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: E9AEC6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 262 | 266 | PF00656 | 0.406 |
CLV_NRD_NRD_1 | 422 | 424 | PF00675 | 0.380 |
CLV_PCSK_KEX2_1 | 422 | 424 | PF00082 | 0.380 |
CLV_PCSK_SKI1_1 | 175 | 179 | PF00082 | 0.407 |
CLV_PCSK_SKI1_1 | 213 | 217 | PF00082 | 0.353 |
CLV_PCSK_SKI1_1 | 318 | 322 | PF00082 | 0.362 |
CLV_PCSK_SKI1_1 | 400 | 404 | PF00082 | 0.401 |
DEG_COP1_1 | 290 | 297 | PF00400 | 0.493 |
DEG_SCF_SKP2-CKS1_1 | 212 | 219 | PF00560 | 0.508 |
DOC_CYCLIN_RxL_1 | 420 | 429 | PF00134 | 0.419 |
DOC_MAPK_gen_1 | 347 | 354 | PF00069 | 0.522 |
DOC_MAPK_MEF2A_6 | 129 | 137 | PF00069 | 0.318 |
DOC_MAPK_MEF2A_6 | 292 | 299 | PF00069 | 0.514 |
DOC_MAPK_MEF2A_6 | 347 | 354 | PF00069 | 0.508 |
DOC_MAPK_MEF2A_6 | 88 | 95 | PF00069 | 0.459 |
DOC_PP1_RVXF_1 | 421 | 428 | PF00149 | 0.500 |
DOC_USP7_MATH_1 | 259 | 263 | PF00917 | 0.508 |
DOC_WW_Pin1_4 | 141 | 146 | PF00397 | 0.648 |
DOC_WW_Pin1_4 | 213 | 218 | PF00397 | 0.555 |
DOC_WW_Pin1_4 | 257 | 262 | PF00397 | 0.553 |
LIG_14-3-3_CanoR_1 | 175 | 181 | PF00244 | 0.418 |
LIG_14-3-3_CanoR_1 | 230 | 235 | PF00244 | 0.542 |
LIG_14-3-3_CanoR_1 | 336 | 343 | PF00244 | 0.563 |
LIG_14-3-3_CanoR_1 | 391 | 399 | PF00244 | 0.479 |
LIG_14-3-3_CanoR_1 | 75 | 83 | PF00244 | 0.486 |
LIG_Actin_WH2_2 | 383 | 399 | PF00022 | 0.523 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.584 |
LIG_BRCT_BRCA1_1 | 24 | 28 | PF00533 | 0.551 |
LIG_CaM_IQ_9 | 222 | 238 | PF13499 | 0.514 |
LIG_FAT_LD_1 | 48 | 56 | PF03623 | 0.569 |
LIG_FHA_1 | 219 | 225 | PF00498 | 0.453 |
LIG_FHA_1 | 270 | 276 | PF00498 | 0.491 |
LIG_FHA_1 | 319 | 325 | PF00498 | 0.360 |
LIG_FHA_1 | 336 | 342 | PF00498 | 0.449 |
LIG_FHA_1 | 346 | 352 | PF00498 | 0.340 |
LIG_FHA_1 | 382 | 388 | PF00498 | 0.484 |
LIG_FHA_1 | 401 | 407 | PF00498 | 0.528 |
LIG_FHA_1 | 64 | 70 | PF00498 | 0.538 |
LIG_FHA_2 | 427 | 433 | PF00498 | 0.418 |
LIG_FHA_2 | 79 | 85 | PF00498 | 0.561 |
LIG_LIR_Gen_1 | 239 | 248 | PF02991 | 0.423 |
LIG_LIR_Gen_1 | 296 | 303 | PF02991 | 0.479 |
LIG_LIR_Gen_1 | 359 | 368 | PF02991 | 0.543 |
LIG_LIR_Nem_3 | 183 | 189 | PF02991 | 0.621 |
LIG_LIR_Nem_3 | 239 | 244 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 25 | 31 | PF02991 | 0.707 |
LIG_LIR_Nem_3 | 296 | 302 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 359 | 363 | PF02991 | 0.472 |
LIG_NRBOX | 297 | 303 | PF00104 | 0.488 |
LIG_PDZ_Class_2 | 436 | 441 | PF00595 | 0.585 |
LIG_Pex14_1 | 431 | 435 | PF04695 | 0.390 |
LIG_Pex14_2 | 427 | 431 | PF04695 | 0.484 |
LIG_SH2_GRB2like | 368 | 371 | PF00017 | 0.623 |
LIG_SH2_NCK_1 | 368 | 372 | PF00017 | 0.629 |
LIG_SH2_STAP1 | 73 | 77 | PF00017 | 0.538 |
LIG_SH2_STAT3 | 223 | 226 | PF00017 | 0.508 |
LIG_SH2_STAT5 | 11 | 14 | PF00017 | 0.589 |
LIG_SH2_STAT5 | 223 | 226 | PF00017 | 0.508 |
LIG_SH2_STAT5 | 254 | 257 | PF00017 | 0.416 |
LIG_SH2_STAT5 | 356 | 359 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 368 | 371 | PF00017 | 0.597 |
LIG_SH2_STAT5 | 420 | 423 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 426 | 429 | PF00017 | 0.394 |
LIG_SH3_3 | 191 | 197 | PF00018 | 0.562 |
LIG_SH3_3 | 55 | 61 | PF00018 | 0.551 |
LIG_SUMO_SIM_anti_2 | 245 | 253 | PF11976 | 0.486 |
LIG_SUMO_SIM_anti_2 | 272 | 277 | PF11976 | 0.410 |
LIG_SUMO_SIM_anti_2 | 348 | 355 | PF11976 | 0.392 |
LIG_SUMO_SIM_par_1 | 110 | 116 | PF11976 | 0.491 |
LIG_SUMO_SIM_par_1 | 348 | 355 | PF11976 | 0.502 |
LIG_SUMO_SIM_par_1 | 91 | 97 | PF11976 | 0.455 |
LIG_TRAF2_1 | 61 | 64 | PF00917 | 0.595 |
LIG_TRAF2_1 | 77 | 80 | PF00917 | 0.329 |
LIG_UBA3_1 | 353 | 362 | PF00899 | 0.327 |
LIG_WRC_WIRS_1 | 203 | 208 | PF05994 | 0.516 |
MOD_CDK_SPxK_1 | 213 | 219 | PF00069 | 0.510 |
MOD_CK1_1 | 144 | 150 | PF00069 | 0.616 |
MOD_CK1_1 | 169 | 175 | PF00069 | 0.437 |
MOD_CK1_1 | 260 | 266 | PF00069 | 0.556 |
MOD_CK1_1 | 325 | 331 | PF00069 | 0.505 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.501 |
MOD_CK1_1 | 78 | 84 | PF00069 | 0.542 |
MOD_CK2_1 | 339 | 345 | PF00069 | 0.581 |
MOD_CK2_1 | 426 | 432 | PF00069 | 0.403 |
MOD_CK2_1 | 78 | 84 | PF00069 | 0.535 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.634 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.491 |
MOD_GlcNHglycan | 304 | 308 | PF01048 | 0.552 |
MOD_GlcNHglycan | 324 | 327 | PF01048 | 0.361 |
MOD_GlcNHglycan | 44 | 47 | PF01048 | 0.550 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.423 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.513 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.465 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.462 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.338 |
MOD_GSK3_1 | 335 | 342 | PF00069 | 0.364 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.529 |
MOD_N-GLC_1 | 169 | 174 | PF02516 | 0.495 |
MOD_N-GLC_1 | 277 | 282 | PF02516 | 0.472 |
MOD_N-GLC_1 | 369 | 374 | PF02516 | 0.608 |
MOD_NEK2_1 | 113 | 118 | PF00069 | 0.376 |
MOD_NEK2_1 | 165 | 170 | PF00069 | 0.456 |
MOD_NEK2_1 | 224 | 229 | PF00069 | 0.496 |
MOD_NEK2_1 | 276 | 281 | PF00069 | 0.433 |
MOD_NEK2_1 | 302 | 307 | PF00069 | 0.519 |
MOD_NEK2_1 | 363 | 368 | PF00069 | 0.481 |
MOD_NEK2_1 | 51 | 56 | PF00069 | 0.524 |
MOD_NEK2_1 | 94 | 99 | PF00069 | 0.438 |
MOD_PIKK_1 | 260 | 266 | PF00454 | 0.634 |
MOD_PIKK_1 | 325 | 331 | PF00454 | 0.425 |
MOD_PIKK_1 | 363 | 369 | PF00454 | 0.504 |
MOD_PIKK_1 | 75 | 81 | PF00454 | 0.443 |
MOD_PKA_2 | 229 | 235 | PF00069 | 0.520 |
MOD_PKA_2 | 335 | 341 | PF00069 | 0.579 |
MOD_PKA_2 | 5 | 11 | PF00069 | 0.658 |
MOD_Plk_1 | 277 | 283 | PF00069 | 0.473 |
MOD_Plk_4 | 199 | 205 | PF00069 | 0.432 |
MOD_Plk_4 | 219 | 225 | PF00069 | 0.496 |
MOD_ProDKin_1 | 141 | 147 | PF00069 | 0.653 |
MOD_ProDKin_1 | 213 | 219 | PF00069 | 0.554 |
MOD_ProDKin_1 | 257 | 263 | PF00069 | 0.560 |
MOD_SUMO_rev_2 | 394 | 399 | PF00179 | 0.486 |
MOD_SUMO_rev_2 | 57 | 66 | PF00179 | 0.568 |
MOD_SUMO_rev_2 | 76 | 83 | PF00179 | 0.327 |
TRG_DiLeu_BaEn_1 | 359 | 364 | PF01217 | 0.527 |
TRG_DiLeu_BaLyEn_6 | 89 | 94 | PF01217 | 0.482 |
TRG_ER_diArg_1 | 31 | 34 | PF00400 | 0.651 |
TRG_ER_diArg_1 | 347 | 350 | PF00400 | 0.514 |
TRG_ER_diArg_1 | 421 | 423 | PF00400 | 0.378 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6Y5 | Leptomonas seymouri | 52% | 96% |
A0A0S4IKI5 | Bodo saltans | 29% | 97% |
A0A1X0P918 | Trypanosomatidae | 36% | 95% |
A0A3Q8IFJ3 | Leishmania donovani | 94% | 100% |
A0A3R7K871 | Trypanosoma rangeli | 39% | 100% |
A4HHR2 | Leishmania braziliensis | 79% | 100% |
A4I4X2 | Leishmania infantum | 94% | 100% |
C9ZKY1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
E9ALG0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
V5BSL0 | Trypanosoma cruzi | 38% | 100% |