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:0005634 | nucleus | 5 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HZS7
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 6 |
GO:0006793 | phosphorus metabolic process | 3 | 6 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 6 |
GO:0006807 | nitrogen compound metabolic process | 2 | 6 |
GO:0008152 | metabolic process | 1 | 6 |
GO:0009987 | cellular process | 1 | 6 |
GO:0016310 | phosphorylation | 5 | 6 |
GO:0019538 | protein metabolic process | 3 | 6 |
GO:0036211 | protein modification process | 4 | 6 |
GO:0043170 | macromolecule metabolic process | 3 | 6 |
GO:0043412 | macromolecule modification | 4 | 6 |
GO:0044237 | cellular metabolic process | 2 | 6 |
GO:0044238 | primary metabolic process | 2 | 6 |
GO:0071704 | organic substance metabolic process | 2 | 6 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 6 |
GO:0007165 | signal transduction | 2 | 1 |
GO:0035556 | intracellular signal transduction | 3 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 6 |
GO:0003824 | catalytic activity | 1 | 6 |
GO:0004672 | protein kinase activity | 3 | 6 |
GO:0005488 | binding | 1 | 6 |
GO:0005524 | ATP binding | 5 | 6 |
GO:0016301 | kinase activity | 4 | 6 |
GO:0016740 | transferase activity | 2 | 6 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 6 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 6 |
GO:0017076 | purine nucleotide binding | 4 | 6 |
GO:0030554 | adenyl nucleotide binding | 5 | 6 |
GO:0032553 | ribonucleotide binding | 3 | 6 |
GO:0032555 | purine ribonucleotide binding | 4 | 6 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 6 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 6 |
GO:0036094 | small molecule binding | 2 | 6 |
GO:0043167 | ion binding | 2 | 6 |
GO:0043168 | anion binding | 3 | 6 |
GO:0097159 | organic cyclic compound binding | 2 | 6 |
GO:0097367 | carbohydrate derivative binding | 2 | 6 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 6 |
GO:1901265 | nucleoside phosphate binding | 3 | 6 |
GO:1901363 | heterocyclic compound binding | 2 | 6 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 1 |
GO:0004707 | MAP kinase activity | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 225 | 229 | PF00656 | 0.791 |
CLV_C14_Caspase3-7 | 427 | 431 | PF00656 | 0.500 |
CLV_C14_Caspase3-7 | 760 | 764 | PF00656 | 0.471 |
CLV_NRD_NRD_1 | 125 | 127 | PF00675 | 0.652 |
CLV_NRD_NRD_1 | 52 | 54 | PF00675 | 0.473 |
CLV_NRD_NRD_1 | 717 | 719 | PF00675 | 0.355 |
CLV_PCSK_FUR_1 | 123 | 127 | PF00082 | 0.617 |
CLV_PCSK_KEX2_1 | 125 | 127 | PF00082 | 0.652 |
CLV_PCSK_KEX2_1 | 193 | 195 | PF00082 | 0.363 |
CLV_PCSK_KEX2_1 | 52 | 54 | PF00082 | 0.473 |
CLV_PCSK_KEX2_1 | 564 | 566 | PF00082 | 0.305 |
CLV_PCSK_KEX2_1 | 717 | 719 | PF00082 | 0.355 |
CLV_PCSK_KEX2_1 | 742 | 744 | PF00082 | 0.296 |
CLV_PCSK_PC1ET2_1 | 193 | 195 | PF00082 | 0.363 |
CLV_PCSK_PC1ET2_1 | 564 | 566 | PF00082 | 0.305 |
CLV_PCSK_PC1ET2_1 | 742 | 744 | PF00082 | 0.296 |
CLV_PCSK_SKI1_1 | 101 | 105 | PF00082 | 0.479 |
CLV_PCSK_SKI1_1 | 11 | 15 | PF00082 | 0.360 |
CLV_PCSK_SKI1_1 | 17 | 21 | PF00082 | 0.412 |
CLV_PCSK_SKI1_1 | 41 | 45 | PF00082 | 0.465 |
CLV_PCSK_SKI1_1 | 438 | 442 | PF00082 | 0.296 |
CLV_PCSK_SKI1_1 | 462 | 466 | PF00082 | 0.336 |
CLV_PCSK_SKI1_1 | 540 | 544 | PF00082 | 0.322 |
CLV_PCSK_SKI1_1 | 645 | 649 | PF00082 | 0.355 |
CLV_PCSK_SKI1_1 | 679 | 683 | PF00082 | 0.243 |
CLV_PCSK_SKI1_1 | 717 | 721 | PF00082 | 0.296 |
CLV_PCSK_SKI1_1 | 72 | 76 | PF00082 | 0.483 |
CLV_PCSK_SKI1_1 | 742 | 746 | PF00082 | 0.355 |
CLV_Separin_Metazoa | 533 | 537 | PF03568 | 0.296 |
DEG_APCC_DBOX_1 | 16 | 24 | PF00400 | 0.421 |
DEG_SCF_FBW7_1 | 89 | 95 | PF00400 | 0.448 |
DEG_SCF_FBW7_2 | 697 | 704 | PF00400 | 0.355 |
DEG_SPOP_SBC_1 | 23 | 27 | PF00917 | 0.439 |
DEG_SPOP_SBC_1 | 242 | 246 | PF00917 | 0.580 |
DEG_SPOP_SBC_1 | 250 | 254 | PF00917 | 0.604 |
DEG_SPOP_SBC_1 | 371 | 375 | PF00917 | 0.738 |
DEG_SPOP_SBC_1 | 92 | 96 | PF00917 | 0.440 |
DOC_CDC14_PxL_1 | 505 | 513 | PF14671 | 0.296 |
DOC_CKS1_1 | 89 | 94 | PF01111 | 0.451 |
DOC_CYCLIN_RxL_1 | 712 | 724 | PF00134 | 0.296 |
DOC_CYCLIN_RxL_1 | 8 | 16 | PF00134 | 0.358 |
DOC_MAPK_DCC_7 | 106 | 116 | PF00069 | 0.457 |
DOC_MAPK_gen_1 | 120 | 130 | PF00069 | 0.535 |
DOC_MAPK_gen_1 | 462 | 471 | PF00069 | 0.296 |
DOC_MAPK_gen_1 | 504 | 513 | PF00069 | 0.296 |
DOC_MAPK_gen_1 | 603 | 612 | PF00069 | 0.355 |
DOC_MAPK_HePTP_8 | 501 | 513 | PF00069 | 0.296 |
DOC_MAPK_MEF2A_6 | 504 | 513 | PF00069 | 0.296 |
DOC_MAPK_MEF2A_6 | 606 | 614 | PF00069 | 0.355 |
DOC_MAPK_RevD_3 | 112 | 126 | PF00069 | 0.494 |
DOC_PP1_RVXF_1 | 439 | 446 | PF00149 | 0.338 |
DOC_PP1_RVXF_1 | 447 | 454 | PF00149 | 0.260 |
DOC_PP2B_LxvP_1 | 559 | 562 | PF13499 | 0.355 |
DOC_PP2B_LxvP_1 | 796 | 799 | PF13499 | 0.383 |
DOC_PP4_FxxP_1 | 104 | 107 | PF00568 | 0.473 |
DOC_PP4_FxxP_1 | 109 | 112 | PF00568 | 0.458 |
DOC_PP4_FxxP_1 | 21 | 24 | PF00568 | 0.443 |
DOC_PP4_FxxP_1 | 682 | 685 | PF00568 | 0.323 |
DOC_USP7_MATH_1 | 135 | 139 | PF00917 | 0.632 |
DOC_USP7_MATH_1 | 154 | 158 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 22 | 26 | PF00917 | 0.442 |
DOC_USP7_MATH_1 | 240 | 244 | PF00917 | 0.664 |
DOC_USP7_MATH_1 | 250 | 254 | PF00917 | 0.575 |
DOC_USP7_MATH_1 | 776 | 780 | PF00917 | 0.588 |
DOC_USP7_UBL2_3 | 189 | 193 | PF12436 | 0.330 |
DOC_USP7_UBL2_3 | 82 | 86 | PF12436 | 0.463 |
DOC_WW_Pin1_4 | 152 | 157 | PF00397 | 0.569 |
DOC_WW_Pin1_4 | 24 | 29 | PF00397 | 0.441 |
DOC_WW_Pin1_4 | 372 | 377 | PF00397 | 0.772 |
DOC_WW_Pin1_4 | 378 | 383 | PF00397 | 0.646 |
DOC_WW_Pin1_4 | 402 | 407 | PF00397 | 0.760 |
DOC_WW_Pin1_4 | 656 | 661 | PF00397 | 0.296 |
DOC_WW_Pin1_4 | 663 | 668 | PF00397 | 0.296 |
DOC_WW_Pin1_4 | 697 | 702 | PF00397 | 0.330 |
DOC_WW_Pin1_4 | 721 | 726 | PF00397 | 0.296 |
DOC_WW_Pin1_4 | 77 | 82 | PF00397 | 0.460 |
DOC_WW_Pin1_4 | 781 | 786 | PF00397 | 0.638 |
DOC_WW_Pin1_4 | 88 | 93 | PF00397 | 0.438 |
LIG_14-3-3_CanoR_1 | 125 | 131 | PF00244 | 0.574 |
LIG_14-3-3_CanoR_1 | 136 | 143 | PF00244 | 0.603 |
LIG_14-3-3_CanoR_1 | 147 | 156 | PF00244 | 0.516 |
LIG_14-3-3_CanoR_1 | 241 | 248 | PF00244 | 0.639 |
LIG_14-3-3_CanoR_1 | 33 | 37 | PF00244 | 0.479 |
LIG_14-3-3_CanoR_1 | 544 | 552 | PF00244 | 0.336 |
LIG_14-3-3_CanoR_1 | 586 | 591 | PF00244 | 0.369 |
LIG_14-3-3_CanoR_1 | 70 | 75 | PF00244 | 0.496 |
LIG_14-3-3_CanoR_1 | 743 | 750 | PF00244 | 0.296 |
LIG_14-3-3_CanoR_1 | 816 | 824 | PF00244 | 0.439 |
LIG_Actin_WH2_2 | 452 | 467 | PF00022 | 0.296 |
LIG_Actin_WH2_2 | 523 | 538 | PF00022 | 0.296 |
LIG_AP2alpha_1 | 755 | 759 | PF02296 | 0.353 |
LIG_BRCT_BRCA1_1 | 15 | 19 | PF00533 | 0.393 |
LIG_BRCT_BRCA1_1 | 243 | 247 | PF00533 | 0.524 |
LIG_BRCT_BRCA1_1 | 300 | 304 | PF00533 | 0.694 |
LIG_BRCT_BRCA1_1 | 95 | 99 | PF00533 | 0.443 |
LIG_deltaCOP1_diTrp_1 | 523 | 527 | PF00928 | 0.296 |
LIG_eIF4E_1 | 506 | 512 | PF01652 | 0.296 |
LIG_FHA_1 | 111 | 117 | PF00498 | 0.509 |
LIG_FHA_1 | 243 | 249 | PF00498 | 0.616 |
LIG_FHA_1 | 473 | 479 | PF00498 | 0.296 |
LIG_FHA_1 | 689 | 695 | PF00498 | 0.355 |
LIG_FHA_1 | 724 | 730 | PF00498 | 0.315 |
LIG_FHA_2 | 223 | 229 | PF00498 | 0.791 |
LIG_FHA_2 | 254 | 260 | PF00498 | 0.558 |
LIG_FHA_2 | 545 | 551 | PF00498 | 0.296 |
LIG_FHA_2 | 691 | 697 | PF00498 | 0.326 |
LIG_FHA_2 | 698 | 704 | PF00498 | 0.321 |
LIG_FHA_2 | 722 | 728 | PF00498 | 0.296 |
LIG_FHA_2 | 743 | 749 | PF00498 | 0.355 |
LIG_FHA_2 | 810 | 816 | PF00498 | 0.356 |
LIG_Integrin_isoDGR_2 | 800 | 802 | PF01839 | 0.402 |
LIG_LIR_Apic_2 | 503 | 509 | PF02991 | 0.296 |
LIG_LIR_Apic_2 | 680 | 685 | PF02991 | 0.323 |
LIG_LIR_Gen_1 | 301 | 312 | PF02991 | 0.515 |
LIG_LIR_Gen_1 | 430 | 440 | PF02991 | 0.340 |
LIG_LIR_Gen_1 | 703 | 714 | PF02991 | 0.296 |
LIG_LIR_Gen_1 | 73 | 81 | PF02991 | 0.470 |
LIG_LIR_Gen_1 | 96 | 107 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 16 | 21 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 174 | 178 | PF02991 | 0.396 |
LIG_LIR_Nem_3 | 276 | 281 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 301 | 307 | PF02991 | 0.568 |
LIG_LIR_Nem_3 | 430 | 435 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 510 | 516 | PF02991 | 0.296 |
LIG_LIR_Nem_3 | 526 | 530 | PF02991 | 0.296 |
LIG_LIR_Nem_3 | 554 | 559 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 700 | 705 | PF02991 | 0.309 |
LIG_LIR_Nem_3 | 73 | 77 | PF02991 | 0.484 |
LIG_LIR_Nem_3 | 85 | 90 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 96 | 102 | PF02991 | 0.456 |
LIG_MLH1_MIPbox_1 | 15 | 19 | PF16413 | 0.393 |
LIG_Pex14_1 | 716 | 720 | PF04695 | 0.296 |
LIG_Pex14_2 | 105 | 109 | PF04695 | 0.473 |
LIG_Pex14_2 | 755 | 759 | PF04695 | 0.353 |
LIG_REV1ctd_RIR_1 | 102 | 106 | PF16727 | 0.452 |
LIG_SH2_CRK | 164 | 168 | PF00017 | 0.441 |
LIG_SH2_CRK | 706 | 710 | PF00017 | 0.296 |
LIG_SH2_NCK_1 | 281 | 285 | PF00017 | 0.464 |
LIG_SH2_NCK_1 | 819 | 823 | PF00017 | 0.441 |
LIG_SH2_STAP1 | 197 | 201 | PF00017 | 0.486 |
LIG_SH2_STAP1 | 819 | 823 | PF00017 | 0.382 |
LIG_SH2_STAT5 | 169 | 172 | PF00017 | 0.401 |
LIG_SH2_STAT5 | 278 | 281 | PF00017 | 0.357 |
LIG_SH2_STAT5 | 342 | 345 | PF00017 | 0.329 |
LIG_SH2_STAT5 | 349 | 352 | PF00017 | 0.331 |
LIG_SH2_STAT5 | 356 | 359 | PF00017 | 0.399 |
LIG_SH2_STAT5 | 361 | 364 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 500 | 503 | PF00017 | 0.321 |
LIG_SH2_STAT5 | 819 | 822 | PF00017 | 0.393 |
LIG_SH2_STAT5 | 87 | 90 | PF00017 | 0.490 |
LIG_SH3_1 | 86 | 92 | PF00018 | 0.455 |
LIG_SH3_2 | 28 | 33 | PF14604 | 0.464 |
LIG_SH3_3 | 104 | 110 | PF00018 | 0.412 |
LIG_SH3_3 | 211 | 217 | PF00018 | 0.643 |
LIG_SH3_3 | 25 | 31 | PF00018 | 0.449 |
LIG_SH3_3 | 330 | 336 | PF00018 | 0.547 |
LIG_SH3_3 | 400 | 406 | PF00018 | 0.669 |
LIG_SH3_3 | 45 | 51 | PF00018 | 0.432 |
LIG_SH3_3 | 747 | 753 | PF00018 | 0.355 |
LIG_SH3_3 | 86 | 92 | PF00018 | 0.455 |
LIG_SUMO_SIM_anti_2 | 205 | 211 | PF11976 | 0.385 |
LIG_SUMO_SIM_anti_2 | 726 | 734 | PF11976 | 0.299 |
LIG_SUMO_SIM_par_1 | 126 | 131 | PF11976 | 0.541 |
LIG_SUMO_SIM_par_1 | 176 | 183 | PF11976 | 0.353 |
LIG_SUMO_SIM_par_1 | 270 | 276 | PF11976 | 0.344 |
LIG_TRAF2_1 | 492 | 495 | PF00917 | 0.355 |
LIG_TRAF2_1 | 618 | 621 | PF00917 | 0.323 |
LIG_TRAF2_1 | 701 | 704 | PF00917 | 0.355 |
LIG_UBA3_1 | 555 | 564 | PF00899 | 0.296 |
LIG_WRC_WIRS_1 | 524 | 529 | PF05994 | 0.296 |
LIG_WRC_WIRS_1 | 71 | 76 | PF05994 | 0.483 |
MOD_CDK_SPK_2 | 402 | 407 | PF00069 | 0.666 |
MOD_CDK_SPK_2 | 77 | 82 | PF00069 | 0.457 |
MOD_CK1_1 | 118 | 124 | PF00069 | 0.669 |
MOD_CK1_1 | 131 | 137 | PF00069 | 0.708 |
MOD_CK1_1 | 138 | 144 | PF00069 | 0.579 |
MOD_CK1_1 | 157 | 163 | PF00069 | 0.722 |
MOD_CK1_1 | 243 | 249 | PF00069 | 0.610 |
MOD_CK1_1 | 251 | 257 | PF00069 | 0.531 |
MOD_CK1_1 | 306 | 312 | PF00069 | 0.530 |
MOD_CK1_1 | 32 | 38 | PF00069 | 0.475 |
MOD_CK1_1 | 320 | 326 | PF00069 | 0.603 |
MOD_CK1_1 | 374 | 380 | PF00069 | 0.606 |
MOD_CK1_1 | 416 | 422 | PF00069 | 0.637 |
MOD_CK1_1 | 589 | 595 | PF00069 | 0.243 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.518 |
MOD_CK1_1 | 654 | 660 | PF00069 | 0.385 |
MOD_CK1_1 | 666 | 672 | PF00069 | 0.226 |
MOD_CK1_1 | 779 | 785 | PF00069 | 0.612 |
MOD_CK1_1 | 94 | 100 | PF00069 | 0.443 |
MOD_CK2_1 | 560 | 566 | PF00069 | 0.296 |
MOD_CK2_1 | 697 | 703 | PF00069 | 0.355 |
MOD_CK2_1 | 721 | 727 | PF00069 | 0.296 |
MOD_CK2_1 | 742 | 748 | PF00069 | 0.355 |
MOD_CK2_1 | 781 | 787 | PF00069 | 0.584 |
MOD_CK2_1 | 809 | 815 | PF00069 | 0.349 |
MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.669 |
MOD_GlcNHglycan | 137 | 140 | PF01048 | 0.603 |
MOD_GlcNHglycan | 248 | 251 | PF01048 | 0.651 |
MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.693 |
MOD_GlcNHglycan | 319 | 322 | PF01048 | 0.596 |
MOD_GlcNHglycan | 333 | 336 | PF01048 | 0.554 |
MOD_GlcNHglycan | 390 | 393 | PF01048 | 0.709 |
MOD_GlcNHglycan | 426 | 429 | PF01048 | 0.637 |
MOD_GlcNHglycan | 484 | 487 | PF01048 | 0.296 |
MOD_GlcNHglycan | 537 | 540 | PF01048 | 0.316 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.489 |
MOD_GlcNHglycan | 595 | 598 | PF01048 | 0.469 |
MOD_GlcNHglycan | 656 | 659 | PF01048 | 0.296 |
MOD_GlcNHglycan | 682 | 685 | PF01048 | 0.355 |
MOD_GlcNHglycan | 759 | 762 | PF01048 | 0.497 |
MOD_GlcNHglycan | 778 | 781 | PF01048 | 0.482 |
MOD_GlcNHglycan | 792 | 795 | PF01048 | 0.404 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.712 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.649 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.806 |
MOD_GSK3_1 | 242 | 249 | PF00069 | 0.532 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.472 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.654 |
MOD_GSK3_1 | 366 | 373 | PF00069 | 0.444 |
MOD_GSK3_1 | 374 | 381 | PF00069 | 0.563 |
MOD_GSK3_1 | 415 | 422 | PF00069 | 0.673 |
MOD_GSK3_1 | 496 | 503 | PF00069 | 0.296 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.477 |
MOD_GSK3_1 | 589 | 596 | PF00069 | 0.243 |
MOD_GSK3_1 | 650 | 657 | PF00069 | 0.325 |
MOD_GSK3_1 | 663 | 670 | PF00069 | 0.244 |
MOD_GSK3_1 | 680 | 687 | PF00069 | 0.213 |
MOD_GSK3_1 | 772 | 779 | PF00069 | 0.619 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.456 |
MOD_N-GLC_1 | 413 | 418 | PF02516 | 0.650 |
MOD_N-GLC_1 | 496 | 501 | PF02516 | 0.296 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.657 |
MOD_NEK2_1 | 13 | 18 | PF00069 | 0.365 |
MOD_NEK2_1 | 145 | 150 | PF00069 | 0.555 |
MOD_NEK2_1 | 248 | 253 | PF00069 | 0.699 |
MOD_NEK2_1 | 345 | 350 | PF00069 | 0.437 |
MOD_NEK2_1 | 370 | 375 | PF00069 | 0.643 |
MOD_NEK2_1 | 535 | 540 | PF00069 | 0.301 |
MOD_NEK2_1 | 578 | 583 | PF00069 | 0.296 |
MOD_NEK2_1 | 731 | 736 | PF00069 | 0.355 |
MOD_NEK2_1 | 93 | 98 | PF00069 | 0.450 |
MOD_NMyristoyl | 1 | 7 | PF02799 | 0.381 |
MOD_PIKK_1 | 154 | 160 | PF00454 | 0.636 |
MOD_PIKK_1 | 36 | 42 | PF00454 | 0.463 |
MOD_PIKK_1 | 651 | 657 | PF00454 | 0.355 |
MOD_PK_1 | 126 | 132 | PF00069 | 0.544 |
MOD_PKA_1 | 52 | 58 | PF00069 | 0.478 |
MOD_PKA_1 | 742 | 748 | PF00069 | 0.296 |
MOD_PKA_2 | 131 | 137 | PF00069 | 0.657 |
MOD_PKA_2 | 171 | 177 | PF00069 | 0.412 |
MOD_PKA_2 | 240 | 246 | PF00069 | 0.635 |
MOD_PKA_2 | 32 | 38 | PF00069 | 0.475 |
MOD_PKA_2 | 419 | 425 | PF00069 | 0.618 |
MOD_PKA_2 | 52 | 58 | PF00069 | 0.447 |
MOD_PKA_2 | 535 | 541 | PF00069 | 0.296 |
MOD_PKA_2 | 742 | 748 | PF00069 | 0.296 |
MOD_PKA_2 | 770 | 776 | PF00069 | 0.508 |
MOD_PKB_1 | 70 | 78 | PF00069 | 0.480 |
MOD_Plk_1 | 118 | 124 | PF00069 | 0.530 |
MOD_Plk_1 | 230 | 236 | PF00069 | 0.574 |
MOD_Plk_1 | 496 | 502 | PF00069 | 0.296 |
MOD_Plk_4 | 208 | 214 | PF00069 | 0.415 |
MOD_Plk_4 | 222 | 228 | PF00069 | 0.710 |
MOD_Plk_4 | 243 | 249 | PF00069 | 0.640 |
MOD_Plk_4 | 345 | 351 | PF00069 | 0.323 |
MOD_Plk_4 | 366 | 372 | PF00069 | 0.378 |
MOD_Plk_4 | 496 | 502 | PF00069 | 0.296 |
MOD_Plk_4 | 731 | 737 | PF00069 | 0.427 |
MOD_Plk_4 | 804 | 810 | PF00069 | 0.462 |
MOD_ProDKin_1 | 152 | 158 | PF00069 | 0.566 |
MOD_ProDKin_1 | 24 | 30 | PF00069 | 0.443 |
MOD_ProDKin_1 | 372 | 378 | PF00069 | 0.770 |
MOD_ProDKin_1 | 402 | 408 | PF00069 | 0.760 |
MOD_ProDKin_1 | 656 | 662 | PF00069 | 0.296 |
MOD_ProDKin_1 | 663 | 669 | PF00069 | 0.296 |
MOD_ProDKin_1 | 697 | 703 | PF00069 | 0.330 |
MOD_ProDKin_1 | 721 | 727 | PF00069 | 0.296 |
MOD_ProDKin_1 | 77 | 83 | PF00069 | 0.461 |
MOD_ProDKin_1 | 781 | 787 | PF00069 | 0.636 |
MOD_ProDKin_1 | 88 | 94 | PF00069 | 0.436 |
MOD_SUMO_rev_2 | 674 | 681 | PF00179 | 0.333 |
TRG_DiLeu_BaEn_1 | 727 | 732 | PF01217 | 0.296 |
TRG_DiLeu_BaLyEn_6 | 8 | 13 | PF01217 | 0.359 |
TRG_ENDOCYTIC_2 | 164 | 167 | PF00928 | 0.443 |
TRG_ENDOCYTIC_2 | 342 | 345 | PF00928 | 0.364 |
TRG_ENDOCYTIC_2 | 349 | 352 | PF00928 | 0.404 |
TRG_ENDOCYTIC_2 | 361 | 364 | PF00928 | 0.436 |
TRG_ENDOCYTIC_2 | 705 | 708 | PF00928 | 0.296 |
TRG_ENDOCYTIC_2 | 87 | 90 | PF00928 | 0.471 |
TRG_ER_diArg_1 | 122 | 125 | PF00400 | 0.639 |
TRG_ER_diArg_1 | 44 | 47 | PF00400 | 0.469 |
TRG_ER_diArg_1 | 51 | 53 | PF00400 | 0.459 |
TRG_ER_diArg_1 | 579 | 582 | PF00400 | 0.355 |
TRG_ER_diArg_1 | 716 | 718 | PF00400 | 0.355 |
TRG_Pf-PMV_PEXEL_1 | 816 | 821 | PF00026 | 0.389 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HU16 | Leptomonas seymouri | 51% | 100% |
A0A3Q8IC49 | Leishmania donovani | 99% | 100% |
E9AVN2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q4QBU7 | Leishmania major | 93% | 100% |