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: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: E9B3M9
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_C14_Caspase3-7 | 19 | 23 | PF00656 | 0.537 |
CLV_NRD_NRD_1 | 343 | 345 | PF00675 | 0.641 |
CLV_NRD_NRD_1 | 431 | 433 | PF00675 | 0.649 |
CLV_NRD_NRD_1 | 649 | 651 | PF00675 | 0.612 |
CLV_NRD_NRD_1 | 823 | 825 | PF00675 | 0.433 |
CLV_PCSK_KEX2_1 | 431 | 433 | PF00082 | 0.649 |
CLV_PCSK_KEX2_1 | 487 | 489 | PF00082 | 0.362 |
CLV_PCSK_KEX2_1 | 634 | 636 | PF00082 | 0.604 |
CLV_PCSK_KEX2_1 | 648 | 650 | PF00082 | 0.485 |
CLV_PCSK_KEX2_1 | 823 | 825 | PF00082 | 0.433 |
CLV_PCSK_PC1ET2_1 | 487 | 489 | PF00082 | 0.349 |
CLV_PCSK_PC1ET2_1 | 634 | 636 | PF00082 | 0.589 |
CLV_PCSK_SKI1_1 | 141 | 145 | PF00082 | 0.632 |
CLV_PCSK_SKI1_1 | 161 | 165 | PF00082 | 0.480 |
CLV_PCSK_SKI1_1 | 188 | 192 | PF00082 | 0.478 |
CLV_PCSK_SKI1_1 | 218 | 222 | PF00082 | 0.597 |
CLV_PCSK_SKI1_1 | 405 | 409 | PF00082 | 0.540 |
CLV_PCSK_SKI1_1 | 431 | 435 | PF00082 | 0.507 |
CLV_PCSK_SKI1_1 | 509 | 513 | PF00082 | 0.351 |
CLV_PCSK_SKI1_1 | 58 | 62 | PF00082 | 0.627 |
CLV_PCSK_SKI1_1 | 595 | 599 | PF00082 | 0.486 |
CLV_PCSK_SKI1_1 | 634 | 638 | PF00082 | 0.495 |
CLV_PCSK_SKI1_1 | 678 | 682 | PF00082 | 0.510 |
CLV_PCSK_SKI1_1 | 712 | 716 | PF00082 | 0.491 |
DEG_APCC_DBOX_1 | 217 | 225 | PF00400 | 0.586 |
DEG_APCC_DBOX_1 | 57 | 65 | PF00400 | 0.602 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.526 |
DEG_SCF_FBW7_1 | 157 | 162 | PF00400 | 0.404 |
DOC_CDC14_PxL_1 | 445 | 453 | PF14671 | 0.674 |
DOC_CYCLIN_RxL_1 | 709 | 717 | PF00134 | 0.488 |
DOC_MAPK_gen_1 | 216 | 224 | PF00069 | 0.581 |
DOC_MAPK_MEF2A_6 | 216 | 224 | PF00069 | 0.581 |
DOC_PP1_RVXF_1 | 430 | 437 | PF00149 | 0.561 |
DOC_PP2B_LxvP_1 | 49 | 52 | PF13499 | 0.635 |
DOC_PP4_FxxP_1 | 390 | 393 | PF00568 | 0.479 |
DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.520 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.665 |
DOC_USP7_MATH_1 | 148 | 152 | PF00917 | 0.379 |
DOC_USP7_MATH_1 | 250 | 254 | PF00917 | 0.664 |
DOC_USP7_MATH_1 | 391 | 395 | PF00917 | 0.657 |
DOC_USP7_MATH_1 | 467 | 471 | PF00917 | 0.519 |
DOC_USP7_MATH_1 | 497 | 501 | PF00917 | 0.547 |
DOC_USP7_MATH_1 | 537 | 541 | PF00917 | 0.424 |
DOC_USP7_MATH_1 | 554 | 558 | PF00917 | 0.447 |
DOC_USP7_MATH_1 | 853 | 857 | PF00917 | 0.408 |
DOC_USP7_MATH_1 | 91 | 95 | PF00917 | 0.632 |
DOC_USP7_UBL2_3 | 483 | 487 | PF12436 | 0.531 |
DOC_WW_Pin1_4 | 12 | 17 | PF00397 | 0.668 |
DOC_WW_Pin1_4 | 127 | 132 | PF00397 | 0.595 |
DOC_WW_Pin1_4 | 155 | 160 | PF00397 | 0.399 |
DOC_WW_Pin1_4 | 307 | 312 | PF00397 | 0.645 |
DOC_WW_Pin1_4 | 415 | 420 | PF00397 | 0.665 |
DOC_WW_Pin1_4 | 530 | 535 | PF00397 | 0.551 |
LIG_14-3-3_CanoR_1 | 161 | 169 | PF00244 | 0.633 |
LIG_14-3-3_CanoR_1 | 198 | 208 | PF00244 | 0.726 |
LIG_14-3-3_CanoR_1 | 216 | 221 | PF00244 | 0.575 |
LIG_14-3-3_CanoR_1 | 44 | 49 | PF00244 | 0.648 |
LIG_14-3-3_CanoR_1 | 635 | 639 | PF00244 | 0.549 |
LIG_14-3-3_CanoR_1 | 648 | 657 | PF00244 | 0.469 |
LIG_14-3-3_CanoR_1 | 661 | 668 | PF00244 | 0.450 |
LIG_14-3-3_CanoR_1 | 860 | 864 | PF00244 | 0.474 |
LIG_Actin_WH2_2 | 359 | 377 | PF00022 | 0.668 |
LIG_APCC_ABBA_1 | 144 | 149 | PF00400 | 0.584 |
LIG_APCC_ABBA_1 | 240 | 245 | PF00400 | 0.446 |
LIG_BIR_III_2 | 388 | 392 | PF00653 | 0.485 |
LIG_BIR_III_4 | 99 | 103 | PF00653 | 0.636 |
LIG_Clathr_ClatBox_1 | 703 | 707 | PF01394 | 0.458 |
LIG_EVH1_1 | 49 | 53 | PF00568 | 0.693 |
LIG_FHA_1 | 176 | 182 | PF00498 | 0.443 |
LIG_FHA_1 | 202 | 208 | PF00498 | 0.448 |
LIG_FHA_1 | 217 | 223 | PF00498 | 0.589 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.669 |
LIG_FHA_1 | 567 | 573 | PF00498 | 0.535 |
LIG_FHA_1 | 618 | 624 | PF00498 | 0.523 |
LIG_FHA_1 | 649 | 655 | PF00498 | 0.496 |
LIG_FHA_1 | 715 | 721 | PF00498 | 0.470 |
LIG_FHA_1 | 849 | 855 | PF00498 | 0.306 |
LIG_FHA_2 | 262 | 268 | PF00498 | 0.458 |
LIG_FHA_2 | 277 | 283 | PF00498 | 0.422 |
LIG_FHA_2 | 689 | 695 | PF00498 | 0.398 |
LIG_FHA_2 | 69 | 75 | PF00498 | 0.465 |
LIG_FHA_2 | 751 | 757 | PF00498 | 0.472 |
LIG_FHA_2 | 869 | 875 | PF00498 | 0.474 |
LIG_Integrin_RGD_1 | 488 | 490 | PF01839 | 0.316 |
LIG_LIR_Apic_2 | 388 | 393 | PF02991 | 0.483 |
LIG_LIR_Gen_1 | 116 | 126 | PF02991 | 0.423 |
LIG_LIR_Gen_1 | 717 | 726 | PF02991 | 0.455 |
LIG_LIR_Gen_1 | 832 | 842 | PF02991 | 0.507 |
LIG_LIR_Nem_3 | 11 | 17 | PF02991 | 0.608 |
LIG_LIR_Nem_3 | 116 | 121 | PF02991 | 0.593 |
LIG_LIR_Nem_3 | 27 | 33 | PF02991 | 0.628 |
LIG_LIR_Nem_3 | 717 | 722 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 832 | 837 | PF02991 | 0.475 |
LIG_LYPXL_SIV_4 | 730 | 738 | PF13949 | 0.490 |
LIG_NRBOX | 220 | 226 | PF00104 | 0.593 |
LIG_NRBOX | 362 | 368 | PF00104 | 0.644 |
LIG_PDZ_Class_3 | 884 | 889 | PF00595 | 0.520 |
LIG_Pex14_1 | 30 | 34 | PF04695 | 0.548 |
LIG_PTAP_UEV_1 | 445 | 450 | PF05743 | 0.606 |
LIG_Rb_LxCxE_1 | 874 | 889 | PF01857 | 0.527 |
LIG_SH2_CRK | 731 | 735 | PF00017 | 0.477 |
LIG_SH2_NCK_1 | 147 | 151 | PF00017 | 0.570 |
LIG_SH2_NCK_1 | 731 | 735 | PF00017 | 0.477 |
LIG_SH2_PTP2 | 834 | 837 | PF00017 | 0.489 |
LIG_SH2_SRC | 147 | 150 | PF00017 | 0.571 |
LIG_SH2_SRC | 239 | 242 | PF00017 | 0.455 |
LIG_SH2_SRC | 565 | 568 | PF00017 | 0.534 |
LIG_SH2_STAP1 | 731 | 735 | PF00017 | 0.477 |
LIG_SH2_STAP1 | 861 | 865 | PF00017 | 0.464 |
LIG_SH2_STAT5 | 239 | 242 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 34 | 37 | PF00017 | 0.535 |
LIG_SH2_STAT5 | 565 | 568 | PF00017 | 0.534 |
LIG_SH2_STAT5 | 774 | 777 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 834 | 837 | PF00017 | 0.489 |
LIG_SH3_2 | 534 | 539 | PF14604 | 0.417 |
LIG_SH3_3 | 4 | 10 | PF00018 | 0.636 |
LIG_SH3_3 | 443 | 449 | PF00018 | 0.682 |
LIG_SH3_3 | 47 | 53 | PF00018 | 0.694 |
LIG_SH3_3 | 531 | 537 | PF00018 | 0.417 |
LIG_SH3_3 | 611 | 617 | PF00018 | 0.393 |
LIG_SH3_3 | 814 | 820 | PF00018 | 0.454 |
LIG_SUMO_SIM_par_1 | 258 | 264 | PF11976 | 0.422 |
LIG_SUMO_SIM_par_1 | 36 | 42 | PF11976 | 0.668 |
LIG_SUMO_SIM_par_1 | 526 | 531 | PF11976 | 0.551 |
LIG_SUMO_SIM_par_1 | 63 | 68 | PF11976 | 0.594 |
LIG_SUMO_SIM_par_1 | 702 | 707 | PF11976 | 0.461 |
LIG_TRAF2_1 | 557 | 560 | PF00917 | 0.551 |
LIG_TRAF2_1 | 753 | 756 | PF00917 | 0.477 |
LIG_TRFH_1 | 238 | 242 | PF08558 | 0.453 |
LIG_WRC_WIRS_1 | 511 | 516 | PF05994 | 0.224 |
LIG_WRC_WIRS_1 | 854 | 859 | PF05994 | 0.478 |
LIG_WW_3 | 465 | 469 | PF00397 | 0.707 |
MOD_CDK_SPxK_1 | 155 | 161 | PF00069 | 0.401 |
MOD_CDK_SPxxK_3 | 307 | 314 | PF00069 | 0.644 |
MOD_CK1_1 | 206 | 212 | PF00069 | 0.574 |
MOD_CK1_1 | 228 | 234 | PF00069 | 0.633 |
MOD_CK1_1 | 444 | 450 | PF00069 | 0.595 |
MOD_CK1_1 | 740 | 746 | PF00069 | 0.482 |
MOD_CK2_1 | 261 | 267 | PF00069 | 0.442 |
MOD_CK2_1 | 554 | 560 | PF00069 | 0.412 |
MOD_CK2_1 | 572 | 578 | PF00069 | 0.338 |
MOD_CK2_1 | 679 | 685 | PF00069 | 0.396 |
MOD_CK2_1 | 749 | 755 | PF00069 | 0.459 |
MOD_CK2_1 | 868 | 874 | PF00069 | 0.469 |
MOD_CK2_1 | 877 | 883 | PF00069 | 0.414 |
MOD_GlcNHglycan | 107 | 111 | PF01048 | 0.489 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.573 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.660 |
MOD_GlcNHglycan | 296 | 299 | PF01048 | 0.654 |
MOD_GlcNHglycan | 346 | 349 | PF01048 | 0.651 |
MOD_GlcNHglycan | 356 | 360 | PF01048 | 0.581 |
MOD_GlcNHglycan | 375 | 378 | PF01048 | 0.441 |
MOD_GlcNHglycan | 393 | 396 | PF01048 | 0.534 |
MOD_GlcNHglycan | 446 | 449 | PF01048 | 0.667 |
MOD_GlcNHglycan | 501 | 504 | PF01048 | 0.392 |
MOD_GlcNHglycan | 556 | 559 | PF01048 | 0.295 |
MOD_GlcNHglycan | 604 | 607 | PF01048 | 0.347 |
MOD_GlcNHglycan | 662 | 665 | PF01048 | 0.538 |
MOD_GlcNHglycan | 742 | 745 | PF01048 | 0.475 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.670 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.527 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.602 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.613 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.418 |
MOD_GSK3_1 | 276 | 283 | PF00069 | 0.501 |
MOD_GSK3_1 | 290 | 297 | PF00069 | 0.574 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.598 |
MOD_GSK3_1 | 415 | 422 | PF00069 | 0.699 |
MOD_GSK3_1 | 499 | 506 | PF00069 | 0.325 |
MOD_GSK3_1 | 566 | 573 | PF00069 | 0.531 |
MOD_GSK3_1 | 617 | 624 | PF00069 | 0.529 |
MOD_GSK3_1 | 655 | 662 | PF00069 | 0.559 |
MOD_GSK3_1 | 710 | 717 | PF00069 | 0.485 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.597 |
MOD_N-GLC_1 | 422 | 427 | PF02516 | 0.661 |
MOD_N-GLC_1 | 503 | 508 | PF02516 | 0.224 |
MOD_NEK2_1 | 224 | 229 | PF00069 | 0.648 |
MOD_NEK2_1 | 33 | 38 | PF00069 | 0.626 |
MOD_NEK2_1 | 373 | 378 | PF00069 | 0.557 |
MOD_NEK2_1 | 572 | 577 | PF00069 | 0.530 |
MOD_NEK2_1 | 579 | 584 | PF00069 | 0.428 |
MOD_NEK2_1 | 729 | 734 | PF00069 | 0.473 |
MOD_NEK2_1 | 738 | 743 | PF00069 | 0.384 |
MOD_NEK2_1 | 749 | 754 | PF00069 | 0.238 |
MOD_NEK2_1 | 775 | 780 | PF00069 | 0.442 |
MOD_NEK2_2 | 261 | 266 | PF00069 | 0.300 |
MOD_OFUCOSY | 645 | 652 | PF10250 | 0.516 |
MOD_PIKK_1 | 572 | 578 | PF00454 | 0.529 |
MOD_PIKK_1 | 590 | 596 | PF00454 | 0.318 |
MOD_PKA_1 | 344 | 350 | PF00069 | 0.595 |
MOD_PKA_1 | 634 | 640 | PF00069 | 0.572 |
MOD_PKA_1 | 648 | 654 | PF00069 | 0.484 |
MOD_PKA_2 | 197 | 203 | PF00069 | 0.575 |
MOD_PKA_2 | 43 | 49 | PF00069 | 0.692 |
MOD_PKA_2 | 467 | 473 | PF00069 | 0.520 |
MOD_PKA_2 | 634 | 640 | PF00069 | 0.572 |
MOD_PKA_2 | 648 | 654 | PF00069 | 0.484 |
MOD_PKA_2 | 660 | 666 | PF00069 | 0.439 |
MOD_PKA_2 | 859 | 865 | PF00069 | 0.474 |
MOD_PKB_1 | 342 | 350 | PF00069 | 0.512 |
MOD_Plk_1 | 106 | 112 | PF00069 | 0.556 |
MOD_Plk_1 | 148 | 154 | PF00069 | 0.574 |
MOD_Plk_1 | 244 | 250 | PF00069 | 0.513 |
MOD_Plk_1 | 26 | 32 | PF00069 | 0.639 |
MOD_Plk_1 | 503 | 509 | PF00069 | 0.355 |
MOD_Plk_1 | 559 | 565 | PF00069 | 0.412 |
MOD_Plk_2-3 | 68 | 74 | PF00069 | 0.533 |
MOD_Plk_4 | 362 | 368 | PF00069 | 0.644 |
MOD_Plk_4 | 44 | 50 | PF00069 | 0.693 |
MOD_Plk_4 | 545 | 551 | PF00069 | 0.412 |
MOD_Plk_4 | 561 | 567 | PF00069 | 0.242 |
MOD_Plk_4 | 634 | 640 | PF00069 | 0.562 |
MOD_Plk_4 | 853 | 859 | PF00069 | 0.465 |
MOD_ProDKin_1 | 12 | 18 | PF00069 | 0.668 |
MOD_ProDKin_1 | 127 | 133 | PF00069 | 0.591 |
MOD_ProDKin_1 | 155 | 161 | PF00069 | 0.401 |
MOD_ProDKin_1 | 307 | 313 | PF00069 | 0.645 |
MOD_ProDKin_1 | 415 | 421 | PF00069 | 0.666 |
MOD_ProDKin_1 | 530 | 536 | PF00069 | 0.412 |
MOD_SUMO_for_1 | 680 | 683 | PF00179 | 0.585 |
MOD_SUMO_rev_2 | 116 | 123 | PF00179 | 0.545 |
MOD_SUMO_rev_2 | 682 | 689 | PF00179 | 0.433 |
MOD_SUMO_rev_2 | 73 | 82 | PF00179 | 0.446 |
TRG_DiLeu_BaEn_1 | 756 | 761 | PF01217 | 0.512 |
TRG_DiLeu_BaEn_1 | 807 | 812 | PF01217 | 0.507 |
TRG_DiLeu_BaEn_1 | 850 | 855 | PF01217 | 0.443 |
TRG_DiLeu_BaEn_1 | 874 | 879 | PF01217 | 0.490 |
TRG_DiLeu_BaLyEn_6 | 763 | 768 | PF01217 | 0.493 |
TRG_ENDOCYTIC_2 | 387 | 390 | PF00928 | 0.490 |
TRG_ENDOCYTIC_2 | 731 | 734 | PF00928 | 0.484 |
TRG_ENDOCYTIC_2 | 774 | 777 | PF00928 | 0.438 |
TRG_ENDOCYTIC_2 | 834 | 837 | PF00928 | 0.489 |
TRG_ER_diArg_1 | 430 | 432 | PF00400 | 0.657 |
TRG_ER_diArg_1 | 585 | 588 | PF00400 | 0.426 |
TRG_ER_diArg_1 | 648 | 650 | PF00400 | 0.599 |
TRG_ER_diArg_1 | 720 | 723 | PF00400 | 0.404 |
TRG_ER_diArg_1 | 822 | 824 | PF00400 | 0.430 |
TRG_Pf-PMV_PEXEL_1 | 608 | 613 | PF00026 | 0.358 |
TRG_Pf-PMV_PEXEL_1 | 670 | 674 | PF00026 | 0.467 |
TRG_Pf-PMV_PEXEL_1 | 701 | 705 | PF00026 | 0.473 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7X6B7 | Leishmania donovani | 85% | 89% |
A4HL86 | Leishmania braziliensis | 70% | 100% |
A4I8R4 | Leishmania infantum | 85% | 89% |
Q4Q4F8 | Leishmania major | 85% | 100% |