Uncharacterized Protein, Uncharacterized
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:0005634 | nucleus | 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: A4I8R4
Term | Name | Level | Count |
---|---|---|---|
GO:0006479 | protein methylation | 4 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0008213 | protein alkylation | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016570 | histone modification | 5 | 1 |
GO:0016571 | histone methylation | 5 | 1 |
GO:0018022 | peptidyl-lysine methylation | 5 | 1 |
GO:0018193 | peptidyl-amino acid modification | 5 | 1 |
GO:0018205 | peptidyl-lysine modification | 6 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0032259 | methylation | 2 | 1 |
GO:0034968 | histone lysine methylation | 6 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0043414 | macromolecule methylation | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 1 |
GO:0008168 | methyltransferase activity | 4 | 1 |
GO:0008170 | N-methyltransferase activity | 5 | 1 |
GO:0008276 | protein methyltransferase activity | 3 | 1 |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 1 |
GO:0016278 | lysine N-methyltransferase activity | 6 | 1 |
GO:0016279 | protein-lysine N-methyltransferase activity | 4 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 1 |
GO:0018024 | obsolete histone lysine N-methyltransferase activity | 5 | 1 |
GO:0042054 | histone methyltransferase activity | 4 | 1 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 147 | 149 | PF00675 | 0.563 |
CLV_NRD_NRD_1 | 433 | 435 | PF00675 | 0.649 |
CLV_NRD_NRD_1 | 458 | 460 | PF00675 | 0.637 |
CLV_NRD_NRD_1 | 546 | 548 | PF00675 | 0.640 |
CLV_NRD_NRD_1 | 764 | 766 | PF00675 | 0.574 |
CLV_NRD_NRD_1 | 8 | 10 | PF00675 | 0.535 |
CLV_PCSK_KEX2_1 | 147 | 149 | PF00082 | 0.563 |
CLV_PCSK_KEX2_1 | 433 | 435 | PF00082 | 0.649 |
CLV_PCSK_KEX2_1 | 546 | 548 | PF00082 | 0.635 |
CLV_PCSK_KEX2_1 | 602 | 604 | PF00082 | 0.594 |
CLV_PCSK_KEX2_1 | 749 | 751 | PF00082 | 0.710 |
CLV_PCSK_KEX2_1 | 763 | 765 | PF00082 | 0.508 |
CLV_PCSK_KEX2_1 | 8 | 10 | PF00082 | 0.535 |
CLV_PCSK_PC1ET2_1 | 602 | 604 | PF00082 | 0.583 |
CLV_PCSK_PC1ET2_1 | 749 | 751 | PF00082 | 0.613 |
CLV_PCSK_PC7_1 | 429 | 435 | PF00082 | 0.548 |
CLV_PCSK_SKI1_1 | 174 | 178 | PF00082 | 0.559 |
CLV_PCSK_SKI1_1 | 194 | 198 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 235 | 239 | PF00082 | 0.466 |
CLV_PCSK_SKI1_1 | 277 | 281 | PF00082 | 0.413 |
CLV_PCSK_SKI1_1 | 334 | 338 | PF00082 | 0.573 |
CLV_PCSK_SKI1_1 | 502 | 506 | PF00082 | 0.547 |
CLV_PCSK_SKI1_1 | 624 | 628 | PF00082 | 0.320 |
CLV_PCSK_SKI1_1 | 703 | 707 | PF00082 | 0.439 |
CLV_PCSK_SKI1_1 | 710 | 714 | PF00082 | 0.408 |
CLV_PCSK_SKI1_1 | 793 | 797 | PF00082 | 0.495 |
CLV_PCSK_SKI1_1 | 8 | 12 | PF00082 | 0.536 |
CLV_PCSK_SKI1_1 | 827 | 831 | PF00082 | 0.481 |
DEG_APCC_DBOX_1 | 173 | 181 | PF00400 | 0.536 |
DEG_APCC_DBOX_1 | 193 | 201 | PF00400 | 0.326 |
DEG_APCC_DBOX_1 | 333 | 341 | PF00400 | 0.548 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.597 |
DEG_SCF_FBW7_2 | 129 | 135 | PF00400 | 0.578 |
DEG_SPOP_SBC_1 | 345 | 349 | PF00917 | 0.515 |
DEG_SPOP_SBC_1 | 57 | 61 | PF00917 | 0.596 |
DOC_CDC14_PxL_1 | 205 | 213 | PF14671 | 0.452 |
DOC_CDC14_PxL_1 | 560 | 568 | PF14671 | 0.615 |
DOC_CKS1_1 | 129 | 134 | PF01111 | 0.577 |
DOC_CKS1_1 | 51 | 56 | PF01111 | 0.557 |
DOC_CYCLIN_RxL_1 | 700 | 708 | PF00134 | 0.418 |
DOC_CYCLIN_RxL_1 | 824 | 832 | PF00134 | 0.473 |
DOC_MAPK_gen_1 | 235 | 243 | PF00069 | 0.480 |
DOC_MAPK_gen_1 | 332 | 340 | PF00069 | 0.502 |
DOC_MAPK_MEF2A_6 | 194 | 202 | PF00069 | 0.487 |
DOC_MAPK_MEF2A_6 | 332 | 340 | PF00069 | 0.493 |
DOC_MAPK_MEF2A_6 | 785 | 794 | PF00069 | 0.417 |
DOC_PP2B_LxvP_1 | 165 | 168 | PF13499 | 0.500 |
DOC_USP7_MATH_1 | 103 | 107 | PF00917 | 0.460 |
DOC_USP7_MATH_1 | 17 | 21 | PF00917 | 0.572 |
DOC_USP7_MATH_1 | 207 | 211 | PF00917 | 0.635 |
DOC_USP7_MATH_1 | 245 | 249 | PF00917 | 0.575 |
DOC_USP7_MATH_1 | 264 | 268 | PF00917 | 0.314 |
DOC_USP7_MATH_1 | 30 | 34 | PF00917 | 0.459 |
DOC_USP7_MATH_1 | 345 | 349 | PF00917 | 0.532 |
DOC_USP7_MATH_1 | 365 | 369 | PF00917 | 0.699 |
DOC_USP7_MATH_1 | 46 | 50 | PF00917 | 0.462 |
DOC_USP7_MATH_1 | 506 | 510 | PF00917 | 0.598 |
DOC_USP7_MATH_1 | 612 | 616 | PF00917 | 0.500 |
DOC_USP7_MATH_1 | 737 | 741 | PF00917 | 0.585 |
DOC_USP7_MATH_1 | 745 | 749 | PF00917 | 0.518 |
DOC_USP7_MATH_1 | 968 | 972 | PF00917 | 0.389 |
DOC_WW_Pin1_4 | 128 | 133 | PF00397 | 0.657 |
DOC_WW_Pin1_4 | 15 | 20 | PF00397 | 0.594 |
DOC_WW_Pin1_4 | 341 | 346 | PF00397 | 0.480 |
DOC_WW_Pin1_4 | 422 | 427 | PF00397 | 0.744 |
DOC_WW_Pin1_4 | 50 | 55 | PF00397 | 0.586 |
DOC_WW_Pin1_4 | 530 | 535 | PF00397 | 0.644 |
DOC_WW_Pin1_4 | 645 | 650 | PF00397 | 0.520 |
LIG_14-3-3_CanoR_1 | 148 | 156 | PF00244 | 0.544 |
LIG_14-3-3_CanoR_1 | 160 | 165 | PF00244 | 0.506 |
LIG_14-3-3_CanoR_1 | 174 | 183 | PF00244 | 0.448 |
LIG_14-3-3_CanoR_1 | 277 | 285 | PF00244 | 0.559 |
LIG_14-3-3_CanoR_1 | 314 | 324 | PF00244 | 0.575 |
LIG_14-3-3_CanoR_1 | 332 | 337 | PF00244 | 0.574 |
LIG_14-3-3_CanoR_1 | 42 | 51 | PF00244 | 0.508 |
LIG_14-3-3_CanoR_1 | 433 | 443 | PF00244 | 0.646 |
LIG_14-3-3_CanoR_1 | 546 | 552 | PF00244 | 0.558 |
LIG_14-3-3_CanoR_1 | 750 | 754 | PF00244 | 0.584 |
LIG_14-3-3_CanoR_1 | 763 | 772 | PF00244 | 0.502 |
LIG_14-3-3_CanoR_1 | 776 | 783 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 8 | 13 | PF00244 | 0.567 |
LIG_14-3-3_CanoR_1 | 975 | 979 | PF00244 | 0.447 |
LIG_Actin_WH2_2 | 474 | 492 | PF00022 | 0.545 |
LIG_APCC_ABBA_1 | 130 | 135 | PF00400 | 0.636 |
LIG_APCC_ABBA_1 | 260 | 265 | PF00400 | 0.479 |
LIG_APCC_ABBA_1 | 355 | 360 | PF00400 | 0.425 |
LIG_BIR_III_2 | 461 | 465 | PF00653 | 0.560 |
LIG_BIR_III_4 | 217 | 221 | PF00653 | 0.622 |
LIG_Clathr_ClatBox_1 | 818 | 822 | PF01394 | 0.363 |
LIG_EH1_1 | 330 | 338 | PF00400 | 0.429 |
LIG_EVH1_1 | 165 | 169 | PF00568 | 0.554 |
LIG_FHA_1 | 151 | 157 | PF00498 | 0.601 |
LIG_FHA_1 | 176 | 182 | PF00498 | 0.552 |
LIG_FHA_1 | 333 | 339 | PF00498 | 0.682 |
LIG_FHA_1 | 409 | 415 | PF00498 | 0.609 |
LIG_FHA_1 | 439 | 445 | PF00498 | 0.630 |
LIG_FHA_1 | 58 | 64 | PF00498 | 0.601 |
LIG_FHA_1 | 682 | 688 | PF00498 | 0.439 |
LIG_FHA_1 | 737 | 743 | PF00498 | 0.548 |
LIG_FHA_1 | 764 | 770 | PF00498 | 0.520 |
LIG_FHA_1 | 830 | 836 | PF00498 | 0.382 |
LIG_FHA_2 | 231 | 237 | PF00498 | 0.495 |
LIG_FHA_2 | 377 | 383 | PF00498 | 0.430 |
LIG_FHA_2 | 866 | 872 | PF00498 | 0.445 |
LIG_FHA_2 | 984 | 990 | PF00498 | 0.453 |
LIG_Integrin_RGD_1 | 603 | 605 | PF01839 | 0.592 |
LIG_LIR_Gen_1 | 832 | 841 | PF02991 | 0.430 |
LIG_LIR_Gen_1 | 947 | 957 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 143 | 149 | PF02991 | 0.594 |
LIG_LIR_Nem_3 | 231 | 237 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 832 | 837 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 947 | 952 | PF02991 | 0.368 |
LIG_LYPXL_SIV_4 | 845 | 853 | PF13949 | 0.399 |
LIG_NRBOX | 336 | 342 | PF00104 | 0.550 |
LIG_NRBOX | 36 | 42 | PF00104 | 0.512 |
LIG_NRBOX | 477 | 483 | PF00104 | 0.584 |
LIG_PCNA_yPIPBox_3 | 784 | 796 | PF02747 | 0.428 |
LIG_PDZ_Class_3 | 999 | 1004 | PF00595 | 0.467 |
LIG_PTAP_UEV_1 | 117 | 122 | PF05743 | 0.568 |
LIG_Rb_LxCxE_1 | 989 | 1004 | PF01857 | 0.508 |
LIG_SH2_CRK | 846 | 850 | PF00017 | 0.379 |
LIG_SH2_NCK_1 | 263 | 267 | PF00017 | 0.470 |
LIG_SH2_NCK_1 | 846 | 850 | PF00017 | 0.379 |
LIG_SH2_PTP2 | 949 | 952 | PF00017 | 0.381 |
LIG_SH2_SRC | 263 | 266 | PF00017 | 0.473 |
LIG_SH2_SRC | 354 | 357 | PF00017 | 0.476 |
LIG_SH2_SRC | 680 | 683 | PF00017 | 0.435 |
LIG_SH2_STAP1 | 846 | 850 | PF00017 | 0.379 |
LIG_SH2_STAP1 | 976 | 980 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 354 | 357 | PF00017 | 0.520 |
LIG_SH2_STAT5 | 680 | 683 | PF00017 | 0.435 |
LIG_SH2_STAT5 | 889 | 892 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 949 | 952 | PF00017 | 0.384 |
LIG_SH3_1 | 115 | 121 | PF00018 | 0.536 |
LIG_SH3_1 | 52 | 58 | PF00018 | 0.558 |
LIG_SH3_3 | 115 | 121 | PF00018 | 0.491 |
LIG_SH3_3 | 123 | 129 | PF00018 | 0.636 |
LIG_SH3_3 | 13 | 19 | PF00018 | 0.606 |
LIG_SH3_3 | 163 | 169 | PF00018 | 0.553 |
LIG_SH3_3 | 206 | 212 | PF00018 | 0.450 |
LIG_SH3_3 | 26 | 32 | PF00018 | 0.489 |
LIG_SH3_3 | 51 | 57 | PF00018 | 0.591 |
LIG_SH3_3 | 558 | 564 | PF00018 | 0.640 |
LIG_SH3_3 | 929 | 935 | PF00018 | 0.367 |
LIG_SH3_3 | 99 | 105 | PF00018 | 0.418 |
LIG_SUMO_SIM_anti_2 | 109 | 115 | PF11976 | 0.453 |
LIG_SUMO_SIM_anti_2 | 272 | 278 | PF11976 | 0.587 |
LIG_SUMO_SIM_par_1 | 152 | 158 | PF11976 | 0.597 |
LIG_SUMO_SIM_par_1 | 178 | 184 | PF11976 | 0.541 |
LIG_SUMO_SIM_par_1 | 373 | 379 | PF11976 | 0.452 |
LIG_SUMO_SIM_par_1 | 641 | 646 | PF11976 | 0.520 |
LIG_SUMO_SIM_par_1 | 663 | 669 | PF11976 | 0.431 |
LIG_SUMO_SIM_par_1 | 817 | 822 | PF11976 | 0.367 |
LIG_SxIP_EBH_1 | 238 | 247 | PF03271 | 0.454 |
LIG_TRAF2_1 | 141 | 144 | PF00917 | 0.595 |
LIG_TRAF2_1 | 672 | 675 | PF00917 | 0.471 |
LIG_TRAF2_1 | 868 | 871 | PF00917 | 0.380 |
LIG_TRFH_1 | 353 | 357 | PF08558 | 0.472 |
LIG_WRC_WIRS_1 | 969 | 974 | PF05994 | 0.381 |
LIG_WW_2 | 29 | 32 | PF00397 | 0.558 |
LIG_WW_3 | 580 | 584 | PF00397 | 0.653 |
MOD_CDK_SPxxK_3 | 422 | 429 | PF00069 | 0.745 |
MOD_CK1_1 | 175 | 181 | PF00069 | 0.505 |
MOD_CK1_1 | 322 | 328 | PF00069 | 0.549 |
MOD_CK1_1 | 344 | 350 | PF00069 | 0.538 |
MOD_CK1_1 | 408 | 414 | PF00069 | 0.604 |
MOD_CK1_1 | 438 | 444 | PF00069 | 0.564 |
MOD_CK1_1 | 519 | 525 | PF00069 | 0.641 |
MOD_CK1_1 | 559 | 565 | PF00069 | 0.571 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.602 |
MOD_CK1_1 | 748 | 754 | PF00069 | 0.512 |
MOD_CK1_1 | 81 | 87 | PF00069 | 0.407 |
MOD_CK1_1 | 855 | 861 | PF00069 | 0.389 |
MOD_CK2_1 | 376 | 382 | PF00069 | 0.420 |
MOD_CK2_1 | 669 | 675 | PF00069 | 0.479 |
MOD_CK2_1 | 687 | 693 | PF00069 | 0.338 |
MOD_CK2_1 | 864 | 870 | PF00069 | 0.562 |
MOD_CK2_1 | 983 | 989 | PF00069 | 0.381 |
MOD_CK2_1 | 992 | 998 | PF00069 | 0.423 |
MOD_GlcNHglycan | 118 | 121 | PF01048 | 0.627 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.619 |
MOD_GlcNHglycan | 19 | 22 | PF01048 | 0.619 |
MOD_GlcNHglycan | 256 | 259 | PF01048 | 0.397 |
MOD_GlcNHglycan | 33 | 36 | PF01048 | 0.435 |
MOD_GlcNHglycan | 411 | 414 | PF01048 | 0.641 |
MOD_GlcNHglycan | 437 | 440 | PF01048 | 0.691 |
MOD_GlcNHglycan | 44 | 47 | PF01048 | 0.600 |
MOD_GlcNHglycan | 471 | 475 | PF01048 | 0.527 |
MOD_GlcNHglycan | 48 | 51 | PF01048 | 0.495 |
MOD_GlcNHglycan | 490 | 493 | PF01048 | 0.412 |
MOD_GlcNHglycan | 508 | 511 | PF01048 | 0.533 |
MOD_GlcNHglycan | 616 | 619 | PF01048 | 0.356 |
MOD_GlcNHglycan | 654 | 657 | PF01048 | 0.292 |
MOD_GlcNHglycan | 671 | 674 | PF01048 | 0.341 |
MOD_GlcNHglycan | 777 | 780 | PF01048 | 0.528 |
MOD_GlcNHglycan | 857 | 860 | PF01048 | 0.380 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.592 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.492 |
MOD_GSK3_1 | 245 | 252 | PF00069 | 0.649 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.452 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.539 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.513 |
MOD_GSK3_1 | 341 | 348 | PF00069 | 0.529 |
MOD_GSK3_1 | 359 | 366 | PF00069 | 0.437 |
MOD_GSK3_1 | 391 | 398 | PF00069 | 0.485 |
MOD_GSK3_1 | 405 | 412 | PF00069 | 0.553 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.480 |
MOD_GSK3_1 | 434 | 441 | PF00069 | 0.619 |
MOD_GSK3_1 | 530 | 537 | PF00069 | 0.772 |
MOD_GSK3_1 | 681 | 688 | PF00069 | 0.437 |
MOD_GSK3_1 | 745 | 752 | PF00069 | 0.625 |
MOD_GSK3_1 | 770 | 777 | PF00069 | 0.672 |
MOD_GSK3_1 | 825 | 832 | PF00069 | 0.471 |
MOD_N-GLC_1 | 537 | 542 | PF02516 | 0.631 |
MOD_NEK2_1 | 149 | 154 | PF00069 | 0.569 |
MOD_NEK2_1 | 172 | 177 | PF00069 | 0.611 |
MOD_NEK2_1 | 230 | 235 | PF00069 | 0.506 |
MOD_NEK2_1 | 243 | 248 | PF00069 | 0.520 |
MOD_NEK2_1 | 275 | 280 | PF00069 | 0.562 |
MOD_NEK2_1 | 346 | 351 | PF00069 | 0.728 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.472 |
MOD_NEK2_1 | 488 | 493 | PF00069 | 0.483 |
MOD_NEK2_1 | 516 | 521 | PF00069 | 0.680 |
MOD_NEK2_1 | 687 | 692 | PF00069 | 0.442 |
MOD_NEK2_1 | 694 | 699 | PF00069 | 0.434 |
MOD_NEK2_1 | 705 | 710 | PF00069 | 0.428 |
MOD_NEK2_1 | 844 | 849 | PF00069 | 0.425 |
MOD_NEK2_1 | 853 | 858 | PF00069 | 0.353 |
MOD_NEK2_1 | 864 | 869 | PF00069 | 0.231 |
MOD_NEK2_1 | 890 | 895 | PF00069 | 0.389 |
MOD_NEK2_2 | 245 | 250 | PF00069 | 0.429 |
MOD_OFUCOSY | 760 | 767 | PF10250 | 0.541 |
MOD_PIKK_1 | 687 | 693 | PF00454 | 0.444 |
MOD_PIKK_1 | 705 | 711 | PF00454 | 0.427 |
MOD_PKA_1 | 749 | 755 | PF00069 | 0.600 |
MOD_PKA_1 | 763 | 769 | PF00069 | 0.516 |
MOD_PKA_1 | 8 | 14 | PF00069 | 0.535 |
MOD_PKA_2 | 159 | 165 | PF00069 | 0.628 |
MOD_PKA_2 | 313 | 319 | PF00069 | 0.478 |
MOD_PKA_2 | 749 | 755 | PF00069 | 0.600 |
MOD_PKA_2 | 763 | 769 | PF00069 | 0.516 |
MOD_PKA_2 | 775 | 781 | PF00069 | 0.395 |
MOD_PKA_2 | 8 | 14 | PF00069 | 0.580 |
MOD_PKA_2 | 974 | 980 | PF00069 | 0.445 |
MOD_Plk_1 | 142 | 148 | PF00069 | 0.616 |
MOD_Plk_1 | 222 | 228 | PF00069 | 0.527 |
MOD_Plk_1 | 264 | 270 | PF00069 | 0.475 |
MOD_Plk_1 | 325 | 331 | PF00069 | 0.496 |
MOD_Plk_1 | 359 | 365 | PF00069 | 0.523 |
MOD_Plk_1 | 619 | 625 | PF00069 | 0.328 |
MOD_Plk_1 | 674 | 680 | PF00069 | 0.307 |
MOD_Plk_1 | 81 | 87 | PF00069 | 0.381 |
MOD_Plk_2-3 | 186 | 192 | PF00069 | 0.500 |
MOD_Plk_4 | 160 | 166 | PF00069 | 0.548 |
MOD_Plk_4 | 19 | 25 | PF00069 | 0.491 |
MOD_Plk_4 | 36 | 42 | PF00069 | 0.495 |
MOD_Plk_4 | 477 | 483 | PF00069 | 0.595 |
MOD_Plk_4 | 59 | 65 | PF00069 | 0.571 |
MOD_Plk_4 | 660 | 666 | PF00069 | 0.307 |
MOD_Plk_4 | 676 | 682 | PF00069 | 0.307 |
MOD_Plk_4 | 737 | 743 | PF00069 | 0.560 |
MOD_Plk_4 | 749 | 755 | PF00069 | 0.580 |
MOD_Plk_4 | 81 | 87 | PF00069 | 0.415 |
MOD_Plk_4 | 968 | 974 | PF00069 | 0.439 |
MOD_ProDKin_1 | 128 | 134 | PF00069 | 0.656 |
MOD_ProDKin_1 | 15 | 21 | PF00069 | 0.597 |
MOD_ProDKin_1 | 341 | 347 | PF00069 | 0.487 |
MOD_ProDKin_1 | 422 | 428 | PF00069 | 0.745 |
MOD_ProDKin_1 | 50 | 56 | PF00069 | 0.587 |
MOD_ProDKin_1 | 530 | 536 | PF00069 | 0.643 |
MOD_ProDKin_1 | 645 | 651 | PF00069 | 0.375 |
MOD_SUMO_for_1 | 795 | 798 | PF00179 | 0.574 |
MOD_SUMO_rev_2 | 231 | 239 | PF00179 | 0.485 |
MOD_SUMO_rev_2 | 527 | 534 | PF00179 | 0.547 |
TRG_DiLeu_BaEn_1 | 721 | 726 | PF01217 | 0.467 |
TRG_DiLeu_BaEn_1 | 871 | 876 | PF01217 | 0.409 |
TRG_DiLeu_BaEn_1 | 922 | 927 | PF01217 | 0.427 |
TRG_DiLeu_BaEn_1 | 965 | 970 | PF01217 | 0.431 |
TRG_DiLeu_BaEn_1 | 989 | 994 | PF01217 | 0.401 |
TRG_DiLeu_BaLyEn_6 | 39 | 44 | PF01217 | 0.509 |
TRG_DiLeu_BaLyEn_6 | 878 | 883 | PF01217 | 0.411 |
TRG_ENDOCYTIC_2 | 846 | 849 | PF00928 | 0.383 |
TRG_ENDOCYTIC_2 | 889 | 892 | PF00928 | 0.409 |
TRG_ENDOCYTIC_2 | 949 | 952 | PF00928 | 0.381 |
TRG_ER_diArg_1 | 146 | 148 | PF00400 | 0.567 |
TRG_ER_diArg_1 | 432 | 434 | PF00400 | 0.632 |
TRG_ER_diArg_1 | 545 | 547 | PF00400 | 0.636 |
TRG_ER_diArg_1 | 763 | 765 | PF00400 | 0.559 |
TRG_ER_diArg_1 | 835 | 838 | PF00400 | 0.338 |
TRG_Pf-PMV_PEXEL_1 | 692 | 696 | PF00026 | 0.386 |
TRG_Pf-PMV_PEXEL_1 | 785 | 789 | PF00026 | 0.420 |
TRG_Pf-PMV_PEXEL_1 | 816 | 820 | PF00026 | 0.379 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEX7 | Leptomonas seymouri | 38% | 100% |
A0A3S7X6B7 | Leishmania donovani | 99% | 100% |
A4HL86 | Leishmania braziliensis | 69% | 100% |
E9B3M9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
Q4Q4F8 | Leishmania major | 89% | 100% |