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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0002189 | ribose phosphate diphosphokinase complex | 5 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0061695 | transferase complex, transferring phosphorus-containing groups | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1990234 | transferase complex | 3 | 1 |
Related structures:
AlphaFold database: A4H5B8
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 9 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 9 |
GO:0006753 | nucleoside phosphate metabolic process | 4 | 9 |
GO:0006793 | phosphorus metabolic process | 3 | 9 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 9 |
GO:0006807 | nitrogen compound metabolic process | 2 | 9 |
GO:0008152 | metabolic process | 1 | 9 |
GO:0009058 | biosynthetic process | 2 | 9 |
GO:0009117 | nucleotide metabolic process | 5 | 9 |
GO:0009165 | nucleotide biosynthetic process | 6 | 9 |
GO:0009987 | cellular process | 1 | 9 |
GO:0016310 | phosphorylation | 5 | 9 |
GO:0018130 | heterocycle biosynthetic process | 4 | 9 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 9 |
GO:0019637 | organophosphate metabolic process | 3 | 9 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 9 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 9 |
GO:0044237 | cellular metabolic process | 2 | 9 |
GO:0044238 | primary metabolic process | 2 | 9 |
GO:0044249 | cellular biosynthetic process | 3 | 9 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 9 |
GO:0044281 | small molecule metabolic process | 2 | 9 |
GO:0046483 | heterocycle metabolic process | 3 | 9 |
GO:0055086 | nucleobase-containing small molecule metabolic process | 3 | 9 |
GO:0071704 | organic substance metabolic process | 2 | 9 |
GO:0090407 | organophosphate biosynthetic process | 4 | 9 |
GO:1901293 | nucleoside phosphate biosynthetic process | 5 | 9 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 9 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 9 |
GO:1901576 | organic substance biosynthetic process | 3 | 9 |
GO:0006015 | 5-phosphoribose 1-diphosphate biosynthetic process | 6 | 1 |
GO:0006163 | purine nucleotide metabolic process | 5 | 1 |
GO:0006164 | purine nucleotide biosynthetic process | 6 | 1 |
GO:0019693 | ribose phosphate metabolic process | 4 | 1 |
GO:0046390 | ribose phosphate biosynthetic process | 5 | 1 |
GO:0046391 | 5-phosphoribose 1-diphosphate metabolic process | 5 | 1 |
GO:0072521 | purine-containing compound metabolic process | 4 | 1 |
GO:0072522 | purine-containing compound biosynthetic process | 5 | 1 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 1 |
GO:1901137 | carbohydrate derivative biosynthetic process | 4 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000287 | magnesium ion binding | 5 | 9 |
GO:0003824 | catalytic activity | 1 | 9 |
GO:0004749 | ribose phosphate diphosphokinase activity | 5 | 9 |
GO:0005488 | binding | 1 | 9 |
GO:0016301 | kinase activity | 4 | 9 |
GO:0016740 | transferase activity | 2 | 9 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 9 |
GO:0016778 | diphosphotransferase activity | 4 | 9 |
GO:0043167 | ion binding | 2 | 9 |
GO:0043169 | cation binding | 3 | 9 |
GO:0046872 | metal ion binding | 4 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 477 | 481 | PF00656 | 0.476 |
CLV_C14_Caspase3-7 | 597 | 601 | PF00656 | 0.521 |
CLV_C14_Caspase3-7 | 631 | 635 | PF00656 | 0.506 |
CLV_NRD_NRD_1 | 193 | 195 | PF00675 | 0.423 |
CLV_NRD_NRD_1 | 502 | 504 | PF00675 | 0.646 |
CLV_NRD_NRD_1 | 674 | 676 | PF00675 | 0.697 |
CLV_NRD_NRD_1 | 768 | 770 | PF00675 | 0.302 |
CLV_PCSK_KEX2_1 | 502 | 504 | PF00082 | 0.573 |
CLV_PCSK_SKI1_1 | 16 | 20 | PF00082 | 0.528 |
CLV_PCSK_SKI1_1 | 194 | 198 | PF00082 | 0.423 |
CLV_PCSK_SKI1_1 | 258 | 262 | PF00082 | 0.567 |
CLV_PCSK_SKI1_1 | 311 | 315 | PF00082 | 0.341 |
CLV_PCSK_SKI1_1 | 669 | 673 | PF00082 | 0.469 |
CLV_PCSK_SKI1_1 | 724 | 728 | PF00082 | 0.302 |
CLV_Separin_Metazoa | 521 | 525 | PF03568 | 0.750 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.710 |
DOC_CKS1_1 | 578 | 583 | PF01111 | 0.489 |
DOC_CKS1_1 | 593 | 598 | PF01111 | 0.530 |
DOC_CYCLIN_RxL_1 | 13 | 21 | PF00134 | 0.528 |
DOC_MAPK_gen_1 | 136 | 144 | PF00069 | 0.490 |
DOC_MAPK_gen_1 | 184 | 193 | PF00069 | 0.378 |
DOC_MAPK_gen_1 | 292 | 300 | PF00069 | 0.377 |
DOC_MAPK_gen_1 | 769 | 776 | PF00069 | 0.514 |
DOC_MAPK_MEF2A_6 | 235 | 243 | PF00069 | 0.538 |
DOC_MAPK_MEF2A_6 | 546 | 554 | PF00069 | 0.523 |
DOC_PP4_FxxP_1 | 431 | 434 | PF00568 | 0.402 |
DOC_PP4_FxxP_1 | 88 | 91 | PF00568 | 0.580 |
DOC_PP4_FxxP_1 | 97 | 100 | PF00568 | 0.573 |
DOC_SPAK_OSR1_1 | 295 | 299 | PF12202 | 0.352 |
DOC_USP7_MATH_1 | 107 | 111 | PF00917 | 0.371 |
DOC_USP7_MATH_1 | 205 | 209 | PF00917 | 0.449 |
DOC_USP7_MATH_1 | 323 | 327 | PF00917 | 0.504 |
DOC_USP7_MATH_1 | 356 | 360 | PF00917 | 0.575 |
DOC_USP7_MATH_1 | 563 | 567 | PF00917 | 0.671 |
DOC_USP7_MATH_1 | 569 | 573 | PF00917 | 0.683 |
DOC_USP7_MATH_1 | 678 | 682 | PF00917 | 0.409 |
DOC_USP7_MATH_1 | 73 | 77 | PF00917 | 0.531 |
DOC_USP7_MATH_1 | 732 | 736 | PF00917 | 0.578 |
DOC_USP7_MATH_1 | 80 | 84 | PF00917 | 0.459 |
DOC_USP7_MATH_2 | 434 | 440 | PF00917 | 0.380 |
DOC_USP7_UBL2_3 | 125 | 129 | PF12436 | 0.321 |
DOC_USP7_UBL2_3 | 195 | 199 | PF12436 | 0.402 |
DOC_USP7_UBL2_3 | 38 | 42 | PF12436 | 0.418 |
DOC_WW_Pin1_4 | 531 | 536 | PF00397 | 0.527 |
DOC_WW_Pin1_4 | 559 | 564 | PF00397 | 0.770 |
DOC_WW_Pin1_4 | 577 | 582 | PF00397 | 0.435 |
DOC_WW_Pin1_4 | 589 | 594 | PF00397 | 0.728 |
DOC_WW_Pin1_4 | 742 | 747 | PF00397 | 0.502 |
DOC_WW_Pin1_4 | 90 | 95 | PF00397 | 0.646 |
DOC_WW_Pin1_4 | 96 | 101 | PF00397 | 0.562 |
LIG_14-3-3_CanoR_1 | 16 | 26 | PF00244 | 0.522 |
LIG_14-3-3_CanoR_1 | 250 | 254 | PF00244 | 0.434 |
LIG_14-3-3_CanoR_1 | 385 | 393 | PF00244 | 0.477 |
LIG_14-3-3_CanoR_1 | 58 | 64 | PF00244 | 0.496 |
LIG_Actin_WH2_2 | 25 | 40 | PF00022 | 0.465 |
LIG_APCC_ABBA_1 | 420 | 425 | PF00400 | 0.434 |
LIG_BIR_III_2 | 285 | 289 | PF00653 | 0.619 |
LIG_BIR_III_4 | 583 | 587 | PF00653 | 0.705 |
LIG_BRCT_BRCA1_1 | 230 | 234 | PF00533 | 0.548 |
LIG_BRCT_BRCA1_1 | 277 | 281 | PF00533 | 0.550 |
LIG_BRCT_BRCA1_1 | 92 | 96 | PF00533 | 0.552 |
LIG_BRCT_BRCA1_1 | 98 | 102 | PF00533 | 0.560 |
LIG_Clathr_ClatBox_1 | 141 | 145 | PF01394 | 0.470 |
LIG_CORNRBOX | 696 | 704 | PF00104 | 0.575 |
LIG_CtBP_PxDLS_1 | 538 | 542 | PF00389 | 0.526 |
LIG_EH1_1 | 348 | 356 | PF00400 | 0.542 |
LIG_eIF4E_1 | 185 | 191 | PF01652 | 0.381 |
LIG_eIF4E_1 | 683 | 689 | PF01652 | 0.413 |
LIG_FHA_1 | 278 | 284 | PF00498 | 0.697 |
LIG_FHA_1 | 302 | 308 | PF00498 | 0.518 |
LIG_FHA_1 | 312 | 318 | PF00498 | 0.473 |
LIG_FHA_1 | 385 | 391 | PF00498 | 0.502 |
LIG_FHA_1 | 394 | 400 | PF00498 | 0.533 |
LIG_FHA_1 | 490 | 496 | PF00498 | 0.562 |
LIG_FHA_1 | 553 | 559 | PF00498 | 0.527 |
LIG_FHA_1 | 653 | 659 | PF00498 | 0.496 |
LIG_FHA_1 | 69 | 75 | PF00498 | 0.744 |
LIG_FHA_1 | 728 | 734 | PF00498 | 0.477 |
LIG_FHA_1 | 751 | 757 | PF00498 | 0.477 |
LIG_FHA_1 | 82 | 88 | PF00498 | 0.715 |
LIG_FHA_2 | 155 | 161 | PF00498 | 0.442 |
LIG_FHA_2 | 2 | 8 | PF00498 | 0.686 |
LIG_FHA_2 | 52 | 58 | PF00498 | 0.571 |
LIG_FHA_2 | 578 | 584 | PF00498 | 0.682 |
LIG_FHA_2 | 629 | 635 | PF00498 | 0.510 |
LIG_FHA_2 | 700 | 706 | PF00498 | 0.455 |
LIG_FHA_2 | 73 | 79 | PF00498 | 0.605 |
LIG_FHA_2 | 793 | 799 | PF00498 | 0.477 |
LIG_Integrin_RGD_1 | 344 | 346 | PF01839 | 0.277 |
LIG_LIR_Apic_2 | 428 | 434 | PF02991 | 0.414 |
LIG_LIR_Apic_2 | 518 | 523 | PF02991 | 0.687 |
LIG_LIR_Apic_2 | 85 | 91 | PF02991 | 0.603 |
LIG_LIR_Gen_1 | 124 | 135 | PF02991 | 0.399 |
LIG_LIR_Gen_1 | 174 | 183 | PF02991 | 0.482 |
LIG_LIR_Gen_1 | 439 | 448 | PF02991 | 0.374 |
LIG_LIR_Gen_1 | 458 | 467 | PF02991 | 0.401 |
LIG_LIR_Gen_1 | 492 | 501 | PF02991 | 0.448 |
LIG_LIR_Gen_1 | 545 | 554 | PF02991 | 0.615 |
LIG_LIR_Gen_1 | 99 | 107 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 124 | 130 | PF02991 | 0.398 |
LIG_LIR_Nem_3 | 132 | 137 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 174 | 179 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 29 | 34 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 439 | 445 | PF02991 | 0.370 |
LIG_LIR_Nem_3 | 458 | 462 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 492 | 497 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 545 | 550 | PF02991 | 0.575 |
LIG_LIR_Nem_3 | 681 | 686 | PF02991 | 0.542 |
LIG_LIR_Nem_3 | 99 | 105 | PF02991 | 0.543 |
LIG_NRBOX | 635 | 641 | PF00104 | 0.510 |
LIG_OCRL_FandH_1 | 126 | 138 | PF00620 | 0.531 |
LIG_PCNA_yPIPBox_3 | 633 | 643 | PF02747 | 0.510 |
LIG_REV1ctd_RIR_1 | 124 | 133 | PF16727 | 0.491 |
LIG_SH2_CRK | 185 | 189 | PF00017 | 0.439 |
LIG_SH2_CRK | 245 | 249 | PF00017 | 0.373 |
LIG_SH2_CRK | 686 | 690 | PF00017 | 0.456 |
LIG_SH2_GRB2like | 263 | 266 | PF00017 | 0.635 |
LIG_SH2_NCK_1 | 686 | 690 | PF00017 | 0.456 |
LIG_SH2_SRC | 171 | 174 | PF00017 | 0.470 |
LIG_SH2_SRC | 589 | 592 | PF00017 | 0.643 |
LIG_SH2_STAP1 | 223 | 227 | PF00017 | 0.545 |
LIG_SH2_STAP1 | 253 | 257 | PF00017 | 0.429 |
LIG_SH2_STAP1 | 395 | 399 | PF00017 | 0.477 |
LIG_SH2_STAT5 | 134 | 137 | PF00017 | 0.404 |
LIG_SH2_STAT5 | 140 | 143 | PF00017 | 0.385 |
LIG_SH2_STAT5 | 171 | 174 | PF00017 | 0.395 |
LIG_SH2_STAT5 | 176 | 179 | PF00017 | 0.374 |
LIG_SH2_STAT5 | 31 | 34 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 392 | 395 | PF00017 | 0.480 |
LIG_SH2_STAT5 | 447 | 450 | PF00017 | 0.419 |
LIG_SH2_STAT5 | 589 | 592 | PF00017 | 0.643 |
LIG_SH2_STAT5 | 59 | 62 | PF00017 | 0.550 |
LIG_SH2_STAT5 | 625 | 628 | PF00017 | 0.562 |
LIG_SH3_1 | 772 | 778 | PF00018 | 0.477 |
LIG_SH3_3 | 224 | 230 | PF00018 | 0.378 |
LIG_SH3_3 | 317 | 323 | PF00018 | 0.542 |
LIG_SH3_3 | 461 | 467 | PF00018 | 0.418 |
LIG_SH3_3 | 532 | 538 | PF00018 | 0.630 |
LIG_SH3_3 | 547 | 553 | PF00018 | 0.743 |
LIG_SH3_3 | 590 | 596 | PF00018 | 0.641 |
LIG_SH3_3 | 613 | 619 | PF00018 | 0.514 |
LIG_SH3_3 | 772 | 778 | PF00018 | 0.477 |
LIG_SH3_3 | 88 | 94 | PF00018 | 0.632 |
LIG_SH3_4 | 38 | 45 | PF00018 | 0.419 |
LIG_SUMO_SIM_anti_2 | 207 | 213 | PF11976 | 0.577 |
LIG_SUMO_SIM_anti_2 | 240 | 245 | PF11976 | 0.518 |
LIG_SUMO_SIM_anti_2 | 370 | 375 | PF11976 | 0.477 |
LIG_SUMO_SIM_anti_2 | 460 | 466 | PF11976 | 0.532 |
LIG_SUMO_SIM_anti_2 | 605 | 614 | PF11976 | 0.715 |
LIG_SUMO_SIM_anti_2 | 723 | 730 | PF11976 | 0.477 |
LIG_SUMO_SIM_anti_2 | 744 | 751 | PF11976 | 0.483 |
LIG_SUMO_SIM_par_1 | 353 | 360 | PF11976 | 0.575 |
LIG_SUMO_SIM_par_1 | 416 | 421 | PF11976 | 0.361 |
LIG_SUMO_SIM_par_1 | 723 | 730 | PF11976 | 0.502 |
LIG_SUMO_SIM_par_1 | 748 | 755 | PF11976 | 0.477 |
LIG_TRFH_1 | 35 | 39 | PF08558 | 0.435 |
LIG_TYR_ITIM | 243 | 248 | PF00017 | 0.519 |
LIG_TYR_ITIM | 32 | 37 | PF00017 | 0.442 |
LIG_WRC_WIRS_1 | 155 | 160 | PF05994 | 0.513 |
MOD_CK1_1 | 225 | 231 | PF00069 | 0.505 |
MOD_CK1_1 | 496 | 502 | PF00069 | 0.436 |
MOD_CK1_1 | 509 | 515 | PF00069 | 0.645 |
MOD_CK1_1 | 570 | 576 | PF00069 | 0.713 |
MOD_CK1_1 | 592 | 598 | PF00069 | 0.695 |
MOD_CK1_1 | 627 | 633 | PF00069 | 0.641 |
MOD_CK1_1 | 65 | 71 | PF00069 | 0.700 |
MOD_CK1_1 | 652 | 658 | PF00069 | 0.583 |
MOD_CK1_1 | 72 | 78 | PF00069 | 0.785 |
MOD_CK1_1 | 789 | 795 | PF00069 | 0.412 |
MOD_CK1_1 | 83 | 89 | PF00069 | 0.548 |
MOD_CK2_1 | 148 | 154 | PF00069 | 0.411 |
MOD_CK2_1 | 533 | 539 | PF00069 | 0.727 |
MOD_CK2_1 | 72 | 78 | PF00069 | 0.734 |
MOD_CK2_1 | 792 | 798 | PF00069 | 0.420 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.424 |
MOD_GlcNHglycan | 235 | 238 | PF01048 | 0.549 |
MOD_GlcNHglycan | 301 | 304 | PF01048 | 0.375 |
MOD_GlcNHglycan | 364 | 367 | PF01048 | 0.241 |
MOD_GlcNHglycan | 402 | 405 | PF01048 | 0.465 |
MOD_GlcNHglycan | 438 | 441 | PF01048 | 0.353 |
MOD_GlcNHglycan | 489 | 492 | PF01048 | 0.621 |
MOD_GlcNHglycan | 565 | 568 | PF01048 | 0.636 |
MOD_GlcNHglycan | 583 | 587 | PF01048 | 0.447 |
MOD_GlcNHglycan | 596 | 599 | PF01048 | 0.688 |
MOD_GlcNHglycan | 613 | 616 | PF01048 | 0.516 |
MOD_GlcNHglycan | 71 | 74 | PF01048 | 0.570 |
MOD_GlcNHglycan | 734 | 737 | PF01048 | 0.308 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.547 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.299 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.522 |
MOD_GSK3_1 | 299 | 306 | PF00069 | 0.459 |
MOD_GSK3_1 | 356 | 363 | PF00069 | 0.532 |
MOD_GSK3_1 | 451 | 458 | PF00069 | 0.555 |
MOD_GSK3_1 | 489 | 496 | PF00069 | 0.628 |
MOD_GSK3_1 | 559 | 566 | PF00069 | 0.681 |
MOD_GSK3_1 | 567 | 574 | PF00069 | 0.605 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.604 |
MOD_GSK3_1 | 624 | 631 | PF00069 | 0.607 |
MOD_N-GLC_1 | 225 | 230 | PF02516 | 0.539 |
MOD_N-GLC_1 | 264 | 269 | PF02516 | 0.638 |
MOD_N-GLC_1 | 360 | 365 | PF02516 | 0.375 |
MOD_N-GLC_1 | 460 | 465 | PF02516 | 0.401 |
MOD_N-GLC_1 | 563 | 568 | PF02516 | 0.699 |
MOD_N-GLC_1 | 628 | 633 | PF02516 | 0.633 |
MOD_N-GLC_2 | 325 | 327 | PF02516 | 0.341 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.700 |
MOD_NEK2_1 | 130 | 135 | PF00069 | 0.392 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.388 |
MOD_NEK2_1 | 301 | 306 | PF00069 | 0.542 |
MOD_NEK2_1 | 362 | 367 | PF00069 | 0.441 |
MOD_NEK2_1 | 374 | 379 | PF00069 | 0.524 |
MOD_NEK2_1 | 393 | 398 | PF00069 | 0.477 |
MOD_NEK2_1 | 408 | 413 | PF00069 | 0.411 |
MOD_NEK2_1 | 51 | 56 | PF00069 | 0.576 |
MOD_NEK2_1 | 727 | 732 | PF00069 | 0.487 |
MOD_NEK2_2 | 303 | 308 | PF00069 | 0.477 |
MOD_PIKK_1 | 225 | 231 | PF00454 | 0.544 |
MOD_PIKK_1 | 275 | 281 | PF00454 | 0.634 |
MOD_PIKK_1 | 489 | 495 | PF00454 | 0.571 |
MOD_PIKK_1 | 503 | 509 | PF00454 | 0.599 |
MOD_PIKK_1 | 6 | 12 | PF00454 | 0.648 |
MOD_PKA_2 | 249 | 255 | PF00069 | 0.428 |
MOD_PKA_2 | 384 | 390 | PF00069 | 0.477 |
MOD_PKA_2 | 57 | 63 | PF00069 | 0.478 |
MOD_Plk_1 | 144 | 150 | PF00069 | 0.302 |
MOD_Plk_1 | 24 | 30 | PF00069 | 0.510 |
MOD_Plk_1 | 333 | 339 | PF00069 | 0.502 |
MOD_Plk_1 | 460 | 466 | PF00069 | 0.394 |
MOD_Plk_1 | 51 | 57 | PF00069 | 0.591 |
MOD_Plk_1 | 789 | 795 | PF00069 | 0.502 |
MOD_Plk_2-3 | 154 | 160 | PF00069 | 0.470 |
MOD_Plk_2-3 | 455 | 461 | PF00069 | 0.585 |
MOD_Plk_4 | 130 | 136 | PF00069 | 0.400 |
MOD_Plk_4 | 144 | 150 | PF00069 | 0.428 |
MOD_Plk_4 | 171 | 177 | PF00069 | 0.496 |
MOD_Plk_4 | 244 | 250 | PF00069 | 0.386 |
MOD_Plk_4 | 277 | 283 | PF00069 | 0.556 |
MOD_Plk_4 | 30 | 36 | PF00069 | 0.492 |
MOD_Plk_4 | 303 | 309 | PF00069 | 0.477 |
MOD_Plk_4 | 350 | 356 | PF00069 | 0.477 |
MOD_Plk_4 | 635 | 641 | PF00069 | 0.536 |
MOD_Plk_4 | 699 | 705 | PF00069 | 0.502 |
MOD_Plk_4 | 792 | 798 | PF00069 | 0.502 |
MOD_Plk_4 | 83 | 89 | PF00069 | 0.675 |
MOD_ProDKin_1 | 531 | 537 | PF00069 | 0.527 |
MOD_ProDKin_1 | 559 | 565 | PF00069 | 0.767 |
MOD_ProDKin_1 | 577 | 583 | PF00069 | 0.431 |
MOD_ProDKin_1 | 589 | 595 | PF00069 | 0.727 |
MOD_ProDKin_1 | 742 | 748 | PF00069 | 0.502 |
MOD_ProDKin_1 | 90 | 96 | PF00069 | 0.640 |
MOD_SUMO_for_1 | 142 | 145 | PF00179 | 0.485 |
MOD_SUMO_for_1 | 177 | 180 | PF00179 | 0.486 |
MOD_SUMO_rev_2 | 33 | 40 | PF00179 | 0.525 |
MOD_SUMO_rev_2 | 98 | 108 | PF00179 | 0.451 |
TRG_DiLeu_BaEn_1 | 370 | 375 | PF01217 | 0.542 |
TRG_DiLeu_BaLyEn_6 | 217 | 222 | PF01217 | 0.554 |
TRG_DiLeu_BaLyEn_6 | 775 | 780 | PF01217 | 0.502 |
TRG_ENDOCYTIC_2 | 134 | 137 | PF00928 | 0.485 |
TRG_ENDOCYTIC_2 | 176 | 179 | PF00928 | 0.391 |
TRG_ENDOCYTIC_2 | 185 | 188 | PF00928 | 0.408 |
TRG_ENDOCYTIC_2 | 245 | 248 | PF00928 | 0.370 |
TRG_ENDOCYTIC_2 | 34 | 37 | PF00928 | 0.441 |
TRG_ENDOCYTIC_2 | 442 | 445 | PF00928 | 0.375 |
TRG_ENDOCYTIC_2 | 485 | 488 | PF00928 | 0.417 |
TRG_ENDOCYTIC_2 | 686 | 689 | PF00928 | 0.542 |
TRG_ER_diArg_1 | 501 | 503 | PF00400 | 0.624 |
TRG_Pf-PMV_PEXEL_1 | 16 | 21 | PF00026 | 0.525 |
TRG_Pf-PMV_PEXEL_1 | 258 | 262 | PF00026 | 0.354 |
TRG_Pf-PMV_PEXEL_1 | 715 | 719 | PF00026 | 0.302 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDZ8 | Leptomonas seymouri | 61% | 94% |
A0A1X0NPK7 | Trypanosomatidae | 47% | 100% |
A0A3R7LSY3 | Trypanosoma rangeli | 46% | 100% |
A0A3S5H655 | Leishmania donovani | 78% | 95% |
A4HTJ9 | Leishmania infantum | 77% | 95% |
E9AMD0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 76% | 95% |
Q4QIB8 | Leishmania major | 76% | 99% |