Could be a sphingosine kinase. Membrane-associated without any TM segments.
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: 5 |
NetGPI | no | yes: 0, no: 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0042721 | TIM22 mitochondrial import inner membrane insertion complex | 4 | 2 |
GO:0098796 | membrane protein complex | 2 | 2 |
GO:0098798 | mitochondrial protein-containing complex | 2 | 2 |
GO:0098800 | inner mitochondrial membrane protein complex | 3 | 2 |
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: Q4QDA8
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 2 |
GO:0006839 | mitochondrial transport | 4 | 2 |
GO:0006886 | intracellular protein transport | 4 | 2 |
GO:0006996 | organelle organization | 4 | 2 |
GO:0007005 | mitochondrion organization | 5 | 2 |
GO:0007006 | mitochondrial membrane organization | 5 | 2 |
GO:0007007 | inner mitochondrial membrane organization | 6 | 2 |
GO:0008104 | protein localization | 4 | 2 |
GO:0009987 | cellular process | 1 | 3 |
GO:0015031 | protein transport | 4 | 2 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0033036 | macromolecule localization | 2 | 2 |
GO:0033365 | protein localization to organelle | 5 | 2 |
GO:0045039 | protein insertion into mitochondrial inner membrane | 6 | 2 |
GO:0045184 | establishment of protein localization | 3 | 2 |
GO:0046907 | intracellular transport | 3 | 2 |
GO:0051179 | localization | 1 | 2 |
GO:0051204 | protein insertion into mitochondrial membrane | 5 | 2 |
GO:0051205 | protein insertion into membrane | 5 | 2 |
GO:0051234 | establishment of localization | 2 | 2 |
GO:0051641 | cellular localization | 2 | 2 |
GO:0051649 | establishment of localization in cell | 3 | 2 |
GO:0051668 | localization within membrane | 3 | 2 |
GO:0061024 | membrane organization | 4 | 2 |
GO:0070585 | protein localization to mitochondrion | 6 | 2 |
GO:0070727 | cellular macromolecule localization | 3 | 2 |
GO:0071702 | organic substance transport | 4 | 2 |
GO:0071705 | nitrogen compound transport | 4 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
GO:0072594 | establishment of protein localization to organelle | 4 | 2 |
GO:0072655 | establishment of protein localization to mitochondrion | 5 | 2 |
GO:0072657 | protein localization to membrane | 4 | 2 |
GO:0090150 | establishment of protein localization to membrane | 4 | 2 |
GO:0090151 | establishment of protein localization to mitochondrial membrane | 4 | 2 |
GO:0006793 | phosphorus metabolic process | 3 | 1 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0016310 | phosphorylation | 5 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 6 |
GO:0016301 | kinase activity | 4 | 6 |
GO:0016740 | transferase activity | 2 | 6 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 6 |
GO:0017050 | D-erythro-sphingosine kinase activity | 5 | 6 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 363 | 367 | PF00656 | 0.619 |
CLV_C14_Caspase3-7 | 493 | 497 | PF00656 | 0.544 |
CLV_C14_Caspase3-7 | 851 | 855 | PF00656 | 0.530 |
CLV_NRD_NRD_1 | 568 | 570 | PF00675 | 0.669 |
CLV_NRD_NRD_1 | 937 | 939 | PF00675 | 0.477 |
CLV_NRD_NRD_1 | 951 | 953 | PF00675 | 0.477 |
CLV_PCSK_FUR_1 | 566 | 570 | PF00082 | 0.650 |
CLV_PCSK_KEX2_1 | 568 | 570 | PF00082 | 0.737 |
CLV_PCSK_KEX2_1 | 937 | 939 | PF00082 | 0.477 |
CLV_PCSK_KEX2_1 | 951 | 953 | PF00082 | 0.497 |
CLV_PCSK_SKI1_1 | 348 | 352 | PF00082 | 0.320 |
CLV_PCSK_SKI1_1 | 411 | 415 | PF00082 | 0.300 |
CLV_PCSK_SKI1_1 | 684 | 688 | PF00082 | 0.732 |
CLV_PCSK_SKI1_1 | 884 | 888 | PF00082 | 0.364 |
DEG_APCC_DBOX_1 | 942 | 950 | PF00400 | 0.656 |
DEG_SPOP_SBC_1 | 28 | 32 | PF00917 | 0.631 |
DEG_SPOP_SBC_1 | 666 | 670 | PF00917 | 0.567 |
DEG_SPOP_SBC_1 | 693 | 697 | PF00917 | 0.560 |
DEG_SPOP_SBC_1 | 92 | 96 | PF00917 | 0.728 |
DOC_ANK_TNKS_1 | 575 | 582 | PF00023 | 0.579 |
DOC_CKS1_1 | 552 | 557 | PF01111 | 0.328 |
DOC_CKS1_1 | 632 | 637 | PF01111 | 0.450 |
DOC_CYCLIN_RxL_1 | 221 | 231 | PF00134 | 0.650 |
DOC_CYCLIN_RxL_1 | 345 | 355 | PF00134 | 0.528 |
DOC_CYCLIN_yCln2_LP_2 | 310 | 316 | PF00134 | 0.534 |
DOC_CYCLIN_yCln2_LP_2 | 598 | 604 | PF00134 | 0.522 |
DOC_MAPK_gen_1 | 222 | 230 | PF00069 | 0.671 |
DOC_MAPK_MEF2A_6 | 222 | 230 | PF00069 | 0.650 |
DOC_MAPK_MEF2A_6 | 35 | 42 | PF00069 | 0.590 |
DOC_MAPK_MEF2A_6 | 468 | 475 | PF00069 | 0.428 |
DOC_PP1_RVXF_1 | 400 | 406 | PF00149 | 0.500 |
DOC_PP1_RVXF_1 | 882 | 888 | PF00149 | 0.499 |
DOC_PP2B_LxvP_1 | 315 | 318 | PF13499 | 0.465 |
DOC_PP2B_LxvP_1 | 598 | 601 | PF13499 | 0.505 |
DOC_PP2B_LxvP_1 | 781 | 784 | PF13499 | 0.334 |
DOC_PP2B_LxvP_1 | 932 | 935 | PF13499 | 0.723 |
DOC_PP4_FxxP_1 | 887 | 890 | PF00568 | 0.492 |
DOC_SPAK_OSR1_1 | 830 | 834 | PF12202 | 0.475 |
DOC_USP7_MATH_1 | 111 | 115 | PF00917 | 0.812 |
DOC_USP7_MATH_1 | 149 | 153 | PF00917 | 0.722 |
DOC_USP7_MATH_1 | 210 | 214 | PF00917 | 0.774 |
DOC_USP7_MATH_1 | 282 | 286 | PF00917 | 0.439 |
DOC_USP7_MATH_1 | 293 | 297 | PF00917 | 0.534 |
DOC_USP7_MATH_1 | 352 | 356 | PF00917 | 0.752 |
DOC_USP7_MATH_1 | 380 | 384 | PF00917 | 0.645 |
DOC_USP7_MATH_1 | 387 | 391 | PF00917 | 0.569 |
DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.699 |
DOC_USP7_MATH_1 | 420 | 424 | PF00917 | 0.547 |
DOC_USP7_MATH_1 | 449 | 453 | PF00917 | 0.408 |
DOC_USP7_MATH_1 | 666 | 670 | PF00917 | 0.510 |
DOC_USP7_MATH_1 | 693 | 697 | PF00917 | 0.517 |
DOC_USP7_MATH_1 | 76 | 80 | PF00917 | 0.580 |
DOC_USP7_MATH_1 | 92 | 96 | PF00917 | 0.662 |
DOC_WW_Pin1_4 | 104 | 109 | PF00397 | 0.712 |
DOC_WW_Pin1_4 | 203 | 208 | PF00397 | 0.738 |
DOC_WW_Pin1_4 | 246 | 251 | PF00397 | 0.562 |
DOC_WW_Pin1_4 | 331 | 336 | PF00397 | 0.475 |
DOC_WW_Pin1_4 | 374 | 379 | PF00397 | 0.722 |
DOC_WW_Pin1_4 | 527 | 532 | PF00397 | 0.566 |
DOC_WW_Pin1_4 | 536 | 541 | PF00397 | 0.468 |
DOC_WW_Pin1_4 | 551 | 556 | PF00397 | 0.307 |
DOC_WW_Pin1_4 | 615 | 620 | PF00397 | 0.592 |
DOC_WW_Pin1_4 | 631 | 636 | PF00397 | 0.368 |
DOC_WW_Pin1_4 | 643 | 648 | PF00397 | 0.461 |
LIG_14-3-3_CanoR_1 | 232 | 238 | PF00244 | 0.746 |
LIG_14-3-3_CanoR_1 | 381 | 387 | PF00244 | 0.723 |
LIG_14-3-3_CanoR_1 | 389 | 396 | PF00244 | 0.544 |
LIG_14-3-3_CanoR_1 | 437 | 442 | PF00244 | 0.545 |
LIG_14-3-3_CanoR_1 | 566 | 575 | PF00244 | 0.544 |
LIG_14-3-3_CanoR_1 | 629 | 633 | PF00244 | 0.566 |
LIG_14-3-3_CanoR_1 | 808 | 813 | PF00244 | 0.444 |
LIG_14-3-3_CanoR_1 | 819 | 826 | PF00244 | 0.450 |
LIG_14-3-3_CanoR_1 | 830 | 839 | PF00244 | 0.477 |
LIG_Actin_WH2_2 | 553 | 570 | PF00022 | 0.408 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.740 |
LIG_BIR_III_2 | 744 | 748 | PF00653 | 0.461 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.702 |
LIG_BIR_III_4 | 578 | 582 | PF00653 | 0.556 |
LIG_BRCT_BRCA1_1 | 669 | 673 | PF00533 | 0.540 |
LIG_CaM_IQ_9 | 424 | 439 | PF13499 | 0.556 |
LIG_Clathr_ClatBox_1 | 758 | 762 | PF01394 | 0.294 |
LIG_DLG_GKlike_1 | 437 | 445 | PF00625 | 0.534 |
LIG_EH1_1 | 636 | 644 | PF00400 | 0.454 |
LIG_eIF4E_1 | 776 | 782 | PF01652 | 0.334 |
LIG_FHA_1 | 162 | 168 | PF00498 | 0.578 |
LIG_FHA_1 | 265 | 271 | PF00498 | 0.542 |
LIG_FHA_1 | 28 | 34 | PF00498 | 0.661 |
LIG_FHA_1 | 527 | 533 | PF00498 | 0.544 |
LIG_FHA_1 | 787 | 793 | PF00498 | 0.312 |
LIG_FHA_1 | 794 | 800 | PF00498 | 0.275 |
LIG_FHA_1 | 844 | 850 | PF00498 | 0.589 |
LIG_FHA_1 | 890 | 896 | PF00498 | 0.668 |
LIG_FHA_1 | 926 | 932 | PF00498 | 0.660 |
LIG_FHA_2 | 260 | 266 | PF00498 | 0.475 |
LIG_FHA_2 | 319 | 325 | PF00498 | 0.475 |
LIG_FHA_2 | 332 | 338 | PF00498 | 0.534 |
LIG_FHA_2 | 491 | 497 | PF00498 | 0.564 |
LIG_FHA_2 | 902 | 908 | PF00498 | 0.650 |
LIG_Integrin_isoDGR_2 | 772 | 774 | PF01839 | 0.475 |
LIG_IRF3_LxIS_1 | 639 | 646 | PF10401 | 0.417 |
LIG_LIR_Gen_1 | 234 | 245 | PF02991 | 0.645 |
LIG_LIR_Gen_1 | 323 | 330 | PF02991 | 0.478 |
LIG_LIR_Gen_1 | 36 | 46 | PF02991 | 0.601 |
LIG_LIR_Gen_1 | 451 | 461 | PF02991 | 0.396 |
LIG_LIR_Gen_1 | 757 | 768 | PF02991 | 0.349 |
LIG_LIR_Nem_3 | 234 | 240 | PF02991 | 0.645 |
LIG_LIR_Nem_3 | 323 | 328 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 36 | 42 | PF02991 | 0.602 |
LIG_LIR_Nem_3 | 451 | 456 | PF02991 | 0.396 |
LIG_LIR_Nem_3 | 757 | 763 | PF02991 | 0.353 |
LIG_NRBOX | 945 | 951 | PF00104 | 0.649 |
LIG_Pex14_2 | 64 | 68 | PF04695 | 0.598 |
LIG_SH2_CRK | 237 | 241 | PF00017 | 0.726 |
LIG_SH2_PTP2 | 39 | 42 | PF00017 | 0.512 |
LIG_SH2_PTP2 | 734 | 737 | PF00017 | 0.398 |
LIG_SH2_SRC | 734 | 737 | PF00017 | 0.493 |
LIG_SH2_STAP1 | 126 | 130 | PF00017 | 0.646 |
LIG_SH2_STAP1 | 396 | 400 | PF00017 | 0.561 |
LIG_SH2_STAP1 | 612 | 616 | PF00017 | 0.498 |
LIG_SH2_STAT3 | 956 | 959 | PF00017 | 0.609 |
LIG_SH2_STAT5 | 39 | 42 | PF00017 | 0.512 |
LIG_SH2_STAT5 | 465 | 468 | PF00017 | 0.326 |
LIG_SH2_STAT5 | 612 | 615 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 734 | 737 | PF00017 | 0.493 |
LIG_SH2_STAT5 | 813 | 816 | PF00017 | 0.335 |
LIG_SH3_1 | 468 | 474 | PF00018 | 0.422 |
LIG_SH3_2 | 601 | 606 | PF14604 | 0.516 |
LIG_SH3_3 | 102 | 108 | PF00018 | 0.693 |
LIG_SH3_3 | 139 | 145 | PF00018 | 0.695 |
LIG_SH3_3 | 195 | 201 | PF00018 | 0.763 |
LIG_SH3_3 | 20 | 26 | PF00018 | 0.734 |
LIG_SH3_3 | 242 | 248 | PF00018 | 0.775 |
LIG_SH3_3 | 40 | 46 | PF00018 | 0.469 |
LIG_SH3_3 | 468 | 474 | PF00018 | 0.457 |
LIG_SH3_3 | 549 | 555 | PF00018 | 0.359 |
LIG_SH3_3 | 574 | 580 | PF00018 | 0.507 |
LIG_SH3_3 | 598 | 604 | PF00018 | 0.605 |
LIG_SH3_3 | 616 | 622 | PF00018 | 0.452 |
LIG_SH3_3 | 758 | 764 | PF00018 | 0.386 |
LIG_SH3_3 | 928 | 934 | PF00018 | 0.656 |
LIG_SUMO_SIM_anti_2 | 451 | 458 | PF11976 | 0.396 |
LIG_SUMO_SIM_anti_2 | 752 | 760 | PF11976 | 0.323 |
LIG_SUMO_SIM_par_1 | 163 | 169 | PF11976 | 0.519 |
LIG_SUMO_SIM_par_1 | 641 | 646 | PF11976 | 0.423 |
LIG_TRAF2_1 | 497 | 500 | PF00917 | 0.540 |
LIG_UBA3_1 | 56 | 62 | PF00899 | 0.340 |
LIG_UBA3_1 | 642 | 649 | PF00899 | 0.480 |
LIG_UBA3_1 | 949 | 958 | PF00899 | 0.553 |
LIG_WW_3 | 469 | 473 | PF00397 | 0.507 |
MOD_CDC14_SPxK_1 | 646 | 649 | PF00782 | 0.504 |
MOD_CDK_SPK_2 | 203 | 208 | PF00069 | 0.582 |
MOD_CDK_SPxK_1 | 643 | 649 | PF00069 | 0.581 |
MOD_CDK_SPxxK_3 | 374 | 381 | PF00069 | 0.660 |
MOD_CDK_SPxxK_3 | 551 | 558 | PF00069 | 0.394 |
MOD_CK1_1 | 122 | 128 | PF00069 | 0.607 |
MOD_CK1_1 | 152 | 158 | PF00069 | 0.528 |
MOD_CK1_1 | 24 | 30 | PF00069 | 0.637 |
MOD_CK1_1 | 264 | 270 | PF00069 | 0.396 |
MOD_CK1_1 | 285 | 291 | PF00069 | 0.439 |
MOD_CK1_1 | 385 | 391 | PF00069 | 0.535 |
MOD_CK1_1 | 452 | 458 | PF00069 | 0.419 |
MOD_CK1_1 | 476 | 482 | PF00069 | 0.696 |
MOD_CK1_1 | 503 | 509 | PF00069 | 0.730 |
MOD_CK1_1 | 526 | 532 | PF00069 | 0.650 |
MOD_CK1_1 | 546 | 552 | PF00069 | 0.533 |
MOD_CK1_1 | 584 | 590 | PF00069 | 0.661 |
MOD_CK1_1 | 688 | 694 | PF00069 | 0.705 |
MOD_CK1_1 | 811 | 817 | PF00069 | 0.307 |
MOD_CK1_1 | 848 | 854 | PF00069 | 0.363 |
MOD_CK1_1 | 891 | 897 | PF00069 | 0.495 |
MOD_CK1_1 | 925 | 931 | PF00069 | 0.708 |
MOD_CK2_1 | 259 | 265 | PF00069 | 0.251 |
MOD_CK2_1 | 45 | 51 | PF00069 | 0.476 |
MOD_CK2_1 | 693 | 699 | PF00069 | 0.732 |
MOD_CK2_1 | 837 | 843 | PF00069 | 0.398 |
MOD_CK2_1 | 901 | 907 | PF00069 | 0.546 |
MOD_CK2_1 | 91 | 97 | PF00069 | 0.797 |
MOD_Cter_Amidation | 935 | 938 | PF01082 | 0.581 |
MOD_GlcNHglycan | 100 | 103 | PF01048 | 0.649 |
MOD_GlcNHglycan | 111 | 114 | PF01048 | 0.712 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.631 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.560 |
MOD_GlcNHglycan | 208 | 211 | PF01048 | 0.726 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.700 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.710 |
MOD_GlcNHglycan | 284 | 287 | PF01048 | 0.292 |
MOD_GlcNHglycan | 384 | 387 | PF01048 | 0.654 |
MOD_GlcNHglycan | 390 | 393 | PF01048 | 0.440 |
MOD_GlcNHglycan | 417 | 421 | PF01048 | 0.394 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.517 |
MOD_GlcNHglycan | 475 | 478 | PF01048 | 0.638 |
MOD_GlcNHglycan | 569 | 572 | PF01048 | 0.678 |
MOD_GlcNHglycan | 589 | 593 | PF01048 | 0.764 |
MOD_GlcNHglycan | 696 | 699 | PF01048 | 0.793 |
MOD_GlcNHglycan | 729 | 732 | PF01048 | 0.614 |
MOD_GlcNHglycan | 834 | 837 | PF01048 | 0.355 |
MOD_GlcNHglycan | 839 | 842 | PF01048 | 0.424 |
MOD_GlcNHglycan | 898 | 901 | PF01048 | 0.488 |
MOD_GlcNHglycan | 924 | 927 | PF01048 | 0.680 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.591 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.674 |
MOD_GSK3_1 | 176 | 183 | PF00069 | 0.401 |
MOD_GSK3_1 | 202 | 209 | PF00069 | 0.661 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.607 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.470 |
MOD_GSK3_1 | 416 | 423 | PF00069 | 0.348 |
MOD_GSK3_1 | 448 | 455 | PF00069 | 0.433 |
MOD_GSK3_1 | 523 | 530 | PF00069 | 0.679 |
MOD_GSK3_1 | 584 | 591 | PF00069 | 0.649 |
MOD_GSK3_1 | 667 | 674 | PF00069 | 0.713 |
MOD_GSK3_1 | 684 | 691 | PF00069 | 0.598 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.451 |
MOD_GSK3_1 | 793 | 800 | PF00069 | 0.377 |
MOD_LATS_1 | 174 | 180 | PF00433 | 0.389 |
MOD_LATS_1 | 435 | 441 | PF00433 | 0.396 |
MOD_LATS_1 | 817 | 823 | PF00433 | 0.381 |
MOD_N-GLC_1 | 134 | 139 | PF02516 | 0.531 |
MOD_N-GLC_2 | 170 | 172 | PF02516 | 0.575 |
MOD_N-GLC_2 | 416 | 418 | PF02516 | 0.443 |
MOD_NEK2_1 | 202 | 207 | PF00069 | 0.635 |
MOD_NEK2_1 | 281 | 286 | PF00069 | 0.356 |
MOD_NEK2_1 | 3 | 8 | PF00069 | 0.683 |
MOD_NEK2_1 | 405 | 410 | PF00069 | 0.411 |
MOD_NEK2_1 | 448 | 453 | PF00069 | 0.429 |
MOD_NEK2_1 | 567 | 572 | PF00069 | 0.734 |
MOD_NEK2_1 | 64 | 69 | PF00069 | 0.488 |
MOD_NEK2_1 | 793 | 798 | PF00069 | 0.313 |
MOD_NEK2_1 | 831 | 836 | PF00069 | 0.396 |
MOD_NEK2_1 | 845 | 850 | PF00069 | 0.301 |
MOD_NEK2_2 | 610 | 615 | PF00069 | 0.608 |
MOD_NEK2_2 | 69 | 74 | PF00069 | 0.504 |
MOD_OFUCOSY | 418 | 424 | PF10250 | 0.436 |
MOD_PIKK_1 | 180 | 186 | PF00454 | 0.449 |
MOD_PIKK_1 | 4 | 10 | PF00454 | 0.527 |
MOD_PIKK_1 | 495 | 501 | PF00454 | 0.687 |
MOD_PK_1 | 821 | 827 | PF00069 | 0.396 |
MOD_PKA_2 | 231 | 237 | PF00069 | 0.727 |
MOD_PKA_2 | 380 | 386 | PF00069 | 0.663 |
MOD_PKA_2 | 388 | 394 | PF00069 | 0.443 |
MOD_PKA_2 | 567 | 573 | PF00069 | 0.661 |
MOD_PKA_2 | 628 | 634 | PF00069 | 0.722 |
MOD_PKA_2 | 659 | 665 | PF00069 | 0.693 |
MOD_PKA_2 | 69 | 75 | PF00069 | 0.451 |
MOD_PKA_2 | 820 | 826 | PF00069 | 0.365 |
MOD_PKB_1 | 725 | 733 | PF00069 | 0.519 |
MOD_PKB_1 | 819 | 827 | PF00069 | 0.363 |
MOD_Plk_4 | 449 | 455 | PF00069 | 0.350 |
MOD_Plk_4 | 763 | 769 | PF00069 | 0.343 |
MOD_Plk_4 | 821 | 827 | PF00069 | 0.403 |
MOD_Plk_4 | 945 | 951 | PF00069 | 0.500 |
MOD_ProDKin_1 | 104 | 110 | PF00069 | 0.645 |
MOD_ProDKin_1 | 203 | 209 | PF00069 | 0.679 |
MOD_ProDKin_1 | 246 | 252 | PF00069 | 0.450 |
MOD_ProDKin_1 | 331 | 337 | PF00069 | 0.313 |
MOD_ProDKin_1 | 374 | 380 | PF00069 | 0.658 |
MOD_ProDKin_1 | 527 | 533 | PF00069 | 0.720 |
MOD_ProDKin_1 | 536 | 542 | PF00069 | 0.577 |
MOD_ProDKin_1 | 551 | 557 | PF00069 | 0.365 |
MOD_ProDKin_1 | 615 | 621 | PF00069 | 0.756 |
MOD_ProDKin_1 | 631 | 637 | PF00069 | 0.444 |
MOD_ProDKin_1 | 643 | 649 | PF00069 | 0.573 |
MOD_SUMO_for_1 | 326 | 329 | PF00179 | 0.263 |
MOD_SUMO_rev_2 | 519 | 527 | PF00179 | 0.541 |
TRG_ENDOCYTIC_2 | 237 | 240 | PF00928 | 0.565 |
TRG_ENDOCYTIC_2 | 39 | 42 | PF00928 | 0.364 |
TRG_ER_diArg_1 | 566 | 569 | PF00400 | 0.602 |
TRG_ER_diArg_1 | 594 | 597 | PF00400 | 0.586 |
TRG_ER_diArg_1 | 937 | 939 | PF00400 | 0.719 |
TRG_ER_diArg_1 | 950 | 952 | PF00400 | 0.636 |
TRG_ER_FFAT_2 | 669 | 678 | PF00635 | 0.576 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IM78 | Leptomonas seymouri | 38% | 100% |
A0A3S7WVF1 | Leishmania donovani | 88% | 100% |
A4HYC4 | Leishmania infantum | 88% | 100% |
E9AS58 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |