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: 3 |
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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: E9B5B8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 139 | 143 | PF00656 | 0.464 |
CLV_NRD_NRD_1 | 165 | 167 | PF00675 | 0.620 |
CLV_NRD_NRD_1 | 205 | 207 | PF00675 | 0.565 |
CLV_PCSK_KEX2_1 | 165 | 167 | PF00082 | 0.583 |
CLV_PCSK_KEX2_1 | 205 | 207 | PF00082 | 0.553 |
CLV_PCSK_KEX2_1 | 469 | 471 | PF00082 | 0.511 |
CLV_PCSK_PC1ET2_1 | 469 | 471 | PF00082 | 0.511 |
CLV_PCSK_SKI1_1 | 108 | 112 | PF00082 | 0.603 |
CLV_PCSK_SKI1_1 | 123 | 127 | PF00082 | 0.543 |
CLV_PCSK_SKI1_1 | 166 | 170 | PF00082 | 0.589 |
CLV_PCSK_SKI1_1 | 179 | 183 | PF00082 | 0.621 |
CLV_PCSK_SKI1_1 | 256 | 260 | PF00082 | 0.599 |
DEG_APCC_DBOX_1 | 178 | 186 | PF00400 | 0.467 |
DOC_ANK_TNKS_1 | 323 | 330 | PF00023 | 0.436 |
DOC_CYCLIN_yCln2_LP_2 | 181 | 184 | PF00134 | 0.378 |
DOC_PP1_RVXF_1 | 233 | 240 | PF00149 | 0.484 |
DOC_PP1_RVXF_1 | 360 | 366 | PF00149 | 0.411 |
DOC_PP2B_LxvP_1 | 126 | 129 | PF13499 | 0.428 |
DOC_PP2B_LxvP_1 | 181 | 184 | PF13499 | 0.378 |
DOC_USP7_MATH_1 | 155 | 159 | PF00917 | 0.402 |
DOC_USP7_MATH_1 | 216 | 220 | PF00917 | 0.406 |
DOC_USP7_MATH_1 | 458 | 462 | PF00917 | 0.589 |
DOC_USP7_MATH_1 | 87 | 91 | PF00917 | 0.525 |
DOC_WW_Pin1_4 | 173 | 178 | PF00397 | 0.435 |
DOC_WW_Pin1_4 | 401 | 406 | PF00397 | 0.599 |
DOC_WW_Pin1_4 | 434 | 439 | PF00397 | 0.669 |
DOC_WW_Pin1_4 | 83 | 88 | PF00397 | 0.488 |
LIG_14-3-3_CanoR_1 | 200 | 207 | PF00244 | 0.451 |
LIG_14-3-3_CanoR_1 | 290 | 295 | PF00244 | 0.405 |
LIG_14-3-3_CanoR_1 | 324 | 328 | PF00244 | 0.395 |
LIG_14-3-3_CanoR_1 | 347 | 357 | PF00244 | 0.437 |
LIG_14-3-3_CanoR_1 | 36 | 44 | PF00244 | 0.429 |
LIG_14-3-3_CanoR_1 | 362 | 368 | PF00244 | 0.341 |
LIG_14-3-3_CanoR_1 | 387 | 396 | PF00244 | 0.695 |
LIG_14-3-3_CanoR_1 | 459 | 467 | PF00244 | 0.602 |
LIG_14-3-3_CanoR_1 | 76 | 80 | PF00244 | 0.364 |
LIG_Actin_WH2_2 | 382 | 399 | PF00022 | 0.685 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.387 |
LIG_BRCT_BRCA1_1 | 305 | 309 | PF00533 | 0.494 |
LIG_Clathr_ClatBox_1 | 110 | 114 | PF01394 | 0.419 |
LIG_CtBP_PxDLS_1 | 438 | 442 | PF00389 | 0.687 |
LIG_deltaCOP1_diTrp_1 | 104 | 113 | PF00928 | 0.343 |
LIG_FHA_1 | 249 | 255 | PF00498 | 0.319 |
LIG_FHA_1 | 25 | 31 | PF00498 | 0.505 |
LIG_FHA_1 | 349 | 355 | PF00498 | 0.455 |
LIG_FHA_1 | 425 | 431 | PF00498 | 0.655 |
LIG_FHA_1 | 446 | 452 | PF00498 | 0.647 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.313 |
LIG_FHA_2 | 421 | 427 | PF00498 | 0.706 |
LIG_FHA_2 | 49 | 55 | PF00498 | 0.452 |
LIG_LIR_Gen_1 | 190 | 197 | PF02991 | 0.471 |
LIG_LIR_Gen_1 | 199 | 207 | PF02991 | 0.452 |
LIG_LIR_Gen_1 | 236 | 246 | PF02991 | 0.368 |
LIG_LIR_Gen_1 | 366 | 375 | PF02991 | 0.358 |
LIG_LIR_Gen_1 | 426 | 436 | PF02991 | 0.681 |
LIG_LIR_Gen_1 | 43 | 49 | PF02991 | 0.365 |
LIG_LIR_Nem_3 | 190 | 194 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 199 | 204 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 236 | 242 | PF02991 | 0.397 |
LIG_LIR_Nem_3 | 366 | 370 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 426 | 432 | PF02991 | 0.686 |
LIG_LIR_Nem_3 | 43 | 47 | PF02991 | 0.361 |
LIG_MLH1_MIPbox_1 | 306 | 310 | PF16413 | 0.490 |
LIG_MYND_3 | 379 | 383 | PF01753 | 0.676 |
LIG_Pex14_1 | 109 | 113 | PF04695 | 0.262 |
LIG_Pex14_1 | 453 | 457 | PF04695 | 0.623 |
LIG_Pex14_2 | 194 | 198 | PF04695 | 0.398 |
LIG_REV1ctd_RIR_1 | 157 | 166 | PF16727 | 0.363 |
LIG_SH2_STAP1 | 44 | 48 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 44 | 47 | PF00017 | 0.454 |
LIG_SH3_3 | 374 | 380 | PF00018 | 0.358 |
LIG_SUMO_SIM_anti_2 | 217 | 227 | PF11976 | 0.390 |
LIG_SUMO_SIM_anti_2 | 67 | 72 | PF11976 | 0.273 |
LIG_SUMO_SIM_par_1 | 114 | 122 | PF11976 | 0.427 |
LIG_SUMO_SIM_par_1 | 26 | 31 | PF11976 | 0.499 |
LIG_SUMO_SIM_par_1 | 356 | 361 | PF11976 | 0.311 |
LIG_SUMO_SIM_par_1 | 437 | 443 | PF11976 | 0.538 |
LIG_TRAF2_1 | 412 | 415 | PF00917 | 0.681 |
LIG_TRAF2_1 | 423 | 426 | PF00917 | 0.722 |
LIG_TRAF2_1 | 61 | 64 | PF00917 | 0.434 |
LIG_UBA3_1 | 37 | 46 | PF00899 | 0.431 |
LIG_WRC_WIRS_1 | 156 | 161 | PF05994 | 0.402 |
MOD_CDK_SPxK_1 | 173 | 179 | PF00069 | 0.441 |
MOD_CK1_1 | 199 | 205 | PF00069 | 0.447 |
MOD_CK1_1 | 248 | 254 | PF00069 | 0.328 |
MOD_CK1_1 | 302 | 308 | PF00069 | 0.443 |
MOD_CK1_1 | 90 | 96 | PF00069 | 0.536 |
MOD_CK2_1 | 418 | 424 | PF00069 | 0.718 |
MOD_CK2_1 | 437 | 443 | PF00069 | 0.527 |
MOD_CK2_1 | 90 | 96 | PF00069 | 0.405 |
MOD_CMANNOS | 106 | 109 | PF00535 | 0.535 |
MOD_CMANNOS | 364 | 367 | PF00535 | 0.411 |
MOD_GlcNHglycan | 145 | 148 | PF01048 | 0.622 |
MOD_GlcNHglycan | 313 | 317 | PF01048 | 0.637 |
MOD_GlcNHglycan | 38 | 41 | PF01048 | 0.662 |
MOD_GlcNHglycan | 391 | 394 | PF01048 | 0.442 |
MOD_GlcNHglycan | 414 | 419 | PF01048 | 0.542 |
MOD_GlcNHglycan | 445 | 448 | PF01048 | 0.449 |
MOD_GlcNHglycan | 56 | 60 | PF01048 | 0.576 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.752 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.438 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.329 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.437 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.440 |
MOD_GSK3_1 | 401 | 408 | PF00069 | 0.653 |
MOD_GSK3_1 | 414 | 421 | PF00069 | 0.756 |
MOD_GSK3_1 | 439 | 446 | PF00069 | 0.681 |
MOD_GSK3_1 | 468 | 475 | PF00069 | 0.571 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.428 |
MOD_GSK3_1 | 83 | 90 | PF00069 | 0.504 |
MOD_N-GLC_1 | 297 | 302 | PF02516 | 0.607 |
MOD_NEK2_1 | 187 | 192 | PF00069 | 0.357 |
MOD_NEK2_1 | 259 | 264 | PF00069 | 0.456 |
MOD_NEK2_1 | 363 | 368 | PF00069 | 0.478 |
MOD_NEK2_1 | 382 | 387 | PF00069 | 0.519 |
MOD_NEK2_1 | 389 | 394 | PF00069 | 0.632 |
MOD_NEK2_2 | 155 | 160 | PF00069 | 0.401 |
MOD_PIKK_1 | 112 | 118 | PF00454 | 0.380 |
MOD_PIKK_1 | 297 | 303 | PF00454 | 0.433 |
MOD_PK_1 | 136 | 142 | PF00069 | 0.340 |
MOD_PKA_2 | 199 | 205 | PF00069 | 0.429 |
MOD_PKA_2 | 323 | 329 | PF00069 | 0.400 |
MOD_PKA_2 | 458 | 464 | PF00069 | 0.605 |
MOD_PKA_2 | 75 | 81 | PF00069 | 0.364 |
MOD_Plk_1 | 216 | 222 | PF00069 | 0.390 |
MOD_Plk_1 | 382 | 388 | PF00069 | 0.677 |
MOD_Plk_2-3 | 26 | 32 | PF00069 | 0.454 |
MOD_Plk_4 | 136 | 142 | PF00069 | 0.347 |
MOD_Plk_4 | 155 | 161 | PF00069 | 0.383 |
MOD_Plk_4 | 424 | 430 | PF00069 | 0.658 |
MOD_Plk_4 | 66 | 72 | PF00069 | 0.360 |
MOD_ProDKin_1 | 173 | 179 | PF00069 | 0.441 |
MOD_ProDKin_1 | 401 | 407 | PF00069 | 0.600 |
MOD_ProDKin_1 | 434 | 440 | PF00069 | 0.667 |
MOD_ProDKin_1 | 83 | 89 | PF00069 | 0.490 |
TRG_DiLeu_BaLyEn_6 | 33 | 38 | PF01217 | 0.438 |
TRG_ENDOCYTIC_2 | 191 | 194 | PF00928 | 0.413 |
TRG_ENDOCYTIC_2 | 44 | 47 | PF00928 | 0.361 |
TRG_ER_diArg_1 | 204 | 206 | PF00400 | 0.349 |
TRG_ER_diArg_1 | 289 | 292 | PF00400 | 0.394 |
TRG_NES_CRM1_1 | 321 | 335 | PF08389 | 0.443 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P448 | Leptomonas seymouri | 33% | 96% |
A0A3S7X8E6 | Leishmania donovani | 85% | 100% |
A4HB48 | Leishmania braziliensis | 67% | 100% |
A4IA96 | Leishmania infantum | 85% | 100% |
Q4Q2L5 | Leishmania major | 84% | 100% |