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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005730 | nucleolus | 5 | 10 |
GO:0043226 | organelle | 2 | 10 |
GO:0043228 | non-membrane-bounded organelle | 3 | 10 |
GO:0043229 | intracellular organelle | 3 | 10 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
Related structures:
AlphaFold database: E9ARB0
Term | Name | Level | Count |
---|---|---|---|
GO:0000054 | ribosomal subunit export from nucleus | 3 | 10 |
GO:0000055 | ribosomal large subunit export from nucleus | 4 | 10 |
GO:0006810 | transport | 3 | 10 |
GO:0006913 | nucleocytoplasmic transport | 5 | 10 |
GO:0006996 | organelle organization | 4 | 10 |
GO:0007010 | cytoskeleton organization | 5 | 10 |
GO:0008104 | protein localization | 4 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0015031 | protein transport | 4 | 10 |
GO:0016043 | cellular component organization | 3 | 10 |
GO:0022613 | ribonucleoprotein complex biogenesis | 4 | 10 |
GO:0030029 | actin filament-based process | 2 | 10 |
GO:0030036 | actin cytoskeleton organization | 3 | 10 |
GO:0031503 | protein-containing complex localization | 2 | 10 |
GO:0033036 | macromolecule localization | 2 | 10 |
GO:0033750 | ribosome localization | 3 | 10 |
GO:0042273 | ribosomal large subunit biogenesis | 5 | 10 |
GO:0044085 | cellular component biogenesis | 3 | 10 |
GO:0045184 | establishment of protein localization | 3 | 10 |
GO:0046907 | intracellular transport | 3 | 10 |
GO:0051168 | nuclear export | 6 | 10 |
GO:0051169 | nuclear transport | 4 | 10 |
GO:0051179 | localization | 1 | 10 |
GO:0051234 | establishment of localization | 2 | 10 |
GO:0051640 | organelle localization | 2 | 10 |
GO:0051641 | cellular localization | 2 | 10 |
GO:0051649 | establishment of localization in cell | 3 | 10 |
GO:0051656 | establishment of organelle localization | 3 | 10 |
GO:0070727 | cellular macromolecule localization | 3 | 10 |
GO:0071702 | organic substance transport | 4 | 10 |
GO:0071705 | nitrogen compound transport | 4 | 10 |
GO:0071840 | cellular component organization or biogenesis | 2 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 395 | 399 | PF00656 | 0.303 |
CLV_C14_Caspase3-7 | 512 | 516 | PF00656 | 0.251 |
CLV_C14_Caspase3-7 | 523 | 527 | PF00656 | 0.198 |
CLV_C14_Caspase3-7 | 568 | 572 | PF00656 | 0.210 |
CLV_C14_Caspase3-7 | 593 | 597 | PF00656 | 0.290 |
CLV_C14_Caspase3-7 | 609 | 613 | PF00656 | 0.243 |
CLV_C14_Caspase3-7 | 684 | 688 | PF00656 | 0.214 |
CLV_NRD_NRD_1 | 130 | 132 | PF00675 | 0.253 |
CLV_NRD_NRD_1 | 142 | 144 | PF00675 | 0.295 |
CLV_NRD_NRD_1 | 18 | 20 | PF00675 | 0.414 |
CLV_NRD_NRD_1 | 189 | 191 | PF00675 | 0.291 |
CLV_NRD_NRD_1 | 275 | 277 | PF00675 | 0.370 |
CLV_NRD_NRD_1 | 744 | 746 | PF00675 | 0.259 |
CLV_NRD_NRD_1 | 793 | 795 | PF00675 | 0.236 |
CLV_NRD_NRD_1 | 803 | 805 | PF00675 | 0.175 |
CLV_PCSK_FUR_1 | 16 | 20 | PF00082 | 0.312 |
CLV_PCSK_FUR_1 | 742 | 746 | PF00082 | 0.403 |
CLV_PCSK_FUR_1 | 859 | 863 | PF00082 | 0.195 |
CLV_PCSK_KEX2_1 | 18 | 20 | PF00082 | 0.354 |
CLV_PCSK_KEX2_1 | 188 | 190 | PF00082 | 0.289 |
CLV_PCSK_KEX2_1 | 262 | 264 | PF00082 | 0.353 |
CLV_PCSK_KEX2_1 | 268 | 270 | PF00082 | 0.340 |
CLV_PCSK_KEX2_1 | 275 | 277 | PF00082 | 0.354 |
CLV_PCSK_KEX2_1 | 412 | 414 | PF00082 | 0.283 |
CLV_PCSK_KEX2_1 | 579 | 581 | PF00082 | 0.242 |
CLV_PCSK_KEX2_1 | 744 | 746 | PF00082 | 0.250 |
CLV_PCSK_KEX2_1 | 754 | 756 | PF00082 | 0.198 |
CLV_PCSK_KEX2_1 | 778 | 780 | PF00082 | 0.195 |
CLV_PCSK_KEX2_1 | 803 | 805 | PF00082 | 0.205 |
CLV_PCSK_KEX2_1 | 819 | 821 | PF00082 | 0.174 |
CLV_PCSK_KEX2_1 | 828 | 830 | PF00082 | 0.195 |
CLV_PCSK_KEX2_1 | 861 | 863 | PF00082 | 0.195 |
CLV_PCSK_PC1ET2_1 | 262 | 264 | PF00082 | 0.365 |
CLV_PCSK_PC1ET2_1 | 268 | 270 | PF00082 | 0.363 |
CLV_PCSK_PC1ET2_1 | 275 | 277 | PF00082 | 0.383 |
CLV_PCSK_PC1ET2_1 | 412 | 414 | PF00082 | 0.283 |
CLV_PCSK_PC1ET2_1 | 579 | 581 | PF00082 | 0.242 |
CLV_PCSK_PC1ET2_1 | 744 | 746 | PF00082 | 0.258 |
CLV_PCSK_PC1ET2_1 | 754 | 756 | PF00082 | 0.235 |
CLV_PCSK_PC1ET2_1 | 778 | 780 | PF00082 | 0.195 |
CLV_PCSK_PC1ET2_1 | 819 | 821 | PF00082 | 0.195 |
CLV_PCSK_PC1ET2_1 | 828 | 830 | PF00082 | 0.195 |
CLV_PCSK_PC1ET2_1 | 861 | 863 | PF00082 | 0.242 |
CLV_PCSK_PC7_1 | 408 | 414 | PF00082 | 0.312 |
CLV_PCSK_SKI1_1 | 132 | 136 | PF00082 | 0.263 |
CLV_PCSK_SKI1_1 | 214 | 218 | PF00082 | 0.250 |
CLV_PCSK_SKI1_1 | 255 | 259 | PF00082 | 0.382 |
CLV_PCSK_SKI1_1 | 265 | 269 | PF00082 | 0.326 |
CLV_PCSK_SKI1_1 | 272 | 276 | PF00082 | 0.322 |
CLV_PCSK_SKI1_1 | 718 | 722 | PF00082 | 0.213 |
CLV_PCSK_SKI1_1 | 783 | 787 | PF00082 | 0.228 |
CLV_PCSK_SKI1_1 | 82 | 86 | PF00082 | 0.209 |
CLV_PCSK_SKI1_1 | 854 | 858 | PF00082 | 0.203 |
CLV_PCSK_SKI1_1 | 94 | 98 | PF00082 | 0.208 |
CLV_Separin_Metazoa | 79 | 83 | PF03568 | 0.213 |
DEG_APCC_DBOX_1 | 217 | 225 | PF00400 | 0.272 |
DEG_APCC_DBOX_1 | 6 | 14 | PF00400 | 0.320 |
DEG_APCC_DBOX_1 | 819 | 827 | PF00400 | 0.195 |
DEG_Kelch_Keap1_1 | 515 | 520 | PF01344 | 0.277 |
DEG_SPOP_SBC_1 | 514 | 518 | PF00917 | 0.192 |
DOC_ANK_TNKS_1 | 568 | 575 | PF00023 | 0.192 |
DOC_CDC14_PxL_1 | 483 | 491 | PF14671 | 0.192 |
DOC_CYCLIN_RxL_1 | 126 | 136 | PF00134 | 0.356 |
DOC_MAPK_DCC_7 | 290 | 298 | PF00069 | 0.318 |
DOC_MAPK_gen_1 | 126 | 135 | PF00069 | 0.271 |
DOC_MAPK_gen_1 | 249 | 256 | PF00069 | 0.309 |
DOC_MAPK_gen_1 | 579 | 589 | PF00069 | 0.135 |
DOC_MAPK_HePTP_8 | 174 | 186 | PF00069 | 0.247 |
DOC_MAPK_MEF2A_6 | 177 | 186 | PF00069 | 0.240 |
DOC_MAPK_MEF2A_6 | 582 | 591 | PF00069 | 0.135 |
DOC_MAPK_MEF2A_6 | 68 | 76 | PF00069 | 0.248 |
DOC_PP1_RVXF_1 | 852 | 859 | PF00149 | 0.195 |
DOC_PP2B_LxvP_1 | 222 | 225 | PF13499 | 0.348 |
DOC_PP2B_LxvP_1 | 340 | 343 | PF13499 | 0.301 |
DOC_PP4_MxPP_1 | 373 | 376 | PF00568 | 0.282 |
DOC_SPAK_OSR1_1 | 319 | 323 | PF12202 | 0.281 |
DOC_USP7_MATH_1 | 522 | 526 | PF00917 | 0.384 |
DOC_USP7_MATH_1 | 539 | 543 | PF00917 | 0.208 |
DOC_USP7_MATH_1 | 592 | 596 | PF00917 | 0.227 |
DOC_USP7_MATH_1 | 654 | 658 | PF00917 | 0.136 |
DOC_USP7_MATH_1 | 703 | 707 | PF00917 | 0.311 |
DOC_USP7_UBL2_3 | 128 | 132 | PF12436 | 0.315 |
DOC_USP7_UBL2_3 | 249 | 253 | PF12436 | 0.350 |
DOC_USP7_UBL2_3 | 255 | 259 | PF12436 | 0.373 |
DOC_USP7_UBL2_3 | 795 | 799 | PF12436 | 0.212 |
DOC_USP7_UBL2_3 | 805 | 809 | PF12436 | 0.182 |
DOC_USP7_UBL2_3 | 849 | 853 | PF12436 | 0.197 |
DOC_USP7_UBL2_3 | 857 | 861 | PF12436 | 0.198 |
DOC_WW_Pin1_4 | 207 | 212 | PF00397 | 0.294 |
DOC_WW_Pin1_4 | 694 | 699 | PF00397 | 0.161 |
LIG_14-3-3_CanoR_1 | 226 | 231 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 315 | 322 | PF00244 | 0.266 |
LIG_14-3-3_CanoR_1 | 332 | 340 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 36 | 43 | PF00244 | 0.400 |
LIG_14-3-3_CanoR_1 | 394 | 402 | PF00244 | 0.433 |
LIG_14-3-3_CanoR_1 | 692 | 698 | PF00244 | 0.171 |
LIG_14-3-3_CanoR_1 | 718 | 725 | PF00244 | 0.182 |
LIG_14-3-3_CanoR_1 | 794 | 802 | PF00244 | 0.301 |
LIG_Actin_WH2_2 | 69 | 84 | PF00022 | 0.301 |
LIG_APCC_ABBA_1 | 116 | 121 | PF00400 | 0.255 |
LIG_APCC_ABBA_1 | 446 | 451 | PF00400 | 0.213 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.532 |
LIG_BIR_III_1 | 1 | 5 | PF00653 | 0.445 |
LIG_BIR_III_2 | 551 | 555 | PF00653 | 0.166 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.445 |
LIG_BIR_III_4 | 571 | 575 | PF00653 | 0.192 |
LIG_BRCT_BRCA1_1 | 316 | 320 | PF00533 | 0.310 |
LIG_BRCT_BRCA1_1 | 796 | 800 | PF00533 | 0.301 |
LIG_FHA_1 | 113 | 119 | PF00498 | 0.310 |
LIG_FHA_1 | 134 | 140 | PF00498 | 0.359 |
LIG_FHA_1 | 195 | 201 | PF00498 | 0.257 |
LIG_FHA_1 | 208 | 214 | PF00498 | 0.270 |
LIG_FHA_1 | 304 | 310 | PF00498 | 0.240 |
LIG_FHA_1 | 358 | 364 | PF00498 | 0.324 |
LIG_FHA_1 | 399 | 405 | PF00498 | 0.263 |
LIG_FHA_1 | 684 | 690 | PF00498 | 0.135 |
LIG_FHA_1 | 7 | 13 | PF00498 | 0.310 |
LIG_FHA_2 | 15 | 21 | PF00498 | 0.312 |
LIG_FHA_2 | 226 | 232 | PF00498 | 0.435 |
LIG_FHA_2 | 331 | 337 | PF00498 | 0.278 |
LIG_FHA_2 | 404 | 410 | PF00498 | 0.251 |
LIG_FHA_2 | 498 | 504 | PF00498 | 0.198 |
LIG_FHA_2 | 521 | 527 | PF00498 | 0.401 |
LIG_FHA_2 | 568 | 574 | PF00498 | 0.418 |
LIG_FHA_2 | 602 | 608 | PF00498 | 0.235 |
LIG_FHA_2 | 651 | 657 | PF00498 | 0.337 |
LIG_FHA_2 | 719 | 725 | PF00498 | 0.213 |
LIG_FHA_2 | 811 | 817 | PF00498 | 0.195 |
LIG_Integrin_RGD_1 | 433 | 435 | PF01839 | 0.195 |
LIG_LIR_Apic_2 | 349 | 354 | PF02991 | 0.284 |
LIG_LIR_Gen_1 | 532 | 543 | PF02991 | 0.242 |
LIG_LIR_Gen_1 | 680 | 689 | PF02991 | 0.243 |
LIG_LIR_Gen_1 | 722 | 731 | PF02991 | 0.195 |
LIG_LIR_Nem_3 | 113 | 119 | PF02991 | 0.280 |
LIG_LIR_Nem_3 | 451 | 456 | PF02991 | 0.242 |
LIG_LIR_Nem_3 | 532 | 538 | PF02991 | 0.242 |
LIG_LIR_Nem_3 | 680 | 685 | PF02991 | 0.243 |
LIG_LIR_Nem_3 | 722 | 728 | PF02991 | 0.195 |
LIG_LRP6_Inhibitor_1 | 402 | 408 | PF00058 | 0.252 |
LIG_LYPXL_S_1 | 452 | 456 | PF13949 | 0.213 |
LIG_LYPXL_yS_3 | 453 | 456 | PF13949 | 0.213 |
LIG_MYND_1 | 454 | 458 | PF01753 | 0.195 |
LIG_MYND_1 | 554 | 558 | PF01753 | 0.242 |
LIG_PALB2_WD40_1 | 677 | 685 | PF16756 | 0.213 |
LIG_Pex14_2 | 116 | 120 | PF04695 | 0.264 |
LIG_PTB_Apo_2 | 46 | 53 | PF02174 | 0.298 |
LIG_SH2_GRB2like | 326 | 329 | PF00017 | 0.284 |
LIG_SH2_NCK_1 | 483 | 487 | PF00017 | 0.192 |
LIG_SH2_SRC | 326 | 329 | PF00017 | 0.284 |
LIG_SH2_STAT3 | 278 | 281 | PF00017 | 0.369 |
LIG_SH2_STAT3 | 429 | 432 | PF00017 | 0.177 |
LIG_SH2_STAT5 | 326 | 329 | PF00017 | 0.284 |
LIG_SH2_STAT5 | 483 | 486 | PF00017 | 0.209 |
LIG_SH2_STAT5 | 58 | 61 | PF00017 | 0.211 |
LIG_SH3_3 | 533 | 539 | PF00018 | 0.187 |
LIG_SUMO_SIM_anti_2 | 100 | 105 | PF11976 | 0.242 |
LIG_SUMO_SIM_anti_2 | 197 | 202 | PF11976 | 0.263 |
LIG_SUMO_SIM_anti_2 | 9 | 14 | PF11976 | 0.296 |
LIG_SUMO_SIM_par_1 | 180 | 185 | PF11976 | 0.237 |
LIG_SUMO_SIM_par_1 | 194 | 202 | PF11976 | 0.261 |
LIG_SUMO_SIM_par_1 | 360 | 366 | PF11976 | 0.287 |
LIG_SUMO_SIM_par_1 | 587 | 593 | PF11976 | 0.287 |
LIG_TRAF2_1 | 542 | 545 | PF00917 | 0.417 |
LIG_TRAF2_1 | 604 | 607 | PF00917 | 0.157 |
LIG_TRAF2_1 | 653 | 656 | PF00917 | 0.181 |
LIG_TRAF2_1 | 657 | 660 | PF00917 | 0.180 |
LIG_TRAF2_1 | 661 | 664 | PF00917 | 0.403 |
LIG_TYR_ITIM | 324 | 329 | PF00017 | 0.287 |
LIG_UBA3_1 | 101 | 107 | PF00899 | 0.238 |
LIG_UBA3_1 | 422 | 430 | PF00899 | 0.213 |
LIG_UBA3_1 | 823 | 828 | PF00899 | 0.195 |
MOD_CDK_SPK_2 | 694 | 699 | PF00069 | 0.161 |
MOD_CDK_SPxxK_3 | 207 | 214 | PF00069 | 0.287 |
MOD_CK1_1 | 207 | 213 | PF00069 | 0.271 |
MOD_CK1_1 | 38 | 44 | PF00069 | 0.400 |
MOD_CK1_1 | 392 | 398 | PF00069 | 0.382 |
MOD_CK1_1 | 507 | 513 | PF00069 | 0.214 |
MOD_CK1_1 | 590 | 596 | PF00069 | 0.255 |
MOD_CK1_1 | 600 | 606 | PF00069 | 0.184 |
MOD_CK1_1 | 702 | 708 | PF00069 | 0.255 |
MOD_CK1_1 | 710 | 716 | PF00069 | 0.287 |
MOD_CK1_1 | 737 | 743 | PF00069 | 0.213 |
MOD_CK2_1 | 258 | 264 | PF00069 | 0.467 |
MOD_CK2_1 | 330 | 336 | PF00069 | 0.254 |
MOD_CK2_1 | 403 | 409 | PF00069 | 0.252 |
MOD_CK2_1 | 502 | 508 | PF00069 | 0.252 |
MOD_CK2_1 | 514 | 520 | PF00069 | 0.184 |
MOD_CK2_1 | 522 | 528 | PF00069 | 0.214 |
MOD_CK2_1 | 538 | 544 | PF00069 | 0.135 |
MOD_CK2_1 | 600 | 606 | PF00069 | 0.271 |
MOD_CK2_1 | 621 | 627 | PF00069 | 0.263 |
MOD_CK2_1 | 638 | 644 | PF00069 | 0.218 |
MOD_CK2_1 | 649 | 655 | PF00069 | 0.202 |
MOD_CK2_1 | 658 | 664 | PF00069 | 0.200 |
MOD_CK2_1 | 795 | 801 | PF00069 | 0.207 |
MOD_CK2_1 | 810 | 816 | PF00069 | 0.169 |
MOD_Cter_Amidation | 742 | 745 | PF01082 | 0.192 |
MOD_GlcNHglycan | 365 | 368 | PF01048 | 0.358 |
MOD_GlcNHglycan | 38 | 41 | PF01048 | 0.398 |
MOD_GlcNHglycan | 395 | 398 | PF01048 | 0.310 |
MOD_GlcNHglycan | 503 | 507 | PF01048 | 0.224 |
MOD_GlcNHglycan | 517 | 520 | PF01048 | 0.192 |
MOD_GlcNHglycan | 541 | 544 | PF01048 | 0.210 |
MOD_GlcNHglycan | 564 | 567 | PF01048 | 0.230 |
MOD_GlcNHglycan | 655 | 659 | PF01048 | 0.155 |
MOD_GlcNHglycan | 668 | 671 | PF01048 | 0.185 |
MOD_GlcNHglycan | 676 | 679 | PF01048 | 0.277 |
MOD_GlcNHglycan | 689 | 692 | PF01048 | 0.163 |
MOD_GlcNHglycan | 701 | 704 | PF01048 | 0.134 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.303 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.274 |
MOD_GSK3_1 | 389 | 396 | PF00069 | 0.295 |
MOD_GSK3_1 | 493 | 500 | PF00069 | 0.189 |
MOD_GSK3_1 | 502 | 509 | PF00069 | 0.201 |
MOD_GSK3_1 | 520 | 527 | PF00069 | 0.310 |
MOD_GSK3_1 | 597 | 604 | PF00069 | 0.268 |
MOD_GSK3_1 | 650 | 657 | PF00069 | 0.205 |
MOD_GSK3_1 | 683 | 690 | PF00069 | 0.190 |
MOD_GSK3_1 | 699 | 706 | PF00069 | 0.213 |
MOD_GSK3_1 | 710 | 717 | PF00069 | 0.197 |
MOD_GSK3_1 | 730 | 737 | PF00069 | 0.182 |
MOD_GSK3_1 | 805 | 812 | PF00069 | 0.195 |
MOD_LATS_1 | 34 | 40 | PF00433 | 0.299 |
MOD_N-GLC_1 | 14 | 19 | PF02516 | 0.306 |
MOD_N-GLC_1 | 497 | 502 | PF02516 | 0.155 |
MOD_N-GLC_1 | 539 | 544 | PF02516 | 0.156 |
MOD_N-GLC_1 | 692 | 697 | PF02516 | 0.243 |
MOD_N-GLC_1 | 810 | 815 | PF02516 | 0.213 |
MOD_NEK2_1 | 133 | 138 | PF00069 | 0.273 |
MOD_NEK2_1 | 163 | 168 | PF00069 | 0.313 |
MOD_NEK2_1 | 267 | 272 | PF00069 | 0.352 |
MOD_NEK2_1 | 35 | 40 | PF00069 | 0.298 |
MOD_NEK2_1 | 357 | 362 | PF00069 | 0.356 |
MOD_NEK2_1 | 363 | 368 | PF00069 | 0.363 |
MOD_NEK2_1 | 382 | 387 | PF00069 | 0.459 |
MOD_NEK2_1 | 461 | 466 | PF00069 | 0.265 |
MOD_NEK2_1 | 599 | 604 | PF00069 | 0.213 |
MOD_NEK2_1 | 6 | 11 | PF00069 | 0.362 |
MOD_NEK2_1 | 714 | 719 | PF00069 | 0.268 |
MOD_NEK2_1 | 810 | 815 | PF00069 | 0.210 |
MOD_NEK2_1 | 824 | 829 | PF00069 | 0.195 |
MOD_NEK2_1 | 837 | 842 | PF00069 | 0.176 |
MOD_NEK2_1 | 97 | 102 | PF00069 | 0.184 |
MOD_NEK2_2 | 403 | 408 | PF00069 | 0.249 |
MOD_PIKK_1 | 352 | 358 | PF00454 | 0.298 |
MOD_PIKK_1 | 41 | 47 | PF00454 | 0.411 |
MOD_PIKK_1 | 590 | 596 | PF00454 | 0.305 |
MOD_PIKK_1 | 730 | 736 | PF00454 | 0.192 |
MOD_PIKK_1 | 827 | 833 | PF00454 | 0.187 |
MOD_PK_1 | 226 | 232 | PF00069 | 0.427 |
MOD_PKA_1 | 258 | 264 | PF00069 | 0.381 |
MOD_PKA_1 | 778 | 784 | PF00069 | 0.202 |
MOD_PKA_1 | 794 | 800 | PF00069 | 0.227 |
MOD_PKA_1 | 803 | 809 | PF00069 | 0.176 |
MOD_PKA_2 | 225 | 231 | PF00069 | 0.476 |
MOD_PKA_2 | 314 | 320 | PF00069 | 0.333 |
MOD_PKA_2 | 35 | 41 | PF00069 | 0.365 |
MOD_PKA_2 | 393 | 399 | PF00069 | 0.410 |
MOD_PKA_2 | 461 | 467 | PF00069 | 0.277 |
MOD_PKA_2 | 6 | 12 | PF00069 | 0.339 |
MOD_PKA_2 | 691 | 697 | PF00069 | 0.140 |
MOD_PKA_2 | 778 | 784 | PF00069 | 0.259 |
MOD_PKA_2 | 803 | 809 | PF00069 | 0.192 |
MOD_PKA_2 | 843 | 849 | PF00069 | 0.301 |
MOD_Plk_1 | 112 | 118 | PF00069 | 0.267 |
MOD_Plk_1 | 126 | 132 | PF00069 | 0.281 |
MOD_Plk_1 | 194 | 200 | PF00069 | 0.265 |
MOD_Plk_2-3 | 194 | 200 | PF00069 | 0.312 |
MOD_Plk_2-3 | 20 | 26 | PF00069 | 0.371 |
MOD_Plk_2-3 | 520 | 526 | PF00069 | 0.257 |
MOD_Plk_2-3 | 546 | 552 | PF00069 | 0.315 |
MOD_Plk_2-3 | 601 | 607 | PF00069 | 0.280 |
MOD_Plk_2-3 | 621 | 627 | PF00069 | 0.158 |
MOD_Plk_2-3 | 638 | 644 | PF00069 | 0.314 |
MOD_Plk_4 | 38 | 44 | PF00069 | 0.350 |
MOD_Plk_4 | 6 | 12 | PF00069 | 0.310 |
MOD_Plk_4 | 97 | 103 | PF00069 | 0.301 |
MOD_ProDKin_1 | 207 | 213 | PF00069 | 0.287 |
MOD_ProDKin_1 | 694 | 700 | PF00069 | 0.161 |
MOD_SUMO_for_1 | 785 | 788 | PF00179 | 0.277 |
MOD_SUMO_rev_2 | 850 | 858 | PF00179 | 0.195 |
TRG_DiLeu_BaEn_4 | 663 | 669 | PF01217 | 0.187 |
TRG_DiLeu_BaLyEn_6 | 294 | 299 | PF01217 | 0.279 |
TRG_DiLeu_BaLyEn_6 | 305 | 310 | PF01217 | 0.269 |
TRG_DiLeu_BaLyEn_6 | 320 | 325 | PF01217 | 0.281 |
TRG_DiLeu_BaLyEn_6 | 378 | 383 | PF01217 | 0.361 |
TRG_DiLeu_BaLyEn_6 | 715 | 720 | PF01217 | 0.301 |
TRG_ENDOCYTIC_2 | 326 | 329 | PF00928 | 0.280 |
TRG_ENDOCYTIC_2 | 345 | 348 | PF00928 | 0.193 |
TRG_ENDOCYTIC_2 | 449 | 452 | PF00928 | 0.201 |
TRG_ENDOCYTIC_2 | 453 | 456 | PF00928 | 0.189 |
TRG_ENDOCYTIC_2 | 483 | 486 | PF00928 | 0.211 |
TRG_ER_diArg_1 | 16 | 19 | PF00400 | 0.332 |
TRG_ER_diArg_1 | 187 | 190 | PF00400 | 0.274 |
TRG_ER_diArg_1 | 580 | 583 | PF00400 | 0.296 |
TRG_ER_diArg_1 | 802 | 804 | PF00400 | 0.206 |
TRG_NLS_Bipartite_1 | 258 | 279 | PF00514 | 0.291 |
TRG_NLS_Bipartite_1 | 794 | 808 | PF00514 | 0.211 |
TRG_NLS_MonoExtC_3 | 578 | 584 | PF00514 | 0.228 |
TRG_NLS_MonoExtN_4 | 272 | 279 | PF00514 | 0.304 |
TRG_NLS_MonoExtN_4 | 577 | 583 | PF00514 | 0.278 |
TRG_NLS_MonoExtN_4 | 803 | 808 | PF00514 | 0.194 |
TRG_Pf-PMV_PEXEL_1 | 297 | 301 | PF00026 | 0.321 |
TRG_Pf-PMV_PEXEL_1 | 424 | 428 | PF00026 | 0.212 |
TRG_Pf-PMV_PEXEL_1 | 443 | 447 | PF00026 | 0.139 |
TRG_Pf-PMV_PEXEL_1 | 46 | 51 | PF00026 | 0.399 |
TRG_Pf-PMV_PEXEL_1 | 718 | 722 | PF00026 | 0.195 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7R9 | Leptomonas seymouri | 73% | 100% |
A0A0S4J2U0 | Bodo saltans | 59% | 97% |
A0A1X0NT40 | Trypanosomatidae | 71% | 100% |
A0A3S5H720 | Leishmania donovani | 91% | 99% |
A4H993 | Leishmania braziliensis | 82% | 99% |
A4HXL4 | Leishmania infantum | 92% | 99% |
C9ZPA8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 60% | 100% |
P53313 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 31% | 100% |
Q4QE53 | Leishmania major | 92% | 100% |
Q6NV26 | Danio rerio | 35% | 100% |