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: E9B3Y7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 235 | 239 | PF00656 | 0.381 |
CLV_C14_Caspase3-7 | 421 | 425 | PF00656 | 0.443 |
CLV_C14_Caspase3-7 | 468 | 472 | PF00656 | 0.392 |
CLV_NRD_NRD_1 | 181 | 183 | PF00675 | 0.506 |
CLV_NRD_NRD_1 | 214 | 216 | PF00675 | 0.570 |
CLV_NRD_NRD_1 | 309 | 311 | PF00675 | 0.579 |
CLV_NRD_NRD_1 | 333 | 335 | PF00675 | 0.431 |
CLV_NRD_NRD_1 | 438 | 440 | PF00675 | 0.447 |
CLV_PCSK_KEX2_1 | 180 | 182 | PF00082 | 0.507 |
CLV_PCSK_KEX2_1 | 213 | 215 | PF00082 | 0.563 |
CLV_PCSK_KEX2_1 | 309 | 311 | PF00082 | 0.583 |
CLV_PCSK_KEX2_1 | 333 | 335 | PF00082 | 0.431 |
CLV_PCSK_PC1ET2_1 | 180 | 182 | PF00082 | 0.507 |
CLV_PCSK_PC7_1 | 176 | 182 | PF00082 | 0.509 |
CLV_PCSK_SKI1_1 | 131 | 135 | PF00082 | 0.649 |
CLV_PCSK_SKI1_1 | 150 | 154 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 181 | 185 | PF00082 | 0.544 |
CLV_PCSK_SKI1_1 | 326 | 330 | PF00082 | 0.557 |
CLV_PCSK_SKI1_1 | 503 | 507 | PF00082 | 0.419 |
CLV_Separin_Metazoa | 210 | 214 | PF03568 | 0.545 |
CLV_Separin_Metazoa | 436 | 440 | PF03568 | 0.450 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.504 |
DEG_SPOP_SBC_1 | 481 | 485 | PF00917 | 0.648 |
DOC_CDC14_PxL_1 | 156 | 164 | PF14671 | 0.573 |
DOC_CYCLIN_RxL_1 | 339 | 350 | PF00134 | 0.453 |
DOC_CYCLIN_RxL_1 | 368 | 378 | PF00134 | 0.398 |
DOC_MAPK_gen_1 | 372 | 381 | PF00069 | 0.410 |
DOC_MAPK_MEF2A_6 | 2 | 9 | PF00069 | 0.468 |
DOC_MAPK_MEF2A_6 | 375 | 383 | PF00069 | 0.401 |
DOC_PP2B_LxvP_1 | 25 | 28 | PF13499 | 0.581 |
DOC_USP7_MATH_1 | 107 | 111 | PF00917 | 0.622 |
DOC_USP7_MATH_1 | 126 | 130 | PF00917 | 0.492 |
DOC_USP7_MATH_1 | 187 | 191 | PF00917 | 0.574 |
DOC_USP7_MATH_1 | 28 | 32 | PF00917 | 0.717 |
DOC_USP7_MATH_1 | 42 | 46 | PF00917 | 0.485 |
DOC_USP7_MATH_1 | 482 | 486 | PF00917 | 0.652 |
DOC_USP7_MATH_1 | 596 | 600 | PF00917 | 0.543 |
DOC_USP7_MATH_1 | 88 | 92 | PF00917 | 0.471 |
DOC_USP7_MATH_2 | 312 | 318 | PF00917 | 0.439 |
DOC_WW_Pin1_4 | 165 | 170 | PF00397 | 0.563 |
DOC_WW_Pin1_4 | 181 | 186 | PF00397 | 0.577 |
DOC_WW_Pin1_4 | 355 | 360 | PF00397 | 0.641 |
DOC_WW_Pin1_4 | 361 | 366 | PF00397 | 0.509 |
DOC_WW_Pin1_4 | 408 | 413 | PF00397 | 0.388 |
DOC_WW_Pin1_4 | 556 | 561 | PF00397 | 0.610 |
LIG_14-3-3_CanoR_1 | 125 | 133 | PF00244 | 0.643 |
LIG_14-3-3_CanoR_1 | 213 | 221 | PF00244 | 0.613 |
LIG_14-3-3_CanoR_1 | 242 | 251 | PF00244 | 0.557 |
LIG_14-3-3_CanoR_1 | 368 | 376 | PF00244 | 0.510 |
LIG_14-3-3_CanoR_1 | 390 | 400 | PF00244 | 0.442 |
LIG_14-3-3_CanoR_1 | 56 | 62 | PF00244 | 0.518 |
LIG_14-3-3_CanoR_1 | 577 | 586 | PF00244 | 0.596 |
LIG_14-3-3_CanoR_1 | 86 | 94 | PF00244 | 0.457 |
LIG_Actin_WH2_2 | 226 | 244 | PF00022 | 0.460 |
LIG_Actin_WH2_2 | 452 | 467 | PF00022 | 0.370 |
LIG_Actin_WH2_2 | 517 | 533 | PF00022 | 0.403 |
LIG_APCC_ABBA_1 | 5 | 10 | PF00400 | 0.454 |
LIG_APCC_ABBA_1 | 506 | 511 | PF00400 | 0.378 |
LIG_BRCT_BRCA1_1 | 51 | 55 | PF00533 | 0.493 |
LIG_CtBP_PxDLS_1 | 560 | 564 | PF00389 | 0.567 |
LIG_deltaCOP1_diTrp_1 | 501 | 509 | PF00928 | 0.459 |
LIG_FHA_1 | 195 | 201 | PF00498 | 0.502 |
LIG_FHA_1 | 216 | 222 | PF00498 | 0.455 |
LIG_FHA_1 | 286 | 292 | PF00498 | 0.524 |
LIG_FHA_1 | 320 | 326 | PF00498 | 0.385 |
LIG_FHA_1 | 341 | 347 | PF00498 | 0.470 |
LIG_FHA_1 | 368 | 374 | PF00498 | 0.438 |
LIG_FHA_1 | 4 | 10 | PF00498 | 0.459 |
LIG_FHA_2 | 166 | 172 | PF00498 | 0.776 |
LIG_FHA_2 | 196 | 202 | PF00498 | 0.466 |
LIG_FHA_2 | 261 | 267 | PF00498 | 0.607 |
LIG_FHA_2 | 419 | 425 | PF00498 | 0.439 |
LIG_FHA_2 | 466 | 472 | PF00498 | 0.480 |
LIG_FHA_2 | 578 | 584 | PF00498 | 0.690 |
LIG_IBAR_NPY_1 | 87 | 89 | PF08397 | 0.432 |
LIG_Integrin_isoDGR_2 | 569 | 571 | PF01839 | 0.535 |
LIG_LIR_Apic_2 | 583 | 589 | PF02991 | 0.608 |
LIG_LIR_Gen_1 | 151 | 161 | PF02991 | 0.539 |
LIG_LIR_Gen_1 | 270 | 280 | PF02991 | 0.536 |
LIG_LIR_Gen_1 | 427 | 433 | PF02991 | 0.300 |
LIG_LIR_Nem_3 | 151 | 156 | PF02991 | 0.508 |
LIG_LIR_Nem_3 | 270 | 276 | PF02991 | 0.562 |
LIG_LIR_Nem_3 | 427 | 431 | PF02991 | 0.295 |
LIG_LYPXL_yS_3 | 447 | 450 | PF13949 | 0.390 |
LIG_NRBOX | 286 | 292 | PF00104 | 0.441 |
LIG_NRBOX | 324 | 330 | PF00104 | 0.460 |
LIG_PCNA_PIPBox_1 | 1 | 10 | PF02747 | 0.535 |
LIG_Pex14_2 | 494 | 498 | PF04695 | 0.442 |
LIG_RPA_C_Plants | 315 | 326 | PF08784 | 0.307 |
LIG_SH2_CRK | 273 | 277 | PF00017 | 0.499 |
LIG_SH2_CRK | 428 | 432 | PF00017 | 0.368 |
LIG_SH2_NCK_1 | 273 | 277 | PF00017 | 0.544 |
LIG_SH2_NCK_1 | 89 | 93 | PF00017 | 0.452 |
LIG_SH2_SRC | 101 | 104 | PF00017 | 0.480 |
LIG_SH2_STAP1 | 273 | 277 | PF00017 | 0.544 |
LIG_SH2_STAP1 | 428 | 432 | PF00017 | 0.408 |
LIG_SH2_STAP1 | 89 | 93 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 458 | 461 | PF00017 | 0.356 |
LIG_SH2_STAT5 | 93 | 96 | PF00017 | 0.438 |
LIG_SH3_3 | 120 | 126 | PF00018 | 0.569 |
LIG_SH3_3 | 261 | 267 | PF00018 | 0.742 |
LIG_Sin3_3 | 70 | 77 | PF02671 | 0.491 |
LIG_SUMO_SIM_anti_2 | 343 | 348 | PF11976 | 0.445 |
LIG_SUMO_SIM_par_1 | 218 | 224 | PF11976 | 0.443 |
LIG_TRAF2_1 | 169 | 172 | PF00917 | 0.749 |
LIG_TYR_ITIM | 445 | 450 | PF00017 | 0.462 |
MOD_CDK_SPxxK_3 | 361 | 368 | PF00069 | 0.565 |
MOD_CK1_1 | 110 | 116 | PF00069 | 0.561 |
MOD_CK1_1 | 33 | 39 | PF00069 | 0.655 |
MOD_CK1_1 | 350 | 356 | PF00069 | 0.701 |
MOD_CK1_1 | 367 | 373 | PF00069 | 0.378 |
MOD_CK1_1 | 41 | 47 | PF00069 | 0.632 |
MOD_CK1_1 | 556 | 562 | PF00069 | 0.663 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.501 |
MOD_CK2_1 | 165 | 171 | PF00069 | 0.778 |
MOD_CK2_1 | 186 | 192 | PF00069 | 0.711 |
MOD_CK2_1 | 195 | 201 | PF00069 | 0.468 |
MOD_CK2_1 | 254 | 260 | PF00069 | 0.585 |
MOD_CK2_1 | 577 | 583 | PF00069 | 0.747 |
MOD_DYRK1A_RPxSP_1 | 165 | 169 | PF00069 | 0.486 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.491 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.509 |
MOD_GlcNHglycan | 157 | 160 | PF01048 | 0.705 |
MOD_GlcNHglycan | 22 | 25 | PF01048 | 0.551 |
MOD_GlcNHglycan | 316 | 319 | PF01048 | 0.575 |
MOD_GlcNHglycan | 349 | 352 | PF01048 | 0.692 |
MOD_GlcNHglycan | 40 | 43 | PF01048 | 0.711 |
MOD_GlcNHglycan | 412 | 415 | PF01048 | 0.386 |
MOD_GlcNHglycan | 484 | 487 | PF01048 | 0.648 |
MOD_GlcNHglycan | 503 | 506 | PF01048 | 0.453 |
MOD_GlcNHglycan | 594 | 597 | PF01048 | 0.602 |
MOD_GlcNHglycan | 598 | 601 | PF01048 | 0.662 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.450 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.473 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.621 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.627 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.639 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.726 |
MOD_GSK3_1 | 355 | 362 | PF00069 | 0.599 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.605 |
MOD_GSK3_1 | 454 | 461 | PF00069 | 0.392 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.503 |
MOD_GSK3_1 | 592 | 599 | PF00069 | 0.532 |
MOD_LATS_1 | 452 | 458 | PF00433 | 0.367 |
MOD_N-GLC_1 | 260 | 265 | PF02516 | 0.766 |
MOD_N-GLC_1 | 33 | 38 | PF02516 | 0.532 |
MOD_N-GLC_1 | 465 | 470 | PF02516 | 0.452 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.554 |
MOD_NEK2_1 | 340 | 345 | PF00069 | 0.433 |
MOD_NEK2_1 | 418 | 423 | PF00069 | 0.429 |
MOD_NEK2_1 | 464 | 469 | PF00069 | 0.390 |
MOD_NEK2_1 | 55 | 60 | PF00069 | 0.581 |
MOD_NEK2_1 | 553 | 558 | PF00069 | 0.628 |
MOD_PIKK_1 | 28 | 34 | PF00454 | 0.640 |
MOD_PIKK_1 | 602 | 608 | PF00454 | 0.508 |
MOD_PK_1 | 375 | 381 | PF00069 | 0.448 |
MOD_PKA_1 | 213 | 219 | PF00069 | 0.590 |
MOD_PKA_2 | 124 | 130 | PF00069 | 0.661 |
MOD_PKA_2 | 213 | 219 | PF00069 | 0.609 |
MOD_PKA_2 | 28 | 34 | PF00069 | 0.595 |
MOD_PKA_2 | 295 | 301 | PF00069 | 0.421 |
MOD_PKA_2 | 314 | 320 | PF00069 | 0.553 |
MOD_PKA_2 | 367 | 373 | PF00069 | 0.531 |
MOD_PKA_2 | 464 | 470 | PF00069 | 0.425 |
MOD_PKA_2 | 496 | 502 | PF00069 | 0.523 |
MOD_PKA_2 | 55 | 61 | PF00069 | 0.570 |
MOD_PKA_2 | 592 | 598 | PF00069 | 0.549 |
MOD_PKB_1 | 213 | 221 | PF00069 | 0.593 |
MOD_PKB_1 | 575 | 583 | PF00069 | 0.578 |
MOD_Plk_1 | 138 | 144 | PF00069 | 0.540 |
MOD_Plk_1 | 260 | 266 | PF00069 | 0.588 |
MOD_Plk_1 | 9 | 15 | PF00069 | 0.450 |
MOD_Plk_2-3 | 138 | 144 | PF00069 | 0.576 |
MOD_Plk_2-3 | 260 | 266 | PF00069 | 0.532 |
MOD_Plk_4 | 268 | 274 | PF00069 | 0.512 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.500 |
MOD_Plk_4 | 375 | 381 | PF00069 | 0.431 |
MOD_Plk_4 | 427 | 433 | PF00069 | 0.378 |
MOD_Plk_4 | 454 | 460 | PF00069 | 0.342 |
MOD_Plk_4 | 613 | 619 | PF00069 | 0.428 |
MOD_ProDKin_1 | 165 | 171 | PF00069 | 0.566 |
MOD_ProDKin_1 | 181 | 187 | PF00069 | 0.574 |
MOD_ProDKin_1 | 355 | 361 | PF00069 | 0.625 |
MOD_ProDKin_1 | 408 | 414 | PF00069 | 0.384 |
MOD_ProDKin_1 | 556 | 562 | PF00069 | 0.615 |
MOD_SUMO_for_1 | 14 | 17 | PF00179 | 0.471 |
TRG_DiLeu_BaEn_1 | 336 | 341 | PF01217 | 0.447 |
TRG_DiLeu_BaLyEn_6 | 414 | 419 | PF01217 | 0.270 |
TRG_DiLeu_BaLyEn_6 | 445 | 450 | PF01217 | 0.401 |
TRG_DiLeu_BaLyEn_6 | 525 | 530 | PF01217 | 0.376 |
TRG_ENDOCYTIC_2 | 101 | 104 | PF00928 | 0.418 |
TRG_ENDOCYTIC_2 | 273 | 276 | PF00928 | 0.569 |
TRG_ENDOCYTIC_2 | 428 | 431 | PF00928 | 0.405 |
TRG_ENDOCYTIC_2 | 447 | 450 | PF00928 | 0.271 |
TRG_ER_diArg_1 | 181 | 183 | PF00400 | 0.511 |
TRG_ER_diArg_1 | 212 | 215 | PF00400 | 0.578 |
TRG_ER_diArg_1 | 308 | 310 | PF00400 | 0.501 |
TRG_ER_diArg_1 | 491 | 494 | PF00400 | 0.536 |
TRG_ER_diArg_1 | 575 | 578 | PF00400 | 0.577 |
TRG_Pf-PMV_PEXEL_1 | 242 | 246 | PF00026 | 0.535 |
TRG_Pf-PMV_PEXEL_1 | 372 | 377 | PF00026 | 0.431 |
TRG_Pf-PMV_PEXEL_1 | 528 | 532 | PF00026 | 0.397 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P490 | Leptomonas seymouri | 36% | 100% |
A0A3Q8IGM0 | Leishmania donovani | 85% | 100% |
A4HLL1 | Leishmania braziliensis | 71% | 98% |
A4I923 | Leishmania infantum | 85% | 100% |
Q4Q437 | Leishmania major | 85% | 100% |