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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9B025
Term | Name | Level | Count |
---|---|---|---|
GO:0006082 | organic acid metabolic process | 3 | 1 |
GO:0006520 | amino acid metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009058 | biosynthetic process | 2 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0019748 | secondary metabolic process | 2 | 1 |
GO:0019752 | carboxylic acid metabolic process | 5 | 1 |
GO:0043038 | amino acid activation | 4 | 1 |
GO:0043041 | amino acid activation for nonribosomal peptide biosynthetic process | 5 | 1 |
GO:0043436 | oxoacid metabolic process | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044281 | small molecule metabolic process | 2 | 1 |
GO:0044550 | secondary metabolite biosynthetic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 1 |
GO:0019842 | vitamin binding | 3 | 1 |
GO:0031177 | phosphopantetheine binding | 3 | 1 |
GO:0033218 | amide binding | 2 | 1 |
GO:0036094 | small molecule binding | 2 | 1 |
GO:0072341 | modified amino acid binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 410 | 414 | PF00656 | 0.210 |
CLV_NRD_NRD_1 | 158 | 160 | PF00675 | 0.395 |
CLV_NRD_NRD_1 | 186 | 188 | PF00675 | 0.307 |
CLV_NRD_NRD_1 | 491 | 493 | PF00675 | 0.376 |
CLV_NRD_NRD_1 | 578 | 580 | PF00675 | 0.485 |
CLV_NRD_NRD_1 | 82 | 84 | PF00675 | 0.517 |
CLV_NRD_NRD_1 | 846 | 848 | PF00675 | 0.485 |
CLV_NRD_NRD_1 | 90 | 92 | PF00675 | 0.452 |
CLV_NRD_NRD_1 | 945 | 947 | PF00675 | 0.673 |
CLV_NRD_NRD_1 | 959 | 961 | PF00675 | 0.644 |
CLV_NRD_NRD_1 | 975 | 977 | PF00675 | 0.597 |
CLV_PCSK_FUR_1 | 156 | 160 | PF00082 | 0.258 |
CLV_PCSK_FUR_1 | 489 | 493 | PF00082 | 0.501 |
CLV_PCSK_FUR_1 | 983 | 987 | PF00082 | 0.641 |
CLV_PCSK_KEX2_1 | 156 | 158 | PF00082 | 0.386 |
CLV_PCSK_KEX2_1 | 491 | 493 | PF00082 | 0.376 |
CLV_PCSK_KEX2_1 | 578 | 580 | PF00082 | 0.485 |
CLV_PCSK_KEX2_1 | 70 | 72 | PF00082 | 0.527 |
CLV_PCSK_KEX2_1 | 81 | 83 | PF00082 | 0.455 |
CLV_PCSK_KEX2_1 | 846 | 848 | PF00082 | 0.485 |
CLV_PCSK_KEX2_1 | 90 | 92 | PF00082 | 0.566 |
CLV_PCSK_KEX2_1 | 943 | 945 | PF00082 | 0.714 |
CLV_PCSK_KEX2_1 | 975 | 977 | PF00082 | 0.724 |
CLV_PCSK_KEX2_1 | 985 | 987 | PF00082 | 0.592 |
CLV_PCSK_PC1ET2_1 | 70 | 72 | PF00082 | 0.527 |
CLV_PCSK_PC1ET2_1 | 81 | 83 | PF00082 | 0.455 |
CLV_PCSK_PC1ET2_1 | 943 | 945 | PF00082 | 0.828 |
CLV_PCSK_PC1ET2_1 | 985 | 987 | PF00082 | 0.719 |
CLV_PCSK_PC7_1 | 153 | 159 | PF00082 | 0.430 |
CLV_PCSK_SKI1_1 | 241 | 245 | PF00082 | 0.501 |
CLV_PCSK_SKI1_1 | 337 | 341 | PF00082 | 0.376 |
CLV_PCSK_SKI1_1 | 502 | 506 | PF00082 | 0.518 |
CLV_PCSK_SKI1_1 | 579 | 583 | PF00082 | 0.483 |
CLV_PCSK_SKI1_1 | 83 | 87 | PF00082 | 0.538 |
CLV_PCSK_SKI1_1 | 846 | 850 | PF00082 | 0.423 |
DEG_APCC_DBOX_1 | 355 | 363 | PF00400 | 0.410 |
DEG_APCC_DBOX_1 | 501 | 509 | PF00400 | 0.516 |
DEG_APCC_DBOX_1 | 772 | 780 | PF00400 | 0.467 |
DEG_SCF_FBW7_2 | 99 | 106 | PF00400 | 0.534 |
DOC_CKS1_1 | 277 | 282 | PF01111 | 0.430 |
DOC_CKS1_1 | 310 | 315 | PF01111 | 0.376 |
DOC_CKS1_1 | 590 | 595 | PF01111 | 0.671 |
DOC_CKS1_1 | 896 | 901 | PF01111 | 0.544 |
DOC_CYCLIN_RxL_1 | 840 | 852 | PF00134 | 0.431 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 232 | 239 | PF00134 | 0.428 |
DOC_CYCLIN_yCln2_LP_2 | 689 | 695 | PF00134 | 0.549 |
DOC_MAPK_DCC_7 | 197 | 207 | PF00069 | 0.210 |
DOC_MAPK_gen_1 | 187 | 194 | PF00069 | 0.307 |
DOC_MAPK_gen_1 | 489 | 498 | PF00069 | 0.385 |
DOC_MAPK_gen_1 | 596 | 604 | PF00069 | 0.551 |
DOC_MAPK_gen_1 | 666 | 675 | PF00069 | 0.443 |
DOC_MAPK_gen_1 | 785 | 795 | PF00069 | 0.636 |
DOC_MAPK_gen_1 | 81 | 87 | PF00069 | 0.321 |
DOC_MAPK_gen_1 | 859 | 869 | PF00069 | 0.376 |
DOC_MAPK_MEF2A_6 | 143 | 151 | PF00069 | 0.506 |
DOC_MAPK_MEF2A_6 | 232 | 239 | PF00069 | 0.210 |
DOC_MAPK_MEF2A_6 | 666 | 675 | PF00069 | 0.466 |
DOC_MAPK_MEF2A_6 | 788 | 797 | PF00069 | 0.595 |
DOC_PP1_RVXF_1 | 577 | 584 | PF00149 | 0.501 |
DOC_PP2B_LxvP_1 | 3 | 6 | PF13499 | 0.449 |
DOC_PP2B_LxvP_1 | 569 | 572 | PF13499 | 0.441 |
DOC_PP2B_LxvP_1 | 644 | 647 | PF13499 | 0.545 |
DOC_PP2B_LxvP_1 | 689 | 692 | PF13499 | 0.633 |
DOC_PP2B_LxvP_1 | 739 | 742 | PF13499 | 0.592 |
DOC_PP4_FxxP_1 | 265 | 268 | PF00568 | 0.430 |
DOC_PP4_FxxP_1 | 574 | 577 | PF00568 | 0.481 |
DOC_USP7_MATH_1 | 409 | 413 | PF00917 | 0.355 |
DOC_USP7_MATH_1 | 448 | 452 | PF00917 | 0.424 |
DOC_USP7_MATH_1 | 796 | 800 | PF00917 | 0.441 |
DOC_USP7_MATH_1 | 838 | 842 | PF00917 | 0.410 |
DOC_USP7_MATH_1 | 870 | 874 | PF00917 | 0.430 |
DOC_WW_Pin1_4 | 195 | 200 | PF00397 | 0.395 |
DOC_WW_Pin1_4 | 260 | 265 | PF00397 | 0.399 |
DOC_WW_Pin1_4 | 276 | 281 | PF00397 | 0.171 |
DOC_WW_Pin1_4 | 309 | 314 | PF00397 | 0.376 |
DOC_WW_Pin1_4 | 451 | 456 | PF00397 | 0.461 |
DOC_WW_Pin1_4 | 531 | 536 | PF00397 | 0.647 |
DOC_WW_Pin1_4 | 589 | 594 | PF00397 | 0.649 |
DOC_WW_Pin1_4 | 788 | 793 | PF00397 | 0.534 |
DOC_WW_Pin1_4 | 824 | 829 | PF00397 | 0.350 |
DOC_WW_Pin1_4 | 895 | 900 | PF00397 | 0.546 |
DOC_WW_Pin1_4 | 99 | 104 | PF00397 | 0.689 |
LIG_14-3-3_CanoR_1 | 344 | 350 | PF00244 | 0.355 |
LIG_14-3-3_CanoR_1 | 474 | 483 | PF00244 | 0.424 |
LIG_14-3-3_CanoR_1 | 527 | 535 | PF00244 | 0.446 |
LIG_14-3-3_CanoR_1 | 634 | 640 | PF00244 | 0.569 |
LIG_14-3-3_CanoR_1 | 788 | 792 | PF00244 | 0.635 |
LIG_14-3-3_CanoR_1 | 82 | 88 | PF00244 | 0.356 |
LIG_14-3-3_CanoR_1 | 822 | 828 | PF00244 | 0.404 |
LIG_14-3-3_CanoR_1 | 862 | 867 | PF00244 | 0.378 |
LIG_14-3-3_CanoR_1 | 90 | 94 | PF00244 | 0.544 |
LIG_14-3-3_CanoR_1 | 960 | 965 | PF00244 | 0.643 |
LIG_APCC_ABBA_1 | 436 | 441 | PF00400 | 0.397 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.665 |
LIG_BIR_III_2 | 615 | 619 | PF00653 | 0.465 |
LIG_BRCT_BRCA1_1 | 261 | 265 | PF00533 | 0.378 |
LIG_BRCT_BRCA1_1 | 411 | 415 | PF00533 | 0.474 |
LIG_BRCT_BRCA1_1 | 452 | 456 | PF00533 | 0.457 |
LIG_deltaCOP1_diTrp_1 | 893 | 902 | PF00928 | 0.490 |
LIG_FHA_1 | 136 | 142 | PF00498 | 0.504 |
LIG_FHA_1 | 305 | 311 | PF00498 | 0.376 |
LIG_FHA_1 | 331 | 337 | PF00498 | 0.210 |
LIG_FHA_1 | 467 | 473 | PF00498 | 0.376 |
LIG_FHA_1 | 509 | 515 | PF00498 | 0.440 |
LIG_FHA_1 | 532 | 538 | PF00498 | 0.612 |
LIG_FHA_1 | 542 | 548 | PF00498 | 0.628 |
LIG_FHA_1 | 592 | 598 | PF00498 | 0.592 |
LIG_FHA_1 | 650 | 656 | PF00498 | 0.551 |
LIG_FHA_1 | 788 | 794 | PF00498 | 0.522 |
LIG_FHA_1 | 807 | 813 | PF00498 | 0.570 |
LIG_FHA_1 | 876 | 882 | PF00498 | 0.424 |
LIG_FHA_1 | 907 | 913 | PF00498 | 0.575 |
LIG_FHA_1 | 918 | 924 | PF00498 | 0.534 |
LIG_FHA_2 | 100 | 106 | PF00498 | 0.656 |
LIG_FHA_2 | 286 | 292 | PF00498 | 0.501 |
LIG_FHA_2 | 350 | 356 | PF00498 | 0.501 |
LIG_FHA_2 | 379 | 385 | PF00498 | 0.501 |
LIG_FHA_2 | 84 | 90 | PF00498 | 0.360 |
LIG_FHA_2 | 961 | 967 | PF00498 | 0.658 |
LIG_GBD_Chelix_1 | 559 | 567 | PF00786 | 0.504 |
LIG_Integrin_RGD_1 | 26 | 28 | PF01839 | 0.494 |
LIG_LIR_Apic_2 | 262 | 268 | PF02991 | 0.430 |
LIG_LIR_Apic_2 | 573 | 577 | PF02991 | 0.569 |
LIG_LIR_Gen_1 | 121 | 131 | PF02991 | 0.433 |
LIG_LIR_Gen_1 | 138 | 147 | PF02991 | 0.527 |
LIG_LIR_Gen_1 | 30 | 41 | PF02991 | 0.353 |
LIG_LIR_Gen_1 | 369 | 379 | PF02991 | 0.353 |
LIG_LIR_Gen_1 | 638 | 648 | PF02991 | 0.516 |
LIG_LIR_Gen_1 | 952 | 959 | PF02991 | 0.677 |
LIG_LIR_Gen_1 | 966 | 974 | PF02991 | 0.633 |
LIG_LIR_Nem_3 | 121 | 127 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 138 | 142 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 30 | 36 | PF02991 | 0.466 |
LIG_LIR_Nem_3 | 358 | 363 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 369 | 374 | PF02991 | 0.305 |
LIG_LIR_Nem_3 | 431 | 436 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 630 | 636 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 753 | 759 | PF02991 | 0.510 |
LIG_LIR_Nem_3 | 952 | 958 | PF02991 | 0.682 |
LIG_LIR_Nem_3 | 963 | 967 | PF02991 | 0.642 |
LIG_MLH1_MIPbox_1 | 262 | 266 | PF16413 | 0.430 |
LIG_NRBOX | 562 | 568 | PF00104 | 0.592 |
LIG_NRBOX | 844 | 850 | PF00104 | 0.430 |
LIG_PCNA_PIPBox_1 | 513 | 522 | PF02747 | 0.518 |
LIG_PCNA_yPIPBox_3 | 513 | 527 | PF02747 | 0.389 |
LIG_Pex3_1 | 563 | 574 | PF04882 | 0.585 |
LIG_REV1ctd_RIR_1 | 464 | 472 | PF16727 | 0.410 |
LIG_REV1ctd_RIR_1 | 752 | 761 | PF16727 | 0.288 |
LIG_RPA_C_Fungi | 551 | 563 | PF08784 | 0.556 |
LIG_RPA_C_Fungi | 835 | 847 | PF08784 | 0.326 |
LIG_SH2_CRK | 124 | 128 | PF00017 | 0.425 |
LIG_SH2_CRK | 633 | 637 | PF00017 | 0.535 |
LIG_SH2_SRC | 654 | 657 | PF00017 | 0.556 |
LIG_SH2_STAP1 | 124 | 128 | PF00017 | 0.425 |
LIG_SH2_STAT3 | 439 | 442 | PF00017 | 0.385 |
LIG_SH2_STAT5 | 217 | 220 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 238 | 241 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 285 | 288 | PF00017 | 0.402 |
LIG_SH2_STAT5 | 654 | 657 | PF00017 | 0.550 |
LIG_SH2_STAT5 | 672 | 675 | PF00017 | 0.345 |
LIG_SH2_STAT5 | 707 | 710 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 964 | 967 | PF00017 | 0.678 |
LIG_SH3_3 | 141 | 147 | PF00018 | 0.518 |
LIG_SH3_3 | 307 | 313 | PF00018 | 0.376 |
LIG_SH3_3 | 587 | 593 | PF00018 | 0.637 |
LIG_SH3_3 | 689 | 695 | PF00018 | 0.511 |
LIG_SUMO_SIM_par_1 | 190 | 196 | PF11976 | 0.307 |
LIG_SUMO_SIM_par_1 | 83 | 89 | PF11976 | 0.343 |
LIG_TRAF2_1 | 178 | 181 | PF00917 | 0.424 |
LIG_TRAF2_1 | 22 | 25 | PF00917 | 0.434 |
LIG_TRAF2_1 | 504 | 507 | PF00917 | 0.507 |
LIG_TRAF2_1 | 562 | 565 | PF00917 | 0.526 |
LIG_TRAF2_1 | 606 | 609 | PF00917 | 0.556 |
LIG_TRAF2_1 | 626 | 629 | PF00917 | 0.535 |
LIG_TYR_ITIM | 965 | 970 | PF00017 | 0.584 |
LIG_TYR_ITSM | 367 | 374 | PF00017 | 0.430 |
LIG_WRC_WIRS_1 | 571 | 576 | PF05994 | 0.569 |
MOD_CDK_SPxK_1 | 195 | 201 | PF00069 | 0.326 |
MOD_CDK_SPxxK_3 | 451 | 458 | PF00069 | 0.210 |
MOD_CDK_SPxxK_3 | 589 | 596 | PF00069 | 0.660 |
MOD_CK1_1 | 119 | 125 | PF00069 | 0.503 |
MOD_CK1_1 | 195 | 201 | PF00069 | 0.330 |
MOD_CK1_1 | 219 | 225 | PF00069 | 0.376 |
MOD_CK1_1 | 317 | 323 | PF00069 | 0.482 |
MOD_CK1_1 | 451 | 457 | PF00069 | 0.440 |
MOD_CK1_1 | 799 | 805 | PF00069 | 0.548 |
MOD_CK1_1 | 921 | 927 | PF00069 | 0.649 |
MOD_CK2_1 | 175 | 181 | PF00069 | 0.492 |
MOD_CK2_1 | 378 | 384 | PF00069 | 0.440 |
MOD_CK2_1 | 474 | 480 | PF00069 | 0.439 |
MOD_CK2_1 | 623 | 629 | PF00069 | 0.695 |
MOD_CK2_1 | 743 | 749 | PF00069 | 0.620 |
MOD_CK2_1 | 945 | 951 | PF00069 | 0.556 |
MOD_CK2_1 | 960 | 966 | PF00069 | 0.693 |
MOD_CK2_1 | 991 | 997 | PF00069 | 0.726 |
MOD_Cter_Amidation | 489 | 492 | PF01082 | 0.376 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.499 |
MOD_GlcNHglycan | 180 | 185 | PF01048 | 0.372 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.376 |
MOD_GlcNHglycan | 427 | 430 | PF01048 | 0.414 |
MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.612 |
MOD_GlcNHglycan | 529 | 532 | PF01048 | 0.671 |
MOD_GlcNHglycan | 746 | 749 | PF01048 | 0.404 |
MOD_GlcNHglycan | 840 | 843 | PF01048 | 0.430 |
MOD_GlcNHglycan | 872 | 875 | PF01048 | 0.380 |
MOD_GlcNHglycan | 947 | 950 | PF01048 | 0.626 |
MOD_GSK3_1 | 163 | 170 | PF00069 | 0.424 |
MOD_GSK3_1 | 176 | 183 | PF00069 | 0.392 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.450 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.378 |
MOD_GSK3_1 | 279 | 286 | PF00069 | 0.383 |
MOD_GSK3_1 | 304 | 311 | PF00069 | 0.408 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.376 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.171 |
MOD_GSK3_1 | 366 | 373 | PF00069 | 0.423 |
MOD_GSK3_1 | 527 | 534 | PF00069 | 0.594 |
MOD_GSK3_1 | 585 | 592 | PF00069 | 0.557 |
MOD_GSK3_1 | 917 | 924 | PF00069 | 0.624 |
MOD_GSK3_1 | 945 | 952 | PF00069 | 0.701 |
MOD_N-GLC_1 | 618 | 623 | PF02516 | 0.549 |
MOD_N-GLC_1 | 949 | 954 | PF02516 | 0.714 |
MOD_NEK2_1 | 127 | 132 | PF00069 | 0.391 |
MOD_NEK2_1 | 135 | 140 | PF00069 | 0.435 |
MOD_NEK2_1 | 216 | 221 | PF00069 | 0.410 |
MOD_NEK2_1 | 259 | 264 | PF00069 | 0.376 |
MOD_NEK2_1 | 349 | 354 | PF00069 | 0.430 |
MOD_NEK2_1 | 41 | 46 | PF00069 | 0.613 |
MOD_NEK2_1 | 425 | 430 | PF00069 | 0.424 |
MOD_NEK2_1 | 49 | 54 | PF00069 | 0.655 |
MOD_NEK2_1 | 665 | 670 | PF00069 | 0.463 |
MOD_NEK2_1 | 836 | 841 | PF00069 | 0.501 |
MOD_NEK2_1 | 917 | 922 | PF00069 | 0.622 |
MOD_PIKK_1 | 116 | 122 | PF00454 | 0.387 |
MOD_PIKK_1 | 285 | 291 | PF00454 | 0.430 |
MOD_PIKK_1 | 343 | 349 | PF00454 | 0.423 |
MOD_PIKK_1 | 518 | 524 | PF00454 | 0.508 |
MOD_PIKK_1 | 597 | 603 | PF00454 | 0.625 |
MOD_PIKK_1 | 713 | 719 | PF00454 | 0.427 |
MOD_PKA_1 | 945 | 951 | PF00069 | 0.733 |
MOD_PKA_1 | 960 | 966 | PF00069 | 0.646 |
MOD_PKA_2 | 343 | 349 | PF00069 | 0.355 |
MOD_PKA_2 | 66 | 72 | PF00069 | 0.474 |
MOD_PKA_2 | 787 | 793 | PF00069 | 0.642 |
MOD_PKA_2 | 821 | 827 | PF00069 | 0.404 |
MOD_PKA_2 | 89 | 95 | PF00069 | 0.566 |
MOD_PKA_2 | 945 | 951 | PF00069 | 0.763 |
MOD_Plk_1 | 167 | 173 | PF00069 | 0.513 |
MOD_Plk_1 | 207 | 213 | PF00069 | 0.444 |
MOD_Plk_1 | 366 | 372 | PF00069 | 0.376 |
MOD_Plk_1 | 876 | 882 | PF00069 | 0.210 |
MOD_Plk_1 | 950 | 956 | PF00069 | 0.646 |
MOD_Plk_1 | 996 | 1002 | PF00069 | 0.576 |
MOD_Plk_2-3 | 966 | 972 | PF00069 | 0.514 |
MOD_Plk_4 | 119 | 125 | PF00069 | 0.447 |
MOD_Plk_4 | 168 | 174 | PF00069 | 0.501 |
MOD_Plk_4 | 279 | 285 | PF00069 | 0.498 |
MOD_Plk_4 | 324 | 330 | PF00069 | 0.444 |
MOD_Plk_4 | 366 | 372 | PF00069 | 0.376 |
MOD_Plk_4 | 570 | 576 | PF00069 | 0.531 |
MOD_Plk_4 | 635 | 641 | PF00069 | 0.566 |
MOD_Plk_4 | 862 | 868 | PF00069 | 0.402 |
MOD_Plk_4 | 960 | 966 | PF00069 | 0.724 |
MOD_ProDKin_1 | 195 | 201 | PF00069 | 0.395 |
MOD_ProDKin_1 | 260 | 266 | PF00069 | 0.399 |
MOD_ProDKin_1 | 276 | 282 | PF00069 | 0.171 |
MOD_ProDKin_1 | 309 | 315 | PF00069 | 0.376 |
MOD_ProDKin_1 | 451 | 457 | PF00069 | 0.461 |
MOD_ProDKin_1 | 531 | 537 | PF00069 | 0.635 |
MOD_ProDKin_1 | 589 | 595 | PF00069 | 0.656 |
MOD_ProDKin_1 | 788 | 794 | PF00069 | 0.524 |
MOD_ProDKin_1 | 824 | 830 | PF00069 | 0.350 |
MOD_ProDKin_1 | 895 | 901 | PF00069 | 0.548 |
MOD_ProDKin_1 | 99 | 105 | PF00069 | 0.695 |
MOD_SUMO_rev_2 | 219 | 228 | PF00179 | 0.376 |
MOD_SUMO_rev_2 | 493 | 498 | PF00179 | 0.501 |
MOD_SUMO_rev_2 | 718 | 726 | PF00179 | 0.691 |
TRG_DiLeu_BaEn_1 | 877 | 882 | PF01217 | 0.430 |
TRG_DiLeu_BaEn_2 | 950 | 956 | PF01217 | 0.466 |
TRG_DiLeu_BaLyEn_6 | 296 | 301 | PF01217 | 0.498 |
TRG_DiLeu_BaLyEn_6 | 733 | 738 | PF01217 | 0.684 |
TRG_DiLeu_BaLyEn_6 | 767 | 772 | PF01217 | 0.582 |
TRG_DiLeu_BaLyEn_6 | 844 | 849 | PF01217 | 0.451 |
TRG_DiLeu_LyEn_5 | 877 | 882 | PF01217 | 0.501 |
TRG_ENDOCYTIC_2 | 124 | 127 | PF00928 | 0.425 |
TRG_ENDOCYTIC_2 | 371 | 374 | PF00928 | 0.353 |
TRG_ENDOCYTIC_2 | 422 | 425 | PF00928 | 0.341 |
TRG_ENDOCYTIC_2 | 433 | 436 | PF00928 | 0.480 |
TRG_ENDOCYTIC_2 | 633 | 636 | PF00928 | 0.538 |
TRG_ENDOCYTIC_2 | 672 | 675 | PF00928 | 0.479 |
TRG_ENDOCYTIC_2 | 967 | 970 | PF00928 | 0.619 |
TRG_ER_diArg_1 | 156 | 159 | PF00400 | 0.388 |
TRG_ER_diArg_1 | 36 | 39 | PF00400 | 0.520 |
TRG_ER_diArg_1 | 395 | 398 | PF00400 | 0.501 |
TRG_ER_diArg_1 | 488 | 491 | PF00400 | 0.451 |
TRG_ER_diArg_1 | 577 | 579 | PF00400 | 0.492 |
TRG_ER_diArg_1 | 82 | 84 | PF00400 | 0.517 |
TRG_ER_diArg_1 | 845 | 847 | PF00400 | 0.424 |
TRG_ER_diArg_1 | 944 | 946 | PF00400 | 0.751 |
TRG_ER_diArg_1 | 975 | 977 | PF00400 | 0.655 |
TRG_NES_CRM1_1 | 806 | 818 | PF08389 | 0.430 |
TRG_NLS_Bipartite_1 | 70 | 85 | PF00514 | 0.402 |
TRG_NLS_Bipartite_1 | 943 | 964 | PF00514 | 0.703 |
TRG_NLS_MonoCore_2 | 942 | 947 | PF00514 | 0.742 |
TRG_NLS_MonoExtN_4 | 957 | 964 | PF00514 | 0.665 |
TRG_Pf-PMV_PEXEL_1 | 241 | 245 | PF00026 | 0.501 |
TRG_Pf-PMV_PEXEL_1 | 846 | 850 | PF00026 | 0.429 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I5E5 | Leptomonas seymouri | 51% | 98% |
A0A0S4JM65 | Bodo saltans | 31% | 84% |
A0A3Q8IEY8 | Leishmania donovani | 91% | 100% |
A4HGQ9 | Leishmania braziliensis | 80% | 100% |
A4I3T3 | Leishmania infantum | 91% | 100% |
Q4Q861 | Leishmania major | 91% | 100% |