A large collection of various protein phosphatases. Very highly expanded in kinetoplastids.
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 2 |
Forrest at al. (procyclic) | no | yes: 2 |
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. | yes | yes: 6 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 13 |
NetGPI | no | yes: 0, no: 13 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 2 |
GO:0005654 | nucleoplasm | 2 | 2 |
GO:0005737 | cytoplasm | 2 | 2 |
GO:0005829 | cytosol | 2 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4QGM7
Term | Name | Level | Count |
---|---|---|---|
GO:0006470 | protein dephosphorylation | 5 | 1 |
GO:0006793 | phosphorus metabolic process | 3 | 1 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016311 | dephosphorylation | 5 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 14 |
GO:0004721 | phosphoprotein phosphatase activity | 3 | 14 |
GO:0004722 | protein serine/threonine phosphatase activity | 4 | 14 |
GO:0005488 | binding | 1 | 9 |
GO:0005509 | calcium ion binding | 5 | 9 |
GO:0016787 | hydrolase activity | 2 | 14 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 14 |
GO:0016791 | phosphatase activity | 5 | 14 |
GO:0017018 | myosin phosphatase activity | 5 | 14 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 14 |
GO:0043167 | ion binding | 2 | 9 |
GO:0043169 | cation binding | 3 | 9 |
GO:0046872 | metal ion binding | 4 | 9 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 14 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 607 | 611 | PF00656 | 0.612 |
CLV_MEL_PAP_1 | 330 | 336 | PF00089 | 0.546 |
CLV_NRD_NRD_1 | 116 | 118 | PF00675 | 0.602 |
CLV_NRD_NRD_1 | 183 | 185 | PF00675 | 0.683 |
CLV_NRD_NRD_1 | 33 | 35 | PF00675 | 0.768 |
CLV_NRD_NRD_1 | 466 | 468 | PF00675 | 0.339 |
CLV_NRD_NRD_1 | 649 | 651 | PF00675 | 0.522 |
CLV_NRD_NRD_1 | 666 | 668 | PF00675 | 0.321 |
CLV_NRD_NRD_1 | 71 | 73 | PF00675 | 0.601 |
CLV_NRD_NRD_1 | 877 | 879 | PF00675 | 0.506 |
CLV_NRD_NRD_1 | 917 | 919 | PF00675 | 0.608 |
CLV_PCSK_KEX2_1 | 116 | 118 | PF00082 | 0.650 |
CLV_PCSK_KEX2_1 | 183 | 185 | PF00082 | 0.683 |
CLV_PCSK_KEX2_1 | 255 | 257 | PF00082 | 0.607 |
CLV_PCSK_KEX2_1 | 33 | 35 | PF00082 | 0.781 |
CLV_PCSK_KEX2_1 | 465 | 467 | PF00082 | 0.318 |
CLV_PCSK_KEX2_1 | 649 | 651 | PF00082 | 0.509 |
CLV_PCSK_KEX2_1 | 666 | 668 | PF00082 | 0.323 |
CLV_PCSK_KEX2_1 | 917 | 919 | PF00082 | 0.653 |
CLV_PCSK_PC1ET2_1 | 255 | 257 | PF00082 | 0.641 |
CLV_PCSK_PC7_1 | 662 | 668 | PF00082 | 0.376 |
CLV_PCSK_SKI1_1 | 163 | 167 | PF00082 | 0.573 |
CLV_PCSK_SKI1_1 | 210 | 214 | PF00082 | 0.499 |
CLV_PCSK_SKI1_1 | 293 | 297 | PF00082 | 0.467 |
CLV_PCSK_SKI1_1 | 298 | 302 | PF00082 | 0.406 |
CLV_PCSK_SKI1_1 | 308 | 312 | PF00082 | 0.263 |
CLV_PCSK_SKI1_1 | 403 | 407 | PF00082 | 0.360 |
CLV_PCSK_SKI1_1 | 433 | 437 | PF00082 | 0.352 |
CLV_PCSK_SKI1_1 | 558 | 562 | PF00082 | 0.365 |
CLV_PCSK_SKI1_1 | 644 | 648 | PF00082 | 0.618 |
CLV_PCSK_SKI1_1 | 695 | 699 | PF00082 | 0.383 |
CLV_PCSK_SKI1_1 | 879 | 883 | PF00082 | 0.471 |
CLV_PCSK_SKI1_1 | 89 | 93 | PF00082 | 0.469 |
DEG_APCC_DBOX_1 | 707 | 715 | PF00400 | 0.532 |
DEG_APCC_DBOX_1 | 844 | 852 | PF00400 | 0.469 |
DEG_SPOP_SBC_1 | 268 | 272 | PF00917 | 0.615 |
DOC_ANK_TNKS_1 | 183 | 190 | PF00023 | 0.548 |
DOC_CDC14_PxL_1 | 720 | 728 | PF14671 | 0.492 |
DOC_CYCLIN_RxL_1 | 638 | 651 | PF00134 | 0.589 |
DOC_CYCLIN_yCln2_LP_2 | 700 | 706 | PF00134 | 0.414 |
DOC_MAPK_gen_1 | 293 | 301 | PF00069 | 0.538 |
DOC_MAPK_gen_1 | 465 | 471 | PF00069 | 0.325 |
DOC_MAPK_gen_1 | 476 | 485 | PF00069 | 0.325 |
DOC_MAPK_MEF2A_6 | 383 | 392 | PF00069 | 0.300 |
DOC_MAPK_MEF2A_6 | 695 | 702 | PF00069 | 0.419 |
DOC_MAPK_NFAT4_5 | 695 | 703 | PF00069 | 0.422 |
DOC_PP1_RVXF_1 | 166 | 172 | PF00149 | 0.665 |
DOC_PP2B_LxvP_1 | 614 | 617 | PF13499 | 0.542 |
DOC_PP2B_LxvP_1 | 700 | 703 | PF13499 | 0.413 |
DOC_PP4_FxxP_1 | 185 | 188 | PF00568 | 0.560 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.658 |
DOC_USP7_MATH_1 | 254 | 258 | PF00917 | 0.600 |
DOC_USP7_MATH_1 | 268 | 272 | PF00917 | 0.536 |
DOC_USP7_MATH_1 | 332 | 336 | PF00917 | 0.547 |
DOC_USP7_MATH_1 | 368 | 372 | PF00917 | 0.384 |
DOC_USP7_MATH_1 | 586 | 590 | PF00917 | 0.364 |
DOC_USP7_MATH_1 | 59 | 63 | PF00917 | 0.651 |
DOC_USP7_UBL2_3 | 159 | 163 | PF12436 | 0.592 |
DOC_USP7_UBL2_3 | 241 | 245 | PF12436 | 0.583 |
DOC_USP7_UBL2_3 | 73 | 77 | PF12436 | 0.620 |
DOC_WW_Pin1_4 | 324 | 329 | PF00397 | 0.440 |
LIG_14-3-3_CanoR_1 | 256 | 261 | PF00244 | 0.677 |
LIG_14-3-3_CanoR_1 | 308 | 317 | PF00244 | 0.366 |
LIG_14-3-3_CanoR_1 | 621 | 626 | PF00244 | 0.618 |
LIG_14-3-3_CanoR_1 | 742 | 746 | PF00244 | 0.467 |
LIG_14-3-3_CanoR_1 | 853 | 861 | PF00244 | 0.576 |
LIG_14-3-3_CanoR_1 | 878 | 884 | PF00244 | 0.520 |
LIG_14-3-3_CanoR_1 | 917 | 921 | PF00244 | 0.634 |
LIG_14-3-3_CanoR_1 | 943 | 948 | PF00244 | 0.654 |
LIG_Actin_WH2_2 | 348 | 365 | PF00022 | 0.453 |
LIG_BRCT_BRCA1_1 | 271 | 275 | PF00533 | 0.494 |
LIG_BRCT_BRCA1_1 | 630 | 634 | PF00533 | 0.753 |
LIG_BRCT_BRCA1_1 | 762 | 766 | PF00533 | 0.550 |
LIG_BRCT_BRCA1_2 | 762 | 768 | PF00533 | 0.549 |
LIG_CaM_IQ_9 | 202 | 217 | PF13499 | 0.456 |
LIG_Clathr_ClatBox_1 | 711 | 715 | PF01394 | 0.528 |
LIG_deltaCOP1_diTrp_1 | 701 | 706 | PF00928 | 0.411 |
LIG_deltaCOP1_diTrp_1 | 735 | 741 | PF00928 | 0.546 |
LIG_DLG_GKlike_1 | 943 | 950 | PF00625 | 0.672 |
LIG_EH1_1 | 285 | 293 | PF00400 | 0.445 |
LIG_FHA_1 | 176 | 182 | PF00498 | 0.499 |
LIG_FHA_1 | 624 | 630 | PF00498 | 0.658 |
LIG_FHA_2 | 427 | 433 | PF00498 | 0.308 |
LIG_FHA_2 | 784 | 790 | PF00498 | 0.407 |
LIG_FHA_2 | 853 | 859 | PF00498 | 0.577 |
LIG_Integrin_isoDGR_2 | 336 | 338 | PF01839 | 0.550 |
LIG_LIR_Apic_2 | 499 | 505 | PF02991 | 0.322 |
LIG_LIR_Apic_2 | 566 | 571 | PF02991 | 0.436 |
LIG_LIR_Apic_2 | 718 | 724 | PF02991 | 0.459 |
LIG_LIR_Gen_1 | 235 | 242 | PF02991 | 0.547 |
LIG_LIR_Gen_1 | 494 | 505 | PF02991 | 0.322 |
LIG_LIR_Gen_1 | 592 | 600 | PF02991 | 0.566 |
LIG_LIR_Gen_1 | 775 | 783 | PF02991 | 0.399 |
LIG_LIR_Gen_1 | 887 | 898 | PF02991 | 0.464 |
LIG_LIR_Gen_1 | 902 | 913 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 220 | 226 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 235 | 240 | PF02991 | 0.551 |
LIG_LIR_Nem_3 | 271 | 277 | PF02991 | 0.570 |
LIG_LIR_Nem_3 | 370 | 376 | PF02991 | 0.341 |
LIG_LIR_Nem_3 | 573 | 578 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 587 | 593 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 701 | 707 | PF02991 | 0.410 |
LIG_LIR_Nem_3 | 775 | 779 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 902 | 908 | PF02991 | 0.423 |
LIG_LIR_Nem_3 | 945 | 950 | PF02991 | 0.559 |
LIG_MLH1_MIPbox_1 | 271 | 275 | PF16413 | 0.494 |
LIG_PCNA_PIPBox_1 | 104 | 113 | PF02747 | 0.562 |
LIG_Pex14_1 | 721 | 725 | PF04695 | 0.394 |
LIG_Pex14_2 | 725 | 729 | PF04695 | 0.353 |
LIG_PTB_Apo_2 | 170 | 177 | PF02174 | 0.636 |
LIG_PTB_Apo_2 | 374 | 381 | PF02174 | 0.300 |
LIG_PTB_Apo_2 | 415 | 422 | PF02174 | 0.322 |
LIG_PTB_Apo_2 | 941 | 948 | PF02174 | 0.593 |
LIG_PTB_Phospho_1 | 374 | 380 | PF10480 | 0.460 |
LIG_PTB_Phospho_1 | 415 | 421 | PF10480 | 0.322 |
LIG_SH2_CRK | 568 | 572 | PF00017 | 0.506 |
LIG_SH2_CRK | 575 | 579 | PF00017 | 0.409 |
LIG_SH2_GRB2like | 416 | 419 | PF00017 | 0.318 |
LIG_SH2_NCK_1 | 488 | 492 | PF00017 | 0.360 |
LIG_SH2_PTP2 | 404 | 407 | PF00017 | 0.334 |
LIG_SH2_SRC | 551 | 554 | PF00017 | 0.428 |
LIG_SH2_SRC | 600 | 603 | PF00017 | 0.585 |
LIG_SH2_STAP1 | 431 | 435 | PF00017 | 0.322 |
LIG_SH2_STAT5 | 274 | 277 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 374 | 377 | PF00017 | 0.349 |
LIG_SH2_STAT5 | 380 | 383 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 404 | 407 | PF00017 | 0.334 |
LIG_SH2_STAT5 | 673 | 676 | PF00017 | 0.396 |
LIG_SH2_STAT5 | 705 | 708 | PF00017 | 0.389 |
LIG_SH2_STAT5 | 710 | 713 | PF00017 | 0.364 |
LIG_SH2_STAT5 | 785 | 788 | PF00017 | 0.418 |
LIG_SH2_STAT5 | 913 | 916 | PF00017 | 0.488 |
LIG_SH3_3 | 248 | 254 | PF00018 | 0.613 |
LIG_SH3_3 | 262 | 268 | PF00018 | 0.483 |
LIG_SH3_3 | 296 | 302 | PF00018 | 0.425 |
LIG_SH3_4 | 144 | 151 | PF00018 | 0.612 |
LIG_SH3_5 | 75 | 79 | PF00018 | 0.553 |
LIG_SUMO_SIM_anti_2 | 389 | 396 | PF11976 | 0.325 |
LIG_SUMO_SIM_par_1 | 128 | 133 | PF11976 | 0.561 |
LIG_SUMO_SIM_par_1 | 344 | 350 | PF11976 | 0.314 |
LIG_SUMO_SIM_par_1 | 389 | 396 | PF11976 | 0.340 |
LIG_SUMO_SIM_par_1 | 558 | 564 | PF11976 | 0.377 |
LIG_SUMO_SIM_par_1 | 601 | 611 | PF11976 | 0.639 |
LIG_SUMO_SIM_par_1 | 710 | 716 | PF11976 | 0.546 |
LIG_TRAF2_1 | 26 | 29 | PF00917 | 0.508 |
LIG_UBA3_1 | 291 | 296 | PF00899 | 0.523 |
LIG_UBA3_1 | 358 | 363 | PF00899 | 0.329 |
LIG_UBA3_1 | 394 | 403 | PF00899 | 0.340 |
LIG_UBA3_1 | 889 | 894 | PF00899 | 0.473 |
LIG_WRC_WIRS_1 | 578 | 583 | PF05994 | 0.503 |
LIG_WRC_WIRS_1 | 622 | 627 | PF05994 | 0.612 |
LIG_WRC_WIRS_1 | 796 | 801 | PF05994 | 0.536 |
LIG_WW_3 | 462 | 466 | PF00397 | 0.304 |
MOD_CK1_1 | 16 | 22 | PF00069 | 0.733 |
MOD_CK1_1 | 37 | 43 | PF00069 | 0.742 |
MOD_CK1_1 | 47 | 53 | PF00069 | 0.735 |
MOD_CK1_1 | 525 | 531 | PF00069 | 0.376 |
MOD_CK1_1 | 589 | 595 | PF00069 | 0.516 |
MOD_CK1_1 | 623 | 629 | PF00069 | 0.693 |
MOD_CK1_1 | 925 | 931 | PF00069 | 0.559 |
MOD_CK2_1 | 2 | 8 | PF00069 | 0.618 |
MOD_CK2_1 | 486 | 492 | PF00069 | 0.331 |
MOD_CK2_1 | 508 | 514 | PF00069 | 0.231 |
MOD_CK2_1 | 546 | 552 | PF00069 | 0.472 |
MOD_CK2_1 | 795 | 801 | PF00069 | 0.508 |
MOD_CK2_1 | 805 | 811 | PF00069 | 0.552 |
MOD_CMANNOS | 94 | 97 | PF00535 | 0.530 |
MOD_Cter_Amidation | 114 | 117 | PF01082 | 0.649 |
MOD_Cter_Amidation | 31 | 34 | PF01082 | 0.621 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.673 |
MOD_GlcNHglycan | 364 | 367 | PF01048 | 0.417 |
MOD_GlcNHglycan | 46 | 49 | PF01048 | 0.776 |
MOD_GlcNHglycan | 548 | 551 | PF01048 | 0.492 |
MOD_GlcNHglycan | 563 | 566 | PF01048 | 0.273 |
MOD_GlcNHglycan | 762 | 765 | PF01048 | 0.562 |
MOD_GlcNHglycan | 807 | 810 | PF01048 | 0.482 |
MOD_GlcNHglycan | 947 | 950 | PF01048 | 0.607 |
MOD_GSK3_1 | 218 | 225 | PF00069 | 0.622 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.667 |
MOD_GSK3_1 | 362 | 369 | PF00069 | 0.449 |
MOD_GSK3_1 | 508 | 515 | PF00069 | 0.231 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.598 |
MOD_GSK3_1 | 600 | 607 | PF00069 | 0.627 |
MOD_GSK3_1 | 608 | 615 | PF00069 | 0.543 |
MOD_GSK3_1 | 621 | 628 | PF00069 | 0.609 |
MOD_GSK3_1 | 636 | 643 | PF00069 | 0.634 |
MOD_GSK3_1 | 677 | 684 | PF00069 | 0.407 |
MOD_GSK3_1 | 756 | 763 | PF00069 | 0.566 |
MOD_GSK3_1 | 843 | 850 | PF00069 | 0.538 |
MOD_GSK3_1 | 89 | 96 | PF00069 | 0.486 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.658 |
MOD_GSK3_1 | 923 | 930 | PF00069 | 0.652 |
MOD_GSK3_1 | 938 | 945 | PF00069 | 0.397 |
MOD_N-GLC_1 | 37 | 42 | PF02516 | 0.635 |
MOD_N-GLC_1 | 486 | 491 | PF02516 | 0.460 |
MOD_N-GLC_1 | 943 | 948 | PF02516 | 0.628 |
MOD_NEK2_1 | 152 | 157 | PF00069 | 0.530 |
MOD_NEK2_1 | 198 | 203 | PF00069 | 0.597 |
MOD_NEK2_1 | 362 | 367 | PF00069 | 0.477 |
MOD_NEK2_1 | 563 | 568 | PF00069 | 0.375 |
MOD_NEK2_1 | 608 | 613 | PF00069 | 0.559 |
MOD_NEK2_1 | 625 | 630 | PF00069 | 0.538 |
MOD_NEK2_1 | 634 | 639 | PF00069 | 0.594 |
MOD_NEK2_1 | 677 | 682 | PF00069 | 0.406 |
MOD_NEK2_1 | 852 | 857 | PF00069 | 0.518 |
MOD_NEK2_1 | 923 | 928 | PF00069 | 0.678 |
MOD_NEK2_1 | 942 | 947 | PF00069 | 0.706 |
MOD_NEK2_2 | 690 | 695 | PF00069 | 0.475 |
MOD_NMyristoyl | 1 | 7 | PF02799 | 0.586 |
MOD_OFUCOSY | 86 | 93 | PF10250 | 0.492 |
MOD_PIKK_1 | 486 | 492 | PF00454 | 0.340 |
MOD_PIKK_1 | 512 | 518 | PF00454 | 0.404 |
MOD_PIKK_1 | 600 | 606 | PF00454 | 0.716 |
MOD_PIKK_1 | 756 | 762 | PF00454 | 0.528 |
MOD_PIKK_1 | 843 | 849 | PF00454 | 0.496 |
MOD_PIKK_1 | 879 | 885 | PF00454 | 0.475 |
MOD_PK_1 | 256 | 262 | PF00069 | 0.587 |
MOD_PK_1 | 467 | 473 | PF00069 | 0.417 |
MOD_PKA_2 | 137 | 143 | PF00069 | 0.621 |
MOD_PKA_2 | 19 | 25 | PF00069 | 0.633 |
MOD_PKA_2 | 32 | 38 | PF00069 | 0.754 |
MOD_PKA_2 | 332 | 338 | PF00069 | 0.571 |
MOD_PKA_2 | 512 | 518 | PF00069 | 0.325 |
MOD_PKA_2 | 620 | 626 | PF00069 | 0.649 |
MOD_PKA_2 | 648 | 654 | PF00069 | 0.549 |
MOD_PKA_2 | 741 | 747 | PF00069 | 0.491 |
MOD_PKA_2 | 852 | 858 | PF00069 | 0.600 |
MOD_PKA_2 | 916 | 922 | PF00069 | 0.640 |
MOD_PKA_2 | 942 | 948 | PF00069 | 0.724 |
MOD_PKB_1 | 465 | 473 | PF00069 | 0.376 |
MOD_Plk_1 | 198 | 204 | PF00069 | 0.578 |
MOD_Plk_1 | 218 | 224 | PF00069 | 0.450 |
MOD_Plk_1 | 472 | 478 | PF00069 | 0.360 |
MOD_Plk_1 | 525 | 531 | PF00069 | 0.328 |
MOD_Plk_1 | 59 | 65 | PF00069 | 0.647 |
MOD_Plk_1 | 600 | 606 | PF00069 | 0.670 |
MOD_Plk_1 | 715 | 721 | PF00069 | 0.455 |
MOD_Plk_1 | 89 | 95 | PF00069 | 0.476 |
MOD_Plk_1 | 901 | 907 | PF00069 | 0.532 |
MOD_Plk_1 | 943 | 949 | PF00069 | 0.626 |
MOD_Plk_2-3 | 508 | 514 | PF00069 | 0.231 |
MOD_Plk_2-3 | 901 | 907 | PF00069 | 0.555 |
MOD_Plk_4 | 161 | 167 | PF00069 | 0.626 |
MOD_Plk_4 | 218 | 224 | PF00069 | 0.479 |
MOD_Plk_4 | 447 | 453 | PF00069 | 0.312 |
MOD_Plk_4 | 558 | 564 | PF00069 | 0.353 |
MOD_Plk_4 | 577 | 583 | PF00069 | 0.372 |
MOD_Plk_4 | 681 | 687 | PF00069 | 0.405 |
MOD_Plk_4 | 775 | 781 | PF00069 | 0.379 |
MOD_Plk_4 | 80 | 86 | PF00069 | 0.566 |
MOD_Plk_4 | 847 | 853 | PF00069 | 0.510 |
MOD_ProDKin_1 | 324 | 330 | PF00069 | 0.451 |
MOD_SPalmitoyl_4 | 1 | 7 | PF01529 | 0.646 |
MOD_SUMO_for_1 | 196 | 199 | PF00179 | 0.475 |
MOD_SUMO_for_1 | 232 | 235 | PF00179 | 0.490 |
MOD_SUMO_rev_2 | 503 | 511 | PF00179 | 0.231 |
TRG_DiLeu_BaLyEn_6 | 434 | 439 | PF01217 | 0.376 |
TRG_DiLeu_BaLyEn_6 | 666 | 671 | PF01217 | 0.438 |
TRG_ENDOCYTIC_2 | 227 | 230 | PF00928 | 0.560 |
TRG_ENDOCYTIC_2 | 274 | 277 | PF00928 | 0.545 |
TRG_ENDOCYTIC_2 | 373 | 376 | PF00928 | 0.351 |
TRG_ENDOCYTIC_2 | 404 | 407 | PF00928 | 0.334 |
TRG_ENDOCYTIC_2 | 575 | 578 | PF00928 | 0.445 |
TRG_ENDOCYTIC_2 | 593 | 596 | PF00928 | 0.362 |
TRG_ENDOCYTIC_2 | 722 | 725 | PF00928 | 0.345 |
TRG_ENDOCYTIC_2 | 773 | 776 | PF00928 | 0.373 |
TRG_ER_diArg_1 | 183 | 185 | PF00400 | 0.569 |
TRG_ER_diArg_1 | 464 | 467 | PF00400 | 0.325 |
TRG_ER_diArg_1 | 666 | 669 | PF00400 | 0.461 |
TRG_NES_CRM1_1 | 220 | 235 | PF08389 | 0.511 |
TRG_NES_CRM1_1 | 350 | 364 | PF08389 | 0.325 |
TRG_NLS_MonoExtN_4 | 254 | 259 | PF00514 | 0.608 |
TRG_Pf-PMV_PEXEL_1 | 109 | 113 | PF00026 | 0.490 |
TRG_Pf-PMV_PEXEL_1 | 657 | 661 | PF00026 | 0.404 |
TRG_Pf-PMV_PEXEL_1 | 748 | 752 | PF00026 | 0.528 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IGT4 | Leptomonas seymouri | 82% | 98% |
A0A0S4JAH8 | Bodo saltans | 31% | 76% |
A0A0S4JE35 | Bodo saltans | 58% | 100% |
A0A1X0NNZ8 | Trypanosomatidae | 62% | 100% |
A0A3Q8I989 | Leishmania donovani | 97% | 99% |
A0A422MRT7 | Trypanosoma rangeli | 59% | 100% |
A4H6X9 | Leishmania braziliensis | 90% | 100% |
C9ZHY0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 59% | 100% |
C9ZUN2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 67% |
E9AGF3 | Leishmania infantum | 97% | 99% |
E9ANZ3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 99% |
V5BP95 | Trypanosoma cruzi | 66% | 100% |