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 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4QAF6
Term | Name | Level | Count |
---|---|---|---|
GO:0006479 | protein methylation | 4 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0008213 | protein alkylation | 5 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016570 | histone modification | 5 | 2 |
GO:0016571 | histone methylation | 5 | 2 |
GO:0018022 | peptidyl-lysine methylation | 5 | 2 |
GO:0018193 | peptidyl-amino acid modification | 5 | 2 |
GO:0018205 | peptidyl-lysine modification | 6 | 2 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0032259 | methylation | 2 | 2 |
GO:0034968 | histone lysine methylation | 6 | 2 |
GO:0036211 | protein modification process | 4 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043412 | macromolecule modification | 4 | 2 |
GO:0043414 | macromolecule methylation | 3 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 2 |
GO:0008168 | methyltransferase activity | 4 | 2 |
GO:0008170 | N-methyltransferase activity | 5 | 2 |
GO:0008276 | protein methyltransferase activity | 3 | 2 |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 2 |
GO:0016278 | lysine N-methyltransferase activity | 6 | 2 |
GO:0016279 | protein-lysine N-methyltransferase activity | 4 | 2 |
GO:0016740 | transferase activity | 2 | 2 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 2 |
GO:0018024 | obsolete histone lysine N-methyltransferase activity | 5 | 2 |
GO:0042054 | histone methyltransferase activity | 4 | 2 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 180 | 184 | PF00656 | 0.588 |
CLV_C14_Caspase3-7 | 366 | 370 | PF00656 | 0.449 |
CLV_NRD_NRD_1 | 123 | 125 | PF00675 | 0.586 |
CLV_NRD_NRD_1 | 289 | 291 | PF00675 | 0.686 |
CLV_NRD_NRD_1 | 379 | 381 | PF00675 | 0.514 |
CLV_NRD_NRD_1 | 705 | 707 | PF00675 | 0.418 |
CLV_PCSK_KEX2_1 | 123 | 125 | PF00082 | 0.586 |
CLV_PCSK_KEX2_1 | 156 | 158 | PF00082 | 0.495 |
CLV_PCSK_KEX2_1 | 289 | 291 | PF00082 | 0.697 |
CLV_PCSK_KEX2_1 | 379 | 381 | PF00082 | 0.514 |
CLV_PCSK_KEX2_1 | 704 | 706 | PF00082 | 0.394 |
CLV_PCSK_PC1ET2_1 | 156 | 158 | PF00082 | 0.495 |
CLV_PCSK_SKI1_1 | 290 | 294 | PF00082 | 0.605 |
CLV_PCSK_SKI1_1 | 452 | 456 | PF00082 | 0.377 |
CLV_PCSK_SKI1_1 | 520 | 524 | PF00082 | 0.508 |
CLV_PCSK_SKI1_1 | 706 | 710 | PF00082 | 0.493 |
DEG_APCC_DBOX_1 | 383 | 391 | PF00400 | 0.404 |
DEG_APCC_DBOX_1 | 428 | 436 | PF00400 | 0.523 |
DEG_SPOP_SBC_1 | 404 | 408 | PF00917 | 0.582 |
DOC_CKS1_1 | 274 | 279 | PF01111 | 0.579 |
DOC_CYCLIN_RxL_1 | 391 | 402 | PF00134 | 0.516 |
DOC_MAPK_gen_1 | 379 | 387 | PF00069 | 0.428 |
DOC_MAPK_MEF2A_6 | 384 | 392 | PF00069 | 0.371 |
DOC_PP1_RVXF_1 | 392 | 399 | PF00149 | 0.505 |
DOC_PP1_RVXF_1 | 413 | 420 | PF00149 | 0.469 |
DOC_PP1_RVXF_1 | 58 | 64 | PF00149 | 0.480 |
DOC_PP4_FxxP_1 | 274 | 277 | PF00568 | 0.538 |
DOC_USP7_MATH_1 | 117 | 121 | PF00917 | 0.696 |
DOC_USP7_MATH_1 | 131 | 135 | PF00917 | 0.755 |
DOC_USP7_MATH_1 | 19 | 23 | PF00917 | 0.674 |
DOC_USP7_MATH_1 | 334 | 338 | PF00917 | 0.479 |
DOC_USP7_MATH_1 | 370 | 374 | PF00917 | 0.498 |
DOC_USP7_MATH_1 | 404 | 408 | PF00917 | 0.612 |
DOC_USP7_MATH_1 | 507 | 511 | PF00917 | 0.635 |
DOC_USP7_MATH_1 | 571 | 575 | PF00917 | 0.636 |
DOC_USP7_MATH_1 | 595 | 599 | PF00917 | 0.560 |
DOC_USP7_MATH_2 | 80 | 86 | PF00917 | 0.662 |
DOC_USP7_UBL2_3 | 94 | 98 | PF12436 | 0.676 |
DOC_WW_Pin1_4 | 118 | 123 | PF00397 | 0.677 |
DOC_WW_Pin1_4 | 127 | 132 | PF00397 | 0.598 |
DOC_WW_Pin1_4 | 198 | 203 | PF00397 | 0.738 |
DOC_WW_Pin1_4 | 207 | 212 | PF00397 | 0.740 |
DOC_WW_Pin1_4 | 252 | 257 | PF00397 | 0.714 |
DOC_WW_Pin1_4 | 273 | 278 | PF00397 | 0.549 |
DOC_WW_Pin1_4 | 4 | 9 | PF00397 | 0.665 |
DOC_WW_Pin1_4 | 405 | 410 | PF00397 | 0.606 |
DOC_WW_Pin1_4 | 497 | 502 | PF00397 | 0.543 |
DOC_WW_Pin1_4 | 503 | 508 | PF00397 | 0.588 |
DOC_WW_Pin1_4 | 554 | 559 | PF00397 | 0.506 |
DOC_WW_Pin1_4 | 625 | 630 | PF00397 | 0.531 |
LIG_14-3-3_CanoR_1 | 191 | 197 | PF00244 | 0.660 |
LIG_14-3-3_CanoR_1 | 257 | 266 | PF00244 | 0.634 |
LIG_14-3-3_CanoR_1 | 290 | 298 | PF00244 | 0.656 |
LIG_14-3-3_CanoR_1 | 456 | 460 | PF00244 | 0.370 |
LIG_Actin_WH2_2 | 440 | 458 | PF00022 | 0.523 |
LIG_BIR_III_4 | 575 | 579 | PF00653 | 0.698 |
LIG_BRCT_BRCA1_1 | 30 | 34 | PF00533 | 0.633 |
LIG_BRCT_BRCA1_1 | 530 | 534 | PF00533 | 0.452 |
LIG_BRCT_BRCA1_1 | 65 | 69 | PF00533 | 0.372 |
LIG_Clathr_ClatBox_1 | 446 | 450 | PF01394 | 0.446 |
LIG_CSL_BTD_1 | 490 | 493 | PF09270 | 0.464 |
LIG_FAT_LD_1 | 182 | 190 | PF03623 | 0.607 |
LIG_FHA_1 | 11 | 17 | PF00498 | 0.660 |
LIG_FHA_1 | 128 | 134 | PF00498 | 0.742 |
LIG_FHA_1 | 211 | 217 | PF00498 | 0.643 |
LIG_FHA_1 | 279 | 285 | PF00498 | 0.606 |
LIG_FHA_1 | 341 | 347 | PF00498 | 0.359 |
LIG_FHA_1 | 473 | 479 | PF00498 | 0.469 |
LIG_FHA_1 | 521 | 527 | PF00498 | 0.518 |
LIG_FHA_1 | 682 | 688 | PF00498 | 0.494 |
LIG_FHA_1 | 694 | 700 | PF00498 | 0.390 |
LIG_FHA_1 | 720 | 726 | PF00498 | 0.383 |
LIG_FHA_2 | 145 | 151 | PF00498 | 0.635 |
LIG_FHA_2 | 243 | 249 | PF00498 | 0.732 |
LIG_FHA_2 | 259 | 265 | PF00498 | 0.582 |
LIG_FHA_2 | 364 | 370 | PF00498 | 0.443 |
LIG_FHA_2 | 510 | 516 | PF00498 | 0.634 |
LIG_FHA_2 | 97 | 103 | PF00498 | 0.667 |
LIG_GBD_Chelix_1 | 388 | 396 | PF00786 | 0.369 |
LIG_LIR_Gen_1 | 212 | 222 | PF02991 | 0.660 |
LIG_LIR_Gen_1 | 458 | 467 | PF02991 | 0.408 |
LIG_LIR_Gen_1 | 472 | 481 | PF02991 | 0.449 |
LIG_LIR_Gen_1 | 684 | 692 | PF02991 | 0.528 |
LIG_LIR_Nem_3 | 106 | 111 | PF02991 | 0.669 |
LIG_LIR_Nem_3 | 212 | 217 | PF02991 | 0.653 |
LIG_LIR_Nem_3 | 458 | 462 | PF02991 | 0.334 |
LIG_LIR_Nem_3 | 463 | 468 | PF02991 | 0.332 |
LIG_LIR_Nem_3 | 472 | 477 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 603 | 609 | PF02991 | 0.503 |
LIG_LIR_Nem_3 | 680 | 686 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 690 | 695 | PF02991 | 0.384 |
LIG_NRBOX | 181 | 187 | PF00104 | 0.592 |
LIG_NRBOX | 386 | 392 | PF00104 | 0.473 |
LIG_PCNA_yPIPBox_3 | 332 | 340 | PF02747 | 0.479 |
LIG_PDZ_Class_2 | 733 | 738 | PF00595 | 0.596 |
LIG_PTB_Apo_2 | 653 | 660 | PF02174 | 0.536 |
LIG_Rb_LxCxE_1 | 463 | 485 | PF01857 | 0.442 |
LIG_SH2_CRK | 108 | 112 | PF00017 | 0.669 |
LIG_SH2_CRK | 474 | 478 | PF00017 | 0.405 |
LIG_SH2_NCK_1 | 643 | 647 | PF00017 | 0.470 |
LIG_SH2_PTP2 | 686 | 689 | PF00017 | 0.367 |
LIG_SH2_SRC | 439 | 442 | PF00017 | 0.546 |
LIG_SH2_STAP1 | 474 | 478 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 242 | 245 | PF00017 | 0.752 |
LIG_SH2_STAT5 | 259 | 262 | PF00017 | 0.611 |
LIG_SH2_STAT5 | 273 | 276 | PF00017 | 0.457 |
LIG_SH2_STAT5 | 474 | 477 | PF00017 | 0.497 |
LIG_SH2_STAT5 | 539 | 542 | PF00017 | 0.357 |
LIG_SH2_STAT5 | 553 | 556 | PF00017 | 0.471 |
LIG_SH2_STAT5 | 560 | 563 | PF00017 | 0.545 |
LIG_SH2_STAT5 | 686 | 689 | PF00017 | 0.370 |
LIG_SH2_STAT5 | 707 | 710 | PF00017 | 0.397 |
LIG_SH3_2 | 410 | 415 | PF14604 | 0.482 |
LIG_SH3_3 | 295 | 301 | PF00018 | 0.643 |
LIG_SH3_3 | 407 | 413 | PF00018 | 0.561 |
LIG_SH3_3 | 552 | 558 | PF00018 | 0.480 |
LIG_SUMO_SIM_anti_2 | 523 | 532 | PF11976 | 0.293 |
LIG_SUMO_SIM_anti_2 | 597 | 603 | PF11976 | 0.620 |
LIG_SUMO_SIM_par_1 | 445 | 450 | PF11976 | 0.454 |
LIG_SUMO_SIM_par_1 | 721 | 727 | PF11976 | 0.324 |
LIG_TRAF2_1 | 147 | 150 | PF00917 | 0.630 |
LIG_TRAF2_2 | 54 | 59 | PF00917 | 0.426 |
LIG_TYR_ITSM | 682 | 689 | PF00017 | 0.545 |
LIG_UBA3_1 | 387 | 394 | PF00899 | 0.477 |
LIG_UBA3_1 | 601 | 607 | PF00899 | 0.559 |
LIG_WRC_WIRS_1 | 347 | 352 | PF05994 | 0.439 |
MOD_CDC14_SPxK_1 | 121 | 124 | PF00782 | 0.572 |
MOD_CDK_SPK_2 | 118 | 123 | PF00069 | 0.677 |
MOD_CDK_SPK_2 | 198 | 203 | PF00069 | 0.685 |
MOD_CDK_SPK_2 | 252 | 257 | PF00069 | 0.681 |
MOD_CDK_SPxK_1 | 118 | 124 | PF00069 | 0.574 |
MOD_CDK_SPxxK_3 | 118 | 125 | PF00069 | 0.681 |
MOD_CDK_SPxxK_3 | 497 | 504 | PF00069 | 0.409 |
MOD_CK1_1 | 132 | 138 | PF00069 | 0.765 |
MOD_CK1_1 | 142 | 148 | PF00069 | 0.809 |
MOD_CK1_1 | 29 | 35 | PF00069 | 0.658 |
MOD_CK1_1 | 373 | 379 | PF00069 | 0.457 |
MOD_CK1_1 | 427 | 433 | PF00069 | 0.451 |
MOD_CK1_1 | 482 | 488 | PF00069 | 0.535 |
MOD_CK1_1 | 510 | 516 | PF00069 | 0.588 |
MOD_CK1_1 | 72 | 78 | PF00069 | 0.597 |
MOD_CK2_1 | 144 | 150 | PF00069 | 0.735 |
MOD_CK2_1 | 190 | 196 | PF00069 | 0.758 |
MOD_CK2_1 | 209 | 215 | PF00069 | 0.611 |
MOD_CK2_1 | 242 | 248 | PF00069 | 0.648 |
MOD_CK2_1 | 280 | 286 | PF00069 | 0.599 |
MOD_CK2_1 | 427 | 433 | PF00069 | 0.521 |
MOD_CK2_1 | 435 | 441 | PF00069 | 0.459 |
MOD_CK2_1 | 497 | 503 | PF00069 | 0.489 |
MOD_CK2_1 | 509 | 515 | PF00069 | 0.582 |
MOD_CK2_1 | 96 | 102 | PF00069 | 0.669 |
MOD_CMANNOS | 563 | 566 | PF00535 | 0.581 |
MOD_Cter_Amidation | 287 | 290 | PF01082 | 0.693 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.526 |
MOD_GlcNHglycan | 316 | 319 | PF01048 | 0.578 |
MOD_GlcNHglycan | 329 | 332 | PF01048 | 0.405 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.638 |
MOD_GlcNHglycan | 401 | 404 | PF01048 | 0.546 |
MOD_GlcNHglycan | 484 | 487 | PF01048 | 0.651 |
MOD_GlcNHglycan | 509 | 512 | PF01048 | 0.601 |
MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.792 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.698 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.770 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.658 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.669 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.511 |
MOD_GSK3_1 | 399 | 406 | PF00069 | 0.488 |
MOD_GSK3_1 | 420 | 427 | PF00069 | 0.341 |
MOD_GSK3_1 | 480 | 487 | PF00069 | 0.564 |
MOD_GSK3_1 | 503 | 510 | PF00069 | 0.601 |
MOD_GSK3_1 | 554 | 561 | PF00069 | 0.493 |
MOD_LATS_1 | 732 | 738 | PF00433 | 0.558 |
MOD_N-GLC_1 | 649 | 654 | PF02516 | 0.274 |
MOD_N-GLC_2 | 77 | 79 | PF02516 | 0.641 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.679 |
MOD_NEK2_1 | 291 | 296 | PF00069 | 0.685 |
MOD_NEK2_1 | 323 | 328 | PF00069 | 0.669 |
MOD_NEK2_1 | 396 | 401 | PF00069 | 0.460 |
MOD_NEK2_1 | 420 | 425 | PF00069 | 0.466 |
MOD_NEK2_1 | 435 | 440 | PF00069 | 0.579 |
MOD_NEK2_1 | 455 | 460 | PF00069 | 0.238 |
MOD_NEK2_1 | 608 | 613 | PF00069 | 0.677 |
MOD_NEK2_1 | 635 | 640 | PF00069 | 0.581 |
MOD_NEK2_1 | 649 | 654 | PF00069 | 0.508 |
MOD_NEK2_1 | 682 | 687 | PF00069 | 0.573 |
MOD_NEK2_1 | 69 | 74 | PF00069 | 0.484 |
MOD_NEK2_2 | 370 | 375 | PF00069 | 0.509 |
MOD_PIKK_1 | 80 | 86 | PF00454 | 0.632 |
MOD_PKA_2 | 142 | 148 | PF00069 | 0.765 |
MOD_PKA_2 | 190 | 196 | PF00069 | 0.720 |
MOD_PKA_2 | 455 | 461 | PF00069 | 0.338 |
MOD_Plk_1 | 177 | 183 | PF00069 | 0.477 |
MOD_Plk_1 | 420 | 426 | PF00069 | 0.422 |
MOD_Plk_1 | 472 | 478 | PF00069 | 0.405 |
MOD_Plk_1 | 63 | 69 | PF00069 | 0.363 |
MOD_Plk_1 | 649 | 655 | PF00069 | 0.463 |
MOD_Plk_2-3 | 190 | 196 | PF00069 | 0.655 |
MOD_Plk_2-3 | 280 | 286 | PF00069 | 0.599 |
MOD_Plk_4 | 280 | 286 | PF00069 | 0.596 |
MOD_Plk_4 | 334 | 340 | PF00069 | 0.454 |
MOD_Plk_4 | 460 | 466 | PF00069 | 0.436 |
MOD_Plk_4 | 487 | 493 | PF00069 | 0.677 |
MOD_Plk_4 | 558 | 564 | PF00069 | 0.486 |
MOD_Plk_4 | 595 | 601 | PF00069 | 0.628 |
MOD_Plk_4 | 64 | 70 | PF00069 | 0.546 |
MOD_Plk_4 | 666 | 672 | PF00069 | 0.548 |
MOD_Plk_4 | 682 | 688 | PF00069 | 0.470 |
MOD_ProDKin_1 | 118 | 124 | PF00069 | 0.679 |
MOD_ProDKin_1 | 127 | 133 | PF00069 | 0.600 |
MOD_ProDKin_1 | 198 | 204 | PF00069 | 0.737 |
MOD_ProDKin_1 | 207 | 213 | PF00069 | 0.740 |
MOD_ProDKin_1 | 252 | 258 | PF00069 | 0.712 |
MOD_ProDKin_1 | 273 | 279 | PF00069 | 0.548 |
MOD_ProDKin_1 | 4 | 10 | PF00069 | 0.666 |
MOD_ProDKin_1 | 405 | 411 | PF00069 | 0.597 |
MOD_ProDKin_1 | 497 | 503 | PF00069 | 0.547 |
MOD_ProDKin_1 | 505 | 511 | PF00069 | 0.622 |
MOD_ProDKin_1 | 554 | 560 | PF00069 | 0.509 |
MOD_ProDKin_1 | 625 | 631 | PF00069 | 0.531 |
MOD_SUMO_rev_2 | 575 | 585 | PF00179 | 0.611 |
TRG_DiLeu_BaEn_1 | 280 | 285 | PF01217 | 0.547 |
TRG_DiLeu_BaEn_1 | 383 | 388 | PF01217 | 0.401 |
TRG_DiLeu_BaEn_1 | 450 | 455 | PF01217 | 0.502 |
TRG_DiLeu_BaEn_3 | 286 | 292 | PF01217 | 0.711 |
TRG_DiLeu_BaEn_4 | 177 | 183 | PF01217 | 0.535 |
TRG_DiLeu_BaLyEn_6 | 167 | 172 | PF01217 | 0.580 |
TRG_ENDOCYTIC_2 | 108 | 111 | PF00928 | 0.671 |
TRG_ENDOCYTIC_2 | 474 | 477 | PF00928 | 0.510 |
TRG_ENDOCYTIC_2 | 539 | 542 | PF00928 | 0.450 |
TRG_ENDOCYTIC_2 | 606 | 609 | PF00928 | 0.537 |
TRG_ENDOCYTIC_2 | 686 | 689 | PF00928 | 0.392 |
TRG_ER_diArg_1 | 122 | 124 | PF00400 | 0.574 |
TRG_ER_diArg_1 | 289 | 291 | PF00400 | 0.686 |
TRG_ER_diArg_1 | 428 | 431 | PF00400 | 0.499 |
TRG_ER_diArg_1 | 703 | 706 | PF00400 | 0.480 |
TRG_NES_CRM1_1 | 715 | 727 | PF08389 | 0.312 |
TRG_Pf-PMV_PEXEL_1 | 203 | 207 | PF00026 | 0.708 |
TRG_Pf-PMV_PEXEL_1 | 60 | 64 | PF00026 | 0.470 |
TRG_Pf-PMV_PEXEL_1 | 706 | 710 | PF00026 | 0.496 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I099 | Leptomonas seymouri | 41% | 100% |
A0A3R7RB97 | Trypanosoma rangeli | 29% | 100% |
A0A3S7WYH5 | Leishmania donovani | 90% | 100% |
A4HDN5 | Leishmania braziliensis | 72% | 100% |
C9ZWC8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
E9AH82 | Leishmania infantum | 90% | 100% |
E9AX20 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 99% |
V5CZP8 | Trypanosoma cruzi | 30% | 100% |