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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: E9B487
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 541 | 545 | PF00656 | 0.561 |
CLV_NRD_NRD_1 | 171 | 173 | PF00675 | 0.516 |
CLV_NRD_NRD_1 | 29 | 31 | PF00675 | 0.532 |
CLV_NRD_NRD_1 | 485 | 487 | PF00675 | 0.533 |
CLV_NRD_NRD_1 | 568 | 570 | PF00675 | 0.363 |
CLV_PCSK_FUR_1 | 11 | 15 | PF00082 | 0.679 |
CLV_PCSK_KEX2_1 | 13 | 15 | PF00082 | 0.738 |
CLV_PCSK_KEX2_1 | 171 | 173 | PF00082 | 0.456 |
CLV_PCSK_KEX2_1 | 29 | 31 | PF00082 | 0.440 |
CLV_PCSK_KEX2_1 | 372 | 374 | PF00082 | 0.617 |
CLV_PCSK_KEX2_1 | 484 | 486 | PF00082 | 0.555 |
CLV_PCSK_PC1ET2_1 | 13 | 15 | PF00082 | 0.679 |
CLV_PCSK_PC1ET2_1 | 372 | 374 | PF00082 | 0.617 |
CLV_PCSK_SKI1_1 | 339 | 343 | PF00082 | 0.490 |
CLV_PCSK_SKI1_1 | 583 | 587 | PF00082 | 0.706 |
CLV_PCSK_SKI1_1 | 99 | 103 | PF00082 | 0.468 |
DEG_SCF_FBW7_2 | 326 | 331 | PF00400 | 0.513 |
DEG_SPOP_SBC_1 | 69 | 73 | PF00917 | 0.569 |
DOC_CYCLIN_yCln2_LP_2 | 116 | 122 | PF00134 | 0.631 |
DOC_MAPK_RevD_3 | 473 | 486 | PF00069 | 0.408 |
DOC_PP1_RVXF_1 | 337 | 344 | PF00149 | 0.613 |
DOC_SPAK_OSR1_1 | 472 | 476 | PF12202 | 0.443 |
DOC_USP7_MATH_1 | 134 | 138 | PF00917 | 0.720 |
DOC_USP7_MATH_1 | 154 | 158 | PF00917 | 0.656 |
DOC_USP7_MATH_1 | 371 | 375 | PF00917 | 0.673 |
DOC_USP7_MATH_1 | 510 | 514 | PF00917 | 0.715 |
DOC_USP7_MATH_1 | 516 | 520 | PF00917 | 0.714 |
DOC_USP7_MATH_1 | 538 | 542 | PF00917 | 0.629 |
DOC_USP7_MATH_1 | 69 | 73 | PF00917 | 0.609 |
DOC_USP7_MATH_1 | 7 | 11 | PF00917 | 0.600 |
DOC_USP7_MATH_2 | 256 | 262 | PF00917 | 0.508 |
DOC_WW_Pin1_4 | 208 | 213 | PF00397 | 0.511 |
DOC_WW_Pin1_4 | 324 | 329 | PF00397 | 0.704 |
DOC_WW_Pin1_4 | 388 | 393 | PF00397 | 0.663 |
DOC_WW_Pin1_4 | 404 | 409 | PF00397 | 0.500 |
LIG_14-3-3_CanoR_1 | 29 | 33 | PF00244 | 0.593 |
LIG_14-3-3_CanoR_1 | 300 | 306 | PF00244 | 0.623 |
LIG_14-3-3_CanoR_1 | 363 | 368 | PF00244 | 0.502 |
LIG_14-3-3_CanoR_1 | 373 | 378 | PF00244 | 0.602 |
LIG_14-3-3_CanoR_1 | 456 | 462 | PF00244 | 0.576 |
LIG_14-3-3_CanoR_1 | 484 | 492 | PF00244 | 0.586 |
LIG_14-3-3_CanoR_1 | 68 | 75 | PF00244 | 0.551 |
LIG_14-3-3_CanoR_1 | 93 | 101 | PF00244 | 0.499 |
LIG_BRCT_BRCA1_1 | 176 | 180 | PF00533 | 0.534 |
LIG_EVH1_1 | 575 | 579 | PF00568 | 0.699 |
LIG_FHA_1 | 148 | 154 | PF00498 | 0.656 |
LIG_FHA_1 | 209 | 215 | PF00498 | 0.552 |
LIG_FHA_1 | 31 | 37 | PF00498 | 0.559 |
LIG_FHA_1 | 385 | 391 | PF00498 | 0.661 |
LIG_FHA_1 | 41 | 47 | PF00498 | 0.542 |
LIG_FHA_1 | 412 | 418 | PF00498 | 0.552 |
LIG_FHA_1 | 547 | 553 | PF00498 | 0.644 |
LIG_FHA_1 | 554 | 560 | PF00498 | 0.500 |
LIG_FHA_1 | 77 | 83 | PF00498 | 0.513 |
LIG_FHA_2 | 310 | 316 | PF00498 | 0.700 |
LIG_FHA_2 | 47 | 53 | PF00498 | 0.396 |
LIG_LIR_Apic_2 | 574 | 578 | PF02991 | 0.604 |
LIG_LIR_Gen_1 | 177 | 187 | PF02991 | 0.469 |
LIG_LIR_Gen_1 | 414 | 424 | PF02991 | 0.513 |
LIG_LIR_Gen_1 | 426 | 436 | PF02991 | 0.487 |
LIG_LIR_Gen_1 | 49 | 55 | PF02991 | 0.607 |
LIG_LIR_Nem_3 | 177 | 183 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 414 | 419 | PF02991 | 0.518 |
LIG_LIR_Nem_3 | 426 | 432 | PF02991 | 0.489 |
LIG_LIR_Nem_3 | 49 | 53 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 547 | 553 | PF02991 | 0.599 |
LIG_LIR_Nem_3 | 55 | 60 | PF02991 | 0.515 |
LIG_MYND_1 | 271 | 275 | PF01753 | 0.481 |
LIG_NRBOX | 473 | 479 | PF00104 | 0.461 |
LIG_PCNA_APIM_2 | 470 | 476 | PF02747 | 0.441 |
LIG_PCNA_PIPBox_1 | 467 | 476 | PF02747 | 0.555 |
LIG_PCNA_yPIPBox_3 | 467 | 476 | PF02747 | 0.555 |
LIG_Pex14_1 | 176 | 180 | PF04695 | 0.534 |
LIG_Pex14_2 | 202 | 206 | PF04695 | 0.595 |
LIG_SH2_CRK | 243 | 247 | PF00017 | 0.463 |
LIG_SH2_CRK | 429 | 433 | PF00017 | 0.540 |
LIG_SH2_NCK_1 | 243 | 247 | PF00017 | 0.608 |
LIG_SH2_NCK_1 | 358 | 362 | PF00017 | 0.338 |
LIG_SH2_NCK_1 | 429 | 433 | PF00017 | 0.540 |
LIG_SH2_STAP1 | 243 | 247 | PF00017 | 0.515 |
LIG_SH2_STAP1 | 32 | 36 | PF00017 | 0.568 |
LIG_SH2_STAP1 | 351 | 355 | PF00017 | 0.484 |
LIG_SH2_STAP1 | 358 | 362 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 163 | 166 | PF00017 | 0.515 |
LIG_SH2_STAT5 | 301 | 304 | PF00017 | 0.603 |
LIG_SH2_STAT5 | 32 | 35 | PF00017 | 0.564 |
LIG_SH2_STAT5 | 358 | 361 | PF00017 | 0.499 |
LIG_SH2_STAT5 | 64 | 67 | PF00017 | 0.654 |
LIG_SH3_3 | 116 | 122 | PF00018 | 0.747 |
LIG_SH3_3 | 268 | 274 | PF00018 | 0.489 |
LIG_SH3_3 | 386 | 392 | PF00018 | 0.658 |
LIG_SH3_3 | 495 | 501 | PF00018 | 0.666 |
LIG_SH3_3 | 573 | 579 | PF00018 | 0.711 |
LIG_SUMO_SIM_anti_2 | 186 | 191 | PF11976 | 0.491 |
LIG_SUMO_SIM_par_1 | 363 | 370 | PF11976 | 0.603 |
LIG_SxIP_EBH_1 | 508 | 521 | PF03271 | 0.581 |
LIG_TRAF2_1 | 376 | 379 | PF00917 | 0.768 |
LIG_TYR_ITIM | 241 | 246 | PF00017 | 0.694 |
MOD_CK1_1 | 110 | 116 | PF00069 | 0.677 |
MOD_CK1_1 | 142 | 148 | PF00069 | 0.688 |
MOD_CK1_1 | 391 | 397 | PF00069 | 0.744 |
MOD_CK1_1 | 457 | 463 | PF00069 | 0.605 |
MOD_CK2_1 | 233 | 239 | PF00069 | 0.576 |
MOD_CK2_1 | 363 | 369 | PF00069 | 0.549 |
MOD_CK2_1 | 373 | 379 | PF00069 | 0.537 |
MOD_CK2_1 | 530 | 536 | PF00069 | 0.490 |
MOD_CK2_1 | 70 | 76 | PF00069 | 0.634 |
MOD_CK2_1 | 86 | 92 | PF00069 | 0.399 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.601 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.749 |
MOD_GlcNHglycan | 190 | 193 | PF01048 | 0.527 |
MOD_GlcNHglycan | 228 | 231 | PF01048 | 0.685 |
MOD_GlcNHglycan | 260 | 263 | PF01048 | 0.569 |
MOD_GlcNHglycan | 333 | 336 | PF01048 | 0.687 |
MOD_GlcNHglycan | 359 | 362 | PF01048 | 0.513 |
MOD_GlcNHglycan | 393 | 396 | PF01048 | 0.544 |
MOD_GlcNHglycan | 450 | 453 | PF01048 | 0.703 |
MOD_GlcNHglycan | 512 | 515 | PF01048 | 0.663 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.582 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.658 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.495 |
MOD_GSK3_1 | 254 | 261 | PF00069 | 0.569 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.552 |
MOD_GSK3_1 | 295 | 302 | PF00069 | 0.492 |
MOD_GSK3_1 | 326 | 333 | PF00069 | 0.603 |
MOD_GSK3_1 | 363 | 370 | PF00069 | 0.622 |
MOD_GSK3_1 | 384 | 391 | PF00069 | 0.700 |
MOD_GSK3_1 | 527 | 534 | PF00069 | 0.734 |
MOD_GSK3_1 | 538 | 545 | PF00069 | 0.651 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.501 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.583 |
MOD_LATS_1 | 66 | 72 | PF00433 | 0.701 |
MOD_N-GLC_1 | 142 | 147 | PF02516 | 0.478 |
MOD_NEK2_1 | 190 | 195 | PF00069 | 0.493 |
MOD_NEK2_1 | 233 | 238 | PF00069 | 0.677 |
MOD_NEK2_1 | 242 | 247 | PF00069 | 0.528 |
MOD_NEK2_1 | 28 | 33 | PF00069 | 0.560 |
MOD_NEK2_1 | 349 | 354 | PF00069 | 0.453 |
MOD_NEK2_1 | 553 | 558 | PF00069 | 0.503 |
MOD_NEK2_1 | 559 | 564 | PF00069 | 0.458 |
MOD_NEK2_2 | 295 | 300 | PF00069 | 0.470 |
MOD_NEK2_2 | 548 | 553 | PF00069 | 0.374 |
MOD_PIKK_1 | 446 | 452 | PF00454 | 0.515 |
MOD_PIKK_1 | 538 | 544 | PF00454 | 0.735 |
MOD_PIKK_1 | 553 | 559 | PF00454 | 0.264 |
MOD_PIKK_1 | 70 | 76 | PF00454 | 0.469 |
MOD_PIKK_1 | 93 | 99 | PF00454 | 0.484 |
MOD_PK_1 | 363 | 369 | PF00069 | 0.549 |
MOD_PK_1 | 373 | 379 | PF00069 | 0.537 |
MOD_PKA_1 | 485 | 491 | PF00069 | 0.493 |
MOD_PKA_2 | 110 | 116 | PF00069 | 0.574 |
MOD_PKA_2 | 28 | 34 | PF00069 | 0.599 |
MOD_PKA_2 | 299 | 305 | PF00069 | 0.616 |
MOD_PKA_2 | 40 | 46 | PF00069 | 0.488 |
MOD_PKA_2 | 446 | 452 | PF00069 | 0.706 |
MOD_PKA_2 | 455 | 461 | PF00069 | 0.552 |
MOD_PKA_2 | 485 | 491 | PF00069 | 0.493 |
MOD_Plk_2-3 | 76 | 82 | PF00069 | 0.487 |
MOD_Plk_4 | 179 | 185 | PF00069 | 0.250 |
MOD_Plk_4 | 349 | 355 | PF00069 | 0.424 |
MOD_Plk_4 | 363 | 369 | PF00069 | 0.539 |
MOD_Plk_4 | 411 | 417 | PF00069 | 0.487 |
MOD_ProDKin_1 | 208 | 214 | PF00069 | 0.515 |
MOD_ProDKin_1 | 324 | 330 | PF00069 | 0.701 |
MOD_ProDKin_1 | 388 | 394 | PF00069 | 0.663 |
MOD_ProDKin_1 | 404 | 410 | PF00069 | 0.492 |
MOD_SUMO_for_1 | 101 | 104 | PF00179 | 0.465 |
MOD_SUMO_for_1 | 321 | 324 | PF00179 | 0.758 |
TRG_DiLeu_BaEn_1 | 221 | 226 | PF01217 | 0.479 |
TRG_DiLeu_BaLyEn_6 | 360 | 365 | PF01217 | 0.515 |
TRG_DiLeu_BaLyEn_6 | 473 | 478 | PF01217 | 0.458 |
TRG_ENDOCYTIC_2 | 243 | 246 | PF00928 | 0.544 |
TRG_ENDOCYTIC_2 | 351 | 354 | PF00928 | 0.473 |
TRG_ENDOCYTIC_2 | 429 | 432 | PF00928 | 0.490 |
TRG_ER_diArg_1 | 171 | 173 | PF00400 | 0.456 |
TRG_ER_diArg_1 | 28 | 30 | PF00400 | 0.523 |
TRG_ER_diArg_1 | 483 | 486 | PF00400 | 0.552 |
TRG_ER_diArg_1 | 521 | 524 | PF00400 | 0.761 |
TRG_Pf-PMV_PEXEL_1 | 476 | 480 | PF00026 | 0.472 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8S0 | Leptomonas seymouri | 36% | 99% |
A0A3S7X715 | Leishmania donovani | 80% | 100% |
A4HLV9 | Leishmania braziliensis | 62% | 99% |
E9AHR6 | Leishmania infantum | 81% | 100% |
Q4Q3T9 | Leishmania major | 82% | 100% |