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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: A4HEK2
Term | Name | Level | Count |
---|---|---|---|
GO:0001510 | RNA methylation | 4 | 8 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 8 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 8 |
GO:0006807 | nitrogen compound metabolic process | 2 | 8 |
GO:0008152 | metabolic process | 1 | 8 |
GO:0009451 | RNA modification | 5 | 8 |
GO:0009987 | cellular process | 1 | 8 |
GO:0016070 | RNA metabolic process | 5 | 8 |
GO:0032259 | methylation | 2 | 8 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 8 |
GO:0043170 | macromolecule metabolic process | 3 | 8 |
GO:0043412 | macromolecule modification | 4 | 8 |
GO:0043414 | macromolecule methylation | 3 | 8 |
GO:0044237 | cellular metabolic process | 2 | 8 |
GO:0044238 | primary metabolic process | 2 | 8 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 8 |
GO:0046483 | heterocycle metabolic process | 3 | 8 |
GO:0071704 | organic substance metabolic process | 2 | 8 |
GO:0090304 | nucleic acid metabolic process | 4 | 8 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 8 |
GO:0003723 | RNA binding | 4 | 8 |
GO:0003824 | catalytic activity | 1 | 8 |
GO:0005488 | binding | 1 | 8 |
GO:0008168 | methyltransferase activity | 4 | 8 |
GO:0016740 | transferase activity | 2 | 8 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 8 |
GO:0097159 | organic cyclic compound binding | 2 | 8 |
GO:1901363 | heterocyclic compound binding | 2 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 541 | 545 | PF00656 | 0.458 |
CLV_C14_Caspase3-7 | 758 | 762 | PF00656 | 0.500 |
CLV_NRD_NRD_1 | 131 | 133 | PF00675 | 0.547 |
CLV_NRD_NRD_1 | 30 | 32 | PF00675 | 0.538 |
CLV_NRD_NRD_1 | 305 | 307 | PF00675 | 0.764 |
CLV_NRD_NRD_1 | 311 | 313 | PF00675 | 0.568 |
CLV_NRD_NRD_1 | 522 | 524 | PF00675 | 0.556 |
CLV_NRD_NRD_1 | 631 | 633 | PF00675 | 0.537 |
CLV_NRD_NRD_1 | 687 | 689 | PF00675 | 0.295 |
CLV_PCSK_FUR_1 | 132 | 136 | PF00082 | 0.530 |
CLV_PCSK_KEX2_1 | 131 | 133 | PF00082 | 0.547 |
CLV_PCSK_KEX2_1 | 134 | 136 | PF00082 | 0.514 |
CLV_PCSK_KEX2_1 | 30 | 32 | PF00082 | 0.538 |
CLV_PCSK_KEX2_1 | 311 | 313 | PF00082 | 0.441 |
CLV_PCSK_KEX2_1 | 357 | 359 | PF00082 | 0.343 |
CLV_PCSK_KEX2_1 | 44 | 46 | PF00082 | 0.473 |
CLV_PCSK_KEX2_1 | 522 | 524 | PF00082 | 0.556 |
CLV_PCSK_KEX2_1 | 631 | 633 | PF00082 | 0.545 |
CLV_PCSK_PC1ET2_1 | 134 | 136 | PF00082 | 0.522 |
CLV_PCSK_PC1ET2_1 | 357 | 359 | PF00082 | 0.343 |
CLV_PCSK_PC1ET2_1 | 44 | 46 | PF00082 | 0.514 |
CLV_PCSK_PC1ET2_1 | 631 | 633 | PF00082 | 0.545 |
CLV_PCSK_SKI1_1 | 375 | 379 | PF00082 | 0.370 |
CLV_PCSK_SKI1_1 | 459 | 463 | PF00082 | 0.472 |
CLV_PCSK_SKI1_1 | 617 | 621 | PF00082 | 0.495 |
CLV_PCSK_SKI1_1 | 632 | 636 | PF00082 | 0.510 |
CLV_PCSK_SKI1_1 | 688 | 692 | PF00082 | 0.295 |
DEG_APCC_DBOX_1 | 310 | 318 | PF00400 | 0.370 |
DEG_APCC_DBOX_1 | 454 | 462 | PF00400 | 0.472 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.490 |
DEG_SCF_FBW7_1 | 64 | 70 | PF00400 | 0.512 |
DEG_SPOP_SBC_1 | 113 | 117 | PF00917 | 0.651 |
DEG_SPOP_SBC_1 | 242 | 246 | PF00917 | 0.473 |
DEG_SPOP_SBC_1 | 638 | 642 | PF00917 | 0.431 |
DEG_SPOP_SBC_1 | 796 | 800 | PF00917 | 0.485 |
DOC_CKS1_1 | 64 | 69 | PF01111 | 0.511 |
DOC_CYCLIN_RxL_1 | 455 | 465 | PF00134 | 0.454 |
DOC_CYCLIN_RxL_1 | 682 | 693 | PF00134 | 0.500 |
DOC_CYCLIN_yClb1_LxF_4 | 722 | 728 | PF00134 | 0.535 |
DOC_CYCLIN_yCln2_LP_2 | 12 | 18 | PF00134 | 0.474 |
DOC_MAPK_gen_1 | 311 | 318 | PF00069 | 0.359 |
DOC_MAPK_gen_1 | 43 | 50 | PF00069 | 0.507 |
DOC_MAPK_gen_1 | 489 | 499 | PF00069 | 0.528 |
DOC_MAPK_gen_1 | 594 | 603 | PF00069 | 0.506 |
DOC_MAPK_MEF2A_6 | 311 | 318 | PF00069 | 0.523 |
DOC_MAPK_MEF2A_6 | 552 | 559 | PF00069 | 0.382 |
DOC_MAPK_MEF2A_6 | 729 | 736 | PF00069 | 0.456 |
DOC_MAPK_MEF2A_6 | 777 | 785 | PF00069 | 0.420 |
DOC_MAPK_NFAT4_5 | 552 | 560 | PF00069 | 0.382 |
DOC_MAPK_RevD_3 | 507 | 523 | PF00069 | 0.301 |
DOC_MIT_MIM_1 | 226 | 236 | PF04212 | 0.428 |
DOC_PP2B_LxvP_1 | 238 | 241 | PF13499 | 0.631 |
DOC_PP2B_LxvP_1 | 332 | 335 | PF13499 | 0.535 |
DOC_PP2B_LxvP_1 | 657 | 660 | PF13499 | 0.461 |
DOC_PP4_FxxP_1 | 257 | 260 | PF00568 | 0.550 |
DOC_PP4_FxxP_1 | 87 | 90 | PF00568 | 0.482 |
DOC_SPAK_OSR1_1 | 45 | 49 | PF12202 | 0.507 |
DOC_USP7_MATH_1 | 184 | 188 | PF00917 | 0.604 |
DOC_USP7_MATH_1 | 412 | 416 | PF00917 | 0.584 |
DOC_USP7_MATH_1 | 637 | 641 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 752 | 756 | PF00917 | 0.628 |
DOC_WW_Pin1_4 | 115 | 120 | PF00397 | 0.504 |
DOC_WW_Pin1_4 | 139 | 144 | PF00397 | 0.477 |
DOC_WW_Pin1_4 | 160 | 165 | PF00397 | 0.549 |
DOC_WW_Pin1_4 | 244 | 249 | PF00397 | 0.571 |
DOC_WW_Pin1_4 | 279 | 284 | PF00397 | 0.602 |
DOC_WW_Pin1_4 | 445 | 450 | PF00397 | 0.449 |
DOC_WW_Pin1_4 | 474 | 479 | PF00397 | 0.769 |
DOC_WW_Pin1_4 | 514 | 519 | PF00397 | 0.498 |
DOC_WW_Pin1_4 | 533 | 538 | PF00397 | 0.651 |
DOC_WW_Pin1_4 | 573 | 578 | PF00397 | 0.573 |
DOC_WW_Pin1_4 | 60 | 65 | PF00397 | 0.501 |
DOC_WW_Pin1_4 | 698 | 703 | PF00397 | 0.535 |
DOC_WW_Pin1_4 | 797 | 802 | PF00397 | 0.527 |
DOC_WW_Pin1_4 | 99 | 104 | PF00397 | 0.619 |
LIG_14-3-3_CanoR_1 | 112 | 121 | PF00244 | 0.539 |
LIG_14-3-3_CanoR_1 | 37 | 46 | PF00244 | 0.521 |
LIG_14-3-3_CanoR_1 | 375 | 382 | PF00244 | 0.451 |
LIG_14-3-3_CanoR_1 | 414 | 418 | PF00244 | 0.563 |
LIG_14-3-3_CanoR_1 | 455 | 459 | PF00244 | 0.457 |
LIG_14-3-3_CanoR_1 | 68 | 72 | PF00244 | 0.521 |
LIG_14-3-3_CanoR_1 | 738 | 747 | PF00244 | 0.495 |
LIG_Actin_WH2_2 | 204 | 221 | PF00022 | 0.332 |
LIG_Actin_WH2_2 | 506 | 524 | PF00022 | 0.515 |
LIG_BRCT_BRCA1_1 | 340 | 344 | PF00533 | 0.515 |
LIG_BRCT_BRCA1_1 | 395 | 399 | PF00533 | 0.458 |
LIG_BRCT_BRCA1_1 | 535 | 539 | PF00533 | 0.406 |
LIG_BRCT_BRCA1_1 | 769 | 773 | PF00533 | 0.427 |
LIG_CSL_BTD_1 | 283 | 286 | PF09270 | 0.500 |
LIG_CtBP_PxDLS_1 | 518 | 522 | PF00389 | 0.331 |
LIG_EVH1_1 | 87 | 91 | PF00568 | 0.480 |
LIG_FHA_1 | 139 | 145 | PF00498 | 0.463 |
LIG_FHA_1 | 165 | 171 | PF00498 | 0.534 |
LIG_FHA_1 | 186 | 192 | PF00498 | 0.502 |
LIG_FHA_1 | 213 | 219 | PF00498 | 0.428 |
LIG_FHA_1 | 228 | 234 | PF00498 | 0.506 |
LIG_FHA_1 | 287 | 293 | PF00498 | 0.699 |
LIG_FHA_1 | 376 | 382 | PF00498 | 0.558 |
LIG_FHA_1 | 414 | 420 | PF00498 | 0.475 |
LIG_FHA_1 | 475 | 481 | PF00498 | 0.672 |
LIG_FHA_1 | 551 | 557 | PF00498 | 0.370 |
LIG_FHA_1 | 614 | 620 | PF00498 | 0.515 |
LIG_FHA_1 | 712 | 718 | PF00498 | 0.485 |
LIG_FHA_1 | 801 | 807 | PF00498 | 0.469 |
LIG_FHA_2 | 361 | 367 | PF00498 | 0.601 |
LIG_FHA_2 | 395 | 401 | PF00498 | 0.456 |
LIG_FHA_2 | 539 | 545 | PF00498 | 0.361 |
LIG_FHA_2 | 713 | 719 | PF00498 | 0.472 |
LIG_FHA_2 | 820 | 826 | PF00498 | 0.465 |
LIG_LIR_Apic_2 | 206 | 212 | PF02991 | 0.424 |
LIG_LIR_Apic_2 | 255 | 260 | PF02991 | 0.526 |
LIG_LIR_Apic_2 | 85 | 90 | PF02991 | 0.490 |
LIG_LIR_Gen_1 | 536 | 547 | PF02991 | 0.321 |
LIG_LIR_Gen_1 | 583 | 591 | PF02991 | 0.363 |
LIG_LIR_Gen_1 | 649 | 660 | PF02991 | 0.361 |
LIG_LIR_Gen_1 | 7 | 18 | PF02991 | 0.476 |
LIG_LIR_Gen_1 | 770 | 781 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 152 | 157 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 173 | 178 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 282 | 287 | PF02991 | 0.652 |
LIG_LIR_Nem_3 | 429 | 433 | PF02991 | 0.536 |
LIG_LIR_Nem_3 | 536 | 542 | PF02991 | 0.351 |
LIG_LIR_Nem_3 | 583 | 588 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 649 | 655 | PF02991 | 0.325 |
LIG_LIR_Nem_3 | 7 | 13 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 730 | 734 | PF02991 | 0.591 |
LIG_LIR_Nem_3 | 770 | 776 | PF02991 | 0.373 |
LIG_LYPXL_yS_3 | 731 | 734 | PF13949 | 0.495 |
LIG_MYND_1 | 478 | 482 | PF01753 | 0.568 |
LIG_MYND_1 | 668 | 672 | PF01753 | 0.470 |
LIG_NRBOX | 457 | 463 | PF00104 | 0.481 |
LIG_NRBOX | 555 | 561 | PF00104 | 0.433 |
LIG_NRBOX | 599 | 605 | PF00104 | 0.408 |
LIG_PCNA_PIPBox_1 | 601 | 610 | PF02747 | 0.504 |
LIG_PCNA_yPIPBox_3 | 592 | 604 | PF02747 | 0.449 |
LIG_PDZ_Class_1 | 837 | 842 | PF00595 | 0.597 |
LIG_Pex14_1 | 10 | 14 | PF04695 | 0.481 |
LIG_Pex14_2 | 46 | 50 | PF04695 | 0.502 |
LIG_Pex14_2 | 830 | 834 | PF04695 | 0.326 |
LIG_SH2_CRK | 161 | 165 | PF00017 | 0.544 |
LIG_SH2_CRK | 209 | 213 | PF00017 | 0.439 |
LIG_SH2_CRK | 96 | 100 | PF00017 | 0.513 |
LIG_SH2_NCK_1 | 161 | 165 | PF00017 | 0.544 |
LIG_SH2_NCK_1 | 209 | 213 | PF00017 | 0.495 |
LIG_SH2_SRC | 159 | 162 | PF00017 | 0.547 |
LIG_SH2_SRC | 333 | 336 | PF00017 | 0.535 |
LIG_SH2_STAP1 | 154 | 158 | PF00017 | 0.445 |
LIG_SH2_STAP1 | 503 | 507 | PF00017 | 0.400 |
LIG_SH2_STAT3 | 157 | 160 | PF00017 | 0.549 |
LIG_SH2_STAT3 | 756 | 759 | PF00017 | 0.681 |
LIG_SH2_STAT5 | 157 | 160 | PF00017 | 0.556 |
LIG_SH2_STAT5 | 270 | 273 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 355 | 358 | PF00017 | 0.497 |
LIG_SH2_STAT5 | 376 | 379 | PF00017 | 0.552 |
LIG_SH2_STAT5 | 614 | 617 | PF00017 | 0.552 |
LIG_SH2_STAT5 | 836 | 839 | PF00017 | 0.483 |
LIG_SH3_1 | 61 | 67 | PF00018 | 0.503 |
LIG_SH3_1 | 699 | 705 | PF00018 | 0.535 |
LIG_SH3_2 | 15 | 20 | PF14604 | 0.477 |
LIG_SH3_2 | 26 | 31 | PF14604 | 0.482 |
LIG_SH3_3 | 12 | 18 | PF00018 | 0.474 |
LIG_SH3_3 | 171 | 177 | PF00018 | 0.476 |
LIG_SH3_3 | 23 | 29 | PF00018 | 0.469 |
LIG_SH3_3 | 280 | 286 | PF00018 | 0.477 |
LIG_SH3_3 | 59 | 65 | PF00018 | 0.499 |
LIG_SH3_3 | 699 | 705 | PF00018 | 0.535 |
LIG_SH3_3 | 85 | 91 | PF00018 | 0.488 |
LIG_SUMO_SIM_anti_2 | 803 | 810 | PF11976 | 0.490 |
LIG_SUMO_SIM_par_1 | 145 | 150 | PF11976 | 0.303 |
LIG_SUMO_SIM_par_1 | 313 | 319 | PF11976 | 0.351 |
LIG_TRAF2_1 | 564 | 567 | PF00917 | 0.562 |
LIG_TRAF2_1 | 595 | 598 | PF00917 | 0.507 |
LIG_TRAF2_1 | 716 | 719 | PF00917 | 0.495 |
LIG_TRFH_1 | 14 | 18 | PF08558 | 0.472 |
LIG_UBA3_1 | 461 | 466 | PF00899 | 0.663 |
MOD_CDK_SPK_2 | 63 | 68 | PF00069 | 0.507 |
MOD_CK1_1 | 162 | 168 | PF00069 | 0.521 |
MOD_CK1_1 | 182 | 188 | PF00069 | 0.410 |
MOD_CK1_1 | 290 | 296 | PF00069 | 0.708 |
MOD_CK1_1 | 302 | 308 | PF00069 | 0.738 |
MOD_CK1_1 | 454 | 460 | PF00069 | 0.529 |
MOD_CK1_1 | 517 | 523 | PF00069 | 0.329 |
MOD_CK1_1 | 676 | 682 | PF00069 | 0.407 |
MOD_CK1_1 | 701 | 707 | PF00069 | 0.370 |
MOD_CK1_1 | 711 | 717 | PF00069 | 0.262 |
MOD_CK1_1 | 755 | 761 | PF00069 | 0.539 |
MOD_CK1_1 | 8 | 14 | PF00069 | 0.480 |
MOD_CK1_1 | 800 | 806 | PF00069 | 0.394 |
MOD_CK1_1 | 83 | 89 | PF00069 | 0.496 |
MOD_CK2_1 | 114 | 120 | PF00069 | 0.638 |
MOD_CK2_1 | 162 | 168 | PF00069 | 0.519 |
MOD_CK2_1 | 297 | 303 | PF00069 | 0.817 |
MOD_CK2_1 | 360 | 366 | PF00069 | 0.586 |
MOD_CK2_1 | 712 | 718 | PF00069 | 0.318 |
MOD_Cter_Amidation | 132 | 135 | PF01082 | 0.536 |
MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.727 |
MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.578 |
MOD_GlcNHglycan | 238 | 241 | PF01048 | 0.566 |
MOD_GlcNHglycan | 422 | 425 | PF01048 | 0.492 |
MOD_GlcNHglycan | 436 | 439 | PF01048 | 0.367 |
MOD_GlcNHglycan | 473 | 477 | PF01048 | 0.610 |
MOD_GlcNHglycan | 641 | 644 | PF01048 | 0.663 |
MOD_GlcNHglycan | 675 | 678 | PF01048 | 0.333 |
MOD_GlcNHglycan | 682 | 685 | PF01048 | 0.308 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.481 |
MOD_GlcNHglycan | 749 | 753 | PF01048 | 0.504 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.500 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.583 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.552 |
MOD_GSK3_1 | 286 | 293 | PF00069 | 0.644 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.753 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.478 |
MOD_GSK3_1 | 434 | 441 | PF00069 | 0.595 |
MOD_GSK3_1 | 468 | 475 | PF00069 | 0.676 |
MOD_GSK3_1 | 551 | 558 | PF00069 | 0.399 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.496 |
MOD_GSK3_1 | 644 | 651 | PF00069 | 0.572 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.485 |
MOD_GSK3_1 | 676 | 683 | PF00069 | 0.384 |
MOD_GSK3_1 | 708 | 715 | PF00069 | 0.351 |
MOD_GSK3_1 | 748 | 755 | PF00069 | 0.493 |
MOD_GSK3_1 | 796 | 803 | PF00069 | 0.482 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.512 |
MOD_LATS_1 | 110 | 116 | PF00433 | 0.543 |
MOD_N-GLC_1 | 501 | 506 | PF02516 | 0.376 |
MOD_NEK2_1 | 170 | 175 | PF00069 | 0.526 |
MOD_NEK2_1 | 434 | 439 | PF00069 | 0.593 |
MOD_NEK2_1 | 555 | 560 | PF00069 | 0.398 |
MOD_NEK2_1 | 571 | 576 | PF00069 | 0.498 |
MOD_NEK2_1 | 690 | 695 | PF00069 | 0.347 |
MOD_NEK2_1 | 708 | 713 | PF00069 | 0.217 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.507 |
MOD_NEK2_1 | 727 | 732 | PF00069 | 0.480 |
MOD_NEK2_1 | 95 | 100 | PF00069 | 0.514 |
MOD_NEK2_2 | 768 | 773 | PF00069 | 0.438 |
MOD_OFUCOSY | 765 | 772 | PF10250 | 0.462 |
MOD_PIKK_1 | 755 | 761 | PF00454 | 0.473 |
MOD_PK_1 | 199 | 205 | PF00069 | 0.657 |
MOD_PK_1 | 262 | 268 | PF00069 | 0.350 |
MOD_PKA_1 | 632 | 638 | PF00069 | 0.538 |
MOD_PKA_2 | 327 | 333 | PF00069 | 0.351 |
MOD_PKA_2 | 413 | 419 | PF00069 | 0.519 |
MOD_PKA_2 | 454 | 460 | PF00069 | 0.498 |
MOD_PKA_2 | 67 | 73 | PF00069 | 0.519 |
MOD_Plk_1 | 199 | 205 | PF00069 | 0.657 |
MOD_Plk_1 | 501 | 507 | PF00069 | 0.373 |
MOD_Plk_1 | 566 | 572 | PF00069 | 0.597 |
MOD_Plk_1 | 748 | 754 | PF00069 | 0.479 |
MOD_Plk_2-3 | 820 | 826 | PF00069 | 0.551 |
MOD_Plk_4 | 413 | 419 | PF00069 | 0.463 |
MOD_Plk_4 | 502 | 508 | PF00069 | 0.367 |
MOD_Plk_4 | 538 | 544 | PF00069 | 0.495 |
MOD_Plk_4 | 551 | 557 | PF00069 | 0.290 |
MOD_Plk_4 | 599 | 605 | PF00069 | 0.505 |
MOD_Plk_4 | 625 | 631 | PF00069 | 0.306 |
MOD_ProDKin_1 | 115 | 121 | PF00069 | 0.503 |
MOD_ProDKin_1 | 139 | 145 | PF00069 | 0.463 |
MOD_ProDKin_1 | 160 | 166 | PF00069 | 0.542 |
MOD_ProDKin_1 | 244 | 250 | PF00069 | 0.563 |
MOD_ProDKin_1 | 279 | 285 | PF00069 | 0.600 |
MOD_ProDKin_1 | 445 | 451 | PF00069 | 0.450 |
MOD_ProDKin_1 | 474 | 480 | PF00069 | 0.769 |
MOD_ProDKin_1 | 514 | 520 | PF00069 | 0.495 |
MOD_ProDKin_1 | 533 | 539 | PF00069 | 0.638 |
MOD_ProDKin_1 | 573 | 579 | PF00069 | 0.568 |
MOD_ProDKin_1 | 60 | 66 | PF00069 | 0.502 |
MOD_ProDKin_1 | 698 | 704 | PF00069 | 0.407 |
MOD_ProDKin_1 | 797 | 803 | PF00069 | 0.521 |
MOD_ProDKin_1 | 99 | 105 | PF00069 | 0.619 |
MOD_SUMO_rev_2 | 40 | 46 | PF00179 | 0.514 |
MOD_SUMO_rev_2 | 423 | 433 | PF00179 | 0.511 |
TRG_DiLeu_BaEn_2 | 494 | 500 | PF01217 | 0.377 |
TRG_DiLeu_BaLyEn_6 | 17 | 22 | PF01217 | 0.488 |
TRG_DiLeu_BaLyEn_6 | 31 | 36 | PF01217 | 0.496 |
TRG_DiLeu_BaLyEn_6 | 802 | 807 | PF01217 | 0.526 |
TRG_ENDOCYTIC_2 | 503 | 506 | PF00928 | 0.404 |
TRG_ENDOCYTIC_2 | 731 | 734 | PF00928 | 0.362 |
TRG_ENDOCYTIC_2 | 96 | 99 | PF00928 | 0.517 |
TRG_ER_diArg_1 | 29 | 31 | PF00400 | 0.519 |
TRG_ER_diArg_1 | 311 | 313 | PF00400 | 0.448 |
TRG_ER_diArg_1 | 521 | 523 | PF00400 | 0.544 |
TRG_ER_diArg_1 | 592 | 595 | PF00400 | 0.475 |
TRG_NLS_MonoExtC_3 | 630 | 636 | PF00514 | 0.559 |
TRG_Pf-PMV_PEXEL_1 | 632 | 636 | PF00026 | 0.541 |
TRG_Pf-PMV_PEXEL_1 | 688 | 692 | PF00026 | 0.351 |
TRG_Pf-PMV_PEXEL_1 | 745 | 749 | PF00026 | 0.444 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PA86 | Leptomonas seymouri | 48% | 100% |
A0A0S4JUU1 | Bodo saltans | 30% | 100% |
A0A1X0NZU0 | Trypanosomatidae | 36% | 100% |
A0A3Q8IGM4 | Leishmania donovani | 78% | 100% |
A4I1J6 | Leishmania infantum | 79% | 100% |
Q4Q9U1 | Leishmania major | 78% | 99% |