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: 1, no: 5 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: A4HS06
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 278 | 282 | PF00656 | 0.498 |
CLV_C14_Caspase3-7 | 510 | 514 | PF00656 | 0.728 |
CLV_NRD_NRD_1 | 11 | 13 | PF00675 | 0.492 |
CLV_NRD_NRD_1 | 20 | 22 | PF00675 | 0.367 |
CLV_NRD_NRD_1 | 432 | 434 | PF00675 | 0.379 |
CLV_NRD_NRD_1 | 50 | 52 | PF00675 | 0.647 |
CLV_NRD_NRD_1 | 539 | 541 | PF00675 | 0.525 |
CLV_NRD_NRD_1 | 562 | 564 | PF00675 | 0.545 |
CLV_NRD_NRD_1 | 574 | 576 | PF00675 | 0.512 |
CLV_PCSK_FUR_1 | 430 | 434 | PF00082 | 0.372 |
CLV_PCSK_FUR_1 | 560 | 564 | PF00082 | 0.544 |
CLV_PCSK_KEX2_1 | 102 | 104 | PF00082 | 0.556 |
CLV_PCSK_KEX2_1 | 11 | 13 | PF00082 | 0.493 |
CLV_PCSK_KEX2_1 | 19 | 21 | PF00082 | 0.489 |
CLV_PCSK_KEX2_1 | 311 | 313 | PF00082 | 0.691 |
CLV_PCSK_KEX2_1 | 430 | 432 | PF00082 | 0.370 |
CLV_PCSK_KEX2_1 | 49 | 51 | PF00082 | 0.654 |
CLV_PCSK_KEX2_1 | 541 | 543 | PF00082 | 0.524 |
CLV_PCSK_KEX2_1 | 562 | 564 | PF00082 | 0.588 |
CLV_PCSK_KEX2_1 | 574 | 576 | PF00082 | 0.529 |
CLV_PCSK_PC1ET2_1 | 102 | 104 | PF00082 | 0.551 |
CLV_PCSK_PC1ET2_1 | 311 | 313 | PF00082 | 0.691 |
CLV_PCSK_PC1ET2_1 | 541 | 543 | PF00082 | 0.496 |
CLV_PCSK_SKI1_1 | 124 | 128 | PF00082 | 0.524 |
CLV_PCSK_SKI1_1 | 20 | 24 | PF00082 | 0.365 |
CLV_PCSK_SKI1_1 | 395 | 399 | PF00082 | 0.680 |
CLV_PCSK_SKI1_1 | 544 | 548 | PF00082 | 0.598 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.718 |
DEG_SPOP_SBC_1 | 507 | 511 | PF00917 | 0.729 |
DOC_CYCLIN_RxL_1 | 392 | 402 | PF00134 | 0.466 |
DOC_MAPK_gen_1 | 19 | 25 | PF00069 | 0.506 |
DOC_MAPK_gen_1 | 431 | 442 | PF00069 | 0.593 |
DOC_MAPK_MEF2A_6 | 122 | 129 | PF00069 | 0.344 |
DOC_MAPK_NFAT4_5 | 122 | 130 | PF00069 | 0.332 |
DOC_PP2B_LxvP_1 | 525 | 528 | PF13499 | 0.642 |
DOC_USP7_MATH_1 | 140 | 144 | PF00917 | 0.452 |
DOC_USP7_MATH_1 | 244 | 248 | PF00917 | 0.464 |
DOC_USP7_MATH_1 | 262 | 266 | PF00917 | 0.412 |
DOC_USP7_MATH_1 | 298 | 302 | PF00917 | 0.403 |
DOC_USP7_MATH_1 | 403 | 407 | PF00917 | 0.453 |
DOC_USP7_MATH_1 | 481 | 485 | PF00917 | 0.775 |
DOC_USP7_MATH_1 | 512 | 516 | PF00917 | 0.772 |
DOC_USP7_MATH_2 | 528 | 534 | PF00917 | 0.782 |
DOC_WW_Pin1_4 | 421 | 426 | PF00397 | 0.604 |
DOC_WW_Pin1_4 | 496 | 501 | PF00397 | 0.693 |
DOC_WW_Pin1_4 | 534 | 539 | PF00397 | 0.785 |
DOC_WW_Pin1_4 | 66 | 71 | PF00397 | 0.496 |
DOC_WW_Pin1_4 | 95 | 100 | PF00397 | 0.463 |
LIG_14-3-3_CanoR_1 | 212 | 220 | PF00244 | 0.494 |
LIG_14-3-3_CanoR_1 | 275 | 284 | PF00244 | 0.438 |
LIG_14-3-3_CanoR_1 | 370 | 376 | PF00244 | 0.453 |
LIG_Actin_WH2_2 | 259 | 277 | PF00022 | 0.408 |
LIG_CSL_BTD_1 | 490 | 493 | PF09270 | 0.704 |
LIG_EVH1_2 | 70 | 74 | PF00568 | 0.457 |
LIG_FHA_1 | 29 | 35 | PF00498 | 0.437 |
LIG_FHA_1 | 318 | 324 | PF00498 | 0.413 |
LIG_FHA_2 | 400 | 406 | PF00498 | 0.341 |
LIG_FHA_2 | 422 | 428 | PF00498 | 0.592 |
LIG_FHA_2 | 508 | 514 | PF00498 | 0.762 |
LIG_FHA_2 | 545 | 551 | PF00498 | 0.760 |
LIG_LIR_Gen_1 | 170 | 181 | PF02991 | 0.341 |
LIG_LIR_Gen_1 | 401 | 412 | PF02991 | 0.327 |
LIG_LIR_Nem_3 | 170 | 176 | PF02991 | 0.342 |
LIG_LIR_Nem_3 | 308 | 313 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 401 | 407 | PF02991 | 0.327 |
LIG_MYND_1 | 71 | 75 | PF01753 | 0.571 |
LIG_NRBOX | 332 | 338 | PF00104 | 0.553 |
LIG_SH2_STAP1 | 173 | 177 | PF00017 | 0.336 |
LIG_SH2_STAT3 | 460 | 463 | PF00017 | 0.733 |
LIG_SH2_STAT5 | 189 | 192 | PF00017 | 0.352 |
LIG_SH2_STAT5 | 418 | 421 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 47 | 50 | PF00017 | 0.487 |
LIG_SH3_3 | 456 | 462 | PF00018 | 0.662 |
LIG_SH3_3 | 494 | 500 | PF00018 | 0.677 |
LIG_SUMO_SIM_anti_2 | 226 | 234 | PF11976 | 0.472 |
LIG_SUMO_SIM_anti_2 | 374 | 380 | PF11976 | 0.501 |
LIG_SUMO_SIM_par_1 | 356 | 361 | PF11976 | 0.329 |
LIG_TRAF2_1 | 435 | 438 | PF00917 | 0.561 |
LIG_WW_3 | 69 | 73 | PF00397 | 0.492 |
MOD_CDK_SPK_2 | 496 | 501 | PF00069 | 0.765 |
MOD_CDK_SPxK_1 | 534 | 540 | PF00069 | 0.787 |
MOD_CDK_SPxK_1 | 66 | 72 | PF00069 | 0.422 |
MOD_CDK_SPxxK_3 | 534 | 541 | PF00069 | 0.789 |
MOD_CDK_SPxxK_3 | 95 | 102 | PF00069 | 0.454 |
MOD_CK1_1 | 148 | 154 | PF00069 | 0.461 |
MOD_CK1_1 | 277 | 283 | PF00069 | 0.410 |
MOD_CK1_1 | 306 | 312 | PF00069 | 0.484 |
MOD_CK1_1 | 515 | 521 | PF00069 | 0.703 |
MOD_CK1_1 | 533 | 539 | PF00069 | 0.808 |
MOD_CK1_1 | 7 | 13 | PF00069 | 0.725 |
MOD_CK2_1 | 220 | 226 | PF00069 | 0.380 |
MOD_CK2_1 | 399 | 405 | PF00069 | 0.427 |
MOD_DYRK1A_RPxSP_1 | 66 | 70 | PF00069 | 0.420 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.676 |
MOD_GlcNHglycan | 155 | 159 | PF01048 | 0.559 |
MOD_GlcNHglycan | 170 | 173 | PF01048 | 0.492 |
MOD_GlcNHglycan | 222 | 225 | PF01048 | 0.574 |
MOD_GlcNHglycan | 270 | 273 | PF01048 | 0.615 |
MOD_GlcNHglycan | 532 | 535 | PF01048 | 0.618 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.467 |
MOD_GSK3_1 | 273 | 280 | PF00069 | 0.403 |
MOD_GSK3_1 | 399 | 406 | PF00069 | 0.461 |
MOD_GSK3_1 | 421 | 428 | PF00069 | 0.687 |
MOD_GSK3_1 | 492 | 499 | PF00069 | 0.758 |
MOD_GSK3_1 | 508 | 515 | PF00069 | 0.745 |
MOD_GSK3_1 | 517 | 524 | PF00069 | 0.650 |
MOD_GSK3_1 | 529 | 536 | PF00069 | 0.782 |
MOD_GSK3_1 | 558 | 565 | PF00069 | 0.753 |
MOD_GSK3_1 | 566 | 573 | PF00069 | 0.694 |
MOD_NEK2_1 | 168 | 173 | PF00069 | 0.345 |
MOD_NEK2_1 | 210 | 215 | PF00069 | 0.507 |
MOD_NEK2_1 | 220 | 225 | PF00069 | 0.280 |
MOD_NEK2_1 | 231 | 236 | PF00069 | 0.391 |
MOD_NEK2_1 | 274 | 279 | PF00069 | 0.413 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.335 |
MOD_NEK2_1 | 399 | 404 | PF00069 | 0.467 |
MOD_NEK2_1 | 407 | 412 | PF00069 | 0.343 |
MOD_NEK2_2 | 425 | 430 | PF00069 | 0.599 |
MOD_NEK2_2 | 566 | 571 | PF00069 | 0.738 |
MOD_OFUCOSY | 355 | 362 | PF10250 | 0.389 |
MOD_PIKK_1 | 148 | 154 | PF00454 | 0.478 |
MOD_PIKK_1 | 231 | 237 | PF00454 | 0.476 |
MOD_PIKK_1 | 303 | 309 | PF00454 | 0.413 |
MOD_PKA_1 | 562 | 568 | PF00069 | 0.740 |
MOD_PKA_2 | 211 | 217 | PF00069 | 0.467 |
MOD_PKA_2 | 274 | 280 | PF00069 | 0.431 |
MOD_PKA_2 | 561 | 567 | PF00069 | 0.742 |
MOD_PKA_2 | 570 | 576 | PF00069 | 0.721 |
MOD_PKA_2 | 7 | 13 | PF00069 | 0.654 |
MOD_PKB_1 | 542 | 550 | PF00069 | 0.695 |
MOD_PKB_1 | 560 | 568 | PF00069 | 0.766 |
MOD_Plk_1 | 117 | 123 | PF00069 | 0.433 |
MOD_Plk_1 | 481 | 487 | PF00069 | 0.707 |
MOD_Plk_4 | 244 | 250 | PF00069 | 0.448 |
MOD_Plk_4 | 371 | 377 | PF00069 | 0.511 |
MOD_Plk_4 | 492 | 498 | PF00069 | 0.711 |
MOD_ProDKin_1 | 421 | 427 | PF00069 | 0.606 |
MOD_ProDKin_1 | 496 | 502 | PF00069 | 0.692 |
MOD_ProDKin_1 | 534 | 540 | PF00069 | 0.787 |
MOD_ProDKin_1 | 66 | 72 | PF00069 | 0.497 |
MOD_ProDKin_1 | 95 | 101 | PF00069 | 0.457 |
TRG_DiLeu_BaEn_1 | 226 | 231 | PF01217 | 0.387 |
TRG_DiLeu_BaEn_4 | 437 | 443 | PF01217 | 0.537 |
TRG_DiLeu_BaLyEn_6 | 382 | 387 | PF01217 | 0.335 |
TRG_ENDOCYTIC_2 | 173 | 176 | PF00928 | 0.336 |
TRG_ER_diArg_1 | 121 | 124 | PF00400 | 0.344 |
TRG_ER_diArg_1 | 18 | 21 | PF00400 | 0.690 |
TRG_ER_diArg_1 | 339 | 342 | PF00400 | 0.529 |
TRG_ER_diArg_1 | 343 | 346 | PF00400 | 0.340 |
TRG_ER_diArg_1 | 393 | 396 | PF00400 | 0.353 |
TRG_ER_diArg_1 | 430 | 433 | PF00400 | 0.614 |
TRG_ER_diArg_1 | 48 | 51 | PF00400 | 0.457 |
TRG_ER_diArg_1 | 542 | 545 | PF00400 | 0.704 |
TRG_ER_diArg_1 | 560 | 563 | PF00400 | 0.774 |
TRG_NLS_MonoExtC_3 | 539 | 544 | PF00514 | 0.699 |
TRG_NLS_MonoExtN_4 | 538 | 545 | PF00514 | 0.697 |
TRG_Pf-PMV_PEXEL_1 | 432 | 437 | PF00026 | 0.431 |
TRG_Pf-PMV_PEXEL_1 | 85 | 89 | PF00026 | 0.615 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3X8 | Leptomonas seymouri | 47% | 92% |
A0A451EJV6 | Leishmania donovani | 100% | 100% |
A4H3T1 | Leishmania braziliensis | 77% | 100% |
E9AJZ4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q9N858 | Leishmania major | 94% | 100% |