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: A0A3Q8ID61
Term | Name | Level | Count |
---|---|---|---|
GO:0006470 | protein dephosphorylation | 5 | 7 |
GO:0006793 | phosphorus metabolic process | 3 | 7 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 7 |
GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0016311 | dephosphorylation | 5 | 7 |
GO:0019538 | protein metabolic process | 3 | 7 |
GO:0036211 | protein modification process | 4 | 7 |
GO:0043170 | macromolecule metabolic process | 3 | 7 |
GO:0043412 | macromolecule modification | 4 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 7 |
GO:0004721 | phosphoprotein phosphatase activity | 3 | 7 |
GO:0004722 | protein serine/threonine phosphatase activity | 4 | 7 |
GO:0016787 | hydrolase activity | 2 | 7 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 7 |
GO:0016791 | phosphatase activity | 5 | 7 |
GO:0017018 | myosin phosphatase activity | 5 | 6 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 7 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 350 | 354 | PF00656 | 0.830 |
CLV_C14_Caspase3-7 | 372 | 376 | PF00656 | 0.747 |
CLV_NRD_NRD_1 | 289 | 291 | PF00675 | 0.755 |
CLV_NRD_NRD_1 | 477 | 479 | PF00675 | 0.514 |
CLV_NRD_NRD_1 | 540 | 542 | PF00675 | 0.389 |
CLV_NRD_NRD_1 | 605 | 607 | PF00675 | 0.412 |
CLV_NRD_NRD_1 | 676 | 678 | PF00675 | 0.478 |
CLV_NRD_NRD_1 | 73 | 75 | PF00675 | 0.676 |
CLV_NRD_NRD_1 | 825 | 827 | PF00675 | 0.697 |
CLV_NRD_NRD_1 | 95 | 97 | PF00675 | 0.794 |
CLV_PCSK_FUR_1 | 538 | 542 | PF00082 | 0.391 |
CLV_PCSK_KEX2_1 | 289 | 291 | PF00082 | 0.755 |
CLV_PCSK_KEX2_1 | 477 | 479 | PF00082 | 0.433 |
CLV_PCSK_KEX2_1 | 538 | 540 | PF00082 | 0.355 |
CLV_PCSK_KEX2_1 | 605 | 607 | PF00082 | 0.412 |
CLV_PCSK_KEX2_1 | 676 | 678 | PF00082 | 0.478 |
CLV_PCSK_KEX2_1 | 73 | 75 | PF00082 | 0.683 |
CLV_PCSK_KEX2_1 | 95 | 97 | PF00082 | 0.819 |
CLV_PCSK_SKI1_1 | 124 | 128 | PF00082 | 0.778 |
CLV_PCSK_SKI1_1 | 188 | 192 | PF00082 | 0.745 |
CLV_PCSK_SKI1_1 | 307 | 311 | PF00082 | 0.613 |
CLV_PCSK_SKI1_1 | 425 | 429 | PF00082 | 0.658 |
CLV_PCSK_SKI1_1 | 514 | 518 | PF00082 | 0.412 |
CLV_PCSK_SKI1_1 | 580 | 584 | PF00082 | 0.412 |
CLV_PCSK_SKI1_1 | 606 | 610 | PF00082 | 0.412 |
CLV_PCSK_SKI1_1 | 725 | 729 | PF00082 | 0.412 |
CLV_PCSK_SKI1_1 | 838 | 842 | PF00082 | 0.673 |
DEG_SPOP_SBC_1 | 195 | 199 | PF00917 | 0.818 |
DOC_MAPK_DCC_7 | 382 | 390 | PF00069 | 0.750 |
DOC_MAPK_gen_1 | 605 | 616 | PF00069 | 0.412 |
DOC_MAPK_MEF2A_6 | 382 | 390 | PF00069 | 0.750 |
DOC_MAPK_MEF2A_6 | 425 | 433 | PF00069 | 0.601 |
DOC_PP2B_LxvP_1 | 191 | 194 | PF13499 | 0.725 |
DOC_USP7_MATH_1 | 111 | 115 | PF00917 | 0.729 |
DOC_USP7_MATH_1 | 150 | 154 | PF00917 | 0.756 |
DOC_USP7_MATH_1 | 164 | 168 | PF00917 | 0.583 |
DOC_USP7_MATH_1 | 195 | 199 | PF00917 | 0.756 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.682 |
DOC_USP7_MATH_1 | 249 | 253 | PF00917 | 0.708 |
DOC_USP7_MATH_1 | 371 | 375 | PF00917 | 0.741 |
DOC_USP7_MATH_1 | 391 | 395 | PF00917 | 0.511 |
DOC_USP7_MATH_1 | 50 | 54 | PF00917 | 0.656 |
DOC_USP7_MATH_1 | 670 | 674 | PF00917 | 0.459 |
DOC_USP7_MATH_1 | 825 | 829 | PF00917 | 0.636 |
DOC_USP7_UBL2_3 | 6 | 10 | PF12436 | 0.607 |
DOC_WW_Pin1_4 | 144 | 149 | PF00397 | 0.796 |
DOC_WW_Pin1_4 | 16 | 21 | PF00397 | 0.711 |
DOC_WW_Pin1_4 | 203 | 208 | PF00397 | 0.667 |
DOC_WW_Pin1_4 | 236 | 241 | PF00397 | 0.715 |
DOC_WW_Pin1_4 | 245 | 250 | PF00397 | 0.699 |
DOC_WW_Pin1_4 | 328 | 333 | PF00397 | 0.801 |
DOC_WW_Pin1_4 | 636 | 641 | PF00397 | 0.426 |
DOC_WW_Pin1_4 | 668 | 673 | PF00397 | 0.473 |
DOC_WW_Pin1_4 | 728 | 733 | PF00397 | 0.353 |
DOC_WW_Pin1_4 | 745 | 750 | PF00397 | 0.353 |
LIG_14-3-3_CanoR_1 | 112 | 117 | PF00244 | 0.688 |
LIG_14-3-3_CanoR_1 | 42 | 48 | PF00244 | 0.669 |
LIG_14-3-3_CanoR_1 | 826 | 830 | PF00244 | 0.692 |
LIG_14-3-3_CanoR_1 | 87 | 91 | PF00244 | 0.746 |
LIG_14-3-3_CanoR_1 | 95 | 103 | PF00244 | 0.769 |
LIG_Actin_WH2_2 | 119 | 136 | PF00022 | 0.802 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.574 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.574 |
LIG_BIR_III_4 | 643 | 647 | PF00653 | 0.330 |
LIG_BRCT_BRCA1_1 | 650 | 654 | PF00533 | 0.514 |
LIG_FHA_1 | 17 | 23 | PF00498 | 0.729 |
LIG_FHA_1 | 240 | 246 | PF00498 | 0.762 |
LIG_FHA_1 | 281 | 287 | PF00498 | 0.823 |
LIG_FHA_1 | 359 | 365 | PF00498 | 0.685 |
LIG_FHA_1 | 39 | 45 | PF00498 | 0.655 |
LIG_FHA_1 | 424 | 430 | PF00498 | 0.555 |
LIG_FHA_1 | 719 | 725 | PF00498 | 0.412 |
LIG_FHA_1 | 729 | 735 | PF00498 | 0.412 |
LIG_FHA_1 | 87 | 93 | PF00498 | 0.808 |
LIG_FHA_2 | 117 | 123 | PF00498 | 0.798 |
LIG_FHA_2 | 444 | 450 | PF00498 | 0.355 |
LIG_FHA_2 | 510 | 516 | PF00498 | 0.412 |
LIG_Integrin_isoDGR_2 | 280 | 282 | PF01839 | 0.760 |
LIG_Integrin_isoDGR_2 | 844 | 846 | PF01839 | 0.694 |
LIG_LIR_Gen_1 | 449 | 460 | PF02991 | 0.401 |
LIG_LIR_Gen_1 | 515 | 522 | PF02991 | 0.402 |
LIG_LIR_Gen_1 | 68 | 77 | PF02991 | 0.586 |
LIG_LIR_Gen_1 | 701 | 711 | PF02991 | 0.412 |
LIG_LIR_LC3C_4 | 41 | 45 | PF02991 | 0.656 |
LIG_LIR_Nem_3 | 449 | 455 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 515 | 520 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 68 | 72 | PF02991 | 0.588 |
LIG_LIR_Nem_3 | 701 | 706 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 709 | 715 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 726 | 730 | PF02991 | 0.260 |
LIG_MYND_1 | 128 | 132 | PF01753 | 0.705 |
LIG_MYND_1 | 20 | 24 | PF01753 | 0.795 |
LIG_Pex14_1 | 486 | 490 | PF04695 | 0.412 |
LIG_Pex14_2 | 632 | 636 | PF04695 | 0.353 |
LIG_Pex14_2 | 723 | 727 | PF04695 | 0.412 |
LIG_PTAP_UEV_1 | 264 | 269 | PF05743 | 0.700 |
LIG_SH2_CRK | 69 | 73 | PF00017 | 0.591 |
LIG_SH2_GRB2like | 36 | 39 | PF00017 | 0.716 |
LIG_SH2_STAP1 | 88 | 92 | PF00017 | 0.736 |
LIG_SH2_STAT5 | 36 | 39 | PF00017 | 0.717 |
LIG_SH2_STAT5 | 490 | 493 | PF00017 | 0.412 |
LIG_SH2_STAT5 | 572 | 575 | PF00017 | 0.412 |
LIG_SH2_STAT5 | 69 | 72 | PF00017 | 0.792 |
LIG_SH2_STAT5 | 730 | 733 | PF00017 | 0.394 |
LIG_SH2_STAT5 | 88 | 91 | PF00017 | 0.737 |
LIG_SH3_3 | 18 | 24 | PF00018 | 0.753 |
LIG_SH3_3 | 262 | 268 | PF00018 | 0.706 |
LIG_SH3_3 | 313 | 319 | PF00018 | 0.654 |
LIG_SH3_3 | 380 | 386 | PF00018 | 0.825 |
LIG_SH3_3 | 42 | 48 | PF00018 | 0.628 |
LIG_SH3_3 | 731 | 737 | PF00018 | 0.412 |
LIG_SUMO_SIM_anti_2 | 466 | 472 | PF11976 | 0.514 |
LIG_SUMO_SIM_anti_2 | 774 | 780 | PF11976 | 0.430 |
LIG_SUMO_SIM_par_1 | 466 | 472 | PF11976 | 0.514 |
LIG_SUMO_SIM_par_1 | 621 | 626 | PF11976 | 0.412 |
LIG_SUMO_SIM_par_1 | 88 | 93 | PF11976 | 0.588 |
LIG_SxIP_EBH_1 | 194 | 208 | PF03271 | 0.819 |
LIG_TRAF2_1 | 645 | 648 | PF00917 | 0.440 |
LIG_TRAF2_1 | 716 | 719 | PF00917 | 0.412 |
LIG_UBA3_1 | 516 | 523 | PF00899 | 0.412 |
LIG_WW_3 | 148 | 152 | PF00397 | 0.769 |
MOD_CDK_SPK_2 | 203 | 208 | PF00069 | 0.821 |
MOD_CDK_SPxxK_3 | 144 | 151 | PF00069 | 0.816 |
MOD_CDK_SPxxK_3 | 236 | 243 | PF00069 | 0.653 |
MOD_CK1_1 | 13 | 19 | PF00069 | 0.818 |
MOD_CK1_1 | 167 | 173 | PF00069 | 0.628 |
MOD_CK1_1 | 203 | 209 | PF00069 | 0.659 |
MOD_CK1_1 | 239 | 245 | PF00069 | 0.775 |
MOD_CK1_1 | 248 | 254 | PF00069 | 0.698 |
MOD_CK1_1 | 366 | 372 | PF00069 | 0.776 |
MOD_CK1_1 | 423 | 429 | PF00069 | 0.520 |
MOD_CK1_1 | 664 | 670 | PF00069 | 0.402 |
MOD_CK1_1 | 745 | 751 | PF00069 | 0.478 |
MOD_CK1_1 | 820 | 826 | PF00069 | 0.666 |
MOD_CK1_1 | 828 | 834 | PF00069 | 0.688 |
MOD_CK2_1 | 263 | 269 | PF00069 | 0.702 |
MOD_CK2_1 | 366 | 372 | PF00069 | 0.798 |
MOD_CK2_1 | 509 | 515 | PF00069 | 0.412 |
MOD_CK2_1 | 713 | 719 | PF00069 | 0.412 |
MOD_CK2_1 | 828 | 834 | PF00069 | 0.581 |
MOD_Cter_Amidation | 475 | 478 | PF01082 | 0.514 |
MOD_Cter_Amidation | 536 | 539 | PF01082 | 0.412 |
MOD_Cter_Amidation | 93 | 96 | PF01082 | 0.727 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.635 |
MOD_GlcNHglycan | 152 | 155 | PF01048 | 0.736 |
MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.725 |
MOD_GlcNHglycan | 251 | 254 | PF01048 | 0.683 |
MOD_GlcNHglycan | 265 | 268 | PF01048 | 0.558 |
MOD_GlcNHglycan | 322 | 326 | PF01048 | 0.752 |
MOD_GlcNHglycan | 368 | 371 | PF01048 | 0.727 |
MOD_GlcNHglycan | 401 | 405 | PF01048 | 0.764 |
MOD_GlcNHglycan | 422 | 425 | PF01048 | 0.615 |
MOD_GlcNHglycan | 436 | 439 | PF01048 | 0.412 |
MOD_GlcNHglycan | 535 | 538 | PF01048 | 0.420 |
MOD_GlcNHglycan | 552 | 555 | PF01048 | 0.438 |
MOD_GlcNHglycan | 663 | 667 | PF01048 | 0.417 |
MOD_GlcNHglycan | 699 | 703 | PF01048 | 0.412 |
MOD_GlcNHglycan | 740 | 743 | PF01048 | 0.412 |
MOD_GlcNHglycan | 793 | 796 | PF01048 | 0.566 |
MOD_GlcNHglycan | 799 | 802 | PF01048 | 0.624 |
MOD_GlcNHglycan | 819 | 822 | PF01048 | 0.826 |
MOD_GlcNHglycan | 91 | 95 | PF01048 | 0.705 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.625 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.786 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.702 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.779 |
MOD_GSK3_1 | 245 | 252 | PF00069 | 0.734 |
MOD_GSK3_1 | 263 | 270 | PF00069 | 0.642 |
MOD_GSK3_1 | 371 | 378 | PF00069 | 0.779 |
MOD_GSK3_1 | 419 | 426 | PF00069 | 0.561 |
MOD_GSK3_1 | 505 | 512 | PF00069 | 0.367 |
MOD_GSK3_1 | 552 | 559 | PF00069 | 0.429 |
MOD_GSK3_1 | 586 | 593 | PF00069 | 0.357 |
MOD_GSK3_1 | 664 | 671 | PF00069 | 0.411 |
MOD_GSK3_1 | 738 | 745 | PF00069 | 0.499 |
MOD_GSK3_1 | 805 | 812 | PF00069 | 0.742 |
MOD_GSK3_1 | 813 | 820 | PF00069 | 0.661 |
MOD_GSK3_1 | 86 | 93 | PF00069 | 0.806 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.712 |
MOD_N-GLC_1 | 173 | 178 | PF02516 | 0.825 |
MOD_N-GLC_1 | 455 | 460 | PF02516 | 0.391 |
MOD_N-GLC_1 | 533 | 538 | PF02516 | 0.440 |
MOD_N-GLC_1 | 661 | 666 | PF02516 | 0.440 |
MOD_N-GLC_1 | 774 | 779 | PF02516 | 0.431 |
MOD_N-GLC_2 | 757 | 759 | PF02516 | 0.412 |
MOD_NEK2_1 | 312 | 317 | PF00069 | 0.698 |
MOD_NEK2_1 | 357 | 362 | PF00069 | 0.687 |
MOD_NEK2_1 | 363 | 368 | PF00069 | 0.686 |
MOD_NEK2_1 | 455 | 460 | PF00069 | 0.348 |
MOD_NEK2_1 | 505 | 510 | PF00069 | 0.412 |
MOD_NEK2_1 | 623 | 628 | PF00069 | 0.390 |
MOD_NEK2_1 | 684 | 689 | PF00069 | 0.412 |
MOD_NEK2_1 | 817 | 822 | PF00069 | 0.825 |
MOD_NEK2_1 | 833 | 838 | PF00069 | 0.504 |
MOD_NEK2_1 | 90 | 95 | PF00069 | 0.584 |
MOD_NEK2_2 | 164 | 169 | PF00069 | 0.719 |
MOD_NEK2_2 | 173 | 178 | PF00069 | 0.632 |
MOD_PIKK_1 | 358 | 364 | PF00454 | 0.659 |
MOD_PIKK_1 | 809 | 815 | PF00454 | 0.814 |
MOD_PKA_1 | 95 | 101 | PF00069 | 0.715 |
MOD_PKA_2 | 111 | 117 | PF00069 | 0.727 |
MOD_PKA_2 | 150 | 156 | PF00069 | 0.824 |
MOD_PKA_2 | 222 | 228 | PF00069 | 0.755 |
MOD_PKA_2 | 443 | 449 | PF00069 | 0.392 |
MOD_PKA_2 | 769 | 775 | PF00069 | 0.412 |
MOD_PKA_2 | 791 | 797 | PF00069 | 0.614 |
MOD_PKA_2 | 825 | 831 | PF00069 | 0.685 |
MOD_PKA_2 | 86 | 92 | PF00069 | 0.772 |
MOD_PKA_2 | 95 | 101 | PF00069 | 0.766 |
MOD_PKB_1 | 110 | 118 | PF00069 | 0.691 |
MOD_PKB_1 | 398 | 406 | PF00069 | 0.713 |
MOD_Plk_1 | 38 | 44 | PF00069 | 0.709 |
MOD_Plk_1 | 455 | 461 | PF00069 | 0.391 |
MOD_Plk_1 | 67 | 73 | PF00069 | 0.591 |
MOD_Plk_1 | 698 | 704 | PF00069 | 0.412 |
MOD_Plk_1 | 774 | 780 | PF00069 | 0.430 |
MOD_Plk_2-3 | 769 | 775 | PF00069 | 0.412 |
MOD_Plk_4 | 173 | 179 | PF00069 | 0.753 |
MOD_Plk_4 | 196 | 202 | PF00069 | 0.766 |
MOD_Plk_4 | 32 | 38 | PF00069 | 0.759 |
MOD_Plk_4 | 463 | 469 | PF00069 | 0.412 |
MOD_Plk_4 | 505 | 511 | PF00069 | 0.412 |
MOD_Plk_4 | 557 | 563 | PF00069 | 0.412 |
MOD_Plk_4 | 774 | 780 | PF00069 | 0.430 |
MOD_Plk_4 | 828 | 834 | PF00069 | 0.646 |
MOD_ProDKin_1 | 144 | 150 | PF00069 | 0.794 |
MOD_ProDKin_1 | 16 | 22 | PF00069 | 0.711 |
MOD_ProDKin_1 | 203 | 209 | PF00069 | 0.656 |
MOD_ProDKin_1 | 236 | 242 | PF00069 | 0.712 |
MOD_ProDKin_1 | 245 | 251 | PF00069 | 0.700 |
MOD_ProDKin_1 | 328 | 334 | PF00069 | 0.802 |
MOD_ProDKin_1 | 636 | 642 | PF00069 | 0.426 |
MOD_ProDKin_1 | 668 | 674 | PF00069 | 0.473 |
MOD_ProDKin_1 | 728 | 734 | PF00069 | 0.353 |
MOD_ProDKin_1 | 745 | 751 | PF00069 | 0.353 |
MOD_SUMO_rev_2 | 121 | 126 | PF00179 | 0.804 |
MOD_SUMO_rev_2 | 593 | 598 | PF00179 | 0.412 |
MOD_SUMO_rev_2 | 631 | 636 | PF00179 | 0.412 |
MOD_SUMO_rev_2 | 641 | 651 | PF00179 | 0.412 |
TRG_DiLeu_BaEn_1 | 39 | 44 | PF01217 | 0.653 |
TRG_DiLeu_BaEn_3 | 718 | 724 | PF01217 | 0.412 |
TRG_DiLeu_BaLyEn_6 | 18 | 23 | PF01217 | 0.634 |
TRG_DiLeu_BaLyEn_6 | 212 | 217 | PF01217 | 0.829 |
TRG_ENDOCYTIC_2 | 69 | 72 | PF00928 | 0.589 |
TRG_ER_diArg_1 | 128 | 131 | PF00400 | 0.708 |
TRG_ER_diArg_1 | 397 | 400 | PF00400 | 0.648 |
TRG_ER_diArg_1 | 477 | 479 | PF00400 | 0.514 |
TRG_ER_diArg_1 | 538 | 541 | PF00400 | 0.412 |
TRG_ER_diArg_1 | 605 | 607 | PF00400 | 0.412 |
TRG_ER_diArg_1 | 676 | 678 | PF00400 | 0.478 |
TRG_ER_diArg_1 | 72 | 74 | PF00400 | 0.583 |
TRG_Pf-PMV_PEXEL_1 | 131 | 135 | PF00026 | 0.801 |
TRG_Pf-PMV_PEXEL_1 | 627 | 631 | PF00026 | 0.412 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2L7 | Leptomonas seymouri | 50% | 81% |
A4H7P3 | Leishmania braziliensis | 71% | 100% |
A4HW33 | Leishmania infantum | 100% | 100% |
E9APT5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q4QFP5 | Leishmania major | 92% | 100% |