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: 5 |
NetGPI | no | yes: 0, no: 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005773 | vacuole | 5 | 1 |
GO:0005776 | autophagosome | 6 | 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: E9AV51
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 6 |
GO:0006793 | phosphorus metabolic process | 3 | 6 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 6 |
GO:0006807 | nitrogen compound metabolic process | 2 | 6 |
GO:0006914 | autophagy | 3 | 5 |
GO:0008152 | metabolic process | 1 | 6 |
GO:0009056 | catabolic process | 2 | 5 |
GO:0009987 | cellular process | 1 | 6 |
GO:0016310 | phosphorylation | 5 | 6 |
GO:0019538 | protein metabolic process | 3 | 6 |
GO:0036211 | protein modification process | 4 | 6 |
GO:0043170 | macromolecule metabolic process | 3 | 6 |
GO:0043412 | macromolecule modification | 4 | 6 |
GO:0044237 | cellular metabolic process | 2 | 6 |
GO:0044238 | primary metabolic process | 2 | 6 |
GO:0044248 | cellular catabolic process | 3 | 5 |
GO:0061919 | process utilizing autophagic mechanism | 2 | 5 |
GO:0071704 | organic substance metabolic process | 2 | 6 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 6 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0007033 | vacuole organization | 5 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0018105 | peptidyl-serine phosphorylation | 6 | 1 |
GO:0018193 | peptidyl-amino acid modification | 5 | 1 |
GO:0018209 | peptidyl-serine modification | 6 | 1 |
GO:0046777 | protein autophosphorylation | 6 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:1905037 | autophagosome organization | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 6 |
GO:0003824 | catalytic activity | 1 | 6 |
GO:0004672 | protein kinase activity | 3 | 6 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 6 |
GO:0005488 | binding | 1 | 6 |
GO:0005524 | ATP binding | 5 | 6 |
GO:0016301 | kinase activity | 4 | 6 |
GO:0016740 | transferase activity | 2 | 6 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 6 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 6 |
GO:0017076 | purine nucleotide binding | 4 | 6 |
GO:0030554 | adenyl nucleotide binding | 5 | 6 |
GO:0032553 | ribonucleotide binding | 3 | 6 |
GO:0032555 | purine ribonucleotide binding | 4 | 6 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 6 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 6 |
GO:0036094 | small molecule binding | 2 | 6 |
GO:0043167 | ion binding | 2 | 6 |
GO:0043168 | anion binding | 3 | 6 |
GO:0097159 | organic cyclic compound binding | 2 | 6 |
GO:0097367 | carbohydrate derivative binding | 2 | 6 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 6 |
GO:1901265 | nucleoside phosphate binding | 3 | 6 |
GO:1901363 | heterocyclic compound binding | 2 | 6 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 458 | 462 | PF00656 | 0.556 |
CLV_C14_Caspase3-7 | 735 | 739 | PF00656 | 0.583 |
CLV_C14_Caspase3-7 | 80 | 84 | PF00656 | 0.540 |
CLV_C14_Caspase3-7 | 826 | 830 | PF00656 | 0.555 |
CLV_NRD_NRD_1 | 143 | 145 | PF00675 | 0.291 |
CLV_NRD_NRD_1 | 217 | 219 | PF00675 | 0.290 |
CLV_NRD_NRD_1 | 479 | 481 | PF00675 | 0.544 |
CLV_NRD_NRD_1 | 516 | 518 | PF00675 | 0.545 |
CLV_NRD_NRD_1 | 881 | 883 | PF00675 | 0.530 |
CLV_NRD_NRD_1 | 962 | 964 | PF00675 | 0.432 |
CLV_PCSK_KEX2_1 | 143 | 145 | PF00082 | 0.302 |
CLV_PCSK_KEX2_1 | 215 | 217 | PF00082 | 0.290 |
CLV_PCSK_KEX2_1 | 881 | 883 | PF00082 | 0.530 |
CLV_PCSK_KEX2_1 | 962 | 964 | PF00082 | 0.432 |
CLV_PCSK_PC1ET2_1 | 215 | 217 | PF00082 | 0.290 |
CLV_PCSK_PC7_1 | 877 | 883 | PF00082 | 0.520 |
CLV_PCSK_SKI1_1 | 137 | 141 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 201 | 205 | PF00082 | 0.290 |
CLV_PCSK_SKI1_1 | 222 | 226 | PF00082 | 0.339 |
CLV_PCSK_SKI1_1 | 304 | 308 | PF00082 | 0.342 |
CLV_PCSK_SKI1_1 | 552 | 556 | PF00082 | 0.685 |
CLV_PCSK_SKI1_1 | 611 | 615 | PF00082 | 0.455 |
CLV_PCSK_SKI1_1 | 877 | 881 | PF00082 | 0.476 |
CLV_PCSK_SKI1_1 | 882 | 886 | PF00082 | 0.477 |
CLV_PCSK_SKI1_1 | 944 | 948 | PF00082 | 0.564 |
CLV_Separin_Metazoa | 325 | 329 | PF03568 | 0.290 |
CLV_Separin_Metazoa | 343 | 347 | PF03568 | 0.290 |
DEG_Kelch_Keap1_1 | 160 | 165 | PF01344 | 0.217 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.669 |
DEG_SCF_FBW7_2 | 60 | 67 | PF00400 | 0.616 |
DEG_SPOP_SBC_1 | 490 | 494 | PF00917 | 0.679 |
DEG_SPOP_SBC_1 | 94 | 98 | PF00917 | 0.653 |
DOC_ANK_TNKS_1 | 900 | 907 | PF00023 | 0.585 |
DOC_CKS1_1 | 294 | 299 | PF01111 | 0.290 |
DOC_CKS1_1 | 61 | 66 | PF01111 | 0.624 |
DOC_CYCLIN_RxL_1 | 608 | 617 | PF00134 | 0.462 |
DOC_CYCLIN_yCln2_LP_2 | 918 | 924 | PF00134 | 0.554 |
DOC_MAPK_DCC_7 | 393 | 403 | PF00069 | 0.609 |
DOC_MAPK_gen_1 | 167 | 175 | PF00069 | 0.299 |
DOC_MAPK_gen_1 | 222 | 231 | PF00069 | 0.335 |
DOC_MAPK_gen_1 | 881 | 887 | PF00069 | 0.465 |
DOC_MAPK_JIP1_4 | 225 | 231 | PF00069 | 0.290 |
DOC_MAPK_MEF2A_6 | 167 | 175 | PF00069 | 0.290 |
DOC_MAPK_MEF2A_6 | 871 | 880 | PF00069 | 0.488 |
DOC_MAPK_MEF2A_6 | 944 | 953 | PF00069 | 0.501 |
DOC_PP1_RVXF_1 | 942 | 948 | PF00149 | 0.568 |
DOC_PP2B_LxvP_1 | 139 | 142 | PF13499 | 0.342 |
DOC_PP2B_LxvP_1 | 776 | 779 | PF13499 | 0.640 |
DOC_PP4_FxxP_1 | 403 | 406 | PF00568 | 0.577 |
DOC_PP4_FxxP_1 | 576 | 579 | PF00568 | 0.604 |
DOC_PP4_FxxP_1 | 99 | 102 | PF00568 | 0.663 |
DOC_USP7_MATH_1 | 153 | 157 | PF00917 | 0.242 |
DOC_USP7_MATH_1 | 486 | 490 | PF00917 | 0.669 |
DOC_USP7_MATH_1 | 509 | 513 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 522 | 526 | PF00917 | 0.564 |
DOC_USP7_MATH_1 | 590 | 594 | PF00917 | 0.527 |
DOC_USP7_MATH_1 | 646 | 650 | PF00917 | 0.528 |
DOC_USP7_MATH_1 | 739 | 743 | PF00917 | 0.584 |
DOC_USP7_MATH_1 | 751 | 755 | PF00917 | 0.621 |
DOC_USP7_MATH_1 | 863 | 867 | PF00917 | 0.636 |
DOC_USP7_MATH_1 | 88 | 92 | PF00917 | 0.684 |
DOC_USP7_MATH_1 | 914 | 918 | PF00917 | 0.630 |
DOC_USP7_MATH_1 | 933 | 937 | PF00917 | 0.483 |
DOC_USP7_MATH_1 | 94 | 98 | PF00917 | 0.758 |
DOC_USP7_MATH_1 | 979 | 983 | PF00917 | 0.555 |
DOC_USP7_MATH_2 | 3 | 9 | PF00917 | 0.504 |
DOC_USP7_UBL2_3 | 514 | 518 | PF12436 | 0.542 |
DOC_WW_Pin1_4 | 104 | 109 | PF00397 | 0.604 |
DOC_WW_Pin1_4 | 157 | 162 | PF00397 | 0.285 |
DOC_WW_Pin1_4 | 284 | 289 | PF00397 | 0.360 |
DOC_WW_Pin1_4 | 293 | 298 | PF00397 | 0.251 |
DOC_WW_Pin1_4 | 424 | 429 | PF00397 | 0.688 |
DOC_WW_Pin1_4 | 558 | 563 | PF00397 | 0.643 |
DOC_WW_Pin1_4 | 60 | 65 | PF00397 | 0.575 |
DOC_WW_Pin1_4 | 817 | 822 | PF00397 | 0.584 |
DOC_WW_Pin1_4 | 848 | 853 | PF00397 | 0.629 |
DOC_WW_Pin1_4 | 905 | 910 | PF00397 | 0.787 |
LIG_14-3-3_CanoR_1 | 201 | 206 | PF00244 | 0.314 |
LIG_14-3-3_CanoR_1 | 369 | 375 | PF00244 | 0.302 |
LIG_14-3-3_CanoR_1 | 378 | 382 | PF00244 | 0.336 |
LIG_14-3-3_CanoR_1 | 386 | 390 | PF00244 | 0.364 |
LIG_14-3-3_CanoR_1 | 470 | 474 | PF00244 | 0.525 |
LIG_14-3-3_CanoR_1 | 480 | 486 | PF00244 | 0.520 |
LIG_14-3-3_CanoR_1 | 611 | 616 | PF00244 | 0.453 |
LIG_14-3-3_CanoR_1 | 686 | 692 | PF00244 | 0.436 |
LIG_14-3-3_CanoR_1 | 789 | 794 | PF00244 | 0.532 |
LIG_14-3-3_CanoR_1 | 845 | 854 | PF00244 | 0.670 |
LIG_14-3-3_CanoR_1 | 858 | 867 | PF00244 | 0.528 |
LIG_14-3-3_CanoR_1 | 962 | 966 | PF00244 | 0.423 |
LIG_14-3-3_CanoR_1 | 974 | 983 | PF00244 | 0.405 |
LIG_APCC_ABBAyCdc20_2 | 217 | 223 | PF00400 | 0.290 |
LIG_BRCT_BRCA1_1 | 168 | 172 | PF00533 | 0.439 |
LIG_BRCT_BRCA1_1 | 286 | 290 | PF00533 | 0.339 |
LIG_BRCT_BRCA1_1 | 95 | 99 | PF00533 | 0.660 |
LIG_CaM_NSCaTE_8 | 698 | 705 | PF13499 | 0.410 |
LIG_EVH1_1 | 920 | 924 | PF00568 | 0.499 |
LIG_EVH1_2 | 399 | 403 | PF00568 | 0.572 |
LIG_FHA_1 | 153 | 159 | PF00498 | 0.334 |
LIG_FHA_1 | 202 | 208 | PF00498 | 0.311 |
LIG_FHA_1 | 238 | 244 | PF00498 | 0.376 |
LIG_FHA_1 | 400 | 406 | PF00498 | 0.645 |
LIG_FHA_1 | 586 | 592 | PF00498 | 0.491 |
LIG_FHA_1 | 682 | 688 | PF00498 | 0.494 |
LIG_FHA_1 | 838 | 844 | PF00498 | 0.584 |
LIG_FHA_1 | 971 | 977 | PF00498 | 0.411 |
LIG_FHA_2 | 230 | 236 | PF00498 | 0.342 |
LIG_FHA_2 | 269 | 275 | PF00498 | 0.402 |
LIG_FHA_2 | 369 | 375 | PF00498 | 0.307 |
LIG_FHA_2 | 456 | 462 | PF00498 | 0.535 |
LIG_FHA_2 | 706 | 712 | PF00498 | 0.550 |
LIG_FHA_2 | 859 | 865 | PF00498 | 0.668 |
LIG_FHA_2 | 884 | 890 | PF00498 | 0.549 |
LIG_GBD_Chelix_1 | 615 | 623 | PF00786 | 0.496 |
LIG_LIR_Apic_2 | 296 | 302 | PF02991 | 0.290 |
LIG_LIR_Apic_2 | 402 | 406 | PF02991 | 0.580 |
LIG_LIR_Apic_2 | 544 | 550 | PF02991 | 0.560 |
LIG_LIR_Apic_2 | 573 | 579 | PF02991 | 0.605 |
LIG_LIR_Apic_2 | 917 | 923 | PF02991 | 0.629 |
LIG_LIR_Apic_2 | 96 | 102 | PF02991 | 0.797 |
LIG_LIR_Gen_1 | 133 | 142 | PF02991 | 0.342 |
LIG_LIR_Gen_1 | 169 | 178 | PF02991 | 0.346 |
LIG_LIR_Gen_1 | 525 | 534 | PF02991 | 0.627 |
LIG_LIR_Gen_1 | 593 | 602 | PF02991 | 0.516 |
LIG_LIR_Nem_3 | 133 | 138 | PF02991 | 0.342 |
LIG_LIR_Nem_3 | 169 | 175 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 284 | 289 | PF02991 | 0.342 |
LIG_LIR_Nem_3 | 347 | 352 | PF02991 | 0.342 |
LIG_LIR_Nem_3 | 525 | 530 | PF02991 | 0.636 |
LIG_LIR_Nem_3 | 593 | 597 | PF02991 | 0.513 |
LIG_MAD2 | 218 | 226 | PF02301 | 0.290 |
LIG_MAD2 | 944 | 952 | PF02301 | 0.564 |
LIG_MYND_1 | 396 | 400 | PF01753 | 0.619 |
LIG_MYND_1 | 905 | 909 | PF01753 | 0.566 |
LIG_MYND_1 | 925 | 929 | PF01753 | 0.632 |
LIG_NRBOX | 618 | 624 | PF00104 | 0.360 |
LIG_NRBOX | 875 | 881 | PF00104 | 0.477 |
LIG_Pex14_2 | 286 | 290 | PF04695 | 0.504 |
LIG_Rb_pABgroove_1 | 112 | 120 | PF01858 | 0.342 |
LIG_SH2_CRK | 39 | 43 | PF00017 | 0.415 |
LIG_SH2_CRK | 547 | 551 | PF00017 | 0.583 |
LIG_SH2_NCK_1 | 24 | 28 | PF00017 | 0.386 |
LIG_SH2_PTP2 | 13 | 16 | PF00017 | 0.487 |
LIG_SH2_SRC | 599 | 602 | PF00017 | 0.478 |
LIG_SH2_STAP1 | 118 | 122 | PF00017 | 0.342 |
LIG_SH2_STAP1 | 627 | 631 | PF00017 | 0.499 |
LIG_SH2_STAP1 | 683 | 687 | PF00017 | 0.485 |
LIG_SH2_STAT3 | 601 | 604 | PF00017 | 0.477 |
LIG_SH2_STAT5 | 13 | 16 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 178 | 181 | PF00017 | 0.323 |
LIG_SH2_STAT5 | 599 | 602 | PF00017 | 0.481 |
LIG_SH2_STAT5 | 618 | 621 | PF00017 | 0.653 |
LIG_SH2_STAT5 | 630 | 633 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 666 | 669 | PF00017 | 0.594 |
LIG_SH2_STAT5 | 683 | 686 | PF00017 | 0.476 |
LIG_SH3_1 | 393 | 399 | PF00018 | 0.602 |
LIG_SH3_1 | 518 | 524 | PF00018 | 0.518 |
LIG_SH3_1 | 547 | 553 | PF00018 | 0.631 |
LIG_SH3_1 | 920 | 926 | PF00018 | 0.562 |
LIG_SH3_2 | 465 | 470 | PF14604 | 0.653 |
LIG_SH3_2 | 521 | 526 | PF14604 | 0.568 |
LIG_SH3_3 | 135 | 141 | PF00018 | 0.496 |
LIG_SH3_3 | 391 | 397 | PF00018 | 0.575 |
LIG_SH3_3 | 450 | 456 | PF00018 | 0.822 |
LIG_SH3_3 | 462 | 468 | PF00018 | 0.590 |
LIG_SH3_3 | 482 | 488 | PF00018 | 0.733 |
LIG_SH3_3 | 518 | 524 | PF00018 | 0.573 |
LIG_SH3_3 | 547 | 553 | PF00018 | 0.583 |
LIG_SH3_3 | 58 | 64 | PF00018 | 0.568 |
LIG_SH3_3 | 725 | 731 | PF00018 | 0.651 |
LIG_SH3_3 | 776 | 782 | PF00018 | 0.635 |
LIG_SH3_3 | 918 | 924 | PF00018 | 0.620 |
LIG_SH3_3 | 946 | 952 | PF00018 | 0.517 |
LIG_SH3_3 | 99 | 105 | PF00018 | 0.638 |
LIG_Sin3_3 | 227 | 234 | PF02671 | 0.342 |
LIG_SUMO_SIM_anti_2 | 112 | 119 | PF11976 | 0.290 |
LIG_SUMO_SIM_anti_2 | 593 | 599 | PF11976 | 0.511 |
LIG_SUMO_SIM_par_1 | 320 | 325 | PF11976 | 0.290 |
LIG_SUMO_SIM_par_1 | 883 | 889 | PF11976 | 0.474 |
LIG_TRAF2_1 | 727 | 730 | PF00917 | 0.596 |
LIG_TRFH_1 | 576 | 580 | PF08558 | 0.607 |
LIG_TYR_ITIM | 37 | 42 | PF00017 | 0.421 |
LIG_TYR_ITIM | 597 | 602 | PF00017 | 0.521 |
LIG_UBA3_1 | 211 | 215 | PF00899 | 0.342 |
LIG_WRC_WIRS_1 | 591 | 596 | PF05994 | 0.515 |
LIG_WW_2 | 396 | 399 | PF00397 | 0.616 |
LIG_WW_3 | 140 | 144 | PF00397 | 0.342 |
MOD_CDC14_SPxK_1 | 301 | 304 | PF00782 | 0.290 |
MOD_CDK_SPxK_1 | 298 | 304 | PF00069 | 0.290 |
MOD_CK1_1 | 148 | 154 | PF00069 | 0.223 |
MOD_CK1_1 | 156 | 162 | PF00069 | 0.240 |
MOD_CK1_1 | 163 | 169 | PF00069 | 0.430 |
MOD_CK1_1 | 437 | 443 | PF00069 | 0.665 |
MOD_CK1_1 | 447 | 453 | PF00069 | 0.530 |
MOD_CK1_1 | 489 | 495 | PF00069 | 0.773 |
MOD_CK1_1 | 737 | 743 | PF00069 | 0.601 |
MOD_CK1_1 | 754 | 760 | PF00069 | 0.551 |
MOD_CK1_1 | 938 | 944 | PF00069 | 0.637 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.806 |
MOD_CK1_1 | 978 | 984 | PF00069 | 0.559 |
MOD_CK2_1 | 159 | 165 | PF00069 | 0.342 |
MOD_CK2_1 | 268 | 274 | PF00069 | 0.367 |
MOD_CK2_1 | 481 | 487 | PF00069 | 0.671 |
MOD_CK2_1 | 706 | 712 | PF00069 | 0.591 |
MOD_CK2_1 | 740 | 746 | PF00069 | 0.559 |
MOD_CK2_1 | 883 | 889 | PF00069 | 0.491 |
MOD_Cter_Amidation | 478 | 481 | PF01082 | 0.545 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.305 |
MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.217 |
MOD_GlcNHglycan | 232 | 235 | PF01048 | 0.342 |
MOD_GlcNHglycan | 263 | 266 | PF01048 | 0.319 |
MOD_GlcNHglycan | 317 | 320 | PF01048 | 0.290 |
MOD_GlcNHglycan | 434 | 437 | PF01048 | 0.829 |
MOD_GlcNHglycan | 449 | 452 | PF01048 | 0.551 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.467 |
MOD_GlcNHglycan | 487 | 491 | PF01048 | 0.615 |
MOD_GlcNHglycan | 543 | 546 | PF01048 | 0.629 |
MOD_GlcNHglycan | 568 | 571 | PF01048 | 0.591 |
MOD_GlcNHglycan | 693 | 696 | PF01048 | 0.532 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.633 |
MOD_GlcNHglycan | 738 | 742 | PF01048 | 0.567 |
MOD_GlcNHglycan | 749 | 752 | PF01048 | 0.557 |
MOD_GlcNHglycan | 898 | 901 | PF01048 | 0.685 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.683 |
MOD_GlcNHglycan | 937 | 940 | PF01048 | 0.504 |
MOD_GlcNHglycan | 977 | 980 | PF01048 | 0.535 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.339 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.283 |
MOD_GSK3_1 | 289 | 296 | PF00069 | 0.355 |
MOD_GSK3_1 | 335 | 342 | PF00069 | 0.342 |
MOD_GSK3_1 | 430 | 437 | PF00069 | 0.680 |
MOD_GSK3_1 | 486 | 493 | PF00069 | 0.687 |
MOD_GSK3_1 | 558 | 565 | PF00069 | 0.585 |
MOD_GSK3_1 | 566 | 573 | PF00069 | 0.556 |
MOD_GSK3_1 | 633 | 640 | PF00069 | 0.567 |
MOD_GSK3_1 | 642 | 649 | PF00069 | 0.431 |
MOD_GSK3_1 | 681 | 688 | PF00069 | 0.398 |
MOD_GSK3_1 | 747 | 754 | PF00069 | 0.597 |
MOD_GSK3_1 | 808 | 815 | PF00069 | 0.580 |
MOD_GSK3_1 | 848 | 855 | PF00069 | 0.581 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.808 |
MOD_GSK3_1 | 953 | 960 | PF00069 | 0.565 |
MOD_GSK3_1 | 970 | 977 | PF00069 | 0.414 |
MOD_N-GLC_1 | 845 | 850 | PF02516 | 0.670 |
MOD_N-GLC_2 | 648 | 650 | PF02516 | 0.538 |
MOD_NEK2_1 | 229 | 234 | PF00069 | 0.348 |
MOD_NEK2_1 | 327 | 332 | PF00069 | 0.301 |
MOD_NEK2_1 | 385 | 390 | PF00069 | 0.313 |
MOD_NEK2_1 | 563 | 568 | PF00069 | 0.758 |
MOD_NEK2_1 | 637 | 642 | PF00069 | 0.527 |
MOD_NEK2_1 | 747 | 752 | PF00069 | 0.670 |
MOD_NEK2_1 | 788 | 793 | PF00069 | 0.585 |
MOD_NEK2_2 | 210 | 215 | PF00069 | 0.290 |
MOD_PIKK_1 | 335 | 341 | PF00454 | 0.290 |
MOD_PIKK_1 | 434 | 440 | PF00454 | 0.672 |
MOD_PIKK_1 | 500 | 506 | PF00454 | 0.603 |
MOD_PK_1 | 481 | 487 | PF00069 | 0.671 |
MOD_PK_1 | 789 | 795 | PF00069 | 0.573 |
MOD_PKA_1 | 480 | 486 | PF00069 | 0.535 |
MOD_PKA_2 | 166 | 172 | PF00069 | 0.290 |
MOD_PKA_2 | 327 | 333 | PF00069 | 0.301 |
MOD_PKA_2 | 368 | 374 | PF00069 | 0.290 |
MOD_PKA_2 | 377 | 383 | PF00069 | 0.290 |
MOD_PKA_2 | 385 | 391 | PF00069 | 0.290 |
MOD_PKA_2 | 469 | 475 | PF00069 | 0.525 |
MOD_PKA_2 | 516 | 522 | PF00069 | 0.669 |
MOD_PKA_2 | 641 | 647 | PF00069 | 0.532 |
MOD_PKA_2 | 685 | 691 | PF00069 | 0.437 |
MOD_PKA_2 | 788 | 794 | PF00069 | 0.580 |
MOD_PKA_2 | 846 | 852 | PF00069 | 0.544 |
MOD_PKA_2 | 857 | 863 | PF00069 | 0.530 |
MOD_PKA_2 | 961 | 967 | PF00069 | 0.424 |
MOD_PKB_1 | 787 | 795 | PF00069 | 0.456 |
MOD_PKB_1 | 845 | 853 | PF00069 | 0.545 |
MOD_Plk_1 | 837 | 843 | PF00069 | 0.557 |
MOD_Plk_1 | 863 | 869 | PF00069 | 0.614 |
MOD_Plk_2-3 | 961 | 967 | PF00069 | 0.549 |
MOD_Plk_4 | 153 | 159 | PF00069 | 0.204 |
MOD_Plk_4 | 385 | 391 | PF00069 | 0.342 |
MOD_Plk_4 | 45 | 51 | PF00069 | 0.453 |
MOD_Plk_4 | 611 | 617 | PF00069 | 0.607 |
MOD_Plk_4 | 812 | 818 | PF00069 | 0.607 |
MOD_ProDKin_1 | 104 | 110 | PF00069 | 0.594 |
MOD_ProDKin_1 | 157 | 163 | PF00069 | 0.285 |
MOD_ProDKin_1 | 284 | 290 | PF00069 | 0.360 |
MOD_ProDKin_1 | 293 | 299 | PF00069 | 0.251 |
MOD_ProDKin_1 | 424 | 430 | PF00069 | 0.688 |
MOD_ProDKin_1 | 558 | 564 | PF00069 | 0.640 |
MOD_ProDKin_1 | 60 | 66 | PF00069 | 0.582 |
MOD_ProDKin_1 | 817 | 823 | PF00069 | 0.584 |
MOD_ProDKin_1 | 848 | 854 | PF00069 | 0.631 |
MOD_ProDKin_1 | 905 | 911 | PF00069 | 0.786 |
MOD_SUMO_for_1 | 334 | 337 | PF00179 | 0.342 |
MOD_SUMO_rev_2 | 77 | 84 | PF00179 | 0.679 |
TRG_DiLeu_BaEn_4 | 729 | 735 | PF01217 | 0.511 |
TRG_DiLeu_BaLyEn_6 | 698 | 703 | PF01217 | 0.474 |
TRG_DiLeu_BaLyEn_6 | 771 | 776 | PF01217 | 0.647 |
TRG_ENDOCYTIC_2 | 13 | 16 | PF00928 | 0.487 |
TRG_ENDOCYTIC_2 | 39 | 42 | PF00928 | 0.416 |
TRG_ENDOCYTIC_2 | 599 | 602 | PF00928 | 0.545 |
TRG_ER_diArg_1 | 142 | 144 | PF00400 | 0.294 |
TRG_ER_diArg_1 | 216 | 218 | PF00400 | 0.290 |
TRG_ER_diArg_1 | 698 | 701 | PF00400 | 0.500 |
TRG_ER_diArg_1 | 787 | 790 | PF00400 | 0.479 |
TRG_ER_diArg_1 | 880 | 882 | PF00400 | 0.527 |
TRG_NLS_MonoCore_2 | 214 | 219 | PF00514 | 0.290 |
TRG_NLS_MonoExtC_3 | 513 | 518 | PF00514 | 0.540 |
TRG_NLS_MonoExtN_4 | 514 | 521 | PF00514 | 0.535 |
TRG_Pf-PMV_PEXEL_1 | 350 | 354 | PF00026 | 0.342 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IGM5 | Leptomonas seymouri | 43% | 92% |
A0A3S7WWM5 | Leishmania donovani | 90% | 100% |
A4HZ84 | Leishmania infantum | 90% | 100% |
Q4QCD0 | Leishmania major | 88% | 99% |