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: 8 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: A4I380
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 127 | 129 | PF00675 | 0.555 |
CLV_NRD_NRD_1 | 13 | 15 | PF00675 | 0.699 |
CLV_NRD_NRD_1 | 347 | 349 | PF00675 | 0.548 |
CLV_NRD_NRD_1 | 455 | 457 | PF00675 | 0.448 |
CLV_PCSK_FUR_1 | 388 | 392 | PF00082 | 0.473 |
CLV_PCSK_FUR_1 | 453 | 457 | PF00082 | 0.483 |
CLV_PCSK_KEX2_1 | 127 | 129 | PF00082 | 0.657 |
CLV_PCSK_KEX2_1 | 13 | 15 | PF00082 | 0.699 |
CLV_PCSK_KEX2_1 | 266 | 268 | PF00082 | 0.477 |
CLV_PCSK_KEX2_1 | 390 | 392 | PF00082 | 0.479 |
CLV_PCSK_KEX2_1 | 455 | 457 | PF00082 | 0.448 |
CLV_PCSK_PC1ET2_1 | 266 | 268 | PF00082 | 0.508 |
CLV_PCSK_PC1ET2_1 | 390 | 392 | PF00082 | 0.479 |
CLV_PCSK_SKI1_1 | 127 | 131 | PF00082 | 0.587 |
CLV_PCSK_SKI1_1 | 257 | 261 | PF00082 | 0.547 |
CLV_PCSK_SKI1_1 | 267 | 271 | PF00082 | 0.279 |
CLV_PCSK_SKI1_1 | 337 | 341 | PF00082 | 0.541 |
CLV_PCSK_SKI1_1 | 344 | 348 | PF00082 | 0.542 |
DEG_APCC_DBOX_1 | 266 | 274 | PF00400 | 0.489 |
DEG_APCC_KENBOX_2 | 329 | 333 | PF00400 | 0.623 |
DEG_SPOP_SBC_1 | 310 | 314 | PF00917 | 0.570 |
DOC_CYCLIN_RxL_1 | 124 | 133 | PF00134 | 0.492 |
DOC_MAPK_DCC_7 | 179 | 189 | PF00069 | 0.487 |
DOC_MAPK_gen_1 | 238 | 246 | PF00069 | 0.575 |
DOC_MAPK_gen_1 | 266 | 272 | PF00069 | 0.472 |
DOC_MAPK_gen_1 | 451 | 459 | PF00069 | 0.427 |
DOC_PP2B_LxvP_1 | 356 | 359 | PF13499 | 0.492 |
DOC_USP7_MATH_1 | 101 | 105 | PF00917 | 0.689 |
DOC_USP7_MATH_1 | 156 | 160 | PF00917 | 0.420 |
DOC_USP7_MATH_1 | 225 | 229 | PF00917 | 0.626 |
DOC_USP7_MATH_1 | 310 | 314 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 467 | 471 | PF00917 | 0.599 |
DOC_USP7_UBL2_3 | 226 | 230 | PF12436 | 0.650 |
DOC_WW_Pin1_4 | 22 | 27 | PF00397 | 0.554 |
DOC_WW_Pin1_4 | 311 | 316 | PF00397 | 0.602 |
DOC_WW_Pin1_4 | 483 | 488 | PF00397 | 0.612 |
LIG_14-3-3_CanoR_1 | 120 | 126 | PF00244 | 0.481 |
LIG_14-3-3_CanoR_1 | 13 | 23 | PF00244 | 0.635 |
LIG_14-3-3_CanoR_1 | 147 | 156 | PF00244 | 0.469 |
LIG_14-3-3_CanoR_1 | 196 | 205 | PF00244 | 0.417 |
LIG_14-3-3_CanoR_1 | 348 | 353 | PF00244 | 0.493 |
LIG_14-3-3_CanoR_1 | 391 | 399 | PF00244 | 0.556 |
LIG_14-3-3_CanoR_1 | 427 | 431 | PF00244 | 0.440 |
LIG_14-3-3_CanoR_1 | 57 | 61 | PF00244 | 0.527 |
LIG_Actin_WH2_2 | 243 | 259 | PF00022 | 0.378 |
LIG_Actin_WH2_2 | 349 | 364 | PF00022 | 0.543 |
LIG_BRCT_BRCA1_1 | 424 | 428 | PF00533 | 0.328 |
LIG_BRCT_BRCA1_1 | 49 | 53 | PF00533 | 0.654 |
LIG_Clathr_ClatBox_1 | 129 | 133 | PF01394 | 0.470 |
LIG_CSL_BTD_1 | 23 | 26 | PF09270 | 0.631 |
LIG_eIF4E_1 | 148 | 154 | PF01652 | 0.491 |
LIG_FHA_1 | 103 | 109 | PF00498 | 0.628 |
LIG_FHA_1 | 163 | 169 | PF00498 | 0.464 |
LIG_FHA_1 | 320 | 326 | PF00498 | 0.612 |
LIG_FHA_1 | 43 | 49 | PF00498 | 0.626 |
LIG_FHA_1 | 452 | 458 | PF00498 | 0.396 |
LIG_FHA_1 | 77 | 83 | PF00498 | 0.705 |
LIG_FHA_2 | 411 | 417 | PF00498 | 0.587 |
LIG_FHA_2 | 470 | 476 | PF00498 | 0.583 |
LIG_LIR_Apic_2 | 478 | 483 | PF02991 | 0.565 |
LIG_LIR_Apic_2 | 69 | 74 | PF02991 | 0.678 |
LIG_LIR_Gen_1 | 149 | 157 | PF02991 | 0.488 |
LIG_LIR_Gen_1 | 167 | 174 | PF02991 | 0.401 |
LIG_LIR_Gen_1 | 195 | 205 | PF02991 | 0.597 |
LIG_LIR_Gen_1 | 297 | 307 | PF02991 | 0.568 |
LIG_LIR_Gen_1 | 429 | 439 | PF02991 | 0.494 |
LIG_LIR_Nem_3 | 115 | 121 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 149 | 153 | PF02991 | 0.410 |
LIG_LIR_Nem_3 | 167 | 173 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 181 | 186 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 195 | 201 | PF02991 | 0.516 |
LIG_LIR_Nem_3 | 233 | 237 | PF02991 | 0.527 |
LIG_LIR_Nem_3 | 297 | 302 | PF02991 | 0.568 |
LIG_LIR_Nem_3 | 429 | 435 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 475 | 480 | PF02991 | 0.577 |
LIG_LIR_Nem_3 | 50 | 56 | PF02991 | 0.655 |
LIG_PDZ_Class_3 | 519 | 524 | PF00595 | 0.783 |
LIG_Pex14_2 | 428 | 432 | PF04695 | 0.362 |
LIG_SH2_CRK | 299 | 303 | PF00017 | 0.545 |
LIG_SH2_SRC | 382 | 385 | PF00017 | 0.353 |
LIG_SH2_STAP1 | 382 | 386 | PF00017 | 0.472 |
LIG_SH2_STAP1 | 477 | 481 | PF00017 | 0.640 |
LIG_SH2_STAP1 | 54 | 58 | PF00017 | 0.614 |
LIG_SH2_STAT5 | 188 | 191 | PF00017 | 0.435 |
LIG_SH2_STAT5 | 288 | 291 | PF00017 | 0.604 |
LIG_SH2_STAT5 | 360 | 363 | PF00017 | 0.520 |
LIG_SH2_STAT5 | 480 | 483 | PF00017 | 0.598 |
LIG_SH2_STAT5 | 496 | 499 | PF00017 | 0.498 |
LIG_SH2_STAT5 | 517 | 520 | PF00017 | 0.694 |
LIG_SH3_3 | 400 | 406 | PF00018 | 0.574 |
LIG_SH3_3 | 58 | 64 | PF00018 | 0.583 |
LIG_SUMO_SIM_anti_2 | 248 | 255 | PF11976 | 0.521 |
LIG_SUMO_SIM_par_1 | 44 | 51 | PF11976 | 0.641 |
LIG_TRFH_1 | 235 | 239 | PF08558 | 0.376 |
LIG_UBA3_1 | 252 | 257 | PF00899 | 0.570 |
MOD_CDC14_SPxK_1 | 314 | 317 | PF00782 | 0.579 |
MOD_CDK_SPxK_1 | 311 | 317 | PF00069 | 0.575 |
MOD_CK1_1 | 123 | 129 | PF00069 | 0.564 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.622 |
MOD_CK1_1 | 178 | 184 | PF00069 | 0.573 |
MOD_CK1_1 | 233 | 239 | PF00069 | 0.580 |
MOD_CK2_1 | 22 | 28 | PF00069 | 0.532 |
MOD_CK2_1 | 320 | 326 | PF00069 | 0.620 |
MOD_CK2_1 | 362 | 368 | PF00069 | 0.574 |
MOD_CK2_1 | 410 | 416 | PF00069 | 0.548 |
MOD_CK2_1 | 469 | 475 | PF00069 | 0.619 |
MOD_GlcNHglycan | 133 | 137 | PF01048 | 0.504 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.689 |
MOD_GlcNHglycan | 143 | 146 | PF01048 | 0.489 |
MOD_GlcNHglycan | 180 | 183 | PF01048 | 0.519 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.516 |
MOD_GlcNHglycan | 227 | 230 | PF01048 | 0.612 |
MOD_GlcNHglycan | 322 | 325 | PF01048 | 0.636 |
MOD_GlcNHglycan | 399 | 402 | PF01048 | 0.537 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.511 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.626 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.444 |
MOD_GSK3_1 | 410 | 417 | PF00069 | 0.522 |
MOD_GSK3_1 | 422 | 429 | PF00069 | 0.443 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.491 |
MOD_NEK2_1 | 12 | 17 | PF00069 | 0.604 |
MOD_NEK2_1 | 146 | 151 | PF00069 | 0.440 |
MOD_NEK2_1 | 208 | 213 | PF00069 | 0.527 |
MOD_NEK2_1 | 335 | 340 | PF00069 | 0.510 |
MOD_NEK2_1 | 347 | 352 | PF00069 | 0.557 |
MOD_NEK2_1 | 4 | 9 | PF00069 | 0.712 |
MOD_NEK2_1 | 430 | 435 | PF00069 | 0.502 |
MOD_NEK2_1 | 460 | 465 | PF00069 | 0.478 |
MOD_NEK2_1 | 56 | 61 | PF00069 | 0.595 |
MOD_NEK2_2 | 288 | 293 | PF00069 | 0.526 |
MOD_PIKK_1 | 362 | 368 | PF00454 | 0.449 |
MOD_PIKK_1 | 422 | 428 | PF00454 | 0.482 |
MOD_PKA_1 | 348 | 354 | PF00069 | 0.529 |
MOD_PKA_1 | 390 | 396 | PF00069 | 0.494 |
MOD_PKA_2 | 119 | 125 | PF00069 | 0.562 |
MOD_PKA_2 | 12 | 18 | PF00069 | 0.693 |
MOD_PKA_2 | 146 | 152 | PF00069 | 0.394 |
MOD_PKA_2 | 178 | 184 | PF00069 | 0.581 |
MOD_PKA_2 | 347 | 353 | PF00069 | 0.532 |
MOD_PKA_2 | 390 | 396 | PF00069 | 0.554 |
MOD_PKA_2 | 426 | 432 | PF00069 | 0.445 |
MOD_PKA_2 | 56 | 62 | PF00069 | 0.527 |
MOD_Plk_1 | 132 | 138 | PF00069 | 0.512 |
MOD_Plk_1 | 294 | 300 | PF00069 | 0.564 |
MOD_Plk_1 | 513 | 519 | PF00069 | 0.758 |
MOD_Plk_2-3 | 490 | 496 | PF00069 | 0.655 |
MOD_Plk_4 | 114 | 120 | PF00069 | 0.547 |
MOD_Plk_4 | 138 | 144 | PF00069 | 0.491 |
MOD_Plk_4 | 164 | 170 | PF00069 | 0.462 |
MOD_Plk_4 | 204 | 210 | PF00069 | 0.460 |
MOD_Plk_4 | 255 | 261 | PF00069 | 0.541 |
MOD_Plk_4 | 348 | 354 | PF00069 | 0.399 |
MOD_Plk_4 | 374 | 380 | PF00069 | 0.445 |
MOD_Plk_4 | 460 | 466 | PF00069 | 0.520 |
MOD_Plk_4 | 56 | 62 | PF00069 | 0.562 |
MOD_ProDKin_1 | 22 | 28 | PF00069 | 0.553 |
MOD_ProDKin_1 | 311 | 317 | PF00069 | 0.608 |
MOD_ProDKin_1 | 483 | 489 | PF00069 | 0.615 |
MOD_SUMO_for_1 | 292 | 295 | PF00179 | 0.624 |
TRG_DiLeu_BaEn_1 | 394 | 399 | PF01217 | 0.533 |
TRG_DiLeu_BaEn_1 | 77 | 82 | PF01217 | 0.706 |
TRG_DiLeu_BaLyEn_6 | 182 | 187 | PF01217 | 0.469 |
TRG_ENDOCYTIC_2 | 188 | 191 | PF00928 | 0.435 |
TRG_ENDOCYTIC_2 | 202 | 205 | PF00928 | 0.310 |
TRG_ENDOCYTIC_2 | 299 | 302 | PF00928 | 0.557 |
TRG_ENDOCYTIC_2 | 382 | 385 | PF00928 | 0.485 |
TRG_ER_diArg_1 | 12 | 14 | PF00400 | 0.718 |
TRG_ER_diArg_1 | 127 | 129 | PF00400 | 0.579 |
TRG_ER_diArg_1 | 453 | 456 | PF00400 | 0.479 |
TRG_NES_CRM1_1 | 37 | 51 | PF08389 | 0.559 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZ13 | Leptomonas seymouri | 55% | 100% |
A0A3R7L246 | Trypanosoma rangeli | 24% | 100% |
A0A3S7X131 | Leishmania donovani | 99% | 100% |
A4HG50 | Leishmania braziliensis | 72% | 100% |
E9AZG8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
Q4Q8R3 | Leishmania major | 87% | 100% |
V5BGK7 | Trypanosoma cruzi | 24% | 100% |