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: 18 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0030117 | membrane coat | 3 | 11 |
GO:0030120 | vesicle coat | 4 | 11 |
GO:0030127 | COPII vesicle coat | 5 | 11 |
GO:0032991 | protein-containing complex | 1 | 11 |
GO:0098796 | membrane protein complex | 2 | 11 |
GO:0070971 | endoplasmic reticulum exit site | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AM57
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 11 |
GO:0006886 | intracellular protein transport | 4 | 11 |
GO:0006888 | endoplasmic reticulum to Golgi vesicle-mediated transport | 4 | 10 |
GO:0008104 | protein localization | 4 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0015031 | protein transport | 4 | 11 |
GO:0016192 | vesicle-mediated transport | 4 | 10 |
GO:0033036 | macromolecule localization | 2 | 11 |
GO:0045184 | establishment of protein localization | 3 | 11 |
GO:0046907 | intracellular transport | 3 | 11 |
GO:0048193 | Golgi vesicle transport | 5 | 10 |
GO:0051179 | localization | 1 | 11 |
GO:0051234 | establishment of localization | 2 | 11 |
GO:0051641 | cellular localization | 2 | 11 |
GO:0051649 | establishment of localization in cell | 3 | 11 |
GO:0070727 | cellular macromolecule localization | 3 | 11 |
GO:0071702 | organic substance transport | 4 | 11 |
GO:0071705 | nitrogen compound transport | 4 | 11 |
GO:0035459 | vesicle cargo loading | 4 | 1 |
GO:0090110 | COPII-coated vesicle cargo loading | 4 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 11 |
GO:0008270 | zinc ion binding | 6 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043169 | cation binding | 3 | 11 |
GO:0046872 | metal ion binding | 4 | 11 |
GO:0046914 | transition metal ion binding | 5 | 11 |
GO:0000149 | SNARE binding | 3 | 1 |
GO:0005515 | protein binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 305 | 309 | PF00656 | 0.423 |
CLV_C14_Caspase3-7 | 503 | 507 | PF00656 | 0.468 |
CLV_C14_Caspase3-7 | 521 | 525 | PF00656 | 0.349 |
CLV_NRD_NRD_1 | 196 | 198 | PF00675 | 0.636 |
CLV_NRD_NRD_1 | 366 | 368 | PF00675 | 0.344 |
CLV_NRD_NRD_1 | 688 | 690 | PF00675 | 0.295 |
CLV_NRD_NRD_1 | 961 | 963 | PF00675 | 0.498 |
CLV_PCSK_FUR_1 | 686 | 690 | PF00082 | 0.312 |
CLV_PCSK_KEX2_1 | 362 | 364 | PF00082 | 0.468 |
CLV_PCSK_KEX2_1 | 366 | 368 | PF00082 | 0.331 |
CLV_PCSK_KEX2_1 | 688 | 690 | PF00082 | 0.295 |
CLV_PCSK_KEX2_1 | 943 | 945 | PF00082 | 0.525 |
CLV_PCSK_PC1ET2_1 | 362 | 364 | PF00082 | 0.560 |
CLV_PCSK_PC1ET2_1 | 943 | 945 | PF00082 | 0.525 |
CLV_PCSK_PC7_1 | 684 | 690 | PF00082 | 0.295 |
CLV_PCSK_SKI1_1 | 367 | 371 | PF00082 | 0.341 |
CLV_PCSK_SKI1_1 | 391 | 395 | PF00082 | 0.384 |
CLV_PCSK_SKI1_1 | 474 | 478 | PF00082 | 0.317 |
CLV_PCSK_SKI1_1 | 610 | 614 | PF00082 | 0.348 |
CLV_PCSK_SKI1_1 | 748 | 752 | PF00082 | 0.329 |
CLV_PCSK_SKI1_1 | 921 | 925 | PF00082 | 0.439 |
DEG_APCC_DBOX_1 | 390 | 398 | PF00400 | 0.384 |
DEG_APCC_DBOX_1 | 473 | 481 | PF00400 | 0.423 |
DEG_SCF_SKP2-CKS1_1 | 882 | 889 | PF00560 | 0.580 |
DOC_CDC14_PxL_1 | 44 | 52 | PF14671 | 0.699 |
DOC_CDC14_PxL_1 | 772 | 780 | PF14671 | 0.312 |
DOC_CKS1_1 | 355 | 360 | PF01111 | 0.501 |
DOC_CYCLIN_RxL_1 | 607 | 616 | PF00134 | 0.462 |
DOC_CYCLIN_yClb3_PxF_3 | 364 | 370 | PF00134 | 0.312 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 417 | 426 | PF00134 | 0.332 |
DOC_CYCLIN_yCln2_LP_2 | 259 | 265 | PF00134 | 0.384 |
DOC_MAPK_gen_1 | 362 | 371 | PF00069 | 0.432 |
DOC_MAPK_gen_1 | 623 | 632 | PF00069 | 0.312 |
DOC_MAPK_gen_1 | 684 | 692 | PF00069 | 0.312 |
DOC_MAPK_gen_1 | 889 | 897 | PF00069 | 0.492 |
DOC_MAPK_gen_1 | 962 | 970 | PF00069 | 0.507 |
DOC_MAPK_JIP1_4 | 367 | 373 | PF00069 | 0.331 |
DOC_MAPK_MEF2A_6 | 366 | 373 | PF00069 | 0.456 |
DOC_MAPK_MEF2A_6 | 642 | 651 | PF00069 | 0.312 |
DOC_MAPK_MEF2A_6 | 691 | 699 | PF00069 | 0.406 |
DOC_PP2B_LxvP_1 | 259 | 262 | PF13499 | 0.389 |
DOC_PP2B_LxvP_1 | 426 | 429 | PF13499 | 0.384 |
DOC_PP2B_LxvP_1 | 630 | 633 | PF13499 | 0.312 |
DOC_PP2B_LxvP_1 | 647 | 650 | PF13499 | 0.312 |
DOC_PP2B_LxvP_1 | 766 | 769 | PF13499 | 0.423 |
DOC_PP4_FxxP_1 | 207 | 210 | PF00568 | 0.514 |
DOC_PP4_FxxP_1 | 270 | 273 | PF00568 | 0.499 |
DOC_PP4_FxxP_1 | 38 | 41 | PF00568 | 0.659 |
DOC_USP7_MATH_1 | 380 | 384 | PF00917 | 0.327 |
DOC_USP7_MATH_1 | 396 | 400 | PF00917 | 0.261 |
DOC_USP7_MATH_1 | 476 | 480 | PF00917 | 0.378 |
DOC_USP7_MATH_1 | 803 | 807 | PF00917 | 0.331 |
DOC_USP7_MATH_1 | 88 | 92 | PF00917 | 0.761 |
DOC_USP7_MATH_1 | 956 | 960 | PF00917 | 0.462 |
DOC_USP7_UBL2_3 | 198 | 202 | PF12436 | 0.653 |
DOC_USP7_UBL2_3 | 738 | 742 | PF12436 | 0.423 |
DOC_USP7_UBL2_3 | 748 | 752 | PF12436 | 0.423 |
DOC_WW_Pin1_4 | 106 | 111 | PF00397 | 0.613 |
DOC_WW_Pin1_4 | 232 | 237 | PF00397 | 0.487 |
DOC_WW_Pin1_4 | 320 | 325 | PF00397 | 0.423 |
DOC_WW_Pin1_4 | 354 | 359 | PF00397 | 0.453 |
DOC_WW_Pin1_4 | 431 | 436 | PF00397 | 0.352 |
DOC_WW_Pin1_4 | 883 | 888 | PF00397 | 0.576 |
DOC_WW_Pin1_4 | 895 | 900 | PF00397 | 0.272 |
DOC_WW_Pin1_4 | 91 | 96 | PF00397 | 0.669 |
LIG_14-3-3_CanoR_1 | 190 | 196 | PF00244 | 0.569 |
LIG_14-3-3_CanoR_1 | 197 | 206 | PF00244 | 0.658 |
LIG_14-3-3_CanoR_1 | 325 | 333 | PF00244 | 0.557 |
LIG_14-3-3_CanoR_1 | 423 | 427 | PF00244 | 0.423 |
LIG_14-3-3_CanoR_1 | 587 | 593 | PF00244 | 0.312 |
LIG_14-3-3_CanoR_1 | 595 | 601 | PF00244 | 0.312 |
LIG_14-3-3_CanoR_1 | 614 | 622 | PF00244 | 0.151 |
LIG_14-3-3_CanoR_1 | 623 | 632 | PF00244 | 0.277 |
LIG_14-3-3_CanoR_1 | 691 | 696 | PF00244 | 0.318 |
LIG_14-3-3_CanoR_1 | 801 | 806 | PF00244 | 0.365 |
LIG_14-3-3_CanoR_1 | 921 | 930 | PF00244 | 0.436 |
LIG_Actin_WH2_2 | 184 | 199 | PF00022 | 0.547 |
LIG_Actin_WH2_2 | 459 | 476 | PF00022 | 0.456 |
LIG_Actin_WH2_2 | 601 | 616 | PF00022 | 0.423 |
LIG_APCC_ABBA_1 | 267 | 272 | PF00400 | 0.371 |
LIG_BIR_III_4 | 506 | 510 | PF00653 | 0.378 |
LIG_BRCT_BRCA1_1 | 350 | 354 | PF00533 | 0.338 |
LIG_BRCT_BRCA1_1 | 658 | 662 | PF00533 | 0.423 |
LIG_BRCT_BRCA1_1 | 770 | 774 | PF00533 | 0.321 |
LIG_Clathr_ClatBox_1 | 371 | 375 | PF01394 | 0.331 |
LIG_CtBP_PxDLS_1 | 769 | 773 | PF00389 | 0.326 |
LIG_EH_1 | 297 | 301 | PF12763 | 0.312 |
LIG_FHA_1 | 235 | 241 | PF00498 | 0.478 |
LIG_FHA_1 | 250 | 256 | PF00498 | 0.343 |
LIG_FHA_1 | 333 | 339 | PF00498 | 0.560 |
LIG_FHA_1 | 457 | 463 | PF00498 | 0.378 |
LIG_FHA_1 | 485 | 491 | PF00498 | 0.308 |
LIG_FHA_1 | 619 | 625 | PF00498 | 0.398 |
LIG_FHA_1 | 692 | 698 | PF00498 | 0.312 |
LIG_FHA_1 | 738 | 744 | PF00498 | 0.354 |
LIG_FHA_1 | 822 | 828 | PF00498 | 0.409 |
LIG_FHA_1 | 949 | 955 | PF00498 | 0.484 |
LIG_FHA_2 | 300 | 306 | PF00498 | 0.312 |
LIG_FHA_2 | 35 | 41 | PF00498 | 0.790 |
LIG_FHA_2 | 435 | 441 | PF00498 | 0.423 |
LIG_FHA_2 | 501 | 507 | PF00498 | 0.410 |
LIG_FHA_2 | 614 | 620 | PF00498 | 0.384 |
LIG_FHA_2 | 871 | 877 | PF00498 | 0.380 |
LIG_GBD_Chelix_1 | 381 | 389 | PF00786 | 0.423 |
LIG_IBAR_NPY_1 | 100 | 102 | PF08397 | 0.772 |
LIG_LIR_Apic_2 | 116 | 121 | PF02991 | 0.774 |
LIG_LIR_Apic_2 | 353 | 358 | PF02991 | 0.439 |
LIG_LIR_Apic_2 | 37 | 41 | PF02991 | 0.753 |
LIG_LIR_Apic_2 | 91 | 95 | PF02991 | 0.722 |
LIG_LIR_Gen_1 | 187 | 196 | PF02991 | 0.561 |
LIG_LIR_Gen_1 | 310 | 320 | PF02991 | 0.390 |
LIG_LIR_Gen_1 | 375 | 386 | PF02991 | 0.317 |
LIG_LIR_Gen_1 | 404 | 413 | PF02991 | 0.165 |
LIG_LIR_Gen_1 | 468 | 477 | PF02991 | 0.302 |
LIG_LIR_Gen_1 | 822 | 830 | PF02991 | 0.454 |
LIG_LIR_Gen_1 | 922 | 932 | PF02991 | 0.537 |
LIG_LIR_LC3C_4 | 459 | 464 | PF02991 | 0.338 |
LIG_LIR_Nem_3 | 187 | 191 | PF02991 | 0.554 |
LIG_LIR_Nem_3 | 310 | 315 | PF02991 | 0.375 |
LIG_LIR_Nem_3 | 375 | 381 | PF02991 | 0.312 |
LIG_LIR_Nem_3 | 404 | 410 | PF02991 | 0.312 |
LIG_LIR_Nem_3 | 416 | 422 | PF02991 | 0.312 |
LIG_LIR_Nem_3 | 468 | 473 | PF02991 | 0.281 |
LIG_LIR_Nem_3 | 822 | 828 | PF02991 | 0.343 |
LIG_LIR_Nem_3 | 922 | 927 | PF02991 | 0.531 |
LIG_LYPXL_yS_3 | 74 | 77 | PF13949 | 0.479 |
LIG_MYND_1 | 213 | 217 | PF01753 | 0.287 |
LIG_PTB_Apo_2 | 182 | 189 | PF02174 | 0.566 |
LIG_REV1ctd_RIR_1 | 417 | 427 | PF16727 | 0.423 |
LIG_REV1ctd_RIR_1 | 780 | 788 | PF16727 | 0.331 |
LIG_SH2_CRK | 118 | 122 | PF00017 | 0.680 |
LIG_SH2_CRK | 138 | 142 | PF00017 | 0.736 |
LIG_SH2_CRK | 152 | 156 | PF00017 | 0.741 |
LIG_SH2_CRK | 175 | 179 | PF00017 | 0.709 |
LIG_SH2_CRK | 407 | 411 | PF00017 | 0.312 |
LIG_SH2_CRK | 45 | 49 | PF00017 | 0.689 |
LIG_SH2_CRK | 470 | 474 | PF00017 | 0.301 |
LIG_SH2_GRB2like | 296 | 299 | PF00017 | 0.312 |
LIG_SH2_NCK_1 | 118 | 122 | PF00017 | 0.584 |
LIG_SH2_NCK_1 | 138 | 142 | PF00017 | 0.705 |
LIG_SH2_NCK_1 | 152 | 156 | PF00017 | 0.774 |
LIG_SH2_NCK_1 | 355 | 359 | PF00017 | 0.501 |
LIG_SH2_NCK_1 | 45 | 49 | PF00017 | 0.658 |
LIG_SH2_NCK_1 | 96 | 100 | PF00017 | 0.736 |
LIG_SH2_PTP2 | 296 | 299 | PF00017 | 0.312 |
LIG_SH2_PTP2 | 92 | 95 | PF00017 | 0.486 |
LIG_SH2_SRC | 118 | 121 | PF00017 | 0.583 |
LIG_SH2_SRC | 296 | 299 | PF00017 | 0.312 |
LIG_SH2_STAP1 | 115 | 119 | PF00017 | 0.721 |
LIG_SH2_STAP1 | 413 | 417 | PF00017 | 0.378 |
LIG_SH2_STAP1 | 543 | 547 | PF00017 | 0.365 |
LIG_SH2_STAP1 | 658 | 662 | PF00017 | 0.331 |
LIG_SH2_STAP1 | 668 | 672 | PF00017 | 0.331 |
LIG_SH2_STAP1 | 9 | 13 | PF00017 | 0.635 |
LIG_SH2_STAT3 | 13 | 16 | PF00017 | 0.604 |
LIG_SH2_STAT3 | 159 | 162 | PF00017 | 0.796 |
LIG_SH2_STAT3 | 180 | 183 | PF00017 | 0.757 |
LIG_SH2_STAT3 | 52 | 55 | PF00017 | 0.787 |
LIG_SH2_STAT3 | 83 | 86 | PF00017 | 0.711 |
LIG_SH2_STAT5 | 296 | 299 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 327 | 330 | PF00017 | 0.393 |
LIG_SH2_STAT5 | 418 | 421 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 45 | 48 | PF00017 | 0.658 |
LIG_SH2_STAT5 | 543 | 546 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 674 | 677 | PF00017 | 0.318 |
LIG_SH2_STAT5 | 681 | 684 | PF00017 | 0.295 |
LIG_SH2_STAT5 | 820 | 823 | PF00017 | 0.356 |
LIG_SH2_STAT5 | 825 | 828 | PF00017 | 0.338 |
LIG_SH2_STAT5 | 854 | 857 | PF00017 | 0.346 |
LIG_SH2_STAT5 | 92 | 95 | PF00017 | 0.525 |
LIG_SH2_STAT5 | 960 | 963 | PF00017 | 0.404 |
LIG_SH3_1 | 118 | 124 | PF00018 | 0.655 |
LIG_SH3_1 | 175 | 181 | PF00018 | 0.737 |
LIG_SH3_1 | 25 | 31 | PF00018 | 0.617 |
LIG_SH3_1 | 362 | 368 | PF00018 | 0.405 |
LIG_SH3_3 | 117 | 123 | PF00018 | 0.780 |
LIG_SH3_3 | 139 | 145 | PF00018 | 0.713 |
LIG_SH3_3 | 175 | 181 | PF00018 | 0.708 |
LIG_SH3_3 | 207 | 213 | PF00018 | 0.501 |
LIG_SH3_3 | 25 | 31 | PF00018 | 0.762 |
LIG_SH3_3 | 362 | 368 | PF00018 | 0.405 |
LIG_SH3_3 | 450 | 456 | PF00018 | 0.423 |
LIG_SH3_3 | 53 | 59 | PF00018 | 0.743 |
LIG_SH3_3 | 638 | 644 | PF00018 | 0.312 |
LIG_SH3_3 | 692 | 698 | PF00018 | 0.456 |
LIG_SH3_3 | 725 | 731 | PF00018 | 0.331 |
LIG_SH3_3 | 792 | 798 | PF00018 | 0.312 |
LIG_SH3_3 | 824 | 830 | PF00018 | 0.369 |
LIG_SH3_3 | 84 | 90 | PF00018 | 0.756 |
LIG_SH3_3 | 924 | 930 | PF00018 | 0.473 |
LIG_SH3_CIN85_PxpxPR_1 | 269 | 274 | PF14604 | 0.538 |
LIG_SUMO_SIM_anti_2 | 645 | 650 | PF11976 | 0.423 |
LIG_SUMO_SIM_par_1 | 370 | 375 | PF11976 | 0.312 |
LIG_SUMO_SIM_par_1 | 461 | 469 | PF11976 | 0.447 |
LIG_TRAF2_1 | 24 | 27 | PF00917 | 0.759 |
LIG_TRAF2_1 | 829 | 832 | PF00917 | 0.529 |
LIG_WRC_WIRS_1 | 300 | 305 | PF05994 | 0.312 |
LIG_WRPW_2 | 267 | 270 | PF00400 | 0.471 |
LIG_WW_3 | 363 | 367 | PF00397 | 0.515 |
MOD_CDK_SPK_2 | 320 | 325 | PF00069 | 0.456 |
MOD_CDK_SPxK_1 | 883 | 889 | PF00069 | 0.664 |
MOD_CDK_SPxxK_3 | 232 | 239 | PF00069 | 0.566 |
MOD_CK1_1 | 434 | 440 | PF00069 | 0.408 |
MOD_CK1_1 | 515 | 521 | PF00069 | 0.323 |
MOD_CK1_1 | 563 | 569 | PF00069 | 0.288 |
MOD_CK1_1 | 656 | 662 | PF00069 | 0.312 |
MOD_CK1_1 | 709 | 715 | PF00069 | 0.343 |
MOD_CK1_1 | 804 | 810 | PF00069 | 0.421 |
MOD_CK1_1 | 840 | 846 | PF00069 | 0.476 |
MOD_CK1_1 | 91 | 97 | PF00069 | 0.751 |
MOD_CK1_1 | 922 | 928 | PF00069 | 0.470 |
MOD_CK2_1 | 299 | 305 | PF00069 | 0.331 |
MOD_CK2_1 | 340 | 346 | PF00069 | 0.463 |
MOD_CK2_1 | 462 | 468 | PF00069 | 0.440 |
MOD_CK2_1 | 483 | 489 | PF00069 | 0.437 |
MOD_CK2_1 | 870 | 876 | PF00069 | 0.328 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.677 |
MOD_GlcNHglycan | 378 | 381 | PF01048 | 0.327 |
MOD_GlcNHglycan | 382 | 385 | PF01048 | 0.295 |
MOD_GlcNHglycan | 562 | 565 | PF01048 | 0.354 |
MOD_GlcNHglycan | 589 | 592 | PF01048 | 0.404 |
MOD_GlcNHglycan | 601 | 604 | PF01048 | 0.312 |
MOD_GlcNHglycan | 699 | 702 | PF01048 | 0.259 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.746 |
MOD_GSK3_1 | 245 | 252 | PF00069 | 0.429 |
MOD_GSK3_1 | 376 | 383 | PF00069 | 0.378 |
MOD_GSK3_1 | 462 | 469 | PF00069 | 0.447 |
MOD_GSK3_1 | 514 | 521 | PF00069 | 0.397 |
MOD_GSK3_1 | 709 | 716 | PF00069 | 0.388 |
MOD_GSK3_1 | 737 | 744 | PF00069 | 0.453 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.548 |
MOD_GSK3_1 | 785 | 792 | PF00069 | 0.423 |
MOD_GSK3_1 | 803 | 810 | PF00069 | 0.331 |
MOD_GSK3_1 | 837 | 844 | PF00069 | 0.490 |
MOD_N-GLC_1 | 14 | 19 | PF02516 | 0.426 |
MOD_N-GLC_1 | 320 | 325 | PF02516 | 0.384 |
MOD_N-GLC_1 | 348 | 353 | PF02516 | 0.436 |
MOD_N-GLC_1 | 919 | 924 | PF02516 | 0.527 |
MOD_N-GLC_1 | 934 | 939 | PF02516 | 0.450 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.686 |
MOD_NEK2_1 | 196 | 201 | PF00069 | 0.710 |
MOD_NEK2_1 | 255 | 260 | PF00069 | 0.417 |
MOD_NEK2_1 | 374 | 379 | PF00069 | 0.312 |
MOD_NEK2_1 | 422 | 427 | PF00069 | 0.358 |
MOD_NEK2_1 | 462 | 467 | PF00069 | 0.458 |
MOD_NEK2_1 | 558 | 563 | PF00069 | 0.312 |
MOD_NEK2_1 | 613 | 618 | PF00069 | 0.461 |
MOD_NEK2_1 | 713 | 718 | PF00069 | 0.353 |
MOD_NEK2_1 | 77 | 82 | PF00069 | 0.709 |
MOD_NEK2_1 | 912 | 917 | PF00069 | 0.443 |
MOD_NEK2_2 | 396 | 401 | PF00069 | 0.328 |
MOD_NEK2_2 | 413 | 418 | PF00069 | 0.247 |
MOD_NEK2_2 | 789 | 794 | PF00069 | 0.423 |
MOD_PIKK_1 | 189 | 195 | PF00454 | 0.538 |
MOD_PIKK_1 | 249 | 255 | PF00454 | 0.431 |
MOD_PIKK_1 | 753 | 759 | PF00454 | 0.265 |
MOD_PIKK_1 | 81 | 87 | PF00454 | 0.748 |
MOD_PIKK_1 | 94 | 100 | PF00454 | 0.692 |
MOD_PKA_1 | 197 | 203 | PF00069 | 0.692 |
MOD_PKA_2 | 189 | 195 | PF00069 | 0.559 |
MOD_PKA_2 | 196 | 202 | PF00069 | 0.671 |
MOD_PKA_2 | 242 | 248 | PF00069 | 0.400 |
MOD_PKA_2 | 422 | 428 | PF00069 | 0.423 |
MOD_PKA_2 | 586 | 592 | PF00069 | 0.312 |
MOD_PKA_2 | 594 | 600 | PF00069 | 0.312 |
MOD_PKA_2 | 613 | 619 | PF00069 | 0.201 |
MOD_PKA_2 | 624 | 630 | PF00069 | 0.264 |
MOD_PKB_1 | 689 | 697 | PF00069 | 0.312 |
MOD_Plk_1 | 348 | 354 | PF00069 | 0.324 |
MOD_Plk_1 | 374 | 380 | PF00069 | 0.312 |
MOD_Plk_1 | 413 | 419 | PF00069 | 0.439 |
MOD_Plk_1 | 541 | 547 | PF00069 | 0.312 |
MOD_Plk_1 | 577 | 583 | PF00069 | 0.358 |
MOD_Plk_1 | 618 | 624 | PF00069 | 0.423 |
MOD_Plk_1 | 653 | 659 | PF00069 | 0.312 |
MOD_Plk_1 | 919 | 925 | PF00069 | 0.530 |
MOD_Plk_1 | 934 | 940 | PF00069 | 0.452 |
MOD_Plk_4 | 413 | 419 | PF00069 | 0.321 |
MOD_Plk_4 | 500 | 506 | PF00069 | 0.384 |
MOD_Plk_4 | 804 | 810 | PF00069 | 0.317 |
MOD_Plk_4 | 837 | 843 | PF00069 | 0.438 |
MOD_Plk_4 | 88 | 94 | PF00069 | 0.604 |
MOD_Plk_4 | 956 | 962 | PF00069 | 0.362 |
MOD_ProDKin_1 | 106 | 112 | PF00069 | 0.615 |
MOD_ProDKin_1 | 232 | 238 | PF00069 | 0.482 |
MOD_ProDKin_1 | 320 | 326 | PF00069 | 0.423 |
MOD_ProDKin_1 | 354 | 360 | PF00069 | 0.454 |
MOD_ProDKin_1 | 431 | 437 | PF00069 | 0.352 |
MOD_ProDKin_1 | 883 | 889 | PF00069 | 0.587 |
MOD_ProDKin_1 | 895 | 901 | PF00069 | 0.265 |
MOD_ProDKin_1 | 91 | 97 | PF00069 | 0.666 |
MOD_SUMO_for_1 | 448 | 451 | PF00179 | 0.331 |
MOD_SUMO_rev_2 | 446 | 450 | PF00179 | 0.447 |
MOD_SUMO_rev_2 | 518 | 527 | PF00179 | 0.335 |
MOD_SUMO_rev_2 | 655 | 664 | PF00179 | 0.370 |
TRG_DiLeu_BaEn_1 | 468 | 473 | PF01217 | 0.456 |
TRG_DiLeu_BaEn_1 | 851 | 856 | PF01217 | 0.407 |
TRG_DiLeu_BaEn_2 | 769 | 775 | PF01217 | 0.326 |
TRG_ENDOCYTIC_2 | 102 | 105 | PF00928 | 0.750 |
TRG_ENDOCYTIC_2 | 407 | 410 | PF00928 | 0.312 |
TRG_ENDOCYTIC_2 | 470 | 473 | PF00928 | 0.281 |
TRG_ENDOCYTIC_2 | 674 | 677 | PF00928 | 0.313 |
TRG_ENDOCYTIC_2 | 74 | 77 | PF00928 | 0.479 |
TRG_ENDOCYTIC_2 | 9 | 12 | PF00928 | 0.638 |
TRG_ENDOCYTIC_2 | 938 | 941 | PF00928 | 0.575 |
TRG_ER_diArg_1 | 365 | 367 | PF00400 | 0.344 |
TRG_ER_diArg_1 | 622 | 625 | PF00400 | 0.324 |
TRG_ER_diArg_1 | 688 | 691 | PF00400 | 0.295 |
TRG_ER_diArg_1 | 905 | 908 | PF00400 | 0.395 |
TRG_NES_CRM1_1 | 440 | 454 | PF08389 | 0.378 |
TRG_Pf-PMV_PEXEL_1 | 773 | 777 | PF00026 | 0.423 |
TRG_Pf-PMV_PEXEL_1 | 794 | 799 | PF00026 | 0.410 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P662 | Leptomonas seymouri | 24% | 94% |
A0A0N1PA55 | Leptomonas seymouri | 72% | 100% |
A0A0S4KJI0 | Bodo saltans | 24% | 88% |
A0A1X0NMN7 | Trypanosomatidae | 24% | 97% |
A0A1X0NZG8 | Trypanosomatidae | 53% | 100% |
A0A3Q8IF67 | Leishmania donovani | 93% | 100% |
A0A3R7KKF1 | Trypanosoma rangeli | 51% | 100% |
A0A3R7MV46 | Trypanosoma rangeli | 26% | 100% |
A0A3S7WZ57 | Leishmania donovani | 23% | 96% |
A1CUC3 | Aspergillus clavatus (strain ATCC 1007 / CBS 513.65 / DSM 816 / NCTC 3887 / NRRL 1 / QM 1276 / 107) | 27% | 100% |
A1DP06 | Neosartorya fischeri (strain ATCC 1020 / DSM 3700 / CBS 544.65 / FGSC A1164 / JCM 1740 / NRRL 181 / WB 181) | 28% | 100% |
A3LRW3 | Scheffersomyces stipitis (strain ATCC 58785 / CBS 6054 / NBRC 10063 / NRRL Y-11545) | 28% | 100% |
A4HE50 | Leishmania braziliensis | 23% | 100% |
A4HH30 | Leishmania braziliensis | 84% | 98% |
A4I1H8 | Leishmania infantum | 23% | 96% |
A4I475 | Leishmania infantum | 93% | 100% |
A4QUL1 | Magnaporthe oryzae (strain 70-15 / ATCC MYA-4617 / FGSC 8958) | 26% | 100% |
A5DPC0 | Meyerozyma guilliermondii (strain ATCC 6260 / CBS 566 / DSM 6381 / JCM 1539 / NBRC 10279 / NRRL Y-324) | 29% | 100% |
A5DSK2 | Lodderomyces elongisporus (strain ATCC 11503 / CBS 2605 / JCM 1781 / NBRC 1676 / NRRL YB-4239) | 27% | 100% |
A6QNT8 | Bos taurus | 27% | 88% |
C9ZJZ2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 100% |
C9ZKQ3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 50% | 100% |
E9ADM4 | Leishmania major | 93% | 99% |
E9AXL3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 95% |
O94855 | Homo sapiens | 26% | 94% |
O95486 | Homo sapiens | 28% | 89% |
P38810 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 24% | 100% |
P40482 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 25% | 100% |
P53953 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 27% | 100% |
P53992 | Homo sapiens | 27% | 89% |
Q0CSL7 | Aspergillus terreus (strain NIH 2624 / FGSC A1156) | 28% | 100% |
Q0PVD8 | Komagataella pastoris | 26% | 100% |
Q1E6U9 | Coccidioides immitis (strain RS) | 27% | 100% |
Q2HH63 | Chaetomium globosum (strain ATCC 6205 / CBS 148.51 / DSM 1962 / NBRC 6347 / NRRL 1970) | 26% | 100% |
Q2ULI0 | Aspergillus oryzae (strain ATCC 42149 / RIB 40) | 27% | 100% |
Q3U2P1 | Mus musculus | 28% | 89% |
Q4P9K4 | Ustilago maydis (strain 521 / FGSC 9021) | 28% | 98% |
Q4Q9V9 | Leishmania major | 23% | 100% |
Q4WLP1 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 27% | 100% |
Q54U61 | Dictyostelium discoideum | 28% | 96% |
Q5AQ76 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 27% | 100% |
Q6BT80 | Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / BCRC 21394 / JCM 1990 / NBRC 0083 / IGC 2968) | 28% | 100% |
Q6C2T4 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 26% | 100% |
Q6CLE0 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 26% | 100% |
Q6FWD3 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 27% | 100% |
Q6FX11 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 25% | 100% |
Q75B16 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 27% | 100% |
Q7S4P3 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 29% | 100% |
Q86ZK8 | Podospora anserina | 26% | 100% |
Q875Q0 | Lachancea kluyveri (strain ATCC 58438 / CBS 3082 / BCRC 21498 / NBRC 1685 / JCM 7257 / NCYC 543 / NRRL Y-12651) | 27% | 100% |
Q875V7 | Naumovozyma castellii (strain ATCC 76901 / BCRC 22586 / CBS 4309 / NBRC 1992 / NRRL Y-12630) | 24% | 100% |
Q875V8 | Naumovozyma castellii (strain ATCC 76901 / BCRC 22586 / CBS 4309 / NBRC 1992 / NRRL Y-12630) | 27% | 100% |
Q876F4 | Saccharomyces uvarum (strain ATCC 76518 / CBS 7001 / CLIB 283 / NBRC 10550 / MCYC 623 / NCYC 2669 / NRRL Y-11845) | 26% | 100% |
Q876F5 | Saccharomyces uvarum (strain ATCC 76518 / CBS 7001 / CLIB 283 / NBRC 10550 / MCYC 623 / NCYC 2669 / NRRL Y-11845) | 25% | 100% |
Q9M081 | Arabidopsis thaliana | 25% | 90% |
Q9M291 | Arabidopsis thaliana | 25% | 89% |
Q9SFU0 | Arabidopsis thaliana | 31% | 94% |
Q9USS7 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 27% | 100% |
Q9UUI5 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 26% | 100% |
V5D902 | Trypanosoma cruzi | 27% | 95% |
V5DLD4 | Trypanosoma cruzi | 54% | 100% |