Homologous to endosomal / ER-localized phospholipid flippases of other Eukaryotes.. These genes only duplicated in Trypasoma conorini and Trypansoma cruzi. Localization: ER (by homology) / Endosomal (by homology)
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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
GO:0005768 | endosome | 7 | 1 |
GO:0005802 | trans-Golgi network | 4 | 1 |
GO:0005886 | plasma membrane | 3 | 1 |
GO:0031410 | cytoplasmic vesicle | 6 | 1 |
GO:0031982 | vesicle | 4 | 1 |
GO:0031984 | organelle subcompartment | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0097708 | intracellular vesicle | 5 | 1 |
GO:0098791 | Golgi apparatus subcompartment | 3 | 1 |
Related structures:
AlphaFold database: A0A3Q8INM6
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 11 |
GO:0006869 | lipid transport | 5 | 11 |
GO:0015748 | organophosphate ester transport | 5 | 11 |
GO:0015914 | phospholipid transport | 6 | 11 |
GO:0051179 | localization | 1 | 11 |
GO:0051234 | establishment of localization | 2 | 11 |
GO:0071702 | organic substance transport | 4 | 11 |
GO:0006890 | retrograde vesicle-mediated transport, Golgi to endoplasmic reticulum | 6 | 1 |
GO:0006897 | endocytosis | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0016192 | vesicle-mediated transport | 4 | 1 |
GO:0034204 | lipid translocation | 4 | 1 |
GO:0045332 | phospholipid translocation | 5 | 1 |
GO:0048193 | Golgi vesicle transport | 5 | 1 |
GO:0061024 | membrane organization | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0065008 | regulation of biological quality | 2 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0097035 | regulation of membrane lipid distribution | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0000287 | magnesium ion binding | 5 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0005215 | transporter activity | 1 | 11 |
GO:0005319 | lipid transporter activity | 2 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0005524 | ATP binding | 5 | 11 |
GO:0016462 | pyrophosphatase activity | 5 | 11 |
GO:0016787 | hydrolase activity | 2 | 11 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 11 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 11 |
GO:0016887 | ATP hydrolysis activity | 7 | 11 |
GO:0017076 | purine nucleotide binding | 4 | 11 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 11 |
GO:0030554 | adenyl nucleotide binding | 5 | 11 |
GO:0032553 | ribonucleotide binding | 3 | 11 |
GO:0032555 | purine ribonucleotide binding | 4 | 11 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 11 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 11 |
GO:0036094 | small molecule binding | 2 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043168 | anion binding | 3 | 11 |
GO:0043169 | cation binding | 3 | 11 |
GO:0046872 | metal ion binding | 4 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:0097367 | carbohydrate derivative binding | 2 | 11 |
GO:0140303 | intramembrane lipid transporter activity | 3 | 11 |
GO:0140326 | ATPase-coupled intramembrane lipid transporter activity | 2 | 11 |
GO:0140657 | ATP-dependent activity | 1 | 11 |
GO:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 246 | 250 | PF00656 | 0.443 |
CLV_C14_Caspase3-7 | 870 | 874 | PF00656 | 0.621 |
CLV_MEL_PAP_1 | 498 | 504 | PF00089 | 0.390 |
CLV_NRD_NRD_1 | 1078 | 1080 | PF00675 | 0.244 |
CLV_NRD_NRD_1 | 116 | 118 | PF00675 | 0.255 |
CLV_NRD_NRD_1 | 184 | 186 | PF00675 | 0.338 |
CLV_NRD_NRD_1 | 624 | 626 | PF00675 | 0.234 |
CLV_NRD_NRD_1 | 74 | 76 | PF00675 | 0.422 |
CLV_PCSK_FUR_1 | 1076 | 1080 | PF00082 | 0.330 |
CLV_PCSK_FUR_1 | 182 | 186 | PF00082 | 0.349 |
CLV_PCSK_KEX2_1 | 1078 | 1080 | PF00082 | 0.243 |
CLV_PCSK_KEX2_1 | 116 | 118 | PF00082 | 0.255 |
CLV_PCSK_KEX2_1 | 181 | 183 | PF00082 | 0.328 |
CLV_PCSK_KEX2_1 | 184 | 186 | PF00082 | 0.317 |
CLV_PCSK_KEX2_1 | 74 | 76 | PF00082 | 0.421 |
CLV_PCSK_PC1ET2_1 | 181 | 183 | PF00082 | 0.340 |
CLV_PCSK_SKI1_1 | 1007 | 1011 | PF00082 | 0.249 |
CLV_PCSK_SKI1_1 | 1018 | 1022 | PF00082 | 0.232 |
CLV_PCSK_SKI1_1 | 1081 | 1085 | PF00082 | 0.330 |
CLV_PCSK_SKI1_1 | 1109 | 1113 | PF00082 | 0.456 |
CLV_PCSK_SKI1_1 | 1140 | 1144 | PF00082 | 0.296 |
CLV_PCSK_SKI1_1 | 174 | 178 | PF00082 | 0.355 |
CLV_PCSK_SKI1_1 | 333 | 337 | PF00082 | 0.304 |
CLV_PCSK_SKI1_1 | 438 | 442 | PF00082 | 0.377 |
CLV_PCSK_SKI1_1 | 492 | 496 | PF00082 | 0.527 |
CLV_PCSK_SKI1_1 | 595 | 599 | PF00082 | 0.304 |
CLV_PCSK_SKI1_1 | 78 | 82 | PF00082 | 0.425 |
CLV_TASPASE1 | 247 | 253 | PF01112 | 0.443 |
DEG_APCC_DBOX_1 | 1017 | 1025 | PF00400 | 0.468 |
DEG_APCC_DBOX_1 | 341 | 349 | PF00400 | 0.456 |
DEG_APCC_DBOX_1 | 491 | 499 | PF00400 | 0.587 |
DEG_APCC_DBOX_1 | 73 | 81 | PF00400 | 0.636 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.750 |
DEG_ODPH_VHL_1 | 85 | 96 | PF01847 | 0.615 |
DOC_ANK_TNKS_1 | 874 | 881 | PF00023 | 0.472 |
DOC_CDC14_PxL_1 | 83 | 91 | PF14671 | 0.520 |
DOC_CYCLIN_RxL_1 | 435 | 445 | PF00134 | 0.575 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 350 | 358 | PF00134 | 0.456 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 426 | 434 | PF00134 | 0.585 |
DOC_CYCLIN_yCln2_LP_2 | 81 | 87 | PF00134 | 0.622 |
DOC_MAPK_gen_1 | 1076 | 1086 | PF00069 | 0.465 |
DOC_MAPK_gen_1 | 184 | 193 | PF00069 | 0.617 |
DOC_MAPK_gen_1 | 452 | 460 | PF00069 | 0.603 |
DOC_MAPK_gen_1 | 583 | 592 | PF00069 | 0.519 |
DOC_MAPK_gen_1 | 625 | 632 | PF00069 | 0.434 |
DOC_MAPK_gen_1 | 74 | 85 | PF00069 | 0.592 |
DOC_MAPK_MEF2A_6 | 583 | 592 | PF00069 | 0.455 |
DOC_MAPK_MEF2A_6 | 625 | 632 | PF00069 | 0.434 |
DOC_MAPK_MEF2A_6 | 78 | 85 | PF00069 | 0.606 |
DOC_MAPK_MEF2A_6 | 916 | 925 | PF00069 | 0.455 |
DOC_MAPK_NFAT4_5 | 78 | 86 | PF00069 | 0.633 |
DOC_PP1_RVXF_1 | 1070 | 1076 | PF00149 | 0.446 |
DOC_PP1_RVXF_1 | 1138 | 1145 | PF00149 | 0.530 |
DOC_PP1_RVXF_1 | 151 | 157 | PF00149 | 0.255 |
DOC_PP1_RVXF_1 | 680 | 687 | PF00149 | 0.475 |
DOC_PP1_RVXF_1 | 920 | 927 | PF00149 | 0.443 |
DOC_PP2B_LxvP_1 | 63 | 66 | PF13499 | 0.576 |
DOC_PP2B_LxvP_1 | 81 | 84 | PF13499 | 0.620 |
DOC_PP2B_PxIxI_1 | 1145 | 1151 | PF00149 | 0.634 |
DOC_SPAK_OSR1_1 | 275 | 279 | PF12202 | 0.545 |
DOC_SPAK_OSR1_1 | 386 | 390 | PF12202 | 0.443 |
DOC_USP7_MATH_1 | 1053 | 1057 | PF00917 | 0.311 |
DOC_USP7_MATH_1 | 259 | 263 | PF00917 | 0.545 |
DOC_USP7_MATH_1 | 335 | 339 | PF00917 | 0.484 |
DOC_USP7_MATH_1 | 500 | 504 | PF00917 | 0.655 |
DOC_USP7_MATH_1 | 58 | 62 | PF00917 | 0.683 |
DOC_USP7_MATH_1 | 620 | 624 | PF00917 | 0.443 |
DOC_USP7_UBL2_3 | 1007 | 1011 | PF12436 | 0.443 |
DOC_USP7_UBL2_3 | 450 | 454 | PF12436 | 0.607 |
DOC_USP7_UBL2_3 | 649 | 653 | PF12436 | 0.457 |
DOC_WW_Pin1_4 | 101 | 106 | PF00397 | 0.609 |
DOC_WW_Pin1_4 | 159 | 164 | PF00397 | 0.319 |
DOC_WW_Pin1_4 | 21 | 26 | PF00397 | 0.769 |
DOC_WW_Pin1_4 | 337 | 342 | PF00397 | 0.545 |
DOC_WW_Pin1_4 | 528 | 533 | PF00397 | 0.491 |
DOC_WW_Pin1_4 | 572 | 577 | PF00397 | 0.441 |
DOC_WW_Pin1_4 | 853 | 858 | PF00397 | 0.488 |
LIG_14-3-3_CanoR_1 | 116 | 121 | PF00244 | 0.455 |
LIG_14-3-3_CanoR_1 | 18 | 27 | PF00244 | 0.779 |
LIG_14-3-3_CanoR_1 | 207 | 213 | PF00244 | 0.513 |
LIG_14-3-3_CanoR_1 | 407 | 413 | PF00244 | 0.494 |
LIG_14-3-3_CanoR_1 | 438 | 448 | PF00244 | 0.551 |
LIG_14-3-3_CanoR_1 | 501 | 505 | PF00244 | 0.718 |
LIG_14-3-3_CanoR_1 | 689 | 696 | PF00244 | 0.524 |
LIG_14-3-3_CanoR_1 | 845 | 851 | PF00244 | 0.531 |
LIG_14-3-3_CanoR_1 | 929 | 933 | PF00244 | 0.443 |
LIG_14-3-3_CanoR_1 | 937 | 943 | PF00244 | 0.443 |
LIG_APCC_ABBA_1 | 217 | 222 | PF00400 | 0.530 |
LIG_APCC_ABBAyCdc20_2 | 46 | 52 | PF00400 | 0.610 |
LIG_BRCT_BRCA1_1 | 1043 | 1047 | PF00533 | 0.345 |
LIG_BRCT_BRCA1_1 | 956 | 960 | PF00533 | 0.295 |
LIG_BRCT_BRCA1_1 | 976 | 980 | PF00533 | 0.113 |
LIG_CtBP_PxDLS_1 | 396 | 400 | PF00389 | 0.443 |
LIG_CtBP_PxDLS_1 | 431 | 435 | PF00389 | 0.474 |
LIG_deltaCOP1_diTrp_1 | 178 | 183 | PF00928 | 0.592 |
LIG_FHA_1 | 1053 | 1059 | PF00498 | 0.286 |
LIG_FHA_1 | 1066 | 1072 | PF00498 | 0.311 |
LIG_FHA_1 | 22 | 28 | PF00498 | 0.770 |
LIG_FHA_1 | 238 | 244 | PF00498 | 0.441 |
LIG_FHA_1 | 261 | 267 | PF00498 | 0.464 |
LIG_FHA_1 | 291 | 297 | PF00498 | 0.510 |
LIG_FHA_1 | 316 | 322 | PF00498 | 0.486 |
LIG_FHA_1 | 443 | 449 | PF00498 | 0.470 |
LIG_FHA_1 | 469 | 475 | PF00498 | 0.649 |
LIG_FHA_1 | 610 | 616 | PF00498 | 0.524 |
LIG_FHA_1 | 775 | 781 | PF00498 | 0.484 |
LIG_FHA_1 | 820 | 826 | PF00498 | 0.479 |
LIG_FHA_1 | 933 | 939 | PF00498 | 0.530 |
LIG_FHA_1 | 962 | 968 | PF00498 | 0.255 |
LIG_FHA_2 | 326 | 332 | PF00498 | 0.434 |
LIG_FHA_2 | 541 | 547 | PF00498 | 0.730 |
LIG_FHA_2 | 591 | 597 | PF00498 | 0.484 |
LIG_FHA_2 | 688 | 694 | PF00498 | 0.542 |
LIG_FHA_2 | 733 | 739 | PF00498 | 0.474 |
LIG_GBD_Chelix_1 | 1090 | 1098 | PF00786 | 0.423 |
LIG_Integrin_RGD_1 | 377 | 379 | PF01839 | 0.330 |
LIG_LIR_Apic_2 | 159 | 163 | PF02991 | 0.311 |
LIG_LIR_Gen_1 | 1044 | 1054 | PF02991 | 0.259 |
LIG_LIR_Gen_1 | 367 | 376 | PF02991 | 0.477 |
LIG_LIR_Gen_1 | 379 | 388 | PF02991 | 0.449 |
LIG_LIR_Gen_1 | 838 | 848 | PF02991 | 0.506 |
LIG_LIR_Gen_1 | 954 | 961 | PF02991 | 0.417 |
LIG_LIR_LC3C_4 | 318 | 323 | PF02991 | 0.545 |
LIG_LIR_Nem_3 | 1001 | 1005 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 102 | 106 | PF02991 | 0.618 |
LIG_LIR_Nem_3 | 1044 | 1050 | PF02991 | 0.273 |
LIG_LIR_Nem_3 | 1051 | 1057 | PF02991 | 0.242 |
LIG_LIR_Nem_3 | 1116 | 1121 | PF02991 | 0.260 |
LIG_LIR_Nem_3 | 121 | 126 | PF02991 | 0.327 |
LIG_LIR_Nem_3 | 159 | 164 | PF02991 | 0.327 |
LIG_LIR_Nem_3 | 178 | 183 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 192 | 197 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 367 | 371 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 593 | 597 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 838 | 843 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 846 | 851 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 954 | 959 | PF02991 | 0.332 |
LIG_LIR_Nem_3 | 966 | 971 | PF02991 | 0.192 |
LIG_LYPXL_yS_3 | 1002 | 1005 | PF13949 | 0.530 |
LIG_NRBOX | 365 | 371 | PF00104 | 0.502 |
LIG_PCNA_yPIPBox_3 | 400 | 409 | PF02747 | 0.491 |
LIG_PCNA_yPIPBox_3 | 678 | 689 | PF02747 | 0.486 |
LIG_Pex14_1 | 1025 | 1029 | PF04695 | 0.295 |
LIG_Pex14_1 | 254 | 258 | PF04695 | 0.443 |
LIG_Pex14_2 | 1107 | 1111 | PF04695 | 0.279 |
LIG_Pex14_2 | 132 | 136 | PF04695 | 0.443 |
LIG_Pex14_2 | 376 | 380 | PF04695 | 0.477 |
LIG_Pex14_2 | 384 | 388 | PF04695 | 0.462 |
LIG_Pex14_2 | 956 | 960 | PF04695 | 0.311 |
LIG_Pex14_2 | 99 | 103 | PF04695 | 0.636 |
LIG_PTB_Apo_2 | 112 | 119 | PF02174 | 0.455 |
LIG_PTB_Apo_2 | 134 | 141 | PF02174 | 0.295 |
LIG_PTB_Phospho_1 | 112 | 118 | PF10480 | 0.455 |
LIG_PTB_Phospho_1 | 134 | 140 | PF10480 | 0.311 |
LIG_SH2_CRK | 1054 | 1058 | PF00017 | 0.295 |
LIG_SH2_CRK | 6 | 10 | PF00017 | 0.740 |
LIG_SH2_CRK | 848 | 852 | PF00017 | 0.477 |
LIG_SH2_CRK | 949 | 953 | PF00017 | 0.293 |
LIG_SH2_CRK | 976 | 980 | PF00017 | 0.311 |
LIG_SH2_NCK_1 | 949 | 953 | PF00017 | 0.295 |
LIG_SH2_NCK_1 | 976 | 980 | PF00017 | 0.282 |
LIG_SH2_STAP1 | 1054 | 1058 | PF00017 | 0.295 |
LIG_SH2_STAP1 | 410 | 414 | PF00017 | 0.477 |
LIG_SH2_STAP1 | 703 | 707 | PF00017 | 0.604 |
LIG_SH2_STAP1 | 848 | 852 | PF00017 | 0.477 |
LIG_SH2_STAP1 | 976 | 980 | PF00017 | 0.311 |
LIG_SH2_STAT5 | 1054 | 1057 | PF00017 | 0.311 |
LIG_SH2_STAT5 | 1141 | 1144 | PF00017 | 0.567 |
LIG_SH2_STAT5 | 118 | 121 | PF00017 | 0.313 |
LIG_SH2_STAT5 | 140 | 143 | PF00017 | 0.296 |
LIG_SH2_STAT5 | 160 | 163 | PF00017 | 0.113 |
LIG_SH2_STAT5 | 327 | 330 | PF00017 | 0.504 |
LIG_SH2_STAT5 | 439 | 442 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 481 | 484 | PF00017 | 0.599 |
LIG_SH2_STAT5 | 788 | 791 | PF00017 | 0.548 |
LIG_SH2_STAT5 | 832 | 835 | PF00017 | 0.563 |
LIG_SH2_STAT5 | 971 | 974 | PF00017 | 0.295 |
LIG_SH2_STAT5 | 98 | 101 | PF00017 | 0.641 |
LIG_SH3_2 | 35 | 40 | PF14604 | 0.662 |
LIG_SH3_3 | 103 | 109 | PF00018 | 0.580 |
LIG_SH3_3 | 1098 | 1104 | PF00018 | 0.417 |
LIG_SH3_3 | 32 | 38 | PF00018 | 0.757 |
LIG_SH3_3 | 415 | 421 | PF00018 | 0.609 |
LIG_SH3_3 | 81 | 87 | PF00018 | 0.620 |
LIG_SUMO_SIM_anti_2 | 1060 | 1066 | PF11976 | 0.285 |
LIG_SUMO_SIM_anti_2 | 1088 | 1095 | PF11976 | 0.411 |
LIG_SUMO_SIM_anti_2 | 215 | 220 | PF11976 | 0.446 |
LIG_SUMO_SIM_anti_2 | 577 | 583 | PF11976 | 0.530 |
LIG_SUMO_SIM_par_1 | 1099 | 1106 | PF11976 | 0.282 |
LIG_SUMO_SIM_par_1 | 202 | 209 | PF11976 | 0.539 |
LIG_SUMO_SIM_par_1 | 361 | 367 | PF11976 | 0.466 |
LIG_SUMO_SIM_par_1 | 536 | 548 | PF11976 | 0.719 |
LIG_SUMO_SIM_par_1 | 821 | 826 | PF11976 | 0.453 |
LIG_SxIP_EBH_1 | 388 | 400 | PF03271 | 0.530 |
LIG_TRAF2_1 | 477 | 480 | PF00917 | 0.625 |
LIG_TRAF2_1 | 643 | 646 | PF00917 | 0.525 |
LIG_TYR_ITIM | 1052 | 1057 | PF00017 | 0.311 |
LIG_TYR_ITIM | 138 | 143 | PF00017 | 0.288 |
LIG_TYR_ITIM | 266 | 271 | PF00017 | 0.417 |
LIG_TYR_ITIM | 4 | 9 | PF00017 | 0.705 |
LIG_TYR_ITIM | 592 | 597 | PF00017 | 0.417 |
LIG_TYR_ITIM | 947 | 952 | PF00017 | 0.381 |
LIG_TYR_ITSM | 844 | 851 | PF00017 | 0.391 |
LIG_UBA3_1 | 1035 | 1043 | PF00899 | 0.438 |
LIG_UBA3_1 | 1133 | 1140 | PF00899 | 0.438 |
LIG_Vh1_VBS_1 | 1084 | 1102 | PF01044 | 0.438 |
LIG_WRC_WIRS_1 | 120 | 125 | PF05994 | 0.295 |
LIG_WRC_WIRS_1 | 287 | 292 | PF05994 | 0.381 |
LIG_WRC_WIRS_1 | 365 | 370 | PF05994 | 0.381 |
MOD_CDK_SPK_2 | 337 | 342 | PF00069 | 0.438 |
MOD_CDK_SPxxK_3 | 337 | 344 | PF00069 | 0.438 |
MOD_CDK_SPxxK_3 | 853 | 860 | PF00069 | 0.351 |
MOD_CK1_1 | 1014 | 1020 | PF00069 | 0.353 |
MOD_CK1_1 | 19 | 25 | PF00069 | 0.732 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.321 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.732 |
MOD_CK1_1 | 442 | 448 | PF00069 | 0.413 |
MOD_CK1_1 | 53 | 59 | PF00069 | 0.591 |
MOD_CK1_1 | 566 | 572 | PF00069 | 0.581 |
MOD_CK1_1 | 640 | 646 | PF00069 | 0.424 |
MOD_CK1_1 | 835 | 841 | PF00069 | 0.485 |
MOD_CK2_1 | 325 | 331 | PF00069 | 0.381 |
MOD_CK2_1 | 540 | 546 | PF00069 | 0.697 |
MOD_CK2_1 | 572 | 578 | PF00069 | 0.282 |
MOD_CK2_1 | 640 | 646 | PF00069 | 0.424 |
MOD_CK2_1 | 687 | 693 | PF00069 | 0.469 |
MOD_CK2_1 | 732 | 738 | PF00069 | 0.357 |
MOD_CMANNOS | 1115 | 1118 | PF00535 | 0.330 |
MOD_GlcNHglycan | 236 | 240 | PF01048 | 0.328 |
MOD_GlcNHglycan | 30 | 33 | PF01048 | 0.752 |
MOD_GlcNHglycan | 333 | 336 | PF01048 | 0.361 |
MOD_GlcNHglycan | 498 | 501 | PF01048 | 0.617 |
MOD_GlcNHglycan | 639 | 642 | PF01048 | 0.421 |
MOD_GSK3_1 | 1048 | 1055 | PF00069 | 0.299 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.388 |
MOD_GSK3_1 | 1085 | 1092 | PF00069 | 0.409 |
MOD_GSK3_1 | 16 | 23 | PF00069 | 0.759 |
MOD_GSK3_1 | 202 | 209 | PF00069 | 0.313 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.317 |
MOD_GSK3_1 | 286 | 293 | PF00069 | 0.358 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.253 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.324 |
MOD_GSK3_1 | 408 | 415 | PF00069 | 0.460 |
MOD_GSK3_1 | 442 | 449 | PF00069 | 0.324 |
MOD_GSK3_1 | 464 | 471 | PF00069 | 0.559 |
MOD_GSK3_1 | 496 | 503 | PF00069 | 0.680 |
MOD_GSK3_1 | 504 | 511 | PF00069 | 0.613 |
MOD_GSK3_1 | 540 | 547 | PF00069 | 0.732 |
MOD_GSK3_1 | 559 | 566 | PF00069 | 0.722 |
MOD_GSK3_1 | 596 | 603 | PF00069 | 0.317 |
MOD_GSK3_1 | 611 | 618 | PF00069 | 0.241 |
MOD_GSK3_1 | 633 | 640 | PF00069 | 0.352 |
MOD_GSK3_1 | 685 | 692 | PF00069 | 0.467 |
MOD_GSK3_1 | 769 | 776 | PF00069 | 0.380 |
MOD_GSK3_1 | 928 | 935 | PF00069 | 0.293 |
MOD_GSK3_1 | 947 | 954 | PF00069 | 0.188 |
MOD_GSK3_1 | 974 | 981 | PF00069 | 0.311 |
MOD_N-GLC_1 | 20 | 25 | PF02516 | 0.755 |
MOD_N-GLC_1 | 260 | 265 | PF02516 | 0.378 |
MOD_N-GLC_1 | 336 | 341 | PF02516 | 0.295 |
MOD_N-GLC_1 | 496 | 501 | PF02516 | 0.693 |
MOD_N-GLC_1 | 528 | 533 | PF02516 | 0.362 |
MOD_N-GLC_1 | 994 | 999 | PF02516 | 0.438 |
MOD_NEK2_1 | 1111 | 1116 | PF00069 | 0.300 |
MOD_NEK2_1 | 143 | 148 | PF00069 | 0.305 |
MOD_NEK2_1 | 156 | 161 | PF00069 | 0.287 |
MOD_NEK2_1 | 260 | 265 | PF00069 | 0.311 |
MOD_NEK2_1 | 336 | 341 | PF00069 | 0.296 |
MOD_NEK2_1 | 364 | 369 | PF00069 | 0.359 |
MOD_NEK2_1 | 390 | 395 | PF00069 | 0.414 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.548 |
MOD_NEK2_1 | 584 | 589 | PF00069 | 0.308 |
MOD_NEK2_1 | 729 | 734 | PF00069 | 0.444 |
MOD_NEK2_1 | 867 | 872 | PF00069 | 0.520 |
MOD_NEK2_1 | 912 | 917 | PF00069 | 0.311 |
MOD_NEK2_1 | 960 | 965 | PF00069 | 0.333 |
MOD_NEK2_1 | 974 | 979 | PF00069 | 0.295 |
MOD_NEK2_2 | 500 | 505 | PF00069 | 0.678 |
MOD_NEK2_2 | 932 | 937 | PF00069 | 0.311 |
MOD_NEK2_2 | 975 | 980 | PF00069 | 0.284 |
MOD_OFUCOSY | 809 | 814 | PF10250 | 0.581 |
MOD_PIKK_1 | 143 | 149 | PF00454 | 0.295 |
MOD_PIKK_1 | 563 | 569 | PF00454 | 0.497 |
MOD_PIKK_1 | 641 | 647 | PF00454 | 0.263 |
MOD_PIKK_1 | 855 | 861 | PF00454 | 0.357 |
MOD_PIKK_1 | 936 | 942 | PF00454 | 0.305 |
MOD_PK_1 | 658 | 664 | PF00069 | 0.454 |
MOD_PK_1 | 69 | 75 | PF00069 | 0.422 |
MOD_PKA_1 | 116 | 122 | PF00069 | 0.311 |
MOD_PKA_1 | 69 | 75 | PF00069 | 0.511 |
MOD_PKA_2 | 116 | 122 | PF00069 | 0.284 |
MOD_PKA_2 | 19 | 25 | PF00069 | 0.578 |
MOD_PKA_2 | 206 | 212 | PF00069 | 0.393 |
MOD_PKA_2 | 329 | 335 | PF00069 | 0.396 |
MOD_PKA_2 | 468 | 474 | PF00069 | 0.568 |
MOD_PKA_2 | 500 | 506 | PF00069 | 0.678 |
MOD_PKA_2 | 663 | 669 | PF00069 | 0.405 |
MOD_PKA_2 | 774 | 780 | PF00069 | 0.365 |
MOD_PKA_2 | 867 | 873 | PF00069 | 0.531 |
MOD_PKA_2 | 928 | 934 | PF00069 | 0.285 |
MOD_PKA_2 | 936 | 942 | PF00069 | 0.277 |
MOD_PKB_1 | 18 | 26 | PF00069 | 0.761 |
MOD_PKB_1 | 633 | 641 | PF00069 | 0.417 |
MOD_Plk_1 | 50 | 56 | PF00069 | 0.707 |
MOD_Plk_1 | 595 | 601 | PF00069 | 0.383 |
MOD_Plk_1 | 727 | 733 | PF00069 | 0.439 |
MOD_Plk_1 | 884 | 890 | PF00069 | 0.370 |
MOD_Plk_1 | 910 | 916 | PF00069 | 0.282 |
MOD_Plk_2-3 | 302 | 308 | PF00069 | 0.330 |
MOD_Plk_4 | 1024 | 1030 | PF00069 | 0.324 |
MOD_Plk_4 | 1053 | 1059 | PF00069 | 0.295 |
MOD_Plk_4 | 1089 | 1095 | PF00069 | 0.318 |
MOD_Plk_4 | 119 | 125 | PF00069 | 0.307 |
MOD_Plk_4 | 168 | 174 | PF00069 | 0.305 |
MOD_Plk_4 | 238 | 244 | PF00069 | 0.417 |
MOD_Plk_4 | 317 | 323 | PF00069 | 0.370 |
MOD_Plk_4 | 364 | 370 | PF00069 | 0.361 |
MOD_Plk_4 | 390 | 396 | PF00069 | 0.388 |
MOD_Plk_4 | 461 | 467 | PF00069 | 0.417 |
MOD_Plk_4 | 58 | 64 | PF00069 | 0.612 |
MOD_Plk_4 | 611 | 617 | PF00069 | 0.398 |
MOD_Plk_4 | 658 | 664 | PF00069 | 0.388 |
MOD_Plk_4 | 813 | 819 | PF00069 | 0.576 |
MOD_Plk_4 | 835 | 841 | PF00069 | 0.437 |
MOD_Plk_4 | 846 | 852 | PF00069 | 0.331 |
MOD_Plk_4 | 862 | 868 | PF00069 | 0.239 |
MOD_Plk_4 | 884 | 890 | PF00069 | 0.357 |
MOD_Plk_4 | 947 | 953 | PF00069 | 0.290 |
MOD_Plk_4 | 963 | 969 | PF00069 | 0.255 |
MOD_Plk_4 | 975 | 981 | PF00069 | 0.282 |
MOD_ProDKin_1 | 101 | 107 | PF00069 | 0.523 |
MOD_ProDKin_1 | 159 | 165 | PF00069 | 0.319 |
MOD_ProDKin_1 | 21 | 27 | PF00069 | 0.754 |
MOD_ProDKin_1 | 337 | 343 | PF00069 | 0.438 |
MOD_ProDKin_1 | 528 | 534 | PF00069 | 0.373 |
MOD_ProDKin_1 | 572 | 578 | PF00069 | 0.292 |
MOD_ProDKin_1 | 853 | 859 | PF00069 | 0.356 |
MOD_SUMO_rev_2 | 175 | 183 | PF00179 | 0.441 |
MOD_SUMO_rev_2 | 249 | 256 | PF00179 | 0.295 |
MOD_SUMO_rev_2 | 622 | 628 | PF00179 | 0.308 |
MOD_SUMO_rev_2 | 899 | 906 | PF00179 | 0.411 |
TRG_DiLeu_BaEn_1 | 1089 | 1094 | PF01217 | 0.417 |
TRG_DiLeu_BaEn_4 | 432 | 438 | PF01217 | 0.353 |
TRG_DiLeu_BaEn_4 | 536 | 542 | PF01217 | 0.669 |
TRG_DiLeu_BaLyEn_6 | 775 | 780 | PF01217 | 0.367 |
TRG_DiLeu_BaLyEn_6 | 919 | 924 | PF01217 | 0.282 |
TRG_ENDOCYTIC_2 | 1002 | 1005 | PF00928 | 0.311 |
TRG_ENDOCYTIC_2 | 1006 | 1009 | PF00928 | 0.279 |
TRG_ENDOCYTIC_2 | 1054 | 1057 | PF00928 | 0.295 |
TRG_ENDOCYTIC_2 | 1141 | 1144 | PF00928 | 0.490 |
TRG_ENDOCYTIC_2 | 140 | 143 | PF00928 | 0.296 |
TRG_ENDOCYTIC_2 | 268 | 271 | PF00928 | 0.381 |
TRG_ENDOCYTIC_2 | 594 | 597 | PF00928 | 0.417 |
TRG_ENDOCYTIC_2 | 6 | 9 | PF00928 | 0.712 |
TRG_ENDOCYTIC_2 | 848 | 851 | PF00928 | 0.345 |
TRG_ENDOCYTIC_2 | 949 | 952 | PF00928 | 0.293 |
TRG_ENDOCYTIC_2 | 971 | 974 | PF00928 | 0.307 |
TRG_ENDOCYTIC_2 | 976 | 979 | PF00928 | 0.311 |
TRG_ER_diArg_1 | 1078 | 1081 | PF00400 | 0.353 |
TRG_ER_diArg_1 | 116 | 118 | PF00400 | 0.330 |
TRG_ER_diArg_1 | 183 | 185 | PF00400 | 0.458 |
TRG_ER_diArg_1 | 436 | 439 | PF00400 | 0.492 |
TRG_ER_diArg_1 | 73 | 75 | PF00400 | 0.573 |
TRG_NES_CRM1_1 | 286 | 300 | PF08389 | 0.389 |
TRG_NLS_MonoExtC_3 | 180 | 185 | PF00514 | 0.458 |
TRG_Pf-PMV_PEXEL_1 | 1072 | 1077 | PF00026 | 0.311 |
TRG_Pf-PMV_PEXEL_1 | 438 | 443 | PF00026 | 0.481 |
TRG_Pf-PMV_PEXEL_1 | 689 | 693 | PF00026 | 0.387 |
TRG_Pf-PMV_PEXEL_1 | 75 | 79 | PF00026 | 0.557 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P450 | Leptomonas seymouri | 74% | 98% |
A0A0N1I0X4 | Leptomonas seymouri | 30% | 100% |
A0A0N1PF54 | Leptomonas seymouri | 27% | 89% |
A0A0S4IM76 | Bodo saltans | 53% | 100% |
A0A0S4ITW3 | Bodo saltans | 27% | 84% |
A0A0S4J0T6 | Bodo saltans | 28% | 90% |
A0A0S4JDQ9 | Bodo saltans | 29% | 100% |
A0A0S4JP22 | Bodo saltans | 30% | 93% |
A0A0S4JUG6 | Bodo saltans | 29% | 100% |
A0A1X0NJY2 | Trypanosomatidae | 29% | 100% |
A0A1X0PAR5 | Trypanosomatidae | 57% | 100% |
A0A3Q8IFQ5 | Leishmania donovani | 27% | 90% |
A0A3R7P4C4 | Trypanosoma rangeli | 29% | 100% |
A0A3S5IS27 | Trypanosoma rangeli | 28% | 95% |
A0A422NNI9 | Trypanosoma rangeli | 56% | 100% |
A1A4J6 | Bos taurus | 41% | 100% |
A3FIN4 | Mus musculus | 28% | 98% |
A4H7E2 | Leishmania braziliensis | 30% | 100% |
A4H7E4 | Leishmania braziliensis | 30% | 100% |
A4HIF8 | Leishmania braziliensis | 27% | 93% |
A4HVT2 | Leishmania infantum | 30% | 100% |
A4I5Q4 | Leishmania infantum | 27% | 90% |
A4IA89 | Leishmania infantum | 100% | 100% |
C7EXK4 | Bos taurus | 30% | 100% |
C9ZM06 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 55% | 100% |
D0A6F9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
D4AA47 | Rattus norvegicus | 27% | 92% |
D4ABB8 | Rattus norvegicus | 41% | 100% |
E9APH7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9B0Z9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 90% |
E9B5B1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
F1Q4S1 | Danio rerio | 42% | 100% |
G5EBH1 | Caenorhabditis elegans | 40% | 100% |
O36028 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 28% | 85% |
O43520 | Homo sapiens | 27% | 92% |
O43861 | Homo sapiens | 41% | 100% |
O70228 | Mus musculus | 40% | 100% |
O75110 | Homo sapiens | 41% | 100% |
O94296 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 30% | 92% |
P32660 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 28% | 74% |
P39524 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 28% | 85% |
P40527 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 37% | 100% |
P57792 | Arabidopsis thaliana | 28% | 98% |
P70704 | Mus musculus | 29% | 99% |
P98195 | Mus musculus | 41% | 100% |
P98196 | Homo sapiens | 27% | 100% |
P98197 | Mus musculus | 27% | 97% |
P98198 | Homo sapiens | 27% | 96% |
P98199 | Mus musculus | 27% | 96% |
P98200 | Mus musculus | 30% | 100% |
P98204 | Arabidopsis thaliana | 28% | 100% |
P98205 | Arabidopsis thaliana | 29% | 100% |
Q09891 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 27% | 83% |
Q10309 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 37% | 100% |
Q12675 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 26% | 72% |
Q148W0 | Mus musculus | 27% | 92% |
Q29449 | Bos taurus | 29% | 100% |
Q4Q2M2 | Leishmania major | 94% | 100% |
Q4Q767 | Leishmania major | 28% | 90% |
Q4QG01 | Leishmania major | 29% | 100% |
Q6DFW5 | Mus musculus | 28% | 98% |
Q6VXY9 | Leishmania donovani | 30% | 100% |
Q8NB49 | Homo sapiens | 27% | 100% |
Q8TF62 | Homo sapiens | 28% | 97% |
Q9LI83 | Arabidopsis thaliana | 27% | 96% |
Q9LK90 | Arabidopsis thaliana | 27% | 97% |
Q9LNQ4 | Arabidopsis thaliana | 26% | 95% |
Q9N0Z4 | Oryctolagus cuniculus | 27% | 99% |
Q9NTI2 | Homo sapiens | 30% | 97% |
Q9QZW0 | Mus musculus | 27% | 100% |
Q9SAF5 | Arabidopsis thaliana | 26% | 96% |
Q9SGG3 | Arabidopsis thaliana | 26% | 94% |
Q9SLK6 | Arabidopsis thaliana | 29% | 93% |
Q9SX33 | Arabidopsis thaliana | 27% | 96% |
Q9U280 | Caenorhabditis elegans | 27% | 100% |
Q9XIE6 | Arabidopsis thaliana | 28% | 95% |
Q9Y2G3 | Homo sapiens | 28% | 98% |
Q9Y2Q0 | Homo sapiens | 29% | 99% |
V5BHI7 | Trypanosoma cruzi | 28% | 100% |
V5BV40 | Trypanosoma cruzi | 58% | 100% |
V5DCY9 | Trypanosoma cruzi | 30% | 100% |