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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: Q4QIQ8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 124 | 126 | PF00675 | 0.676 |
CLV_NRD_NRD_1 | 263 | 265 | PF00675 | 0.718 |
CLV_NRD_NRD_1 | 578 | 580 | PF00675 | 0.741 |
CLV_NRD_NRD_1 | 598 | 600 | PF00675 | 0.384 |
CLV_PCSK_KEX2_1 | 124 | 126 | PF00082 | 0.676 |
CLV_PCSK_KEX2_1 | 247 | 249 | PF00082 | 0.663 |
CLV_PCSK_KEX2_1 | 263 | 265 | PF00082 | 0.491 |
CLV_PCSK_KEX2_1 | 275 | 277 | PF00082 | 0.581 |
CLV_PCSK_KEX2_1 | 47 | 49 | PF00082 | 0.713 |
CLV_PCSK_KEX2_1 | 578 | 580 | PF00082 | 0.741 |
CLV_PCSK_KEX2_1 | 598 | 600 | PF00082 | 0.384 |
CLV_PCSK_PC1ET2_1 | 247 | 249 | PF00082 | 0.663 |
CLV_PCSK_PC1ET2_1 | 275 | 277 | PF00082 | 0.751 |
CLV_PCSK_PC1ET2_1 | 47 | 49 | PF00082 | 0.713 |
CLV_PCSK_SKI1_1 | 148 | 152 | PF00082 | 0.654 |
DEG_SCF_FBW7_1 | 451 | 457 | PF00400 | 0.635 |
DOC_ANK_TNKS_1 | 532 | 539 | PF00023 | 0.686 |
DOC_CKS1_1 | 443 | 448 | PF01111 | 0.724 |
DOC_CKS1_1 | 451 | 456 | PF01111 | 0.611 |
DOC_PP1_RVXF_1 | 41 | 47 | PF00149 | 0.694 |
DOC_PP4_FxxP_1 | 8 | 11 | PF00568 | 0.732 |
DOC_USP7_MATH_1 | 320 | 324 | PF00917 | 0.732 |
DOC_USP7_MATH_1 | 380 | 384 | PF00917 | 0.729 |
DOC_USP7_MATH_1 | 395 | 399 | PF00917 | 0.559 |
DOC_USP7_MATH_1 | 437 | 441 | PF00917 | 0.729 |
DOC_USP7_MATH_1 | 503 | 507 | PF00917 | 0.791 |
DOC_USP7_MATH_1 | 618 | 622 | PF00917 | 0.742 |
DOC_USP7_MATH_1 | 64 | 68 | PF00917 | 0.714 |
DOC_USP7_UBL2_3 | 148 | 152 | PF12436 | 0.654 |
DOC_USP7_UBL2_3 | 188 | 192 | PF12436 | 0.790 |
DOC_USP7_UBL2_3 | 193 | 197 | PF12436 | 0.658 |
DOC_USP7_UBL2_3 | 255 | 259 | PF12436 | 0.668 |
DOC_USP7_UBL2_3 | 43 | 47 | PF12436 | 0.688 |
DOC_WW_Pin1_4 | 311 | 316 | PF00397 | 0.637 |
DOC_WW_Pin1_4 | 442 | 447 | PF00397 | 0.683 |
DOC_WW_Pin1_4 | 450 | 455 | PF00397 | 0.577 |
DOC_WW_Pin1_4 | 499 | 504 | PF00397 | 0.774 |
DOC_WW_Pin1_4 | 537 | 542 | PF00397 | 0.772 |
DOC_WW_Pin1_4 | 579 | 584 | PF00397 | 0.720 |
LIG_14-3-3_CanoR_1 | 382 | 386 | PF00244 | 0.754 |
LIG_14-3-3_CanoR_1 | 623 | 629 | PF00244 | 0.696 |
LIG_Actin_WH2_2 | 151 | 168 | PF00022 | 0.523 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.737 |
LIG_BRCT_BRCA1_1 | 549 | 553 | PF00533 | 0.750 |
LIG_BRCT_BRCA1_1 | 620 | 624 | PF00533 | 0.750 |
LIG_BRCT_BRCA1_1 | 649 | 653 | PF00533 | 0.612 |
LIG_deltaCOP1_diTrp_1 | 33 | 39 | PF00928 | 0.674 |
LIG_deltaCOP1_diTrp_1 | 643 | 653 | PF00928 | 0.698 |
LIG_FHA_1 | 199 | 205 | PF00498 | 0.652 |
LIG_FHA_1 | 511 | 517 | PF00498 | 0.768 |
LIG_FHA_1 | 625 | 631 | PF00498 | 0.696 |
LIG_FHA_1 | 71 | 77 | PF00498 | 0.701 |
LIG_FHA_1 | 90 | 96 | PF00498 | 0.461 |
LIG_FHA_2 | 340 | 346 | PF00498 | 0.769 |
LIG_LIR_Apic_2 | 60 | 64 | PF02991 | 0.716 |
LIG_LIR_Apic_2 | 638 | 644 | PF02991 | 0.601 |
LIG_LIR_Apic_2 | 7 | 11 | PF02991 | 0.734 |
LIG_LIR_Gen_1 | 141 | 150 | PF02991 | 0.626 |
LIG_LIR_Gen_1 | 584 | 593 | PF02991 | 0.687 |
LIG_LIR_Gen_1 | 67 | 76 | PF02991 | 0.693 |
LIG_LIR_Nem_3 | 141 | 146 | PF02991 | 0.623 |
LIG_LIR_Nem_3 | 584 | 590 | PF02991 | 0.694 |
LIG_LIR_Nem_3 | 67 | 72 | PF02991 | 0.693 |
LIG_MYND_1 | 537 | 541 | PF01753 | 0.705 |
LIG_PCNA_yPIPBox_3 | 225 | 235 | PF02747 | 0.610 |
LIG_Pex14_1 | 35 | 39 | PF04695 | 0.670 |
LIG_Pex14_2 | 624 | 628 | PF04695 | 0.761 |
LIG_SH2_CRK | 132 | 136 | PF00017 | 0.606 |
LIG_SH2_CRK | 162 | 166 | PF00017 | 0.583 |
LIG_SH2_CRK | 568 | 572 | PF00017 | 0.747 |
LIG_SH2_CRK | 587 | 591 | PF00017 | 0.415 |
LIG_SH2_PTP2 | 61 | 64 | PF00017 | 0.708 |
LIG_SH2_SRC | 61 | 64 | PF00017 | 0.708 |
LIG_SH2_STAP1 | 132 | 136 | PF00017 | 0.606 |
LIG_SH2_STAT5 | 157 | 160 | PF00017 | 0.585 |
LIG_SH2_STAT5 | 524 | 527 | PF00017 | 0.727 |
LIG_SH2_STAT5 | 61 | 64 | PF00017 | 0.708 |
LIG_SH3_1 | 448 | 454 | PF00018 | 0.740 |
LIG_SH3_2 | 443 | 448 | PF14604 | 0.798 |
LIG_SH3_3 | 290 | 296 | PF00018 | 0.768 |
LIG_SH3_3 | 440 | 446 | PF00018 | 0.787 |
LIG_SH3_3 | 448 | 454 | PF00018 | 0.693 |
LIG_SxIP_EBH_1 | 435 | 448 | PF03271 | 0.682 |
LIG_TRAF2_1 | 342 | 345 | PF00917 | 0.784 |
LIG_TYR_ITIM | 130 | 135 | PF00017 | 0.590 |
LIG_UBA3_1 | 146 | 152 | PF00899 | 0.643 |
LIG_UBA3_1 | 235 | 244 | PF00899 | 0.622 |
LIG_UBA3_1 | 429 | 436 | PF00899 | 0.654 |
LIG_WRC_WIRS_1 | 5 | 10 | PF05994 | 0.741 |
LIG_WRC_WIRS_1 | 94 | 99 | PF05994 | 0.712 |
MOD_CDC14_SPxK_1 | 582 | 585 | PF00782 | 0.645 |
MOD_CDK_SPxK_1 | 442 | 448 | PF00069 | 0.797 |
MOD_CDK_SPxK_1 | 579 | 585 | PF00069 | 0.718 |
MOD_CK1_1 | 288 | 294 | PF00069 | 0.707 |
MOD_CK1_1 | 323 | 329 | PF00069 | 0.705 |
MOD_CK1_1 | 381 | 387 | PF00069 | 0.756 |
MOD_CK1_1 | 435 | 441 | PF00069 | 0.580 |
MOD_CK1_1 | 444 | 450 | PF00069 | 0.570 |
MOD_CK1_1 | 547 | 553 | PF00069 | 0.748 |
MOD_CK1_1 | 635 | 641 | PF00069 | 0.617 |
MOD_CK2_1 | 339 | 345 | PF00069 | 0.768 |
MOD_CK2_1 | 616 | 622 | PF00069 | 0.741 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.703 |
MOD_GlcNHglycan | 180 | 183 | PF01048 | 0.669 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.631 |
MOD_GlcNHglycan | 322 | 325 | PF01048 | 0.713 |
MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.668 |
MOD_GlcNHglycan | 422 | 425 | PF01048 | 0.648 |
MOD_GlcNHglycan | 486 | 489 | PF01048 | 0.737 |
MOD_GlcNHglycan | 549 | 552 | PF01048 | 0.681 |
MOD_GSK3_1 | 178 | 185 | PF00069 | 0.737 |
MOD_GSK3_1 | 238 | 245 | PF00069 | 0.648 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.756 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.628 |
MOD_GSK3_1 | 307 | 314 | PF00069 | 0.608 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.672 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.661 |
MOD_GSK3_1 | 345 | 352 | PF00069 | 0.740 |
MOD_GSK3_1 | 416 | 423 | PF00069 | 0.697 |
MOD_GSK3_1 | 431 | 438 | PF00069 | 0.593 |
MOD_GSK3_1 | 450 | 457 | PF00069 | 0.533 |
MOD_GSK3_1 | 495 | 502 | PF00069 | 0.714 |
MOD_GSK3_1 | 647 | 654 | PF00069 | 0.763 |
MOD_GSK3_1 | 89 | 96 | PF00069 | 0.729 |
MOD_N-GLC_1 | 182 | 187 | PF02516 | 0.737 |
MOD_N-GLC_1 | 334 | 339 | PF02516 | 0.695 |
MOD_N-GLC_1 | 97 | 102 | PF02516 | 0.619 |
MOD_NEK2_1 | 146 | 151 | PF00069 | 0.643 |
MOD_NEK2_1 | 289 | 294 | PF00069 | 0.674 |
MOD_NEK2_1 | 494 | 499 | PF00069 | 0.707 |
MOD_NEK2_1 | 76 | 81 | PF00069 | 0.700 |
MOD_NEK2_1 | 97 | 102 | PF00069 | 0.695 |
MOD_NEK2_2 | 395 | 400 | PF00069 | 0.673 |
MOD_PIKK_1 | 62 | 68 | PF00454 | 0.696 |
MOD_PIKK_1 | 70 | 76 | PF00454 | 0.581 |
MOD_PK_1 | 608 | 614 | PF00069 | 0.477 |
MOD_PKA_1 | 280 | 286 | PF00069 | 0.682 |
MOD_PKA_2 | 381 | 387 | PF00069 | 0.756 |
MOD_Plk_1 | 334 | 340 | PF00069 | 0.726 |
MOD_Plk_1 | 70 | 76 | PF00069 | 0.694 |
MOD_Plk_2-3 | 87 | 93 | PF00069 | 0.718 |
MOD_Plk_4 | 35 | 41 | PF00069 | 0.677 |
MOD_Plk_4 | 402 | 408 | PF00069 | 0.656 |
MOD_ProDKin_1 | 311 | 317 | PF00069 | 0.638 |
MOD_ProDKin_1 | 442 | 448 | PF00069 | 0.687 |
MOD_ProDKin_1 | 450 | 456 | PF00069 | 0.575 |
MOD_ProDKin_1 | 499 | 505 | PF00069 | 0.774 |
MOD_ProDKin_1 | 537 | 543 | PF00069 | 0.771 |
MOD_ProDKin_1 | 579 | 585 | PF00069 | 0.718 |
MOD_SUMO_for_1 | 274 | 277 | PF00179 | 0.748 |
MOD_SUMO_for_1 | 279 | 282 | PF00179 | 0.673 |
MOD_SUMO_for_1 | 590 | 593 | PF00179 | 0.604 |
MOD_SUMO_rev_2 | 540 | 547 | PF00179 | 0.690 |
TRG_ENDOCYTIC_2 | 132 | 135 | PF00928 | 0.600 |
TRG_ENDOCYTIC_2 | 162 | 165 | PF00928 | 0.572 |
TRG_ENDOCYTIC_2 | 568 | 571 | PF00928 | 0.750 |
TRG_ENDOCYTIC_2 | 587 | 590 | PF00928 | 0.418 |
TRG_ER_diArg_1 | 124 | 126 | PF00400 | 0.674 |
TRG_ER_diArg_1 | 263 | 265 | PF00400 | 0.718 |
TRG_ER_diArg_1 | 578 | 580 | PF00400 | 0.741 |
TRG_Pf-PMV_PEXEL_1 | 263 | 267 | PF00026 | 0.719 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S5H5X4 | Leishmania donovani | 95% | 100% |
A4H4Y1 | Leishmania braziliensis | 70% | 100% |
A4HT32 | Leishmania infantum | 95% | 100% |
E9AL46 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |