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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000139 | Golgi membrane | 5 | 10 |
GO:0016020 | membrane | 2 | 10 |
GO:0017119 | Golgi transport complex | 3 | 10 |
GO:0031090 | organelle membrane | 3 | 10 |
GO:0032991 | protein-containing complex | 1 | 10 |
GO:0098588 | bounding membrane of organelle | 4 | 10 |
GO:0099023 | vesicle tethering complex | 2 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
Related structures:
AlphaFold database: E9AYC7
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 10 |
GO:0006886 | intracellular protein transport | 4 | 10 |
GO:0008104 | protein localization | 4 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0015031 | protein transport | 4 | 10 |
GO:0033036 | macromolecule localization | 2 | 10 |
GO:0045184 | establishment of protein localization | 3 | 10 |
GO:0046907 | intracellular transport | 3 | 10 |
GO:0051179 | localization | 1 | 10 |
GO:0051234 | establishment of localization | 2 | 10 |
GO:0051641 | cellular localization | 2 | 10 |
GO:0051649 | establishment of localization in cell | 3 | 10 |
GO:0070727 | cellular macromolecule localization | 3 | 10 |
GO:0071702 | organic substance transport | 4 | 10 |
GO:0071705 | nitrogen compound transport | 4 | 10 |
GO:0006890 | retrograde vesicle-mediated transport, Golgi to endoplasmic reticulum | 6 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0007030 | Golgi organization | 5 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0016192 | vesicle-mediated transport | 4 | 1 |
GO:0048193 | Golgi vesicle transport | 5 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 861 | 865 | PF00656 | 0.590 |
CLV_NRD_NRD_1 | 112 | 114 | PF00675 | 0.622 |
CLV_NRD_NRD_1 | 405 | 407 | PF00675 | 0.434 |
CLV_NRD_NRD_1 | 428 | 430 | PF00675 | 0.470 |
CLV_NRD_NRD_1 | 702 | 704 | PF00675 | 0.499 |
CLV_NRD_NRD_1 | 847 | 849 | PF00675 | 0.518 |
CLV_NRD_NRD_1 | 933 | 935 | PF00675 | 0.368 |
CLV_PCSK_KEX2_1 | 209 | 211 | PF00082 | 0.487 |
CLV_PCSK_KEX2_1 | 405 | 407 | PF00082 | 0.434 |
CLV_PCSK_KEX2_1 | 428 | 430 | PF00082 | 0.470 |
CLV_PCSK_KEX2_1 | 67 | 69 | PF00082 | 0.503 |
CLV_PCSK_KEX2_1 | 701 | 703 | PF00082 | 0.465 |
CLV_PCSK_KEX2_1 | 847 | 849 | PF00082 | 0.518 |
CLV_PCSK_KEX2_1 | 933 | 935 | PF00082 | 0.368 |
CLV_PCSK_PC1ET2_1 | 209 | 211 | PF00082 | 0.421 |
CLV_PCSK_PC1ET2_1 | 67 | 69 | PF00082 | 0.503 |
CLV_PCSK_PC1ET2_1 | 701 | 703 | PF00082 | 0.429 |
CLV_PCSK_SKI1_1 | 161 | 165 | PF00082 | 0.433 |
CLV_PCSK_SKI1_1 | 276 | 280 | PF00082 | 0.479 |
CLV_PCSK_SKI1_1 | 299 | 303 | PF00082 | 0.496 |
CLV_PCSK_SKI1_1 | 345 | 349 | PF00082 | 0.507 |
CLV_PCSK_SKI1_1 | 418 | 422 | PF00082 | 0.550 |
CLV_PCSK_SKI1_1 | 584 | 588 | PF00082 | 0.479 |
CLV_PCSK_SKI1_1 | 760 | 764 | PF00082 | 0.506 |
CLV_PCSK_SKI1_1 | 768 | 772 | PF00082 | 0.526 |
CLV_PCSK_SKI1_1 | 950 | 954 | PF00082 | 0.362 |
CLV_Separin_Metazoa | 402 | 406 | PF03568 | 0.505 |
DEG_APCC_DBOX_1 | 294 | 302 | PF00400 | 0.429 |
DEG_APCC_DBOX_1 | 767 | 775 | PF00400 | 0.436 |
DEG_APCC_DBOX_1 | 949 | 957 | PF00400 | 0.481 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.625 |
DEG_SCF_FBW7_1 | 682 | 689 | PF00400 | 0.474 |
DEG_SIAH_1 | 903 | 911 | PF03145 | 0.394 |
DEG_SPOP_SBC_1 | 454 | 458 | PF00917 | 0.642 |
DEG_SPOP_SBC_1 | 562 | 566 | PF00917 | 0.474 |
DOC_CKS1_1 | 465 | 470 | PF01111 | 0.507 |
DOC_CKS1_1 | 568 | 573 | PF01111 | 0.575 |
DOC_CKS1_1 | 683 | 688 | PF01111 | 0.485 |
DOC_CYCLIN_RxL_1 | 111 | 120 | PF00134 | 0.586 |
DOC_CYCLIN_RxL_1 | 415 | 425 | PF00134 | 0.422 |
DOC_MAPK_gen_1 | 151 | 159 | PF00069 | 0.449 |
DOC_MAPK_gen_1 | 894 | 902 | PF00069 | 0.495 |
DOC_MAPK_MEF2A_6 | 894 | 902 | PF00069 | 0.401 |
DOC_PP1_RVXF_1 | 416 | 423 | PF00149 | 0.417 |
DOC_PP2B_LxvP_1 | 150 | 153 | PF13499 | 0.362 |
DOC_PP2B_LxvP_1 | 24 | 27 | PF13499 | 0.634 |
DOC_PP2B_LxvP_1 | 743 | 746 | PF13499 | 0.309 |
DOC_PP4_FxxP_1 | 568 | 571 | PF00568 | 0.584 |
DOC_USP7_MATH_1 | 103 | 107 | PF00917 | 0.593 |
DOC_USP7_MATH_1 | 17 | 21 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 200 | 204 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 33 | 37 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 381 | 385 | PF00917 | 0.529 |
DOC_USP7_MATH_1 | 39 | 43 | PF00917 | 0.654 |
DOC_USP7_MATH_1 | 414 | 418 | PF00917 | 0.432 |
DOC_USP7_MATH_1 | 439 | 443 | PF00917 | 0.731 |
DOC_USP7_MATH_1 | 463 | 467 | PF00917 | 0.762 |
DOC_USP7_MATH_1 | 5 | 9 | PF00917 | 0.746 |
DOC_USP7_MATH_1 | 512 | 516 | PF00917 | 0.338 |
DOC_USP7_MATH_1 | 562 | 566 | PF00917 | 0.685 |
DOC_USP7_MATH_1 | 684 | 688 | PF00917 | 0.533 |
DOC_USP7_MATH_1 | 711 | 715 | PF00917 | 0.440 |
DOC_USP7_MATH_1 | 754 | 758 | PF00917 | 0.490 |
DOC_USP7_MATH_1 | 776 | 780 | PF00917 | 0.408 |
DOC_USP7_MATH_1 | 790 | 794 | PF00917 | 0.635 |
DOC_USP7_MATH_1 | 801 | 805 | PF00917 | 0.690 |
DOC_USP7_MATH_1 | 815 | 819 | PF00917 | 0.597 |
DOC_USP7_MATH_1 | 86 | 90 | PF00917 | 0.552 |
DOC_USP7_MATH_1 | 904 | 908 | PF00917 | 0.610 |
DOC_USP7_MATH_1 | 923 | 927 | PF00917 | 0.580 |
DOC_USP7_MATH_2 | 477 | 483 | PF00917 | 0.483 |
DOC_WW_Pin1_4 | 270 | 275 | PF00397 | 0.574 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.532 |
DOC_WW_Pin1_4 | 435 | 440 | PF00397 | 0.547 |
DOC_WW_Pin1_4 | 464 | 469 | PF00397 | 0.636 |
DOC_WW_Pin1_4 | 567 | 572 | PF00397 | 0.586 |
DOC_WW_Pin1_4 | 629 | 634 | PF00397 | 0.396 |
DOC_WW_Pin1_4 | 682 | 687 | PF00397 | 0.488 |
DOC_WW_Pin1_4 | 794 | 799 | PF00397 | 0.716 |
DOC_WW_Pin1_4 | 9 | 14 | PF00397 | 0.732 |
DOC_WW_Pin1_4 | 90 | 95 | PF00397 | 0.594 |
LIG_14-3-3_CanoR_1 | 129 | 137 | PF00244 | 0.440 |
LIG_14-3-3_CanoR_1 | 151 | 159 | PF00244 | 0.488 |
LIG_14-3-3_CanoR_1 | 161 | 169 | PF00244 | 0.404 |
LIG_14-3-3_CanoR_1 | 198 | 205 | PF00244 | 0.557 |
LIG_14-3-3_CanoR_1 | 345 | 351 | PF00244 | 0.504 |
LIG_14-3-3_CanoR_1 | 380 | 390 | PF00244 | 0.622 |
LIG_14-3-3_CanoR_1 | 428 | 432 | PF00244 | 0.553 |
LIG_14-3-3_CanoR_1 | 625 | 633 | PF00244 | 0.426 |
LIG_14-3-3_CanoR_1 | 68 | 78 | PF00244 | 0.492 |
LIG_14-3-3_CanoR_1 | 710 | 716 | PF00244 | 0.420 |
LIG_14-3-3_CanoR_1 | 727 | 735 | PF00244 | 0.451 |
LIG_14-3-3_CanoR_1 | 933 | 942 | PF00244 | 0.395 |
LIG_14-3-3_CanoR_1 | 990 | 995 | PF00244 | 0.441 |
LIG_Actin_WH2_2 | 283 | 301 | PF00022 | 0.483 |
LIG_APCC_ABBAyCdc20_2 | 113 | 119 | PF00400 | 0.543 |
LIG_BRCT_BRCA1_1 | 564 | 568 | PF00533 | 0.594 |
LIG_FHA_1 | 154 | 160 | PF00498 | 0.504 |
LIG_FHA_1 | 168 | 174 | PF00498 | 0.554 |
LIG_FHA_1 | 568 | 574 | PF00498 | 0.572 |
LIG_FHA_1 | 643 | 649 | PF00498 | 0.441 |
LIG_FHA_1 | 719 | 725 | PF00498 | 0.488 |
LIG_FHA_1 | 765 | 771 | PF00498 | 0.476 |
LIG_FHA_1 | 795 | 801 | PF00498 | 0.503 |
LIG_FHA_1 | 934 | 940 | PF00498 | 0.435 |
LIG_FHA_1 | 941 | 947 | PF00498 | 0.452 |
LIG_FHA_2 | 153 | 159 | PF00498 | 0.430 |
LIG_FHA_2 | 197 | 203 | PF00498 | 0.601 |
LIG_FHA_2 | 300 | 306 | PF00498 | 0.549 |
LIG_FHA_2 | 428 | 434 | PF00498 | 0.624 |
LIG_FHA_2 | 526 | 532 | PF00498 | 0.515 |
LIG_FHA_2 | 555 | 561 | PF00498 | 0.660 |
LIG_FHA_2 | 572 | 578 | PF00498 | 0.689 |
LIG_FHA_2 | 633 | 639 | PF00498 | 0.681 |
LIG_FHA_2 | 721 | 727 | PF00498 | 0.541 |
LIG_FHA_2 | 942 | 948 | PF00498 | 0.483 |
LIG_GBD_Chelix_1 | 332 | 340 | PF00786 | 0.439 |
LIG_LIR_Apic_2 | 565 | 571 | PF02991 | 0.587 |
LIG_LIR_Nem_3 | 317 | 322 | PF02991 | 0.531 |
LIG_LIR_Nem_3 | 741 | 747 | PF02991 | 0.371 |
LIG_LRP6_Inhibitor_1 | 984 | 990 | PF00058 | 0.291 |
LIG_MAD2 | 625 | 633 | PF02301 | 0.355 |
LIG_MAD2 | 896 | 904 | PF02301 | 0.442 |
LIG_NRBOX | 121 | 127 | PF00104 | 0.527 |
LIG_PCNA_PIPBox_1 | 690 | 699 | PF02747 | 0.383 |
LIG_PCNA_yPIPBox_3 | 67 | 78 | PF02747 | 0.520 |
LIG_PCNA_yPIPBox_3 | 690 | 703 | PF02747 | 0.561 |
LIG_PCNA_yPIPBox_3 | 705 | 719 | PF02747 | 0.481 |
LIG_Pex14_2 | 594 | 598 | PF04695 | 0.461 |
LIG_PTB_Apo_2 | 221 | 228 | PF02174 | 0.482 |
LIG_PTB_Phospho_1 | 221 | 227 | PF10480 | 0.481 |
LIG_RPA_C_Fungi | 387 | 399 | PF08784 | 0.494 |
LIG_SH2_CRK | 777 | 781 | PF00017 | 0.509 |
LIG_SH2_NCK_1 | 510 | 514 | PF00017 | 0.378 |
LIG_SH2_SRC | 322 | 325 | PF00017 | 0.456 |
LIG_SH2_SRC | 510 | 513 | PF00017 | 0.316 |
LIG_SH2_SRC | 696 | 699 | PF00017 | 0.370 |
LIG_SH2_STAP1 | 607 | 611 | PF00017 | 0.460 |
LIG_SH2_STAP1 | 935 | 939 | PF00017 | 0.491 |
LIG_SH2_STAT3 | 312 | 315 | PF00017 | 0.527 |
LIG_SH2_STAT3 | 363 | 366 | PF00017 | 0.502 |
LIG_SH2_STAT5 | 191 | 194 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 211 | 214 | PF00017 | 0.303 |
LIG_SH2_STAT5 | 227 | 230 | PF00017 | 0.514 |
LIG_SH2_STAT5 | 322 | 325 | PF00017 | 0.513 |
LIG_SH2_STAT5 | 696 | 699 | PF00017 | 0.497 |
LIG_SH2_STAT5 | 777 | 780 | PF00017 | 0.586 |
LIG_SH2_STAT5 | 810 | 813 | PF00017 | 0.580 |
LIG_SH2_STAT5 | 935 | 938 | PF00017 | 0.417 |
LIG_SH2_STAT5 | 948 | 951 | PF00017 | 0.368 |
LIG_SH3_1 | 459 | 465 | PF00018 | 0.512 |
LIG_SH3_3 | 13 | 19 | PF00018 | 0.727 |
LIG_SH3_3 | 459 | 465 | PF00018 | 0.529 |
LIG_SH3_3 | 608 | 614 | PF00018 | 0.432 |
LIG_SH3_3 | 627 | 633 | PF00018 | 0.407 |
LIG_SH3_3 | 654 | 660 | PF00018 | 0.503 |
LIG_SH3_3 | 92 | 98 | PF00018 | 0.503 |
LIG_SUMO_SIM_anti_2 | 500 | 506 | PF11976 | 0.460 |
LIG_SUMO_SIM_par_1 | 830 | 837 | PF11976 | 0.411 |
LIG_TRAF2_1 | 326 | 329 | PF00917 | 0.479 |
LIG_TRAF2_1 | 430 | 433 | PF00917 | 0.494 |
LIG_TRAF2_1 | 450 | 453 | PF00917 | 0.631 |
LIG_TRAF2_1 | 651 | 654 | PF00917 | 0.482 |
LIG_TYR_ITIM | 694 | 699 | PF00017 | 0.374 |
LIG_UBA3_1 | 693 | 701 | PF00899 | 0.492 |
LIG_WRC_WIRS_1 | 889 | 894 | PF05994 | 0.409 |
MOD_CDC14_SPxK_1 | 273 | 276 | PF00782 | 0.471 |
MOD_CDC14_SPxK_1 | 438 | 441 | PF00782 | 0.582 |
MOD_CDK_SPxK_1 | 270 | 276 | PF00069 | 0.480 |
MOD_CDK_SPxK_1 | 435 | 441 | PF00069 | 0.555 |
MOD_CK1_1 | 106 | 112 | PF00069 | 0.504 |
MOD_CK1_1 | 201 | 207 | PF00069 | 0.496 |
MOD_CK1_1 | 25 | 31 | PF00069 | 0.610 |
MOD_CK1_1 | 466 | 472 | PF00069 | 0.744 |
MOD_CK1_1 | 545 | 551 | PF00069 | 0.586 |
MOD_CK1_1 | 563 | 569 | PF00069 | 0.608 |
MOD_CK1_1 | 632 | 638 | PF00069 | 0.658 |
MOD_CK1_1 | 643 | 649 | PF00069 | 0.514 |
MOD_CK1_1 | 689 | 695 | PF00069 | 0.432 |
MOD_CK1_1 | 720 | 726 | PF00069 | 0.499 |
MOD_CK1_1 | 793 | 799 | PF00069 | 0.667 |
MOD_CK1_1 | 855 | 861 | PF00069 | 0.458 |
MOD_CK1_1 | 960 | 966 | PF00069 | 0.529 |
MOD_CK2_1 | 152 | 158 | PF00069 | 0.431 |
MOD_CK2_1 | 196 | 202 | PF00069 | 0.566 |
MOD_CK2_1 | 304 | 310 | PF00069 | 0.465 |
MOD_CK2_1 | 427 | 433 | PF00069 | 0.484 |
MOD_CK2_1 | 554 | 560 | PF00069 | 0.651 |
MOD_CK2_1 | 632 | 638 | PF00069 | 0.603 |
MOD_CK2_1 | 720 | 726 | PF00069 | 0.511 |
MOD_CK2_1 | 923 | 929 | PF00069 | 0.481 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.536 |
MOD_GlcNHglycan | 136 | 140 | PF01048 | 0.487 |
MOD_GlcNHglycan | 240 | 243 | PF01048 | 0.754 |
MOD_GlcNHglycan | 270 | 273 | PF01048 | 0.638 |
MOD_GlcNHglycan | 384 | 387 | PF01048 | 0.555 |
MOD_GlcNHglycan | 441 | 444 | PF01048 | 0.742 |
MOD_GlcNHglycan | 469 | 472 | PF01048 | 0.757 |
MOD_GlcNHglycan | 481 | 484 | PF01048 | 0.700 |
MOD_GlcNHglycan | 536 | 539 | PF01048 | 0.491 |
MOD_GlcNHglycan | 544 | 547 | PF01048 | 0.454 |
MOD_GlcNHglycan | 627 | 630 | PF01048 | 0.499 |
MOD_GlcNHglycan | 730 | 733 | PF01048 | 0.521 |
MOD_GlcNHglycan | 788 | 791 | PF01048 | 0.600 |
MOD_GlcNHglycan | 818 | 821 | PF01048 | 0.540 |
MOD_GlcNHglycan | 840 | 843 | PF01048 | 0.516 |
MOD_GlcNHglycan | 857 | 860 | PF01048 | 0.516 |
MOD_GlcNHglycan | 925 | 928 | PF01048 | 0.590 |
MOD_GlcNHglycan | 953 | 956 | PF01048 | 0.499 |
MOD_GlcNHglycan | 995 | 999 | PF01048 | 0.690 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.454 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.477 |
MOD_GSK3_1 | 153 | 160 | PF00069 | 0.501 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.451 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.707 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.721 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.609 |
MOD_GSK3_1 | 341 | 348 | PF00069 | 0.518 |
MOD_GSK3_1 | 414 | 421 | PF00069 | 0.515 |
MOD_GSK3_1 | 435 | 442 | PF00069 | 0.683 |
MOD_GSK3_1 | 453 | 460 | PF00069 | 0.767 |
MOD_GSK3_1 | 463 | 470 | PF00069 | 0.758 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.788 |
MOD_GSK3_1 | 563 | 570 | PF00069 | 0.673 |
MOD_GSK3_1 | 621 | 628 | PF00069 | 0.546 |
MOD_GSK3_1 | 642 | 649 | PF00069 | 0.578 |
MOD_GSK3_1 | 661 | 668 | PF00069 | 0.519 |
MOD_GSK3_1 | 682 | 689 | PF00069 | 0.498 |
MOD_GSK3_1 | 734 | 741 | PF00069 | 0.385 |
MOD_GSK3_1 | 754 | 761 | PF00069 | 0.539 |
MOD_GSK3_1 | 786 | 793 | PF00069 | 0.592 |
MOD_GSK3_1 | 834 | 841 | PF00069 | 0.491 |
MOD_GSK3_1 | 86 | 93 | PF00069 | 0.706 |
MOD_GSK3_1 | 883 | 890 | PF00069 | 0.376 |
MOD_GSK3_1 | 904 | 911 | PF00069 | 0.707 |
MOD_GSK3_1 | 917 | 924 | PF00069 | 0.636 |
MOD_GSK3_1 | 990 | 997 | PF00069 | 0.662 |
MOD_LATS_1 | 127 | 133 | PF00433 | 0.570 |
MOD_N-GLC_1 | 236 | 241 | PF02516 | 0.600 |
MOD_N-GLC_1 | 242 | 247 | PF02516 | 0.594 |
MOD_N-GLC_1 | 268 | 273 | PF02516 | 0.656 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.577 |
MOD_NEK2_1 | 157 | 162 | PF00069 | 0.420 |
MOD_NEK2_1 | 346 | 351 | PF00069 | 0.498 |
MOD_NEK2_1 | 422 | 427 | PF00069 | 0.432 |
MOD_NEK2_1 | 554 | 559 | PF00069 | 0.760 |
MOD_NEK2_1 | 838 | 843 | PF00069 | 0.518 |
MOD_PIKK_1 | 131 | 137 | PF00454 | 0.499 |
MOD_PIKK_1 | 366 | 372 | PF00454 | 0.418 |
MOD_PIKK_1 | 686 | 692 | PF00454 | 0.558 |
MOD_PIKK_1 | 808 | 814 | PF00454 | 0.670 |
MOD_PIKK_1 | 908 | 914 | PF00454 | 0.684 |
MOD_PIKK_1 | 917 | 923 | PF00454 | 0.680 |
MOD_PK_1 | 175 | 181 | PF00069 | 0.340 |
MOD_PKA_1 | 933 | 939 | PF00069 | 0.341 |
MOD_PKA_2 | 153 | 159 | PF00069 | 0.562 |
MOD_PKA_2 | 231 | 237 | PF00069 | 0.528 |
MOD_PKA_2 | 252 | 258 | PF00069 | 0.669 |
MOD_PKA_2 | 341 | 347 | PF00069 | 0.490 |
MOD_PKA_2 | 427 | 433 | PF00069 | 0.548 |
MOD_PKA_2 | 665 | 671 | PF00069 | 0.481 |
MOD_PKA_2 | 933 | 939 | PF00069 | 0.366 |
MOD_PKB_1 | 725 | 733 | PF00069 | 0.371 |
MOD_Plk_1 | 157 | 163 | PF00069 | 0.497 |
MOD_Plk_1 | 201 | 207 | PF00069 | 0.520 |
MOD_Plk_1 | 299 | 305 | PF00069 | 0.487 |
MOD_Plk_1 | 418 | 424 | PF00069 | 0.382 |
MOD_Plk_1 | 640 | 646 | PF00069 | 0.553 |
MOD_Plk_1 | 758 | 764 | PF00069 | 0.282 |
MOD_Plk_1 | 957 | 963 | PF00069 | 0.487 |
MOD_Plk_4 | 145 | 151 | PF00069 | 0.553 |
MOD_Plk_4 | 175 | 181 | PF00069 | 0.427 |
MOD_Plk_4 | 346 | 352 | PF00069 | 0.609 |
MOD_Plk_4 | 418 | 424 | PF00069 | 0.382 |
MOD_Plk_4 | 643 | 649 | PF00069 | 0.479 |
MOD_Plk_4 | 689 | 695 | PF00069 | 0.387 |
MOD_Plk_4 | 758 | 764 | PF00069 | 0.441 |
MOD_Plk_4 | 880 | 886 | PF00069 | 0.462 |
MOD_Plk_4 | 888 | 894 | PF00069 | 0.480 |
MOD_ProDKin_1 | 270 | 276 | PF00069 | 0.572 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.534 |
MOD_ProDKin_1 | 435 | 441 | PF00069 | 0.555 |
MOD_ProDKin_1 | 464 | 470 | PF00069 | 0.637 |
MOD_ProDKin_1 | 567 | 573 | PF00069 | 0.580 |
MOD_ProDKin_1 | 629 | 635 | PF00069 | 0.401 |
MOD_ProDKin_1 | 682 | 688 | PF00069 | 0.480 |
MOD_ProDKin_1 | 794 | 800 | PF00069 | 0.716 |
MOD_ProDKin_1 | 90 | 96 | PF00069 | 0.585 |
MOD_SUMO_for_1 | 747 | 750 | PF00179 | 0.487 |
MOD_SUMO_rev_2 | 296 | 301 | PF00179 | 0.471 |
TRG_DiLeu_BaLyEn_6 | 516 | 521 | PF01217 | 0.497 |
TRG_ENDOCYTIC_2 | 510 | 513 | PF00928 | 0.415 |
TRG_ENDOCYTIC_2 | 696 | 699 | PF00928 | 0.370 |
TRG_ENDOCYTIC_2 | 777 | 780 | PF00928 | 0.496 |
TRG_ER_diArg_1 | 404 | 406 | PF00400 | 0.413 |
TRG_ER_diArg_1 | 427 | 429 | PF00400 | 0.462 |
TRG_ER_diArg_1 | 702 | 705 | PF00400 | 0.507 |
TRG_ER_diArg_1 | 933 | 935 | PF00400 | 0.368 |
TRG_NLS_MonoExtC_3 | 700 | 705 | PF00514 | 0.420 |
TRG_Pf-PMV_PEXEL_1 | 429 | 433 | PF00026 | 0.562 |
TRG_Pf-PMV_PEXEL_1 | 57 | 62 | PF00026 | 0.569 |
TRG_Pf-PMV_PEXEL_1 | 870 | 874 | PF00026 | 0.532 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I8B9 | Leptomonas seymouri | 53% | 98% |
A0A1X0NS38 | Trypanosomatidae | 24% | 100% |
A0A3Q8IP82 | Leishmania donovani | 89% | 99% |
A0A422NIU2 | Trypanosoma rangeli | 26% | 100% |
A4HF03 | Leishmania braziliensis | 73% | 100% |
A4I282 | Leishmania infantum | 89% | 99% |
C9ZRR4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
Q4Q946 | Leishmania major | 88% | 100% |