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: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: A0A3Q8IFJ3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 422 | 424 | PF00675 | 0.365 |
CLV_PCSK_KEX2_1 | 422 | 424 | PF00082 | 0.365 |
CLV_PCSK_SKI1_1 | 175 | 179 | PF00082 | 0.391 |
CLV_PCSK_SKI1_1 | 318 | 322 | PF00082 | 0.351 |
CLV_PCSK_SKI1_1 | 400 | 404 | PF00082 | 0.382 |
DEG_COP1_1 | 290 | 297 | PF00400 | 0.464 |
DEG_SCF_SKP2-CKS1_1 | 212 | 219 | PF00560 | 0.467 |
DOC_CYCLIN_RxL_1 | 420 | 429 | PF00134 | 0.397 |
DOC_MAPK_gen_1 | 347 | 354 | PF00069 | 0.438 |
DOC_MAPK_MEF2A_6 | 292 | 299 | PF00069 | 0.481 |
DOC_MAPK_MEF2A_6 | 347 | 354 | PF00069 | 0.473 |
DOC_MAPK_MEF2A_6 | 88 | 95 | PF00069 | 0.437 |
DOC_PP1_RVXF_1 | 421 | 428 | PF00149 | 0.489 |
DOC_USP7_MATH_1 | 146 | 150 | PF00917 | 0.545 |
DOC_USP7_MATH_1 | 181 | 185 | PF00917 | 0.578 |
DOC_USP7_MATH_1 | 202 | 206 | PF00917 | 0.400 |
DOC_USP7_UBL2_3 | 362 | 366 | PF12436 | 0.495 |
DOC_WW_Pin1_4 | 142 | 147 | PF00397 | 0.586 |
DOC_WW_Pin1_4 | 213 | 218 | PF00397 | 0.523 |
LIG_14-3-3_CanoR_1 | 175 | 181 | PF00244 | 0.403 |
LIG_14-3-3_CanoR_1 | 230 | 235 | PF00244 | 0.490 |
LIG_14-3-3_CanoR_1 | 391 | 399 | PF00244 | 0.493 |
LIG_14-3-3_CanoR_1 | 75 | 83 | PF00244 | 0.502 |
LIG_Actin_WH2_2 | 383 | 399 | PF00022 | 0.504 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.577 |
LIG_CaM_IQ_9 | 222 | 238 | PF13499 | 0.480 |
LIG_DLG_GKlike_1 | 230 | 238 | PF00625 | 0.400 |
LIG_EVH1_1 | 258 | 262 | PF00568 | 0.350 |
LIG_FAT_LD_1 | 48 | 56 | PF03623 | 0.536 |
LIG_FHA_1 | 219 | 225 | PF00498 | 0.435 |
LIG_FHA_1 | 270 | 276 | PF00498 | 0.455 |
LIG_FHA_1 | 319 | 325 | PF00498 | 0.340 |
LIG_FHA_1 | 336 | 342 | PF00498 | 0.515 |
LIG_FHA_1 | 346 | 352 | PF00498 | 0.327 |
LIG_FHA_1 | 382 | 388 | PF00498 | 0.506 |
LIG_FHA_1 | 401 | 407 | PF00498 | 0.528 |
LIG_FHA_1 | 64 | 70 | PF00498 | 0.524 |
LIG_FHA_1 | 85 | 91 | PF00498 | 0.441 |
LIG_FHA_2 | 427 | 433 | PF00498 | 0.396 |
LIG_FHA_2 | 79 | 85 | PF00498 | 0.525 |
LIG_GBD_Chelix_1 | 136 | 144 | PF00786 | 0.338 |
LIG_GBD_Chelix_1 | 203 | 211 | PF00786 | 0.395 |
LIG_LIR_Gen_1 | 239 | 248 | PF02991 | 0.404 |
LIG_LIR_Gen_1 | 296 | 303 | PF02991 | 0.476 |
LIG_LIR_Gen_1 | 359 | 368 | PF02991 | 0.543 |
LIG_LIR_Nem_3 | 183 | 189 | PF02991 | 0.584 |
LIG_LIR_Nem_3 | 239 | 244 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 296 | 302 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 359 | 363 | PF02991 | 0.461 |
LIG_NRBOX | 297 | 303 | PF00104 | 0.468 |
LIG_PDZ_Class_2 | 436 | 441 | PF00595 | 0.576 |
LIG_Pex14_1 | 431 | 435 | PF04695 | 0.369 |
LIG_Pex14_2 | 427 | 431 | PF04695 | 0.468 |
LIG_SH2_GRB2like | 368 | 371 | PF00017 | 0.622 |
LIG_SH2_NCK_1 | 368 | 372 | PF00017 | 0.624 |
LIG_SH2_STAP1 | 73 | 77 | PF00017 | 0.530 |
LIG_SH2_STAT3 | 223 | 226 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 11 | 14 | PF00017 | 0.559 |
LIG_SH2_STAT5 | 223 | 226 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 356 | 359 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 368 | 371 | PF00017 | 0.624 |
LIG_SH2_STAT5 | 420 | 423 | PF00017 | 0.397 |
LIG_SH2_STAT5 | 426 | 429 | PF00017 | 0.386 |
LIG_SH3_1 | 256 | 262 | PF00018 | 0.430 |
LIG_SH3_3 | 140 | 146 | PF00018 | 0.400 |
LIG_SH3_3 | 194 | 200 | PF00018 | 0.510 |
LIG_SH3_3 | 256 | 262 | PF00018 | 0.430 |
LIG_SH3_3 | 55 | 61 | PF00018 | 0.529 |
LIG_SUMO_SIM_anti_2 | 245 | 253 | PF11976 | 0.481 |
LIG_SUMO_SIM_anti_2 | 272 | 277 | PF11976 | 0.400 |
LIG_SUMO_SIM_anti_2 | 348 | 355 | PF11976 | 0.379 |
LIG_SUMO_SIM_par_1 | 110 | 116 | PF11976 | 0.488 |
LIG_SUMO_SIM_par_1 | 348 | 355 | PF11976 | 0.467 |
LIG_SUMO_SIM_par_1 | 91 | 97 | PF11976 | 0.440 |
LIG_TRAF2_1 | 61 | 64 | PF00917 | 0.583 |
LIG_TRAF2_1 | 77 | 80 | PF00917 | 0.315 |
LIG_WRC_WIRS_1 | 203 | 208 | PF05994 | 0.478 |
MOD_CDK_SPxK_1 | 213 | 219 | PF00069 | 0.467 |
MOD_CK1_1 | 169 | 175 | PF00069 | 0.428 |
MOD_CK1_1 | 210 | 216 | PF00069 | 0.363 |
MOD_CK1_1 | 325 | 331 | PF00069 | 0.546 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.484 |
MOD_CK1_1 | 78 | 84 | PF00069 | 0.530 |
MOD_CK2_1 | 181 | 187 | PF00069 | 0.405 |
MOD_CK2_1 | 339 | 345 | PF00069 | 0.554 |
MOD_CK2_1 | 426 | 432 | PF00069 | 0.388 |
MOD_CK2_1 | 78 | 84 | PF00069 | 0.521 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.483 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.401 |
MOD_GlcNHglycan | 304 | 308 | PF01048 | 0.545 |
MOD_GlcNHglycan | 324 | 327 | PF01048 | 0.368 |
MOD_GlcNHglycan | 341 | 344 | PF01048 | 0.537 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.405 |
MOD_GSK3_1 | 142 | 149 | PF00069 | 0.565 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.452 |
MOD_GSK3_1 | 303 | 310 | PF00069 | 0.472 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.328 |
MOD_GSK3_1 | 335 | 342 | PF00069 | 0.466 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.517 |
MOD_N-GLC_1 | 169 | 174 | PF02516 | 0.486 |
MOD_N-GLC_1 | 277 | 282 | PF02516 | 0.454 |
MOD_N-GLC_1 | 369 | 374 | PF02516 | 0.649 |
MOD_NEK2_1 | 113 | 118 | PF00069 | 0.362 |
MOD_NEK2_1 | 165 | 170 | PF00069 | 0.476 |
MOD_NEK2_1 | 224 | 229 | PF00069 | 0.465 |
MOD_NEK2_1 | 276 | 281 | PF00069 | 0.431 |
MOD_NEK2_1 | 302 | 307 | PF00069 | 0.497 |
MOD_NEK2_1 | 51 | 56 | PF00069 | 0.497 |
MOD_NEK2_1 | 94 | 99 | PF00069 | 0.420 |
MOD_PIKK_1 | 260 | 266 | PF00454 | 0.568 |
MOD_PIKK_1 | 307 | 313 | PF00454 | 0.377 |
MOD_PIKK_1 | 325 | 331 | PF00454 | 0.510 |
MOD_PIKK_1 | 75 | 81 | PF00454 | 0.422 |
MOD_PKA_2 | 229 | 235 | PF00069 | 0.485 |
MOD_PKA_2 | 335 | 341 | PF00069 | 0.571 |
MOD_PKA_2 | 5 | 11 | PF00069 | 0.675 |
MOD_Plk_1 | 277 | 283 | PF00069 | 0.459 |
MOD_Plk_4 | 139 | 145 | PF00069 | 0.584 |
MOD_Plk_4 | 202 | 208 | PF00069 | 0.468 |
MOD_Plk_4 | 219 | 225 | PF00069 | 0.471 |
MOD_ProDKin_1 | 142 | 148 | PF00069 | 0.588 |
MOD_ProDKin_1 | 213 | 219 | PF00069 | 0.524 |
MOD_SUMO_rev_2 | 394 | 399 | PF00179 | 0.494 |
MOD_SUMO_rev_2 | 57 | 66 | PF00179 | 0.554 |
MOD_SUMO_rev_2 | 76 | 83 | PF00179 | 0.308 |
TRG_DiLeu_BaEn_1 | 359 | 364 | PF01217 | 0.498 |
TRG_DiLeu_BaLyEn_6 | 89 | 94 | PF01217 | 0.464 |
TRG_ER_diArg_1 | 31 | 34 | PF00400 | 0.574 |
TRG_ER_diArg_1 | 347 | 350 | PF00400 | 0.502 |
TRG_ER_diArg_1 | 421 | 423 | PF00400 | 0.369 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6Y5 | Leptomonas seymouri | 51% | 96% |
A0A0S4IKI5 | Bodo saltans | 27% | 97% |
A0A1X0P918 | Trypanosomatidae | 35% | 95% |
A0A3R7K871 | Trypanosoma rangeli | 38% | 100% |
A4HHR2 | Leishmania braziliensis | 79% | 100% |
A4I4X2 | Leishmania infantum | 100% | 100% |
C9ZKY1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
E9AEC6 | Leishmania major | 94% | 100% |
E9ALG0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
V5BSL0 | Trypanosoma cruzi | 37% | 100% |