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: A0A3Q8IGL6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 341 | 345 | PF00656 | 0.360 |
CLV_NRD_NRD_1 | 100 | 102 | PF00675 | 0.473 |
CLV_NRD_NRD_1 | 148 | 150 | PF00675 | 0.486 |
CLV_NRD_NRD_1 | 294 | 296 | PF00675 | 0.555 |
CLV_NRD_NRD_1 | 418 | 420 | PF00675 | 0.431 |
CLV_NRD_NRD_1 | 516 | 518 | PF00675 | 0.326 |
CLV_NRD_NRD_1 | 88 | 90 | PF00675 | 0.456 |
CLV_PCSK_KEX2_1 | 100 | 102 | PF00082 | 0.371 |
CLV_PCSK_KEX2_1 | 148 | 150 | PF00082 | 0.433 |
CLV_PCSK_KEX2_1 | 516 | 518 | PF00082 | 0.326 |
CLV_PCSK_KEX2_1 | 537 | 539 | PF00082 | 0.376 |
CLV_PCSK_KEX2_1 | 88 | 90 | PF00082 | 0.389 |
CLV_PCSK_PC1ET2_1 | 537 | 539 | PF00082 | 0.378 |
CLV_PCSK_SKI1_1 | 118 | 122 | PF00082 | 0.395 |
CLV_PCSK_SKI1_1 | 149 | 153 | PF00082 | 0.475 |
CLV_PCSK_SKI1_1 | 162 | 166 | PF00082 | 0.488 |
CLV_PCSK_SKI1_1 | 419 | 423 | PF00082 | 0.349 |
CLV_PCSK_SKI1_1 | 488 | 492 | PF00082 | 0.453 |
CLV_PCSK_SKI1_1 | 529 | 533 | PF00082 | 0.381 |
DEG_APCC_DBOX_1 | 148 | 156 | PF00400 | 0.463 |
DEG_APCC_DBOX_1 | 161 | 169 | PF00400 | 0.481 |
DEG_APCC_DBOX_1 | 528 | 536 | PF00400 | 0.436 |
DEG_SCF_FBW7_1 | 75 | 81 | PF00400 | 0.470 |
DOC_CDC14_PxL_1 | 449 | 457 | PF14671 | 0.393 |
DOC_CKS1_1 | 75 | 80 | PF01111 | 0.477 |
DOC_CYCLIN_RxL_1 | 364 | 372 | PF00134 | 0.431 |
DOC_CYCLIN_yCln2_LP_2 | 304 | 310 | PF00134 | 0.368 |
DOC_MAPK_DCC_7 | 173 | 181 | PF00069 | 0.423 |
DOC_MAPK_gen_1 | 300 | 310 | PF00069 | 0.495 |
DOC_MAPK_gen_1 | 537 | 548 | PF00069 | 0.458 |
DOC_MAPK_MEF2A_6 | 228 | 235 | PF00069 | 0.293 |
DOC_MAPK_MEF2A_6 | 541 | 550 | PF00069 | 0.451 |
DOC_MAPK_NFAT4_5 | 228 | 236 | PF00069 | 0.288 |
DOC_MAPK_RevD_3 | 405 | 420 | PF00069 | 0.396 |
DOC_PP1_RVXF_1 | 417 | 424 | PF00149 | 0.375 |
DOC_USP7_MATH_1 | 120 | 124 | PF00917 | 0.520 |
DOC_USP7_MATH_1 | 207 | 211 | PF00917 | 0.530 |
DOC_USP7_MATH_1 | 445 | 449 | PF00917 | 0.388 |
DOC_USP7_MATH_1 | 78 | 82 | PF00917 | 0.521 |
DOC_USP7_UBL2_3 | 296 | 300 | PF12436 | 0.562 |
DOC_WW_Pin1_4 | 210 | 215 | PF00397 | 0.375 |
DOC_WW_Pin1_4 | 303 | 308 | PF00397 | 0.539 |
DOC_WW_Pin1_4 | 74 | 79 | PF00397 | 0.546 |
DOC_WW_Pin1_4 | 8 | 13 | PF00397 | 0.532 |
LIG_14-3-3_CanoR_1 | 19 | 24 | PF00244 | 0.491 |
LIG_14-3-3_CanoR_1 | 199 | 205 | PF00244 | 0.528 |
LIG_14-3-3_CanoR_1 | 425 | 430 | PF00244 | 0.387 |
LIG_14-3-3_CanoR_1 | 475 | 480 | PF00244 | 0.320 |
LIG_14-3-3_CanoR_1 | 517 | 523 | PF00244 | 0.417 |
LIG_Actin_WH2_2 | 184 | 201 | PF00022 | 0.480 |
LIG_Actin_WH2_2 | 472 | 490 | PF00022 | 0.353 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.465 |
LIG_BRCT_BRCA1_1 | 1 | 5 | PF00533 | 0.610 |
LIG_BRCT_BRCA1_1 | 212 | 216 | PF00533 | 0.281 |
LIG_Clathr_ClatBox_1 | 353 | 357 | PF01394 | 0.322 |
LIG_FHA_1 | 122 | 128 | PF00498 | 0.434 |
LIG_FHA_1 | 349 | 355 | PF00498 | 0.319 |
LIG_FHA_1 | 356 | 362 | PF00498 | 0.292 |
LIG_FHA_1 | 390 | 396 | PF00498 | 0.452 |
LIG_FHA_1 | 487 | 493 | PF00498 | 0.420 |
LIG_FHA_2 | 220 | 226 | PF00498 | 0.402 |
LIG_FHA_2 | 243 | 249 | PF00498 | 0.456 |
LIG_FHA_2 | 397 | 403 | PF00498 | 0.342 |
LIG_FHA_2 | 42 | 48 | PF00498 | 0.405 |
LIG_FHA_2 | 498 | 504 | PF00498 | 0.416 |
LIG_HCF-1_HBM_1 | 372 | 375 | PF13415 | 0.485 |
LIG_LIR_Gen_1 | 213 | 223 | PF02991 | 0.397 |
LIG_LIR_Gen_1 | 22 | 30 | PF02991 | 0.383 |
LIG_LIR_Gen_1 | 254 | 264 | PF02991 | 0.389 |
LIG_LIR_Gen_1 | 267 | 277 | PF02991 | 0.416 |
LIG_LIR_Gen_1 | 309 | 319 | PF02991 | 0.432 |
LIG_LIR_Gen_1 | 372 | 383 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 213 | 219 | PF02991 | 0.285 |
LIG_LIR_Nem_3 | 22 | 26 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 254 | 259 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 267 | 272 | PF02991 | 0.367 |
LIG_LIR_Nem_3 | 309 | 314 | PF02991 | 0.396 |
LIG_LIR_Nem_3 | 372 | 377 | PF02991 | 0.398 |
LIG_LIR_Nem_3 | 62 | 68 | PF02991 | 0.388 |
LIG_LYPXL_yS_3 | 382 | 385 | PF13949 | 0.342 |
LIG_MYND_1 | 552 | 556 | PF01753 | 0.468 |
LIG_NRBOX | 131 | 137 | PF00104 | 0.556 |
LIG_NRBOX | 506 | 512 | PF00104 | 0.458 |
LIG_OCRL_FandH_1 | 187 | 199 | PF00620 | 0.286 |
LIG_PCNA_PIPBox_1 | 368 | 377 | PF02747 | 0.429 |
LIG_PCNA_yPIPBox_3 | 250 | 264 | PF02747 | 0.416 |
LIG_PCNA_yPIPBox_3 | 366 | 375 | PF02747 | 0.384 |
LIG_SH2_CRK | 256 | 260 | PF00017 | 0.366 |
LIG_SH2_CRK | 66 | 70 | PF00017 | 0.379 |
LIG_SH2_STAP1 | 264 | 268 | PF00017 | 0.449 |
LIG_SH2_STAP1 | 325 | 329 | PF00017 | 0.417 |
LIG_SH2_STAP1 | 335 | 339 | PF00017 | 0.448 |
LIG_SH2_STAT3 | 377 | 380 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 36 | 39 | PF00017 | 0.573 |
LIG_SH2_STAT5 | 436 | 439 | PF00017 | 0.377 |
LIG_SH2_STAT5 | 486 | 489 | PF00017 | 0.365 |
LIG_SH2_STAT5 | 518 | 521 | PF00017 | 0.498 |
LIG_SH3_2 | 75 | 80 | PF14604 | 0.442 |
LIG_SH3_3 | 37 | 43 | PF00018 | 0.455 |
LIG_SH3_3 | 390 | 396 | PF00018 | 0.403 |
LIG_SH3_3 | 519 | 525 | PF00018 | 0.307 |
LIG_SH3_3 | 69 | 75 | PF00018 | 0.414 |
LIG_SUMO_SIM_anti_2 | 22 | 28 | PF11976 | 0.459 |
LIG_SUMO_SIM_anti_2 | 351 | 358 | PF11976 | 0.292 |
LIG_SUMO_SIM_par_1 | 351 | 358 | PF11976 | 0.292 |
LIG_TRAF2_1 | 222 | 225 | PF00917 | 0.437 |
LIG_TYR_ITIM | 63 | 68 | PF00017 | 0.353 |
LIG_UBA3_1 | 219 | 228 | PF00899 | 0.452 |
LIG_UBA3_1 | 361 | 367 | PF00899 | 0.461 |
LIG_UBA3_1 | 507 | 512 | PF00899 | 0.330 |
LIG_UBA3_1 | 531 | 537 | PF00899 | 0.353 |
MOD_CDK_SPxK_1 | 74 | 80 | PF00069 | 0.494 |
MOD_CK1_1 | 210 | 216 | PF00069 | 0.368 |
MOD_CK1_1 | 338 | 344 | PF00069 | 0.528 |
MOD_CK1_1 | 58 | 64 | PF00069 | 0.417 |
MOD_CK2_1 | 219 | 225 | PF00069 | 0.425 |
MOD_CK2_1 | 242 | 248 | PF00069 | 0.428 |
MOD_CK2_1 | 396 | 402 | PF00069 | 0.339 |
MOD_CK2_1 | 41 | 47 | PF00069 | 0.419 |
MOD_CK2_1 | 497 | 503 | PF00069 | 0.423 |
MOD_DYRK1A_RPxSP_1 | 8 | 12 | PF00069 | 0.448 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.485 |
MOD_GlcNHglycan | 108 | 111 | PF01048 | 0.549 |
MOD_GlcNHglycan | 195 | 198 | PF01048 | 0.475 |
MOD_GlcNHglycan | 216 | 219 | PF01048 | 0.337 |
MOD_GlcNHglycan | 242 | 245 | PF01048 | 0.534 |
MOD_GlcNHglycan | 344 | 347 | PF01048 | 0.403 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.414 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.440 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.389 |
MOD_GSK3_1 | 219 | 226 | PF00069 | 0.404 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.386 |
MOD_GSK3_1 | 338 | 345 | PF00069 | 0.200 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.505 |
MOD_GSK3_1 | 421 | 428 | PF00069 | 0.345 |
MOD_GSK3_1 | 475 | 482 | PF00069 | 0.428 |
MOD_GSK3_1 | 486 | 493 | PF00069 | 0.357 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.386 |
MOD_GSK3_1 | 74 | 81 | PF00069 | 0.479 |
MOD_N-GLC_1 | 251 | 256 | PF02516 | 0.557 |
MOD_NEK2_1 | 121 | 126 | PF00069 | 0.445 |
MOD_NEK2_1 | 141 | 146 | PF00069 | 0.232 |
MOD_NEK2_1 | 15 | 20 | PF00069 | 0.393 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.335 |
MOD_NEK2_1 | 198 | 203 | PF00069 | 0.441 |
MOD_NEK2_1 | 223 | 228 | PF00069 | 0.433 |
MOD_NEK2_1 | 242 | 247 | PF00069 | 0.245 |
MOD_NEK2_1 | 319 | 324 | PF00069 | 0.396 |
MOD_NEK2_1 | 421 | 426 | PF00069 | 0.321 |
MOD_NEK2_1 | 496 | 501 | PF00069 | 0.508 |
MOD_NEK2_2 | 320 | 325 | PF00069 | 0.386 |
MOD_NEK2_2 | 518 | 523 | PF00069 | 0.500 |
MOD_PIKK_1 | 55 | 61 | PF00454 | 0.369 |
MOD_PK_1 | 475 | 481 | PF00069 | 0.364 |
MOD_PKA_1 | 537 | 543 | PF00069 | 0.343 |
MOD_PKA_2 | 198 | 204 | PF00069 | 0.433 |
MOD_PKA_2 | 294 | 300 | PF00069 | 0.623 |
MOD_PKA_2 | 537 | 543 | PF00069 | 0.363 |
MOD_Plk_1 | 142 | 148 | PF00069 | 0.488 |
MOD_Plk_1 | 251 | 257 | PF00069 | 0.551 |
MOD_Plk_1 | 78 | 84 | PF00069 | 0.524 |
MOD_Plk_4 | 131 | 137 | PF00069 | 0.468 |
MOD_Plk_4 | 19 | 25 | PF00069 | 0.440 |
MOD_Plk_4 | 251 | 257 | PF00069 | 0.501 |
MOD_Plk_4 | 313 | 319 | PF00069 | 0.467 |
MOD_Plk_4 | 320 | 326 | PF00069 | 0.377 |
MOD_Plk_4 | 338 | 344 | PF00069 | 0.297 |
MOD_Plk_4 | 389 | 395 | PF00069 | 0.465 |
MOD_Plk_4 | 425 | 431 | PF00069 | 0.343 |
MOD_Plk_4 | 50 | 56 | PF00069 | 0.465 |
MOD_Plk_4 | 59 | 65 | PF00069 | 0.288 |
MOD_Plk_4 | 78 | 84 | PF00069 | 0.397 |
MOD_ProDKin_1 | 210 | 216 | PF00069 | 0.370 |
MOD_ProDKin_1 | 303 | 309 | PF00069 | 0.541 |
MOD_ProDKin_1 | 74 | 80 | PF00069 | 0.550 |
MOD_ProDKin_1 | 8 | 14 | PF00069 | 0.532 |
TRG_DiLeu_BaLyEn_6 | 137 | 142 | PF01217 | 0.381 |
TRG_DiLeu_BaLyEn_6 | 526 | 531 | PF01217 | 0.433 |
TRG_ENDOCYTIC_2 | 256 | 259 | PF00928 | 0.362 |
TRG_ENDOCYTIC_2 | 269 | 272 | PF00928 | 0.338 |
TRG_ENDOCYTIC_2 | 375 | 378 | PF00928 | 0.347 |
TRG_ENDOCYTIC_2 | 382 | 385 | PF00928 | 0.330 |
TRG_ENDOCYTIC_2 | 457 | 460 | PF00928 | 0.355 |
TRG_ENDOCYTIC_2 | 65 | 68 | PF00928 | 0.369 |
TRG_ER_diArg_1 | 148 | 150 | PF00400 | 0.489 |
TRG_ER_diArg_1 | 284 | 287 | PF00400 | 0.554 |
TRG_ER_diArg_1 | 515 | 517 | PF00400 | 0.313 |
TRG_ER_diArg_1 | 87 | 89 | PF00400 | 0.497 |
TRG_ER_diArg_1 | 99 | 101 | PF00400 | 0.547 |
TRG_NLS_MonoExtN_4 | 293 | 299 | PF00514 | 0.451 |
TRG_Pf-PMV_PEXEL_1 | 101 | 105 | PF00026 | 0.521 |
TRG_Pf-PMV_PEXEL_1 | 288 | 292 | PF00026 | 0.618 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1II47 | Leptomonas seymouri | 57% | 100% |
A0A0S4JG92 | Bodo saltans | 22% | 77% |
A0A1X0NRZ6 | Trypanosomatidae | 40% | 99% |
A0A422NHU1 | Trypanosoma rangeli | 42% | 98% |
A4HL31 | Leishmania braziliensis | 82% | 100% |
A4I8L2 | Leishmania infantum | 100% | 100% |
D0AAK3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 92% |
E9B3H2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
Q4Q4M8 | Leishmania major | 95% | 100% |
V5BI03 | Trypanosoma cruzi | 42% | 98% |