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: 4 |
NetGPI | no | yes: 0, no: 4 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0016592 | mediator complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 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 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
Related structures:
AlphaFold database: E9AMN0
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 5 |
GO:0006793 | phosphorus metabolic process | 3 | 5 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 5 |
GO:0006807 | nitrogen compound metabolic process | 2 | 5 |
GO:0008152 | metabolic process | 1 | 5 |
GO:0009987 | cellular process | 1 | 5 |
GO:0016310 | phosphorylation | 5 | 5 |
GO:0019538 | protein metabolic process | 3 | 5 |
GO:0036211 | protein modification process | 4 | 5 |
GO:0043170 | macromolecule metabolic process | 3 | 5 |
GO:0043412 | macromolecule modification | 4 | 5 |
GO:0044237 | cellular metabolic process | 2 | 5 |
GO:0044238 | primary metabolic process | 2 | 5 |
GO:0071704 | organic substance metabolic process | 2 | 5 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 5 |
GO:0006810 | transport | 3 | 1 |
GO:0006897 | endocytosis | 5 | 1 |
GO:0016192 | vesicle-mediated transport | 4 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 5 |
GO:0003824 | catalytic activity | 1 | 5 |
GO:0004672 | protein kinase activity | 3 | 5 |
GO:0005488 | binding | 1 | 5 |
GO:0005524 | ATP binding | 5 | 5 |
GO:0016301 | kinase activity | 4 | 5 |
GO:0016740 | transferase activity | 2 | 5 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 5 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 5 |
GO:0017076 | purine nucleotide binding | 4 | 5 |
GO:0030554 | adenyl nucleotide binding | 5 | 5 |
GO:0032553 | ribonucleotide binding | 3 | 5 |
GO:0032555 | purine ribonucleotide binding | 4 | 5 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 5 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 5 |
GO:0036094 | small molecule binding | 2 | 5 |
GO:0043167 | ion binding | 2 | 5 |
GO:0043168 | anion binding | 3 | 5 |
GO:0097159 | organic cyclic compound binding | 2 | 5 |
GO:0097367 | carbohydrate derivative binding | 2 | 5 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 5 |
GO:1901265 | nucleoside phosphate binding | 3 | 5 |
GO:1901363 | heterocyclic compound binding | 2 | 5 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 1 |
GO:0004693 | cyclin-dependent protein serine/threonine kinase activity | 5 | 1 |
GO:0008353 | RNA polymerase II CTD heptapeptide repeat kinase activity | 5 | 1 |
GO:0097472 | cyclin-dependent protein kinase activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 136 | 140 | PF00656 | 0.526 |
CLV_NRD_NRD_1 | 304 | 306 | PF00675 | 0.701 |
CLV_NRD_NRD_1 | 429 | 431 | PF00675 | 0.705 |
CLV_NRD_NRD_1 | 575 | 577 | PF00675 | 0.524 |
CLV_NRD_NRD_1 | 596 | 598 | PF00675 | 0.399 |
CLV_NRD_NRD_1 | 6 | 8 | PF00675 | 0.729 |
CLV_NRD_NRD_1 | 801 | 803 | PF00675 | 0.399 |
CLV_NRD_NRD_1 | 861 | 863 | PF00675 | 0.495 |
CLV_NRD_NRD_1 | 878 | 880 | PF00675 | 0.581 |
CLV_PCSK_KEX2_1 | 202 | 204 | PF00082 | 0.715 |
CLV_PCSK_KEX2_1 | 429 | 431 | PF00082 | 0.705 |
CLV_PCSK_KEX2_1 | 479 | 481 | PF00082 | 0.399 |
CLV_PCSK_KEX2_1 | 488 | 490 | PF00082 | 0.309 |
CLV_PCSK_KEX2_1 | 575 | 577 | PF00082 | 0.524 |
CLV_PCSK_KEX2_1 | 6 | 8 | PF00082 | 0.729 |
CLV_PCSK_KEX2_1 | 801 | 803 | PF00082 | 0.397 |
CLV_PCSK_KEX2_1 | 861 | 863 | PF00082 | 0.495 |
CLV_PCSK_KEX2_1 | 878 | 880 | PF00082 | 0.581 |
CLV_PCSK_PC1ET2_1 | 202 | 204 | PF00082 | 0.715 |
CLV_PCSK_PC1ET2_1 | 479 | 481 | PF00082 | 0.399 |
CLV_PCSK_PC1ET2_1 | 488 | 490 | PF00082 | 0.309 |
CLV_PCSK_SKI1_1 | 241 | 245 | PF00082 | 0.593 |
CLV_PCSK_SKI1_1 | 413 | 417 | PF00082 | 0.608 |
CLV_PCSK_SKI1_1 | 453 | 457 | PF00082 | 0.468 |
CLV_PCSK_SKI1_1 | 488 | 492 | PF00082 | 0.399 |
CLV_PCSK_SKI1_1 | 590 | 594 | PF00082 | 0.424 |
CLV_PCSK_SKI1_1 | 607 | 611 | PF00082 | 0.229 |
CLV_Separin_Metazoa | 827 | 831 | PF03568 | 0.399 |
DEG_SCF_FBW7_2 | 850 | 857 | PF00400 | 0.552 |
DEG_SPOP_SBC_1 | 157 | 161 | PF00917 | 0.533 |
DEG_SPOP_SBC_1 | 243 | 247 | PF00917 | 0.602 |
DEG_SPOP_SBC_1 | 62 | 66 | PF00917 | 0.710 |
DEG_SPOP_SBC_1 | 83 | 87 | PF00917 | 0.532 |
DOC_CDC14_PxL_1 | 837 | 845 | PF14671 | 0.531 |
DOC_CKS1_1 | 117 | 122 | PF01111 | 0.699 |
DOC_CKS1_1 | 645 | 650 | PF01111 | 0.399 |
DOC_CKS1_1 | 851 | 856 | PF01111 | 0.501 |
DOC_CYCLIN_yCln2_LP_2 | 95 | 101 | PF00134 | 0.528 |
DOC_MAPK_DCC_7 | 351 | 361 | PF00069 | 0.530 |
DOC_MAPK_gen_1 | 429 | 438 | PF00069 | 0.698 |
DOC_MAPK_gen_1 | 479 | 487 | PF00069 | 0.399 |
DOC_MAPK_gen_1 | 554 | 563 | PF00069 | 0.399 |
DOC_MAPK_gen_1 | 590 | 596 | PF00069 | 0.399 |
DOC_MAPK_gen_1 | 597 | 604 | PF00069 | 0.329 |
DOC_MAPK_gen_1 | 607 | 616 | PF00069 | 0.229 |
DOC_MAPK_gen_1 | 861 | 868 | PF00069 | 0.384 |
DOC_MAPK_HePTP_8 | 551 | 563 | PF00069 | 0.399 |
DOC_MAPK_MEF2A_6 | 429 | 438 | PF00069 | 0.648 |
DOC_MAPK_MEF2A_6 | 554 | 563 | PF00069 | 0.399 |
DOC_MAPK_RevD_3 | 585 | 598 | PF00069 | 0.349 |
DOC_PP2B_LxvP_1 | 686 | 689 | PF13499 | 0.399 |
DOC_PP2B_LxvP_1 | 829 | 832 | PF13499 | 0.399 |
DOC_USP7_MATH_1 | 157 | 161 | PF00917 | 0.727 |
DOC_USP7_MATH_1 | 206 | 210 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 243 | 247 | PF00917 | 0.695 |
DOC_USP7_MATH_1 | 281 | 285 | PF00917 | 0.583 |
DOC_USP7_MATH_1 | 500 | 504 | PF00917 | 0.399 |
DOC_USP7_MATH_1 | 541 | 545 | PF00917 | 0.399 |
DOC_USP7_MATH_1 | 566 | 570 | PF00917 | 0.474 |
DOC_USP7_MATH_1 | 62 | 66 | PF00917 | 0.710 |
DOC_USP7_MATH_1 | 634 | 638 | PF00917 | 0.389 |
DOC_USP7_MATH_1 | 706 | 710 | PF00917 | 0.399 |
DOC_USP7_MATH_1 | 84 | 88 | PF00917 | 0.527 |
DOC_USP7_UBL2_3 | 475 | 479 | PF12436 | 0.399 |
DOC_WW_Pin1_4 | 113 | 118 | PF00397 | 0.701 |
DOC_WW_Pin1_4 | 158 | 163 | PF00397 | 0.564 |
DOC_WW_Pin1_4 | 214 | 219 | PF00397 | 0.679 |
DOC_WW_Pin1_4 | 254 | 259 | PF00397 | 0.764 |
DOC_WW_Pin1_4 | 314 | 319 | PF00397 | 0.672 |
DOC_WW_Pin1_4 | 323 | 328 | PF00397 | 0.634 |
DOC_WW_Pin1_4 | 354 | 359 | PF00397 | 0.649 |
DOC_WW_Pin1_4 | 374 | 379 | PF00397 | 0.549 |
DOC_WW_Pin1_4 | 413 | 418 | PF00397 | 0.575 |
DOC_WW_Pin1_4 | 423 | 428 | PF00397 | 0.606 |
DOC_WW_Pin1_4 | 446 | 451 | PF00397 | 0.458 |
DOC_WW_Pin1_4 | 578 | 583 | PF00397 | 0.399 |
DOC_WW_Pin1_4 | 58 | 63 | PF00397 | 0.715 |
DOC_WW_Pin1_4 | 644 | 649 | PF00397 | 0.399 |
DOC_WW_Pin1_4 | 850 | 855 | PF00397 | 0.524 |
LIG_14-3-3_CanoR_1 | 110 | 120 | PF00244 | 0.665 |
LIG_14-3-3_CanoR_1 | 241 | 251 | PF00244 | 0.602 |
LIG_14-3-3_CanoR_1 | 366 | 371 | PF00244 | 0.704 |
LIG_14-3-3_CanoR_1 | 411 | 416 | PF00244 | 0.553 |
LIG_14-3-3_CanoR_1 | 708 | 717 | PF00244 | 0.399 |
LIG_14-3-3_CanoR_1 | 719 | 727 | PF00244 | 0.289 |
LIG_14-3-3_CanoR_1 | 78 | 84 | PF00244 | 0.676 |
LIG_BRCT_BRCA1_1 | 200 | 204 | PF00533 | 0.527 |
LIG_BRCT_BRCA1_1 | 444 | 448 | PF00533 | 0.659 |
LIG_deltaCOP1_diTrp_1 | 193 | 204 | PF00928 | 0.531 |
LIG_EVH1_1 | 178 | 182 | PF00568 | 0.525 |
LIG_FHA_1 | 130 | 136 | PF00498 | 0.713 |
LIG_FHA_1 | 141 | 147 | PF00498 | 0.600 |
LIG_FHA_1 | 167 | 173 | PF00498 | 0.718 |
LIG_FHA_1 | 227 | 233 | PF00498 | 0.683 |
LIG_FHA_1 | 302 | 308 | PF00498 | 0.611 |
LIG_FHA_1 | 355 | 361 | PF00498 | 0.683 |
LIG_FHA_1 | 378 | 384 | PF00498 | 0.675 |
LIG_FHA_1 | 479 | 485 | PF00498 | 0.224 |
LIG_FHA_1 | 53 | 59 | PF00498 | 0.669 |
LIG_FHA_1 | 535 | 541 | PF00498 | 0.389 |
LIG_FHA_1 | 565 | 571 | PF00498 | 0.399 |
LIG_FHA_1 | 645 | 651 | PF00498 | 0.399 |
LIG_FHA_1 | 719 | 725 | PF00498 | 0.399 |
LIG_FHA_1 | 83 | 89 | PF00498 | 0.639 |
LIG_FHA_2 | 315 | 321 | PF00498 | 0.570 |
LIG_FHA_2 | 452 | 458 | PF00498 | 0.527 |
LIG_FHA_2 | 467 | 473 | PF00498 | 0.249 |
LIG_FHA_2 | 579 | 585 | PF00498 | 0.506 |
LIG_FHA_2 | 663 | 669 | PF00498 | 0.399 |
LIG_FHA_2 | 710 | 716 | PF00498 | 0.399 |
LIG_FHA_2 | 768 | 774 | PF00498 | 0.399 |
LIG_FHA_2 | 822 | 828 | PF00498 | 0.372 |
LIG_FHA_2 | 833 | 839 | PF00498 | 0.425 |
LIG_LIR_Apic_2 | 194 | 200 | PF02991 | 0.651 |
LIG_LIR_Apic_2 | 642 | 648 | PF02991 | 0.343 |
LIG_LIR_Apic_2 | 652 | 658 | PF02991 | 0.356 |
LIG_LIR_Gen_1 | 217 | 227 | PF02991 | 0.536 |
LIG_LIR_Gen_1 | 406 | 417 | PF02991 | 0.569 |
LIG_LIR_Gen_1 | 775 | 784 | PF02991 | 0.399 |
LIG_LIR_Gen_1 | 845 | 854 | PF02991 | 0.538 |
LIG_LIR_Nem_3 | 201 | 207 | PF02991 | 0.528 |
LIG_LIR_Nem_3 | 406 | 412 | PF02991 | 0.627 |
LIG_LIR_Nem_3 | 445 | 451 | PF02991 | 0.640 |
LIG_LIR_Nem_3 | 467 | 473 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 775 | 781 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 845 | 849 | PF02991 | 0.572 |
LIG_MYND_1 | 122 | 126 | PF01753 | 0.605 |
LIG_NRBOX | 675 | 681 | PF00104 | 0.399 |
LIG_PCNA_yPIPBox_3 | 452 | 464 | PF02747 | 0.517 |
LIG_PCNA_yPIPBox_3 | 501 | 511 | PF02747 | 0.349 |
LIG_Pex14_2 | 772 | 776 | PF04695 | 0.399 |
LIG_Pex14_2 | 784 | 788 | PF04695 | 0.279 |
LIG_SH2_CRK | 846 | 850 | PF00017 | 0.624 |
LIG_SH2_NCK_1 | 565 | 569 | PF00017 | 0.399 |
LIG_SH2_STAP1 | 667 | 671 | PF00017 | 0.399 |
LIG_SH2_STAT3 | 552 | 555 | PF00017 | 0.399 |
LIG_SH2_STAT5 | 23 | 26 | PF00017 | 0.662 |
LIG_SH2_STAT5 | 684 | 687 | PF00017 | 0.337 |
LIG_SH2_STAT5 | 833 | 836 | PF00017 | 0.486 |
LIG_SH3_1 | 148 | 154 | PF00018 | 0.742 |
LIG_SH3_1 | 324 | 330 | PF00018 | 0.603 |
LIG_SH3_1 | 848 | 854 | PF00018 | 0.535 |
LIG_SH3_2 | 851 | 856 | PF14604 | 0.501 |
LIG_SH3_3 | 114 | 120 | PF00018 | 0.722 |
LIG_SH3_3 | 148 | 154 | PF00018 | 0.742 |
LIG_SH3_3 | 176 | 182 | PF00018 | 0.631 |
LIG_SH3_3 | 280 | 286 | PF00018 | 0.522 |
LIG_SH3_3 | 295 | 301 | PF00018 | 0.530 |
LIG_SH3_3 | 324 | 330 | PF00018 | 0.647 |
LIG_SH3_3 | 367 | 373 | PF00018 | 0.687 |
LIG_SH3_3 | 433 | 439 | PF00018 | 0.694 |
LIG_SH3_3 | 68 | 74 | PF00018 | 0.555 |
LIG_SH3_3 | 723 | 729 | PF00018 | 0.392 |
LIG_SH3_3 | 848 | 854 | PF00018 | 0.535 |
LIG_SUMO_SIM_anti_2 | 558 | 563 | PF11976 | 0.399 |
LIG_SUMO_SIM_par_1 | 357 | 362 | PF11976 | 0.528 |
LIG_TRAF2_1 | 297 | 300 | PF00917 | 0.727 |
LIG_TRFH_1 | 684 | 688 | PF08558 | 0.399 |
LIG_WRPW_2 | 204 | 207 | PF00400 | 0.525 |
LIG_WW_1 | 688 | 691 | PF00397 | 0.399 |
LIG_WW_3 | 75 | 79 | PF00397 | 0.662 |
MOD_CDC14_SPxK_1 | 426 | 429 | PF00782 | 0.698 |
MOD_CDK_SPxK_1 | 423 | 429 | PF00069 | 0.706 |
MOD_CDK_SPxK_1 | 850 | 856 | PF00069 | 0.558 |
MOD_CDK_SPxxK_3 | 254 | 261 | PF00069 | 0.548 |
MOD_CDK_SPxxK_3 | 423 | 430 | PF00069 | 0.706 |
MOD_CDK_SPxxK_3 | 446 | 453 | PF00069 | 0.449 |
MOD_CK1_1 | 116 | 122 | PF00069 | 0.648 |
MOD_CK1_1 | 155 | 161 | PF00069 | 0.709 |
MOD_CK1_1 | 246 | 252 | PF00069 | 0.690 |
MOD_CK1_1 | 326 | 332 | PF00069 | 0.663 |
MOD_CK1_1 | 354 | 360 | PF00069 | 0.631 |
MOD_CK1_1 | 362 | 368 | PF00069 | 0.690 |
MOD_CK1_1 | 377 | 383 | PF00069 | 0.560 |
MOD_CK1_1 | 385 | 391 | PF00069 | 0.667 |
MOD_CK1_1 | 407 | 413 | PF00069 | 0.594 |
MOD_CK1_1 | 466 | 472 | PF00069 | 0.399 |
MOD_CK1_1 | 56 | 62 | PF00069 | 0.716 |
MOD_CK1_1 | 637 | 643 | PF00069 | 0.373 |
MOD_CK1_1 | 649 | 655 | PF00069 | 0.283 |
MOD_CK1_1 | 67 | 73 | PF00069 | 0.622 |
MOD_CK1_1 | 709 | 715 | PF00069 | 0.399 |
MOD_CK1_1 | 718 | 724 | PF00069 | 0.309 |
MOD_CK2_1 | 333 | 339 | PF00069 | 0.534 |
MOD_CK2_1 | 451 | 457 | PF00069 | 0.503 |
MOD_CK2_1 | 466 | 472 | PF00069 | 0.287 |
MOD_CK2_1 | 500 | 506 | PF00069 | 0.399 |
MOD_CK2_1 | 578 | 584 | PF00069 | 0.449 |
MOD_CK2_1 | 615 | 621 | PF00069 | 0.412 |
MOD_CK2_1 | 67 | 73 | PF00069 | 0.731 |
MOD_CK2_1 | 709 | 715 | PF00069 | 0.349 |
MOD_CK2_1 | 767 | 773 | PF00069 | 0.399 |
MOD_CK2_1 | 821 | 827 | PF00069 | 0.399 |
MOD_DYRK1A_RPxSP_1 | 413 | 417 | PF00069 | 0.608 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.623 |
MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.738 |
MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.714 |
MOD_GlcNHglycan | 234 | 237 | PF01048 | 0.607 |
MOD_GlcNHglycan | 271 | 274 | PF01048 | 0.609 |
MOD_GlcNHglycan | 283 | 286 | PF01048 | 0.562 |
MOD_GlcNHglycan | 331 | 334 | PF01048 | 0.640 |
MOD_GlcNHglycan | 361 | 364 | PF01048 | 0.571 |
MOD_GlcNHglycan | 384 | 387 | PF01048 | 0.716 |
MOD_GlcNHglycan | 397 | 400 | PF01048 | 0.581 |
MOD_GlcNHglycan | 406 | 409 | PF01048 | 0.524 |
MOD_GlcNHglycan | 639 | 642 | PF01048 | 0.346 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.727 |
MOD_GlcNHglycan | 707 | 711 | PF01048 | 0.399 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.595 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.695 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.660 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.586 |
MOD_GSK3_1 | 242 | 249 | PF00069 | 0.636 |
MOD_GSK3_1 | 329 | 336 | PF00069 | 0.570 |
MOD_GSK3_1 | 362 | 369 | PF00069 | 0.640 |
MOD_GSK3_1 | 403 | 410 | PF00069 | 0.626 |
MOD_GSK3_1 | 411 | 418 | PF00069 | 0.507 |
MOD_GSK3_1 | 442 | 449 | PF00069 | 0.649 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.722 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.700 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.612 |
MOD_GSK3_1 | 635 | 642 | PF00069 | 0.361 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.559 |
MOD_N-GLC_1 | 281 | 286 | PF02516 | 0.693 |
MOD_NEK2_1 | 212 | 217 | PF00069 | 0.589 |
MOD_NEK2_1 | 227 | 232 | PF00069 | 0.604 |
MOD_NEK2_1 | 242 | 247 | PF00069 | 0.650 |
MOD_NEK2_1 | 379 | 384 | PF00069 | 0.544 |
MOD_NEK2_1 | 404 | 409 | PF00069 | 0.598 |
MOD_NEK2_1 | 492 | 497 | PF00069 | 0.287 |
MOD_NEK2_1 | 63 | 68 | PF00069 | 0.716 |
MOD_NEK2_1 | 661 | 666 | PF00069 | 0.399 |
MOD_NEK2_1 | 792 | 797 | PF00069 | 0.399 |
MOD_NEK2_1 | 842 | 847 | PF00069 | 0.568 |
MOD_NEK2_1 | 90 | 95 | PF00069 | 0.693 |
MOD_NEK2_2 | 166 | 171 | PF00069 | 0.649 |
MOD_NEK2_2 | 500 | 505 | PF00069 | 0.399 |
MOD_PIKK_1 | 385 | 391 | PF00454 | 0.672 |
MOD_PIKK_1 | 541 | 547 | PF00454 | 0.399 |
MOD_PIKK_1 | 801 | 807 | PF00454 | 0.399 |
MOD_PIKK_1 | 873 | 879 | PF00454 | 0.682 |
MOD_PK_1 | 261 | 267 | PF00069 | 0.544 |
MOD_PK_1 | 366 | 372 | PF00069 | 0.653 |
MOD_PK_1 | 44 | 50 | PF00069 | 0.726 |
MOD_PK_1 | 646 | 652 | PF00069 | 0.399 |
MOD_PKA_1 | 6 | 12 | PF00069 | 0.728 |
MOD_PKA_1 | 801 | 807 | PF00069 | 0.399 |
MOD_PKA_2 | 111 | 117 | PF00069 | 0.730 |
MOD_PKA_2 | 172 | 178 | PF00069 | 0.608 |
MOD_PKA_2 | 312 | 318 | PF00069 | 0.632 |
MOD_PKA_2 | 6 | 12 | PF00069 | 0.728 |
MOD_PKA_2 | 718 | 724 | PF00069 | 0.399 |
MOD_PKA_2 | 801 | 807 | PF00069 | 0.399 |
MOD_PKA_2 | 821 | 827 | PF00069 | 0.199 |
MOD_Plk_1 | 541 | 547 | PF00069 | 0.487 |
MOD_Plk_4 | 646 | 652 | PF00069 | 0.354 |
MOD_Plk_4 | 728 | 734 | PF00069 | 0.349 |
MOD_Plk_4 | 767 | 773 | PF00069 | 0.430 |
MOD_ProDKin_1 | 113 | 119 | PF00069 | 0.700 |
MOD_ProDKin_1 | 158 | 164 | PF00069 | 0.564 |
MOD_ProDKin_1 | 214 | 220 | PF00069 | 0.681 |
MOD_ProDKin_1 | 254 | 260 | PF00069 | 0.763 |
MOD_ProDKin_1 | 314 | 320 | PF00069 | 0.676 |
MOD_ProDKin_1 | 323 | 329 | PF00069 | 0.633 |
MOD_ProDKin_1 | 354 | 360 | PF00069 | 0.651 |
MOD_ProDKin_1 | 374 | 380 | PF00069 | 0.552 |
MOD_ProDKin_1 | 413 | 419 | PF00069 | 0.587 |
MOD_ProDKin_1 | 423 | 429 | PF00069 | 0.606 |
MOD_ProDKin_1 | 446 | 452 | PF00069 | 0.456 |
MOD_ProDKin_1 | 578 | 584 | PF00069 | 0.399 |
MOD_ProDKin_1 | 58 | 64 | PF00069 | 0.716 |
MOD_ProDKin_1 | 644 | 650 | PF00069 | 0.399 |
MOD_ProDKin_1 | 850 | 856 | PF00069 | 0.517 |
MOD_SUMO_rev_2 | 664 | 671 | PF00179 | 0.399 |
TRG_DiLeu_BaEn_1 | 584 | 589 | PF01217 | 0.399 |
TRG_DiLeu_BaLyEn_6 | 119 | 124 | PF01217 | 0.660 |
TRG_DiLeu_BaLyEn_6 | 838 | 843 | PF01217 | 0.596 |
TRG_ENDOCYTIC_2 | 470 | 473 | PF00928 | 0.399 |
TRG_ENDOCYTIC_2 | 778 | 781 | PF00928 | 0.399 |
TRG_ENDOCYTIC_2 | 846 | 849 | PF00928 | 0.631 |
TRG_ER_diArg_1 | 170 | 173 | PF00400 | 0.678 |
TRG_ER_diArg_1 | 429 | 432 | PF00400 | 0.654 |
TRG_ER_diArg_1 | 5 | 7 | PF00400 | 0.713 |
TRG_ER_diArg_1 | 691 | 694 | PF00400 | 0.399 |
TRG_ER_diArg_1 | 801 | 803 | PF00400 | 0.394 |
TRG_ER_diArg_1 | 860 | 862 | PF00400 | 0.481 |
TRG_ER_diArg_1 | 878 | 880 | PF00400 | 0.571 |
TRG_NLS_MonoExtC_3 | 201 | 206 | PF00514 | 0.699 |
TRG_NLS_MonoExtN_4 | 199 | 206 | PF00514 | 0.691 |
TRG_Pf-PMV_PEXEL_1 | 305 | 309 | PF00026 | 0.616 |
TRG_Pf-PMV_PEXEL_1 | 597 | 601 | PF00026 | 0.399 |
TRG_Pf-PMV_PEXEL_1 | 742 | 746 | PF00026 | 0.399 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7WQK2 | Leishmania donovani | 88% | 100% |
A4H5K5 | Leishmania braziliensis | 77% | 100% |
Q4QHZ5 | Leishmania major | 89% | 100% |