Fast evolving protein with mostly disordered structure. Possibly coat proteins.
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: 2 |
NetGPI | no | yes: 0, no: 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005789 | endoplasmic reticulum membrane | 4 | 1 |
GO:0016020 | membrane | 2 | 1 |
GO:0031090 | organelle membrane | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HT83
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0006950 | response to stress | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0009057 | macromolecule catabolic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010033 | response to organic substance | 3 | 1 |
GO:0010243 | response to organonitrogen compound | 4 | 1 |
GO:0010498 | proteasomal protein catabolic process | 5 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0030163 | protein catabolic process | 4 | 1 |
GO:0033554 | cellular response to stress | 3 | 1 |
GO:0034976 | response to endoplasmic reticulum stress | 4 | 1 |
GO:0036503 | ERAD pathway | 5 | 1 |
GO:0042221 | response to chemical | 2 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0050896 | response to stimulus | 1 | 1 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 1 |
GO:0051716 | cellular response to stimulus | 2 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
GO:1901565 | organonitrogen compound catabolic process | 4 | 1 |
GO:1901575 | organic substance catabolic process | 3 | 1 |
GO:1901698 | response to nitrogen compound | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 218 | 222 | PF00656 | 0.836 |
CLV_C14_Caspase3-7 | 393 | 397 | PF00656 | 0.876 |
CLV_C14_Caspase3-7 | 402 | 406 | PF00656 | 0.692 |
CLV_C14_Caspase3-7 | 41 | 45 | PF00656 | 0.549 |
CLV_C14_Caspase3-7 | 462 | 466 | PF00656 | 0.658 |
CLV_NRD_NRD_1 | 100 | 102 | PF00675 | 0.648 |
CLV_NRD_NRD_1 | 138 | 140 | PF00675 | 0.549 |
CLV_NRD_NRD_1 | 179 | 181 | PF00675 | 0.549 |
CLV_NRD_NRD_1 | 274 | 276 | PF00675 | 0.549 |
CLV_NRD_NRD_1 | 96 | 98 | PF00675 | 0.722 |
CLV_PCSK_FUR_1 | 379 | 383 | PF00082 | 0.856 |
CLV_PCSK_KEX2_1 | 100 | 102 | PF00082 | 0.718 |
CLV_PCSK_KEX2_1 | 138 | 140 | PF00082 | 0.549 |
CLV_PCSK_KEX2_1 | 179 | 181 | PF00082 | 0.549 |
CLV_PCSK_KEX2_1 | 274 | 276 | PF00082 | 0.549 |
CLV_PCSK_KEX2_1 | 381 | 383 | PF00082 | 0.862 |
CLV_PCSK_KEX2_1 | 768 | 770 | PF00082 | 0.844 |
CLV_PCSK_PC1ET2_1 | 381 | 383 | PF00082 | 0.629 |
CLV_PCSK_PC1ET2_1 | 768 | 770 | PF00082 | 0.844 |
CLV_PCSK_SKI1_1 | 179 | 183 | PF00082 | 0.549 |
CLV_PCSK_SKI1_1 | 274 | 278 | PF00082 | 0.549 |
CLV_PCSK_SKI1_1 | 279 | 283 | PF00082 | 0.462 |
CLV_PCSK_SKI1_1 | 532 | 536 | PF00082 | 0.644 |
CLV_PCSK_SKI1_1 | 769 | 773 | PF00082 | 0.838 |
CLV_Separin_Metazoa | 621 | 625 | PF03568 | 0.775 |
DEG_APCC_DBOX_1 | 100 | 108 | PF00400 | 0.679 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.437 |
DEG_SPOP_SBC_1 | 446 | 450 | PF00917 | 0.773 |
DOC_CYCLIN_RxL_1 | 270 | 278 | PF00134 | 0.549 |
DOC_CYCLIN_RxL_1 | 310 | 321 | PF00134 | 0.639 |
DOC_CYCLIN_RxL_1 | 97 | 106 | PF00134 | 0.699 |
DOC_CYCLIN_yCln2_LP_2 | 501 | 507 | PF00134 | 0.466 |
DOC_MAPK_gen_1 | 21 | 28 | PF00069 | 0.549 |
DOC_MAPK_gen_1 | 75 | 84 | PF00069 | 0.811 |
DOC_MAPK_gen_1 | 97 | 107 | PF00069 | 0.693 |
DOC_MAPK_MEF2A_6 | 21 | 28 | PF00069 | 0.491 |
DOC_MAPK_MEF2A_6 | 692 | 699 | PF00069 | 0.712 |
DOC_MAPK_NFAT4_5 | 21 | 29 | PF00069 | 0.549 |
DOC_PP4_FxxP_1 | 410 | 413 | PF00568 | 0.788 |
DOC_USP7_MATH_1 | 377 | 381 | PF00917 | 0.616 |
DOC_USP7_MATH_1 | 403 | 407 | PF00917 | 0.617 |
DOC_USP7_MATH_1 | 466 | 470 | PF00917 | 0.620 |
DOC_USP7_MATH_1 | 493 | 497 | PF00917 | 0.759 |
DOC_USP7_MATH_1 | 520 | 524 | PF00917 | 0.430 |
DOC_USP7_MATH_1 | 54 | 58 | PF00917 | 0.771 |
DOC_USP7_MATH_1 | 732 | 736 | PF00917 | 0.842 |
DOC_USP7_MATH_1 | 91 | 95 | PF00917 | 0.742 |
DOC_WW_Pin1_4 | 168 | 173 | PF00397 | 0.549 |
DOC_WW_Pin1_4 | 482 | 487 | PF00397 | 0.733 |
DOC_WW_Pin1_4 | 509 | 514 | PF00397 | 0.510 |
DOC_WW_Pin1_4 | 557 | 562 | PF00397 | 0.549 |
DOC_WW_Pin1_4 | 645 | 650 | PF00397 | 0.790 |
DOC_WW_Pin1_4 | 724 | 729 | PF00397 | 0.844 |
LIG_14-3-3_CanoR_1 | 320 | 325 | PF00244 | 0.668 |
LIG_14-3-3_CanoR_1 | 412 | 421 | PF00244 | 0.734 |
LIG_14-3-3_CanoR_1 | 664 | 670 | PF00244 | 0.752 |
LIG_BIR_III_4 | 796 | 800 | PF00653 | 0.765 |
LIG_BRCT_BRCA1_1 | 647 | 651 | PF00533 | 0.782 |
LIG_BRCT_BRCA1_1 | 80 | 84 | PF00533 | 0.794 |
LIG_CaM_IQ_9 | 703 | 719 | PF13499 | 0.704 |
LIG_EH1_1 | 712 | 720 | PF00400 | 0.520 |
LIG_eIF4E_1 | 254 | 260 | PF01652 | 0.549 |
LIG_FHA_1 | 402 | 408 | PF00498 | 0.616 |
LIG_FHA_1 | 446 | 452 | PF00498 | 0.760 |
LIG_FHA_1 | 603 | 609 | PF00498 | 0.749 |
LIG_FHA_1 | 682 | 688 | PF00498 | 0.580 |
LIG_FHA_1 | 778 | 784 | PF00498 | 0.531 |
LIG_FHA_2 | 216 | 222 | PF00498 | 0.824 |
LIG_LIR_Apic_2 | 803 | 807 | PF02991 | 0.511 |
LIG_LIR_Gen_1 | 121 | 131 | PF02991 | 0.549 |
LIG_LIR_Gen_1 | 4 | 12 | PF02991 | 0.639 |
LIG_LIR_Gen_1 | 416 | 427 | PF02991 | 0.712 |
LIG_LIR_Gen_1 | 453 | 461 | PF02991 | 0.656 |
LIG_LIR_Gen_1 | 469 | 476 | PF02991 | 0.334 |
LIG_LIR_Gen_1 | 477 | 487 | PF02991 | 0.563 |
LIG_LIR_Gen_1 | 524 | 535 | PF02991 | 0.620 |
LIG_LIR_Nem_3 | 121 | 127 | PF02991 | 0.549 |
LIG_LIR_Nem_3 | 130 | 134 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 405 | 411 | PF02991 | 0.706 |
LIG_LIR_Nem_3 | 416 | 422 | PF02991 | 0.653 |
LIG_LIR_Nem_3 | 453 | 457 | PF02991 | 0.671 |
LIG_LIR_Nem_3 | 469 | 473 | PF02991 | 0.329 |
LIG_LIR_Nem_3 | 477 | 482 | PF02991 | 0.527 |
LIG_LIR_Nem_3 | 524 | 530 | PF02991 | 0.603 |
LIG_LIR_Nem_3 | 803 | 808 | PF02991 | 0.510 |
LIG_LIR_Nem_3 | 81 | 87 | PF02991 | 0.793 |
LIG_MYND_1 | 172 | 176 | PF01753 | 0.549 |
LIG_NRBOX | 121 | 127 | PF00104 | 0.549 |
LIG_NRBOX | 525 | 531 | PF00104 | 0.610 |
LIG_PCNA_yPIPBox_3 | 282 | 296 | PF02747 | 0.630 |
LIG_Pex14_2 | 588 | 592 | PF04695 | 0.614 |
LIG_PTB_Apo_2 | 550 | 557 | PF02174 | 0.549 |
LIG_PTB_Apo_2 | 586 | 593 | PF02174 | 0.607 |
LIG_PTB_Phospho_1 | 550 | 556 | PF10480 | 0.549 |
LIG_REV1ctd_RIR_1 | 82 | 92 | PF16727 | 0.784 |
LIG_SH2_CRK | 131 | 135 | PF00017 | 0.549 |
LIG_SH2_CRK | 408 | 412 | PF00017 | 0.691 |
LIG_SH2_CRK | 419 | 423 | PF00017 | 0.647 |
LIG_SH2_CRK | 527 | 531 | PF00017 | 0.614 |
LIG_SH2_CRK | 814 | 818 | PF00017 | 0.719 |
LIG_SH2_GRB2like | 626 | 629 | PF00017 | 0.535 |
LIG_SH2_NCK_1 | 626 | 630 | PF00017 | 0.777 |
LIG_SH2_SRC | 479 | 482 | PF00017 | 0.664 |
LIG_SH2_STAP1 | 3 | 7 | PF00017 | 0.631 |
LIG_SH2_STAP1 | 683 | 687 | PF00017 | 0.618 |
LIG_SH2_STAT3 | 208 | 211 | PF00017 | 0.644 |
LIG_SH2_STAT5 | 124 | 127 | PF00017 | 0.549 |
LIG_SH2_STAT5 | 143 | 146 | PF00017 | 0.217 |
LIG_SH2_STAT5 | 208 | 211 | PF00017 | 0.644 |
LIG_SH2_STAT5 | 243 | 246 | PF00017 | 0.624 |
LIG_SH2_STAT5 | 475 | 478 | PF00017 | 0.642 |
LIG_SH2_STAT5 | 479 | 482 | PF00017 | 0.594 |
LIG_SH2_STAT5 | 515 | 518 | PF00017 | 0.666 |
LIG_SH2_STAT5 | 548 | 551 | PF00017 | 0.549 |
LIG_SH2_STAT5 | 626 | 629 | PF00017 | 0.769 |
LIG_SH2_STAT5 | 644 | 647 | PF00017 | 0.465 |
LIG_SH2_STAT5 | 677 | 680 | PF00017 | 0.644 |
LIG_SH2_STAT5 | 683 | 686 | PF00017 | 0.506 |
LIG_SH3_3 | 170 | 176 | PF00018 | 0.549 |
LIG_SUMO_SIM_anti_2 | 453 | 459 | PF11976 | 0.667 |
LIG_SUMO_SIM_anti_2 | 818 | 823 | PF11976 | 0.724 |
LIG_SUMO_SIM_par_1 | 456 | 463 | PF11976 | 0.652 |
LIG_TRAF2_1 | 432 | 435 | PF00917 | 0.748 |
LIG_TRAF2_1 | 612 | 615 | PF00917 | 0.762 |
LIG_TYR_ITIM | 122 | 127 | PF00017 | 0.549 |
LIG_TYR_ITIM | 525 | 530 | PF00017 | 0.604 |
LIG_TYR_ITIM | 571 | 576 | PF00017 | 0.549 |
LIG_TYR_ITIM | 812 | 817 | PF00017 | 0.715 |
LIG_UBA3_1 | 104 | 108 | PF00899 | 0.663 |
LIG_WRC_WIRS_1 | 2 | 7 | PF05994 | 0.639 |
LIG_WRC_WIRS_1 | 451 | 456 | PF05994 | 0.695 |
LIG_WW_1 | 641 | 644 | PF00397 | 0.771 |
MOD_CK1_1 | 297 | 303 | PF00069 | 0.748 |
MOD_CK1_1 | 31 | 37 | PF00069 | 0.549 |
MOD_CK1_1 | 323 | 329 | PF00069 | 0.748 |
MOD_CK1_1 | 436 | 442 | PF00069 | 0.811 |
MOD_CK1_1 | 450 | 456 | PF00069 | 0.456 |
MOD_CK1_1 | 724 | 730 | PF00069 | 0.844 |
MOD_CK1_1 | 735 | 741 | PF00069 | 0.648 |
MOD_CK2_1 | 219 | 225 | PF00069 | 0.622 |
MOD_CK2_1 | 386 | 392 | PF00069 | 0.876 |
MOD_CK2_1 | 412 | 418 | PF00069 | 0.741 |
MOD_CK2_1 | 436 | 442 | PF00069 | 0.811 |
MOD_CK2_1 | 450 | 456 | PF00069 | 0.456 |
MOD_CK2_1 | 609 | 615 | PF00069 | 0.768 |
MOD_CK2_1 | 738 | 744 | PF00069 | 0.837 |
MOD_Cter_Amidation | 136 | 139 | PF01082 | 0.549 |
MOD_Cter_Amidation | 766 | 769 | PF01082 | 0.610 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.639 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.789 |
MOD_GlcNHglycan | 33 | 36 | PF01048 | 0.549 |
MOD_GlcNHglycan | 336 | 339 | PF01048 | 0.636 |
MOD_GlcNHglycan | 387 | 391 | PF01048 | 0.865 |
MOD_GlcNHglycan | 495 | 498 | PF01048 | 0.725 |
MOD_GlcNHglycan | 516 | 519 | PF01048 | 0.550 |
MOD_GlcNHglycan | 56 | 59 | PF01048 | 0.799 |
MOD_GlcNHglycan | 611 | 614 | PF01048 | 0.760 |
MOD_GlcNHglycan | 665 | 668 | PF01048 | 0.747 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.563 |
MOD_GlcNHglycan | 724 | 727 | PF01048 | 0.829 |
MOD_GlcNHglycan | 732 | 735 | PF01048 | 0.692 |
MOD_GlcNHglycan | 737 | 740 | PF01048 | 0.604 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.712 |
MOD_GlcNHglycan | 796 | 800 | PF01048 | 0.532 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.584 |
MOD_GSK3_1 | 382 | 389 | PF00069 | 0.870 |
MOD_GSK3_1 | 433 | 440 | PF00069 | 0.779 |
MOD_GSK3_1 | 446 | 453 | PF00069 | 0.524 |
MOD_GSK3_1 | 456 | 463 | PF00069 | 0.477 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.678 |
MOD_GSK3_1 | 535 | 542 | PF00069 | 0.684 |
MOD_GSK3_1 | 724 | 731 | PF00069 | 0.846 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.811 |
MOD_GSK3_1 | 775 | 782 | PF00069 | 0.757 |
MOD_LATS_1 | 489 | 495 | PF00433 | 0.558 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.498 |
MOD_NEK2_1 | 244 | 249 | PF00069 | 0.616 |
MOD_NEK2_1 | 375 | 380 | PF00069 | 0.614 |
MOD_NEK2_1 | 530 | 535 | PF00069 | 0.635 |
MOD_NEK2_1 | 651 | 656 | PF00069 | 0.515 |
MOD_NEK2_1 | 713 | 718 | PF00069 | 0.644 |
MOD_NEK2_1 | 722 | 727 | PF00069 | 0.783 |
MOD_NEK2_1 | 779 | 784 | PF00069 | 0.705 |
MOD_NEK2_2 | 403 | 408 | PF00069 | 0.615 |
MOD_NEK2_2 | 683 | 688 | PF00069 | 0.631 |
MOD_NEK2_2 | 80 | 85 | PF00069 | 0.790 |
MOD_PK_1 | 282 | 288 | PF00069 | 0.549 |
MOD_PKA_2 | 334 | 340 | PF00069 | 0.639 |
MOD_PKA_2 | 602 | 608 | PF00069 | 0.739 |
MOD_PKA_2 | 663 | 669 | PF00069 | 0.753 |
MOD_PKA_2 | 691 | 697 | PF00069 | 0.722 |
MOD_Plk_1 | 433 | 439 | PF00069 | 0.775 |
MOD_Plk_1 | 750 | 756 | PF00069 | 0.825 |
MOD_Plk_2-3 | 456 | 462 | PF00069 | 0.647 |
MOD_Plk_4 | 282 | 288 | PF00069 | 0.549 |
MOD_Plk_4 | 403 | 409 | PF00069 | 0.615 |
MOD_Plk_4 | 433 | 439 | PF00069 | 0.775 |
MOD_Plk_4 | 450 | 456 | PF00069 | 0.404 |
MOD_Plk_4 | 466 | 472 | PF00069 | 0.339 |
MOD_Plk_4 | 750 | 756 | PF00069 | 0.825 |
MOD_Plk_4 | 797 | 803 | PF00069 | 0.765 |
MOD_Plk_4 | 80 | 86 | PF00069 | 0.789 |
MOD_ProDKin_1 | 168 | 174 | PF00069 | 0.549 |
MOD_ProDKin_1 | 482 | 488 | PF00069 | 0.743 |
MOD_ProDKin_1 | 509 | 515 | PF00069 | 0.505 |
MOD_ProDKin_1 | 557 | 563 | PF00069 | 0.549 |
MOD_ProDKin_1 | 645 | 651 | PF00069 | 0.787 |
MOD_ProDKin_1 | 724 | 730 | PF00069 | 0.844 |
TRG_DiLeu_BaEn_1 | 418 | 423 | PF01217 | 0.711 |
TRG_DiLeu_BaLyEn_6 | 170 | 175 | PF01217 | 0.549 |
TRG_DiLeu_BaLyEn_6 | 370 | 375 | PF01217 | 0.615 |
TRG_DiLeu_BaLyEn_6 | 714 | 719 | PF01217 | 0.757 |
TRG_ENDOCYTIC_2 | 124 | 127 | PF00928 | 0.549 |
TRG_ENDOCYTIC_2 | 131 | 134 | PF00928 | 0.427 |
TRG_ENDOCYTIC_2 | 2 | 5 | PF00928 | 0.652 |
TRG_ENDOCYTIC_2 | 408 | 411 | PF00928 | 0.693 |
TRG_ENDOCYTIC_2 | 419 | 422 | PF00928 | 0.651 |
TRG_ENDOCYTIC_2 | 479 | 482 | PF00928 | 0.664 |
TRG_ENDOCYTIC_2 | 527 | 530 | PF00928 | 0.606 |
TRG_ENDOCYTIC_2 | 548 | 551 | PF00928 | 0.549 |
TRG_ENDOCYTIC_2 | 573 | 576 | PF00928 | 0.549 |
TRG_ENDOCYTIC_2 | 805 | 808 | PF00928 | 0.739 |
TRG_ENDOCYTIC_2 | 814 | 817 | PF00928 | 0.558 |
TRG_ER_diArg_1 | 100 | 102 | PF00400 | 0.718 |
TRG_ER_diArg_1 | 178 | 180 | PF00400 | 0.549 |
TRG_ER_diArg_1 | 274 | 276 | PF00400 | 0.549 |
TRG_ER_diArg_1 | 411 | 414 | PF00400 | 0.778 |
TRG_NES_CRM1_1 | 117 | 130 | PF08389 | 0.549 |
TRG_NES_CRM1_1 | 177 | 191 | PF08389 | 0.549 |
TRG_NLS_MonoExtC_3 | 96 | 101 | PF00514 | 0.718 |
TRG_Pf-PMV_PEXEL_1 | 274 | 278 | PF00026 | 0.549 |
TRG_Pf-PMV_PEXEL_1 | 717 | 721 | PF00026 | 0.795 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
Q4QIN3 | Leishmania major | 94% | 66% |