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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005739 | mitochondrion | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HKL4
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006396 | RNA processing | 6 | 1 |
GO:0006399 | tRNA metabolic process | 7 | 1 |
GO:0006400 | tRNA modification | 6 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008033 | tRNA processing | 8 | 1 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009451 | RNA modification | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0019988 | charged-tRNA amino acid modification | 7 | 1 |
GO:0034470 | ncRNA processing | 7 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0034660 | ncRNA metabolic process | 6 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0071951 | conversion of methionyl-tRNA to N-formyl-methionyl-tRNA | 8 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
GO:0009058 | biosynthetic process | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 7 |
GO:0004479 | methionyl-tRNA formyltransferase activity | 5 | 6 |
GO:0016740 | transferase activity | 2 | 7 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 6 |
GO:0016742 | hydroxymethyl-, formyl- and related transferase activity | 4 | 6 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 6 |
GO:0140101 | catalytic activity, acting on a tRNA | 4 | 6 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 6 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 116 | 120 | PF00656 | 0.344 |
CLV_C14_Caspase3-7 | 17 | 21 | PF00656 | 0.548 |
CLV_C14_Caspase3-7 | 261 | 265 | PF00656 | 0.516 |
CLV_C14_Caspase3-7 | 52 | 56 | PF00656 | 0.587 |
CLV_C14_Caspase3-7 | 561 | 565 | PF00656 | 0.536 |
CLV_C14_Caspase3-7 | 791 | 795 | PF00656 | 0.509 |
CLV_MEL_PAP_1 | 756 | 762 | PF00089 | 0.515 |
CLV_NRD_NRD_1 | 645 | 647 | PF00675 | 0.453 |
CLV_NRD_NRD_1 | 649 | 651 | PF00675 | 0.435 |
CLV_NRD_NRD_1 | 770 | 772 | PF00675 | 0.556 |
CLV_NRD_NRD_1 | 804 | 806 | PF00675 | 0.604 |
CLV_NRD_NRD_1 | 952 | 954 | PF00675 | 0.543 |
CLV_PCSK_FUR_1 | 802 | 806 | PF00082 | 0.532 |
CLV_PCSK_KEX2_1 | 122 | 124 | PF00082 | 0.517 |
CLV_PCSK_KEX2_1 | 645 | 647 | PF00082 | 0.453 |
CLV_PCSK_KEX2_1 | 649 | 651 | PF00082 | 0.435 |
CLV_PCSK_KEX2_1 | 770 | 772 | PF00082 | 0.556 |
CLV_PCSK_KEX2_1 | 804 | 806 | PF00082 | 0.604 |
CLV_PCSK_PC1ET2_1 | 122 | 124 | PF00082 | 0.517 |
CLV_PCSK_PC7_1 | 645 | 651 | PF00082 | 0.468 |
CLV_PCSK_SKI1_1 | 110 | 114 | PF00082 | 0.443 |
CLV_PCSK_SKI1_1 | 115 | 119 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 207 | 211 | PF00082 | 0.269 |
CLV_PCSK_SKI1_1 | 212 | 216 | PF00082 | 0.269 |
CLV_PCSK_SKI1_1 | 645 | 649 | PF00082 | 0.447 |
CLV_PCSK_SKI1_1 | 650 | 654 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 785 | 789 | PF00082 | 0.586 |
DEG_APCC_DBOX_1 | 486 | 494 | PF00400 | 0.481 |
DEG_APCC_DBOX_1 | 644 | 652 | PF00400 | 0.432 |
DEG_COP1_1 | 886 | 896 | PF00400 | 0.628 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.480 |
DEG_SPOP_SBC_1 | 150 | 154 | PF00917 | 0.519 |
DOC_ANK_TNKS_1 | 243 | 250 | PF00023 | 0.414 |
DOC_CKS1_1 | 724 | 729 | PF01111 | 0.400 |
DOC_CYCLIN_RxL_1 | 782 | 791 | PF00134 | 0.583 |
DOC_MAPK_gen_1 | 487 | 495 | PF00069 | 0.515 |
DOC_MAPK_gen_1 | 508 | 518 | PF00069 | 0.521 |
DOC_MAPK_gen_1 | 528 | 535 | PF00069 | 0.483 |
DOC_MAPK_gen_1 | 645 | 653 | PF00069 | 0.356 |
DOC_MAPK_gen_1 | 770 | 776 | PF00069 | 0.516 |
DOC_MAPK_HePTP_8 | 950 | 967 | PF00069 | 0.537 |
DOC_MAPK_MEF2A_6 | 528 | 535 | PF00069 | 0.483 |
DOC_MAPK_MEF2A_6 | 804 | 812 | PF00069 | 0.517 |
DOC_MAPK_MEF2A_6 | 945 | 952 | PF00069 | 0.534 |
DOC_MAPK_MEF2A_6 | 959 | 967 | PF00069 | 0.542 |
DOC_MAPK_NFAT4_5 | 528 | 536 | PF00069 | 0.476 |
DOC_PP1_RVXF_1 | 281 | 287 | PF00149 | 0.421 |
DOC_PP1_RVXF_1 | 771 | 777 | PF00149 | 0.595 |
DOC_PP2B_LxvP_1 | 216 | 219 | PF13499 | 0.414 |
DOC_PP2B_LxvP_1 | 493 | 496 | PF13499 | 0.502 |
DOC_PP2B_LxvP_1 | 907 | 910 | PF13499 | 0.499 |
DOC_SPAK_OSR1_1 | 759 | 763 | PF12202 | 0.527 |
DOC_USP7_MATH_1 | 128 | 132 | PF00917 | 0.588 |
DOC_USP7_MATH_1 | 151 | 155 | PF00917 | 0.603 |
DOC_USP7_MATH_1 | 171 | 175 | PF00917 | 0.548 |
DOC_USP7_MATH_1 | 262 | 266 | PF00917 | 0.469 |
DOC_USP7_MATH_1 | 31 | 35 | PF00917 | 0.570 |
DOC_USP7_MATH_1 | 316 | 320 | PF00917 | 0.510 |
DOC_USP7_MATH_1 | 324 | 328 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 330 | 334 | PF00917 | 0.563 |
DOC_USP7_MATH_1 | 457 | 461 | PF00917 | 0.653 |
DOC_USP7_MATH_1 | 626 | 630 | PF00917 | 0.510 |
DOC_USP7_MATH_1 | 792 | 796 | PF00917 | 0.507 |
DOC_USP7_MATH_1 | 823 | 827 | PF00917 | 0.535 |
DOC_USP7_MATH_1 | 879 | 883 | PF00917 | 0.556 |
DOC_USP7_UBL2_3 | 168 | 172 | PF12436 | 0.650 |
DOC_USP7_UBL2_3 | 941 | 945 | PF12436 | 0.549 |
DOC_WW_Pin1_4 | 161 | 166 | PF00397 | 0.593 |
DOC_WW_Pin1_4 | 181 | 186 | PF00397 | 0.548 |
DOC_WW_Pin1_4 | 233 | 238 | PF00397 | 0.469 |
DOC_WW_Pin1_4 | 320 | 325 | PF00397 | 0.558 |
DOC_WW_Pin1_4 | 362 | 367 | PF00397 | 0.586 |
DOC_WW_Pin1_4 | 473 | 478 | PF00397 | 0.595 |
DOC_WW_Pin1_4 | 497 | 502 | PF00397 | 0.653 |
DOC_WW_Pin1_4 | 554 | 559 | PF00397 | 0.550 |
DOC_WW_Pin1_4 | 634 | 639 | PF00397 | 0.488 |
DOC_WW_Pin1_4 | 723 | 728 | PF00397 | 0.421 |
LIG_14-3-3_CanoR_1 | 489 | 494 | PF00244 | 0.714 |
LIG_14-3-3_CanoR_1 | 602 | 607 | PF00244 | 0.497 |
LIG_14-3-3_CanoR_1 | 655 | 662 | PF00244 | 0.471 |
LIG_14-3-3_CanoR_1 | 725 | 731 | PF00244 | 0.484 |
LIG_14-3-3_CanoR_1 | 849 | 854 | PF00244 | 0.665 |
LIG_APCC_ABBA_1 | 556 | 561 | PF00400 | 0.548 |
LIG_APCC_ABBA_1 | 965 | 970 | PF00400 | 0.537 |
LIG_BIR_III_4 | 20 | 24 | PF00653 | 0.522 |
LIG_BRCT_BRCA1_1 | 177 | 181 | PF00533 | 0.502 |
LIG_BRCT_BRCA1_1 | 235 | 239 | PF00533 | 0.469 |
LIG_deltaCOP1_diTrp_1 | 561 | 566 | PF00928 | 0.534 |
LIG_deltaCOP1_diTrp_1 | 769 | 776 | PF00928 | 0.513 |
LIG_deltaCOP1_diTrp_1 | 930 | 935 | PF00928 | 0.514 |
LIG_EVH1_2 | 780 | 784 | PF00568 | 0.483 |
LIG_FHA_1 | 199 | 205 | PF00498 | 0.519 |
LIG_FHA_1 | 313 | 319 | PF00498 | 0.585 |
LIG_FHA_1 | 490 | 496 | PF00498 | 0.494 |
LIG_FHA_1 | 66 | 72 | PF00498 | 0.373 |
LIG_FHA_1 | 729 | 735 | PF00498 | 0.473 |
LIG_FHA_1 | 958 | 964 | PF00498 | 0.609 |
LIG_FHA_2 | 259 | 265 | PF00498 | 0.516 |
LIG_FHA_2 | 43 | 49 | PF00498 | 0.513 |
LIG_FHA_2 | 541 | 547 | PF00498 | 0.477 |
LIG_FHA_2 | 686 | 692 | PF00498 | 0.476 |
LIG_FHA_2 | 716 | 722 | PF00498 | 0.516 |
LIG_LIR_Apic_2 | 205 | 211 | PF02991 | 0.469 |
LIG_LIR_Apic_2 | 586 | 592 | PF02991 | 0.488 |
LIG_LIR_Apic_2 | 622 | 626 | PF02991 | 0.503 |
LIG_LIR_Gen_1 | 236 | 247 | PF02991 | 0.474 |
LIG_LIR_Gen_1 | 580 | 589 | PF02991 | 0.503 |
LIG_LIR_Gen_1 | 729 | 738 | PF02991 | 0.500 |
LIG_LIR_Nem_3 | 205 | 209 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 236 | 242 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 365 | 371 | PF02991 | 0.613 |
LIG_LIR_Nem_3 | 577 | 581 | PF02991 | 0.619 |
LIG_LIR_Nem_3 | 729 | 733 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 920 | 926 | PF02991 | 0.495 |
LIG_MYND_1 | 226 | 230 | PF01753 | 0.469 |
LIG_MYND_1 | 736 | 740 | PF01753 | 0.495 |
LIG_NRBOX | 647 | 653 | PF00104 | 0.346 |
LIG_PCNA_yPIPBox_3 | 625 | 634 | PF02747 | 0.399 |
LIG_PDZ_Class_3 | 967 | 972 | PF00595 | 0.464 |
LIG_Pex14_1 | 562 | 566 | PF04695 | 0.580 |
LIG_Pex14_1 | 772 | 776 | PF04695 | 0.518 |
LIG_Pex14_2 | 566 | 570 | PF04695 | 0.527 |
LIG_Rb_LxCxE_1 | 543 | 561 | PF01857 | 0.478 |
LIG_Rb_LxCxE_1 | 921 | 937 | PF01857 | 0.497 |
LIG_SH2_CRK | 589 | 593 | PF00017 | 0.515 |
LIG_SH2_CRK | 777 | 781 | PF00017 | 0.572 |
LIG_SH2_CRK | 923 | 927 | PF00017 | 0.479 |
LIG_SH2_PTP2 | 964 | 967 | PF00017 | 0.540 |
LIG_SH2_STAP1 | 198 | 202 | PF00017 | 0.469 |
LIG_SH2_STAP1 | 568 | 572 | PF00017 | 0.535 |
LIG_SH2_STAT3 | 915 | 918 | PF00017 | 0.605 |
LIG_SH2_STAT5 | 208 | 211 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 285 | 288 | PF00017 | 0.400 |
LIG_SH2_STAT5 | 623 | 626 | PF00017 | 0.501 |
LIG_SH2_STAT5 | 892 | 895 | PF00017 | 0.626 |
LIG_SH2_STAT5 | 91 | 94 | PF00017 | 0.408 |
LIG_SH2_STAT5 | 915 | 918 | PF00017 | 0.558 |
LIG_SH2_STAT5 | 964 | 967 | PF00017 | 0.540 |
LIG_SH3_1 | 589 | 595 | PF00018 | 0.525 |
LIG_SH3_3 | 271 | 277 | PF00018 | 0.472 |
LIG_SH3_3 | 305 | 311 | PF00018 | 0.520 |
LIG_SH3_3 | 315 | 321 | PF00018 | 0.747 |
LIG_SH3_3 | 461 | 467 | PF00018 | 0.601 |
LIG_SH3_3 | 552 | 558 | PF00018 | 0.594 |
LIG_SH3_3 | 589 | 595 | PF00018 | 0.461 |
LIG_SH3_3 | 61 | 67 | PF00018 | 0.418 |
LIG_SH3_3 | 730 | 736 | PF00018 | 0.532 |
LIG_SH3_3 | 95 | 101 | PF00018 | 0.404 |
LIG_SH3_5 | 194 | 198 | PF00018 | 0.318 |
LIG_SUMO_SIM_anti_2 | 199 | 205 | PF11976 | 0.496 |
LIG_SUMO_SIM_anti_2 | 60 | 66 | PF11976 | 0.416 |
LIG_SUMO_SIM_anti_2 | 705 | 710 | PF11976 | 0.387 |
LIG_SUMO_SIM_par_1 | 199 | 205 | PF11976 | 0.516 |
LIG_TRAF2_1 | 447 | 450 | PF00917 | 0.584 |
LIG_TYR_ITIM | 962 | 967 | PF00017 | 0.539 |
LIG_UBA3_1 | 113 | 122 | PF00899 | 0.502 |
LIG_UBA3_1 | 253 | 257 | PF00899 | 0.411 |
LIG_WRC_WIRS_1 | 203 | 208 | PF05994 | 0.469 |
LIG_WW_3 | 756 | 760 | PF00397 | 0.511 |
MOD_CDK_SPxK_1 | 634 | 640 | PF00069 | 0.488 |
MOD_CDK_SPxxK_3 | 161 | 168 | PF00069 | 0.517 |
MOD_CK1_1 | 174 | 180 | PF00069 | 0.684 |
MOD_CK1_1 | 312 | 318 | PF00069 | 0.578 |
MOD_CK1_1 | 323 | 329 | PF00069 | 0.543 |
MOD_CK1_1 | 331 | 337 | PF00069 | 0.590 |
MOD_CK1_1 | 359 | 365 | PF00069 | 0.650 |
MOD_CK1_1 | 392 | 398 | PF00069 | 0.681 |
MOD_CK1_1 | 442 | 448 | PF00069 | 0.682 |
MOD_CK1_1 | 554 | 560 | PF00069 | 0.552 |
MOD_CK1_1 | 670 | 676 | PF00069 | 0.573 |
MOD_CK1_1 | 761 | 767 | PF00069 | 0.516 |
MOD_CK1_1 | 843 | 849 | PF00069 | 0.660 |
MOD_CK1_1 | 919 | 925 | PF00069 | 0.433 |
MOD_CK2_1 | 444 | 450 | PF00069 | 0.641 |
MOD_CK2_1 | 540 | 546 | PF00069 | 0.477 |
MOD_CK2_1 | 715 | 721 | PF00069 | 0.517 |
MOD_CMANNOS | 932 | 935 | PF00535 | 0.504 |
MOD_Cter_Amidation | 120 | 123 | PF01082 | 0.418 |
MOD_DYRK1A_RPxSP_1 | 473 | 477 | PF00069 | 0.515 |
MOD_GlcNHglycan | 110 | 113 | PF01048 | 0.610 |
MOD_GlcNHglycan | 119 | 122 | PF01048 | 0.501 |
MOD_GlcNHglycan | 126 | 129 | PF01048 | 0.481 |
MOD_GlcNHglycan | 178 | 181 | PF01048 | 0.653 |
MOD_GlcNHglycan | 239 | 242 | PF01048 | 0.211 |
MOD_GlcNHglycan | 264 | 267 | PF01048 | 0.304 |
MOD_GlcNHglycan | 330 | 333 | PF01048 | 0.584 |
MOD_GlcNHglycan | 358 | 361 | PF01048 | 0.525 |
MOD_GlcNHglycan | 501 | 504 | PF01048 | 0.522 |
MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.454 |
MOD_GlcNHglycan | 628 | 631 | PF01048 | 0.403 |
MOD_GlcNHglycan | 751 | 755 | PF01048 | 0.656 |
MOD_GlcNHglycan | 790 | 793 | PF01048 | 0.609 |
MOD_GlcNHglycan | 794 | 797 | PF01048 | 0.622 |
MOD_GlcNHglycan | 868 | 871 | PF01048 | 0.536 |
MOD_GlcNHglycan | 880 | 884 | PF01048 | 0.544 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.447 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.462 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.674 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.734 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.621 |
MOD_GSK3_1 | 198 | 205 | PF00069 | 0.494 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.469 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.516 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.571 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.566 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.648 |
MOD_GSK3_1 | 331 | 338 | PF00069 | 0.618 |
MOD_GSK3_1 | 388 | 395 | PF00069 | 0.773 |
MOD_GSK3_1 | 413 | 420 | PF00069 | 0.592 |
MOD_GSK3_1 | 562 | 569 | PF00069 | 0.582 |
MOD_GSK3_1 | 715 | 722 | PF00069 | 0.427 |
MOD_GSK3_1 | 788 | 795 | PF00069 | 0.570 |
MOD_GSK3_1 | 840 | 847 | PF00069 | 0.630 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.452 |
MOD_N-GLC_1 | 14 | 19 | PF02516 | 0.534 |
MOD_N-GLC_1 | 442 | 447 | PF02516 | 0.547 |
MOD_N-GLC_1 | 792 | 797 | PF02516 | 0.563 |
MOD_NEK2_1 | 108 | 113 | PF00069 | 0.433 |
MOD_NEK2_1 | 117 | 122 | PF00069 | 0.446 |
MOD_NEK2_1 | 124 | 129 | PF00069 | 0.557 |
MOD_NEK2_1 | 176 | 181 | PF00069 | 0.503 |
MOD_NEK2_1 | 335 | 340 | PF00069 | 0.527 |
MOD_NEK2_1 | 413 | 418 | PF00069 | 0.702 |
MOD_NEK2_1 | 439 | 444 | PF00069 | 0.644 |
MOD_NEK2_1 | 516 | 521 | PF00069 | 0.558 |
MOD_NEK2_1 | 566 | 571 | PF00069 | 0.529 |
MOD_NEK2_1 | 632 | 637 | PF00069 | 0.389 |
MOD_NEK2_1 | 788 | 793 | PF00069 | 0.584 |
MOD_NEK2_1 | 9 | 14 | PF00069 | 0.482 |
MOD_NEK2_2 | 720 | 725 | PF00069 | 0.523 |
MOD_PIKK_1 | 287 | 293 | PF00454 | 0.389 |
MOD_PIKK_1 | 437 | 443 | PF00454 | 0.528 |
MOD_PIKK_1 | 728 | 734 | PF00454 | 0.476 |
MOD_PIKK_1 | 761 | 767 | PF00454 | 0.606 |
MOD_PIKK_1 | 794 | 800 | PF00454 | 0.537 |
MOD_PIKK_1 | 900 | 906 | PF00454 | 0.677 |
MOD_PKA_2 | 309 | 315 | PF00069 | 0.619 |
MOD_PKA_2 | 328 | 334 | PF00069 | 0.748 |
MOD_PKA_2 | 601 | 607 | PF00069 | 0.492 |
MOD_PKA_2 | 758 | 764 | PF00069 | 0.604 |
MOD_PKA_2 | 9 | 15 | PF00069 | 0.491 |
MOD_PKB_1 | 487 | 495 | PF00069 | 0.485 |
MOD_Plk_1 | 198 | 204 | PF00069 | 0.516 |
MOD_Plk_1 | 316 | 322 | PF00069 | 0.604 |
MOD_Plk_1 | 720 | 726 | PF00069 | 0.523 |
MOD_Plk_1 | 919 | 925 | PF00069 | 0.515 |
MOD_Plk_4 | 184 | 190 | PF00069 | 0.514 |
MOD_Plk_4 | 198 | 204 | PF00069 | 0.434 |
MOD_Plk_4 | 210 | 216 | PF00069 | 0.495 |
MOD_Plk_4 | 224 | 230 | PF00069 | 0.470 |
MOD_Plk_4 | 249 | 255 | PF00069 | 0.411 |
MOD_Plk_4 | 364 | 370 | PF00069 | 0.605 |
MOD_Plk_4 | 389 | 395 | PF00069 | 0.789 |
MOD_Plk_4 | 551 | 557 | PF00069 | 0.589 |
MOD_Plk_4 | 562 | 568 | PF00069 | 0.608 |
MOD_ProDKin_1 | 161 | 167 | PF00069 | 0.594 |
MOD_ProDKin_1 | 181 | 187 | PF00069 | 0.534 |
MOD_ProDKin_1 | 233 | 239 | PF00069 | 0.469 |
MOD_ProDKin_1 | 320 | 326 | PF00069 | 0.558 |
MOD_ProDKin_1 | 362 | 368 | PF00069 | 0.584 |
MOD_ProDKin_1 | 473 | 479 | PF00069 | 0.591 |
MOD_ProDKin_1 | 497 | 503 | PF00069 | 0.653 |
MOD_ProDKin_1 | 554 | 560 | PF00069 | 0.551 |
MOD_ProDKin_1 | 634 | 640 | PF00069 | 0.488 |
MOD_ProDKin_1 | 723 | 729 | PF00069 | 0.424 |
MOD_SUMO_rev_2 | 103 | 108 | PF00179 | 0.514 |
MOD_SUMO_rev_2 | 831 | 841 | PF00179 | 0.536 |
TRG_DiLeu_BaEn_2 | 45 | 51 | PF01217 | 0.519 |
TRG_DiLeu_BaEn_3 | 52 | 58 | PF01217 | 0.359 |
TRG_DiLeu_BaLyEn_6 | 138 | 143 | PF01217 | 0.542 |
TRG_DiLeu_BaLyEn_6 | 589 | 594 | PF01217 | 0.451 |
TRG_DiLeu_BaLyEn_6 | 647 | 652 | PF01217 | 0.339 |
TRG_ENDOCYTIC_2 | 285 | 288 | PF00928 | 0.400 |
TRG_ENDOCYTIC_2 | 581 | 584 | PF00928 | 0.566 |
TRG_ENDOCYTIC_2 | 923 | 926 | PF00928 | 0.468 |
TRG_ENDOCYTIC_2 | 964 | 967 | PF00928 | 0.540 |
TRG_ER_diArg_1 | 371 | 374 | PF00400 | 0.572 |
TRG_ER_diArg_1 | 644 | 646 | PF00400 | 0.457 |
TRG_ER_diArg_1 | 648 | 650 | PF00400 | 0.437 |
TRG_ER_diArg_1 | 770 | 772 | PF00400 | 0.556 |
TRG_ER_diArg_1 | 773 | 776 | PF00400 | 0.557 |
TRG_ER_diArg_1 | 803 | 805 | PF00400 | 0.647 |
TRG_Pf-PMV_PEXEL_1 | 193 | 197 | PF00026 | 0.413 |
TRG_Pf-PMV_PEXEL_1 | 649 | 654 | PF00026 | 0.353 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCE1 | Leptomonas seymouri | 48% | 83% |
A0A3Q8IG07 | Leishmania donovani | 69% | 99% |
A4I847 | Leishmania infantum | 69% | 99% |
E9B305 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 67% | 99% |
Q4Q551 | Leishmania major | 68% | 99% |