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: A0A3Q8IET1
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 7 |
GO:0003723 | RNA binding | 4 | 7 |
GO:0005488 | binding | 1 | 7 |
GO:0097159 | organic cyclic compound binding | 2 | 7 |
GO:1901363 | heterocyclic compound binding | 2 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 384 | 388 | PF00656 | 0.713 |
CLV_MEL_PAP_1 | 472 | 478 | PF00089 | 0.407 |
CLV_NRD_NRD_1 | 229 | 231 | PF00675 | 0.605 |
CLV_NRD_NRD_1 | 246 | 248 | PF00675 | 0.415 |
CLV_NRD_NRD_1 | 393 | 395 | PF00675 | 0.468 |
CLV_NRD_NRD_1 | 474 | 476 | PF00675 | 0.490 |
CLV_NRD_NRD_1 | 556 | 558 | PF00675 | 0.647 |
CLV_NRD_NRD_1 | 649 | 651 | PF00675 | 0.597 |
CLV_PCSK_KEX2_1 | 229 | 231 | PF00082 | 0.603 |
CLV_PCSK_KEX2_1 | 393 | 395 | PF00082 | 0.468 |
CLV_PCSK_KEX2_1 | 473 | 475 | PF00082 | 0.621 |
CLV_PCSK_KEX2_1 | 555 | 557 | PF00082 | 0.635 |
CLV_PCSK_KEX2_1 | 649 | 651 | PF00082 | 0.597 |
CLV_PCSK_PC1ET2_1 | 555 | 557 | PF00082 | 0.635 |
CLV_PCSK_SKI1_1 | 229 | 233 | PF00082 | 0.591 |
CLV_PCSK_SKI1_1 | 433 | 437 | PF00082 | 0.421 |
CLV_PCSK_SKI1_1 | 656 | 660 | PF00082 | 0.552 |
CLV_PCSK_SKI1_1 | 728 | 732 | PF00082 | 0.616 |
DEG_APCC_DBOX_1 | 655 | 663 | PF00400 | 0.553 |
DEG_COP1_1 | 9 | 19 | PF00400 | 0.695 |
DOC_CYCLIN_yCln2_LP_2 | 349 | 355 | PF00134 | 0.738 |
DOC_MAPK_FxFP_2 | 353 | 356 | PF00069 | 0.605 |
DOC_MAPK_gen_1 | 393 | 400 | PF00069 | 0.443 |
DOC_MAPK_gen_1 | 503 | 511 | PF00069 | 0.535 |
DOC_MAPK_gen_1 | 555 | 564 | PF00069 | 0.632 |
DOC_MAPK_MEF2A_6 | 555 | 564 | PF00069 | 0.632 |
DOC_MAPK_MEF2A_6 | 656 | 665 | PF00069 | 0.551 |
DOC_PP1_RVXF_1 | 726 | 733 | PF00149 | 0.634 |
DOC_PP2B_LxvP_1 | 349 | 352 | PF13499 | 0.735 |
DOC_PP4_FxxP_1 | 353 | 356 | PF00568 | 0.753 |
DOC_USP7_MATH_1 | 206 | 210 | PF00917 | 0.712 |
DOC_USP7_MATH_1 | 214 | 218 | PF00917 | 0.586 |
DOC_USP7_MATH_1 | 233 | 237 | PF00917 | 0.599 |
DOC_USP7_MATH_1 | 242 | 246 | PF00917 | 0.455 |
DOC_USP7_MATH_1 | 341 | 345 | PF00917 | 0.597 |
DOC_USP7_MATH_1 | 41 | 45 | PF00917 | 0.631 |
DOC_USP7_MATH_1 | 549 | 553 | PF00917 | 0.674 |
DOC_USP7_MATH_1 | 563 | 567 | PF00917 | 0.521 |
DOC_WW_Pin1_4 | 15 | 20 | PF00397 | 0.641 |
DOC_WW_Pin1_4 | 155 | 160 | PF00397 | 0.475 |
DOC_WW_Pin1_4 | 175 | 180 | PF00397 | 0.604 |
DOC_WW_Pin1_4 | 202 | 207 | PF00397 | 0.700 |
DOC_WW_Pin1_4 | 357 | 362 | PF00397 | 0.580 |
DOC_WW_Pin1_4 | 490 | 495 | PF00397 | 0.484 |
DOC_WW_Pin1_4 | 9 | 14 | PF00397 | 0.744 |
LIG_14-3-3_CanoR_1 | 408 | 415 | PF00244 | 0.482 |
LIG_14-3-3_CanoR_1 | 454 | 461 | PF00244 | 0.533 |
LIG_14-3-3_CanoR_1 | 598 | 606 | PF00244 | 0.584 |
LIG_14-3-3_CanoR_1 | 687 | 695 | PF00244 | 0.505 |
LIG_Actin_WH2_2 | 361 | 378 | PF00022 | 0.591 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.697 |
LIG_BIR_III_2 | 38 | 42 | PF00653 | 0.521 |
LIG_BIR_III_2 | 478 | 482 | PF00653 | 0.616 |
LIG_BRCT_BRCA1_1 | 405 | 409 | PF00533 | 0.493 |
LIG_BRCT_BRCA1_1 | 634 | 638 | PF00533 | 0.625 |
LIG_EH1_1 | 462 | 470 | PF00400 | 0.368 |
LIG_eIF4E_1 | 657 | 663 | PF01652 | 0.548 |
LIG_FHA_1 | 21 | 27 | PF00498 | 0.645 |
LIG_FHA_1 | 421 | 427 | PF00498 | 0.443 |
LIG_FHA_1 | 446 | 452 | PF00498 | 0.660 |
LIG_FHA_1 | 495 | 501 | PF00498 | 0.525 |
LIG_FHA_1 | 51 | 57 | PF00498 | 0.635 |
LIG_FHA_1 | 642 | 648 | PF00498 | 0.505 |
LIG_FHA_1 | 687 | 693 | PF00498 | 0.385 |
LIG_FHA_1 | 78 | 84 | PF00498 | 0.445 |
LIG_FHA_2 | 189 | 195 | PF00498 | 0.746 |
LIG_FHA_2 | 416 | 422 | PF00498 | 0.411 |
LIG_GBD_Chelix_1 | 464 | 472 | PF00786 | 0.398 |
LIG_Integrin_isoDGR_2 | 685 | 687 | PF01839 | 0.473 |
LIG_LIR_Gen_1 | 104 | 110 | PF02991 | 0.630 |
LIG_LIR_LC3C_4 | 194 | 199 | PF02991 | 0.607 |
LIG_LIR_Nem_3 | 104 | 108 | PF02991 | 0.541 |
LIG_LIR_Nem_3 | 268 | 273 | PF02991 | 0.573 |
LIG_LIR_Nem_3 | 651 | 657 | PF02991 | 0.578 |
LIG_LIR_Nem_3 | 755 | 761 | PF02991 | 0.605 |
LIG_NRBOX | 421 | 427 | PF00104 | 0.569 |
LIG_PCNA_yPIPBox_3 | 91 | 99 | PF02747 | 0.525 |
LIG_PDZ_Class_2 | 767 | 772 | PF00595 | 0.489 |
LIG_Pex14_1 | 120 | 124 | PF04695 | 0.630 |
LIG_Pex14_2 | 733 | 737 | PF04695 | 0.576 |
LIG_SH2_STAP1 | 170 | 174 | PF00017 | 0.562 |
LIG_SH2_STAP1 | 633 | 637 | PF00017 | 0.600 |
LIG_SH2_STAT5 | 105 | 108 | PF00017 | 0.630 |
LIG_SH2_STAT5 | 139 | 142 | PF00017 | 0.506 |
LIG_SH2_STAT5 | 657 | 660 | PF00017 | 0.452 |
LIG_SH3_1 | 557 | 563 | PF00018 | 0.630 |
LIG_SH3_2 | 145 | 150 | PF14604 | 0.547 |
LIG_SH3_3 | 13 | 19 | PF00018 | 0.692 |
LIG_SH3_3 | 142 | 148 | PF00018 | 0.643 |
LIG_SH3_3 | 297 | 303 | PF00018 | 0.612 |
LIG_SH3_3 | 34 | 40 | PF00018 | 0.559 |
LIG_SH3_3 | 557 | 563 | PF00018 | 0.630 |
LIG_SUMO_SIM_anti_2 | 194 | 201 | PF11976 | 0.587 |
LIG_SUMO_SIM_par_1 | 194 | 201 | PF11976 | 0.614 |
LIG_SUMO_SIM_par_1 | 27 | 34 | PF11976 | 0.552 |
LIG_SUMO_SIM_par_1 | 747 | 755 | PF11976 | 0.385 |
LIG_TRAF2_1 | 510 | 513 | PF00917 | 0.497 |
LIG_TRAF2_1 | 668 | 671 | PF00917 | 0.593 |
LIG_WRC_WIRS_1 | 487 | 492 | PF05994 | 0.483 |
LIG_WRC_WIRS_1 | 564 | 569 | PF05994 | 0.649 |
MOD_CDC14_SPxK_1 | 158 | 161 | PF00782 | 0.484 |
MOD_CDK_SPK_2 | 202 | 207 | PF00069 | 0.634 |
MOD_CDK_SPxK_1 | 155 | 161 | PF00069 | 0.483 |
MOD_CK1_1 | 236 | 242 | PF00069 | 0.441 |
MOD_CK1_1 | 289 | 295 | PF00069 | 0.652 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.817 |
MOD_CK1_1 | 378 | 384 | PF00069 | 0.624 |
MOD_CK1_1 | 420 | 426 | PF00069 | 0.388 |
MOD_CK1_1 | 44 | 50 | PF00069 | 0.637 |
MOD_CK1_1 | 57 | 63 | PF00069 | 0.523 |
MOD_CK1_1 | 624 | 630 | PF00069 | 0.650 |
MOD_CK1_1 | 64 | 70 | PF00069 | 0.576 |
MOD_CK1_1 | 641 | 647 | PF00069 | 0.512 |
MOD_CK2_1 | 415 | 421 | PF00069 | 0.520 |
MOD_CK2_1 | 572 | 578 | PF00069 | 0.666 |
MOD_CK2_1 | 586 | 592 | PF00069 | 0.615 |
MOD_CK2_1 | 69 | 75 | PF00069 | 0.621 |
MOD_CK2_1 | 9 | 15 | PF00069 | 0.702 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.737 |
MOD_GlcNHglycan | 200 | 203 | PF01048 | 0.644 |
MOD_GlcNHglycan | 216 | 219 | PF01048 | 0.677 |
MOD_GlcNHglycan | 235 | 238 | PF01048 | 0.449 |
MOD_GlcNHglycan | 258 | 261 | PF01048 | 0.606 |
MOD_GlcNHglycan | 290 | 294 | PF01048 | 0.723 |
MOD_GlcNHglycan | 318 | 321 | PF01048 | 0.629 |
MOD_GlcNHglycan | 343 | 346 | PF01048 | 0.636 |
MOD_GlcNHglycan | 377 | 380 | PF01048 | 0.721 |
MOD_GlcNHglycan | 405 | 408 | PF01048 | 0.498 |
MOD_GlcNHglycan | 443 | 446 | PF01048 | 0.691 |
MOD_GlcNHglycan | 465 | 468 | PF01048 | 0.321 |
MOD_GlcNHglycan | 623 | 627 | PF01048 | 0.800 |
MOD_GlcNHglycan | 640 | 643 | PF01048 | 0.450 |
MOD_GlcNHglycan | 678 | 681 | PF01048 | 0.612 |
MOD_GlcNHglycan | 725 | 728 | PF01048 | 0.672 |
MOD_GSK3_1 | 198 | 205 | PF00069 | 0.718 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.592 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.617 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.553 |
MOD_GSK3_1 | 403 | 410 | PF00069 | 0.490 |
MOD_GSK3_1 | 441 | 448 | PF00069 | 0.555 |
MOD_GSK3_1 | 486 | 493 | PF00069 | 0.478 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.627 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.555 |
MOD_GSK3_1 | 622 | 629 | PF00069 | 0.661 |
MOD_N-GLC_1 | 175 | 180 | PF02516 | 0.591 |
MOD_N-GLC_1 | 50 | 55 | PF02516 | 0.594 |
MOD_N-GLC_1 | 57 | 62 | PF02516 | 0.570 |
MOD_N-GLC_1 | 723 | 728 | PF02516 | 0.584 |
MOD_N-GLC_2 | 262 | 264 | PF02516 | 0.586 |
MOD_NEK2_1 | 31 | 36 | PF00069 | 0.714 |
MOD_NEK2_1 | 339 | 344 | PF00069 | 0.558 |
MOD_NEK2_1 | 375 | 380 | PF00069 | 0.744 |
MOD_NEK2_1 | 403 | 408 | PF00069 | 0.587 |
MOD_NEK2_1 | 428 | 433 | PF00069 | 0.477 |
MOD_NEK2_1 | 520 | 525 | PF00069 | 0.603 |
MOD_NEK2_1 | 621 | 626 | PF00069 | 0.646 |
MOD_NEK2_1 | 69 | 74 | PF00069 | 0.739 |
MOD_NEK2_1 | 737 | 742 | PF00069 | 0.358 |
MOD_NEK2_1 | 77 | 82 | PF00069 | 0.528 |
MOD_NEK2_2 | 242 | 247 | PF00069 | 0.448 |
MOD_OFUCOSY | 263 | 269 | PF10250 | 0.558 |
MOD_OFUCOSY | 309 | 315 | PF10250 | 0.518 |
MOD_PIKK_1 | 381 | 387 | PF00454 | 0.603 |
MOD_PIKK_1 | 420 | 426 | PF00454 | 0.497 |
MOD_PIKK_1 | 453 | 459 | PF00454 | 0.569 |
MOD_PIKK_1 | 50 | 56 | PF00454 | 0.633 |
MOD_PIKK_1 | 520 | 526 | PF00454 | 0.575 |
MOD_PIKK_1 | 742 | 748 | PF00454 | 0.462 |
MOD_PKA_2 | 375 | 381 | PF00069 | 0.619 |
MOD_PKA_2 | 407 | 413 | PF00069 | 0.501 |
MOD_PKA_2 | 453 | 459 | PF00069 | 0.542 |
MOD_PKA_2 | 597 | 603 | PF00069 | 0.586 |
MOD_PKA_2 | 686 | 692 | PF00069 | 0.408 |
MOD_PKA_2 | 69 | 75 | PF00069 | 0.518 |
MOD_PKA_2 | 751 | 757 | PF00069 | 0.478 |
MOD_Plk_1 | 188 | 194 | PF00069 | 0.597 |
MOD_Plk_1 | 420 | 426 | PF00069 | 0.438 |
MOD_Plk_1 | 50 | 56 | PF00069 | 0.606 |
MOD_Plk_1 | 57 | 63 | PF00069 | 0.603 |
MOD_Plk_1 | 650 | 656 | PF00069 | 0.427 |
MOD_Plk_1 | 728 | 734 | PF00069 | 0.470 |
MOD_Plk_4 | 41 | 47 | PF00069 | 0.632 |
MOD_Plk_4 | 494 | 500 | PF00069 | 0.510 |
MOD_Plk_4 | 549 | 555 | PF00069 | 0.632 |
MOD_Plk_4 | 563 | 569 | PF00069 | 0.586 |
MOD_Plk_4 | 572 | 578 | PF00069 | 0.714 |
MOD_Plk_4 | 64 | 70 | PF00069 | 0.646 |
MOD_Plk_4 | 728 | 734 | PF00069 | 0.452 |
MOD_Plk_4 | 765 | 771 | PF00069 | 0.460 |
MOD_ProDKin_1 | 155 | 161 | PF00069 | 0.483 |
MOD_ProDKin_1 | 175 | 181 | PF00069 | 0.597 |
MOD_ProDKin_1 | 202 | 208 | PF00069 | 0.703 |
MOD_ProDKin_1 | 357 | 363 | PF00069 | 0.574 |
MOD_ProDKin_1 | 490 | 496 | PF00069 | 0.481 |
MOD_ProDKin_1 | 9 | 15 | PF00069 | 0.748 |
TRG_DiLeu_BaEn_1 | 421 | 426 | PF01217 | 0.435 |
TRG_DiLeu_BaEn_1 | 694 | 699 | PF01217 | 0.497 |
TRG_DiLeu_BaLyEn_6 | 744 | 749 | PF01217 | 0.456 |
TRG_ENDOCYTIC_2 | 105 | 108 | PF00928 | 0.637 |
TRG_ENDOCYTIC_2 | 122 | 125 | PF00928 | 0.434 |
TRG_ENDOCYTIC_2 | 139 | 142 | PF00928 | 0.380 |
TRG_ER_diArg_1 | 106 | 109 | PF00400 | 0.630 |
TRG_ER_diArg_1 | 229 | 231 | PF00400 | 0.603 |
TRG_ER_diArg_1 | 472 | 475 | PF00400 | 0.460 |
TRG_ER_diArg_1 | 500 | 503 | PF00400 | 0.534 |
TRG_ER_diArg_1 | 556 | 558 | PF00400 | 0.552 |
TRG_NES_CRM1_1 | 478 | 492 | PF08389 | 0.527 |
TRG_Pf-PMV_PEXEL_1 | 271 | 275 | PF00026 | 0.609 |
TRG_Pf-PMV_PEXEL_1 | 93 | 97 | PF00026 | 0.305 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7X4F6 | Leishmania donovani | 32% | 86% |
A4I6M7 | Leishmania infantum | 32% | 86% |
A4I6M8 | Leishmania infantum | 99% | 100% |
E9B1Q1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 99% |
Q4Q6F9 | Leishmania major | 89% | 100% |