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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0002189 | ribose phosphate diphosphokinase complex | 5 | 2 |
GO:0005737 | cytoplasm | 2 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0061695 | transferase complex, transferring phosphorus-containing groups | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:1902494 | catalytic complex | 2 | 2 |
GO:1990234 | transferase complex | 3 | 2 |
Related structures:
AlphaFold database: Q4QIB8
Term | Name | Level | Count |
---|---|---|---|
GO:0006015 | 5-phosphoribose 1-diphosphate biosynthetic process | 6 | 2 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 7 |
GO:0006163 | purine nucleotide metabolic process | 5 | 2 |
GO:0006164 | purine nucleotide biosynthetic process | 6 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 7 |
GO:0006753 | nucleoside phosphate metabolic process | 4 | 7 |
GO:0006793 | phosphorus metabolic process | 3 | 7 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 7 |
GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0009058 | biosynthetic process | 2 | 7 |
GO:0009117 | nucleotide metabolic process | 5 | 7 |
GO:0009165 | nucleotide biosynthetic process | 6 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0016310 | phosphorylation | 5 | 7 |
GO:0018130 | heterocycle biosynthetic process | 4 | 7 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 7 |
GO:0019637 | organophosphate metabolic process | 3 | 7 |
GO:0019693 | ribose phosphate metabolic process | 4 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 7 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0044249 | cellular biosynthetic process | 3 | 7 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 7 |
GO:0044281 | small molecule metabolic process | 2 | 7 |
GO:0046390 | ribose phosphate biosynthetic process | 5 | 2 |
GO:0046391 | 5-phosphoribose 1-diphosphate metabolic process | 5 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 7 |
GO:0055086 | nucleobase-containing small molecule metabolic process | 3 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:0072521 | purine-containing compound metabolic process | 4 | 2 |
GO:0072522 | purine-containing compound biosynthetic process | 5 | 2 |
GO:0090407 | organophosphate biosynthetic process | 4 | 7 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 2 |
GO:1901137 | carbohydrate derivative biosynthetic process | 4 | 2 |
GO:1901293 | nucleoside phosphate biosynthetic process | 5 | 7 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 7 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 7 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 2 |
GO:1901576 | organic substance biosynthetic process | 3 | 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000287 | magnesium ion binding | 5 | 7 |
GO:0003824 | catalytic activity | 1 | 7 |
GO:0004749 | ribose phosphate diphosphokinase activity | 5 | 7 |
GO:0005488 | binding | 1 | 7 |
GO:0016301 | kinase activity | 4 | 7 |
GO:0016740 | transferase activity | 2 | 7 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 7 |
GO:0016778 | diphosphotransferase activity | 4 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043169 | cation binding | 3 | 7 |
GO:0046872 | metal ion binding | 4 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 516 | 520 | PF00656 | 0.481 |
CLV_NRD_NRD_1 | 117 | 119 | PF00675 | 0.645 |
CLV_NRD_NRD_1 | 232 | 234 | PF00675 | 0.500 |
CLV_NRD_NRD_1 | 541 | 543 | PF00675 | 0.661 |
CLV_NRD_NRD_1 | 569 | 571 | PF00675 | 0.598 |
CLV_NRD_NRD_1 | 710 | 712 | PF00675 | 0.790 |
CLV_NRD_NRD_1 | 804 | 806 | PF00675 | 0.346 |
CLV_PCSK_FUR_1 | 175 | 179 | PF00082 | 0.521 |
CLV_PCSK_KEX2_1 | 117 | 119 | PF00082 | 0.645 |
CLV_PCSK_KEX2_1 | 177 | 179 | PF00082 | 0.603 |
CLV_PCSK_KEX2_1 | 300 | 302 | PF00082 | 0.433 |
CLV_PCSK_KEX2_1 | 541 | 543 | PF00082 | 0.559 |
CLV_PCSK_KEX2_1 | 569 | 571 | PF00082 | 0.598 |
CLV_PCSK_PC1ET2_1 | 177 | 179 | PF00082 | 0.603 |
CLV_PCSK_PC1ET2_1 | 300 | 302 | PF00082 | 0.433 |
CLV_PCSK_SKI1_1 | 16 | 20 | PF00082 | 0.630 |
CLV_PCSK_SKI1_1 | 233 | 237 | PF00082 | 0.500 |
CLV_PCSK_SKI1_1 | 297 | 301 | PF00082 | 0.652 |
CLV_PCSK_SKI1_1 | 350 | 354 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 48 | 52 | PF00082 | 0.555 |
CLV_PCSK_SKI1_1 | 721 | 725 | PF00082 | 0.263 |
CLV_PCSK_SKI1_1 | 760 | 764 | PF00082 | 0.346 |
CLV_Separin_Metazoa | 205 | 209 | PF03568 | 0.550 |
CLV_Separin_Metazoa | 560 | 564 | PF03568 | 0.805 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.675 |
DEG_SCF_FBW7_1 | 600 | 606 | PF00400 | 0.628 |
DEG_SPOP_SBC_1 | 603 | 607 | PF00917 | 0.704 |
DOC_CKS1_1 | 136 | 141 | PF01111 | 0.553 |
DOC_CKS1_1 | 600 | 605 | PF01111 | 0.761 |
DOC_CKS1_1 | 618 | 623 | PF01111 | 0.587 |
DOC_CKS1_1 | 633 | 638 | PF01111 | 0.611 |
DOC_CYCLIN_RxL_1 | 13 | 21 | PF00134 | 0.629 |
DOC_MAPK_DCC_7 | 208 | 216 | PF00069 | 0.500 |
DOC_MAPK_gen_1 | 175 | 183 | PF00069 | 0.490 |
DOC_MAPK_gen_1 | 729 | 736 | PF00069 | 0.530 |
DOC_MAPK_gen_1 | 805 | 812 | PF00069 | 0.565 |
DOC_MAPK_MEF2A_6 | 208 | 216 | PF00069 | 0.500 |
DOC_MAPK_MEF2A_6 | 274 | 282 | PF00069 | 0.588 |
DOC_MAPK_MEF2A_6 | 729 | 736 | PF00069 | 0.530 |
DOC_PP2B_LxvP_1 | 378 | 381 | PF13499 | 0.563 |
DOC_PP4_FxxP_1 | 127 | 130 | PF00568 | 0.625 |
DOC_PP4_FxxP_1 | 136 | 139 | PF00568 | 0.604 |
DOC_PP4_FxxP_1 | 470 | 473 | PF00568 | 0.497 |
DOC_USP7_MATH_1 | 244 | 248 | PF00917 | 0.502 |
DOC_USP7_MATH_1 | 362 | 366 | PF00917 | 0.516 |
DOC_USP7_MATH_1 | 395 | 399 | PF00917 | 0.619 |
DOC_USP7_MATH_1 | 433 | 437 | PF00917 | 0.563 |
DOC_USP7_MATH_1 | 473 | 477 | PF00917 | 0.501 |
DOC_USP7_MATH_1 | 50 | 54 | PF00917 | 0.564 |
DOC_USP7_MATH_1 | 603 | 607 | PF00917 | 0.718 |
DOC_USP7_MATH_1 | 641 | 645 | PF00917 | 0.721 |
DOC_USP7_MATH_1 | 768 | 772 | PF00917 | 0.619 |
DOC_USP7_MATH_2 | 473 | 479 | PF00917 | 0.470 |
DOC_USP7_UBL2_3 | 145 | 149 | PF12436 | 0.598 |
DOC_USP7_UBL2_3 | 230 | 234 | PF12436 | 0.522 |
DOC_USP7_UBL2_3 | 38 | 42 | PF12436 | 0.514 |
DOC_WW_Pin1_4 | 106 | 111 | PF00397 | 0.687 |
DOC_WW_Pin1_4 | 129 | 134 | PF00397 | 0.706 |
DOC_WW_Pin1_4 | 135 | 140 | PF00397 | 0.590 |
DOC_WW_Pin1_4 | 599 | 604 | PF00397 | 0.809 |
DOC_WW_Pin1_4 | 617 | 622 | PF00397 | 0.711 |
DOC_WW_Pin1_4 | 629 | 634 | PF00397 | 0.734 |
DOC_WW_Pin1_4 | 65 | 70 | PF00397 | 0.608 |
DOC_WW_Pin1_4 | 778 | 783 | PF00397 | 0.619 |
DOC_WW_Pin1_4 | 93 | 98 | PF00397 | 0.678 |
LIG_14-3-3_CanoR_1 | 16 | 26 | PF00244 | 0.618 |
LIG_14-3-3_CanoR_1 | 289 | 293 | PF00244 | 0.532 |
LIG_14-3-3_CanoR_1 | 424 | 432 | PF00244 | 0.546 |
LIG_14-3-3_CanoR_1 | 687 | 693 | PF00244 | 0.642 |
LIG_Actin_WH2_2 | 25 | 40 | PF00022 | 0.560 |
LIG_APCC_ABBA_1 | 459 | 464 | PF00400 | 0.489 |
LIG_BIR_III_2 | 324 | 328 | PF00653 | 0.626 |
LIG_BIR_III_4 | 623 | 627 | PF00653 | 0.838 |
LIG_BRCT_BRCA1_1 | 131 | 135 | PF00533 | 0.581 |
LIG_BRCT_BRCA1_1 | 269 | 273 | PF00533 | 0.613 |
LIG_BRCT_BRCA1_1 | 316 | 320 | PF00533 | 0.594 |
LIG_BRCT_BRCA1_1 | 506 | 510 | PF00533 | 0.482 |
LIG_Clathr_ClatBox_1 | 180 | 184 | PF01394 | 0.464 |
LIG_CORNRBOX | 732 | 740 | PF00104 | 0.619 |
LIG_CtBP_PxDLS_1 | 782 | 786 | PF00389 | 0.563 |
LIG_EH1_1 | 387 | 395 | PF00400 | 0.546 |
LIG_eIF4E_1 | 719 | 725 | PF01652 | 0.546 |
LIG_FHA_1 | 126 | 132 | PF00498 | 0.615 |
LIG_FHA_1 | 317 | 323 | PF00498 | 0.700 |
LIG_FHA_1 | 332 | 338 | PF00498 | 0.505 |
LIG_FHA_1 | 341 | 347 | PF00498 | 0.521 |
LIG_FHA_1 | 351 | 357 | PF00498 | 0.475 |
LIG_FHA_1 | 424 | 430 | PF00498 | 0.546 |
LIG_FHA_1 | 433 | 439 | PF00498 | 0.546 |
LIG_FHA_1 | 529 | 535 | PF00498 | 0.613 |
LIG_FHA_1 | 543 | 549 | PF00498 | 0.513 |
LIG_FHA_1 | 611 | 617 | PF00498 | 0.749 |
LIG_FHA_1 | 670 | 676 | PF00498 | 0.824 |
LIG_FHA_1 | 68 | 74 | PF00498 | 0.798 |
LIG_FHA_1 | 689 | 695 | PF00498 | 0.576 |
LIG_FHA_1 | 764 | 770 | PF00498 | 0.546 |
LIG_FHA_1 | 787 | 793 | PF00498 | 0.546 |
LIG_FHA_2 | 145 | 151 | PF00498 | 0.539 |
LIG_FHA_2 | 194 | 200 | PF00498 | 0.526 |
LIG_FHA_2 | 2 | 8 | PF00498 | 0.644 |
LIG_FHA_2 | 618 | 624 | PF00498 | 0.779 |
LIG_FHA_2 | 72 | 78 | PF00498 | 0.721 |
LIG_FHA_2 | 829 | 835 | PF00498 | 0.546 |
LIG_FHA_2 | 97 | 103 | PF00498 | 0.575 |
LIG_Integrin_RGD_1 | 383 | 385 | PF01839 | 0.346 |
LIG_LIR_Apic_2 | 124 | 130 | PF02991 | 0.613 |
LIG_LIR_Apic_2 | 467 | 473 | PF02991 | 0.509 |
LIG_LIR_Gen_1 | 138 | 148 | PF02991 | 0.522 |
LIG_LIR_Gen_1 | 163 | 174 | PF02991 | 0.477 |
LIG_LIR_Gen_1 | 213 | 222 | PF02991 | 0.574 |
LIG_LIR_Gen_1 | 478 | 487 | PF02991 | 0.460 |
LIG_LIR_Gen_1 | 497 | 506 | PF02991 | 0.497 |
LIG_LIR_Gen_1 | 531 | 540 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 138 | 144 | PF02991 | 0.509 |
LIG_LIR_Nem_3 | 163 | 169 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 171 | 176 | PF02991 | 0.398 |
LIG_LIR_Nem_3 | 213 | 218 | PF02991 | 0.509 |
LIG_LIR_Nem_3 | 29 | 34 | PF02991 | 0.576 |
LIG_LIR_Nem_3 | 478 | 484 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 497 | 501 | PF02991 | 0.538 |
LIG_LIR_Nem_3 | 531 | 536 | PF02991 | 0.523 |
LIG_LIR_Nem_3 | 716 | 722 | PF02991 | 0.548 |
LIG_OCRL_FandH_1 | 165 | 177 | PF00620 | 0.585 |
LIG_PCNA_APIM_2 | 176 | 182 | PF02747 | 0.514 |
LIG_Rb_pABgroove_1 | 827 | 835 | PF01858 | 0.530 |
LIG_REV1ctd_RIR_1 | 163 | 172 | PF16727 | 0.486 |
LIG_SH2_CRK | 224 | 228 | PF00017 | 0.593 |
LIG_SH2_CRK | 284 | 288 | PF00017 | 0.470 |
LIG_SH2_GRB2like | 302 | 305 | PF00017 | 0.672 |
LIG_SH2_GRB2like | 55 | 58 | PF00017 | 0.475 |
LIG_SH2_PTP2 | 173 | 176 | PF00017 | 0.389 |
LIG_SH2_PTP2 | 722 | 725 | PF00017 | 0.563 |
LIG_SH2_SRC | 210 | 213 | PF00017 | 0.463 |
LIG_SH2_SRC | 517 | 520 | PF00017 | 0.494 |
LIG_SH2_SRC | 559 | 562 | PF00017 | 0.728 |
LIG_SH2_STAP1 | 262 | 266 | PF00017 | 0.609 |
LIG_SH2_STAP1 | 292 | 296 | PF00017 | 0.518 |
LIG_SH2_STAP1 | 434 | 438 | PF00017 | 0.546 |
LIG_SH2_STAP1 | 517 | 521 | PF00017 | 0.494 |
LIG_SH2_STAP1 | 89 | 93 | PF00017 | 0.567 |
LIG_SH2_STAT5 | 173 | 176 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 179 | 182 | PF00017 | 0.486 |
LIG_SH2_STAT5 | 210 | 213 | PF00017 | 0.463 |
LIG_SH2_STAT5 | 215 | 218 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 31 | 34 | PF00017 | 0.571 |
LIG_SH2_STAT5 | 431 | 434 | PF00017 | 0.555 |
LIG_SH2_STAT5 | 486 | 489 | PF00017 | 0.468 |
LIG_SH2_STAT5 | 722 | 725 | PF00017 | 0.563 |
LIG_SH3_1 | 104 | 110 | PF00018 | 0.694 |
LIG_SH3_1 | 627 | 633 | PF00018 | 0.607 |
LIG_SH3_1 | 808 | 814 | PF00018 | 0.546 |
LIG_SH3_3 | 104 | 110 | PF00018 | 0.735 |
LIG_SH3_3 | 127 | 133 | PF00018 | 0.606 |
LIG_SH3_3 | 356 | 362 | PF00018 | 0.546 |
LIG_SH3_3 | 500 | 506 | PF00018 | 0.471 |
LIG_SH3_3 | 590 | 596 | PF00018 | 0.788 |
LIG_SH3_3 | 597 | 603 | PF00018 | 0.626 |
LIG_SH3_3 | 61 | 67 | PF00018 | 0.716 |
LIG_SH3_3 | 615 | 621 | PF00018 | 0.737 |
LIG_SH3_3 | 627 | 633 | PF00018 | 0.681 |
LIG_SH3_3 | 776 | 782 | PF00018 | 0.536 |
LIG_SH3_3 | 80 | 86 | PF00018 | 0.446 |
LIG_SH3_3 | 808 | 814 | PF00018 | 0.546 |
LIG_SH3_4 | 38 | 45 | PF00018 | 0.509 |
LIG_SUMO_SIM_anti_2 | 246 | 252 | PF11976 | 0.601 |
LIG_SUMO_SIM_anti_2 | 279 | 284 | PF11976 | 0.576 |
LIG_SUMO_SIM_anti_2 | 409 | 414 | PF11976 | 0.546 |
LIG_SUMO_SIM_anti_2 | 446 | 452 | PF11976 | 0.445 |
LIG_SUMO_SIM_anti_2 | 499 | 505 | PF11976 | 0.589 |
LIG_SUMO_SIM_anti_2 | 644 | 654 | PF11976 | 0.787 |
LIG_SUMO_SIM_anti_2 | 759 | 766 | PF11976 | 0.546 |
LIG_SUMO_SIM_anti_2 | 780 | 787 | PF11976 | 0.558 |
LIG_SUMO_SIM_par_1 | 392 | 399 | PF11976 | 0.619 |
LIG_SUMO_SIM_par_1 | 455 | 460 | PF11976 | 0.446 |
LIG_SUMO_SIM_par_1 | 70 | 77 | PF11976 | 0.727 |
LIG_SUMO_SIM_par_1 | 759 | 766 | PF11976 | 0.546 |
LIG_SUMO_SIM_par_1 | 784 | 791 | PF11976 | 0.546 |
LIG_TRFH_1 | 35 | 39 | PF08558 | 0.532 |
LIG_TYR_ITIM | 222 | 227 | PF00017 | 0.451 |
LIG_TYR_ITIM | 282 | 287 | PF00017 | 0.581 |
LIG_TYR_ITIM | 32 | 37 | PF00017 | 0.548 |
LIG_WRC_WIRS_1 | 194 | 199 | PF05994 | 0.512 |
MOD_CDK_SPxK_1 | 111 | 117 | PF00069 | 0.614 |
MOD_CDK_SPxxK_3 | 111 | 118 | PF00069 | 0.715 |
MOD_CK1_1 | 264 | 270 | PF00069 | 0.614 |
MOD_CK1_1 | 535 | 541 | PF00069 | 0.489 |
MOD_CK1_1 | 604 | 610 | PF00069 | 0.759 |
MOD_CK1_1 | 632 | 638 | PF00069 | 0.729 |
MOD_CK1_1 | 658 | 664 | PF00069 | 0.757 |
MOD_CK1_1 | 68 | 74 | PF00069 | 0.790 |
MOD_CK1_1 | 688 | 694 | PF00069 | 0.660 |
MOD_CK2_1 | 144 | 150 | PF00069 | 0.541 |
MOD_CK2_1 | 193 | 199 | PF00069 | 0.515 |
MOD_CK2_1 | 30 | 36 | PF00069 | 0.588 |
MOD_CK2_1 | 573 | 579 | PF00069 | 0.787 |
MOD_CK2_1 | 71 | 77 | PF00069 | 0.735 |
MOD_CK2_1 | 778 | 784 | PF00069 | 0.563 |
MOD_GlcNHglycan | 274 | 277 | PF01048 | 0.596 |
MOD_GlcNHglycan | 340 | 343 | PF01048 | 0.414 |
MOD_GlcNHglycan | 415 | 418 | PF01048 | 0.383 |
MOD_GlcNHglycan | 441 | 444 | PF01048 | 0.456 |
MOD_GlcNHglycan | 475 | 478 | PF01048 | 0.478 |
MOD_GlcNHglycan | 506 | 509 | PF01048 | 0.490 |
MOD_GlcNHglycan | 528 | 531 | PF01048 | 0.677 |
MOD_GlcNHglycan | 576 | 579 | PF01048 | 0.717 |
MOD_GlcNHglycan | 596 | 599 | PF01048 | 0.725 |
MOD_GlcNHglycan | 770 | 773 | PF01048 | 0.419 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.723 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.384 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.601 |
MOD_GSK3_1 | 338 | 345 | PF00069 | 0.507 |
MOD_GSK3_1 | 395 | 402 | PF00069 | 0.546 |
MOD_GSK3_1 | 433 | 440 | PF00069 | 0.619 |
MOD_GSK3_1 | 490 | 497 | PF00069 | 0.635 |
MOD_GSK3_1 | 528 | 535 | PF00069 | 0.644 |
MOD_GSK3_1 | 599 | 606 | PF00069 | 0.722 |
MOD_GSK3_1 | 607 | 614 | PF00069 | 0.707 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.735 |
MOD_GSK3_1 | 651 | 658 | PF00069 | 0.741 |
MOD_GSK3_1 | 660 | 667 | PF00069 | 0.684 |
MOD_GSK3_1 | 89 | 96 | PF00069 | 0.677 |
MOD_LATS_1 | 329 | 335 | PF00433 | 0.609 |
MOD_N-GLC_1 | 264 | 269 | PF02516 | 0.609 |
MOD_N-GLC_1 | 303 | 308 | PF02516 | 0.691 |
MOD_N-GLC_1 | 399 | 404 | PF02516 | 0.419 |
MOD_N-GLC_1 | 499 | 504 | PF02516 | 0.493 |
MOD_N-GLC_1 | 744 | 749 | PF02516 | 0.280 |
MOD_N-GLC_2 | 364 | 366 | PF02516 | 0.346 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.650 |
MOD_NEK2_1 | 154 | 159 | PF00069 | 0.415 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.520 |
MOD_NEK2_1 | 340 | 345 | PF00069 | 0.546 |
MOD_NEK2_1 | 413 | 418 | PF00069 | 0.583 |
MOD_NEK2_1 | 432 | 437 | PF00069 | 0.546 |
MOD_NEK2_1 | 51 | 56 | PF00069 | 0.625 |
MOD_NEK2_1 | 548 | 553 | PF00069 | 0.680 |
MOD_NEK2_1 | 565 | 570 | PF00069 | 0.553 |
MOD_NEK2_1 | 685 | 690 | PF00069 | 0.667 |
MOD_NEK2_1 | 763 | 768 | PF00069 | 0.546 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.630 |
MOD_NEK2_2 | 342 | 347 | PF00069 | 0.546 |
MOD_PIKK_1 | 264 | 270 | PF00454 | 0.614 |
MOD_PIKK_1 | 314 | 320 | PF00454 | 0.592 |
MOD_PIKK_1 | 528 | 534 | PF00454 | 0.622 |
MOD_PIKK_1 | 542 | 548 | PF00454 | 0.559 |
MOD_PIKK_1 | 6 | 12 | PF00454 | 0.620 |
MOD_PIKK_1 | 651 | 657 | PF00454 | 0.722 |
MOD_PIKK_1 | 96 | 102 | PF00454 | 0.569 |
MOD_PKA_1 | 711 | 717 | PF00069 | 0.667 |
MOD_PKA_2 | 288 | 294 | PF00069 | 0.527 |
MOD_PKA_2 | 423 | 429 | PF00069 | 0.546 |
MOD_PKA_2 | 686 | 692 | PF00069 | 0.767 |
MOD_Plk_1 | 24 | 30 | PF00069 | 0.592 |
MOD_Plk_1 | 372 | 378 | PF00069 | 0.546 |
MOD_Plk_1 | 499 | 505 | PF00069 | 0.486 |
MOD_Plk_1 | 51 | 57 | PF00069 | 0.633 |
MOD_Plk_1 | 825 | 831 | PF00069 | 0.619 |
MOD_Plk_1 | 89 | 95 | PF00069 | 0.587 |
MOD_Plk_2-3 | 193 | 199 | PF00069 | 0.521 |
MOD_Plk_2-3 | 494 | 500 | PF00069 | 0.654 |
MOD_Plk_4 | 122 | 128 | PF00069 | 0.739 |
MOD_Plk_4 | 150 | 156 | PF00069 | 0.443 |
MOD_Plk_4 | 169 | 175 | PF00069 | 0.570 |
MOD_Plk_4 | 210 | 216 | PF00069 | 0.560 |
MOD_Plk_4 | 283 | 289 | PF00069 | 0.483 |
MOD_Plk_4 | 30 | 36 | PF00069 | 0.665 |
MOD_Plk_4 | 316 | 322 | PF00069 | 0.605 |
MOD_Plk_4 | 342 | 348 | PF00069 | 0.546 |
MOD_Plk_4 | 389 | 395 | PF00069 | 0.546 |
MOD_Plk_4 | 735 | 741 | PF00069 | 0.546 |
MOD_Plk_4 | 828 | 834 | PF00069 | 0.546 |
MOD_ProDKin_1 | 106 | 112 | PF00069 | 0.687 |
MOD_ProDKin_1 | 129 | 135 | PF00069 | 0.698 |
MOD_ProDKin_1 | 599 | 605 | PF00069 | 0.805 |
MOD_ProDKin_1 | 617 | 623 | PF00069 | 0.713 |
MOD_ProDKin_1 | 629 | 635 | PF00069 | 0.734 |
MOD_ProDKin_1 | 65 | 71 | PF00069 | 0.607 |
MOD_ProDKin_1 | 778 | 784 | PF00069 | 0.619 |
MOD_ProDKin_1 | 93 | 99 | PF00069 | 0.677 |
MOD_SUMO_for_1 | 181 | 184 | PF00179 | 0.480 |
MOD_SUMO_for_1 | 216 | 219 | PF00179 | 0.430 |
MOD_SUMO_rev_2 | 33 | 40 | PF00179 | 0.605 |
MOD_SUMO_rev_2 | 577 | 586 | PF00179 | 0.695 |
TRG_DiLeu_BaEn_1 | 150 | 155 | PF01217 | 0.539 |
TRG_DiLeu_BaEn_1 | 409 | 414 | PF01217 | 0.546 |
TRG_DiLeu_BaEn_1 | 446 | 451 | PF01217 | 0.481 |
TRG_DiLeu_BaEn_1 | 759 | 764 | PF01217 | 0.530 |
TRG_DiLeu_BaLyEn_6 | 256 | 261 | PF01217 | 0.600 |
TRG_DiLeu_BaLyEn_6 | 811 | 816 | PF01217 | 0.546 |
TRG_ENDOCYTIC_2 | 173 | 176 | PF00928 | 0.482 |
TRG_ENDOCYTIC_2 | 215 | 218 | PF00928 | 0.469 |
TRG_ENDOCYTIC_2 | 224 | 227 | PF00928 | 0.454 |
TRG_ENDOCYTIC_2 | 284 | 287 | PF00928 | 0.467 |
TRG_ENDOCYTIC_2 | 34 | 37 | PF00928 | 0.537 |
TRG_ENDOCYTIC_2 | 481 | 484 | PF00928 | 0.463 |
TRG_ENDOCYTIC_2 | 524 | 527 | PF00928 | 0.521 |
TRG_ENDOCYTIC_2 | 722 | 725 | PF00928 | 0.546 |
TRG_ER_diArg_1 | 116 | 118 | PF00400 | 0.661 |
TRG_ER_diArg_1 | 540 | 542 | PF00400 | 0.640 |
TRG_NES_CRM1_1 | 150 | 163 | PF08389 | 0.370 |
TRG_NES_CRM1_1 | 246 | 258 | PF08389 | 0.516 |
TRG_Pf-PMV_PEXEL_1 | 16 | 21 | PF00026 | 0.630 |
TRG_Pf-PMV_PEXEL_1 | 751 | 755 | PF00026 | 0.346 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDZ8 | Leptomonas seymouri | 62% | 98% |
A0A3S5H655 | Leishmania donovani | 94% | 100% |
A4H5B8 | Leishmania braziliensis | 76% | 100% |
A4HTJ9 | Leishmania infantum | 94% | 100% |
E9AMD0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |