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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005840 | ribosome | 5 | 12 |
GO:0032991 | protein-containing complex | 1 | 12 |
GO:0043226 | organelle | 2 | 12 |
GO:0043228 | non-membrane-bounded organelle | 3 | 12 |
GO:0043229 | intracellular organelle | 3 | 12 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:1990904 | ribonucleoprotein complex | 2 | 12 |
GO:0035869 | ciliary transition zone | 2 | 2 |
Related structures:
AlphaFold database: A4HLH9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 414 | 418 | PF00656 | 0.531 |
CLV_NRD_NRD_1 | 165 | 167 | PF00675 | 0.572 |
CLV_NRD_NRD_1 | 57 | 59 | PF00675 | 0.548 |
CLV_NRD_NRD_1 | 696 | 698 | PF00675 | 0.649 |
CLV_NRD_NRD_1 | 716 | 718 | PF00675 | 0.477 |
CLV_PCSK_KEX2_1 | 466 | 468 | PF00082 | 0.598 |
CLV_PCSK_KEX2_1 | 57 | 59 | PF00082 | 0.548 |
CLV_PCSK_KEX2_1 | 671 | 673 | PF00082 | 0.573 |
CLV_PCSK_KEX2_1 | 696 | 698 | PF00082 | 0.649 |
CLV_PCSK_KEX2_1 | 715 | 717 | PF00082 | 0.649 |
CLV_PCSK_PC1ET2_1 | 466 | 468 | PF00082 | 0.531 |
CLV_PCSK_PC1ET2_1 | 671 | 673 | PF00082 | 0.573 |
CLV_PCSK_PC7_1 | 462 | 468 | PF00082 | 0.509 |
CLV_PCSK_SKI1_1 | 189 | 193 | PF00082 | 0.318 |
CLV_PCSK_SKI1_1 | 742 | 746 | PF00082 | 0.610 |
CLV_PCSK_SKI1_1 | 754 | 758 | PF00082 | 0.633 |
CLV_Separin_Metazoa | 54 | 58 | PF03568 | 0.531 |
DEG_APCC_DBOX_1 | 445 | 453 | PF00400 | 0.387 |
DEG_APCC_DBOX_1 | 716 | 724 | PF00400 | 0.660 |
DEG_Kelch_Keap1_1 | 142 | 147 | PF01344 | 0.494 |
DEG_SPOP_SBC_1 | 534 | 538 | PF00917 | 0.678 |
DEG_SPOP_SBC_1 | 549 | 553 | PF00917 | 0.573 |
DEG_SPOP_SBC_1 | 580 | 584 | PF00917 | 0.670 |
DEG_SPOP_SBC_1 | 626 | 630 | PF00917 | 0.635 |
DEG_SPOP_SBC_1 | 756 | 760 | PF00917 | 0.713 |
DEG_SPOP_SBC_1 | 761 | 765 | PF00917 | 0.786 |
DOC_CDC14_PxL_1 | 503 | 511 | PF14671 | 0.475 |
DOC_CYCLIN_yCln2_LP_2 | 20 | 26 | PF00134 | 0.476 |
DOC_CYCLIN_yCln2_LP_2 | 554 | 560 | PF00134 | 0.658 |
DOC_MAPK_DCC_7 | 715 | 725 | PF00069 | 0.660 |
DOC_MAPK_gen_1 | 715 | 725 | PF00069 | 0.636 |
DOC_MAPK_MEF2A_6 | 282 | 291 | PF00069 | 0.324 |
DOC_MAPK_MEF2A_6 | 488 | 495 | PF00069 | 0.537 |
DOC_MAPK_MEF2A_6 | 716 | 725 | PF00069 | 0.635 |
DOC_MAPK_NFAT4_5 | 488 | 496 | PF00069 | 0.543 |
DOC_PP1_RVXF_1 | 347 | 354 | PF00149 | 0.491 |
DOC_PP2B_LxvP_1 | 113 | 116 | PF13499 | 0.448 |
DOC_PP2B_LxvP_1 | 20 | 23 | PF13499 | 0.498 |
DOC_PP2B_LxvP_1 | 493 | 496 | PF13499 | 0.582 |
DOC_PP2B_LxvP_1 | 558 | 561 | PF13499 | 0.705 |
DOC_SPAK_OSR1_1 | 349 | 353 | PF12202 | 0.466 |
DOC_USP7_MATH_1 | 171 | 175 | PF00917 | 0.450 |
DOC_USP7_MATH_1 | 220 | 224 | PF00917 | 0.502 |
DOC_USP7_MATH_1 | 386 | 390 | PF00917 | 0.445 |
DOC_USP7_MATH_1 | 550 | 554 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 570 | 574 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 627 | 631 | PF00917 | 0.620 |
DOC_USP7_MATH_1 | 634 | 638 | PF00917 | 0.664 |
DOC_USP7_MATH_1 | 701 | 705 | PF00917 | 0.641 |
DOC_WW_Pin1_4 | 154 | 159 | PF00397 | 0.483 |
DOC_WW_Pin1_4 | 387 | 392 | PF00397 | 0.552 |
DOC_WW_Pin1_4 | 515 | 520 | PF00397 | 0.799 |
DOC_WW_Pin1_4 | 572 | 577 | PF00397 | 0.552 |
DOC_WW_Pin1_4 | 699 | 704 | PF00397 | 0.644 |
LIG_14-3-3_CanoR_1 | 166 | 175 | PF00244 | 0.431 |
LIG_14-3-3_CanoR_1 | 203 | 210 | PF00244 | 0.293 |
LIG_14-3-3_CanoR_1 | 296 | 301 | PF00244 | 0.417 |
LIG_14-3-3_CanoR_1 | 425 | 431 | PF00244 | 0.537 |
LIG_14-3-3_CanoR_1 | 467 | 471 | PF00244 | 0.600 |
LIG_14-3-3_CanoR_1 | 501 | 507 | PF00244 | 0.579 |
LIG_14-3-3_CanoR_1 | 747 | 755 | PF00244 | 0.723 |
LIG_BIR_III_4 | 271 | 275 | PF00653 | 0.412 |
LIG_BRCT_BRCA1_1 | 427 | 431 | PF00533 | 0.544 |
LIG_deltaCOP1_diTrp_1 | 34 | 40 | PF00928 | 0.433 |
LIG_EVH1_1 | 623 | 627 | PF00568 | 0.545 |
LIG_FHA_1 | 167 | 173 | PF00498 | 0.390 |
LIG_FHA_1 | 231 | 237 | PF00498 | 0.511 |
LIG_FHA_1 | 241 | 247 | PF00498 | 0.448 |
LIG_FHA_1 | 313 | 319 | PF00498 | 0.429 |
LIG_FHA_1 | 329 | 335 | PF00498 | 0.494 |
LIG_FHA_1 | 401 | 407 | PF00498 | 0.532 |
LIG_FHA_1 | 478 | 484 | PF00498 | 0.451 |
LIG_FHA_1 | 50 | 56 | PF00498 | 0.548 |
LIG_FHA_1 | 509 | 515 | PF00498 | 0.608 |
LIG_FHA_1 | 518 | 524 | PF00498 | 0.640 |
LIG_FHA_1 | 560 | 566 | PF00498 | 0.590 |
LIG_FHA_1 | 581 | 587 | PF00498 | 0.665 |
LIG_FHA_1 | 66 | 72 | PF00498 | 0.626 |
LIG_FHA_1 | 705 | 711 | PF00498 | 0.575 |
LIG_FHA_1 | 761 | 767 | PF00498 | 0.799 |
LIG_FHA_1 | 81 | 87 | PF00498 | 0.477 |
LIG_FHA_2 | 29 | 35 | PF00498 | 0.463 |
LIG_FHA_2 | 371 | 377 | PF00498 | 0.475 |
LIG_FHA_2 | 448 | 454 | PF00498 | 0.443 |
LIG_FHA_2 | 508 | 514 | PF00498 | 0.656 |
LIG_FHA_2 | 738 | 744 | PF00498 | 0.684 |
LIG_LIR_Apic_2 | 684 | 688 | PF02991 | 0.560 |
LIG_LIR_Gen_1 | 34 | 45 | PF02991 | 0.510 |
LIG_LIR_Gen_1 | 367 | 377 | PF02991 | 0.540 |
LIG_LIR_LC3C_4 | 17 | 22 | PF02991 | 0.507 |
LIG_LIR_Nem_3 | 122 | 128 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 177 | 181 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 34 | 40 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 389 | 395 | PF02991 | 0.561 |
LIG_MYND_1 | 597 | 601 | PF01753 | 0.518 |
LIG_NRBOX | 160 | 166 | PF00104 | 0.473 |
LIG_PCNA_yPIPBox_3 | 687 | 697 | PF02747 | 0.528 |
LIG_SH2_SRC | 181 | 184 | PF00017 | 0.349 |
LIG_SH2_SRC | 219 | 222 | PF00017 | 0.554 |
LIG_SH2_STAT5 | 181 | 184 | PF00017 | 0.407 |
LIG_SH2_STAT5 | 249 | 252 | PF00017 | 0.458 |
LIG_SH2_STAT5 | 517 | 520 | PF00017 | 0.632 |
LIG_SH2_STAT5 | 693 | 696 | PF00017 | 0.632 |
LIG_SH3_3 | 19 | 25 | PF00018 | 0.434 |
LIG_SH3_3 | 338 | 344 | PF00018 | 0.442 |
LIG_SH3_3 | 544 | 550 | PF00018 | 0.656 |
LIG_SH3_3 | 560 | 566 | PF00018 | 0.667 |
LIG_SH3_3 | 585 | 591 | PF00018 | 0.653 |
LIG_SH3_3 | 594 | 600 | PF00018 | 0.655 |
LIG_SH3_3 | 621 | 627 | PF00018 | 0.710 |
LIG_SH3_3 | 729 | 735 | PF00018 | 0.561 |
LIG_SUMO_SIM_anti_2 | 17 | 23 | PF11976 | 0.510 |
LIG_SUMO_SIM_anti_2 | 479 | 485 | PF11976 | 0.452 |
LIG_SUMO_SIM_anti_2 | 602 | 607 | PF11976 | 0.546 |
LIG_SUMO_SIM_par_1 | 111 | 117 | PF11976 | 0.530 |
LIG_SUMO_SIM_par_1 | 25 | 31 | PF11976 | 0.427 |
LIG_SUMO_SIM_par_1 | 337 | 342 | PF11976 | 0.309 |
LIG_UBA3_1 | 161 | 167 | PF00899 | 0.471 |
LIG_UBA3_1 | 85 | 90 | PF00899 | 0.492 |
MOD_CDK_SPxK_1 | 387 | 393 | PF00069 | 0.557 |
MOD_CDK_SPxxK_3 | 699 | 706 | PF00069 | 0.643 |
MOD_CK1_1 | 139 | 145 | PF00069 | 0.600 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.505 |
MOD_CK1_1 | 309 | 315 | PF00069 | 0.435 |
MOD_CK1_1 | 387 | 393 | PF00069 | 0.557 |
MOD_CK1_1 | 540 | 546 | PF00069 | 0.751 |
MOD_CK1_1 | 629 | 635 | PF00069 | 0.768 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.800 |
MOD_CK1_1 | 704 | 710 | PF00069 | 0.575 |
MOD_CK1_1 | 8 | 14 | PF00069 | 0.664 |
MOD_CK1_1 | 93 | 99 | PF00069 | 0.547 |
MOD_CK2_1 | 141 | 147 | PF00069 | 0.497 |
MOD_CK2_1 | 171 | 177 | PF00069 | 0.478 |
MOD_CK2_1 | 181 | 187 | PF00069 | 0.345 |
MOD_CK2_1 | 370 | 376 | PF00069 | 0.569 |
MOD_CK2_1 | 447 | 453 | PF00069 | 0.440 |
MOD_CK2_1 | 737 | 743 | PF00069 | 0.732 |
MOD_GlcNHglycan | 104 | 107 | PF01048 | 0.477 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.706 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.352 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.320 |
MOD_GlcNHglycan | 253 | 256 | PF01048 | 0.459 |
MOD_GlcNHglycan | 268 | 271 | PF01048 | 0.384 |
MOD_GlcNHglycan | 272 | 275 | PF01048 | 0.415 |
MOD_GlcNHglycan | 293 | 296 | PF01048 | 0.508 |
MOD_GlcNHglycan | 308 | 311 | PF01048 | 0.357 |
MOD_GlcNHglycan | 322 | 325 | PF01048 | 0.486 |
MOD_GlcNHglycan | 353 | 356 | PF01048 | 0.404 |
MOD_GlcNHglycan | 386 | 389 | PF01048 | 0.493 |
MOD_GlcNHglycan | 529 | 532 | PF01048 | 0.689 |
MOD_GlcNHglycan | 539 | 542 | PF01048 | 0.723 |
MOD_GlcNHglycan | 567 | 570 | PF01048 | 0.792 |
MOD_GlcNHglycan | 572 | 575 | PF01048 | 0.645 |
MOD_GlcNHglycan | 610 | 613 | PF01048 | 0.703 |
MOD_GlcNHglycan | 63 | 66 | PF01048 | 0.579 |
MOD_GlcNHglycan | 636 | 639 | PF01048 | 0.597 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.645 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.652 |
MOD_GlcNHglycan | 747 | 750 | PF01048 | 0.721 |
MOD_GlcNHglycan | 95 | 98 | PF01048 | 0.562 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.554 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.649 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.575 |
MOD_GSK3_1 | 220 | 227 | PF00069 | 0.503 |
MOD_GSK3_1 | 240 | 247 | PF00069 | 0.501 |
MOD_GSK3_1 | 266 | 273 | PF00069 | 0.419 |
MOD_GSK3_1 | 308 | 315 | PF00069 | 0.378 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.523 |
MOD_GSK3_1 | 437 | 444 | PF00069 | 0.526 |
MOD_GSK3_1 | 533 | 540 | PF00069 | 0.762 |
MOD_GSK3_1 | 561 | 568 | PF00069 | 0.669 |
MOD_GSK3_1 | 595 | 602 | PF00069 | 0.564 |
MOD_GSK3_1 | 61 | 68 | PF00069 | 0.505 |
MOD_GSK3_1 | 625 | 632 | PF00069 | 0.656 |
MOD_GSK3_1 | 634 | 641 | PF00069 | 0.637 |
MOD_GSK3_1 | 701 | 708 | PF00069 | 0.641 |
MOD_GSK3_1 | 743 | 750 | PF00069 | 0.712 |
MOD_GSK3_1 | 755 | 762 | PF00069 | 0.660 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.616 |
MOD_N-GLC_1 | 150 | 155 | PF02516 | 0.607 |
MOD_N-GLC_2 | 130 | 132 | PF02516 | 0.433 |
MOD_NEK2_1 | 126 | 131 | PF00069 | 0.463 |
MOD_NEK2_1 | 141 | 146 | PF00069 | 0.597 |
MOD_NEK2_1 | 204 | 209 | PF00069 | 0.404 |
MOD_NEK2_1 | 244 | 249 | PF00069 | 0.448 |
MOD_NEK2_1 | 525 | 530 | PF00069 | 0.661 |
MOD_NEK2_1 | 579 | 584 | PF00069 | 0.571 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.513 |
MOD_NEK2_2 | 240 | 245 | PF00069 | 0.417 |
MOD_PIKK_1 | 249 | 255 | PF00454 | 0.429 |
MOD_PIKK_1 | 400 | 406 | PF00454 | 0.588 |
MOD_PIKK_1 | 437 | 443 | PF00454 | 0.432 |
MOD_PKA_1 | 166 | 172 | PF00069 | 0.441 |
MOD_PKA_1 | 466 | 472 | PF00069 | 0.386 |
MOD_PKA_2 | 244 | 250 | PF00069 | 0.478 |
MOD_PKA_2 | 466 | 472 | PF00069 | 0.593 |
MOD_PKA_2 | 47 | 53 | PF00069 | 0.630 |
MOD_PKA_2 | 705 | 711 | PF00069 | 0.637 |
MOD_Plk_1 | 230 | 236 | PF00069 | 0.510 |
MOD_Plk_4 | 104 | 110 | PF00069 | 0.486 |
MOD_Plk_4 | 15 | 21 | PF00069 | 0.434 |
MOD_Plk_4 | 221 | 227 | PF00069 | 0.420 |
MOD_Plk_4 | 380 | 386 | PF00069 | 0.580 |
MOD_Plk_4 | 426 | 432 | PF00069 | 0.600 |
MOD_Plk_4 | 550 | 556 | PF00069 | 0.603 |
MOD_Plk_4 | 601 | 607 | PF00069 | 0.562 |
MOD_Plk_4 | 762 | 768 | PF00069 | 0.646 |
MOD_ProDKin_1 | 154 | 160 | PF00069 | 0.467 |
MOD_ProDKin_1 | 387 | 393 | PF00069 | 0.557 |
MOD_ProDKin_1 | 515 | 521 | PF00069 | 0.800 |
MOD_ProDKin_1 | 572 | 578 | PF00069 | 0.552 |
MOD_ProDKin_1 | 699 | 705 | PF00069 | 0.642 |
MOD_SUMO_for_1 | 711 | 714 | PF00179 | 0.631 |
MOD_SUMO_for_1 | 723 | 726 | PF00179 | 0.684 |
MOD_SUMO_rev_2 | 41 | 45 | PF00179 | 0.365 |
MOD_SUMO_rev_2 | 746 | 756 | PF00179 | 0.609 |
TRG_DiLeu_BaEn_1 | 221 | 226 | PF01217 | 0.626 |
TRG_DiLeu_BaEn_1 | 490 | 495 | PF01217 | 0.540 |
TRG_ENDOCYTIC_2 | 369 | 372 | PF00928 | 0.574 |
TRG_ENDOCYTIC_2 | 392 | 395 | PF00928 | 0.524 |
TRG_ER_diArg_1 | 455 | 458 | PF00400 | 0.537 |
TRG_ER_diArg_1 | 56 | 58 | PF00400 | 0.566 |
TRG_ER_diArg_1 | 696 | 698 | PF00400 | 0.649 |
TRG_ER_diArg_1 | 715 | 717 | PF00400 | 0.649 |
TRG_ER_diArg_1 | 734 | 737 | PF00400 | 0.696 |
TRG_Pf-PMV_PEXEL_1 | 189 | 193 | PF00026 | 0.284 |
TRG_Pf-PMV_PEXEL_1 | 216 | 221 | PF00026 | 0.311 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I4G0 | Leptomonas seymouri | 61% | 98% |
A0A3Q8IGU1 | Leishmania donovani | 31% | 100% |
A0A3S7X6R5 | Leishmania donovani | 75% | 100% |
A4HLH8 | Leishmania braziliensis | 31% | 100% |
A4I8Y8 | Leishmania infantum | 30% | 100% |
A4I8Y9 | Leishmania infantum | 75% | 100% |
E9B3V7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E9B3V8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 76% | 89% |
Q4Q466 | Leishmania major | 74% | 100% |
Q4Q467 | Leishmania major | 32% | 100% |