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 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: Q4QFP5
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 | 352 | 356 | PF00656 | 0.683 |
CLV_C14_Caspase3-7 | 374 | 378 | PF00656 | 0.650 |
CLV_NRD_NRD_1 | 291 | 293 | PF00675 | 0.788 |
CLV_NRD_NRD_1 | 479 | 481 | PF00675 | 0.375 |
CLV_NRD_NRD_1 | 542 | 544 | PF00675 | 0.372 |
CLV_NRD_NRD_1 | 607 | 609 | PF00675 | 0.386 |
CLV_NRD_NRD_1 | 679 | 681 | PF00675 | 0.399 |
CLV_NRD_NRD_1 | 73 | 75 | PF00675 | 0.680 |
CLV_NRD_NRD_1 | 828 | 830 | PF00675 | 0.637 |
CLV_NRD_NRD_1 | 95 | 97 | PF00675 | 0.673 |
CLV_PCSK_FUR_1 | 540 | 544 | PF00082 | 0.335 |
CLV_PCSK_KEX2_1 | 291 | 293 | PF00082 | 0.794 |
CLV_PCSK_KEX2_1 | 479 | 481 | PF00082 | 0.375 |
CLV_PCSK_KEX2_1 | 540 | 542 | PF00082 | 0.375 |
CLV_PCSK_KEX2_1 | 607 | 609 | PF00082 | 0.386 |
CLV_PCSK_KEX2_1 | 679 | 681 | PF00082 | 0.412 |
CLV_PCSK_KEX2_1 | 73 | 75 | PF00082 | 0.641 |
CLV_PCSK_KEX2_1 | 95 | 97 | PF00082 | 0.673 |
CLV_PCSK_SKI1_1 | 124 | 128 | PF00082 | 0.649 |
CLV_PCSK_SKI1_1 | 188 | 192 | PF00082 | 0.697 |
CLV_PCSK_SKI1_1 | 292 | 296 | PF00082 | 0.615 |
CLV_PCSK_SKI1_1 | 309 | 313 | PF00082 | 0.606 |
CLV_PCSK_SKI1_1 | 427 | 431 | PF00082 | 0.502 |
CLV_PCSK_SKI1_1 | 516 | 520 | PF00082 | 0.375 |
CLV_PCSK_SKI1_1 | 582 | 586 | PF00082 | 0.379 |
CLV_PCSK_SKI1_1 | 608 | 612 | PF00082 | 0.386 |
CLV_PCSK_SKI1_1 | 728 | 732 | PF00082 | 0.375 |
CLV_PCSK_SKI1_1 | 841 | 845 | PF00082 | 0.564 |
DEG_SPOP_SBC_1 | 195 | 199 | PF00917 | 0.687 |
DOC_MAPK_DCC_7 | 384 | 392 | PF00069 | 0.656 |
DOC_MAPK_gen_1 | 607 | 618 | PF00069 | 0.386 |
DOC_MAPK_MEF2A_6 | 384 | 392 | PF00069 | 0.685 |
DOC_MAPK_MEF2A_6 | 427 | 435 | PF00069 | 0.579 |
DOC_PP2B_LxvP_1 | 191 | 194 | PF13499 | 0.688 |
DOC_USP7_MATH_1 | 111 | 115 | PF00917 | 0.703 |
DOC_USP7_MATH_1 | 150 | 154 | PF00917 | 0.647 |
DOC_USP7_MATH_1 | 164 | 168 | PF00917 | 0.625 |
DOC_USP7_MATH_1 | 195 | 199 | PF00917 | 0.777 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.645 |
DOC_USP7_MATH_1 | 249 | 253 | PF00917 | 0.638 |
DOC_USP7_MATH_1 | 373 | 377 | PF00917 | 0.646 |
DOC_USP7_MATH_1 | 50 | 54 | PF00917 | 0.660 |
DOC_USP7_MATH_1 | 534 | 538 | PF00917 | 0.258 |
DOC_USP7_MATH_1 | 672 | 676 | PF00917 | 0.403 |
DOC_USP7_MATH_1 | 809 | 813 | PF00917 | 0.562 |
DOC_USP7_MATH_1 | 828 | 832 | PF00917 | 0.675 |
DOC_WW_Pin1_4 | 144 | 149 | PF00397 | 0.808 |
DOC_WW_Pin1_4 | 16 | 21 | PF00397 | 0.661 |
DOC_WW_Pin1_4 | 203 | 208 | PF00397 | 0.686 |
DOC_WW_Pin1_4 | 245 | 250 | PF00397 | 0.617 |
DOC_WW_Pin1_4 | 330 | 335 | PF00397 | 0.624 |
DOC_WW_Pin1_4 | 640 | 645 | PF00397 | 0.330 |
DOC_WW_Pin1_4 | 670 | 675 | PF00397 | 0.372 |
DOC_WW_Pin1_4 | 731 | 736 | PF00397 | 0.375 |
DOC_WW_Pin1_4 | 748 | 753 | PF00397 | 0.355 |
LIG_14-3-3_CanoR_1 | 112 | 117 | PF00244 | 0.543 |
LIG_14-3-3_CanoR_1 | 243 | 249 | PF00244 | 0.573 |
LIG_14-3-3_CanoR_1 | 42 | 48 | PF00244 | 0.672 |
LIG_14-3-3_CanoR_1 | 829 | 833 | PF00244 | 0.650 |
LIG_14-3-3_CanoR_1 | 87 | 91 | PF00244 | 0.639 |
LIG_14-3-3_CanoR_1 | 95 | 103 | PF00244 | 0.588 |
LIG_Actin_WH2_2 | 119 | 136 | PF00022 | 0.749 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.563 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.563 |
LIG_BRCT_BRCA1_1 | 246 | 250 | PF00533 | 0.573 |
LIG_BRCT_BRCA1_1 | 652 | 656 | PF00533 | 0.375 |
LIG_FHA_1 | 17 | 23 | PF00498 | 0.644 |
LIG_FHA_1 | 240 | 246 | PF00498 | 0.648 |
LIG_FHA_1 | 283 | 289 | PF00498 | 0.743 |
LIG_FHA_1 | 361 | 367 | PF00498 | 0.656 |
LIG_FHA_1 | 39 | 45 | PF00498 | 0.599 |
LIG_FHA_1 | 426 | 432 | PF00498 | 0.581 |
LIG_FHA_1 | 722 | 728 | PF00498 | 0.375 |
LIG_FHA_1 | 732 | 738 | PF00498 | 0.305 |
LIG_FHA_1 | 87 | 93 | PF00498 | 0.677 |
LIG_FHA_2 | 117 | 123 | PF00498 | 0.666 |
LIG_FHA_2 | 446 | 452 | PF00498 | 0.404 |
LIG_FHA_2 | 512 | 518 | PF00498 | 0.375 |
LIG_FHA_2 | 645 | 651 | PF00498 | 0.258 |
LIG_Integrin_isoDGR_2 | 282 | 284 | PF01839 | 0.647 |
LIG_Integrin_isoDGR_2 | 847 | 849 | PF01839 | 0.652 |
LIG_Integrin_isoDGR_2 | 93 | 95 | PF01839 | 0.585 |
LIG_LIR_Gen_1 | 451 | 462 | PF02991 | 0.375 |
LIG_LIR_Gen_1 | 517 | 524 | PF02991 | 0.372 |
LIG_LIR_Gen_1 | 547 | 554 | PF02991 | 0.296 |
LIG_LIR_Gen_1 | 704 | 714 | PF02991 | 0.404 |
LIG_LIR_LC3C_4 | 41 | 45 | PF02991 | 0.602 |
LIG_LIR_Nem_3 | 451 | 457 | PF02991 | 0.375 |
LIG_LIR_Nem_3 | 517 | 522 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 704 | 709 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 712 | 718 | PF02991 | 0.322 |
LIG_LIR_Nem_3 | 729 | 733 | PF02991 | 0.225 |
LIG_MYND_1 | 128 | 132 | PF01753 | 0.674 |
LIG_MYND_1 | 20 | 24 | PF01753 | 0.704 |
LIG_Pex14_1 | 488 | 492 | PF04695 | 0.475 |
LIG_Pex14_2 | 634 | 638 | PF04695 | 0.375 |
LIG_Pex14_2 | 726 | 730 | PF04695 | 0.375 |
LIG_PTAP_UEV_1 | 264 | 269 | PF05743 | 0.611 |
LIG_SH2_GRB2like | 36 | 39 | PF00017 | 0.670 |
LIG_SH2_STAP1 | 88 | 92 | PF00017 | 0.638 |
LIG_SH2_STAT5 | 36 | 39 | PF00017 | 0.631 |
LIG_SH2_STAT5 | 492 | 495 | PF00017 | 0.481 |
LIG_SH2_STAT5 | 574 | 577 | PF00017 | 0.393 |
LIG_SH2_STAT5 | 69 | 72 | PF00017 | 0.681 |
LIG_SH2_STAT5 | 733 | 736 | PF00017 | 0.501 |
LIG_SH2_STAT5 | 88 | 91 | PF00017 | 0.641 |
LIG_SH3_3 | 20 | 26 | PF00018 | 0.696 |
LIG_SH3_3 | 262 | 268 | PF00018 | 0.619 |
LIG_SH3_3 | 382 | 388 | PF00018 | 0.718 |
LIG_SH3_3 | 389 | 395 | PF00018 | 0.649 |
LIG_SH3_3 | 42 | 48 | PF00018 | 0.633 |
LIG_SH3_3 | 666 | 672 | PF00018 | 0.291 |
LIG_SH3_3 | 734 | 740 | PF00018 | 0.471 |
LIG_SUMO_SIM_anti_2 | 468 | 474 | PF11976 | 0.383 |
LIG_SUMO_SIM_anti_2 | 777 | 783 | PF11976 | 0.418 |
LIG_SUMO_SIM_par_1 | 468 | 474 | PF11976 | 0.382 |
LIG_SUMO_SIM_par_1 | 623 | 628 | PF11976 | 0.404 |
LIG_SxIP_EBH_1 | 194 | 208 | PF03271 | 0.686 |
LIG_TRAF2_1 | 647 | 650 | PF00917 | 0.335 |
LIG_TRAF2_1 | 719 | 722 | PF00917 | 0.375 |
LIG_UBA3_1 | 518 | 525 | PF00899 | 0.375 |
LIG_WW_3 | 148 | 152 | PF00397 | 0.650 |
MOD_CDK_SPK_2 | 203 | 208 | PF00069 | 0.686 |
MOD_CDK_SPxxK_3 | 144 | 151 | PF00069 | 0.681 |
MOD_CK1_1 | 13 | 19 | PF00069 | 0.700 |
MOD_CK1_1 | 167 | 173 | PF00069 | 0.611 |
MOD_CK1_1 | 203 | 209 | PF00069 | 0.683 |
MOD_CK1_1 | 248 | 254 | PF00069 | 0.606 |
MOD_CK1_1 | 368 | 374 | PF00069 | 0.662 |
MOD_CK1_1 | 425 | 431 | PF00069 | 0.542 |
MOD_CK1_1 | 673 | 679 | PF00069 | 0.420 |
MOD_CK1_1 | 748 | 754 | PF00069 | 0.355 |
MOD_CK1_1 | 812 | 818 | PF00069 | 0.640 |
MOD_CK1_1 | 831 | 837 | PF00069 | 0.692 |
MOD_CK2_1 | 251 | 257 | PF00069 | 0.594 |
MOD_CK2_1 | 263 | 269 | PF00069 | 0.607 |
MOD_CK2_1 | 368 | 374 | PF00069 | 0.693 |
MOD_CK2_1 | 511 | 517 | PF00069 | 0.375 |
MOD_CK2_1 | 644 | 650 | PF00069 | 0.281 |
MOD_CK2_1 | 716 | 722 | PF00069 | 0.381 |
MOD_CK2_1 | 831 | 837 | PF00069 | 0.607 |
MOD_Cter_Amidation | 477 | 480 | PF01082 | 0.375 |
MOD_Cter_Amidation | 538 | 541 | PF01082 | 0.375 |
MOD_Cter_Amidation | 93 | 96 | PF01082 | 0.644 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.679 |
MOD_GlcNHglycan | 152 | 155 | PF01048 | 0.645 |
MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.688 |
MOD_GlcNHglycan | 251 | 254 | PF01048 | 0.733 |
MOD_GlcNHglycan | 265 | 268 | PF01048 | 0.577 |
MOD_GlcNHglycan | 370 | 373 | PF01048 | 0.684 |
MOD_GlcNHglycan | 403 | 407 | PF01048 | 0.653 |
MOD_GlcNHglycan | 424 | 427 | PF01048 | 0.551 |
MOD_GlcNHglycan | 438 | 441 | PF01048 | 0.389 |
MOD_GlcNHglycan | 537 | 540 | PF01048 | 0.339 |
MOD_GlcNHglycan | 554 | 557 | PF01048 | 0.252 |
MOD_GlcNHglycan | 665 | 669 | PF01048 | 0.479 |
MOD_GlcNHglycan | 702 | 706 | PF01048 | 0.383 |
MOD_GlcNHglycan | 743 | 746 | PF01048 | 0.400 |
MOD_GlcNHglycan | 796 | 799 | PF01048 | 0.509 |
MOD_GlcNHglycan | 802 | 805 | PF01048 | 0.593 |
MOD_GlcNHglycan | 811 | 814 | PF01048 | 0.576 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.708 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.645 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.656 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.679 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.717 |
MOD_GSK3_1 | 263 | 270 | PF00069 | 0.565 |
MOD_GSK3_1 | 326 | 333 | PF00069 | 0.553 |
MOD_GSK3_1 | 373 | 380 | PF00069 | 0.660 |
MOD_GSK3_1 | 390 | 397 | PF00069 | 0.625 |
MOD_GSK3_1 | 421 | 428 | PF00069 | 0.535 |
MOD_GSK3_1 | 507 | 514 | PF00069 | 0.450 |
MOD_GSK3_1 | 554 | 561 | PF00069 | 0.375 |
MOD_GSK3_1 | 588 | 595 | PF00069 | 0.375 |
MOD_GSK3_1 | 640 | 647 | PF00069 | 0.258 |
MOD_GSK3_1 | 741 | 748 | PF00069 | 0.396 |
MOD_GSK3_1 | 808 | 815 | PF00069 | 0.671 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.674 |
MOD_N-GLC_1 | 173 | 178 | PF02516 | 0.682 |
MOD_N-GLC_1 | 457 | 462 | PF02516 | 0.335 |
MOD_N-GLC_1 | 535 | 540 | PF02516 | 0.335 |
MOD_N-GLC_1 | 644 | 649 | PF02516 | 0.280 |
MOD_N-GLC_1 | 663 | 668 | PF02516 | 0.280 |
MOD_N-GLC_1 | 777 | 782 | PF02516 | 0.423 |
MOD_N-GLC_2 | 760 | 762 | PF02516 | 0.375 |
MOD_NEK2_1 | 244 | 249 | PF00069 | 0.571 |
MOD_NEK2_1 | 314 | 319 | PF00069 | 0.622 |
MOD_NEK2_1 | 359 | 364 | PF00069 | 0.658 |
MOD_NEK2_1 | 457 | 462 | PF00069 | 0.455 |
MOD_NEK2_1 | 507 | 512 | PF00069 | 0.419 |
MOD_NEK2_1 | 625 | 630 | PF00069 | 0.404 |
MOD_NEK2_1 | 687 | 692 | PF00069 | 0.375 |
MOD_NEK2_1 | 743 | 748 | PF00069 | 0.264 |
MOD_NEK2_1 | 820 | 825 | PF00069 | 0.693 |
MOD_NEK2_1 | 836 | 841 | PF00069 | 0.629 |
MOD_NEK2_2 | 164 | 169 | PF00069 | 0.626 |
MOD_NEK2_2 | 173 | 178 | PF00069 | 0.517 |
MOD_PIKK_1 | 231 | 237 | PF00454 | 0.591 |
MOD_PIKK_1 | 360 | 366 | PF00454 | 0.654 |
MOD_PIKK_1 | 812 | 818 | PF00454 | 0.629 |
MOD_PKA_1 | 95 | 101 | PF00069 | 0.680 |
MOD_PKA_2 | 111 | 117 | PF00069 | 0.553 |
MOD_PKA_2 | 150 | 156 | PF00069 | 0.648 |
MOD_PKA_2 | 222 | 228 | PF00069 | 0.678 |
MOD_PKA_2 | 445 | 451 | PF00069 | 0.448 |
MOD_PKA_2 | 61 | 67 | PF00069 | 0.583 |
MOD_PKA_2 | 772 | 778 | PF00069 | 0.375 |
MOD_PKA_2 | 794 | 800 | PF00069 | 0.494 |
MOD_PKA_2 | 828 | 834 | PF00069 | 0.664 |
MOD_PKA_2 | 86 | 92 | PF00069 | 0.656 |
MOD_PKA_2 | 95 | 101 | PF00069 | 0.623 |
MOD_PKB_1 | 110 | 118 | PF00069 | 0.650 |
MOD_Plk_1 | 38 | 44 | PF00069 | 0.628 |
MOD_Plk_1 | 457 | 463 | PF00069 | 0.335 |
MOD_Plk_1 | 701 | 707 | PF00069 | 0.375 |
MOD_Plk_1 | 777 | 783 | PF00069 | 0.422 |
MOD_Plk_2-3 | 772 | 778 | PF00069 | 0.375 |
MOD_Plk_4 | 173 | 179 | PF00069 | 0.644 |
MOD_Plk_4 | 196 | 202 | PF00069 | 0.700 |
MOD_Plk_4 | 32 | 38 | PF00069 | 0.639 |
MOD_Plk_4 | 465 | 471 | PF00069 | 0.383 |
MOD_Plk_4 | 507 | 513 | PF00069 | 0.375 |
MOD_Plk_4 | 559 | 565 | PF00069 | 0.375 |
MOD_Plk_4 | 777 | 783 | PF00069 | 0.475 |
MOD_Plk_4 | 831 | 837 | PF00069 | 0.607 |
MOD_ProDKin_1 | 144 | 150 | PF00069 | 0.804 |
MOD_ProDKin_1 | 16 | 22 | PF00069 | 0.662 |
MOD_ProDKin_1 | 203 | 209 | PF00069 | 0.683 |
MOD_ProDKin_1 | 245 | 251 | PF00069 | 0.614 |
MOD_ProDKin_1 | 330 | 336 | PF00069 | 0.626 |
MOD_ProDKin_1 | 640 | 646 | PF00069 | 0.330 |
MOD_ProDKin_1 | 670 | 676 | PF00069 | 0.372 |
MOD_ProDKin_1 | 731 | 737 | PF00069 | 0.375 |
MOD_ProDKin_1 | 748 | 754 | PF00069 | 0.355 |
MOD_SUMO_rev_2 | 121 | 126 | PF00179 | 0.674 |
MOD_SUMO_rev_2 | 595 | 600 | PF00179 | 0.399 |
MOD_SUMO_rev_2 | 633 | 638 | PF00179 | 0.375 |
MOD_SUMO_rev_2 | 643 | 653 | PF00179 | 0.287 |
TRG_DiLeu_BaEn_1 | 39 | 44 | PF01217 | 0.597 |
TRG_DiLeu_BaEn_3 | 721 | 727 | PF01217 | 0.375 |
TRG_DiLeu_BaLyEn_6 | 212 | 217 | PF01217 | 0.699 |
TRG_ER_diArg_1 | 479 | 481 | PF00400 | 0.393 |
TRG_ER_diArg_1 | 540 | 543 | PF00400 | 0.375 |
TRG_ER_diArg_1 | 607 | 609 | PF00400 | 0.386 |
TRG_ER_diArg_1 | 679 | 681 | PF00400 | 0.401 |
TRG_Pf-PMV_PEXEL_1 | 131 | 135 | PF00026 | 0.674 |
TRG_Pf-PMV_PEXEL_1 | 629 | 633 | PF00026 | 0.404 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8ID61 | Leishmania donovani | 92% | 100% |
A4H7P3 | Leishmania braziliensis | 72% | 91% |
A4HKF6 | Leishmania braziliensis | 25% | 100% |
A4HW33 | Leishmania infantum | 92% | 88% |
E9APT5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 88% |