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: A0A3Q8IJ91
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 579 | 583 | PF00656 | 0.598 |
CLV_NRD_NRD_1 | 178 | 180 | PF00675 | 0.765 |
CLV_NRD_NRD_1 | 302 | 304 | PF00675 | 0.618 |
CLV_NRD_NRD_1 | 345 | 347 | PF00675 | 0.565 |
CLV_NRD_NRD_1 | 387 | 389 | PF00675 | 0.459 |
CLV_NRD_NRD_1 | 464 | 466 | PF00675 | 0.572 |
CLV_NRD_NRD_1 | 487 | 489 | PF00675 | 0.636 |
CLV_NRD_NRD_1 | 531 | 533 | PF00675 | 0.568 |
CLV_PCSK_FUR_1 | 176 | 180 | PF00082 | 0.769 |
CLV_PCSK_KEX2_1 | 178 | 180 | PF00082 | 0.769 |
CLV_PCSK_KEX2_1 | 301 | 303 | PF00082 | 0.619 |
CLV_PCSK_KEX2_1 | 386 | 388 | PF00082 | 0.486 |
CLV_PCSK_KEX2_1 | 464 | 466 | PF00082 | 0.572 |
CLV_PCSK_KEX2_1 | 487 | 489 | PF00082 | 0.674 |
CLV_PCSK_KEX2_1 | 533 | 535 | PF00082 | 0.587 |
CLV_PCSK_KEX2_1 | 586 | 588 | PF00082 | 0.840 |
CLV_PCSK_PC1ET2_1 | 386 | 388 | PF00082 | 0.558 |
CLV_PCSK_PC1ET2_1 | 533 | 535 | PF00082 | 0.514 |
CLV_PCSK_PC1ET2_1 | 586 | 588 | PF00082 | 0.840 |
CLV_PCSK_PC7_1 | 383 | 389 | PF00082 | 0.559 |
CLV_PCSK_SKI1_1 | 114 | 118 | PF00082 | 0.441 |
CLV_PCSK_SKI1_1 | 292 | 296 | PF00082 | 0.723 |
CLV_PCSK_SKI1_1 | 356 | 360 | PF00082 | 0.718 |
CLV_PCSK_SKI1_1 | 387 | 391 | PF00082 | 0.511 |
CLV_PCSK_SKI1_1 | 434 | 438 | PF00082 | 0.506 |
CLV_PCSK_SKI1_1 | 465 | 469 | PF00082 | 0.591 |
CLV_PCSK_SKI1_1 | 489 | 493 | PF00082 | 0.769 |
CLV_PCSK_SKI1_1 | 534 | 538 | PF00082 | 0.571 |
DEG_SPOP_SBC_1 | 490 | 494 | PF00917 | 0.616 |
DEG_SPOP_SBC_1 | 576 | 580 | PF00917 | 0.824 |
DOC_CKS1_1 | 235 | 240 | PF01111 | 0.513 |
DOC_CYCLIN_yCln2_LP_2 | 235 | 241 | PF00134 | 0.507 |
DOC_MAPK_MEF2A_6 | 423 | 432 | PF00069 | 0.577 |
DOC_MAPK_NFAT4_5 | 423 | 431 | PF00069 | 0.677 |
DOC_PP1_RVXF_1 | 432 | 439 | PF00149 | 0.532 |
DOC_PP2B_LxvP_1 | 82 | 85 | PF13499 | 0.763 |
DOC_USP7_MATH_1 | 163 | 167 | PF00917 | 0.763 |
DOC_USP7_MATH_1 | 231 | 235 | PF00917 | 0.532 |
DOC_USP7_MATH_1 | 334 | 338 | PF00917 | 0.707 |
DOC_USP7_MATH_1 | 36 | 40 | PF00917 | 0.571 |
DOC_USP7_MATH_1 | 398 | 402 | PF00917 | 0.729 |
DOC_USP7_MATH_1 | 490 | 494 | PF00917 | 0.732 |
DOC_USP7_MATH_1 | 576 | 580 | PF00917 | 0.824 |
DOC_USP7_MATH_1 | 592 | 596 | PF00917 | 0.600 |
DOC_USP7_MATH_1 | 7 | 11 | PF00917 | 0.651 |
DOC_USP7_MATH_1 | 75 | 79 | PF00917 | 0.675 |
DOC_USP7_UBL2_3 | 468 | 472 | PF12436 | 0.755 |
DOC_USP7_UBL2_3 | 629 | 633 | PF12436 | 0.665 |
DOC_WW_Pin1_4 | 153 | 158 | PF00397 | 0.597 |
DOC_WW_Pin1_4 | 234 | 239 | PF00397 | 0.521 |
DOC_WW_Pin1_4 | 322 | 327 | PF00397 | 0.671 |
DOC_WW_Pin1_4 | 392 | 397 | PF00397 | 0.595 |
DOC_WW_Pin1_4 | 491 | 496 | PF00397 | 0.748 |
DOC_WW_Pin1_4 | 502 | 507 | PF00397 | 0.699 |
DOC_WW_Pin1_4 | 510 | 515 | PF00397 | 0.603 |
DOC_WW_Pin1_4 | 555 | 560 | PF00397 | 0.724 |
LIG_14-3-3_CanoR_1 | 143 | 153 | PF00244 | 0.445 |
LIG_14-3-3_CanoR_1 | 203 | 211 | PF00244 | 0.597 |
LIG_14-3-3_CanoR_1 | 292 | 298 | PF00244 | 0.624 |
LIG_14-3-3_CanoR_1 | 387 | 396 | PF00244 | 0.576 |
LIG_14-3-3_CanoR_1 | 593 | 601 | PF00244 | 0.611 |
LIG_Actin_WH2_2 | 419 | 435 | PF00022 | 0.655 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.646 |
LIG_BRCT_BRCA1_1 | 457 | 461 | PF00533 | 0.576 |
LIG_FHA_1 | 235 | 241 | PF00498 | 0.529 |
LIG_FHA_1 | 411 | 417 | PF00498 | 0.486 |
LIG_FHA_1 | 48 | 54 | PF00498 | 0.528 |
LIG_FHA_1 | 507 | 513 | PF00498 | 0.646 |
LIG_FHA_1 | 620 | 626 | PF00498 | 0.649 |
LIG_FHA_2 | 116 | 122 | PF00498 | 0.458 |
LIG_Integrin_isoDGR_2 | 571 | 573 | PF01839 | 0.751 |
LIG_LIR_Apic_2 | 227 | 231 | PF02991 | 0.598 |
LIG_LIR_Gen_1 | 6 | 15 | PF02991 | 0.521 |
LIG_LIR_LC3C_4 | 106 | 109 | PF02991 | 0.663 |
LIG_LIR_LC3C_4 | 237 | 242 | PF02991 | 0.591 |
LIG_LIR_Nem_3 | 325 | 331 | PF02991 | 0.708 |
LIG_LIR_Nem_3 | 6 | 11 | PF02991 | 0.538 |
LIG_SH2_CRK | 15 | 19 | PF00017 | 0.483 |
LIG_SH2_PTP2 | 228 | 231 | PF00017 | 0.602 |
LIG_SH2_PTP2 | 328 | 331 | PF00017 | 0.671 |
LIG_SH2_SRC | 406 | 409 | PF00017 | 0.627 |
LIG_SH2_STAT3 | 133 | 136 | PF00017 | 0.495 |
LIG_SH2_STAT3 | 215 | 218 | PF00017 | 0.395 |
LIG_SH2_STAT5 | 200 | 203 | PF00017 | 0.488 |
LIG_SH2_STAT5 | 228 | 231 | PF00017 | 0.602 |
LIG_SH2_STAT5 | 328 | 331 | PF00017 | 0.748 |
LIG_SH2_STAT5 | 406 | 409 | PF00017 | 0.579 |
LIG_SH2_STAT5 | 528 | 531 | PF00017 | 0.598 |
LIG_SH2_STAT5 | 606 | 609 | PF00017 | 0.603 |
LIG_SH3_3 | 124 | 130 | PF00018 | 0.435 |
LIG_SH3_3 | 280 | 286 | PF00018 | 0.800 |
LIG_SH3_3 | 320 | 326 | PF00018 | 0.577 |
LIG_SUMO_SIM_anti_2 | 208 | 215 | PF11976 | 0.566 |
LIG_SUMO_SIM_anti_2 | 236 | 243 | PF11976 | 0.602 |
LIG_SUMO_SIM_anti_2 | 339 | 345 | PF11976 | 0.604 |
LIG_SUMO_SIM_anti_2 | 513 | 519 | PF11976 | 0.639 |
LIG_SUMO_SIM_anti_2 | 622 | 631 | PF11976 | 0.701 |
LIG_TRAF2_1 | 312 | 315 | PF00917 | 0.735 |
LIG_UBA3_1 | 428 | 434 | PF00899 | 0.544 |
LIG_UBA3_1 | 473 | 481 | PF00899 | 0.666 |
LIG_WRC_WIRS_1 | 294 | 299 | PF05994 | 0.583 |
LIG_WRC_WIRS_1 | 566 | 571 | PF05994 | 0.739 |
LIG_WRC_WIRS_1 | 8 | 13 | PF05994 | 0.661 |
MOD_CDK_SPxK_1 | 491 | 497 | PF00069 | 0.718 |
MOD_CK1_1 | 234 | 240 | PF00069 | 0.616 |
MOD_CK1_1 | 493 | 499 | PF00069 | 0.597 |
MOD_CK1_1 | 553 | 559 | PF00069 | 0.621 |
MOD_CK1_1 | 585 | 591 | PF00069 | 0.684 |
MOD_CK1_1 | 599 | 605 | PF00069 | 0.616 |
MOD_CK1_1 | 74 | 80 | PF00069 | 0.645 |
MOD_CK2_1 | 115 | 121 | PF00069 | 0.496 |
MOD_CK2_1 | 163 | 169 | PF00069 | 0.656 |
MOD_CK2_1 | 279 | 285 | PF00069 | 0.700 |
MOD_CK2_1 | 472 | 478 | PF00069 | 0.578 |
MOD_CK2_1 | 502 | 508 | PF00069 | 0.749 |
MOD_CK2_1 | 510 | 516 | PF00069 | 0.606 |
MOD_GlcNHglycan | 28 | 32 | PF01048 | 0.543 |
MOD_GlcNHglycan | 336 | 339 | PF01048 | 0.557 |
MOD_GlcNHglycan | 353 | 356 | PF01048 | 0.605 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.461 |
MOD_GlcNHglycan | 408 | 411 | PF01048 | 0.540 |
MOD_GlcNHglycan | 455 | 458 | PF01048 | 0.637 |
MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.579 |
MOD_GlcNHglycan | 552 | 555 | PF01048 | 0.634 |
MOD_GlcNHglycan | 587 | 590 | PF01048 | 0.716 |
MOD_GlcNHglycan | 596 | 599 | PF01048 | 0.671 |
MOD_GlcNHglycan | 601 | 604 | PF01048 | 0.566 |
MOD_GlcNHglycan | 630 | 633 | PF01048 | 0.769 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.730 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.695 |
MOD_GSK3_1 | 202 | 209 | PF00069 | 0.524 |
MOD_GSK3_1 | 229 | 236 | PF00069 | 0.614 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.600 |
MOD_GSK3_1 | 392 | 399 | PF00069 | 0.598 |
MOD_GSK3_1 | 402 | 409 | PF00069 | 0.601 |
MOD_GSK3_1 | 449 | 456 | PF00069 | 0.626 |
MOD_GSK3_1 | 489 | 496 | PF00069 | 0.683 |
MOD_GSK3_1 | 502 | 509 | PF00069 | 0.590 |
MOD_GSK3_1 | 578 | 585 | PF00069 | 0.703 |
MOD_GSK3_1 | 592 | 599 | PF00069 | 0.774 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.717 |
MOD_N-GLC_1 | 163 | 168 | PF02516 | 0.662 |
MOD_N-GLC_1 | 18 | 23 | PF02516 | 0.548 |
MOD_N-GLC_2 | 446 | 448 | PF02516 | 0.520 |
MOD_NEK2_1 | 202 | 207 | PF00069 | 0.450 |
MOD_NEK2_1 | 233 | 238 | PF00069 | 0.640 |
MOD_NEK2_1 | 418 | 423 | PF00069 | 0.650 |
MOD_NEK2_1 | 453 | 458 | PF00069 | 0.608 |
MOD_NEK2_1 | 507 | 512 | PF00069 | 0.696 |
MOD_NEK2_1 | 627 | 632 | PF00069 | 0.678 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.593 |
MOD_NEK2_2 | 192 | 197 | PF00069 | 0.464 |
MOD_NEK2_2 | 449 | 454 | PF00069 | 0.572 |
MOD_NEK2_2 | 7 | 12 | PF00069 | 0.675 |
MOD_PIKK_1 | 455 | 461 | PF00454 | 0.756 |
MOD_PIKK_1 | 47 | 53 | PF00454 | 0.568 |
MOD_PK_1 | 134 | 140 | PF00069 | 0.519 |
MOD_PKA_1 | 178 | 184 | PF00069 | 0.670 |
MOD_PKA_1 | 387 | 393 | PF00069 | 0.516 |
MOD_PKA_2 | 178 | 184 | PF00069 | 0.701 |
MOD_PKA_2 | 202 | 208 | PF00069 | 0.501 |
MOD_PKA_2 | 387 | 393 | PF00069 | 0.597 |
MOD_PKA_2 | 592 | 598 | PF00069 | 0.730 |
MOD_PKB_1 | 176 | 184 | PF00069 | 0.713 |
MOD_Plk_1 | 18 | 24 | PF00069 | 0.544 |
MOD_Plk_1 | 370 | 376 | PF00069 | 0.587 |
MOD_Plk_1 | 507 | 513 | PF00069 | 0.632 |
MOD_Plk_2-3 | 279 | 285 | PF00069 | 0.802 |
MOD_Plk_4 | 224 | 230 | PF00069 | 0.517 |
MOD_Plk_4 | 293 | 299 | PF00069 | 0.710 |
MOD_Plk_4 | 402 | 408 | PF00069 | 0.570 |
MOD_ProDKin_1 | 153 | 159 | PF00069 | 0.604 |
MOD_ProDKin_1 | 234 | 240 | PF00069 | 0.514 |
MOD_ProDKin_1 | 322 | 328 | PF00069 | 0.674 |
MOD_ProDKin_1 | 392 | 398 | PF00069 | 0.605 |
MOD_ProDKin_1 | 491 | 497 | PF00069 | 0.750 |
MOD_ProDKin_1 | 502 | 508 | PF00069 | 0.694 |
MOD_ProDKin_1 | 510 | 516 | PF00069 | 0.591 |
MOD_ProDKin_1 | 555 | 561 | PF00069 | 0.727 |
TRG_DiLeu_BaEn_1 | 425 | 430 | PF01217 | 0.670 |
TRG_DiLeu_BaEn_1 | 623 | 628 | PF01217 | 0.683 |
TRG_DiLeu_BaLyEn_6 | 235 | 240 | PF01217 | 0.513 |
TRG_DiLeu_BaLyEn_6 | 424 | 429 | PF01217 | 0.553 |
TRG_ENDOCYTIC_2 | 15 | 18 | PF00928 | 0.567 |
TRG_ENDOCYTIC_2 | 328 | 331 | PF00928 | 0.710 |
TRG_ENDOCYTIC_2 | 606 | 609 | PF00928 | 0.501 |
TRG_ER_diArg_1 | 177 | 179 | PF00400 | 0.764 |
TRG_ER_diArg_1 | 301 | 303 | PF00400 | 0.598 |
TRG_ER_diArg_1 | 387 | 389 | PF00400 | 0.472 |
TRG_ER_diArg_1 | 53 | 56 | PF00400 | 0.535 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCD2 | Leptomonas seymouri | 45% | 100% |
A4HMZ7 | Leishmania braziliensis | 71% | 99% |
A4IBM0 | Leishmania infantum | 99% | 100% |
E9AFF4 | Leishmania major | 90% | 100% |
E9B6K9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |