Metal Binding, 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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4IDC4
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0016567 | protein ubiquitination | 7 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0032446 | protein modification by small protein conjugation | 6 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 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 | 7 |
GO:0008270 | zinc ion binding | 6 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043169 | cation binding | 3 | 7 |
GO:0046872 | metal ion binding | 4 | 7 |
GO:0046914 | transition metal ion binding | 5 | 7 |
GO:0003824 | catalytic activity | 1 | 1 |
GO:0004842 | ubiquitin-protein transferase activity | 4 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
GO:0019787 | ubiquitin-like protein transferase activity | 3 | 1 |
GO:0061630 | ubiquitin protein ligase activity | 5 | 1 |
GO:0061659 | ubiquitin-like protein ligase activity | 4 | 1 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 679 | 683 | PF00656 | 0.636 |
CLV_C14_Caspase3-7 | 783 | 787 | PF00656 | 0.724 |
CLV_C14_Caspase3-7 | 821 | 825 | PF00656 | 0.641 |
CLV_NRD_NRD_1 | 273 | 275 | PF00675 | 0.583 |
CLV_NRD_NRD_1 | 397 | 399 | PF00675 | 0.533 |
CLV_NRD_NRD_1 | 421 | 423 | PF00675 | 0.571 |
CLV_NRD_NRD_1 | 812 | 814 | PF00675 | 0.799 |
CLV_NRD_NRD_1 | 839 | 841 | PF00675 | 0.734 |
CLV_PCSK_FUR_1 | 419 | 423 | PF00082 | 0.571 |
CLV_PCSK_KEX2_1 | 272 | 274 | PF00082 | 0.581 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.685 |
CLV_PCSK_KEX2_1 | 397 | 399 | PF00082 | 0.533 |
CLV_PCSK_KEX2_1 | 421 | 423 | PF00082 | 0.571 |
CLV_PCSK_KEX2_1 | 498 | 500 | PF00082 | 0.648 |
CLV_PCSK_KEX2_1 | 839 | 841 | PF00082 | 0.731 |
CLV_PCSK_PC1ET2_1 | 3 | 5 | PF00082 | 0.685 |
CLV_PCSK_PC1ET2_1 | 498 | 500 | PF00082 | 0.640 |
CLV_PCSK_SKI1_1 | 374 | 378 | PF00082 | 0.529 |
CLV_PCSK_SKI1_1 | 40 | 44 | PF00082 | 0.712 |
CLV_PCSK_SKI1_1 | 498 | 502 | PF00082 | 0.638 |
CLV_PCSK_SKI1_1 | 596 | 600 | PF00082 | 0.614 |
CLV_PCSK_SKI1_1 | 703 | 707 | PF00082 | 0.644 |
CLV_PCSK_SKI1_1 | 743 | 747 | PF00082 | 0.572 |
CLV_PCSK_SKI1_1 | 774 | 778 | PF00082 | 0.664 |
DOC_CKS1_1 | 597 | 602 | PF01111 | 0.749 |
DOC_CYCLIN_RxL_1 | 771 | 782 | PF00134 | 0.805 |
DOC_CYCLIN_RxL_1 | 803 | 816 | PF00134 | 0.584 |
DOC_CYCLIN_yCln2_LP_2 | 80 | 86 | PF00134 | 0.521 |
DOC_MAPK_gen_1 | 3 | 11 | PF00069 | 0.700 |
DOC_MAPK_gen_1 | 734 | 742 | PF00069 | 0.775 |
DOC_MAPK_gen_1 | 839 | 846 | PF00069 | 0.730 |
DOC_MAPK_MEF2A_6 | 839 | 848 | PF00069 | 0.725 |
DOC_MAPK_RevD_3 | 383 | 398 | PF00069 | 0.562 |
DOC_PP2B_LxvP_1 | 62 | 65 | PF13499 | 0.714 |
DOC_PP2B_LxvP_1 | 827 | 830 | PF13499 | 0.699 |
DOC_PP4_FxxP_1 | 70 | 73 | PF00568 | 0.483 |
DOC_USP7_MATH_1 | 188 | 192 | PF00917 | 0.495 |
DOC_USP7_MATH_1 | 219 | 223 | PF00917 | 0.698 |
DOC_USP7_MATH_1 | 22 | 26 | PF00917 | 0.709 |
DOC_USP7_MATH_1 | 225 | 229 | PF00917 | 0.497 |
DOC_USP7_MATH_1 | 598 | 602 | PF00917 | 0.735 |
DOC_USP7_MATH_1 | 606 | 610 | PF00917 | 0.678 |
DOC_USP7_MATH_1 | 73 | 77 | PF00917 | 0.610 |
DOC_USP7_MATH_1 | 791 | 795 | PF00917 | 0.737 |
DOC_USP7_MATH_1 | 822 | 826 | PF00917 | 0.782 |
DOC_WW_Pin1_4 | 145 | 150 | PF00397 | 0.734 |
DOC_WW_Pin1_4 | 221 | 226 | PF00397 | 0.585 |
DOC_WW_Pin1_4 | 425 | 430 | PF00397 | 0.549 |
DOC_WW_Pin1_4 | 485 | 490 | PF00397 | 0.674 |
DOC_WW_Pin1_4 | 596 | 601 | PF00397 | 0.749 |
DOC_WW_Pin1_4 | 723 | 728 | PF00397 | 0.583 |
DOC_WW_Pin1_4 | 92 | 97 | PF00397 | 0.739 |
LIG_14-3-3_CanoR_1 | 252 | 260 | PF00244 | 0.615 |
LIG_14-3-3_CanoR_1 | 278 | 285 | PF00244 | 0.474 |
LIG_14-3-3_CanoR_1 | 387 | 395 | PF00244 | 0.548 |
LIG_14-3-3_CanoR_1 | 397 | 406 | PF00244 | 0.481 |
LIG_14-3-3_CanoR_1 | 4 | 11 | PF00244 | 0.562 |
LIG_14-3-3_CanoR_1 | 40 | 47 | PF00244 | 0.715 |
LIG_14-3-3_CanoR_1 | 448 | 454 | PF00244 | 0.547 |
LIG_14-3-3_CanoR_1 | 477 | 482 | PF00244 | 0.649 |
LIG_14-3-3_CanoR_1 | 629 | 636 | PF00244 | 0.814 |
LIG_14-3-3_CanoR_1 | 797 | 807 | PF00244 | 0.723 |
LIG_14-3-3_CanoR_1 | 839 | 846 | PF00244 | 0.725 |
LIG_Actin_WH2_2 | 359 | 376 | PF00022 | 0.511 |
LIG_Actin_WH2_2 | 388 | 405 | PF00022 | 0.638 |
LIG_APCC_ABBA_1 | 287 | 292 | PF00400 | 0.411 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.686 |
LIG_BIR_III_4 | 342 | 346 | PF00653 | 0.512 |
LIG_BRCT_BRCA1_1 | 66 | 70 | PF00533 | 0.648 |
LIG_deltaCOP1_diTrp_1 | 118 | 127 | PF00928 | 0.510 |
LIG_DLG_GKlike_1 | 477 | 484 | PF00625 | 0.646 |
LIG_EH1_1 | 406 | 414 | PF00400 | 0.530 |
LIG_EVH1_2 | 642 | 646 | PF00568 | 0.597 |
LIG_FHA_1 | 449 | 455 | PF00498 | 0.597 |
LIG_FHA_1 | 585 | 591 | PF00498 | 0.791 |
LIG_FHA_1 | 597 | 603 | PF00498 | 0.664 |
LIG_FHA_1 | 659 | 665 | PF00498 | 0.776 |
LIG_FHA_1 | 687 | 693 | PF00498 | 0.816 |
LIG_FHA_1 | 799 | 805 | PF00498 | 0.707 |
LIG_FHA_1 | 839 | 845 | PF00498 | 0.701 |
LIG_FHA_2 | 101 | 107 | PF00498 | 0.672 |
LIG_FHA_2 | 166 | 172 | PF00498 | 0.465 |
LIG_FHA_2 | 3 | 9 | PF00498 | 0.601 |
LIG_FHA_2 | 436 | 442 | PF00498 | 0.553 |
LIG_FHA_2 | 486 | 492 | PF00498 | 0.646 |
LIG_FHA_2 | 50 | 56 | PF00498 | 0.668 |
LIG_LIR_Apic_2 | 67 | 73 | PF02991 | 0.511 |
LIG_LIR_Gen_1 | 224 | 233 | PF02991 | 0.535 |
LIG_LIR_Gen_1 | 480 | 489 | PF02991 | 0.616 |
LIG_LIR_Gen_1 | 572 | 581 | PF02991 | 0.580 |
LIG_LIR_Nem_3 | 145 | 150 | PF02991 | 0.642 |
LIG_LIR_Nem_3 | 224 | 229 | PF02991 | 0.537 |
LIG_LIR_Nem_3 | 349 | 355 | PF02991 | 0.532 |
LIG_LIR_Nem_3 | 480 | 484 | PF02991 | 0.618 |
LIG_LIR_Nem_3 | 572 | 578 | PF02991 | 0.573 |
LIG_LIR_Nem_3 | 67 | 71 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 697 | 702 | PF02991 | 0.791 |
LIG_MYND_1 | 69 | 73 | PF01753 | 0.483 |
LIG_MYND_2 | 747 | 751 | PF01753 | 0.587 |
LIG_PDZ_Class_2 | 843 | 848 | PF00595 | 0.722 |
LIG_Pex14_2 | 348 | 352 | PF04695 | 0.405 |
LIG_PTAP_UEV_1 | 215 | 220 | PF05743 | 0.778 |
LIG_SH2_CRK | 497 | 501 | PF00017 | 0.616 |
LIG_SH2_STAP1 | 355 | 359 | PF00017 | 0.607 |
LIG_SH2_STAP1 | 662 | 666 | PF00017 | 0.813 |
LIG_SH2_STAT5 | 197 | 200 | PF00017 | 0.557 |
LIG_SH2_STAT5 | 806 | 809 | PF00017 | 0.697 |
LIG_SH3_3 | 210 | 216 | PF00018 | 0.778 |
LIG_SH3_3 | 510 | 516 | PF00018 | 0.701 |
LIG_SH3_3 | 594 | 600 | PF00018 | 0.825 |
LIG_SH3_3 | 637 | 643 | PF00018 | 0.724 |
LIG_SH3_3 | 741 | 747 | PF00018 | 0.688 |
LIG_SUMO_SIM_par_1 | 82 | 88 | PF11976 | 0.646 |
LIG_TRAF2_1 | 438 | 441 | PF00917 | 0.445 |
LIG_WRC_WIRS_1 | 478 | 483 | PF05994 | 0.655 |
LIG_WW_3 | 746 | 750 | PF00397 | 0.696 |
MOD_CK1_1 | 148 | 154 | PF00069 | 0.617 |
MOD_CK1_1 | 204 | 210 | PF00069 | 0.659 |
MOD_CK1_1 | 25 | 31 | PF00069 | 0.725 |
MOD_CK1_1 | 386 | 392 | PF00069 | 0.487 |
MOD_CK1_1 | 428 | 434 | PF00069 | 0.635 |
MOD_CK1_1 | 447 | 453 | PF00069 | 0.432 |
MOD_CK1_1 | 522 | 528 | PF00069 | 0.817 |
MOD_CK1_1 | 632 | 638 | PF00069 | 0.788 |
MOD_CK1_1 | 651 | 657 | PF00069 | 0.767 |
MOD_CK1_1 | 790 | 796 | PF00069 | 0.670 |
MOD_CK1_1 | 825 | 831 | PF00069 | 0.717 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.729 |
MOD_CK2_1 | 100 | 106 | PF00069 | 0.681 |
MOD_CK2_1 | 2 | 8 | PF00069 | 0.630 |
MOD_CK2_1 | 225 | 231 | PF00069 | 0.604 |
MOD_CK2_1 | 412 | 418 | PF00069 | 0.531 |
MOD_CK2_1 | 435 | 441 | PF00069 | 0.605 |
MOD_CK2_1 | 49 | 55 | PF00069 | 0.719 |
MOD_CK2_1 | 73 | 79 | PF00069 | 0.585 |
MOD_CK2_1 | 760 | 766 | PF00069 | 0.739 |
MOD_Cter_Amidation | 395 | 398 | PF01082 | 0.544 |
MOD_DYRK1A_RPxSP_1 | 596 | 600 | PF00069 | 0.614 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.493 |
MOD_GlcNHglycan | 150 | 153 | PF01048 | 0.661 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.637 |
MOD_GlcNHglycan | 216 | 219 | PF01048 | 0.653 |
MOD_GlcNHglycan | 221 | 224 | PF01048 | 0.546 |
MOD_GlcNHglycan | 390 | 394 | PF01048 | 0.493 |
MOD_GlcNHglycan | 403 | 406 | PF01048 | 0.475 |
MOD_GlcNHglycan | 508 | 512 | PF01048 | 0.626 |
MOD_GlcNHglycan | 521 | 524 | PF01048 | 0.628 |
MOD_GlcNHglycan | 631 | 634 | PF01048 | 0.745 |
MOD_GlcNHglycan | 678 | 681 | PF01048 | 0.761 |
MOD_GlcNHglycan | 686 | 689 | PF01048 | 0.713 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.513 |
MOD_GlcNHglycan | 789 | 792 | PF01048 | 0.681 |
MOD_GlcNHglycan | 827 | 830 | PF01048 | 0.650 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.683 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.519 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.646 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.578 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.531 |
MOD_GSK3_1 | 397 | 404 | PF00069 | 0.494 |
MOD_GSK3_1 | 444 | 451 | PF00069 | 0.611 |
MOD_GSK3_1 | 462 | 469 | PF00069 | 0.400 |
MOD_GSK3_1 | 553 | 560 | PF00069 | 0.627 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.686 |
MOD_GSK3_1 | 608 | 615 | PF00069 | 0.770 |
MOD_GSK3_1 | 631 | 638 | PF00069 | 0.718 |
MOD_GSK3_1 | 644 | 651 | PF00069 | 0.752 |
MOD_GSK3_1 | 682 | 689 | PF00069 | 0.691 |
MOD_GSK3_1 | 787 | 794 | PF00069 | 0.679 |
MOD_GSK3_1 | 834 | 841 | PF00069 | 0.697 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.685 |
MOD_N-GLC_1 | 166 | 171 | PF02516 | 0.597 |
MOD_N-GLC_1 | 629 | 634 | PF02516 | 0.611 |
MOD_N-GLC_1 | 780 | 785 | PF02516 | 0.700 |
MOD_N-GLC_2 | 474 | 476 | PF02516 | 0.587 |
MOD_NEK2_1 | 135 | 140 | PF00069 | 0.754 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.464 |
MOD_NEK2_1 | 165 | 170 | PF00069 | 0.540 |
MOD_NEK2_1 | 175 | 180 | PF00069 | 0.593 |
MOD_NEK2_1 | 246 | 251 | PF00069 | 0.428 |
MOD_NEK2_1 | 290 | 295 | PF00069 | 0.420 |
MOD_NEK2_1 | 412 | 417 | PF00069 | 0.617 |
MOD_NEK2_1 | 631 | 636 | PF00069 | 0.718 |
MOD_NEK2_1 | 823 | 828 | PF00069 | 0.729 |
MOD_NEK2_2 | 369 | 374 | PF00069 | 0.611 |
MOD_OFUCOSY | 163 | 170 | PF10250 | 0.504 |
MOD_OFUCOSY | 291 | 297 | PF10250 | 0.411 |
MOD_PIKK_1 | 197 | 203 | PF00454 | 0.683 |
MOD_PIKK_1 | 277 | 283 | PF00454 | 0.474 |
MOD_PIKK_1 | 325 | 331 | PF00454 | 0.586 |
MOD_PIKK_1 | 34 | 40 | PF00454 | 0.746 |
MOD_PIKK_1 | 606 | 612 | PF00454 | 0.646 |
MOD_PIKK_1 | 635 | 641 | PF00454 | 0.769 |
MOD_PIKK_1 | 649 | 655 | PF00454 | 0.802 |
MOD_PIKK_1 | 834 | 840 | PF00454 | 0.833 |
MOD_PKA_1 | 397 | 403 | PF00069 | 0.531 |
MOD_PKA_1 | 813 | 819 | PF00069 | 0.799 |
MOD_PKA_1 | 839 | 845 | PF00069 | 0.730 |
MOD_PKA_2 | 195 | 201 | PF00069 | 0.653 |
MOD_PKA_2 | 251 | 257 | PF00069 | 0.600 |
MOD_PKA_2 | 277 | 283 | PF00069 | 0.419 |
MOD_PKA_2 | 386 | 392 | PF00069 | 0.569 |
MOD_PKA_2 | 396 | 402 | PF00069 | 0.515 |
MOD_PKA_2 | 447 | 453 | PF00069 | 0.550 |
MOD_PKA_2 | 590 | 596 | PF00069 | 0.726 |
MOD_PKA_2 | 736 | 742 | PF00069 | 0.787 |
MOD_PKA_2 | 838 | 844 | PF00069 | 0.669 |
MOD_PKB_1 | 621 | 629 | PF00069 | 0.735 |
MOD_Plk_1 | 170 | 176 | PF00069 | 0.574 |
MOD_Plk_1 | 188 | 194 | PF00069 | 0.695 |
MOD_Plk_1 | 389 | 395 | PF00069 | 0.567 |
MOD_Plk_1 | 455 | 461 | PF00069 | 0.534 |
MOD_Plk_1 | 48 | 54 | PF00069 | 0.732 |
MOD_Plk_1 | 584 | 590 | PF00069 | 0.745 |
MOD_Plk_1 | 612 | 618 | PF00069 | 0.745 |
MOD_Plk_1 | 760 | 766 | PF00069 | 0.739 |
MOD_Plk_1 | 780 | 786 | PF00069 | 0.702 |
MOD_Plk_1 | 823 | 829 | PF00069 | 0.700 |
MOD_Plk_2-3 | 49 | 55 | PF00069 | 0.572 |
MOD_Plk_2-3 | 760 | 766 | PF00069 | 0.739 |
MOD_Plk_4 | 142 | 148 | PF00069 | 0.584 |
MOD_Plk_4 | 156 | 162 | PF00069 | 0.647 |
MOD_Plk_4 | 170 | 176 | PF00069 | 0.488 |
MOD_Plk_4 | 188 | 194 | PF00069 | 0.656 |
MOD_Plk_4 | 347 | 353 | PF00069 | 0.540 |
MOD_Plk_4 | 428 | 434 | PF00069 | 0.451 |
MOD_Plk_4 | 477 | 483 | PF00069 | 0.740 |
MOD_Plk_4 | 584 | 590 | PF00069 | 0.783 |
MOD_ProDKin_1 | 145 | 151 | PF00069 | 0.731 |
MOD_ProDKin_1 | 221 | 227 | PF00069 | 0.565 |
MOD_ProDKin_1 | 425 | 431 | PF00069 | 0.544 |
MOD_ProDKin_1 | 485 | 491 | PF00069 | 0.670 |
MOD_ProDKin_1 | 596 | 602 | PF00069 | 0.751 |
MOD_ProDKin_1 | 723 | 729 | PF00069 | 0.586 |
MOD_ProDKin_1 | 92 | 98 | PF00069 | 0.738 |
MOD_SUMO_rev_2 | 228 | 236 | PF00179 | 0.494 |
MOD_SUMO_rev_2 | 350 | 359 | PF00179 | 0.532 |
MOD_SUMO_rev_2 | 697 | 705 | PF00179 | 0.615 |
TRG_DiLeu_BaEn_1 | 585 | 590 | PF01217 | 0.748 |
TRG_DiLeu_BaLyEn_6 | 655 | 660 | PF01217 | 0.724 |
TRG_DiLeu_BaLyEn_6 | 746 | 751 | PF01217 | 0.583 |
TRG_ENDOCYTIC_2 | 497 | 500 | PF00928 | 0.566 |
TRG_ER_diArg_1 | 193 | 196 | PF00400 | 0.441 |
TRG_ER_diArg_1 | 272 | 274 | PF00400 | 0.581 |
TRG_ER_diArg_1 | 419 | 422 | PF00400 | 0.578 |
TRG_ER_diArg_1 | 618 | 621 | PF00400 | 0.749 |
TRG_Pf-PMV_PEXEL_1 | 452 | 456 | PF00026 | 0.634 |
TRG_Pf-PMV_PEXEL_1 | 499 | 503 | PF00026 | 0.709 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZ00 | Leptomonas seymouri | 35% | 97% |
A0A3S7XAN9 | Leishmania donovani | 99% | 100% |
A4HP15 | Leishmania braziliensis | 64% | 100% |
E9ASS5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
Q4Q1S1 | Leishmania major | 88% | 100% |