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 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pescher et al. (upgregulation) | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Lahav et al. - mRNA
- Protein
|
Related structures:
AlphaFold database: A4HW33
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 | 469 | 473 | PF00656 | 0.761 |
CLV_C14_Caspase3-7 | 491 | 495 | PF00656 | 0.669 |
CLV_NRD_NRD_1 | 192 | 194 | PF00675 | 0.630 |
CLV_NRD_NRD_1 | 2 | 4 | PF00675 | 0.552 |
CLV_NRD_NRD_1 | 214 | 216 | PF00675 | 0.699 |
CLV_NRD_NRD_1 | 408 | 410 | PF00675 | 0.720 |
CLV_NRD_NRD_1 | 5 | 7 | PF00675 | 0.538 |
CLV_NRD_NRD_1 | 596 | 598 | PF00675 | 0.400 |
CLV_NRD_NRD_1 | 659 | 661 | PF00675 | 0.348 |
CLV_NRD_NRD_1 | 724 | 726 | PF00675 | 0.280 |
CLV_NRD_NRD_1 | 795 | 797 | PF00675 | 0.418 |
CLV_NRD_NRD_1 | 944 | 946 | PF00675 | 0.617 |
CLV_NRD_NRD_1 | 98 | 100 | PF00675 | 0.689 |
CLV_PCSK_FUR_1 | 657 | 661 | PF00082 | 0.259 |
CLV_PCSK_FUR_1 | 96 | 100 | PF00082 | 0.557 |
CLV_PCSK_KEX2_1 | 110 | 112 | PF00082 | 0.506 |
CLV_PCSK_KEX2_1 | 192 | 194 | PF00082 | 0.593 |
CLV_PCSK_KEX2_1 | 214 | 216 | PF00082 | 0.721 |
CLV_PCSK_KEX2_1 | 408 | 410 | PF00082 | 0.720 |
CLV_PCSK_KEX2_1 | 596 | 598 | PF00082 | 0.400 |
CLV_PCSK_KEX2_1 | 657 | 659 | PF00082 | 0.280 |
CLV_PCSK_KEX2_1 | 724 | 726 | PF00082 | 0.280 |
CLV_PCSK_KEX2_1 | 795 | 797 | PF00082 | 0.418 |
CLV_PCSK_KEX2_1 | 98 | 100 | PF00082 | 0.689 |
CLV_PCSK_PC1ET2_1 | 110 | 112 | PF00082 | 0.554 |
CLV_PCSK_SKI1_1 | 243 | 247 | PF00082 | 0.672 |
CLV_PCSK_SKI1_1 | 307 | 311 | PF00082 | 0.607 |
CLV_PCSK_SKI1_1 | 426 | 430 | PF00082 | 0.523 |
CLV_PCSK_SKI1_1 | 544 | 548 | PF00082 | 0.533 |
CLV_PCSK_SKI1_1 | 633 | 637 | PF00082 | 0.280 |
CLV_PCSK_SKI1_1 | 699 | 703 | PF00082 | 0.280 |
CLV_PCSK_SKI1_1 | 725 | 729 | PF00082 | 0.280 |
CLV_PCSK_SKI1_1 | 844 | 848 | PF00082 | 0.280 |
CLV_PCSK_SKI1_1 | 957 | 961 | PF00082 | 0.519 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.678 |
DEG_SPOP_SBC_1 | 314 | 318 | PF00917 | 0.699 |
DOC_MAPK_DCC_7 | 501 | 509 | PF00069 | 0.653 |
DOC_MAPK_gen_1 | 724 | 735 | PF00069 | 0.280 |
DOC_MAPK_MEF2A_6 | 501 | 509 | PF00069 | 0.653 |
DOC_MAPK_MEF2A_6 | 544 | 552 | PF00069 | 0.521 |
DOC_PP2B_LxvP_1 | 310 | 313 | PF13499 | 0.604 |
DOC_PP4_FxxP_1 | 64 | 67 | PF00568 | 0.602 |
DOC_USP7_MATH_1 | 121 | 125 | PF00917 | 0.582 |
DOC_USP7_MATH_1 | 169 | 173 | PF00917 | 0.574 |
DOC_USP7_MATH_1 | 21 | 25 | PF00917 | 0.536 |
DOC_USP7_MATH_1 | 230 | 234 | PF00917 | 0.669 |
DOC_USP7_MATH_1 | 269 | 273 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 283 | 287 | PF00917 | 0.472 |
DOC_USP7_MATH_1 | 314 | 318 | PF00917 | 0.702 |
DOC_USP7_MATH_1 | 368 | 372 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 490 | 494 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 510 | 514 | PF00917 | 0.455 |
DOC_USP7_MATH_1 | 68 | 72 | PF00917 | 0.585 |
DOC_USP7_MATH_1 | 789 | 793 | PF00917 | 0.379 |
DOC_USP7_MATH_1 | 944 | 948 | PF00917 | 0.533 |
DOC_USP7_UBL2_3 | 125 | 129 | PF12436 | 0.504 |
DOC_WW_Pin1_4 | 135 | 140 | PF00397 | 0.578 |
DOC_WW_Pin1_4 | 263 | 268 | PF00397 | 0.686 |
DOC_WW_Pin1_4 | 322 | 327 | PF00397 | 0.596 |
DOC_WW_Pin1_4 | 355 | 360 | PF00397 | 0.600 |
DOC_WW_Pin1_4 | 36 | 41 | PF00397 | 0.609 |
DOC_WW_Pin1_4 | 364 | 369 | PF00397 | 0.602 |
DOC_WW_Pin1_4 | 447 | 452 | PF00397 | 0.650 |
DOC_WW_Pin1_4 | 63 | 68 | PF00397 | 0.723 |
DOC_WW_Pin1_4 | 755 | 760 | PF00397 | 0.327 |
DOC_WW_Pin1_4 | 787 | 792 | PF00397 | 0.361 |
DOC_WW_Pin1_4 | 847 | 852 | PF00397 | 0.280 |
DOC_WW_Pin1_4 | 864 | 869 | PF00397 | 0.280 |
LIG_14-3-3_CanoR_1 | 161 | 167 | PF00244 | 0.575 |
LIG_14-3-3_CanoR_1 | 206 | 210 | PF00244 | 0.582 |
LIG_14-3-3_CanoR_1 | 214 | 222 | PF00244 | 0.546 |
LIG_14-3-3_CanoR_1 | 23 | 30 | PF00244 | 0.481 |
LIG_14-3-3_CanoR_1 | 231 | 236 | PF00244 | 0.571 |
LIG_14-3-3_CanoR_1 | 77 | 85 | PF00244 | 0.471 |
LIG_14-3-3_CanoR_1 | 945 | 949 | PF00244 | 0.597 |
LIG_Actin_WH2_2 | 238 | 255 | PF00022 | 0.672 |
LIG_Actin_WH2_2 | 7 | 25 | PF00022 | 0.466 |
LIG_BIR_III_4 | 762 | 766 | PF00653 | 0.248 |
LIG_BRCT_BRCA1_1 | 769 | 773 | PF00533 | 0.400 |
LIG_FHA_1 | 136 | 142 | PF00498 | 0.628 |
LIG_FHA_1 | 206 | 212 | PF00498 | 0.642 |
LIG_FHA_1 | 24 | 30 | PF00498 | 0.526 |
LIG_FHA_1 | 359 | 365 | PF00498 | 0.644 |
LIG_FHA_1 | 400 | 406 | PF00498 | 0.714 |
LIG_FHA_1 | 478 | 484 | PF00498 | 0.556 |
LIG_FHA_1 | 543 | 549 | PF00498 | 0.483 |
LIG_FHA_1 | 838 | 844 | PF00498 | 0.280 |
LIG_FHA_1 | 848 | 854 | PF00498 | 0.280 |
LIG_FHA_2 | 236 | 242 | PF00498 | 0.673 |
LIG_FHA_2 | 563 | 569 | PF00498 | 0.280 |
LIG_FHA_2 | 629 | 635 | PF00498 | 0.280 |
LIG_Integrin_isoDGR_2 | 399 | 401 | PF01839 | 0.653 |
LIG_Integrin_isoDGR_2 | 963 | 965 | PF01839 | 0.533 |
LIG_LIR_Apic_2 | 63 | 67 | PF02991 | 0.538 |
LIG_LIR_Gen_1 | 187 | 196 | PF02991 | 0.524 |
LIG_LIR_Gen_1 | 568 | 579 | PF02991 | 0.280 |
LIG_LIR_Gen_1 | 634 | 641 | PF02991 | 0.270 |
LIG_LIR_Gen_1 | 820 | 830 | PF02991 | 0.280 |
LIG_LIR_Nem_3 | 187 | 191 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 568 | 574 | PF02991 | 0.280 |
LIG_LIR_Nem_3 | 634 | 639 | PF02991 | 0.280 |
LIG_LIR_Nem_3 | 820 | 825 | PF02991 | 0.280 |
LIG_LIR_Nem_3 | 828 | 834 | PF02991 | 0.280 |
LIG_LIR_Nem_3 | 845 | 849 | PF02991 | 0.280 |
LIG_MYND_1 | 139 | 143 | PF01753 | 0.683 |
LIG_MYND_1 | 247 | 251 | PF01753 | 0.562 |
LIG_Pex14_1 | 605 | 609 | PF04695 | 0.280 |
LIG_Pex14_2 | 751 | 755 | PF04695 | 0.280 |
LIG_Pex14_2 | 842 | 846 | PF04695 | 0.280 |
LIG_PTAP_UEV_1 | 383 | 388 | PF05743 | 0.610 |
LIG_SH2_CRK | 188 | 192 | PF00017 | 0.526 |
LIG_SH2_GRB2like | 155 | 158 | PF00017 | 0.578 |
LIG_SH2_SRC | 57 | 60 | PF00017 | 0.507 |
LIG_SH2_STAP1 | 207 | 211 | PF00017 | 0.576 |
LIG_SH2_STAP1 | 52 | 56 | PF00017 | 0.493 |
LIG_SH2_STAT5 | 155 | 158 | PF00017 | 0.617 |
LIG_SH2_STAT5 | 188 | 191 | PF00017 | 0.705 |
LIG_SH2_STAT5 | 207 | 210 | PF00017 | 0.592 |
LIG_SH2_STAT5 | 609 | 612 | PF00017 | 0.280 |
LIG_SH2_STAT5 | 691 | 694 | PF00017 | 0.280 |
LIG_SH2_STAT5 | 849 | 852 | PF00017 | 0.280 |
LIG_SH3_3 | 137 | 143 | PF00018 | 0.617 |
LIG_SH3_3 | 161 | 167 | PF00018 | 0.575 |
LIG_SH3_3 | 381 | 387 | PF00018 | 0.613 |
LIG_SH3_3 | 432 | 438 | PF00018 | 0.514 |
LIG_SH3_3 | 499 | 505 | PF00018 | 0.710 |
LIG_SH3_3 | 53 | 59 | PF00018 | 0.510 |
LIG_SH3_3 | 850 | 856 | PF00018 | 0.280 |
LIG_SUMO_SIM_anti_2 | 585 | 591 | PF11976 | 0.400 |
LIG_SUMO_SIM_anti_2 | 893 | 899 | PF11976 | 0.298 |
LIG_SUMO_SIM_par_1 | 207 | 212 | PF11976 | 0.460 |
LIG_SUMO_SIM_par_1 | 585 | 591 | PF11976 | 0.400 |
LIG_SUMO_SIM_par_1 | 740 | 745 | PF11976 | 0.280 |
LIG_SxIP_EBH_1 | 313 | 327 | PF03271 | 0.707 |
LIG_TRAF2_1 | 764 | 767 | PF00917 | 0.339 |
LIG_TRAF2_1 | 835 | 838 | PF00917 | 0.280 |
LIG_UBA3_1 | 635 | 642 | PF00899 | 0.280 |
LIG_WW_3 | 267 | 271 | PF00397 | 0.673 |
MOD_CDK_SPK_2 | 322 | 327 | PF00069 | 0.707 |
MOD_CDK_SPxxK_3 | 263 | 270 | PF00069 | 0.708 |
MOD_CDK_SPxxK_3 | 355 | 362 | PF00069 | 0.550 |
MOD_CK1_1 | 132 | 138 | PF00069 | 0.741 |
MOD_CK1_1 | 286 | 292 | PF00069 | 0.547 |
MOD_CK1_1 | 322 | 328 | PF00069 | 0.605 |
MOD_CK1_1 | 358 | 364 | PF00069 | 0.610 |
MOD_CK1_1 | 367 | 373 | PF00069 | 0.595 |
MOD_CK1_1 | 485 | 491 | PF00069 | 0.678 |
MOD_CK1_1 | 542 | 548 | PF00069 | 0.560 |
MOD_CK1_1 | 60 | 66 | PF00069 | 0.556 |
MOD_CK1_1 | 783 | 789 | PF00069 | 0.248 |
MOD_CK1_1 | 864 | 870 | PF00069 | 0.370 |
MOD_CK1_1 | 939 | 945 | PF00069 | 0.543 |
MOD_CK1_1 | 947 | 953 | PF00069 | 0.612 |
MOD_CK2_1 | 382 | 388 | PF00069 | 0.591 |
MOD_CK2_1 | 485 | 491 | PF00069 | 0.696 |
MOD_CK2_1 | 628 | 634 | PF00069 | 0.280 |
MOD_CK2_1 | 832 | 838 | PF00069 | 0.280 |
MOD_CK2_1 | 947 | 953 | PF00069 | 0.495 |
MOD_Cter_Amidation | 212 | 215 | PF01082 | 0.621 |
MOD_Cter_Amidation | 4 | 7 | PF01082 | 0.604 |
MOD_Cter_Amidation | 594 | 597 | PF01082 | 0.400 |
MOD_Cter_Amidation | 655 | 658 | PF01082 | 0.280 |
MOD_GlcNHglycan | 210 | 214 | PF01048 | 0.591 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.583 |
MOD_GlcNHglycan | 222 | 225 | PF01048 | 0.581 |
MOD_GlcNHglycan | 271 | 274 | PF01048 | 0.661 |
MOD_GlcNHglycan | 310 | 313 | PF01048 | 0.612 |
MOD_GlcNHglycan | 370 | 373 | PF01048 | 0.613 |
MOD_GlcNHglycan | 384 | 387 | PF01048 | 0.493 |
MOD_GlcNHglycan | 441 | 445 | PF01048 | 0.592 |
MOD_GlcNHglycan | 487 | 490 | PF01048 | 0.714 |
MOD_GlcNHglycan | 520 | 524 | PF01048 | 0.662 |
MOD_GlcNHglycan | 541 | 544 | PF01048 | 0.597 |
MOD_GlcNHglycan | 555 | 558 | PF01048 | 0.280 |
MOD_GlcNHglycan | 654 | 657 | PF01048 | 0.281 |
MOD_GlcNHglycan | 671 | 674 | PF01048 | 0.219 |
MOD_GlcNHglycan | 70 | 73 | PF01048 | 0.642 |
MOD_GlcNHglycan | 782 | 786 | PF01048 | 0.286 |
MOD_GlcNHglycan | 818 | 822 | PF01048 | 0.280 |
MOD_GlcNHglycan | 859 | 862 | PF01048 | 0.280 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.438 |
MOD_GlcNHglycan | 912 | 915 | PF01048 | 0.514 |
MOD_GlcNHglycan | 918 | 921 | PF01048 | 0.560 |
MOD_GlcNHglycan | 938 | 941 | PF01048 | 0.728 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.480 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.610 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.560 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.601 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.503 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.688 |
MOD_GSK3_1 | 341 | 348 | PF00069 | 0.773 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.651 |
MOD_GSK3_1 | 382 | 389 | PF00069 | 0.466 |
MOD_GSK3_1 | 490 | 497 | PF00069 | 0.657 |
MOD_GSK3_1 | 538 | 545 | PF00069 | 0.592 |
MOD_GSK3_1 | 624 | 631 | PF00069 | 0.280 |
MOD_GSK3_1 | 671 | 678 | PF00069 | 0.400 |
MOD_GSK3_1 | 705 | 712 | PF00069 | 0.280 |
MOD_GSK3_1 | 783 | 790 | PF00069 | 0.348 |
MOD_GSK3_1 | 857 | 864 | PF00069 | 0.400 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.519 |
MOD_GSK3_1 | 924 | 931 | PF00069 | 0.686 |
MOD_GSK3_1 | 932 | 939 | PF00069 | 0.595 |
MOD_N-GLC_1 | 106 | 111 | PF02516 | 0.534 |
MOD_N-GLC_1 | 292 | 297 | PF02516 | 0.711 |
MOD_N-GLC_1 | 574 | 579 | PF02516 | 0.259 |
MOD_N-GLC_1 | 60 | 65 | PF02516 | 0.567 |
MOD_N-GLC_1 | 652 | 657 | PF02516 | 0.339 |
MOD_N-GLC_1 | 68 | 73 | PF02516 | 0.528 |
MOD_N-GLC_1 | 780 | 785 | PF02516 | 0.253 |
MOD_N-GLC_1 | 893 | 898 | PF02516 | 0.298 |
MOD_N-GLC_2 | 876 | 878 | PF02516 | 0.280 |
MOD_NEK2_1 | 106 | 111 | PF00069 | 0.554 |
MOD_NEK2_1 | 209 | 214 | PF00069 | 0.477 |
MOD_NEK2_1 | 22 | 27 | PF00069 | 0.475 |
MOD_NEK2_1 | 431 | 436 | PF00069 | 0.559 |
MOD_NEK2_1 | 476 | 481 | PF00069 | 0.574 |
MOD_NEK2_1 | 482 | 487 | PF00069 | 0.587 |
MOD_NEK2_1 | 574 | 579 | PF00069 | 0.259 |
MOD_NEK2_1 | 624 | 629 | PF00069 | 0.280 |
MOD_NEK2_1 | 742 | 747 | PF00069 | 0.280 |
MOD_NEK2_1 | 803 | 808 | PF00069 | 0.280 |
MOD_NEK2_1 | 936 | 941 | PF00069 | 0.726 |
MOD_NEK2_1 | 952 | 957 | PF00069 | 0.409 |
MOD_NEK2_2 | 283 | 288 | PF00069 | 0.620 |
MOD_NEK2_2 | 292 | 297 | PF00069 | 0.551 |
MOD_NEK2_2 | 52 | 57 | PF00069 | 0.495 |
MOD_PIKK_1 | 477 | 483 | PF00454 | 0.635 |
MOD_PIKK_1 | 928 | 934 | PF00454 | 0.621 |
MOD_PK_1 | 99 | 105 | PF00069 | 0.619 |
MOD_PKA_1 | 110 | 116 | PF00069 | 0.506 |
MOD_PKA_1 | 214 | 220 | PF00069 | 0.684 |
MOD_PKA_2 | 110 | 116 | PF00069 | 0.533 |
MOD_PKA_2 | 205 | 211 | PF00069 | 0.606 |
MOD_PKA_2 | 214 | 220 | PF00069 | 0.616 |
MOD_PKA_2 | 22 | 28 | PF00069 | 0.476 |
MOD_PKA_2 | 230 | 236 | PF00069 | 0.613 |
MOD_PKA_2 | 269 | 275 | PF00069 | 0.716 |
MOD_PKA_2 | 341 | 347 | PF00069 | 0.714 |
MOD_PKA_2 | 5 | 11 | PF00069 | 0.463 |
MOD_PKA_2 | 562 | 568 | PF00069 | 0.260 |
MOD_PKA_2 | 76 | 82 | PF00069 | 0.589 |
MOD_PKA_2 | 888 | 894 | PF00069 | 0.280 |
MOD_PKA_2 | 910 | 916 | PF00069 | 0.506 |
MOD_PKA_2 | 944 | 950 | PF00069 | 0.590 |
MOD_PKB_1 | 229 | 237 | PF00069 | 0.571 |
MOD_PKB_1 | 517 | 525 | PF00069 | 0.623 |
MOD_Plk_1 | 157 | 163 | PF00069 | 0.608 |
MOD_Plk_1 | 186 | 192 | PF00069 | 0.525 |
MOD_Plk_1 | 52 | 58 | PF00069 | 0.537 |
MOD_Plk_1 | 574 | 580 | PF00069 | 0.259 |
MOD_Plk_1 | 60 | 66 | PF00069 | 0.504 |
MOD_Plk_1 | 817 | 823 | PF00069 | 0.280 |
MOD_Plk_1 | 893 | 899 | PF00069 | 0.298 |
MOD_Plk_2-3 | 888 | 894 | PF00069 | 0.280 |
MOD_Plk_4 | 151 | 157 | PF00069 | 0.630 |
MOD_Plk_4 | 292 | 298 | PF00069 | 0.709 |
MOD_Plk_4 | 315 | 321 | PF00069 | 0.707 |
MOD_Plk_4 | 52 | 58 | PF00069 | 0.533 |
MOD_Plk_4 | 582 | 588 | PF00069 | 0.280 |
MOD_Plk_4 | 60 | 66 | PF00069 | 0.493 |
MOD_Plk_4 | 624 | 630 | PF00069 | 0.280 |
MOD_Plk_4 | 676 | 682 | PF00069 | 0.280 |
MOD_Plk_4 | 893 | 899 | PF00069 | 0.298 |
MOD_Plk_4 | 947 | 953 | PF00069 | 0.576 |
MOD_ProDKin_1 | 135 | 141 | PF00069 | 0.579 |
MOD_ProDKin_1 | 263 | 269 | PF00069 | 0.685 |
MOD_ProDKin_1 | 322 | 328 | PF00069 | 0.593 |
MOD_ProDKin_1 | 355 | 361 | PF00069 | 0.598 |
MOD_ProDKin_1 | 36 | 42 | PF00069 | 0.605 |
MOD_ProDKin_1 | 364 | 370 | PF00069 | 0.600 |
MOD_ProDKin_1 | 447 | 453 | PF00069 | 0.651 |
MOD_ProDKin_1 | 63 | 69 | PF00069 | 0.726 |
MOD_ProDKin_1 | 755 | 761 | PF00069 | 0.327 |
MOD_ProDKin_1 | 787 | 793 | PF00069 | 0.361 |
MOD_ProDKin_1 | 847 | 853 | PF00069 | 0.280 |
MOD_ProDKin_1 | 864 | 870 | PF00069 | 0.280 |
MOD_SUMO_rev_2 | 240 | 245 | PF00179 | 0.665 |
MOD_SUMO_rev_2 | 712 | 717 | PF00179 | 0.280 |
MOD_SUMO_rev_2 | 750 | 755 | PF00179 | 0.280 |
MOD_SUMO_rev_2 | 760 | 770 | PF00179 | 0.280 |
TRG_DiLeu_BaEn_3 | 837 | 843 | PF01217 | 0.280 |
TRG_DiLeu_BaLyEn_6 | 137 | 142 | PF01217 | 0.548 |
TRG_DiLeu_BaLyEn_6 | 331 | 336 | PF01217 | 0.714 |
TRG_ENDOCYTIC_2 | 188 | 191 | PF00928 | 0.522 |
TRG_ER_diArg_1 | 191 | 193 | PF00400 | 0.551 |
TRG_ER_diArg_1 | 247 | 250 | PF00400 | 0.562 |
TRG_ER_diArg_1 | 516 | 519 | PF00400 | 0.562 |
TRG_ER_diArg_1 | 596 | 598 | PF00400 | 0.400 |
TRG_ER_diArg_1 | 657 | 660 | PF00400 | 0.280 |
TRG_ER_diArg_1 | 724 | 726 | PF00400 | 0.280 |
TRG_ER_diArg_1 | 795 | 797 | PF00400 | 0.418 |
TRG_ER_diArg_1 | 96 | 99 | PF00400 | 0.615 |
TRG_NLS_Bipartite_1 | 945 | 961 | PF00514 | 0.390 |
TRG_NLS_MonoExtC_3 | 2 | 7 | PF00514 | 0.563 |
TRG_Pf-PMV_PEXEL_1 | 250 | 254 | PF00026 | 0.682 |
TRG_Pf-PMV_PEXEL_1 | 746 | 750 | PF00026 | 0.280 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2L7 | Leptomonas seymouri | 49% | 92% |
A0A3Q8ID61 | Leishmania donovani | 100% | 100% |
A4H7P3 | Leishmania braziliensis | 70% | 97% |
E9APT5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q4QFP5 | Leishmania major | 92% | 100% |