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: 1, no: 9 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: E9ANJ1
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0003909 | DNA ligase activity | 4 | 8 |
GO:0003910 | DNA ligase (ATP) activity | 5 | 8 |
GO:0016874 | ligase activity | 2 | 11 |
GO:0016886 | ligase activity, forming phosphoric ester bonds | 3 | 8 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 8 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 150 | 154 | PF00656 | 0.594 |
CLV_C14_Caspase3-7 | 164 | 168 | PF00656 | 0.702 |
CLV_C14_Caspase3-7 | 181 | 185 | PF00656 | 0.706 |
CLV_C14_Caspase3-7 | 268 | 272 | PF00656 | 0.440 |
CLV_C14_Caspase3-7 | 285 | 289 | PF00656 | 0.303 |
CLV_C14_Caspase3-7 | 54 | 58 | PF00656 | 0.553 |
CLV_NRD_NRD_1 | 168 | 170 | PF00675 | 0.772 |
CLV_NRD_NRD_1 | 175 | 177 | PF00675 | 0.806 |
CLV_NRD_NRD_1 | 353 | 355 | PF00675 | 0.708 |
CLV_NRD_NRD_1 | 445 | 447 | PF00675 | 0.755 |
CLV_NRD_NRD_1 | 463 | 465 | PF00675 | 0.624 |
CLV_NRD_NRD_1 | 527 | 529 | PF00675 | 0.595 |
CLV_NRD_NRD_1 | 618 | 620 | PF00675 | 0.586 |
CLV_PCSK_KEX2_1 | 175 | 177 | PF00082 | 0.808 |
CLV_PCSK_KEX2_1 | 445 | 447 | PF00082 | 0.755 |
CLV_PCSK_KEX2_1 | 463 | 465 | PF00082 | 0.579 |
CLV_PCSK_KEX2_1 | 527 | 529 | PF00082 | 0.575 |
CLV_PCSK_KEX2_1 | 618 | 620 | PF00082 | 0.538 |
CLV_PCSK_PC1ET2_1 | 618 | 620 | PF00082 | 0.538 |
CLV_PCSK_SKI1_1 | 175 | 179 | PF00082 | 0.687 |
CLV_PCSK_SKI1_1 | 478 | 482 | PF00082 | 0.648 |
CLV_PCSK_SKI1_1 | 528 | 532 | PF00082 | 0.558 |
CLV_PCSK_SKI1_1 | 539 | 543 | PF00082 | 0.519 |
CLV_PCSK_SKI1_1 | 545 | 549 | PF00082 | 0.459 |
CLV_PCSK_SKI1_1 | 558 | 562 | PF00082 | 0.309 |
CLV_PCSK_SKI1_1 | 614 | 618 | PF00082 | 0.784 |
CLV_PCSK_SKI1_1 | 659 | 663 | PF00082 | 0.418 |
DEG_SCF_FBW7_2 | 607 | 613 | PF00400 | 0.578 |
DEG_SPOP_SBC_1 | 89 | 93 | PF00917 | 0.757 |
DOC_CDC14_PxL_1 | 217 | 225 | PF14671 | 0.498 |
DOC_CKS1_1 | 607 | 612 | PF01111 | 0.682 |
DOC_CYCLIN_RxL_1 | 552 | 565 | PF00134 | 0.518 |
DOC_CYCLIN_yCln2_LP_2 | 584 | 590 | PF00134 | 0.481 |
DOC_MAPK_gen_1 | 463 | 473 | PF00069 | 0.657 |
DOC_MAPK_gen_1 | 566 | 576 | PF00069 | 0.538 |
DOC_MAPK_MEF2A_6 | 466 | 475 | PF00069 | 0.701 |
DOC_MAPK_NFAT4_5 | 468 | 476 | PF00069 | 0.698 |
DOC_PP2B_LxvP_1 | 241 | 244 | PF13499 | 0.632 |
DOC_PP2B_LxvP_1 | 431 | 434 | PF13499 | 0.634 |
DOC_PP4_FxxP_1 | 229 | 232 | PF00568 | 0.494 |
DOC_PP4_FxxP_1 | 61 | 64 | PF00568 | 0.380 |
DOC_SPAK_OSR1_1 | 225 | 229 | PF12202 | 0.261 |
DOC_USP7_MATH_1 | 155 | 159 | PF00917 | 0.504 |
DOC_USP7_MATH_1 | 177 | 181 | PF00917 | 0.713 |
DOC_USP7_MATH_1 | 262 | 266 | PF00917 | 0.459 |
DOC_USP7_MATH_1 | 32 | 36 | PF00917 | 0.796 |
DOC_USP7_MATH_1 | 537 | 541 | PF00917 | 0.599 |
DOC_USP7_MATH_1 | 623 | 627 | PF00917 | 0.766 |
DOC_USP7_MATH_1 | 704 | 708 | PF00917 | 0.620 |
DOC_USP7_UBL2_3 | 263 | 267 | PF12436 | 0.635 |
DOC_USP7_UBL2_3 | 421 | 425 | PF12436 | 0.626 |
DOC_USP7_UBL2_3 | 562 | 566 | PF12436 | 0.511 |
DOC_USP7_UBL2_3 | 614 | 618 | PF12436 | 0.700 |
DOC_USP7_UBL2_3 | 691 | 695 | PF12436 | 0.652 |
DOC_WW_Pin1_4 | 100 | 105 | PF00397 | 0.612 |
DOC_WW_Pin1_4 | 232 | 237 | PF00397 | 0.581 |
DOC_WW_Pin1_4 | 24 | 29 | PF00397 | 0.776 |
DOC_WW_Pin1_4 | 302 | 307 | PF00397 | 0.554 |
DOC_WW_Pin1_4 | 324 | 329 | PF00397 | 0.507 |
DOC_WW_Pin1_4 | 482 | 487 | PF00397 | 0.766 |
DOC_WW_Pin1_4 | 503 | 508 | PF00397 | 0.713 |
DOC_WW_Pin1_4 | 60 | 65 | PF00397 | 0.393 |
DOC_WW_Pin1_4 | 603 | 608 | PF00397 | 0.728 |
DOC_WW_Pin1_4 | 678 | 683 | PF00397 | 0.725 |
DOC_WW_Pin1_4 | 76 | 81 | PF00397 | 0.587 |
DOC_WW_Pin1_4 | 82 | 87 | PF00397 | 0.694 |
LIG_14-3-3_CanoR_1 | 281 | 290 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 310 | 315 | PF00244 | 0.516 |
LIG_14-3-3_CanoR_1 | 539 | 547 | PF00244 | 0.558 |
LIG_14-3-3_CanoR_1 | 70 | 75 | PF00244 | 0.436 |
LIG_Actin_WH2_2 | 424 | 439 | PF00022 | 0.651 |
LIG_APCC_ABBA_1 | 398 | 403 | PF00400 | 0.474 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.555 |
LIG_BIR_III_4 | 182 | 186 | PF00653 | 0.628 |
LIG_BRCT_BRCA1_1 | 629 | 633 | PF00533 | 0.482 |
LIG_Clathr_ClatBox_1 | 120 | 124 | PF01394 | 0.470 |
LIG_FHA_1 | 189 | 195 | PF00498 | 0.440 |
LIG_FHA_1 | 285 | 291 | PF00498 | 0.480 |
LIG_FHA_1 | 3 | 9 | PF00498 | 0.637 |
LIG_FHA_1 | 345 | 351 | PF00498 | 0.643 |
LIG_FHA_1 | 392 | 398 | PF00498 | 0.480 |
LIG_FHA_1 | 475 | 481 | PF00498 | 0.626 |
LIG_FHA_1 | 568 | 574 | PF00498 | 0.638 |
LIG_FHA_2 | 148 | 154 | PF00498 | 0.609 |
LIG_FHA_2 | 511 | 517 | PF00498 | 0.735 |
LIG_FHA_2 | 546 | 552 | PF00498 | 0.619 |
LIG_FHA_2 | 623 | 629 | PF00498 | 0.609 |
LIG_FHA_2 | 721 | 727 | PF00498 | 0.575 |
LIG_FHA_2 | 97 | 103 | PF00498 | 0.486 |
LIG_GSK3_LRP6_1 | 76 | 81 | PF00069 | 0.466 |
LIG_LIR_Apic_2 | 111 | 116 | PF02991 | 0.439 |
LIG_LIR_Apic_2 | 73 | 77 | PF02991 | 0.599 |
LIG_LIR_Gen_1 | 191 | 200 | PF02991 | 0.423 |
LIG_LIR_Gen_1 | 713 | 724 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 108 | 113 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 191 | 196 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 551 | 557 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 630 | 636 | PF02991 | 0.513 |
LIG_LIR_Nem_3 | 713 | 719 | PF02991 | 0.423 |
LIG_LYPXL_yS_3 | 554 | 557 | PF13949 | 0.547 |
LIG_MYND_1 | 555 | 559 | PF01753 | 0.572 |
LIG_NRBOX | 316 | 322 | PF00104 | 0.374 |
LIG_NRBOX | 661 | 667 | PF00104 | 0.443 |
LIG_PCNA_PIPBox_1 | 658 | 667 | PF02747 | 0.444 |
LIG_Pex14_2 | 189 | 193 | PF04695 | 0.579 |
LIG_SH2_CRK | 113 | 117 | PF00017 | 0.552 |
LIG_SH2_CRK | 384 | 388 | PF00017 | 0.457 |
LIG_SH2_CRK | 716 | 720 | PF00017 | 0.414 |
LIG_SH2_NCK_1 | 40 | 44 | PF00017 | 0.606 |
LIG_SH2_PTP2 | 74 | 77 | PF00017 | 0.586 |
LIG_SH2_SRC | 219 | 222 | PF00017 | 0.498 |
LIG_SH2_SRC | 401 | 404 | PF00017 | 0.547 |
LIG_SH2_SRC | 74 | 77 | PF00017 | 0.557 |
LIG_SH2_STAT3 | 146 | 149 | PF00017 | 0.518 |
LIG_SH2_STAT3 | 634 | 637 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 146 | 149 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 219 | 222 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 316 | 319 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 401 | 404 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 74 | 77 | PF00017 | 0.579 |
LIG_SH3_1 | 218 | 224 | PF00018 | 0.431 |
LIG_SH3_1 | 74 | 80 | PF00018 | 0.428 |
LIG_SH3_3 | 160 | 166 | PF00018 | 0.568 |
LIG_SH3_3 | 218 | 224 | PF00018 | 0.502 |
LIG_SH3_3 | 237 | 243 | PF00018 | 0.665 |
LIG_SH3_3 | 498 | 504 | PF00018 | 0.737 |
LIG_SH3_3 | 53 | 59 | PF00018 | 0.558 |
LIG_SH3_3 | 571 | 577 | PF00018 | 0.484 |
LIG_SH3_3 | 584 | 590 | PF00018 | 0.498 |
LIG_SH3_3 | 604 | 610 | PF00018 | 0.624 |
LIG_SH3_3 | 645 | 651 | PF00018 | 0.409 |
LIG_SH3_3 | 74 | 80 | PF00018 | 0.548 |
LIG_SUMO_SIM_anti_2 | 4 | 10 | PF11976 | 0.577 |
LIG_SUMO_SIM_anti_2 | 516 | 521 | PF11976 | 0.642 |
LIG_SUMO_SIM_par_1 | 4 | 10 | PF11976 | 0.581 |
LIG_SUMO_SIM_par_1 | 471 | 477 | PF11976 | 0.600 |
LIG_SUMO_SIM_par_1 | 707 | 713 | PF11976 | 0.526 |
LIG_SxIP_EBH_1 | 375 | 388 | PF03271 | 0.524 |
LIG_TRAF2_1 | 211 | 214 | PF00917 | 0.414 |
LIG_TYR_ITIM | 382 | 387 | PF00017 | 0.412 |
LIG_UBA3_1 | 556 | 562 | PF00899 | 0.438 |
MOD_CDK_SPK_2 | 24 | 29 | PF00069 | 0.674 |
MOD_CDK_SPK_2 | 60 | 65 | PF00069 | 0.384 |
MOD_CDK_SPxxK_3 | 24 | 31 | PF00069 | 0.502 |
MOD_CDK_SPxxK_3 | 324 | 331 | PF00069 | 0.436 |
MOD_CK1_1 | 253 | 259 | PF00069 | 0.657 |
MOD_CK1_1 | 284 | 290 | PF00069 | 0.412 |
MOD_CK1_1 | 474 | 480 | PF00069 | 0.664 |
MOD_CK1_1 | 591 | 597 | PF00069 | 0.706 |
MOD_CK1_1 | 722 | 728 | PF00069 | 0.551 |
MOD_CK1_1 | 90 | 96 | PF00069 | 0.784 |
MOD_CK2_1 | 510 | 516 | PF00069 | 0.727 |
MOD_CK2_1 | 622 | 628 | PF00069 | 0.579 |
MOD_CK2_1 | 720 | 726 | PF00069 | 0.485 |
MOD_CK2_1 | 76 | 82 | PF00069 | 0.569 |
MOD_CK2_1 | 96 | 102 | PF00069 | 0.498 |
MOD_Cter_Amidation | 167 | 170 | PF01082 | 0.587 |
MOD_Cter_Amidation | 461 | 464 | PF01082 | 0.706 |
MOD_Cter_Amidation | 525 | 528 | PF01082 | 0.668 |
MOD_GlcNHglycan | 196 | 199 | PF01048 | 0.412 |
MOD_GlcNHglycan | 236 | 239 | PF01048 | 0.477 |
MOD_GlcNHglycan | 252 | 255 | PF01048 | 0.604 |
MOD_GlcNHglycan | 337 | 340 | PF01048 | 0.406 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.766 |
MOD_GlcNHglycan | 367 | 370 | PF01048 | 0.677 |
MOD_GlcNHglycan | 40 | 43 | PF01048 | 0.550 |
MOD_GlcNHglycan | 459 | 463 | PF01048 | 0.791 |
MOD_GlcNHglycan | 590 | 593 | PF01048 | 0.580 |
MOD_GlcNHglycan | 625 | 628 | PF01048 | 0.684 |
MOD_GlcNHglycan | 666 | 669 | PF01048 | 0.613 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.683 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.338 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.767 |
MOD_GSK3_1 | 386 | 393 | PF00069 | 0.470 |
MOD_GSK3_1 | 572 | 579 | PF00069 | 0.513 |
MOD_GSK3_1 | 623 | 630 | PF00069 | 0.703 |
MOD_GSK3_1 | 704 | 711 | PF00069 | 0.601 |
MOD_GSK3_1 | 715 | 722 | PF00069 | 0.405 |
MOD_GSK3_1 | 78 | 85 | PF00069 | 0.627 |
MOD_GSK3_1 | 89 | 96 | PF00069 | 0.615 |
MOD_N-GLC_1 | 302 | 307 | PF02516 | 0.388 |
MOD_N-GLC_1 | 38 | 43 | PF02516 | 0.622 |
MOD_N-GLC_1 | 646 | 651 | PF02516 | 0.468 |
MOD_N-GLC_2 | 201 | 203 | PF02516 | 0.290 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.470 |
MOD_NEK2_1 | 18 | 23 | PF00069 | 0.694 |
MOD_NEK2_1 | 194 | 199 | PF00069 | 0.407 |
MOD_NEK2_1 | 390 | 395 | PF00069 | 0.533 |
MOD_NEK2_1 | 450 | 455 | PF00069 | 0.681 |
MOD_NEK2_1 | 471 | 476 | PF00069 | 0.679 |
MOD_NEK2_1 | 646 | 651 | PF00069 | 0.481 |
MOD_NEK2_1 | 715 | 720 | PF00069 | 0.424 |
MOD_NEK2_2 | 105 | 110 | PF00069 | 0.563 |
MOD_NEK2_2 | 262 | 267 | PF00069 | 0.460 |
MOD_OFUCOSY | 203 | 208 | PF10250 | 0.327 |
MOD_PIKK_1 | 269 | 275 | PF00454 | 0.585 |
MOD_PIKK_1 | 305 | 311 | PF00454 | 0.389 |
MOD_PIKK_1 | 391 | 397 | PF00454 | 0.565 |
MOD_PK_1 | 731 | 737 | PF00069 | 0.570 |
MOD_PKA_1 | 354 | 360 | PF00069 | 0.495 |
MOD_PKA_1 | 614 | 620 | PF00069 | 0.770 |
MOD_PKA_2 | 155 | 161 | PF00069 | 0.495 |
MOD_PKA_2 | 203 | 209 | PF00069 | 0.569 |
MOD_PKA_2 | 450 | 456 | PF00069 | 0.779 |
MOD_PKB_1 | 202 | 210 | PF00069 | 0.554 |
MOD_Plk_1 | 135 | 141 | PF00069 | 0.539 |
MOD_Plk_1 | 646 | 652 | PF00069 | 0.480 |
MOD_Plk_4 | 135 | 141 | PF00069 | 0.474 |
MOD_Plk_4 | 628 | 634 | PF00069 | 0.362 |
MOD_Plk_4 | 657 | 663 | PF00069 | 0.500 |
MOD_ProDKin_1 | 100 | 106 | PF00069 | 0.601 |
MOD_ProDKin_1 | 232 | 238 | PF00069 | 0.603 |
MOD_ProDKin_1 | 24 | 30 | PF00069 | 0.776 |
MOD_ProDKin_1 | 302 | 308 | PF00069 | 0.553 |
MOD_ProDKin_1 | 324 | 330 | PF00069 | 0.505 |
MOD_ProDKin_1 | 482 | 488 | PF00069 | 0.767 |
MOD_ProDKin_1 | 503 | 509 | PF00069 | 0.713 |
MOD_ProDKin_1 | 60 | 66 | PF00069 | 0.392 |
MOD_ProDKin_1 | 603 | 609 | PF00069 | 0.730 |
MOD_ProDKin_1 | 678 | 684 | PF00069 | 0.725 |
MOD_ProDKin_1 | 76 | 82 | PF00069 | 0.594 |
TRG_DiLeu_BaEn_1 | 125 | 130 | PF01217 | 0.358 |
TRG_DiLeu_BaEn_4 | 125 | 131 | PF01217 | 0.342 |
TRG_DiLeu_BaLyEn_6 | 431 | 436 | PF01217 | 0.539 |
TRG_DiLeu_BaLyEn_6 | 556 | 561 | PF01217 | 0.432 |
TRG_DiLeu_BaLyEn_6 | 67 | 72 | PF01217 | 0.544 |
TRG_DiLeu_LyEn_5 | 125 | 130 | PF01217 | 0.418 |
TRG_ENDOCYTIC_2 | 118 | 121 | PF00928 | 0.494 |
TRG_ENDOCYTIC_2 | 384 | 387 | PF00928 | 0.462 |
TRG_ENDOCYTIC_2 | 554 | 557 | PF00928 | 0.430 |
TRG_ENDOCYTIC_2 | 716 | 719 | PF00928 | 0.403 |
TRG_ER_diArg_1 | 445 | 448 | PF00400 | 0.699 |
TRG_ER_diArg_1 | 463 | 466 | PF00400 | 0.715 |
TRG_ER_diArg_1 | 568 | 571 | PF00400 | 0.589 |
TRG_NLS_MonoExtC_3 | 168 | 173 | PF00514 | 0.678 |
TRG_NLS_MonoExtN_4 | 166 | 173 | PF00514 | 0.629 |
TRG_NLS_MonoExtN_4 | 615 | 622 | PF00514 | 0.593 |
TRG_Pf-PMV_PEXEL_1 | 131 | 136 | PF00026 | 0.363 |
TRG_Pf-PMV_PEXEL_1 | 528 | 532 | PF00026 | 0.668 |
TRG_Pf-PMV_PEXEL_1 | 558 | 563 | PF00026 | 0.580 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZN9 | Leptomonas seymouri | 52% | 97% |
A0A1X0NVK9 | Trypanosomatidae | 36% | 100% |
A0A3R7NRR1 | Trypanosoma rangeli | 37% | 100% |
A0A3S7WRI1 | Leishmania donovani | 88% | 100% |
A4H6G1 | Leishmania braziliensis | 74% | 100% |
A4HUV6 | Leishmania infantum | 89% | 100% |
D0A7J8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
Q4QH35 | Leishmania major | 86% | 100% |
V5BB55 | Trypanosoma cruzi | 35% | 100% |