |
DOC_PP2B_LxvP_1 | 318 | 321 | PF13499 | 0.445 |
DOC_PP4_FxxP_1 | 223 | 226 | PF00568 | 0.296 |
DOC_PP4_FxxP_1 | 74 | 77 | PF00568 | 0.405 |
DOC_PP4_MxPP_1 | 1 | 4 | PF00568 | 0.442 |
DOC_USP7_MATH_1 | 456 | 460 | PF00917 | 0.504 |
DOC_USP7_UBL2_3 | 15 | 19 | PF12436 | 0.546 |
DOC_USP7_UBL2_3 | 398 | 402 | PF12436 | 0.367 |
DOC_WW_Pin1_4 | 167 | 172 | PF00397 | 0.513 |
DOC_WW_Pin1_4 | 202 | 207 | PF00397 | 0.444 |
DOC_WW_Pin1_4 | 236 | 241 | PF00397 | 0.436 |
DOC_WW_Pin1_4 | 79 | 84 | PF00397 | 0.469 |
DOC_WW_Pin1_4 | 97 | 102 | PF00397 | 0.414 |
LIG_14-3-3_CanoR_1 | 209 | 216 | PF00244 | 0.406 |
LIG_14-3-3_CanoR_1 | 35 | 41 | PF00244 | 0.436 |
LIG_14-3-3_CanoR_1 | 362 | 368 | PF00244 | 0.524 |
LIG_14-3-3_CanoR_1 | 436 | 441 | PF00244 | 0.530 |
LIG_14-3-3_CanoR_1 | 90 | 95 | PF00244 | 0.513 |
LIG_Actin_WH2_2 | 114 | 131 | PF00022 | 0.372 |
LIG_APCC_ABBA_1 | 25 | 30 | PF00400 | 0.408 |
LIG_BRCT_BRCA1_1 | 109 | 113 | PF00533 | 0.381 |
LIG_deltaCOP1_diTrp_1 | 29 | 40 | PF00928 | 0.417 |
LIG_EH_1 | 218 | 222 | PF12763 | 0.364 |
LIG_eIF4E_1 | 250 | 256 | PF01652 | 0.324 |
LIG_FHA_1 | 100 | 106 | PF00498 | 0.470 |
LIG_FHA_1 | 442 | 448 | PF00498 | 0.567 |
LIG_FHA_2 | 157 | 163 | PF00498 | 0.600 |
LIG_FHA_2 | 257 | 263 | PF00498 | 0.382 |
LIG_LIR_Apic_2 | 72 | 77 | PF02991 | 0.401 |
LIG_LIR_Gen_1 | 133 | 143 | PF02991 | 0.335 |
LIG_LIR_Gen_1 | 380 | 390 | PF02991 | 0.351 |
LIG_LIR_Gen_1 | 64 | 75 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 110 | 116 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 133 | 138 | PF02991 | 0.345 |
LIG_LIR_Nem_3 | 199 | 204 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 380 | 386 | PF02991 | 0.336 |
LIG_LIR_Nem_3 | 394 | 400 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 64 | 70 | PF02991 | 0.383 |
LIG_LYPXL_SIV_4 | 378 | 386 | PF13949 | 0.424 |
LIG_PCNA_PIPBox_1 | 106 | 115 | PF02747 | 0.488 |
LIG_PCNA_yPIPBox_3 | 421 | 429 | PF02747 | 0.534 |
LIG_Pex14_2 | 221 | 225 | PF04695 | 0.334 |
LIG_Pex14_2 | 397 | 401 | PF04695 | 0.499 |
LIG_SH2_CRK | 379 | 383 | PF00017 | 0.337 |
LIG_SH2_CRK | 67 | 71 | PF00017 | 0.365 |
LIG_SH2_NCK_1 | 150 | 154 | PF00017 | 0.445 |
LIG_SH2_NCK_1 | 379 | 383 | PF00017 | 0.315 |
LIG_SH2_NCK_1 | 67 | 71 | PF00017 | 0.364 |
LIG_SH2_SRC | 150 | 153 | PF00017 | 0.441 |
LIG_SH2_STAP1 | 23 | 27 | PF00017 | 0.422 |
LIG_SH2_STAP1 | 250 | 254 | PF00017 | 0.321 |
LIG_SH2_STAP1 | 379 | 383 | PF00017 | 0.337 |
LIG_SH2_STAT5 | 146 | 149 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 235 | 238 | PF00017 | 0.523 |
LIG_SH2_STAT5 | 379 | 382 | PF00017 | 0.338 |
LIG_SH2_STAT5 | 383 | 386 | PF00017 | 0.338 |
LIG_SH2_STAT5 | 67 | 70 | PF00017 | 0.347 |
LIG_SH3_3 | 384 | 390 | PF00018 | 0.474 |
LIG_SH3_3 | 82 | 88 | PF00018 | 0.441 |
LIG_TYR_ITIM | 377 | 382 | PF00017 | 0.338 |
LIG_TYR_ITSM | 63 | 70 | PF00017 | 0.356 |
LIG_UBA3_1 | 340 | 345 | PF00899 | 0.410 |
LIG_WRC_WIRS_1 | 325 | 330 | PF05994 | 0.453 |
MOD_CDK_SPxK_1 | 236 | 242 | PF00069 | 0.428 |
MOD_CDK_SPxxK_3 | 202 | 209 | PF00069 | 0.442 |
MOD_CDK_SPxxK_3 | 97 | 104 | PF00069 | 0.402 |
MOD_CK2_1 | 97 | 103 | PF00069 | 0.428 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.463 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.500 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.539 |
MOD_GSK3_1 | 441 | 448 | PF00069 | 0.622 |
MOD_NEK2_1 | 117 | 122 | PF00069 | 0.460 |
MOD_NEK2_1 | 165 | 170 | PF00069 | 0.526 |
MOD_NEK2_1 | 256 | 261 | PF00069 | 0.380 |
MOD_NEK2_1 | 312 | 317 | PF00069 | 0.381 |
MOD_NEK2_1 | 377 | 382 | PF00069 | 0.346 |
MOD_NEK2_1 | 441 | 446 | PF00069 | 0.488 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.544 |
MOD_NEK2_2 | 245 | 250 | PF00069 | 0.356 |
MOD_PIKK_1 | 156 | 162 | PF00454 | 0.562 |
MOD_PIKK_1 | 348 | 354 | PF00454 | 0.507 |
MOD_PK_1 | 49 | 55 | PF00069 | 0.420 |
MOD_PKA_1 | 36 | 42 | PF00069 | 0.454 |
MOD_PKA_2 | 208 | 214 | PF00069 | 0.410 |
MOD_PKA_2 | 267 | 273 | PF00069 | 0.622 |
MOD_PKA_2 | 36 | 42 | PF00069 | 0.423 |
MOD_PKA_2 | 361 | 367 | PF00069 | 0.540 |
MOD_PKA_2 | 48 | 54 | PF00069 | 0.407 |
MOD_Plk_1 | 17 | 23 | PF00069 | 0.549 |
MOD_Plk_1 | 196 | 202 | PF00069 | 0.443 |
MOD_Plk_1 | 29 | 35 | PF00069 | 0.439 |
MOD_Plk_1 | 330 | 336 | PF00069 | 0.488 |
MOD_Plk_1 | 65 | 71 | PF00069 | 0.363 |
MOD_Plk_2-3 | 186 | 192 | PF00069 | 0.452 |
MOD_Plk_4 | 196 | 202 | PF00069 | 0.486 |
MOD_Plk_4 | 250 | 256 | PF00069 | 0.343 |
MOD_Plk_4 | 377 | 383 | PF00069 | 0.338 |
MOD_Plk_4 | 436 | 442 | PF00069 | 0.525 |
MOD_Plk_4 | 49 | 55 | PF00069 | 0.405 |
MOD_Plk_4 | 65 | 71 | PF00069 | 0.358 |
MOD_Plk_4 | 90 | 96 | PF00069 | 0.511 |
MOD_ProDKin_1 | 167 | 173 | PF00069 | 0.505 |
MOD_ProDKin_1 | 202 | 208 | PF00069 | 0.438 |
MOD_ProDKin_1 | 236 | 242 | PF00069 | 0.431 |
MOD_ProDKin_1 | 79 | 85 | PF00069 | 0.469 |
MOD_ProDKin_1 | 97 | 103 | PF00069 | 0.416 |
MOD_SUMO_for_1 | 334 | 337 | PF00179 | 0.439 |
MOD_SUMO_rev_2 | 158 | 166 | PF00179 | 0.644 |
MOD_SUMO_rev_2 | 18 | 27 | PF00179 | 0.428 |
MOD_SUMO_rev_2 | 337 | 347 | PF00179 | 0.415 |
MOD_SUMO_rev_2 | 459 | 464 | PF00179 | 0.538 |
MOD_SUMO_rev_2 | 8 | 17 | PF00179 | 0.459 |
TRG_DiLeu_BaEn_1 | 420 | 425 | PF01217 | 0.449 |
TRG_DiLeu_BaEn_2 | 196 | 202 | PF01217 | 0.375 |
TRG_DiLeu_BaEn_2 | 341 | 347 | PF01217 | 0.414 |
TRG_DiLeu_BaEn_4 | 342 | 348 | PF01217 | 0.419 |
TRG_DiLeu_BaLyEn_6 | 112 | 117 | PF01217 | 0.349 |
TRG_ENDOCYTIC_2 | 150 | 153 | PF00928 | 0.461 |
TRG_ENDOCYTIC_2 | 28 | 31 | PF00928 | 0.412 |
TRG_ENDOCYTIC_2 | 379 | 382 | PF00928 | 0.337 |
TRG_ENDOCYTIC_2 | 383 | 386 | PF00928 | 0.337 |
TRG_ENDOCYTIC_2 | 389 | 392 | PF00928 | 0.374 |
TRG_ENDOCYTIC_2 | 67 | 70 | PF00928 | 0.366 |
TRG_ER_diArg_1 | 182 | 185 | PF00400 | 0.417 |
TRG_ER_diArg_1 | 33 | 35 | PF00400 | 0.437 |
TRG_ER_diArg_1 | 461 | 464 | PF00400 | 0.482 |
TRG_ER_diArg_1 | 54 | 57 | PF00400 | 0.411 |
TRG_NLS_MonoExtN_4 | 34 | 39 | PF00514 | 0.490 |
TRG_Pf-PMV_PEXEL_1 | 302 | 306 | PF00026 | 0.465 |
TRG_Pf-PMV_PEXEL_1 | 338 | 342 | PF00026 | 0.408 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PA50 | Leptomonas seymouri | 89% | 94% |
A0A0N1PBN6 | Leptomonas seymouri | 26% | 67% |
A0A0S4JJ07 | Bodo saltans | 70% | 100% |
A0A1X0NY35 | Trypanosomatidae | 25% | 67% |
A0A1X0P990 | Trypanosomatidae | 73% | 96% |
A0A3Q8IE69 | Leishmania donovani | 100% | 100% |
A0A3R7MZ34 | Trypanosoma rangeli | 28% | 69% |
A0A3R7N7Y7 | Trypanosoma rangeli | 71% | 97% |
A4HAI4 | Leishmania braziliensis | 93% | 100% |
C9ZN08 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 69% | 98% |
C9ZVC0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 68% |
E9AWF4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 69% |
E9B4P5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
Q4Q3D1 | Leishmania major | 97% | 100% |
Q4QB18 | Leishmania major | 27% | 68% |
V5BJD7 | Trypanosoma cruzi | 72% | 97% |