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:0016020 | membrane | 2 | 4 |
GO:0110165 | cellular anatomical entity | 1 | 4 |
Related structures:
AlphaFold database: A4HT52
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006163 | purine nucleotide metabolic process | 5 | 1 |
GO:0006195 | purine nucleotide catabolic process | 6 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006753 | nucleoside phosphate metabolic process | 4 | 1 |
GO:0006793 | phosphorus metabolic process | 3 | 1 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0009117 | nucleotide metabolic process | 5 | 1 |
GO:0009150 | purine ribonucleotide metabolic process | 6 | 1 |
GO:0009154 | purine ribonucleotide catabolic process | 6 | 1 |
GO:0009166 | nucleotide catabolic process | 6 | 1 |
GO:0009259 | ribonucleotide metabolic process | 5 | 1 |
GO:0009261 | ribonucleotide catabolic process | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0015936 | coenzyme A metabolic process | 6 | 1 |
GO:0015938 | coenzyme A catabolic process | 7 | 1 |
GO:0019439 | aromatic compound catabolic process | 4 | 1 |
GO:0019637 | organophosphate metabolic process | 3 | 1 |
GO:0019693 | ribose phosphate metabolic process | 4 | 1 |
GO:0033865 | nucleoside bisphosphate metabolic process | 5 | 1 |
GO:0033869 | nucleoside bisphosphate catabolic process | 6 | 1 |
GO:0033875 | ribonucleoside bisphosphate metabolic process | 6 | 1 |
GO:0034031 | ribonucleoside bisphosphate catabolic process | 7 | 1 |
GO:0034032 | purine nucleoside bisphosphate metabolic process | 5 | 1 |
GO:0034034 | purine nucleoside bisphosphate catabolic process | 6 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0034655 | nucleobase-containing compound catabolic process | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044248 | cellular catabolic process | 3 | 1 |
GO:0044270 | cellular nitrogen compound catabolic process | 4 | 1 |
GO:0044281 | small molecule metabolic process | 2 | 1 |
GO:0046434 | organophosphate catabolic process | 4 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0046700 | heterocycle catabolic process | 4 | 1 |
GO:0055086 | nucleobase-containing small molecule metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0072521 | purine-containing compound metabolic process | 4 | 1 |
GO:0072523 | purine-containing compound catabolic process | 5 | 1 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 1 |
GO:1901136 | carbohydrate derivative catabolic process | 4 | 1 |
GO:1901292 | nucleoside phosphate catabolic process | 5 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
GO:1901361 | organic cyclic compound catabolic process | 4 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
GO:1901565 | organonitrogen compound catabolic process | 4 | 1 |
GO:1901575 | organic substance catabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 7 |
GO:0010945 | CoA pyrophosphatase activity | 6 | 7 |
GO:0016462 | pyrophosphatase activity | 5 | 7 |
GO:0016787 | hydrolase activity | 2 | 7 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 7 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 7 |
GO:0003986 | acetyl-CoA hydrolase activity | 6 | 1 |
GO:0016289 | CoA hydrolase activity | 5 | 1 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 1 |
GO:0016790 | thiolester hydrolase activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 273 | 277 | PF00656 | 0.640 |
CLV_C14_Caspase3-7 | 719 | 723 | PF00656 | 0.674 |
CLV_C14_Caspase3-7 | 729 | 733 | PF00656 | 0.695 |
CLV_C14_Caspase3-7 | 813 | 817 | PF00656 | 0.649 |
CLV_MEL_PAP_1 | 176 | 182 | PF00089 | 0.353 |
CLV_NRD_NRD_1 | 160 | 162 | PF00675 | 0.406 |
CLV_NRD_NRD_1 | 170 | 172 | PF00675 | 0.327 |
CLV_NRD_NRD_1 | 201 | 203 | PF00675 | 0.435 |
CLV_NRD_NRD_1 | 296 | 298 | PF00675 | 0.322 |
CLV_NRD_NRD_1 | 308 | 310 | PF00675 | 0.243 |
CLV_NRD_NRD_1 | 37 | 39 | PF00675 | 0.590 |
CLV_NRD_NRD_1 | 609 | 611 | PF00675 | 0.366 |
CLV_NRD_NRD_1 | 678 | 680 | PF00675 | 0.416 |
CLV_NRD_NRD_1 | 694 | 696 | PF00675 | 0.497 |
CLV_NRD_NRD_1 | 787 | 789 | PF00675 | 0.606 |
CLV_NRD_NRD_1 | 908 | 910 | PF00675 | 0.420 |
CLV_PCSK_FUR_1 | 692 | 696 | PF00082 | 0.485 |
CLV_PCSK_KEX2_1 | 160 | 162 | PF00082 | 0.406 |
CLV_PCSK_KEX2_1 | 170 | 172 | PF00082 | 0.327 |
CLV_PCSK_KEX2_1 | 201 | 203 | PF00082 | 0.435 |
CLV_PCSK_KEX2_1 | 289 | 291 | PF00082 | 0.269 |
CLV_PCSK_KEX2_1 | 296 | 298 | PF00082 | 0.284 |
CLV_PCSK_KEX2_1 | 308 | 310 | PF00082 | 0.343 |
CLV_PCSK_KEX2_1 | 37 | 39 | PF00082 | 0.590 |
CLV_PCSK_KEX2_1 | 609 | 611 | PF00082 | 0.366 |
CLV_PCSK_KEX2_1 | 677 | 679 | PF00082 | 0.423 |
CLV_PCSK_KEX2_1 | 694 | 696 | PF00082 | 0.504 |
CLV_PCSK_KEX2_1 | 786 | 788 | PF00082 | 0.610 |
CLV_PCSK_KEX2_1 | 908 | 910 | PF00082 | 0.420 |
CLV_PCSK_PC1ET2_1 | 289 | 291 | PF00082 | 0.256 |
CLV_PCSK_PC7_1 | 166 | 172 | PF00082 | 0.359 |
CLV_PCSK_SKI1_1 | 186 | 190 | PF00082 | 0.354 |
CLV_PCSK_SKI1_1 | 196 | 200 | PF00082 | 0.360 |
CLV_PCSK_SKI1_1 | 363 | 367 | PF00082 | 0.275 |
CLV_PCSK_SKI1_1 | 392 | 396 | PF00082 | 0.377 |
CLV_PCSK_SKI1_1 | 599 | 603 | PF00082 | 0.337 |
DEG_SCF_FBW7_2 | 626 | 632 | PF00400 | 0.609 |
DEG_SPOP_SBC_1 | 111 | 115 | PF00917 | 0.567 |
DEG_SPOP_SBC_1 | 238 | 242 | PF00917 | 0.611 |
DEG_SPOP_SBC_1 | 444 | 448 | PF00917 | 0.755 |
DOC_ANK_TNKS_1 | 244 | 251 | PF00023 | 0.654 |
DOC_CKS1_1 | 626 | 631 | PF01111 | 0.612 |
DOC_MAPK_gen_1 | 170 | 178 | PF00069 | 0.548 |
DOC_MAPK_gen_1 | 296 | 304 | PF00069 | 0.495 |
DOC_MAPK_MEF2A_6 | 171 | 180 | PF00069 | 0.523 |
DOC_MAPK_MEF2A_6 | 23 | 31 | PF00069 | 0.373 |
DOC_MAPK_RevD_3 | 145 | 161 | PF00069 | 0.527 |
DOC_PP2B_LxvP_1 | 437 | 440 | PF13499 | 0.578 |
DOC_PP4_FxxP_1 | 411 | 414 | PF00568 | 0.635 |
DOC_PP4_FxxP_1 | 507 | 510 | PF00568 | 0.573 |
DOC_USP7_MATH_1 | 103 | 107 | PF00917 | 0.569 |
DOC_USP7_MATH_1 | 111 | 115 | PF00917 | 0.563 |
DOC_USP7_MATH_1 | 118 | 122 | PF00917 | 0.577 |
DOC_USP7_MATH_1 | 212 | 216 | PF00917 | 0.671 |
DOC_USP7_MATH_1 | 221 | 225 | PF00917 | 0.684 |
DOC_USP7_MATH_1 | 234 | 238 | PF00917 | 0.608 |
DOC_USP7_MATH_1 | 239 | 243 | PF00917 | 0.592 |
DOC_USP7_MATH_1 | 244 | 248 | PF00917 | 0.587 |
DOC_USP7_MATH_1 | 27 | 31 | PF00917 | 0.364 |
DOC_USP7_MATH_1 | 382 | 386 | PF00917 | 0.452 |
DOC_USP7_MATH_1 | 407 | 411 | PF00917 | 0.634 |
DOC_USP7_MATH_1 | 41 | 45 | PF00917 | 0.393 |
DOC_USP7_MATH_1 | 443 | 447 | PF00917 | 0.682 |
DOC_USP7_MATH_1 | 654 | 658 | PF00917 | 0.255 |
DOC_USP7_MATH_1 | 698 | 702 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 8 | 12 | PF00917 | 0.371 |
DOC_USP7_MATH_1 | 812 | 816 | PF00917 | 0.716 |
DOC_WW_Pin1_4 | 122 | 127 | PF00397 | 0.583 |
DOC_WW_Pin1_4 | 133 | 138 | PF00397 | 0.564 |
DOC_WW_Pin1_4 | 29 | 34 | PF00397 | 0.377 |
DOC_WW_Pin1_4 | 370 | 375 | PF00397 | 0.475 |
DOC_WW_Pin1_4 | 473 | 478 | PF00397 | 0.727 |
DOC_WW_Pin1_4 | 479 | 484 | PF00397 | 0.633 |
DOC_WW_Pin1_4 | 52 | 57 | PF00397 | 0.337 |
DOC_WW_Pin1_4 | 625 | 630 | PF00397 | 0.607 |
DOC_WW_Pin1_4 | 824 | 829 | PF00397 | 0.719 |
LIG_14-3-3_CanoR_1 | 170 | 178 | PF00244 | 0.576 |
LIG_14-3-3_CanoR_1 | 196 | 204 | PF00244 | 0.604 |
LIG_14-3-3_CanoR_1 | 392 | 399 | PF00244 | 0.471 |
LIG_14-3-3_CanoR_1 | 541 | 550 | PF00244 | 0.601 |
LIG_14-3-3_CanoR_1 | 583 | 587 | PF00244 | 0.772 |
LIG_14-3-3_CanoR_1 | 750 | 758 | PF00244 | 0.685 |
LIG_14-3-3_CanoR_1 | 763 | 769 | PF00244 | 0.661 |
LIG_14-3-3_CanoR_1 | 788 | 798 | PF00244 | 0.711 |
LIG_14-3-3_CanoR_1 | 811 | 821 | PF00244 | 0.690 |
LIG_Actin_WH2_2 | 890 | 906 | PF00022 | 0.629 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.361 |
LIG_BIR_III_2 | 474 | 478 | PF00653 | 0.657 |
LIG_BRCT_BRCA1_1 | 113 | 117 | PF00533 | 0.564 |
LIG_BRCT_BRCA1_1 | 227 | 231 | PF00533 | 0.718 |
LIG_BRCT_BRCA1_1 | 355 | 359 | PF00533 | 0.512 |
LIG_Clathr_ClatBox_1 | 498 | 502 | PF01394 | 0.511 |
LIG_CORNRBOX | 104 | 112 | PF00104 | 0.572 |
LIG_deltaCOP1_diTrp_1 | 249 | 259 | PF00928 | 0.583 |
LIG_deltaCOP1_diTrp_1 | 508 | 511 | PF00928 | 0.589 |
LIG_FHA_1 | 152 | 158 | PF00498 | 0.575 |
LIG_FHA_1 | 187 | 193 | PF00498 | 0.553 |
LIG_FHA_1 | 251 | 257 | PF00498 | 0.596 |
LIG_FHA_1 | 371 | 377 | PF00498 | 0.475 |
LIG_FHA_1 | 52 | 58 | PF00498 | 0.333 |
LIG_FHA_1 | 66 | 72 | PF00498 | 0.186 |
LIG_FHA_1 | 763 | 769 | PF00498 | 0.721 |
LIG_FHA_1 | 833 | 839 | PF00498 | 0.718 |
LIG_FHA_1 | 844 | 850 | PF00498 | 0.585 |
LIG_FHA_2 | 289 | 295 | PF00498 | 0.495 |
LIG_FHA_2 | 322 | 328 | PF00498 | 0.493 |
LIG_FHA_2 | 469 | 475 | PF00498 | 0.762 |
LIG_FHA_2 | 492 | 498 | PF00498 | 0.569 |
LIG_FHA_2 | 750 | 756 | PF00498 | 0.668 |
LIG_FHA_2 | 789 | 795 | PF00498 | 0.699 |
LIG_FHA_2 | 811 | 817 | PF00498 | 0.740 |
LIG_FXI_DFP_1 | 314 | 318 | PF00024 | 0.329 |
LIG_GBD_Chelix_1 | 104 | 112 | PF00786 | 0.372 |
LIG_HP1_1 | 27 | 31 | PF01393 | 0.372 |
LIG_Integrin_RGD_1 | 868 | 870 | PF01839 | 0.450 |
LIG_LIR_Apic_2 | 249 | 255 | PF02991 | 0.605 |
LIG_LIR_Apic_2 | 410 | 414 | PF02991 | 0.635 |
LIG_LIR_Gen_1 | 257 | 263 | PF02991 | 0.487 |
LIG_LIR_Gen_1 | 315 | 325 | PF02991 | 0.475 |
LIG_LIR_Gen_1 | 337 | 345 | PF02991 | 0.483 |
LIG_LIR_Gen_1 | 430 | 439 | PF02991 | 0.549 |
LIG_LIR_Gen_1 | 608 | 618 | PF02991 | 0.547 |
LIG_LIR_Nem_3 | 257 | 262 | PF02991 | 0.563 |
LIG_LIR_Nem_3 | 315 | 320 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 323 | 328 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 337 | 341 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 385 | 391 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 430 | 434 | PF02991 | 0.615 |
LIG_LIR_Nem_3 | 508 | 512 | PF02991 | 0.669 |
LIG_LIR_Nem_3 | 532 | 538 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 608 | 614 | PF02991 | 0.533 |
LIG_MYND_1 | 128 | 132 | PF01753 | 0.579 |
LIG_PCNA_PIPBox_1 | 795 | 804 | PF02747 | 0.697 |
LIG_Pex14_2 | 507 | 511 | PF04695 | 0.586 |
LIG_SH2_CRK | 521 | 525 | PF00017 | 0.542 |
LIG_SH2_CRK | 611 | 615 | PF00017 | 0.589 |
LIG_SH2_NCK_1 | 204 | 208 | PF00017 | 0.686 |
LIG_SH2_NCK_1 | 325 | 329 | PF00017 | 0.529 |
LIG_SH2_NCK_1 | 649 | 653 | PF00017 | 0.329 |
LIG_SH2_SRC | 204 | 207 | PF00017 | 0.685 |
LIG_SH2_SRC | 325 | 328 | PF00017 | 0.495 |
LIG_SH2_STAP1 | 271 | 275 | PF00017 | 0.581 |
LIG_SH2_STAP1 | 531 | 535 | PF00017 | 0.512 |
LIG_SH2_STAP1 | 649 | 653 | PF00017 | 0.329 |
LIG_SH2_STAP1 | 682 | 686 | PF00017 | 0.540 |
LIG_SH2_STAT3 | 910 | 913 | PF00017 | 0.678 |
LIG_SH2_STAT5 | 122 | 125 | PF00017 | 0.589 |
LIG_SH2_STAT5 | 261 | 264 | PF00017 | 0.587 |
LIG_SH2_STAT5 | 431 | 434 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 649 | 652 | PF00017 | 0.403 |
LIG_SH3_1 | 623 | 629 | PF00018 | 0.557 |
LIG_SH3_2 | 129 | 134 | PF14604 | 0.587 |
LIG_SH3_2 | 33 | 38 | PF14604 | 0.381 |
LIG_SH3_3 | 123 | 129 | PF00018 | 0.579 |
LIG_SH3_3 | 161 | 167 | PF00018 | 0.613 |
LIG_SH3_3 | 30 | 36 | PF00018 | 0.377 |
LIG_SH3_3 | 401 | 407 | PF00018 | 0.568 |
LIG_SH3_3 | 437 | 443 | PF00018 | 0.555 |
LIG_SH3_3 | 474 | 480 | PF00018 | 0.725 |
LIG_SH3_3 | 520 | 526 | PF00018 | 0.538 |
LIG_SH3_3 | 623 | 629 | PF00018 | 0.555 |
LIG_SH3_3 | 817 | 823 | PF00018 | 0.722 |
LIG_SH3_3 | 875 | 881 | PF00018 | 0.731 |
LIG_SH3_3 | 9 | 15 | PF00018 | 0.370 |
LIG_Sin3_3 | 618 | 625 | PF02671 | 0.533 |
LIG_SUMO_SIM_anti_2 | 146 | 151 | PF11976 | 0.585 |
LIG_SUMO_SIM_par_1 | 27 | 32 | PF11976 | 0.373 |
LIG_SUMO_SIM_par_1 | 497 | 503 | PF11976 | 0.534 |
LIG_SUMO_SIM_par_1 | 822 | 827 | PF11976 | 0.658 |
LIG_SUMO_SIM_par_1 | 845 | 850 | PF11976 | 0.617 |
LIG_TRAF2_1 | 324 | 327 | PF00917 | 0.495 |
LIG_TYR_ITIM | 519 | 524 | PF00017 | 0.403 |
LIG_UBA3_1 | 285 | 289 | PF00899 | 0.312 |
LIG_WRC_WIRS_1 | 192 | 197 | PF05994 | 0.392 |
LIG_WRC_WIRS_1 | 408 | 413 | PF05994 | 0.533 |
LIG_WW_2 | 128 | 131 | PF00397 | 0.455 |
LIG_WW_3 | 34 | 38 | PF00397 | 0.462 |
MOD_CDC14_SPxK_1 | 827 | 830 | PF00782 | 0.589 |
MOD_CDK_SPxK_1 | 824 | 830 | PF00069 | 0.594 |
MOD_CDK_SPxxK_3 | 479 | 486 | PF00069 | 0.487 |
MOD_CK1_1 | 106 | 112 | PF00069 | 0.447 |
MOD_CK1_1 | 113 | 119 | PF00069 | 0.439 |
MOD_CK1_1 | 169 | 175 | PF00069 | 0.483 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.773 |
MOD_CK1_1 | 237 | 243 | PF00069 | 0.521 |
MOD_CK1_1 | 433 | 439 | PF00069 | 0.529 |
MOD_CK1_1 | 446 | 452 | PF00069 | 0.526 |
MOD_CK1_1 | 476 | 482 | PF00069 | 0.611 |
MOD_CK1_1 | 500 | 506 | PF00069 | 0.635 |
MOD_CK1_1 | 51 | 57 | PF00069 | 0.406 |
MOD_CK1_1 | 577 | 583 | PF00069 | 0.721 |
MOD_CK1_1 | 589 | 595 | PF00069 | 0.452 |
MOD_CK1_1 | 727 | 733 | PF00069 | 0.618 |
MOD_CK1_1 | 829 | 835 | PF00069 | 0.711 |
MOD_CK1_1 | 842 | 848 | PF00069 | 0.480 |
MOD_CK2_1 | 288 | 294 | PF00069 | 0.340 |
MOD_CK2_1 | 321 | 327 | PF00069 | 0.337 |
MOD_CK2_1 | 491 | 497 | PF00069 | 0.369 |
MOD_CK2_1 | 602 | 608 | PF00069 | 0.417 |
MOD_CK2_1 | 749 | 755 | PF00069 | 0.586 |
MOD_CK2_1 | 761 | 767 | PF00069 | 0.574 |
MOD_CK2_1 | 788 | 794 | PF00069 | 0.640 |
MOD_CMANNOS | 485 | 488 | PF00535 | 0.443 |
MOD_CMANNOS | 540 | 543 | PF00535 | 0.388 |
MOD_Cter_Amidation | 306 | 309 | PF01082 | 0.302 |
MOD_GlcNHglycan | 118 | 121 | PF01048 | 0.461 |
MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.469 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.377 |
MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.644 |
MOD_GlcNHglycan | 223 | 226 | PF01048 | 0.768 |
MOD_GlcNHglycan | 232 | 235 | PF01048 | 0.494 |
MOD_GlcNHglycan | 236 | 239 | PF01048 | 0.497 |
MOD_GlcNHglycan | 246 | 249 | PF01048 | 0.465 |
MOD_GlcNHglycan | 298 | 301 | PF01048 | 0.388 |
MOD_GlcNHglycan | 448 | 451 | PF01048 | 0.634 |
MOD_GlcNHglycan | 50 | 53 | PF01048 | 0.435 |
MOD_GlcNHglycan | 579 | 582 | PF01048 | 0.670 |
MOD_GlcNHglycan | 584 | 587 | PF01048 | 0.587 |
MOD_GlcNHglycan | 616 | 619 | PF01048 | 0.453 |
MOD_GlcNHglycan | 656 | 659 | PF01048 | 0.300 |
MOD_GlcNHglycan | 700 | 703 | PF01048 | 0.598 |
MOD_GlcNHglycan | 718 | 721 | PF01048 | 0.624 |
MOD_GlcNHglycan | 758 | 761 | PF01048 | 0.628 |
MOD_GlcNHglycan | 778 | 781 | PF01048 | 0.491 |
MOD_GlcNHglycan | 806 | 809 | PF01048 | 0.624 |
MOD_GlcNHglycan | 841 | 844 | PF01048 | 0.784 |
MOD_GlcNHglycan | 856 | 859 | PF01048 | 0.530 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.445 |
MOD_GSK3_1 | 118 | 125 | PF00069 | 0.459 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.418 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.441 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.650 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.767 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.685 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.480 |
MOD_GSK3_1 | 444 | 451 | PF00069 | 0.670 |
MOD_GSK3_1 | 570 | 577 | PF00069 | 0.679 |
MOD_GSK3_1 | 582 | 589 | PF00069 | 0.606 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.418 |
MOD_GSK3_1 | 724 | 731 | PF00069 | 0.783 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.500 |
MOD_GSK3_1 | 800 | 807 | PF00069 | 0.626 |
MOD_GSK3_1 | 822 | 829 | PF00069 | 0.714 |
MOD_GSK3_1 | 832 | 839 | PF00069 | 0.669 |
MOD_N-GLC_1 | 708 | 713 | PF02516 | 0.586 |
MOD_NEK2_1 | 110 | 115 | PF00069 | 0.443 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.340 |
MOD_NEK2_1 | 47 | 52 | PF00069 | 0.462 |
MOD_NEK2_1 | 511 | 516 | PF00069 | 0.414 |
MOD_NEK2_1 | 575 | 580 | PF00069 | 0.675 |
MOD_NEK2_1 | 602 | 607 | PF00069 | 0.445 |
MOD_NEK2_1 | 65 | 70 | PF00069 | 0.184 |
MOD_NEK2_1 | 73 | 78 | PF00069 | 0.433 |
MOD_NEK2_1 | 741 | 746 | PF00069 | 0.603 |
MOD_NEK2_1 | 838 | 843 | PF00069 | 0.790 |
MOD_NEK2_2 | 191 | 196 | PF00069 | 0.390 |
MOD_NEK2_2 | 382 | 387 | PF00069 | 0.279 |
MOD_NEK2_2 | 488 | 493 | PF00069 | 0.470 |
MOD_PIKK_1 | 148 | 154 | PF00454 | 0.458 |
MOD_PIKK_1 | 181 | 187 | PF00454 | 0.495 |
MOD_PKA_1 | 296 | 302 | PF00069 | 0.371 |
MOD_PKA_2 | 13 | 19 | PF00069 | 0.438 |
MOD_PKA_2 | 169 | 175 | PF00069 | 0.490 |
MOD_PKA_2 | 225 | 231 | PF00069 | 0.649 |
MOD_PKA_2 | 244 | 250 | PF00069 | 0.568 |
MOD_PKA_2 | 296 | 302 | PF00069 | 0.305 |
MOD_PKA_2 | 321 | 327 | PF00069 | 0.388 |
MOD_PKA_2 | 582 | 588 | PF00069 | 0.663 |
MOD_PKA_2 | 727 | 733 | PF00069 | 0.602 |
MOD_PKA_2 | 741 | 747 | PF00069 | 0.579 |
MOD_PKA_2 | 749 | 755 | PF00069 | 0.563 |
MOD_PKA_2 | 762 | 768 | PF00069 | 0.568 |
MOD_PKA_2 | 810 | 816 | PF00069 | 0.572 |
MOD_PKB_1 | 786 | 794 | PF00069 | 0.629 |
MOD_PKB_1 | 909 | 917 | PF00069 | 0.597 |
MOD_Plk_2-3 | 497 | 503 | PF00069 | 0.424 |
MOD_Plk_2-3 | 703 | 709 | PF00069 | 0.624 |
MOD_Plk_4 | 427 | 433 | PF00069 | 0.390 |
MOD_Plk_4 | 713 | 719 | PF00069 | 0.620 |
MOD_Plk_4 | 8 | 14 | PF00069 | 0.448 |
MOD_ProDKin_1 | 122 | 128 | PF00069 | 0.461 |
MOD_ProDKin_1 | 133 | 139 | PF00069 | 0.421 |
MOD_ProDKin_1 | 29 | 35 | PF00069 | 0.454 |
MOD_ProDKin_1 | 370 | 376 | PF00069 | 0.312 |
MOD_ProDKin_1 | 473 | 479 | PF00069 | 0.657 |
MOD_ProDKin_1 | 52 | 58 | PF00069 | 0.393 |
MOD_ProDKin_1 | 625 | 631 | PF00069 | 0.499 |
MOD_ProDKin_1 | 824 | 830 | PF00069 | 0.655 |
MOD_SUMO_rev_2 | 206 | 215 | PF00179 | 0.582 |
MOD_SUMO_rev_2 | 900 | 906 | PF00179 | 0.542 |
TRG_AP2beta_CARGO_1 | 257 | 266 | PF09066 | 0.336 |
TRG_DiLeu_BaEn_3 | 901 | 907 | PF01217 | 0.587 |
TRG_DiLeu_BaLyEn_6 | 514 | 519 | PF01217 | 0.475 |
TRG_DiLeu_BaLyEn_6 | 770 | 775 | PF01217 | 0.560 |
TRG_ENDOCYTIC_2 | 271 | 274 | PF00928 | 0.462 |
TRG_ENDOCYTIC_2 | 325 | 328 | PF00928 | 0.388 |
TRG_ENDOCYTIC_2 | 431 | 434 | PF00928 | 0.362 |
TRG_ENDOCYTIC_2 | 521 | 524 | PF00928 | 0.459 |
TRG_ENDOCYTIC_2 | 530 | 533 | PF00928 | 0.315 |
TRG_ENDOCYTIC_2 | 611 | 614 | PF00928 | 0.389 |
TRG_ER_diArg_1 | 160 | 162 | PF00400 | 0.496 |
TRG_ER_diArg_1 | 296 | 298 | PF00400 | 0.336 |
TRG_ER_diArg_1 | 36 | 38 | PF00400 | 0.467 |
TRG_ER_diArg_1 | 401 | 404 | PF00400 | 0.475 |
TRG_ER_diArg_1 | 548 | 551 | PF00400 | 0.532 |
TRG_ER_diArg_1 | 595 | 598 | PF00400 | 0.449 |
TRG_ER_diArg_1 | 609 | 611 | PF00400 | 0.394 |
TRG_ER_diArg_1 | 677 | 679 | PF00400 | 0.520 |
TRG_ER_diArg_1 | 691 | 694 | PF00400 | 0.610 |
TRG_ER_diArg_1 | 786 | 788 | PF00400 | 0.768 |
TRG_ER_diArg_1 | 907 | 909 | PF00400 | 0.522 |
TRG_Pf-PMV_PEXEL_1 | 155 | 159 | PF00026 | 0.434 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I6E0 | Leptomonas seymouri | 39% | 100% |
A0A3S7WPU2 | Leishmania donovani | 99% | 100% |
A4H4X9 | Leishmania braziliensis | 64% | 100% |
E9AL44 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 99% |
Q4QIR0 | Leishmania major | 87% | 100% |