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: 7 |
NetGPI | no | yes: 0, no: 7 |
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: E9AMD0
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 8 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 8 |
GO:0006753 | nucleoside phosphate metabolic process | 4 | 8 |
GO:0006793 | phosphorus metabolic process | 3 | 8 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 8 |
GO:0006807 | nitrogen compound metabolic process | 2 | 8 |
GO:0008152 | metabolic process | 1 | 8 |
GO:0009058 | biosynthetic process | 2 | 8 |
GO:0009117 | nucleotide metabolic process | 5 | 8 |
GO:0009165 | nucleotide biosynthetic process | 6 | 8 |
GO:0009987 | cellular process | 1 | 8 |
GO:0016310 | phosphorylation | 5 | 8 |
GO:0018130 | heterocycle biosynthetic process | 4 | 8 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 8 |
GO:0019637 | organophosphate metabolic process | 3 | 8 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 8 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 8 |
GO:0044237 | cellular metabolic process | 2 | 8 |
GO:0044238 | primary metabolic process | 2 | 8 |
GO:0044249 | cellular biosynthetic process | 3 | 8 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 8 |
GO:0044281 | small molecule metabolic process | 2 | 8 |
GO:0046483 | heterocycle metabolic process | 3 | 8 |
GO:0055086 | nucleobase-containing small molecule metabolic process | 3 | 8 |
GO:0071704 | organic substance metabolic process | 2 | 8 |
GO:0090407 | organophosphate biosynthetic process | 4 | 8 |
GO:1901293 | nucleoside phosphate biosynthetic process | 5 | 8 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 8 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 8 |
GO:1901576 | organic substance biosynthetic process | 3 | 8 |
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 | 8 |
GO:0003824 | catalytic activity | 1 | 8 |
GO:0004749 | ribose phosphate diphosphokinase activity | 5 | 8 |
GO:0005488 | binding | 1 | 8 |
GO:0016301 | kinase activity | 4 | 8 |
GO:0016740 | transferase activity | 2 | 8 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 8 |
GO:0016778 | diphosphotransferase activity | 4 | 8 |
GO:0043167 | ion binding | 2 | 8 |
GO:0043169 | cation binding | 3 | 8 |
GO:0046872 | metal ion binding | 4 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 516 | 520 | PF00656 | 0.428 |
CLV_NRD_NRD_1 | 100 | 102 | PF00675 | 0.560 |
CLV_NRD_NRD_1 | 117 | 119 | PF00675 | 0.597 |
CLV_NRD_NRD_1 | 157 | 159 | PF00675 | 0.364 |
CLV_NRD_NRD_1 | 232 | 234 | PF00675 | 0.371 |
CLV_NRD_NRD_1 | 541 | 543 | PF00675 | 0.531 |
CLV_NRD_NRD_1 | 569 | 571 | PF00675 | 0.601 |
CLV_NRD_NRD_1 | 712 | 714 | PF00675 | 0.644 |
CLV_NRD_NRD_1 | 806 | 808 | PF00675 | 0.290 |
CLV_PCSK_FUR_1 | 175 | 179 | PF00082 | 0.399 |
CLV_PCSK_KEX2_1 | 100 | 102 | PF00082 | 0.560 |
CLV_PCSK_KEX2_1 | 117 | 119 | PF00082 | 0.597 |
CLV_PCSK_KEX2_1 | 157 | 159 | PF00082 | 0.392 |
CLV_PCSK_KEX2_1 | 177 | 179 | PF00082 | 0.308 |
CLV_PCSK_KEX2_1 | 541 | 543 | PF00082 | 0.510 |
CLV_PCSK_KEX2_1 | 569 | 571 | PF00082 | 0.540 |
CLV_PCSK_PC1ET2_1 | 177 | 179 | PF00082 | 0.408 |
CLV_PCSK_SKI1_1 | 142 | 146 | PF00082 | 0.588 |
CLV_PCSK_SKI1_1 | 16 | 20 | PF00082 | 0.482 |
CLV_PCSK_SKI1_1 | 233 | 237 | PF00082 | 0.375 |
CLV_PCSK_SKI1_1 | 297 | 301 | PF00082 | 0.590 |
CLV_PCSK_SKI1_1 | 350 | 354 | PF00082 | 0.308 |
CLV_PCSK_SKI1_1 | 48 | 52 | PF00082 | 0.446 |
CLV_PCSK_SKI1_1 | 762 | 766 | PF00082 | 0.308 |
CLV_PCSK_SKI1_1 | 802 | 806 | PF00082 | 0.189 |
CLV_Separin_Metazoa | 205 | 209 | PF03568 | 0.456 |
CLV_Separin_Metazoa | 560 | 564 | PF03568 | 0.678 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.655 |
DOC_CKS1_1 | 112 | 117 | PF01111 | 0.623 |
DOC_CKS1_1 | 598 | 603 | PF01111 | 0.646 |
DOC_CKS1_1 | 631 | 636 | PF01111 | 0.554 |
DOC_CYCLIN_RxL_1 | 13 | 21 | PF00134 | 0.475 |
DOC_MAPK_DCC_7 | 208 | 216 | PF00069 | 0.403 |
DOC_MAPK_gen_1 | 175 | 183 | PF00069 | 0.427 |
DOC_MAPK_gen_1 | 731 | 738 | PF00069 | 0.450 |
DOC_MAPK_gen_1 | 807 | 814 | PF00069 | 0.475 |
DOC_MAPK_MEF2A_6 | 208 | 216 | PF00069 | 0.403 |
DOC_MAPK_MEF2A_6 | 274 | 282 | PF00069 | 0.466 |
DOC_MAPK_MEF2A_6 | 731 | 738 | PF00069 | 0.450 |
DOC_PP2B_LxvP_1 | 378 | 381 | PF13499 | 0.487 |
DOC_PP4_FxxP_1 | 127 | 130 | PF00568 | 0.579 |
DOC_PP4_FxxP_1 | 136 | 139 | PF00568 | 0.571 |
DOC_PP4_FxxP_1 | 470 | 473 | PF00568 | 0.384 |
DOC_USP7_MATH_1 | 244 | 248 | PF00917 | 0.404 |
DOC_USP7_MATH_1 | 362 | 366 | PF00917 | 0.467 |
DOC_USP7_MATH_1 | 395 | 399 | PF00917 | 0.523 |
DOC_USP7_MATH_1 | 433 | 437 | PF00917 | 0.487 |
DOC_USP7_MATH_1 | 473 | 477 | PF00917 | 0.395 |
DOC_USP7_MATH_1 | 50 | 54 | PF00917 | 0.452 |
DOC_USP7_MATH_1 | 60 | 64 | PF00917 | 0.504 |
DOC_USP7_MATH_1 | 601 | 605 | PF00917 | 0.647 |
DOC_USP7_MATH_1 | 639 | 643 | PF00917 | 0.690 |
DOC_USP7_MATH_1 | 770 | 774 | PF00917 | 0.559 |
DOC_USP7_MATH_2 | 473 | 479 | PF00917 | 0.359 |
DOC_USP7_UBL2_3 | 145 | 149 | PF12436 | 0.489 |
DOC_USP7_UBL2_3 | 230 | 234 | PF12436 | 0.391 |
DOC_USP7_UBL2_3 | 38 | 42 | PF12436 | 0.395 |
DOC_WW_Pin1_4 | 111 | 116 | PF00397 | 0.646 |
DOC_WW_Pin1_4 | 129 | 134 | PF00397 | 0.701 |
DOC_WW_Pin1_4 | 597 | 602 | PF00397 | 0.677 |
DOC_WW_Pin1_4 | 615 | 620 | PF00397 | 0.688 |
DOC_WW_Pin1_4 | 627 | 632 | PF00397 | 0.735 |
DOC_WW_Pin1_4 | 65 | 70 | PF00397 | 0.586 |
DOC_WW_Pin1_4 | 780 | 785 | PF00397 | 0.508 |
DOC_WW_Pin1_4 | 93 | 98 | PF00397 | 0.626 |
LIG_14-3-3_CanoR_1 | 118 | 127 | PF00244 | 0.509 |
LIG_14-3-3_CanoR_1 | 16 | 26 | PF00244 | 0.468 |
LIG_14-3-3_CanoR_1 | 289 | 293 | PF00244 | 0.436 |
LIG_14-3-3_CanoR_1 | 424 | 432 | PF00244 | 0.465 |
LIG_14-3-3_CanoR_1 | 594 | 601 | PF00244 | 0.586 |
LIG_14-3-3_CanoR_1 | 689 | 695 | PF00244 | 0.604 |
LIG_Actin_WH2_2 | 25 | 40 | PF00022 | 0.420 |
LIG_APCC_ABBA_1 | 459 | 464 | PF00400 | 0.376 |
LIG_BIR_III_2 | 324 | 328 | PF00653 | 0.577 |
LIG_BIR_III_4 | 621 | 625 | PF00653 | 0.711 |
LIG_BRCT_BRCA1_1 | 131 | 135 | PF00533 | 0.566 |
LIG_BRCT_BRCA1_1 | 269 | 273 | PF00533 | 0.468 |
LIG_BRCT_BRCA1_1 | 316 | 320 | PF00533 | 0.490 |
LIG_BRCT_BRCA1_1 | 506 | 510 | PF00533 | 0.428 |
LIG_CORNRBOX | 734 | 742 | PF00104 | 0.523 |
LIG_CtBP_PxDLS_1 | 784 | 788 | PF00389 | 0.491 |
LIG_EH1_1 | 387 | 395 | PF00400 | 0.508 |
LIG_eIF4E_1 | 721 | 727 | PF01652 | 0.508 |
LIG_FHA_1 | 121 | 127 | PF00498 | 0.711 |
LIG_FHA_1 | 317 | 323 | PF00498 | 0.584 |
LIG_FHA_1 | 332 | 338 | PF00498 | 0.443 |
LIG_FHA_1 | 341 | 347 | PF00498 | 0.482 |
LIG_FHA_1 | 351 | 357 | PF00498 | 0.439 |
LIG_FHA_1 | 424 | 430 | PF00498 | 0.483 |
LIG_FHA_1 | 433 | 439 | PF00498 | 0.502 |
LIG_FHA_1 | 609 | 615 | PF00498 | 0.641 |
LIG_FHA_1 | 639 | 645 | PF00498 | 0.600 |
LIG_FHA_1 | 68 | 74 | PF00498 | 0.679 |
LIG_FHA_1 | 691 | 697 | PF00498 | 0.564 |
LIG_FHA_1 | 766 | 772 | PF00498 | 0.465 |
LIG_FHA_1 | 789 | 795 | PF00498 | 0.465 |
LIG_FHA_2 | 145 | 151 | PF00498 | 0.570 |
LIG_FHA_2 | 194 | 200 | PF00498 | 0.430 |
LIG_FHA_2 | 2 | 8 | PF00498 | 0.630 |
LIG_FHA_2 | 72 | 78 | PF00498 | 0.556 |
LIG_FHA_2 | 738 | 744 | PF00498 | 0.446 |
LIG_FHA_2 | 831 | 837 | PF00498 | 0.474 |
LIG_Integrin_RGD_1 | 383 | 385 | PF01839 | 0.265 |
LIG_LIR_Apic_2 | 124 | 130 | PF02991 | 0.591 |
LIG_LIR_Apic_2 | 467 | 473 | PF02991 | 0.395 |
LIG_LIR_Apic_2 | 558 | 562 | PF02991 | 0.638 |
LIG_LIR_Apic_2 | 595 | 601 | PF02991 | 0.585 |
LIG_LIR_Gen_1 | 163 | 174 | PF02991 | 0.367 |
LIG_LIR_Gen_1 | 213 | 222 | PF02991 | 0.423 |
LIG_LIR_Gen_1 | 478 | 487 | PF02991 | 0.352 |
LIG_LIR_Gen_1 | 497 | 506 | PF02991 | 0.377 |
LIG_LIR_LC3C_4 | 786 | 789 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 163 | 169 | PF02991 | 0.365 |
LIG_LIR_Nem_3 | 171 | 176 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 213 | 218 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 29 | 34 | PF02991 | 0.410 |
LIG_LIR_Nem_3 | 478 | 484 | PF02991 | 0.351 |
LIG_LIR_Nem_3 | 497 | 501 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 720 | 724 | PF02991 | 0.510 |
LIG_OCRL_FandH_1 | 165 | 177 | PF00620 | 0.445 |
LIG_PCNA_APIM_2 | 176 | 182 | PF02747 | 0.397 |
LIG_Rb_pABgroove_1 | 829 | 837 | PF01858 | 0.491 |
LIG_REV1ctd_RIR_1 | 163 | 172 | PF16727 | 0.428 |
LIG_SH2_CRK | 141 | 145 | PF00017 | 0.345 |
LIG_SH2_CRK | 224 | 228 | PF00017 | 0.422 |
LIG_SH2_CRK | 284 | 288 | PF00017 | 0.371 |
LIG_SH2_GRB2like | 302 | 305 | PF00017 | 0.572 |
LIG_SH2_GRB2like | 663 | 666 | PF00017 | 0.507 |
LIG_SH2_PTP2 | 173 | 176 | PF00017 | 0.313 |
LIG_SH2_PTP2 | 724 | 727 | PF00017 | 0.487 |
LIG_SH2_SRC | 210 | 213 | PF00017 | 0.418 |
LIG_SH2_SRC | 517 | 520 | PF00017 | 0.388 |
LIG_SH2_SRC | 559 | 562 | PF00017 | 0.629 |
LIG_SH2_STAP1 | 262 | 266 | PF00017 | 0.456 |
LIG_SH2_STAP1 | 292 | 296 | PF00017 | 0.417 |
LIG_SH2_STAP1 | 434 | 438 | PF00017 | 0.465 |
LIG_SH2_STAP1 | 517 | 521 | PF00017 | 0.387 |
LIG_SH2_STAT5 | 173 | 176 | PF00017 | 0.362 |
LIG_SH2_STAT5 | 179 | 182 | PF00017 | 0.360 |
LIG_SH2_STAT5 | 210 | 213 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 215 | 218 | PF00017 | 0.351 |
LIG_SH2_STAT5 | 31 | 34 | PF00017 | 0.389 |
LIG_SH2_STAT5 | 431 | 434 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 486 | 489 | PF00017 | 0.419 |
LIG_SH2_STAT5 | 663 | 666 | PF00017 | 0.557 |
LIG_SH2_STAT5 | 724 | 727 | PF00017 | 0.487 |
LIG_SH3_1 | 810 | 816 | PF00018 | 0.465 |
LIG_SH3_3 | 109 | 115 | PF00018 | 0.645 |
LIG_SH3_3 | 127 | 133 | PF00018 | 0.623 |
LIG_SH3_3 | 356 | 362 | PF00018 | 0.508 |
LIG_SH3_3 | 500 | 506 | PF00018 | 0.371 |
LIG_SH3_3 | 61 | 67 | PF00018 | 0.606 |
LIG_SH3_3 | 613 | 619 | PF00018 | 0.740 |
LIG_SH3_3 | 625 | 631 | PF00018 | 0.650 |
LIG_SH3_3 | 810 | 816 | PF00018 | 0.465 |
LIG_SH3_4 | 38 | 45 | PF00018 | 0.391 |
LIG_SUMO_SIM_anti_2 | 246 | 252 | PF11976 | 0.481 |
LIG_SUMO_SIM_anti_2 | 279 | 284 | PF11976 | 0.450 |
LIG_SUMO_SIM_anti_2 | 409 | 414 | PF11976 | 0.465 |
LIG_SUMO_SIM_anti_2 | 446 | 452 | PF11976 | 0.392 |
LIG_SUMO_SIM_anti_2 | 499 | 505 | PF11976 | 0.452 |
LIG_SUMO_SIM_anti_2 | 641 | 652 | PF11976 | 0.668 |
LIG_SUMO_SIM_anti_2 | 761 | 768 | PF11976 | 0.465 |
LIG_SUMO_SIM_anti_2 | 782 | 789 | PF11976 | 0.473 |
LIG_SUMO_SIM_par_1 | 392 | 399 | PF11976 | 0.523 |
LIG_SUMO_SIM_par_1 | 455 | 460 | PF11976 | 0.336 |
LIG_SUMO_SIM_par_1 | 70 | 77 | PF11976 | 0.635 |
LIG_SUMO_SIM_par_1 | 761 | 768 | PF11976 | 0.508 |
LIG_SUMO_SIM_par_1 | 786 | 793 | PF11976 | 0.465 |
LIG_TRFH_1 | 35 | 39 | PF08558 | 0.414 |
LIG_TYR_ITIM | 222 | 227 | PF00017 | 0.358 |
LIG_TYR_ITIM | 282 | 287 | PF00017 | 0.460 |
LIG_TYR_ITIM | 32 | 37 | PF00017 | 0.401 |
MOD_CDK_SPxK_1 | 111 | 117 | PF00069 | 0.562 |
MOD_CDK_SPxxK_3 | 111 | 118 | PF00069 | 0.674 |
MOD_CDK_SPxxK_3 | 93 | 100 | PF00069 | 0.557 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.734 |
MOD_CK1_1 | 264 | 270 | PF00069 | 0.460 |
MOD_CK1_1 | 535 | 541 | PF00069 | 0.436 |
MOD_CK1_1 | 604 | 610 | PF00069 | 0.667 |
MOD_CK1_1 | 630 | 636 | PF00069 | 0.637 |
MOD_CK1_1 | 656 | 662 | PF00069 | 0.664 |
MOD_CK1_1 | 68 | 74 | PF00069 | 0.675 |
MOD_CK1_1 | 690 | 696 | PF00069 | 0.573 |
MOD_CK2_1 | 144 | 150 | PF00069 | 0.500 |
MOD_CK2_1 | 161 | 167 | PF00069 | 0.257 |
MOD_CK2_1 | 193 | 199 | PF00069 | 0.418 |
MOD_CK2_1 | 30 | 36 | PF00069 | 0.445 |
MOD_CK2_1 | 573 | 579 | PF00069 | 0.660 |
MOD_CK2_1 | 60 | 66 | PF00069 | 0.599 |
MOD_CK2_1 | 71 | 77 | PF00069 | 0.697 |
MOD_CK2_1 | 780 | 786 | PF00069 | 0.487 |
MOD_GlcNHglycan | 105 | 109 | PF01048 | 0.737 |
MOD_GlcNHglycan | 274 | 277 | PF01048 | 0.513 |
MOD_GlcNHglycan | 340 | 343 | PF01048 | 0.323 |
MOD_GlcNHglycan | 415 | 418 | PF01048 | 0.312 |
MOD_GlcNHglycan | 441 | 444 | PF01048 | 0.409 |
MOD_GlcNHglycan | 477 | 480 | PF01048 | 0.336 |
MOD_GlcNHglycan | 506 | 509 | PF01048 | 0.436 |
MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.361 |
MOD_GlcNHglycan | 528 | 531 | PF01048 | 0.522 |
MOD_GlcNHglycan | 576 | 579 | PF01048 | 0.618 |
MOD_GlcNHglycan | 603 | 606 | PF01048 | 0.629 |
MOD_GlcNHglycan | 772 | 775 | PF01048 | 0.333 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.548 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.614 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.467 |
MOD_GSK3_1 | 338 | 345 | PF00069 | 0.383 |
MOD_GSK3_1 | 395 | 402 | PF00069 | 0.502 |
MOD_GSK3_1 | 433 | 440 | PF00069 | 0.542 |
MOD_GSK3_1 | 490 | 497 | PF00069 | 0.490 |
MOD_GSK3_1 | 544 | 551 | PF00069 | 0.551 |
MOD_GSK3_1 | 593 | 600 | PF00069 | 0.590 |
MOD_GSK3_1 | 601 | 608 | PF00069 | 0.697 |
MOD_GSK3_1 | 649 | 656 | PF00069 | 0.795 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.624 |
MOD_GSK3_1 | 684 | 691 | PF00069 | 0.641 |
MOD_GSK3_1 | 89 | 96 | PF00069 | 0.625 |
MOD_LATS_1 | 329 | 335 | PF00433 | 0.547 |
MOD_N-GLC_1 | 264 | 269 | PF02516 | 0.454 |
MOD_N-GLC_1 | 303 | 308 | PF02516 | 0.614 |
MOD_N-GLC_1 | 399 | 404 | PF02516 | 0.323 |
MOD_N-GLC_1 | 499 | 504 | PF02516 | 0.376 |
MOD_N-GLC_1 | 601 | 606 | PF02516 | 0.674 |
MOD_N-GLC_1 | 666 | 671 | PF02516 | 0.682 |
MOD_N-GLC_1 | 746 | 751 | PF02516 | 0.233 |
MOD_N-GLC_2 | 364 | 366 | PF02516 | 0.308 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.642 |
MOD_NEK2_1 | 106 | 111 | PF00069 | 0.498 |
MOD_NEK2_1 | 161 | 166 | PF00069 | 0.362 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.378 |
MOD_NEK2_1 | 340 | 345 | PF00069 | 0.508 |
MOD_NEK2_1 | 413 | 418 | PF00069 | 0.512 |
MOD_NEK2_1 | 432 | 437 | PF00069 | 0.465 |
MOD_NEK2_1 | 655 | 660 | PF00069 | 0.500 |
MOD_NEK2_1 | 765 | 770 | PF00069 | 0.491 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.584 |
MOD_NEK2_2 | 342 | 347 | PF00069 | 0.465 |
MOD_PIKK_1 | 264 | 270 | PF00454 | 0.460 |
MOD_PIKK_1 | 314 | 320 | PF00454 | 0.551 |
MOD_PIKK_1 | 6 | 12 | PF00454 | 0.571 |
MOD_PIKK_1 | 649 | 655 | PF00454 | 0.623 |
MOD_PIKK_1 | 684 | 690 | PF00454 | 0.678 |
MOD_PKA_1 | 713 | 719 | PF00069 | 0.553 |
MOD_PKA_2 | 288 | 294 | PF00069 | 0.427 |
MOD_PKA_2 | 423 | 429 | PF00069 | 0.465 |
MOD_PKA_2 | 593 | 599 | PF00069 | 0.591 |
MOD_PKA_2 | 688 | 694 | PF00069 | 0.758 |
MOD_Plk_1 | 24 | 30 | PF00069 | 0.450 |
MOD_Plk_1 | 372 | 378 | PF00069 | 0.465 |
MOD_Plk_1 | 499 | 505 | PF00069 | 0.370 |
MOD_Plk_1 | 746 | 752 | PF00069 | 0.393 |
MOD_Plk_1 | 827 | 833 | PF00069 | 0.508 |
MOD_Plk_1 | 89 | 95 | PF00069 | 0.598 |
MOD_Plk_2-3 | 193 | 199 | PF00069 | 0.424 |
MOD_Plk_2-3 | 494 | 500 | PF00069 | 0.504 |
MOD_Plk_4 | 107 | 113 | PF00069 | 0.500 |
MOD_Plk_4 | 122 | 128 | PF00069 | 0.639 |
MOD_Plk_4 | 161 | 167 | PF00069 | 0.395 |
MOD_Plk_4 | 169 | 175 | PF00069 | 0.392 |
MOD_Plk_4 | 210 | 216 | PF00069 | 0.450 |
MOD_Plk_4 | 283 | 289 | PF00069 | 0.383 |
MOD_Plk_4 | 30 | 36 | PF00069 | 0.469 |
MOD_Plk_4 | 316 | 322 | PF00069 | 0.503 |
MOD_Plk_4 | 342 | 348 | PF00069 | 0.465 |
MOD_Plk_4 | 389 | 395 | PF00069 | 0.465 |
MOD_Plk_4 | 737 | 743 | PF00069 | 0.475 |
MOD_Plk_4 | 830 | 836 | PF00069 | 0.508 |
MOD_ProDKin_1 | 111 | 117 | PF00069 | 0.647 |
MOD_ProDKin_1 | 129 | 135 | PF00069 | 0.697 |
MOD_ProDKin_1 | 597 | 603 | PF00069 | 0.676 |
MOD_ProDKin_1 | 615 | 621 | PF00069 | 0.691 |
MOD_ProDKin_1 | 627 | 633 | PF00069 | 0.735 |
MOD_ProDKin_1 | 65 | 71 | PF00069 | 0.588 |
MOD_ProDKin_1 | 780 | 786 | PF00069 | 0.508 |
MOD_ProDKin_1 | 93 | 99 | PF00069 | 0.626 |
MOD_SUMO_for_1 | 181 | 184 | PF00179 | 0.425 |
MOD_SUMO_for_1 | 216 | 219 | PF00179 | 0.430 |
MOD_SUMO_rev_2 | 33 | 40 | PF00179 | 0.462 |
TRG_DiLeu_BaEn_1 | 150 | 155 | PF01217 | 0.451 |
TRG_DiLeu_BaEn_1 | 409 | 414 | PF01217 | 0.508 |
TRG_DiLeu_BaEn_1 | 446 | 451 | PF01217 | 0.385 |
TRG_DiLeu_BaEn_1 | 761 | 766 | PF01217 | 0.491 |
TRG_DiLeu_BaLyEn_6 | 256 | 261 | PF01217 | 0.459 |
TRG_DiLeu_BaLyEn_6 | 674 | 679 | PF01217 | 0.524 |
TRG_DiLeu_BaLyEn_6 | 813 | 818 | PF01217 | 0.489 |
TRG_ENDOCYTIC_2 | 141 | 144 | PF00928 | 0.344 |
TRG_ENDOCYTIC_2 | 173 | 176 | PF00928 | 0.418 |
TRG_ENDOCYTIC_2 | 215 | 218 | PF00928 | 0.363 |
TRG_ENDOCYTIC_2 | 224 | 227 | PF00928 | 0.369 |
TRG_ENDOCYTIC_2 | 284 | 287 | PF00928 | 0.369 |
TRG_ENDOCYTIC_2 | 34 | 37 | PF00928 | 0.409 |
TRG_ENDOCYTIC_2 | 481 | 484 | PF00928 | 0.355 |
TRG_ENDOCYTIC_2 | 524 | 527 | PF00928 | 0.397 |
TRG_ENDOCYTIC_2 | 724 | 727 | PF00928 | 0.508 |
TRG_ER_diArg_1 | 157 | 159 | PF00400 | 0.364 |
TRG_ER_diArg_1 | 540 | 542 | PF00400 | 0.506 |
TRG_NES_CRM1_1 | 246 | 258 | PF08389 | 0.415 |
TRG_Pf-PMV_PEXEL_1 | 142 | 146 | PF00026 | 0.429 |
TRG_Pf-PMV_PEXEL_1 | 149 | 153 | PF00026 | 0.364 |
TRG_Pf-PMV_PEXEL_1 | 16 | 21 | PF00026 | 0.478 |
TRG_Pf-PMV_PEXEL_1 | 195 | 199 | PF00026 | 0.474 |
TRG_Pf-PMV_PEXEL_1 | 753 | 758 | PF00026 | 0.308 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDZ8 | Leptomonas seymouri | 62% | 98% |
A0A3R7LSY3 | Trypanosoma rangeli | 43% | 100% |
A0A3S5H655 | Leishmania donovani | 91% | 100% |
A4H5B8 | Leishmania braziliensis | 76% | 95% |
A4HTJ9 | Leishmania infantum | 91% | 100% |
Q4QIB8 | Leishmania major | 90% | 100% |