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: 5 |
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: 8 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
GO:0005886 | plasma membrane | 3 | 4 |
Related structures:
AlphaFold database: E9AK92
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 4 |
GO:0006811 | monoatomic ion transport | 4 | 4 |
GO:0006812 | monoatomic cation transport | 5 | 4 |
GO:0006873 | intracellular monoatomic ion homeostasis | 4 | 1 |
GO:0006885 | regulation of pH | 8 | 1 |
GO:0009987 | cellular process | 1 | 4 |
GO:0019725 | cellular homeostasis | 2 | 1 |
GO:0030003 | intracellular monoatomic cation homeostasis | 5 | 1 |
GO:0030004 | obsolete cellular monovalent inorganic cation homeostasis | 6 | 1 |
GO:0030641 | regulation of cellular pH | 7 | 1 |
GO:0034220 | monoatomic ion transmembrane transport | 3 | 4 |
GO:0042592 | homeostatic process | 3 | 1 |
GO:0048878 | chemical homeostasis | 4 | 1 |
GO:0050801 | monoatomic ion homeostasis | 5 | 1 |
GO:0051179 | localization | 1 | 4 |
GO:0051234 | establishment of localization | 2 | 4 |
GO:0051453 | regulation of intracellular pH | 8 | 1 |
GO:0055067 | obsolete monovalent inorganic cation homeostasis | 7 | 1 |
GO:0055080 | monoatomic cation homeostasis | 6 | 1 |
GO:0055082 | intracellular chemical homeostasis | 3 | 1 |
GO:0055085 | transmembrane transport | 2 | 4 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0065008 | regulation of biological quality | 2 | 1 |
GO:0098655 | monoatomic cation transmembrane transport | 4 | 4 |
GO:0098660 | inorganic ion transmembrane transport | 4 | 4 |
GO:0098662 | inorganic cation transmembrane transport | 5 | 4 |
GO:0098771 | inorganic ion homeostasis | 6 | 1 |
GO:1902600 | proton transmembrane transport | 6 | 4 |
GO:0120029 | proton export across plasma membrane | 4 | 3 |
GO:0140115 | export across plasma membrane | 3 | 3 |
GO:0140352 | export from cell | 2 | 3 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 9 |
GO:0003824 | catalytic activity | 1 | 9 |
GO:0005488 | binding | 1 | 9 |
GO:0005524 | ATP binding | 5 | 9 |
GO:0016462 | pyrophosphatase activity | 5 | 9 |
GO:0016787 | hydrolase activity | 2 | 9 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 9 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 9 |
GO:0016887 | ATP hydrolysis activity | 7 | 9 |
GO:0017076 | purine nucleotide binding | 4 | 9 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 9 |
GO:0030554 | adenyl nucleotide binding | 5 | 9 |
GO:0032553 | ribonucleotide binding | 3 | 9 |
GO:0032555 | purine ribonucleotide binding | 4 | 9 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 9 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 9 |
GO:0036094 | small molecule binding | 2 | 9 |
GO:0043167 | ion binding | 2 | 9 |
GO:0043168 | anion binding | 3 | 9 |
GO:0097159 | organic cyclic compound binding | 2 | 9 |
GO:0097367 | carbohydrate derivative binding | 2 | 9 |
GO:1901265 | nucleoside phosphate binding | 3 | 9 |
GO:1901363 | heterocyclic compound binding | 2 | 9 |
GO:0005215 | transporter activity | 1 | 4 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 4 |
GO:0008553 | P-type proton-exporting transporter activity | 4 | 4 |
GO:0009678 | pyrophosphate hydrolysis-driven proton transmembrane transporter activity | 5 | 4 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 4 |
GO:0015078 | proton transmembrane transporter activity | 5 | 4 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 4 |
GO:0015399 | primary active transmembrane transporter activity | 4 | 4 |
GO:0015662 | P-type ion transporter activity | 4 | 4 |
GO:0019829 | ATPase-coupled monoatomic cation transmembrane transporter activity | 3 | 4 |
GO:0022804 | active transmembrane transporter activity | 3 | 4 |
GO:0022853 | active monoatomic ion transmembrane transporter activity | 4 | 4 |
GO:0022857 | transmembrane transporter activity | 2 | 4 |
GO:0022890 | inorganic cation transmembrane transporter activity | 4 | 4 |
GO:0042626 | ATPase-coupled transmembrane transporter activity | 2 | 4 |
GO:0140358 | P-type transmembrane transporter activity | 3 | 4 |
GO:0140657 | ATP-dependent activity | 1 | 4 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 674 | 678 | PF00656 | 0.475 |
CLV_C14_Caspase3-7 | 881 | 885 | PF00656 | 0.549 |
CLV_NRD_NRD_1 | 365 | 367 | PF00675 | 0.477 |
CLV_NRD_NRD_1 | 636 | 638 | PF00675 | 0.584 |
CLV_NRD_NRD_1 | 70 | 72 | PF00675 | 0.337 |
CLV_NRD_NRD_1 | 862 | 864 | PF00675 | 0.461 |
CLV_NRD_NRD_1 | 875 | 877 | PF00675 | 0.394 |
CLV_PCSK_FUR_1 | 68 | 72 | PF00082 | 0.330 |
CLV_PCSK_KEX2_1 | 330 | 332 | PF00082 | 0.309 |
CLV_PCSK_KEX2_1 | 364 | 366 | PF00082 | 0.423 |
CLV_PCSK_KEX2_1 | 636 | 638 | PF00082 | 0.584 |
CLV_PCSK_KEX2_1 | 70 | 72 | PF00082 | 0.337 |
CLV_PCSK_KEX2_1 | 862 | 864 | PF00082 | 0.461 |
CLV_PCSK_KEX2_1 | 875 | 877 | PF00082 | 0.394 |
CLV_PCSK_PC1ET2_1 | 330 | 332 | PF00082 | 0.291 |
CLV_PCSK_PC7_1 | 66 | 72 | PF00082 | 0.323 |
CLV_PCSK_SKI1_1 | 268 | 272 | PF00082 | 0.276 |
CLV_PCSK_SKI1_1 | 331 | 335 | PF00082 | 0.327 |
CLV_PCSK_SKI1_1 | 379 | 383 | PF00082 | 0.317 |
CLV_PCSK_SKI1_1 | 399 | 403 | PF00082 | 0.376 |
CLV_PCSK_SKI1_1 | 530 | 534 | PF00082 | 0.242 |
CLV_PCSK_SKI1_1 | 577 | 581 | PF00082 | 0.305 |
CLV_PCSK_SKI1_1 | 603 | 607 | PF00082 | 0.306 |
CLV_PCSK_SKI1_1 | 777 | 781 | PF00082 | 0.282 |
DEG_APCC_DBOX_1 | 378 | 386 | PF00400 | 0.503 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.469 |
DOC_ANK_TNKS_1 | 73 | 80 | PF00023 | 0.506 |
DOC_ANK_TNKS_1 | 834 | 841 | PF00023 | 0.543 |
DOC_CKS1_1 | 235 | 240 | PF01111 | 0.402 |
DOC_CYCLIN_RxL_1 | 265 | 275 | PF00134 | 0.475 |
DOC_CYCLIN_RxL_1 | 600 | 608 | PF00134 | 0.537 |
DOC_CYCLIN_yCln2_LP_2 | 235 | 241 | PF00134 | 0.433 |
DOC_MAPK_gen_1 | 266 | 273 | PF00069 | 0.476 |
DOC_MAPK_gen_1 | 364 | 373 | PF00069 | 0.568 |
DOC_MAPK_gen_1 | 377 | 384 | PF00069 | 0.476 |
DOC_MAPK_gen_1 | 769 | 778 | PF00069 | 0.542 |
DOC_MAPK_MEF2A_6 | 259 | 267 | PF00069 | 0.482 |
DOC_MAPK_MEF2A_6 | 448 | 455 | PF00069 | 0.558 |
DOC_MAPK_MEF2A_6 | 481 | 488 | PF00069 | 0.650 |
DOC_MAPK_MEF2A_6 | 558 | 566 | PF00069 | 0.537 |
DOC_MAPK_MEF2A_6 | 772 | 780 | PF00069 | 0.555 |
DOC_MAPK_NFAT4_5 | 775 | 783 | PF00069 | 0.426 |
DOC_PP1_RVXF_1 | 397 | 403 | PF00149 | 0.492 |
DOC_PP2B_LxvP_1 | 648 | 651 | PF13499 | 0.386 |
DOC_PP4_FxxP_1 | 431 | 434 | PF00568 | 0.567 |
DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.520 |
DOC_USP7_MATH_1 | 509 | 513 | PF00917 | 0.556 |
DOC_USP7_MATH_1 | 586 | 590 | PF00917 | 0.493 |
DOC_USP7_MATH_1 | 639 | 643 | PF00917 | 0.472 |
DOC_USP7_MATH_1 | 905 | 909 | PF00917 | 0.558 |
DOC_WW_Pin1_4 | 18 | 23 | PF00397 | 0.284 |
DOC_WW_Pin1_4 | 234 | 239 | PF00397 | 0.402 |
DOC_WW_Pin1_4 | 492 | 497 | PF00397 | 0.607 |
DOC_WW_Pin1_4 | 6 | 11 | PF00397 | 0.582 |
DOC_WW_Pin1_4 | 726 | 731 | PF00397 | 0.374 |
DOC_WW_Pin1_4 | 759 | 764 | PF00397 | 0.351 |
DOC_WW_Pin1_4 | 864 | 869 | PF00397 | 0.705 |
LIG_14-3-3_CanoR_1 | 132 | 137 | PF00244 | 0.396 |
LIG_14-3-3_CanoR_1 | 268 | 274 | PF00244 | 0.484 |
LIG_14-3-3_CanoR_1 | 372 | 378 | PF00244 | 0.507 |
LIG_14-3-3_CanoR_1 | 494 | 504 | PF00244 | 0.614 |
LIG_14-3-3_CanoR_1 | 5 | 9 | PF00244 | 0.540 |
LIG_14-3-3_CanoR_1 | 558 | 566 | PF00244 | 0.600 |
LIG_14-3-3_CanoR_1 | 862 | 868 | PF00244 | 0.654 |
LIG_14-3-3_CanoR_1 | 875 | 880 | PF00244 | 0.574 |
LIG_BIR_III_2 | 438 | 442 | PF00653 | 0.484 |
LIG_BIR_III_4 | 871 | 875 | PF00653 | 0.617 |
LIG_BRCT_BRCA1_1 | 108 | 112 | PF00533 | 0.433 |
LIG_BRCT_BRCA1_1 | 610 | 614 | PF00533 | 0.451 |
LIG_eIF4E_1 | 118 | 124 | PF01652 | 0.451 |
LIG_FHA_1 | 169 | 175 | PF00498 | 0.490 |
LIG_FHA_1 | 193 | 199 | PF00498 | 0.435 |
LIG_FHA_1 | 203 | 209 | PF00498 | 0.393 |
LIG_FHA_1 | 22 | 28 | PF00498 | 0.289 |
LIG_FHA_1 | 282 | 288 | PF00498 | 0.513 |
LIG_FHA_1 | 627 | 633 | PF00498 | 0.271 |
LIG_FHA_1 | 744 | 750 | PF00498 | 0.289 |
LIG_FHA_1 | 789 | 795 | PF00498 | 0.337 |
LIG_FHA_1 | 86 | 92 | PF00498 | 0.406 |
LIG_FHA_2 | 131 | 137 | PF00498 | 0.556 |
LIG_FHA_2 | 160 | 166 | PF00498 | 0.451 |
LIG_FHA_2 | 344 | 350 | PF00498 | 0.538 |
LIG_FHA_2 | 428 | 434 | PF00498 | 0.538 |
LIG_FHA_2 | 592 | 598 | PF00498 | 0.398 |
LIG_GBD_Chelix_1 | 263 | 271 | PF00786 | 0.221 |
LIG_GBD_Chelix_1 | 709 | 717 | PF00786 | 0.264 |
LIG_Integrin_RGD_1 | 436 | 438 | PF01839 | 0.230 |
LIG_LIR_Apic_2 | 430 | 434 | PF02991 | 0.562 |
LIG_LIR_Gen_1 | 229 | 239 | PF02991 | 0.370 |
LIG_LIR_Gen_1 | 343 | 351 | PF02991 | 0.586 |
LIG_LIR_Gen_1 | 608 | 618 | PF02991 | 0.513 |
LIG_LIR_Gen_1 | 86 | 97 | PF02991 | 0.467 |
LIG_LIR_LC3C_4 | 597 | 601 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 195 | 199 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 229 | 235 | PF02991 | 0.383 |
LIG_LIR_Nem_3 | 343 | 348 | PF02991 | 0.582 |
LIG_LIR_Nem_3 | 604 | 609 | PF02991 | 0.503 |
LIG_LIR_Nem_3 | 611 | 616 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 699 | 705 | PF02991 | 0.267 |
LIG_LIR_Nem_3 | 746 | 751 | PF02991 | 0.427 |
LIG_LIR_Nem_3 | 783 | 789 | PF02991 | 0.170 |
LIG_LIR_Nem_3 | 86 | 92 | PF02991 | 0.467 |
LIG_MLH1_MIPbox_1 | 610 | 614 | PF16413 | 0.451 |
LIG_NRBOX | 230 | 236 | PF00104 | 0.433 |
LIG_NRBOX | 266 | 272 | PF00104 | 0.497 |
LIG_NRBOX | 424 | 430 | PF00104 | 0.472 |
LIG_SH2_CRK | 34 | 38 | PF00017 | 0.224 |
LIG_SH2_CRK | 807 | 811 | PF00017 | 0.242 |
LIG_SH2_GRB2like | 662 | 665 | PF00017 | 0.420 |
LIG_SH2_GRB2like | 751 | 754 | PF00017 | 0.264 |
LIG_SH2_SRC | 350 | 353 | PF00017 | 0.538 |
LIG_SH2_SRC | 662 | 665 | PF00017 | 0.436 |
LIG_SH2_STAP1 | 610 | 614 | PF00017 | 0.433 |
LIG_SH2_STAP1 | 690 | 694 | PF00017 | 0.576 |
LIG_SH2_STAT3 | 842 | 845 | PF00017 | 0.497 |
LIG_SH2_STAT5 | 161 | 164 | PF00017 | 0.596 |
LIG_SH2_STAT5 | 196 | 199 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 246 | 249 | PF00017 | 0.433 |
LIG_SH2_STAT5 | 301 | 304 | PF00017 | 0.559 |
LIG_SH2_STAT5 | 345 | 348 | PF00017 | 0.494 |
LIG_SH2_STAT5 | 350 | 353 | PF00017 | 0.494 |
LIG_SH2_STAT5 | 662 | 665 | PF00017 | 0.264 |
LIG_SH2_STAT5 | 748 | 751 | PF00017 | 0.322 |
LIG_SH2_STAT5 | 807 | 810 | PF00017 | 0.372 |
LIG_SH2_STAT5 | 827 | 830 | PF00017 | 0.446 |
LIG_SH3_3 | 382 | 388 | PF00018 | 0.522 |
LIG_SH3_3 | 629 | 635 | PF00018 | 0.264 |
LIG_Sin3_3 | 60 | 67 | PF02671 | 0.268 |
LIG_SUMO_SIM_anti_2 | 171 | 176 | PF11976 | 0.433 |
LIG_SUMO_SIM_anti_2 | 380 | 386 | PF11976 | 0.519 |
LIG_SUMO_SIM_anti_2 | 452 | 457 | PF11976 | 0.433 |
LIG_SUMO_SIM_anti_2 | 597 | 602 | PF11976 | 0.461 |
LIG_SUMO_SIM_anti_2 | 691 | 696 | PF11976 | 0.567 |
LIG_SUMO_SIM_par_1 | 170 | 176 | PF11976 | 0.433 |
LIG_SUMO_SIM_par_1 | 269 | 275 | PF11976 | 0.482 |
LIG_SUMO_SIM_par_1 | 277 | 282 | PF11976 | 0.472 |
LIG_SUMO_SIM_par_1 | 597 | 602 | PF11976 | 0.479 |
LIG_SUMO_SIM_par_1 | 731 | 739 | PF11976 | 0.288 |
LIG_SUMO_SIM_par_1 | 778 | 783 | PF11976 | 0.170 |
LIG_TYR_ITIM | 32 | 37 | PF00017 | 0.225 |
LIG_TYR_ITIM | 749 | 754 | PF00017 | 0.264 |
LIG_WRC_WIRS_1 | 428 | 433 | PF05994 | 0.511 |
LIG_WRC_WIRS_1 | 744 | 749 | PF05994 | 0.298 |
MOD_CDC14_SPxK_1 | 762 | 765 | PF00782 | 0.289 |
MOD_CDK_SPxK_1 | 759 | 765 | PF00069 | 0.289 |
MOD_CDK_SPxxK_3 | 6 | 13 | PF00069 | 0.494 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.417 |
MOD_CK1_1 | 21 | 27 | PF00069 | 0.289 |
MOD_CK1_1 | 272 | 278 | PF00069 | 0.491 |
MOD_CK1_1 | 495 | 501 | PF00069 | 0.636 |
MOD_CK1_1 | 759 | 765 | PF00069 | 0.264 |
MOD_CK1_1 | 866 | 872 | PF00069 | 0.708 |
MOD_CK1_1 | 877 | 883 | PF00069 | 0.540 |
MOD_CK2_1 | 130 | 136 | PF00069 | 0.564 |
MOD_CK2_1 | 159 | 165 | PF00069 | 0.433 |
MOD_CK2_1 | 454 | 460 | PF00069 | 0.482 |
MOD_CK2_1 | 484 | 490 | PF00069 | 0.556 |
MOD_CK2_1 | 509 | 515 | PF00069 | 0.556 |
MOD_CK2_1 | 591 | 597 | PF00069 | 0.407 |
MOD_CK2_1 | 639 | 645 | PF00069 | 0.403 |
MOD_CK2_1 | 904 | 910 | PF00069 | 0.593 |
MOD_CMANNOS | 768 | 771 | PF00535 | 0.369 |
MOD_Cter_Amidation | 873 | 876 | PF01082 | 0.414 |
MOD_GlcNHglycan | 108 | 111 | PF01048 | 0.283 |
MOD_GlcNHglycan | 253 | 256 | PF01048 | 0.343 |
MOD_GlcNHglycan | 288 | 291 | PF01048 | 0.365 |
MOD_GlcNHglycan | 335 | 338 | PF01048 | 0.310 |
MOD_GlcNHglycan | 359 | 362 | PF01048 | 0.353 |
MOD_GlcNHglycan | 389 | 392 | PF01048 | 0.412 |
MOD_GlcNHglycan | 406 | 409 | PF01048 | 0.301 |
MOD_GlcNHglycan | 456 | 459 | PF01048 | 0.331 |
MOD_GlcNHglycan | 478 | 481 | PF01048 | 0.337 |
MOD_GlcNHglycan | 497 | 500 | PF01048 | 0.381 |
MOD_GlcNHglycan | 505 | 509 | PF01048 | 0.449 |
MOD_GlcNHglycan | 511 | 514 | PF01048 | 0.326 |
MOD_GlcNHglycan | 539 | 542 | PF01048 | 0.251 |
MOD_GlcNHglycan | 567 | 570 | PF01048 | 0.335 |
MOD_GlcNHglycan | 652 | 655 | PF01048 | 0.561 |
MOD_GlcNHglycan | 853 | 859 | PF01048 | 0.420 |
MOD_GlcNHglycan | 907 | 910 | PF01048 | 0.381 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.309 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.465 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.466 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.498 |
MOD_GSK3_1 | 322 | 329 | PF00069 | 0.515 |
MOD_GSK3_1 | 472 | 479 | PF00069 | 0.495 |
MOD_GSK3_1 | 500 | 507 | PF00069 | 0.617 |
MOD_GSK3_1 | 862 | 869 | PF00069 | 0.662 |
MOD_GSK3_1 | 874 | 881 | PF00069 | 0.578 |
MOD_N-GLC_1 | 118 | 123 | PF02516 | 0.166 |
MOD_NEK2_1 | 257 | 262 | PF00069 | 0.493 |
MOD_NEK2_1 | 326 | 331 | PF00069 | 0.509 |
MOD_NEK2_1 | 402 | 407 | PF00069 | 0.496 |
MOD_NEK2_1 | 43 | 48 | PF00069 | 0.450 |
MOD_NEK2_1 | 537 | 542 | PF00069 | 0.451 |
MOD_NEK2_1 | 605 | 610 | PF00069 | 0.491 |
MOD_NEK2_1 | 614 | 619 | PF00069 | 0.289 |
MOD_NEK2_1 | 621 | 626 | PF00069 | 0.289 |
MOD_NEK2_1 | 688 | 693 | PF00069 | 0.516 |
MOD_NEK2_1 | 695 | 700 | PF00069 | 0.450 |
MOD_NEK2_1 | 754 | 759 | PF00069 | 0.380 |
MOD_NEK2_1 | 780 | 785 | PF00069 | 0.303 |
MOD_NEK2_1 | 788 | 793 | PF00069 | 0.445 |
MOD_NEK2_2 | 113 | 118 | PF00069 | 0.433 |
MOD_NEK2_2 | 743 | 748 | PF00069 | 0.299 |
MOD_NEK2_2 | 818 | 823 | PF00069 | 0.486 |
MOD_PIKK_1 | 257 | 263 | PF00454 | 0.507 |
MOD_PIKK_1 | 343 | 349 | PF00454 | 0.527 |
MOD_PIKK_1 | 37 | 43 | PF00454 | 0.232 |
MOD_PIKK_1 | 402 | 408 | PF00454 | 0.536 |
MOD_PK_1 | 377 | 383 | PF00069 | 0.498 |
MOD_PK_1 | 875 | 881 | PF00069 | 0.592 |
MOD_PKA_1 | 862 | 868 | PF00069 | 0.657 |
MOD_PKA_1 | 875 | 881 | PF00069 | 0.571 |
MOD_PKA_2 | 159 | 165 | PF00069 | 0.451 |
MOD_PKA_2 | 186 | 192 | PF00069 | 0.433 |
MOD_PKA_2 | 226 | 232 | PF00069 | 0.431 |
MOD_PKA_2 | 357 | 363 | PF00069 | 0.555 |
MOD_PKA_2 | 371 | 377 | PF00069 | 0.593 |
MOD_PKA_2 | 4 | 10 | PF00069 | 0.531 |
MOD_PKA_2 | 557 | 563 | PF00069 | 0.463 |
MOD_PKA_2 | 771 | 777 | PF00069 | 0.539 |
MOD_PKA_2 | 861 | 867 | PF00069 | 0.658 |
MOD_PKA_2 | 874 | 880 | PF00069 | 0.579 |
MOD_PKB_1 | 320 | 328 | PF00069 | 0.512 |
MOD_Plk_1 | 113 | 119 | PF00069 | 0.487 |
MOD_Plk_1 | 227 | 233 | PF00069 | 0.454 |
MOD_Plk_1 | 343 | 349 | PF00069 | 0.640 |
MOD_Plk_1 | 444 | 450 | PF00069 | 0.579 |
MOD_Plk_1 | 451 | 457 | PF00069 | 0.441 |
MOD_Plk_1 | 85 | 91 | PF00069 | 0.433 |
MOD_Plk_2-3 | 734 | 740 | PF00069 | 0.286 |
MOD_Plk_4 | 113 | 119 | PF00069 | 0.457 |
MOD_Plk_4 | 163 | 169 | PF00069 | 0.571 |
MOD_Plk_4 | 192 | 198 | PF00069 | 0.426 |
MOD_Plk_4 | 218 | 224 | PF00069 | 0.433 |
MOD_Plk_4 | 227 | 233 | PF00069 | 0.397 |
MOD_Plk_4 | 43 | 49 | PF00069 | 0.187 |
MOD_Plk_4 | 451 | 457 | PF00069 | 0.469 |
MOD_Plk_4 | 484 | 490 | PF00069 | 0.561 |
MOD_Plk_4 | 605 | 611 | PF00069 | 0.506 |
MOD_Plk_4 | 621 | 627 | PF00069 | 0.297 |
MOD_Plk_4 | 656 | 662 | PF00069 | 0.374 |
MOD_Plk_4 | 664 | 670 | PF00069 | 0.279 |
MOD_Plk_4 | 676 | 682 | PF00069 | 0.531 |
MOD_Plk_4 | 780 | 786 | PF00069 | 0.224 |
MOD_ProDKin_1 | 18 | 24 | PF00069 | 0.284 |
MOD_ProDKin_1 | 234 | 240 | PF00069 | 0.402 |
MOD_ProDKin_1 | 492 | 498 | PF00069 | 0.606 |
MOD_ProDKin_1 | 6 | 12 | PF00069 | 0.581 |
MOD_ProDKin_1 | 726 | 732 | PF00069 | 0.370 |
MOD_ProDKin_1 | 759 | 765 | PF00069 | 0.351 |
MOD_ProDKin_1 | 864 | 870 | PF00069 | 0.706 |
MOD_SUMO_for_1 | 473 | 476 | PF00179 | 0.547 |
MOD_SUMO_rev_2 | 892 | 898 | PF00179 | 0.586 |
TRG_ENDOCYTIC_2 | 196 | 199 | PF00928 | 0.438 |
TRG_ENDOCYTIC_2 | 34 | 37 | PF00928 | 0.285 |
TRG_ENDOCYTIC_2 | 345 | 348 | PF00928 | 0.583 |
TRG_ENDOCYTIC_2 | 522 | 525 | PF00928 | 0.460 |
TRG_ENDOCYTIC_2 | 610 | 613 | PF00928 | 0.471 |
TRG_ENDOCYTIC_2 | 751 | 754 | PF00928 | 0.308 |
TRG_ENDOCYTIC_2 | 807 | 810 | PF00928 | 0.340 |
TRG_ER_diArg_1 | 185 | 188 | PF00400 | 0.504 |
TRG_ER_diArg_1 | 265 | 268 | PF00400 | 0.494 |
TRG_ER_diArg_1 | 363 | 366 | PF00400 | 0.535 |
TRG_ER_diArg_1 | 635 | 637 | PF00400 | 0.379 |
TRG_ER_diArg_1 | 66 | 69 | PF00400 | 0.512 |
TRG_ER_diArg_1 | 70 | 72 | PF00400 | 0.490 |
TRG_ER_diArg_1 | 775 | 778 | PF00400 | 0.508 |
TRG_ER_diArg_1 | 861 | 863 | PF00400 | 0.664 |
TRG_ER_diArg_1 | 900 | 903 | PF00400 | 0.620 |
TRG_NES_CRM1_1 | 590 | 604 | PF08389 | 0.468 |
TRG_Pf-PMV_PEXEL_1 | 535 | 539 | PF00026 | 0.233 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1X4 | Leptomonas seymouri | 44% | 90% |
A0A0S4IVK7 | Bodo saltans | 27% | 100% |
A0A0S4JRV4 | Bodo saltans | 21% | 90% |
A0A1X0NL00 | Trypanosomatidae | 28% | 100% |
A0A381MFJ0 | Leishmania infantum | 27% | 93% |
A0A3S5H5E7 | Leishmania donovani | 90% | 95% |
A0A3S7WV61 | Leishmania donovani | 27% | 93% |
A0A3S7WV68 | Leishmania donovani | 28% | 93% |
A0R3A7 | Mycolicibacterium smegmatis (strain ATCC 700084 / mc(2)155) | 24% | 100% |
A4HSA9 | Leishmania infantum | 90% | 95% |
A4HY23 | Leishmania infantum | 28% | 100% |
A7L9Z8 | Mus musculus | 22% | 96% |
D0ZTB2 | Salmonella typhimurium (strain 14028s / SGSC 2262) | 25% | 100% |
O59868 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 26% | 100% |
O75185 | Homo sapiens | 22% | 96% |
O81108 | Arabidopsis thaliana | 21% | 90% |
O97198 | Leishmania major | 89% | 100% |
P0ABB8 | Escherichia coli (strain K12) | 26% | 100% |
P0ABB9 | Escherichia coli O157:H7 | 26% | 100% |
P13586 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 21% | 96% |
P22036 | Salmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720) | 27% | 100% |
P22180 | Solanum lycopersicum | 26% | 95% |
P36640 | Salmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720) | 25% | 100% |
P37367 | Synechocystis sp. (strain PCC 6803 / Kazusa) | 25% | 100% |
P54211 | Dunaliella bioculata | 25% | 80% |
P54678 | Dictyostelium discoideum | 22% | 82% |
P63688 | Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) | 27% | 100% |
P83970 | Triticum aestivum | 27% | 96% |
P98194 | Homo sapiens | 23% | 99% |
P9WPS8 | Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) | 27% | 100% |
P9WPS9 | Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) | 27% | 100% |
Q08435 | Nicotiana plumbaginifolia | 26% | 95% |
Q37145 | Arabidopsis thaliana | 22% | 89% |
Q43128 | Arabidopsis thaliana | 24% | 96% |
Q47H39 | Dechloromonas aromatica (strain RCB) | 23% | 100% |
Q65X71 | Oryza sativa subsp. japonica | 21% | 89% |
Q6ATV4 | Oryza sativa subsp. japonica | 23% | 88% |
Q73E41 | Bacillus cereus (strain ATCC 10987 / NRS 248) | 22% | 100% |
Q7XEK4 | Oryza sativa subsp. japonica | 27% | 88% |
Q7XPY2 | Oryza sativa subsp. japonica | 27% | 96% |
Q8R4C1 | Rattus norvegicus | 22% | 96% |
Q8Y8Q5 | Listeria monocytogenes serovar 1/2a (strain ATCC BAA-679 / EGD-e) | 22% | 100% |
Q98GX6 | Mesorhizobium japonicum (strain LMG 29417 / CECT 9101 / MAFF 303099) | 23% | 100% |
Q9LIK7 | Arabidopsis thaliana | 23% | 89% |
Q9LV11 | Arabidopsis thaliana | 26% | 95% |
Q9M2L4 | Arabidopsis thaliana | 21% | 89% |
Q9RZP0 | Deinococcus radiodurans (strain ATCC 13939 / DSM 20539 / JCM 16871 / LMG 4051 / NBRC 15346 / NCIMB 9279 / R1 / VKM B-1422) | 25% | 100% |
Q9SU58 | Arabidopsis thaliana | 27% | 95% |
Q9SZR1 | Arabidopsis thaliana | 23% | 85% |