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: A4I3T3
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 | 411 | 415 | PF00656 | 0.476 |
CLV_C14_Caspase3-7 | 478 | 482 | PF00656 | 0.494 |
CLV_C14_Caspase3-7 | 486 | 490 | PF00656 | 0.528 |
CLV_NRD_NRD_1 | 24 | 26 | PF00675 | 0.371 |
CLV_NRD_NRD_1 | 357 | 359 | PF00675 | 0.352 |
CLV_NRD_NRD_1 | 444 | 446 | PF00675 | 0.446 |
CLV_NRD_NRD_1 | 650 | 652 | PF00675 | 0.590 |
CLV_NRD_NRD_1 | 712 | 714 | PF00675 | 0.461 |
CLV_NRD_NRD_1 | 811 | 813 | PF00675 | 0.617 |
CLV_NRD_NRD_1 | 825 | 827 | PF00675 | 0.510 |
CLV_NRD_NRD_1 | 841 | 843 | PF00675 | 0.464 |
CLV_PCSK_FUR_1 | 355 | 359 | PF00082 | 0.478 |
CLV_PCSK_FUR_1 | 849 | 853 | PF00082 | 0.500 |
CLV_PCSK_KEX2_1 | 23 | 25 | PF00082 | 0.370 |
CLV_PCSK_KEX2_1 | 357 | 359 | PF00082 | 0.352 |
CLV_PCSK_KEX2_1 | 444 | 446 | PF00082 | 0.446 |
CLV_PCSK_KEX2_1 | 650 | 652 | PF00082 | 0.590 |
CLV_PCSK_KEX2_1 | 712 | 714 | PF00082 | 0.461 |
CLV_PCSK_KEX2_1 | 809 | 811 | PF00082 | 0.681 |
CLV_PCSK_KEX2_1 | 841 | 843 | PF00082 | 0.590 |
CLV_PCSK_KEX2_1 | 851 | 853 | PF00082 | 0.458 |
CLV_PCSK_PC1ET2_1 | 809 | 811 | PF00082 | 0.795 |
CLV_PCSK_PC1ET2_1 | 851 | 853 | PF00082 | 0.584 |
CLV_PCSK_PC7_1 | 19 | 25 | PF00082 | 0.525 |
CLV_PCSK_SKI1_1 | 107 | 111 | PF00082 | 0.478 |
CLV_PCSK_SKI1_1 | 203 | 207 | PF00082 | 0.352 |
CLV_PCSK_SKI1_1 | 368 | 372 | PF00082 | 0.496 |
CLV_PCSK_SKI1_1 | 445 | 449 | PF00082 | 0.450 |
CLV_PCSK_SKI1_1 | 712 | 716 | PF00082 | 0.399 |
DEG_APCC_DBOX_1 | 221 | 229 | PF00400 | 0.387 |
DEG_APCC_DBOX_1 | 367 | 375 | PF00400 | 0.492 |
DEG_APCC_DBOX_1 | 638 | 646 | PF00400 | 0.405 |
DOC_CKS1_1 | 143 | 148 | PF01111 | 0.406 |
DOC_CKS1_1 | 176 | 181 | PF01111 | 0.352 |
DOC_CKS1_1 | 456 | 461 | PF01111 | 0.657 |
DOC_CKS1_1 | 762 | 767 | PF01111 | 0.471 |
DOC_CYCLIN_RxL_1 | 442 | 450 | PF00134 | 0.391 |
DOC_CYCLIN_RxL_1 | 706 | 718 | PF00134 | 0.407 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 98 | 105 | PF00134 | 0.404 |
DOC_CYCLIN_yCln2_LP_2 | 555 | 561 | PF00134 | 0.502 |
DOC_MAPK_gen_1 | 355 | 364 | PF00069 | 0.361 |
DOC_MAPK_gen_1 | 462 | 470 | PF00069 | 0.521 |
DOC_MAPK_gen_1 | 532 | 541 | PF00069 | 0.394 |
DOC_MAPK_gen_1 | 650 | 661 | PF00069 | 0.604 |
DOC_MAPK_gen_1 | 725 | 735 | PF00069 | 0.352 |
DOC_MAPK_MEF2A_6 | 532 | 541 | PF00069 | 0.417 |
DOC_MAPK_MEF2A_6 | 654 | 663 | PF00069 | 0.555 |
DOC_MAPK_MEF2A_6 | 9 | 17 | PF00069 | 0.487 |
DOC_PP1_RVXF_1 | 443 | 450 | PF00149 | 0.464 |
DOC_PP2B_LxvP_1 | 435 | 438 | PF13499 | 0.396 |
DOC_PP2B_LxvP_1 | 510 | 513 | PF13499 | 0.490 |
DOC_PP2B_LxvP_1 | 555 | 558 | PF13499 | 0.589 |
DOC_PP2B_LxvP_1 | 605 | 608 | PF13499 | 0.556 |
DOC_PP4_FxxP_1 | 131 | 134 | PF00568 | 0.406 |
DOC_PP4_FxxP_1 | 440 | 443 | PF00568 | 0.447 |
DOC_USP7_MATH_1 | 314 | 318 | PF00917 | 0.400 |
DOC_USP7_MATH_1 | 617 | 621 | PF00917 | 0.567 |
DOC_USP7_MATH_1 | 662 | 666 | PF00917 | 0.407 |
DOC_USP7_MATH_1 | 704 | 708 | PF00917 | 0.387 |
DOC_USP7_MATH_1 | 736 | 740 | PF00917 | 0.406 |
DOC_WW_Pin1_4 | 126 | 131 | PF00397 | 0.376 |
DOC_WW_Pin1_4 | 142 | 147 | PF00397 | 0.147 |
DOC_WW_Pin1_4 | 175 | 180 | PF00397 | 0.352 |
DOC_WW_Pin1_4 | 317 | 322 | PF00397 | 0.437 |
DOC_WW_Pin1_4 | 397 | 402 | PF00397 | 0.593 |
DOC_WW_Pin1_4 | 455 | 460 | PF00397 | 0.636 |
DOC_WW_Pin1_4 | 61 | 66 | PF00397 | 0.371 |
DOC_WW_Pin1_4 | 654 | 659 | PF00397 | 0.487 |
DOC_WW_Pin1_4 | 761 | 766 | PF00397 | 0.478 |
LIG_14-3-3_CanoR_1 | 210 | 216 | PF00244 | 0.331 |
LIG_14-3-3_CanoR_1 | 340 | 349 | PF00244 | 0.400 |
LIG_14-3-3_CanoR_1 | 500 | 506 | PF00244 | 0.513 |
LIG_14-3-3_CanoR_1 | 654 | 658 | PF00244 | 0.586 |
LIG_14-3-3_CanoR_1 | 688 | 694 | PF00244 | 0.380 |
LIG_14-3-3_CanoR_1 | 728 | 733 | PF00244 | 0.354 |
LIG_14-3-3_CanoR_1 | 826 | 831 | PF00244 | 0.530 |
LIG_BRCT_BRCA1_1 | 127 | 131 | PF00533 | 0.354 |
LIG_BRCT_BRCA1_1 | 277 | 281 | PF00533 | 0.450 |
LIG_BRCT_BRCA1_1 | 318 | 322 | PF00533 | 0.433 |
LIG_deltaCOP1_diTrp_1 | 759 | 768 | PF00928 | 0.428 |
LIG_FHA_1 | 171 | 177 | PF00498 | 0.352 |
LIG_FHA_1 | 2 | 8 | PF00498 | 0.549 |
LIG_FHA_1 | 333 | 339 | PF00498 | 0.352 |
LIG_FHA_1 | 398 | 404 | PF00498 | 0.566 |
LIG_FHA_1 | 408 | 414 | PF00498 | 0.562 |
LIG_FHA_1 | 458 | 464 | PF00498 | 0.576 |
LIG_FHA_1 | 516 | 522 | PF00498 | 0.498 |
LIG_FHA_1 | 654 | 660 | PF00498 | 0.478 |
LIG_FHA_1 | 673 | 679 | PF00498 | 0.529 |
LIG_FHA_1 | 742 | 748 | PF00498 | 0.400 |
LIG_FHA_1 | 773 | 779 | PF00498 | 0.497 |
LIG_FHA_2 | 152 | 158 | PF00498 | 0.478 |
LIG_FHA_2 | 216 | 222 | PF00498 | 0.478 |
LIG_FHA_2 | 245 | 251 | PF00498 | 0.478 |
LIG_FHA_2 | 833 | 839 | PF00498 | 0.480 |
LIG_GBD_Chelix_1 | 425 | 433 | PF00786 | 0.438 |
LIG_LIR_Apic_2 | 128 | 134 | PF02991 | 0.406 |
LIG_LIR_Apic_2 | 439 | 443 | PF02991 | 0.532 |
LIG_LIR_Gen_1 | 235 | 245 | PF02991 | 0.330 |
LIG_LIR_Gen_1 | 4 | 13 | PF02991 | 0.540 |
LIG_LIR_Gen_1 | 504 | 514 | PF02991 | 0.463 |
LIG_LIR_Gen_1 | 818 | 825 | PF02991 | 0.533 |
LIG_LIR_Nem_3 | 224 | 229 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 235 | 240 | PF02991 | 0.281 |
LIG_LIR_Nem_3 | 297 | 302 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 4 | 8 | PF02991 | 0.531 |
LIG_LIR_Nem_3 | 496 | 502 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 619 | 625 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 818 | 824 | PF02991 | 0.540 |
LIG_LIR_Nem_3 | 829 | 833 | PF02991 | 0.533 |
LIG_MLH1_MIPbox_1 | 128 | 132 | PF16413 | 0.406 |
LIG_NRBOX | 428 | 434 | PF00104 | 0.530 |
LIG_NRBOX | 710 | 716 | PF00104 | 0.406 |
LIG_PCNA_PIPBox_1 | 379 | 388 | PF02747 | 0.477 |
LIG_Pex3_1 | 429 | 440 | PF04882 | 0.534 |
LIG_REV1ctd_RIR_1 | 330 | 338 | PF16727 | 0.387 |
LIG_RPA_C_Fungi | 417 | 429 | PF08784 | 0.486 |
LIG_RPA_C_Fungi | 701 | 713 | PF08784 | 0.303 |
LIG_SH2_CRK | 499 | 503 | PF00017 | 0.470 |
LIG_SH2_SRC | 520 | 523 | PF00017 | 0.495 |
LIG_SH2_STAT5 | 104 | 107 | PF00017 | 0.352 |
LIG_SH2_STAT5 | 151 | 154 | PF00017 | 0.379 |
LIG_SH2_STAT5 | 520 | 523 | PF00017 | 0.488 |
LIG_SH2_STAT5 | 538 | 541 | PF00017 | 0.290 |
LIG_SH2_STAT5 | 573 | 576 | PF00017 | 0.414 |
LIG_SH2_STAT5 | 784 | 787 | PF00017 | 0.485 |
LIG_SH2_STAT5 | 81 | 84 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 830 | 833 | PF00017 | 0.574 |
LIG_SH3_3 | 173 | 179 | PF00018 | 0.352 |
LIG_SH3_3 | 453 | 459 | PF00018 | 0.615 |
LIG_SH3_3 | 555 | 561 | PF00018 | 0.464 |
LIG_SH3_3 | 7 | 13 | PF00018 | 0.519 |
LIG_TRAF2_1 | 282 | 285 | PF00917 | 0.361 |
LIG_TRAF2_1 | 370 | 373 | PF00917 | 0.485 |
LIG_TRAF2_1 | 428 | 431 | PF00917 | 0.457 |
LIG_TRAF2_1 | 44 | 47 | PF00917 | 0.400 |
LIG_TRAF2_1 | 475 | 478 | PF00917 | 0.501 |
LIG_TYR_ITIM | 831 | 836 | PF00017 | 0.454 |
LIG_TYR_ITSM | 233 | 240 | PF00017 | 0.406 |
LIG_WRC_WIRS_1 | 437 | 442 | PF05994 | 0.530 |
MOD_CDK_SPxK_1 | 61 | 67 | PF00069 | 0.303 |
MOD_CDK_SPxxK_3 | 455 | 462 | PF00069 | 0.644 |
MOD_CK1_1 | 183 | 189 | PF00069 | 0.459 |
MOD_CK1_1 | 317 | 323 | PF00069 | 0.416 |
MOD_CK1_1 | 665 | 671 | PF00069 | 0.503 |
MOD_CK1_1 | 787 | 793 | PF00069 | 0.619 |
MOD_CK1_1 | 85 | 91 | PF00069 | 0.352 |
MOD_CK2_1 | 244 | 250 | PF00069 | 0.416 |
MOD_CK2_1 | 340 | 346 | PF00069 | 0.415 |
MOD_CK2_1 | 41 | 47 | PF00069 | 0.468 |
MOD_CK2_1 | 587 | 593 | PF00069 | 0.665 |
MOD_CK2_1 | 609 | 615 | PF00069 | 0.596 |
MOD_CK2_1 | 832 | 838 | PF00069 | 0.586 |
MOD_CK2_1 | 857 | 863 | PF00069 | 0.572 |
MOD_Cter_Amidation | 355 | 358 | PF01082 | 0.352 |
MOD_GlcNHglycan | 293 | 296 | PF01048 | 0.390 |
MOD_GlcNHglycan | 395 | 398 | PF01048 | 0.607 |
MOD_GlcNHglycan | 43 | 46 | PF01048 | 0.341 |
MOD_GlcNHglycan | 706 | 709 | PF01048 | 0.406 |
MOD_GlcNHglycan | 738 | 741 | PF01048 | 0.356 |
MOD_GlcNHglycan | 787 | 790 | PF01048 | 0.614 |
MOD_GlcNHglycan | 792 | 795 | PF01048 | 0.612 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.352 |
MOD_GlcNHglycan | 863 | 867 | PF01048 | 0.535 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.360 |
MOD_GSK3_1 | 170 | 177 | PF00069 | 0.384 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.352 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.147 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.399 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.400 |
MOD_GSK3_1 | 393 | 400 | PF00069 | 0.534 |
MOD_GSK3_1 | 447 | 454 | PF00069 | 0.510 |
MOD_GSK3_1 | 457 | 464 | PF00069 | 0.573 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.426 |
MOD_GSK3_1 | 783 | 790 | PF00069 | 0.546 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.354 |
MOD_GSK3_1 | 815 | 822 | PF00069 | 0.548 |
MOD_N-GLC_1 | 47 | 52 | PF02516 | 0.395 |
MOD_N-GLC_1 | 815 | 820 | PF02516 | 0.599 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.499 |
MOD_NEK2_1 | 125 | 130 | PF00069 | 0.352 |
MOD_NEK2_1 | 215 | 220 | PF00069 | 0.406 |
MOD_NEK2_1 | 291 | 296 | PF00069 | 0.400 |
MOD_NEK2_1 | 447 | 452 | PF00069 | 0.357 |
MOD_NEK2_1 | 531 | 536 | PF00069 | 0.419 |
MOD_NEK2_1 | 702 | 707 | PF00069 | 0.478 |
MOD_NEK2_1 | 783 | 788 | PF00069 | 0.534 |
MOD_NEK2_2 | 617 | 622 | PF00069 | 0.460 |
MOD_NEK2_2 | 832 | 837 | PF00069 | 0.433 |
MOD_PIKK_1 | 151 | 157 | PF00454 | 0.406 |
MOD_PIKK_1 | 209 | 215 | PF00454 | 0.399 |
MOD_PIKK_1 | 384 | 390 | PF00454 | 0.469 |
MOD_PIKK_1 | 463 | 469 | PF00454 | 0.596 |
MOD_PKA_1 | 826 | 832 | PF00069 | 0.544 |
MOD_PKA_2 | 209 | 215 | PF00069 | 0.331 |
MOD_PKA_2 | 653 | 659 | PF00069 | 0.590 |
MOD_PKA_2 | 687 | 693 | PF00069 | 0.380 |
MOD_PKA_2 | 819 | 825 | PF00069 | 0.556 |
MOD_Plk_1 | 232 | 238 | PF00069 | 0.352 |
MOD_Plk_1 | 33 | 39 | PF00069 | 0.489 |
MOD_Plk_1 | 73 | 79 | PF00069 | 0.420 |
MOD_Plk_4 | 145 | 151 | PF00069 | 0.474 |
MOD_Plk_4 | 190 | 196 | PF00069 | 0.420 |
MOD_Plk_4 | 232 | 238 | PF00069 | 0.352 |
MOD_Plk_4 | 34 | 40 | PF00069 | 0.478 |
MOD_Plk_4 | 436 | 442 | PF00069 | 0.491 |
MOD_Plk_4 | 617 | 623 | PF00069 | 0.451 |
MOD_Plk_4 | 728 | 734 | PF00069 | 0.379 |
MOD_Plk_4 | 826 | 832 | PF00069 | 0.622 |
MOD_ProDKin_1 | 126 | 132 | PF00069 | 0.376 |
MOD_ProDKin_1 | 142 | 148 | PF00069 | 0.147 |
MOD_ProDKin_1 | 175 | 181 | PF00069 | 0.352 |
MOD_ProDKin_1 | 317 | 323 | PF00069 | 0.437 |
MOD_ProDKin_1 | 397 | 403 | PF00069 | 0.583 |
MOD_ProDKin_1 | 455 | 461 | PF00069 | 0.642 |
MOD_ProDKin_1 | 61 | 67 | PF00069 | 0.371 |
MOD_ProDKin_1 | 654 | 660 | PF00069 | 0.480 |
MOD_ProDKin_1 | 761 | 767 | PF00069 | 0.476 |
MOD_SUMO_rev_2 | 359 | 364 | PF00179 | 0.478 |
MOD_SUMO_rev_2 | 583 | 592 | PF00179 | 0.655 |
MOD_SUMO_rev_2 | 85 | 94 | PF00179 | 0.352 |
TRG_DiLeu_BaEn_1 | 743 | 748 | PF01217 | 0.406 |
TRG_DiLeu_BaLyEn_6 | 162 | 167 | PF01217 | 0.474 |
TRG_DiLeu_BaLyEn_6 | 599 | 604 | PF01217 | 0.666 |
TRG_DiLeu_BaLyEn_6 | 633 | 638 | PF01217 | 0.516 |
TRG_DiLeu_BaLyEn_6 | 710 | 715 | PF01217 | 0.428 |
TRG_DiLeu_LyEn_5 | 743 | 748 | PF01217 | 0.478 |
TRG_ENDOCYTIC_2 | 237 | 240 | PF00928 | 0.330 |
TRG_ENDOCYTIC_2 | 299 | 302 | PF00928 | 0.456 |
TRG_ENDOCYTIC_2 | 499 | 502 | PF00928 | 0.471 |
TRG_ENDOCYTIC_2 | 538 | 541 | PF00928 | 0.423 |
TRG_ENDOCYTIC_2 | 833 | 836 | PF00928 | 0.461 |
TRG_ER_diArg_1 | 23 | 25 | PF00400 | 0.373 |
TRG_ER_diArg_1 | 261 | 264 | PF00400 | 0.478 |
TRG_ER_diArg_1 | 354 | 357 | PF00400 | 0.428 |
TRG_ER_diArg_1 | 443 | 445 | PF00400 | 0.455 |
TRG_ER_diArg_1 | 711 | 713 | PF00400 | 0.400 |
TRG_ER_diArg_1 | 810 | 812 | PF00400 | 0.704 |
TRG_ER_diArg_1 | 841 | 843 | PF00400 | 0.521 |
TRG_NES_CRM1_1 | 672 | 684 | PF08389 | 0.406 |
TRG_NLS_Bipartite_1 | 809 | 830 | PF00514 | 0.600 |
TRG_NLS_MonoCore_2 | 808 | 813 | PF00514 | 0.698 |
TRG_NLS_MonoExtN_4 | 823 | 830 | PF00514 | 0.541 |
TRG_Pf-PMV_PEXEL_1 | 107 | 111 | PF00026 | 0.478 |
TRG_Pf-PMV_PEXEL_1 | 712 | 716 | PF00026 | 0.405 |
TRG_Pf-PMV_PEXEL_1 | 746 | 750 | PF00026 | 0.361 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I5E5 | Leptomonas seymouri | 54% | 85% |
A0A0S4JM65 | Bodo saltans | 30% | 73% |
A0A3Q8IEY8 | Leishmania donovani | 99% | 87% |
A4HGQ9 | Leishmania braziliensis | 80% | 100% |
E9B025 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
M1W600 | Claviceps purpurea (strain 20.1) | 24% | 67% |
Q4Q861 | Leishmania major | 95% | 100% |
Q8J0L6 | Claviceps purpurea | 24% | 66% |