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:0005634 | nucleus | 5 | 1 |
GO:0005654 | nucleoplasm | 2 | 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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000724 | double-strand break repair via homologous recombination | 7 | 10 |
GO:0000725 | recombinational repair | 6 | 10 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 10 |
GO:0006259 | DNA metabolic process | 4 | 10 |
GO:0006281 | DNA repair | 5 | 10 |
GO:0006302 | double-strand break repair | 6 | 10 |
GO:0006310 | DNA recombination | 5 | 10 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 10 |
GO:0006807 | nitrogen compound metabolic process | 2 | 10 |
GO:0006950 | response to stress | 2 | 10 |
GO:0006974 | DNA damage response | 4 | 10 |
GO:0008152 | metabolic process | 1 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0033554 | cellular response to stress | 3 | 10 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 10 |
GO:0043170 | macromolecule metabolic process | 3 | 10 |
GO:0044237 | cellular metabolic process | 2 | 10 |
GO:0044238 | primary metabolic process | 2 | 10 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 10 |
GO:0046483 | heterocycle metabolic process | 3 | 10 |
GO:0050896 | response to stimulus | 1 | 10 |
GO:0051716 | cellular response to stimulus | 2 | 10 |
GO:0071704 | organic substance metabolic process | 2 | 10 |
GO:0090304 | nucleic acid metabolic process | 4 | 10 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 10 |
GO:0006355 | regulation of DNA-templated transcription | 6 | 1 |
GO:0009605 | response to external stimulus | 2 | 1 |
GO:0009607 | response to biotic stimulus | 2 | 1 |
GO:0009889 | regulation of biosynthetic process | 4 | 1 |
GO:0010468 | regulation of gene expression | 5 | 1 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 1 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0020033 | antigenic variation | 7 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 1 |
GO:0042783 | evasion of host immune response | 6 | 1 |
GO:0043207 | response to external biotic stimulus | 3 | 1 |
GO:0044403 | biological process involved in symbiotic interaction | 2 | 1 |
GO:0044419 | biological process involved in interspecies interaction between organisms | 1 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
GO:0051252 | regulation of RNA metabolic process | 5 | 1 |
GO:0051701 | biological process involved in interaction with host | 3 | 1 |
GO:0051707 | response to other organism | 2 | 1 |
GO:0052173 | response to defenses of other organism | 3 | 1 |
GO:0052200 | response to host defenses | 4 | 1 |
GO:0052572 | response to host immune response | 5 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0075136 | response to host | 3 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:1903506 | regulation of nucleic acid-templated transcription | 7 | 1 |
GO:2001141 | regulation of RNA biosynthetic process | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003677 | DNA binding | 4 | 1 |
GO:0003684 | damaged DNA binding | 5 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 469 | 473 | PF00656 | 0.525 |
CLV_C14_Caspase3-7 | 587 | 591 | PF00656 | 0.531 |
CLV_NRD_NRD_1 | 1003 | 1005 | PF00675 | 0.475 |
CLV_NRD_NRD_1 | 1091 | 1093 | PF00675 | 0.505 |
CLV_NRD_NRD_1 | 133 | 135 | PF00675 | 0.325 |
CLV_NRD_NRD_1 | 27 | 29 | PF00675 | 0.480 |
CLV_NRD_NRD_1 | 278 | 280 | PF00675 | 0.568 |
CLV_NRD_NRD_1 | 286 | 288 | PF00675 | 0.609 |
CLV_NRD_NRD_1 | 435 | 437 | PF00675 | 0.325 |
CLV_NRD_NRD_1 | 45 | 47 | PF00675 | 0.636 |
CLV_NRD_NRD_1 | 617 | 619 | PF00675 | 0.513 |
CLV_NRD_NRD_1 | 705 | 707 | PF00675 | 0.493 |
CLV_NRD_NRD_1 | 721 | 723 | PF00675 | 0.425 |
CLV_NRD_NRD_1 | 856 | 858 | PF00675 | 0.422 |
CLV_NRD_NRD_1 | 931 | 933 | PF00675 | 0.545 |
CLV_PCSK_FUR_1 | 615 | 619 | PF00082 | 0.500 |
CLV_PCSK_KEX2_1 | 1003 | 1005 | PF00082 | 0.451 |
CLV_PCSK_KEX2_1 | 1091 | 1093 | PF00082 | 0.449 |
CLV_PCSK_KEX2_1 | 133 | 135 | PF00082 | 0.325 |
CLV_PCSK_KEX2_1 | 278 | 280 | PF00082 | 0.570 |
CLV_PCSK_KEX2_1 | 286 | 288 | PF00082 | 0.611 |
CLV_PCSK_KEX2_1 | 29 | 31 | PF00082 | 0.514 |
CLV_PCSK_KEX2_1 | 617 | 619 | PF00082 | 0.590 |
CLV_PCSK_KEX2_1 | 721 | 723 | PF00082 | 0.458 |
CLV_PCSK_KEX2_1 | 856 | 858 | PF00082 | 0.295 |
CLV_PCSK_KEX2_1 | 931 | 933 | PF00082 | 0.617 |
CLV_PCSK_PC1ET2_1 | 29 | 31 | PF00082 | 0.506 |
CLV_PCSK_PC7_1 | 25 | 31 | PF00082 | 0.486 |
CLV_PCSK_SKI1_1 | 1101 | 1105 | PF00082 | 0.397 |
CLV_PCSK_SKI1_1 | 128 | 132 | PF00082 | 0.322 |
CLV_PCSK_SKI1_1 | 166 | 170 | PF00082 | 0.596 |
CLV_PCSK_SKI1_1 | 224 | 228 | PF00082 | 0.488 |
CLV_PCSK_SKI1_1 | 385 | 389 | PF00082 | 0.365 |
CLV_PCSK_SKI1_1 | 432 | 436 | PF00082 | 0.300 |
CLV_PCSK_SKI1_1 | 466 | 470 | PF00082 | 0.297 |
CLV_PCSK_SKI1_1 | 506 | 510 | PF00082 | 0.259 |
CLV_PCSK_SKI1_1 | 598 | 602 | PF00082 | 0.506 |
CLV_PCSK_SKI1_1 | 632 | 636 | PF00082 | 0.320 |
CLV_PCSK_SKI1_1 | 660 | 664 | PF00082 | 0.551 |
CLV_PCSK_SKI1_1 | 700 | 704 | PF00082 | 0.400 |
CLV_PCSK_SKI1_1 | 833 | 837 | PF00082 | 0.440 |
CLV_Separin_Metazoa | 1153 | 1157 | PF03568 | 0.428 |
DEG_APCC_DBOX_1 | 133 | 141 | PF00400 | 0.488 |
DEG_APCC_DBOX_1 | 431 | 439 | PF00400 | 0.276 |
DEG_APCC_DBOX_1 | 789 | 797 | PF00400 | 0.449 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.552 |
DEG_SPOP_SBC_1 | 190 | 194 | PF00917 | 0.588 |
DEG_SPOP_SBC_1 | 940 | 944 | PF00917 | 0.487 |
DOC_ANK_TNKS_1 | 435 | 442 | PF00023 | 0.487 |
DOC_CKS1_1 | 1109 | 1114 | PF01111 | 0.315 |
DOC_CKS1_1 | 199 | 204 | PF01111 | 0.490 |
DOC_CKS1_1 | 536 | 541 | PF01111 | 0.550 |
DOC_CYCLIN_RxL_1 | 776 | 787 | PF00134 | 0.451 |
DOC_CYCLIN_yCln2_LP_2 | 1009 | 1015 | PF00134 | 0.575 |
DOC_CYCLIN_yCln2_LP_2 | 1109 | 1115 | PF00134 | 0.452 |
DOC_CYCLIN_yCln2_LP_2 | 266 | 272 | PF00134 | 0.514 |
DOC_CYCLIN_yCln2_LP_2 | 548 | 554 | PF00134 | 0.440 |
DOC_CYCLIN_yCln2_LP_2 | 86 | 89 | PF00134 | 0.471 |
DOC_MAPK_gen_1 | 1091 | 1098 | PF00069 | 0.435 |
DOC_MAPK_gen_1 | 17 | 26 | PF00069 | 0.499 |
DOC_MAPK_gen_1 | 931 | 941 | PF00069 | 0.654 |
DOC_MAPK_MEF2A_6 | 17 | 26 | PF00069 | 0.558 |
DOC_MAPK_RevD_3 | 1077 | 1092 | PF00069 | 0.424 |
DOC_PP1_RVXF_1 | 1084 | 1091 | PF00149 | 0.424 |
DOC_PP1_RVXF_1 | 698 | 704 | PF00149 | 0.460 |
DOC_PP2B_LxvP_1 | 266 | 269 | PF13499 | 0.610 |
DOC_PP2B_LxvP_1 | 548 | 551 | PF13499 | 0.440 |
DOC_PP2B_LxvP_1 | 770 | 773 | PF13499 | 0.496 |
DOC_PP2B_LxvP_1 | 781 | 784 | PF13499 | 0.414 |
DOC_PP2B_LxvP_1 | 86 | 89 | PF13499 | 0.518 |
DOC_PP2B_LxvP_1 | 886 | 889 | PF13499 | 0.487 |
DOC_PP4_FxxP_1 | 11 | 14 | PF00568 | 0.522 |
DOC_PP4_FxxP_1 | 199 | 202 | PF00568 | 0.493 |
DOC_PP4_FxxP_1 | 281 | 284 | PF00568 | 0.524 |
DOC_PP4_FxxP_1 | 54 | 57 | PF00568 | 0.520 |
DOC_USP7_MATH_1 | 171 | 175 | PF00917 | 0.666 |
DOC_USP7_MATH_1 | 189 | 193 | PF00917 | 0.575 |
DOC_USP7_MATH_1 | 237 | 241 | PF00917 | 0.583 |
DOC_USP7_MATH_1 | 262 | 266 | PF00917 | 0.584 |
DOC_USP7_MATH_1 | 294 | 298 | PF00917 | 0.584 |
DOC_USP7_MATH_1 | 325 | 329 | PF00917 | 0.414 |
DOC_USP7_MATH_1 | 387 | 391 | PF00917 | 0.494 |
DOC_USP7_MATH_1 | 399 | 403 | PF00917 | 0.365 |
DOC_USP7_MATH_1 | 405 | 409 | PF00917 | 0.310 |
DOC_USP7_MATH_1 | 484 | 488 | PF00917 | 0.386 |
DOC_USP7_MATH_1 | 686 | 690 | PF00917 | 0.410 |
DOC_USP7_MATH_1 | 773 | 777 | PF00917 | 0.423 |
DOC_USP7_MATH_1 | 92 | 96 | PF00917 | 0.658 |
DOC_USP7_MATH_1 | 981 | 985 | PF00917 | 0.578 |
DOC_USP7_MATH_2 | 220 | 226 | PF00917 | 0.491 |
DOC_WW_Pin1_4 | 1108 | 1113 | PF00397 | 0.447 |
DOC_WW_Pin1_4 | 198 | 203 | PF00397 | 0.655 |
DOC_WW_Pin1_4 | 244 | 249 | PF00397 | 0.677 |
DOC_WW_Pin1_4 | 258 | 263 | PF00397 | 0.532 |
DOC_WW_Pin1_4 | 323 | 328 | PF00397 | 0.508 |
DOC_WW_Pin1_4 | 372 | 377 | PF00397 | 0.446 |
DOC_WW_Pin1_4 | 408 | 413 | PF00397 | 0.390 |
DOC_WW_Pin1_4 | 459 | 464 | PF00397 | 0.488 |
DOC_WW_Pin1_4 | 53 | 58 | PF00397 | 0.625 |
DOC_WW_Pin1_4 | 535 | 540 | PF00397 | 0.504 |
DOC_WW_Pin1_4 | 67 | 72 | PF00397 | 0.597 |
DOC_WW_Pin1_4 | 691 | 696 | PF00397 | 0.341 |
DOC_WW_Pin1_4 | 906 | 911 | PF00397 | 0.812 |
LIG_14-3-3_CanoR_1 | 1159 | 1167 | PF00244 | 0.623 |
LIG_14-3-3_CanoR_1 | 286 | 293 | PF00244 | 0.555 |
LIG_14-3-3_CanoR_1 | 466 | 471 | PF00244 | 0.502 |
LIG_14-3-3_CanoR_1 | 598 | 604 | PF00244 | 0.543 |
LIG_14-3-3_CanoR_1 | 636 | 641 | PF00244 | 0.336 |
LIG_14-3-3_CanoR_1 | 722 | 730 | PF00244 | 0.349 |
LIG_14-3-3_CanoR_1 | 779 | 784 | PF00244 | 0.477 |
LIG_Actin_WH2_2 | 1143 | 1158 | PF00022 | 0.422 |
LIG_Actin_WH2_2 | 463 | 480 | PF00022 | 0.510 |
LIG_Actin_WH2_2 | 481 | 497 | PF00022 | 0.371 |
LIG_BIR_III_2 | 847 | 851 | PF00653 | 0.471 |
LIG_BIR_III_2 | 898 | 902 | PF00653 | 0.510 |
LIG_BRCT_BRCA1_1 | 333 | 337 | PF00533 | 0.497 |
LIG_BRCT_BRCA1_1 | 406 | 410 | PF00533 | 0.550 |
LIG_CSL_BTD_1 | 1005 | 1008 | PF09270 | 0.504 |
LIG_CSL_BTD_1 | 1124 | 1127 | PF09270 | 0.448 |
LIG_CtBP_PxDLS_1 | 220 | 224 | PF00389 | 0.494 |
LIG_CtBP_PxDLS_1 | 551 | 555 | PF00389 | 0.481 |
LIG_CtBP_PxDLS_1 | 975 | 979 | PF00389 | 0.469 |
LIG_EVH1_1 | 214 | 218 | PF00568 | 0.504 |
LIG_FHA_1 | 1008 | 1014 | PF00498 | 0.507 |
LIG_FHA_1 | 1043 | 1049 | PF00498 | 0.461 |
LIG_FHA_1 | 191 | 197 | PF00498 | 0.599 |
LIG_FHA_1 | 233 | 239 | PF00498 | 0.686 |
LIG_FHA_1 | 355 | 361 | PF00498 | 0.381 |
LIG_FHA_1 | 412 | 418 | PF00498 | 0.514 |
LIG_FHA_1 | 444 | 450 | PF00498 | 0.443 |
LIG_FHA_1 | 478 | 484 | PF00498 | 0.461 |
LIG_FHA_1 | 636 | 642 | PF00498 | 0.368 |
LIG_FHA_1 | 71 | 77 | PF00498 | 0.567 |
LIG_FHA_1 | 754 | 760 | PF00498 | 0.399 |
LIG_FHA_1 | 786 | 792 | PF00498 | 0.379 |
LIG_FHA_1 | 819 | 825 | PF00498 | 0.332 |
LIG_FHA_1 | 931 | 937 | PF00498 | 0.756 |
LIG_FHA_1 | 97 | 103 | PF00498 | 0.518 |
LIG_FHA_2 | 1054 | 1060 | PF00498 | 0.401 |
LIG_FHA_2 | 1109 | 1115 | PF00498 | 0.383 |
LIG_FHA_2 | 146 | 152 | PF00498 | 0.587 |
LIG_FHA_2 | 467 | 473 | PF00498 | 0.525 |
LIG_FHA_2 | 514 | 520 | PF00498 | 0.525 |
LIG_FHA_2 | 53 | 59 | PF00498 | 0.643 |
LIG_FHA_2 | 585 | 591 | PF00498 | 0.455 |
LIG_FHA_2 | 662 | 668 | PF00498 | 0.698 |
LIG_FHA_2 | 800 | 806 | PF00498 | 0.488 |
LIG_HP1_1 | 792 | 796 | PF01393 | 0.241 |
LIG_LIR_Apic_2 | 10 | 14 | PF02991 | 0.589 |
LIG_LIR_Apic_2 | 197 | 202 | PF02991 | 0.497 |
LIG_LIR_Apic_2 | 53 | 57 | PF02991 | 0.522 |
LIG_LIR_Gen_1 | 525 | 535 | PF02991 | 0.574 |
LIG_LIR_Gen_1 | 675 | 686 | PF02991 | 0.459 |
LIG_LIR_Gen_1 | 727 | 736 | PF02991 | 0.528 |
LIG_LIR_Gen_1 | 756 | 762 | PF02991 | 0.337 |
LIG_LIR_Gen_1 | 765 | 775 | PF02991 | 0.331 |
LIG_LIR_Gen_1 | 819 | 828 | PF02991 | 0.355 |
LIG_LIR_LC3C_4 | 445 | 450 | PF02991 | 0.485 |
LIG_LIR_LC3C_4 | 638 | 643 | PF02991 | 0.253 |
LIG_LIR_Nem_3 | 1025 | 1030 | PF02991 | 0.325 |
LIG_LIR_Nem_3 | 1097 | 1103 | PF02991 | 0.327 |
LIG_LIR_Nem_3 | 407 | 413 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 525 | 531 | PF02991 | 0.574 |
LIG_LIR_Nem_3 | 675 | 681 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 727 | 733 | PF02991 | 0.538 |
LIG_LIR_Nem_3 | 756 | 760 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 765 | 770 | PF02991 | 0.320 |
LIG_LIR_Nem_3 | 819 | 823 | PF02991 | 0.318 |
LIG_LIR_Nem_3 | 859 | 864 | PF02991 | 0.496 |
LIG_LIR_Nem_3 | 984 | 990 | PF02991 | 0.361 |
LIG_NRBOX | 222 | 228 | PF00104 | 0.489 |
LIG_NRBOX | 347 | 353 | PF00104 | 0.390 |
LIG_Pex14_1 | 1099 | 1103 | PF04695 | 0.436 |
LIG_Pex14_1 | 678 | 682 | PF04695 | 0.458 |
LIG_PTB_Apo_2 | 761 | 768 | PF02174 | 0.406 |
LIG_PTB_Apo_2 | 794 | 801 | PF02174 | 0.323 |
LIG_PTB_Phospho_1 | 761 | 767 | PF10480 | 0.411 |
LIG_Rb_pABgroove_1 | 991 | 999 | PF01858 | 0.487 |
LIG_REV1ctd_RIR_1 | 700 | 711 | PF16727 | 0.480 |
LIG_SH2_CRK | 528 | 532 | PF00017 | 0.551 |
LIG_SH2_CRK | 730 | 734 | PF00017 | 0.369 |
LIG_SH2_CRK | 767 | 771 | PF00017 | 0.426 |
LIG_SH2_CRK | 820 | 824 | PF00017 | 0.372 |
LIG_SH2_CRK | 987 | 991 | PF00017 | 0.458 |
LIG_SH2_NCK_1 | 730 | 734 | PF00017 | 0.369 |
LIG_SH2_PTP2 | 1029 | 1032 | PF00017 | 0.332 |
LIG_SH2_SRC | 710 | 713 | PF00017 | 0.444 |
LIG_SH2_STAP1 | 820 | 824 | PF00017 | 0.383 |
LIG_SH2_STAT3 | 923 | 926 | PF00017 | 0.657 |
LIG_SH2_STAT5 | 1029 | 1032 | PF00017 | 0.292 |
LIG_SH2_STAT5 | 1122 | 1125 | PF00017 | 0.271 |
LIG_SH2_STAT5 | 710 | 713 | PF00017 | 0.441 |
LIG_SH2_STAT5 | 77 | 80 | PF00017 | 0.489 |
LIG_SH2_STAT5 | 820 | 823 | PF00017 | 0.358 |
LIG_SH2_STAT5 | 923 | 926 | PF00017 | 0.685 |
LIG_SH3_3 | 100 | 106 | PF00018 | 0.685 |
LIG_SH3_3 | 204 | 210 | PF00018 | 0.757 |
LIG_SH3_3 | 212 | 218 | PF00018 | 0.575 |
LIG_SH3_3 | 490 | 496 | PF00018 | 0.488 |
LIG_SH3_3 | 617 | 623 | PF00018 | 0.392 |
LIG_SH3_3 | 86 | 92 | PF00018 | 0.740 |
LIG_SH3_3 | 886 | 892 | PF00018 | 0.601 |
LIG_SH3_3 | 898 | 904 | PF00018 | 0.524 |
LIG_SH3_3 | 907 | 913 | PF00018 | 0.508 |
LIG_SH3_3 | 943 | 949 | PF00018 | 0.628 |
LIG_SUMO_SIM_anti_2 | 411 | 417 | PF11976 | 0.466 |
LIG_SUMO_SIM_anti_2 | 444 | 452 | PF11976 | 0.442 |
LIG_SUMO_SIM_anti_2 | 638 | 645 | PF11976 | 0.459 |
LIG_SUMO_SIM_anti_2 | 756 | 762 | PF11976 | 0.267 |
LIG_SUMO_SIM_par_1 | 219 | 225 | PF11976 | 0.574 |
LIG_SUMO_SIM_par_1 | 466 | 472 | PF11976 | 0.520 |
LIG_SUMO_SIM_par_1 | 638 | 645 | PF11976 | 0.459 |
LIG_TRAF2_1 | 1063 | 1066 | PF00917 | 0.422 |
LIG_TYR_ITIM | 526 | 531 | PF00017 | 0.525 |
LIG_TYR_ITSM | 726 | 733 | PF00017 | 0.356 |
LIG_WRC_WIRS_1 | 573 | 578 | PF05994 | 0.439 |
MOD_CDK_SPK_2 | 244 | 249 | PF00069 | 0.540 |
MOD_CDK_SPxxK_3 | 459 | 466 | PF00069 | 0.480 |
MOD_CDK_SPxxK_3 | 691 | 698 | PF00069 | 0.307 |
MOD_CK1_1 | 1037 | 1043 | PF00069 | 0.556 |
MOD_CK1_1 | 123 | 129 | PF00069 | 0.515 |
MOD_CK1_1 | 194 | 200 | PF00069 | 0.613 |
MOD_CK1_1 | 319 | 325 | PF00069 | 0.413 |
MOD_CK1_1 | 328 | 334 | PF00069 | 0.384 |
MOD_CK1_1 | 38 | 44 | PF00069 | 0.734 |
MOD_CK1_1 | 408 | 414 | PF00069 | 0.410 |
MOD_CK1_1 | 444 | 450 | PF00069 | 0.544 |
MOD_CK1_1 | 585 | 591 | PF00069 | 0.512 |
MOD_CK1_1 | 677 | 683 | PF00069 | 0.408 |
MOD_CK1_1 | 70 | 76 | PF00069 | 0.581 |
MOD_CK1_1 | 731 | 737 | PF00069 | 0.529 |
MOD_CK1_1 | 876 | 882 | PF00069 | 0.534 |
MOD_CK1_1 | 930 | 936 | PF00069 | 0.648 |
MOD_CK2_1 | 1053 | 1059 | PF00069 | 0.496 |
MOD_CK2_1 | 257 | 263 | PF00069 | 0.671 |
MOD_CK2_1 | 352 | 358 | PF00069 | 0.592 |
MOD_CK2_1 | 452 | 458 | PF00069 | 0.446 |
MOD_CK2_1 | 513 | 519 | PF00069 | 0.490 |
MOD_CK2_1 | 52 | 58 | PF00069 | 0.639 |
MOD_CK2_1 | 884 | 890 | PF00069 | 0.561 |
MOD_CK2_1 | 91 | 97 | PF00069 | 0.505 |
MOD_GlcNHglycan | 1036 | 1039 | PF01048 | 0.550 |
MOD_GlcNHglycan | 1050 | 1054 | PF01048 | 0.328 |
MOD_GlcNHglycan | 111 | 114 | PF01048 | 0.541 |
MOD_GlcNHglycan | 1150 | 1153 | PF01048 | 0.510 |
MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.285 |
MOD_GlcNHglycan | 180 | 183 | PF01048 | 0.700 |
MOD_GlcNHglycan | 193 | 196 | PF01048 | 0.660 |
MOD_GlcNHglycan | 203 | 206 | PF01048 | 0.595 |
MOD_GlcNHglycan | 239 | 242 | PF01048 | 0.559 |
MOD_GlcNHglycan | 296 | 299 | PF01048 | 0.629 |
MOD_GlcNHglycan | 354 | 357 | PF01048 | 0.482 |
MOD_GlcNHglycan | 389 | 392 | PF01048 | 0.414 |
MOD_GlcNHglycan | 40 | 43 | PF01048 | 0.624 |
MOD_GlcNHglycan | 402 | 405 | PF01048 | 0.576 |
MOD_GlcNHglycan | 407 | 410 | PF01048 | 0.488 |
MOD_GlcNHglycan | 583 | 587 | PF01048 | 0.548 |
MOD_GlcNHglycan | 868 | 872 | PF01048 | 0.615 |
MOD_GlcNHglycan | 886 | 889 | PF01048 | 0.585 |
MOD_GSK3_1 | 1049 | 1056 | PF00069 | 0.440 |
MOD_GSK3_1 | 1077 | 1084 | PF00069 | 0.438 |
MOD_GSK3_1 | 116 | 123 | PF00069 | 0.557 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.709 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.528 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.482 |
MOD_GSK3_1 | 252 | 259 | PF00069 | 0.781 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.355 |
MOD_GSK3_1 | 327 | 334 | PF00069 | 0.386 |
MOD_GSK3_1 | 335 | 342 | PF00069 | 0.383 |
MOD_GSK3_1 | 352 | 359 | PF00069 | 0.365 |
MOD_GSK3_1 | 400 | 407 | PF00069 | 0.444 |
MOD_GSK3_1 | 572 | 579 | PF00069 | 0.383 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.775 |
MOD_GSK3_1 | 599 | 606 | PF00069 | 0.480 |
MOD_GSK3_1 | 724 | 731 | PF00069 | 0.510 |
MOD_GSK3_1 | 78 | 85 | PF00069 | 0.695 |
MOD_GSK3_1 | 799 | 806 | PF00069 | 0.461 |
MOD_GSK3_1 | 874 | 881 | PF00069 | 0.650 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.692 |
MOD_LATS_1 | 1157 | 1163 | PF00433 | 0.493 |
MOD_LATS_1 | 464 | 470 | PF00433 | 0.522 |
MOD_N-GLC_1 | 763 | 768 | PF02516 | 0.417 |
MOD_N-GLC_1 | 796 | 801 | PF02516 | 0.326 |
MOD_N-GLC_1 | 927 | 932 | PF02516 | 0.516 |
MOD_N-GLC_2 | 377 | 379 | PF02516 | 0.365 |
MOD_NEK2_1 | 1103 | 1108 | PF00069 | 0.333 |
MOD_NEK2_1 | 1146 | 1151 | PF00069 | 0.363 |
MOD_NEK2_1 | 121 | 126 | PF00069 | 0.456 |
MOD_NEK2_1 | 159 | 164 | PF00069 | 0.749 |
MOD_NEK2_1 | 257 | 262 | PF00069 | 0.670 |
MOD_NEK2_1 | 335 | 340 | PF00069 | 0.539 |
MOD_NEK2_1 | 352 | 357 | PF00069 | 0.440 |
MOD_NEK2_1 | 397 | 402 | PF00069 | 0.332 |
MOD_NEK2_1 | 451 | 456 | PF00069 | 0.455 |
MOD_NEK2_1 | 635 | 640 | PF00069 | 0.364 |
MOD_NEK2_1 | 701 | 706 | PF00069 | 0.474 |
MOD_NEK2_1 | 796 | 801 | PF00069 | 0.443 |
MOD_NEK2_1 | 824 | 829 | PF00069 | 0.510 |
MOD_NEK2_1 | 873 | 878 | PF00069 | 0.708 |
MOD_NEK2_1 | 941 | 946 | PF00069 | 0.501 |
MOD_NEK2_1 | 96 | 101 | PF00069 | 0.581 |
MOD_NEK2_2 | 262 | 267 | PF00069 | 0.523 |
MOD_NEK2_2 | 960 | 965 | PF00069 | 0.495 |
MOD_PIKK_1 | 1117 | 1123 | PF00454 | 0.313 |
MOD_PIKK_1 | 576 | 582 | PF00454 | 0.359 |
MOD_PKA_1 | 133 | 139 | PF00069 | 0.525 |
MOD_PKA_1 | 286 | 292 | PF00069 | 0.523 |
MOD_PKA_1 | 29 | 35 | PF00069 | 0.588 |
MOD_PKA_2 | 1034 | 1040 | PF00069 | 0.600 |
MOD_PKA_2 | 133 | 139 | PF00069 | 0.525 |
MOD_PKA_2 | 286 | 292 | PF00069 | 0.764 |
MOD_PKA_2 | 29 | 35 | PF00069 | 0.497 |
MOD_PKA_2 | 603 | 609 | PF00069 | 0.354 |
MOD_PKA_2 | 635 | 641 | PF00069 | 0.362 |
MOD_PKA_2 | 78 | 84 | PF00069 | 0.478 |
MOD_PKA_2 | 930 | 936 | PF00069 | 0.579 |
MOD_Plk_1 | 1049 | 1055 | PF00069 | 0.431 |
MOD_Plk_1 | 1077 | 1083 | PF00069 | 0.449 |
MOD_Plk_1 | 262 | 268 | PF00069 | 0.597 |
MOD_Plk_1 | 728 | 734 | PF00069 | 0.399 |
MOD_Plk_1 | 763 | 769 | PF00069 | 0.411 |
MOD_Plk_1 | 796 | 802 | PF00069 | 0.352 |
MOD_Plk_1 | 803 | 809 | PF00069 | 0.375 |
MOD_Plk_1 | 818 | 824 | PF00069 | 0.394 |
MOD_Plk_1 | 92 | 98 | PF00069 | 0.596 |
MOD_Plk_2-3 | 222 | 228 | PF00069 | 0.489 |
MOD_Plk_4 | 1053 | 1059 | PF00069 | 0.455 |
MOD_Plk_4 | 1066 | 1072 | PF00069 | 0.488 |
MOD_Plk_4 | 1094 | 1100 | PF00069 | 0.373 |
MOD_Plk_4 | 117 | 123 | PF00069 | 0.543 |
MOD_Plk_4 | 194 | 200 | PF00069 | 0.502 |
MOD_Plk_4 | 303 | 309 | PF00069 | 0.665 |
MOD_Plk_4 | 343 | 349 | PF00069 | 0.508 |
MOD_Plk_4 | 411 | 417 | PF00069 | 0.372 |
MOD_Plk_4 | 444 | 450 | PF00069 | 0.476 |
MOD_Plk_4 | 484 | 490 | PF00069 | 0.391 |
MOD_Plk_4 | 504 | 510 | PF00069 | 0.553 |
MOD_Plk_4 | 550 | 556 | PF00069 | 0.476 |
MOD_Plk_4 | 572 | 578 | PF00069 | 0.384 |
MOD_Plk_4 | 636 | 642 | PF00069 | 0.333 |
MOD_Plk_4 | 674 | 680 | PF00069 | 0.357 |
MOD_Plk_4 | 7 | 13 | PF00069 | 0.535 |
MOD_Plk_4 | 753 | 759 | PF00069 | 0.271 |
MOD_Plk_4 | 796 | 802 | PF00069 | 0.310 |
MOD_Plk_4 | 818 | 824 | PF00069 | 0.366 |
MOD_ProDKin_1 | 1108 | 1114 | PF00069 | 0.449 |
MOD_ProDKin_1 | 198 | 204 | PF00069 | 0.654 |
MOD_ProDKin_1 | 244 | 250 | PF00069 | 0.678 |
MOD_ProDKin_1 | 258 | 264 | PF00069 | 0.531 |
MOD_ProDKin_1 | 323 | 329 | PF00069 | 0.501 |
MOD_ProDKin_1 | 372 | 378 | PF00069 | 0.448 |
MOD_ProDKin_1 | 408 | 414 | PF00069 | 0.390 |
MOD_ProDKin_1 | 459 | 465 | PF00069 | 0.488 |
MOD_ProDKin_1 | 53 | 59 | PF00069 | 0.626 |
MOD_ProDKin_1 | 535 | 541 | PF00069 | 0.504 |
MOD_ProDKin_1 | 67 | 73 | PF00069 | 0.596 |
MOD_ProDKin_1 | 691 | 697 | PF00069 | 0.341 |
MOD_ProDKin_1 | 906 | 912 | PF00069 | 0.810 |
MOD_SUMO_rev_2 | 41 | 49 | PF00179 | 0.528 |
MOD_SUMO_rev_2 | 627 | 634 | PF00179 | 0.472 |
TRG_DiLeu_BaEn_1 | 222 | 227 | PF01217 | 0.491 |
TRG_DiLeu_BaEn_1 | 819 | 824 | PF01217 | 0.246 |
TRG_DiLeu_BaEn_4 | 519 | 525 | PF01217 | 0.433 |
TRG_DiLeu_BaLyEn_6 | 1083 | 1088 | PF01217 | 0.280 |
TRG_DiLeu_BaLyEn_6 | 1156 | 1161 | PF01217 | 0.475 |
TRG_DiLeu_BaLyEn_6 | 22 | 27 | PF01217 | 0.549 |
TRG_DiLeu_BaLyEn_6 | 943 | 948 | PF01217 | 0.477 |
TRG_DiLeu_BaLyEn_6 | 996 | 1001 | PF01217 | 0.444 |
TRG_DiLeu_LyEn_5 | 630 | 635 | PF01217 | 0.357 |
TRG_ENDOCYTIC_2 | 1029 | 1032 | PF00928 | 0.268 |
TRG_ENDOCYTIC_2 | 528 | 531 | PF00928 | 0.551 |
TRG_ENDOCYTIC_2 | 730 | 733 | PF00928 | 0.377 |
TRG_ENDOCYTIC_2 | 767 | 770 | PF00928 | 0.365 |
TRG_ENDOCYTIC_2 | 820 | 823 | PF00928 | 0.376 |
TRG_ENDOCYTIC_2 | 987 | 990 | PF00928 | 0.457 |
TRG_ER_diArg_1 | 1090 | 1092 | PF00400 | 0.424 |
TRG_ER_diArg_1 | 132 | 134 | PF00400 | 0.500 |
TRG_ER_diArg_1 | 27 | 30 | PF00400 | 0.483 |
TRG_ER_diArg_1 | 595 | 598 | PF00400 | 0.538 |
TRG_ER_diArg_1 | 615 | 618 | PF00400 | 0.315 |
TRG_ER_diArg_1 | 720 | 722 | PF00400 | 0.484 |
TRG_Pf-PMV_PEXEL_1 | 1159 | 1163 | PF00026 | 0.469 |
TRG_Pf-PMV_PEXEL_1 | 224 | 228 | PF00026 | 0.543 |
TRG_Pf-PMV_PEXEL_1 | 660 | 665 | PF00026 | 0.567 |
TRG_Pf-PMV_PEXEL_1 | 721 | 725 | PF00026 | 0.329 |
TRG_Pf-PMV_PEXEL_1 | 843 | 847 | PF00026 | 0.452 |
TRG_Pf-PMV_PEXEL_1 | 862 | 866 | PF00026 | 0.305 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAP2 | Leptomonas seymouri | 50% | 95% |
A0A1X0NWJ4 | Trypanosomatidae | 27% | 100% |
A0A3S7WVQ6 | Leishmania donovani | 74% | 100% |
A0A422N7U4 | Trypanosoma rangeli | 30% | 100% |
A4HYJ9 | Leishmania infantum | 74% | 100% |
E9AUE6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 74% | 100% |
Q4QD38 | Leishmania major | 74% | 99% |
V5BQX8 | Trypanosoma cruzi | 29% | 100% |