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: 20 |
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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: A4HAV7
Term | Name | Level | Count |
---|---|---|---|
GO:0006414 | translational elongation | 5 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009058 | biosynthetic process | 2 | 1 |
GO:0009059 | macromolecule biosynthetic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0034645 | obsolete cellular macromolecule biosynthetic process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044249 | cellular biosynthetic process | 3 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901576 | organic substance biosynthetic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 10 |
GO:0003824 | catalytic activity | 1 | 10 |
GO:0003924 | GTPase activity | 7 | 10 |
GO:0005488 | binding | 1 | 10 |
GO:0005525 | GTP binding | 5 | 10 |
GO:0016462 | pyrophosphatase activity | 5 | 10 |
GO:0016787 | hydrolase activity | 2 | 10 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 10 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 10 |
GO:0017076 | purine nucleotide binding | 4 | 10 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 10 |
GO:0019001 | guanyl nucleotide binding | 5 | 10 |
GO:0032553 | ribonucleotide binding | 3 | 10 |
GO:0032555 | purine ribonucleotide binding | 4 | 10 |
GO:0032561 | guanyl ribonucleotide binding | 5 | 10 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 10 |
GO:0036094 | small molecule binding | 2 | 10 |
GO:0043167 | ion binding | 2 | 10 |
GO:0043168 | anion binding | 3 | 10 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:0097367 | carbohydrate derivative binding | 2 | 10 |
GO:1901265 | nucleoside phosphate binding | 3 | 10 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
GO:0003676 | nucleic acid binding | 3 | 2 |
GO:0003746 | translation elongation factor activity | 4 | 2 |
GO:0008135 | translation factor activity, RNA binding | 3 | 2 |
GO:0045182 | translation regulator activity | 1 | 2 |
GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 113 | 117 | PF00656 | 0.582 |
CLV_C14_Caspase3-7 | 442 | 446 | PF00656 | 0.529 |
CLV_C14_Caspase3-7 | 528 | 532 | PF00656 | 0.545 |
CLV_C14_Caspase3-7 | 760 | 764 | PF00656 | 0.762 |
CLV_C14_Caspase3-7 | 788 | 792 | PF00656 | 0.547 |
CLV_NRD_NRD_1 | 227 | 229 | PF00675 | 0.563 |
CLV_NRD_NRD_1 | 311 | 313 | PF00675 | 0.565 |
CLV_NRD_NRD_1 | 460 | 462 | PF00675 | 0.282 |
CLV_NRD_NRD_1 | 59 | 61 | PF00675 | 0.669 |
CLV_PCSK_KEX2_1 | 227 | 229 | PF00082 | 0.563 |
CLV_PCSK_KEX2_1 | 311 | 313 | PF00082 | 0.565 |
CLV_PCSK_KEX2_1 | 59 | 61 | PF00082 | 0.669 |
CLV_PCSK_SKI1_1 | 258 | 262 | PF00082 | 0.592 |
CLV_PCSK_SKI1_1 | 439 | 443 | PF00082 | 0.266 |
CLV_PCSK_SKI1_1 | 452 | 456 | PF00082 | 0.207 |
CLV_PCSK_SKI1_1 | 773 | 777 | PF00082 | 0.508 |
CLV_PCSK_SKI1_1 | 779 | 783 | PF00082 | 0.490 |
DEG_APCC_DBOX_1 | 596 | 604 | PF00400 | 0.509 |
DEG_SCF_FBW7_1 | 427 | 434 | PF00400 | 0.470 |
DEG_SCF_FBW7_1 | 561 | 568 | PF00400 | 0.560 |
DEG_SPOP_SBC_1 | 408 | 412 | PF00917 | 0.380 |
DEG_SPOP_SBC_1 | 556 | 560 | PF00917 | 0.564 |
DOC_CKS1_1 | 490 | 495 | PF01111 | 0.537 |
DOC_CKS1_1 | 562 | 567 | PF01111 | 0.560 |
DOC_CKS1_1 | 810 | 815 | PF01111 | 0.379 |
DOC_CYCLIN_RxL_1 | 773 | 785 | PF00134 | 0.491 |
DOC_CYCLIN_yCln2_LP_2 | 389 | 395 | PF00134 | 0.463 |
DOC_MAPK_gen_1 | 461 | 468 | PF00069 | 0.537 |
DOC_MAPK_gen_1 | 643 | 651 | PF00069 | 0.495 |
DOC_MAPK_gen_1 | 742 | 750 | PF00069 | 0.488 |
DOC_MAPK_HePTP_8 | 458 | 470 | PF00069 | 0.537 |
DOC_MAPK_MEF2A_6 | 333 | 341 | PF00069 | 0.457 |
DOC_MAPK_MEF2A_6 | 461 | 470 | PF00069 | 0.537 |
DOC_PP2B_LxvP_1 | 108 | 111 | PF13499 | 0.480 |
DOC_PP2B_LxvP_1 | 577 | 580 | PF13499 | 0.537 |
DOC_PP2B_LxvP_1 | 612 | 615 | PF13499 | 0.616 |
DOC_PP2B_LxvP_1 | 76 | 79 | PF13499 | 0.503 |
DOC_PP2B_LxvP_1 | 92 | 95 | PF13499 | 0.480 |
DOC_USP7_MATH_1 | 165 | 169 | PF00917 | 0.634 |
DOC_USP7_MATH_1 | 328 | 332 | PF00917 | 0.502 |
DOC_USP7_MATH_1 | 407 | 411 | PF00917 | 0.453 |
DOC_USP7_MATH_1 | 414 | 418 | PF00917 | 0.444 |
DOC_USP7_MATH_1 | 475 | 479 | PF00917 | 0.528 |
DOC_USP7_MATH_1 | 51 | 55 | PF00917 | 0.616 |
DOC_USP7_MATH_1 | 722 | 726 | PF00917 | 0.529 |
DOC_USP7_MATH_1 | 8 | 12 | PF00917 | 0.741 |
DOC_USP7_MATH_1 | 95 | 99 | PF00917 | 0.525 |
DOC_WW_Pin1_4 | 153 | 158 | PF00397 | 0.719 |
DOC_WW_Pin1_4 | 218 | 223 | PF00397 | 0.477 |
DOC_WW_Pin1_4 | 267 | 272 | PF00397 | 0.674 |
DOC_WW_Pin1_4 | 383 | 388 | PF00397 | 0.518 |
DOC_WW_Pin1_4 | 397 | 402 | PF00397 | 0.455 |
DOC_WW_Pin1_4 | 418 | 423 | PF00397 | 0.543 |
DOC_WW_Pin1_4 | 425 | 430 | PF00397 | 0.547 |
DOC_WW_Pin1_4 | 434 | 439 | PF00397 | 0.371 |
DOC_WW_Pin1_4 | 489 | 494 | PF00397 | 0.537 |
DOC_WW_Pin1_4 | 557 | 562 | PF00397 | 0.542 |
DOC_WW_Pin1_4 | 606 | 611 | PF00397 | 0.527 |
DOC_WW_Pin1_4 | 78 | 83 | PF00397 | 0.712 |
DOC_WW_Pin1_4 | 809 | 814 | PF00397 | 0.356 |
DOC_WW_Pin1_4 | 85 | 90 | PF00397 | 0.654 |
LIG_14-3-3_CanoR_1 | 353 | 357 | PF00244 | 0.521 |
LIG_14-3-3_CanoR_1 | 367 | 372 | PF00244 | 0.528 |
LIG_14-3-3_CanoR_1 | 374 | 379 | PF00244 | 0.509 |
LIG_14-3-3_CanoR_1 | 391 | 399 | PF00244 | 0.466 |
LIG_14-3-3_CanoR_1 | 439 | 444 | PF00244 | 0.492 |
LIG_14-3-3_CanoR_1 | 50 | 56 | PF00244 | 0.656 |
LIG_14-3-3_CanoR_1 | 597 | 607 | PF00244 | 0.510 |
LIG_14-3-3_CanoR_1 | 74 | 79 | PF00244 | 0.647 |
LIG_14-3-3_CanoR_1 | 749 | 754 | PF00244 | 0.321 |
LIG_14-3-3_CanoR_1 | 806 | 811 | PF00244 | 0.558 |
LIG_Actin_WH2_2 | 14 | 32 | PF00022 | 0.486 |
LIG_APCC_ABBA_1 | 480 | 485 | PF00400 | 0.533 |
LIG_BIR_III_4 | 160 | 164 | PF00653 | 0.497 |
LIG_BIR_III_4 | 445 | 449 | PF00653 | 0.537 |
LIG_BRCT_BRCA1_1 | 321 | 325 | PF00533 | 0.422 |
LIG_FHA_1 | 340 | 346 | PF00498 | 0.488 |
LIG_FHA_1 | 366 | 372 | PF00498 | 0.449 |
LIG_FHA_1 | 472 | 478 | PF00498 | 0.537 |
LIG_FHA_1 | 490 | 496 | PF00498 | 0.537 |
LIG_FHA_1 | 557 | 563 | PF00498 | 0.547 |
LIG_FHA_1 | 688 | 694 | PF00498 | 0.395 |
LIG_FHA_1 | 721 | 727 | PF00498 | 0.356 |
LIG_FHA_2 | 257 | 263 | PF00498 | 0.550 |
LIG_FHA_2 | 276 | 282 | PF00498 | 0.562 |
LIG_FHA_2 | 294 | 300 | PF00498 | 0.643 |
LIG_FHA_2 | 440 | 446 | PF00498 | 0.498 |
LIG_FHA_2 | 497 | 503 | PF00498 | 0.457 |
LIG_FHA_2 | 558 | 564 | PF00498 | 0.477 |
LIG_FHA_2 | 98 | 104 | PF00498 | 0.489 |
LIG_GSK3_LRP6_1 | 606 | 611 | PF00069 | 0.666 |
LIG_Integrin_isoDGR_2 | 662 | 664 | PF01839 | 0.304 |
LIG_Integrin_RGD_1 | 158 | 160 | PF01839 | 0.500 |
LIG_LIR_Apic_2 | 654 | 659 | PF02991 | 0.486 |
LIG_LIR_Gen_1 | 16 | 26 | PF02991 | 0.492 |
LIG_LIR_Gen_1 | 190 | 199 | PF02991 | 0.444 |
LIG_LIR_Gen_1 | 270 | 280 | PF02991 | 0.731 |
LIG_LIR_Gen_1 | 373 | 382 | PF02991 | 0.477 |
LIG_LIR_Gen_1 | 464 | 472 | PF02991 | 0.516 |
LIG_LIR_Gen_1 | 481 | 490 | PF02991 | 0.488 |
LIG_LIR_Gen_1 | 492 | 498 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 16 | 21 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 190 | 195 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 270 | 275 | PF02991 | 0.732 |
LIG_LIR_Nem_3 | 373 | 379 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 464 | 468 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 481 | 486 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 492 | 497 | PF02991 | 0.458 |
LIG_MYND_1 | 610 | 614 | PF01753 | 0.690 |
LIG_PDZ_Class_2 | 811 | 816 | PF00595 | 0.602 |
LIG_Rb_LxCxE_1 | 299 | 316 | PF01857 | 0.455 |
LIG_SH2_CRK | 166 | 170 | PF00017 | 0.704 |
LIG_SH2_CRK | 272 | 276 | PF00017 | 0.760 |
LIG_SH2_CRK | 666 | 670 | PF00017 | 0.493 |
LIG_SH2_NCK_1 | 272 | 276 | PF00017 | 0.507 |
LIG_SH2_PTP2 | 465 | 468 | PF00017 | 0.537 |
LIG_SH2_PTP2 | 656 | 659 | PF00017 | 0.476 |
LIG_SH2_SRC | 483 | 486 | PF00017 | 0.533 |
LIG_SH2_STAP1 | 22 | 26 | PF00017 | 0.480 |
LIG_SH2_STAP1 | 666 | 670 | PF00017 | 0.454 |
LIG_SH2_STAP1 | 740 | 744 | PF00017 | 0.455 |
LIG_SH2_STAT3 | 286 | 289 | PF00017 | 0.501 |
LIG_SH2_STAT5 | 465 | 468 | PF00017 | 0.537 |
LIG_SH2_STAT5 | 539 | 542 | PF00017 | 0.537 |
LIG_SH2_STAT5 | 598 | 601 | PF00017 | 0.560 |
LIG_SH2_STAT5 | 656 | 659 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 740 | 743 | PF00017 | 0.426 |
LIG_SH3_1 | 140 | 146 | PF00018 | 0.761 |
LIG_SH3_3 | 140 | 146 | PF00018 | 0.764 |
LIG_SH3_3 | 379 | 385 | PF00018 | 0.398 |
LIG_SH3_3 | 416 | 422 | PF00018 | 0.565 |
LIG_SH3_3 | 426 | 432 | PF00018 | 0.521 |
LIG_SH3_3 | 559 | 565 | PF00018 | 0.408 |
LIG_SH3_3 | 604 | 610 | PF00018 | 0.501 |
LIG_SH3_3 | 642 | 648 | PF00018 | 0.278 |
LIG_SH3_3 | 707 | 713 | PF00018 | 0.521 |
LIG_SH3_3 | 750 | 756 | PF00018 | 0.557 |
LIG_SH3_3 | 76 | 82 | PF00018 | 0.755 |
LIG_SH3_3 | 807 | 813 | PF00018 | 0.467 |
LIG_SUMO_SIM_anti_2 | 440 | 445 | PF11976 | 0.509 |
LIG_SUMO_SIM_anti_2 | 723 | 728 | PF11976 | 0.292 |
LIG_SUMO_SIM_anti_2 | 90 | 98 | PF11976 | 0.731 |
LIG_SUMO_SIM_par_1 | 494 | 499 | PF11976 | 0.536 |
LIG_SUMO_SIM_par_1 | 722 | 728 | PF11976 | 0.287 |
LIG_SUMO_SIM_par_1 | 90 | 98 | PF11976 | 0.720 |
LIG_TRAF2_1 | 757 | 760 | PF00917 | 0.723 |
LIG_TYR_ITIM | 164 | 169 | PF00017 | 0.675 |
LIG_UBA3_1 | 454 | 462 | PF00899 | 0.537 |
LIG_WRC_WIRS_1 | 15 | 20 | PF05994 | 0.499 |
MOD_CDK_SPK_2 | 153 | 158 | PF00069 | 0.506 |
MOD_CDK_SPK_2 | 397 | 402 | PF00069 | 0.560 |
MOD_CDK_SPK_2 | 434 | 439 | PF00069 | 0.537 |
MOD_CDK_SPxxK_3 | 267 | 274 | PF00069 | 0.761 |
MOD_CK1_1 | 11 | 17 | PF00069 | 0.612 |
MOD_CK1_1 | 131 | 137 | PF00069 | 0.740 |
MOD_CK1_1 | 147 | 153 | PF00069 | 0.779 |
MOD_CK1_1 | 233 | 239 | PF00069 | 0.396 |
MOD_CK1_1 | 331 | 337 | PF00069 | 0.491 |
MOD_CK1_1 | 370 | 376 | PF00069 | 0.483 |
MOD_CK1_1 | 412 | 418 | PF00069 | 0.572 |
MOD_CK1_1 | 437 | 443 | PF00069 | 0.511 |
MOD_CK1_1 | 478 | 484 | PF00069 | 0.560 |
MOD_CK1_1 | 613 | 619 | PF00069 | 0.657 |
MOD_CK1_1 | 725 | 731 | PF00069 | 0.554 |
MOD_CK1_1 | 762 | 768 | PF00069 | 0.697 |
MOD_CK1_1 | 809 | 815 | PF00069 | 0.370 |
MOD_CK1_1 | 97 | 103 | PF00069 | 0.748 |
MOD_CK2_1 | 275 | 281 | PF00069 | 0.756 |
MOD_CK2_1 | 293 | 299 | PF00069 | 0.418 |
MOD_CK2_1 | 557 | 563 | PF00069 | 0.411 |
MOD_CK2_1 | 754 | 760 | PF00069 | 0.666 |
MOD_CK2_1 | 97 | 103 | PF00069 | 0.553 |
MOD_DYRK1A_RPxSP_1 | 267 | 271 | PF00069 | 0.507 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.672 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.765 |
MOD_GlcNHglycan | 186 | 190 | PF01048 | 0.368 |
MOD_GlcNHglycan | 222 | 225 | PF01048 | 0.432 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.561 |
MOD_GlcNHglycan | 330 | 333 | PF01048 | 0.246 |
MOD_GlcNHglycan | 393 | 396 | PF01048 | 0.299 |
MOD_GlcNHglycan | 536 | 539 | PF01048 | 0.277 |
MOD_GlcNHglycan | 572 | 575 | PF01048 | 0.240 |
MOD_GlcNHglycan | 628 | 631 | PF01048 | 0.467 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.503 |
MOD_GlcNHglycan | 787 | 790 | PF01048 | 0.547 |
MOD_GlcNHglycan | 9 | 13 | PF01048 | 0.690 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.681 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.651 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.688 |
MOD_GSK3_1 | 214 | 221 | PF00069 | 0.558 |
MOD_GSK3_1 | 256 | 263 | PF00069 | 0.413 |
MOD_GSK3_1 | 328 | 335 | PF00069 | 0.471 |
MOD_GSK3_1 | 362 | 369 | PF00069 | 0.458 |
MOD_GSK3_1 | 370 | 377 | PF00069 | 0.461 |
MOD_GSK3_1 | 393 | 400 | PF00069 | 0.501 |
MOD_GSK3_1 | 408 | 415 | PF00069 | 0.501 |
MOD_GSK3_1 | 427 | 434 | PF00069 | 0.439 |
MOD_GSK3_1 | 471 | 478 | PF00069 | 0.542 |
MOD_GSK3_1 | 557 | 564 | PF00069 | 0.515 |
MOD_GSK3_1 | 606 | 613 | PF00069 | 0.621 |
MOD_GSK3_1 | 74 | 81 | PF00069 | 0.640 |
MOD_GSK3_1 | 751 | 758 | PF00069 | 0.558 |
MOD_GSK3_1 | 759 | 766 | PF00069 | 0.683 |
MOD_GSK3_1 | 805 | 812 | PF00069 | 0.573 |
MOD_N-GLC_1 | 230 | 235 | PF02516 | 0.550 |
MOD_N-GLC_1 | 275 | 280 | PF02516 | 0.502 |
MOD_NEK2_1 | 13 | 18 | PF00069 | 0.635 |
MOD_NEK2_1 | 136 | 141 | PF00069 | 0.760 |
MOD_NEK2_1 | 230 | 235 | PF00069 | 0.478 |
MOD_NEK2_1 | 246 | 251 | PF00069 | 0.448 |
MOD_NEK2_1 | 340 | 345 | PF00069 | 0.554 |
MOD_NEK2_1 | 534 | 539 | PF00069 | 0.434 |
MOD_NEK2_1 | 582 | 587 | PF00069 | 0.457 |
MOD_NEK2_1 | 626 | 631 | PF00069 | 0.401 |
MOD_NEK2_1 | 720 | 725 | PF00069 | 0.460 |
MOD_NEK2_1 | 727 | 732 | PF00069 | 0.483 |
MOD_NEK2_2 | 51 | 56 | PF00069 | 0.615 |
MOD_PIKK_1 | 194 | 200 | PF00454 | 0.424 |
MOD_PIKK_1 | 39 | 45 | PF00454 | 0.687 |
MOD_PIKK_1 | 393 | 399 | PF00454 | 0.392 |
MOD_PIKK_1 | 725 | 731 | PF00454 | 0.489 |
MOD_PK_1 | 749 | 755 | PF00069 | 0.330 |
MOD_PK_1 | 806 | 812 | PF00069 | 0.456 |
MOD_PKA_2 | 182 | 188 | PF00069 | 0.406 |
MOD_PKA_2 | 201 | 207 | PF00069 | 0.509 |
MOD_PKA_2 | 352 | 358 | PF00069 | 0.521 |
MOD_PKA_2 | 366 | 372 | PF00069 | 0.531 |
MOD_PKA_2 | 748 | 754 | PF00069 | 0.338 |
MOD_PKA_2 | 805 | 811 | PF00069 | 0.520 |
MOD_Plk_1 | 230 | 236 | PF00069 | 0.472 |
MOD_Plk_1 | 246 | 252 | PF00069 | 0.441 |
MOD_Plk_1 | 319 | 325 | PF00069 | 0.508 |
MOD_Plk_1 | 478 | 484 | PF00069 | 0.484 |
MOD_Plk_1 | 687 | 693 | PF00069 | 0.409 |
MOD_Plk_1 | 95 | 101 | PF00069 | 0.482 |
MOD_Plk_4 | 165 | 171 | PF00069 | 0.556 |
MOD_Plk_4 | 17 | 23 | PF00069 | 0.672 |
MOD_Plk_4 | 233 | 239 | PF00069 | 0.410 |
MOD_Plk_4 | 246 | 252 | PF00069 | 0.452 |
MOD_Plk_4 | 332 | 338 | PF00069 | 0.457 |
MOD_Plk_4 | 352 | 358 | PF00069 | 0.324 |
MOD_Plk_4 | 450 | 456 | PF00069 | 0.517 |
MOD_Plk_4 | 478 | 484 | PF00069 | 0.522 |
MOD_Plk_4 | 529 | 535 | PF00069 | 0.542 |
MOD_Plk_4 | 722 | 728 | PF00069 | 0.539 |
MOD_Plk_4 | 806 | 812 | PF00069 | 0.442 |
MOD_Plk_4 | 87 | 93 | PF00069 | 0.708 |
MOD_ProDKin_1 | 153 | 159 | PF00069 | 0.715 |
MOD_ProDKin_1 | 218 | 224 | PF00069 | 0.470 |
MOD_ProDKin_1 | 267 | 273 | PF00069 | 0.673 |
MOD_ProDKin_1 | 383 | 389 | PF00069 | 0.518 |
MOD_ProDKin_1 | 397 | 403 | PF00069 | 0.455 |
MOD_ProDKin_1 | 418 | 424 | PF00069 | 0.543 |
MOD_ProDKin_1 | 425 | 431 | PF00069 | 0.547 |
MOD_ProDKin_1 | 434 | 440 | PF00069 | 0.371 |
MOD_ProDKin_1 | 489 | 495 | PF00069 | 0.537 |
MOD_ProDKin_1 | 557 | 563 | PF00069 | 0.542 |
MOD_ProDKin_1 | 606 | 612 | PF00069 | 0.533 |
MOD_ProDKin_1 | 78 | 84 | PF00069 | 0.709 |
MOD_ProDKin_1 | 809 | 815 | PF00069 | 0.370 |
MOD_ProDKin_1 | 85 | 91 | PF00069 | 0.656 |
TRG_DiLeu_BaEn_1 | 508 | 513 | PF01217 | 0.537 |
TRG_DiLeu_BaEn_4 | 103 | 109 | PF01217 | 0.496 |
TRG_DiLeu_BaEn_4 | 24 | 30 | PF01217 | 0.492 |
TRG_DiLeu_BaLyEn_6 | 140 | 145 | PF01217 | 0.741 |
TRG_DiLeu_BaLyEn_6 | 607 | 612 | PF01217 | 0.685 |
TRG_ENDOCYTIC_2 | 166 | 169 | PF00928 | 0.710 |
TRG_ENDOCYTIC_2 | 272 | 275 | PF00928 | 0.761 |
TRG_ENDOCYTIC_2 | 465 | 468 | PF00928 | 0.509 |
TRG_ENDOCYTIC_2 | 483 | 486 | PF00928 | 0.457 |
TRG_ENDOCYTIC_2 | 666 | 669 | PF00928 | 0.459 |
TRG_ER_diArg_1 | 226 | 228 | PF00400 | 0.557 |
TRG_ER_diArg_1 | 545 | 548 | PF00400 | 0.537 |
TRG_ER_diArg_1 | 576 | 579 | PF00400 | 0.537 |
TRG_ER_diArg_1 | 59 | 61 | PF00400 | 0.647 |
TRG_NES_CRM1_1 | 235 | 247 | PF08389 | 0.426 |
TRG_NES_CRM1_1 | 508 | 521 | PF08389 | 0.488 |
TRG_Pf-PMV_PEXEL_1 | 773 | 777 | PF00026 | 0.285 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8Y7 | Leptomonas seymouri | 65% | 97% |
A0A0S4JNB2 | Bodo saltans | 34% | 100% |
A0A1X0PAM4 | Trypanosomatidae | 40% | 100% |
A0A3R7MTY6 | Trypanosoma rangeli | 39% | 100% |
A0A3S7X814 | Leishmania donovani | 79% | 93% |
A4IA17 | Leishmania infantum | 79% | 93% |
C9ZMK5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
D2XV59 | Rattus norvegicus | 26% | 100% |
E9B532 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 93% |
O00178 | Homo sapiens | 26% | 100% |
O08582 | Mus musculus | 26% | 100% |
Q3UJK4 | Mus musculus | 26% | 100% |
Q4Q2V4 | Leishmania major | 77% | 100% |
Q58DC5 | Bos taurus | 26% | 100% |
Q5R8Q7 | Pongo abelii | 26% | 100% |
Q5XGS8 | Xenopus laevis | 25% | 100% |
Q9BX10 | Homo sapiens | 26% | 100% |