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:0005768 | endosome | 7 | 2 |
GO:0005802 | trans-Golgi network | 4 | 2 |
GO:0005886 | plasma membrane | 3 | 2 |
GO:0016020 | membrane | 2 | 11 |
GO:0031410 | cytoplasmic vesicle | 6 | 2 |
GO:0031982 | vesicle | 4 | 2 |
GO:0031984 | organelle subcompartment | 2 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0097708 | intracellular vesicle | 5 | 2 |
GO:0098791 | Golgi apparatus subcompartment | 3 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
Related structures:
AlphaFold database: Q4Q2M2
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 11 |
GO:0006869 | lipid transport | 5 | 11 |
GO:0006890 | retrograde vesicle-mediated transport, Golgi to endoplasmic reticulum | 6 | 2 |
GO:0006897 | endocytosis | 5 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0015748 | organophosphate ester transport | 5 | 11 |
GO:0015914 | phospholipid transport | 6 | 11 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0016192 | vesicle-mediated transport | 4 | 2 |
GO:0034204 | lipid translocation | 4 | 2 |
GO:0045332 | phospholipid translocation | 5 | 2 |
GO:0048193 | Golgi vesicle transport | 5 | 2 |
GO:0051179 | localization | 1 | 11 |
GO:0051234 | establishment of localization | 2 | 11 |
GO:0061024 | membrane organization | 4 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0065008 | regulation of biological quality | 2 | 2 |
GO:0071702 | organic substance transport | 4 | 11 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
GO:0097035 | regulation of membrane lipid distribution | 3 | 2 |
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 | 247 | 251 | PF00656 | 0.447 |
CLV_C14_Caspase3-7 | 870 | 874 | PF00656 | 0.630 |
CLV_NRD_NRD_1 | 1078 | 1080 | PF00675 | 0.248 |
CLV_NRD_NRD_1 | 117 | 119 | PF00675 | 0.258 |
CLV_NRD_NRD_1 | 185 | 187 | PF00675 | 0.337 |
CLV_NRD_NRD_1 | 2 | 4 | PF00675 | 0.530 |
CLV_NRD_NRD_1 | 624 | 626 | PF00675 | 0.248 |
CLV_NRD_NRD_1 | 75 | 77 | PF00675 | 0.418 |
CLV_NRD_NRD_1 | 799 | 801 | PF00675 | 0.321 |
CLV_PCSK_FUR_1 | 1076 | 1080 | PF00082 | 0.334 |
CLV_PCSK_FUR_1 | 183 | 187 | PF00082 | 0.352 |
CLV_PCSK_FUR_1 | 343 | 347 | PF00082 | 0.206 |
CLV_PCSK_KEX2_1 | 1078 | 1080 | PF00082 | 0.247 |
CLV_PCSK_KEX2_1 | 117 | 119 | PF00082 | 0.258 |
CLV_PCSK_KEX2_1 | 182 | 184 | PF00082 | 0.330 |
CLV_PCSK_KEX2_1 | 185 | 187 | PF00082 | 0.319 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.530 |
CLV_PCSK_KEX2_1 | 345 | 347 | PF00082 | 0.206 |
CLV_PCSK_KEX2_1 | 75 | 77 | PF00082 | 0.398 |
CLV_PCSK_KEX2_1 | 799 | 801 | PF00082 | 0.321 |
CLV_PCSK_PC1ET2_1 | 182 | 184 | PF00082 | 0.358 |
CLV_PCSK_PC1ET2_1 | 345 | 347 | PF00082 | 0.206 |
CLV_PCSK_SKI1_1 | 1007 | 1011 | PF00082 | 0.253 |
CLV_PCSK_SKI1_1 | 1018 | 1022 | PF00082 | 0.235 |
CLV_PCSK_SKI1_1 | 1081 | 1085 | PF00082 | 0.334 |
CLV_PCSK_SKI1_1 | 1109 | 1113 | PF00082 | 0.472 |
CLV_PCSK_SKI1_1 | 1140 | 1144 | PF00082 | 0.308 |
CLV_PCSK_SKI1_1 | 175 | 179 | PF00082 | 0.361 |
CLV_PCSK_SKI1_1 | 334 | 338 | PF00082 | 0.334 |
CLV_PCSK_SKI1_1 | 439 | 443 | PF00082 | 0.382 |
CLV_PCSK_SKI1_1 | 493 | 497 | PF00082 | 0.525 |
CLV_PCSK_SKI1_1 | 595 | 599 | PF00082 | 0.308 |
CLV_PCSK_SKI1_1 | 79 | 83 | PF00082 | 0.432 |
CLV_TASPASE1 | 248 | 254 | PF01112 | 0.447 |
DEG_APCC_DBOX_1 | 1017 | 1025 | PF00400 | 0.472 |
DEG_APCC_DBOX_1 | 74 | 82 | PF00400 | 0.634 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.750 |
DEG_ODPH_VHL_1 | 86 | 97 | PF01847 | 0.620 |
DEG_SPOP_SBC_1 | 28 | 32 | PF00917 | 0.621 |
DOC_ANK_TNKS_1 | 874 | 881 | PF00023 | 0.478 |
DOC_CYCLIN_RxL_1 | 436 | 446 | PF00134 | 0.580 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 427 | 435 | PF00134 | 0.592 |
DOC_MAPK_gen_1 | 1076 | 1086 | PF00069 | 0.460 |
DOC_MAPK_gen_1 | 185 | 194 | PF00069 | 0.605 |
DOC_MAPK_gen_1 | 45 | 52 | PF00069 | 0.620 |
DOC_MAPK_gen_1 | 453 | 461 | PF00069 | 0.607 |
DOC_MAPK_gen_1 | 583 | 592 | PF00069 | 0.553 |
DOC_MAPK_gen_1 | 625 | 632 | PF00069 | 0.447 |
DOC_MAPK_gen_1 | 75 | 86 | PF00069 | 0.593 |
DOC_MAPK_MEF2A_6 | 583 | 592 | PF00069 | 0.472 |
DOC_MAPK_MEF2A_6 | 625 | 632 | PF00069 | 0.447 |
DOC_MAPK_MEF2A_6 | 79 | 86 | PF00069 | 0.608 |
DOC_MAPK_MEF2A_6 | 916 | 925 | PF00069 | 0.458 |
DOC_MAPK_NFAT4_5 | 79 | 87 | PF00069 | 0.635 |
DOC_PP1_RVXF_1 | 1070 | 1076 | PF00149 | 0.450 |
DOC_PP1_RVXF_1 | 1138 | 1145 | PF00149 | 0.534 |
DOC_PP1_RVXF_1 | 152 | 158 | PF00149 | 0.258 |
DOC_PP1_RVXF_1 | 491 | 497 | PF00149 | 0.610 |
DOC_PP1_RVXF_1 | 680 | 687 | PF00149 | 0.479 |
DOC_PP1_RVXF_1 | 920 | 927 | PF00149 | 0.447 |
DOC_PP2B_LxvP_1 | 64 | 67 | PF13499 | 0.577 |
DOC_PP2B_PxIxI_1 | 163 | 169 | PF00149 | 0.242 |
DOC_SPAK_OSR1_1 | 276 | 280 | PF12202 | 0.549 |
DOC_SPAK_OSR1_1 | 387 | 391 | PF12202 | 0.447 |
DOC_USP7_MATH_1 | 1053 | 1057 | PF00917 | 0.315 |
DOC_USP7_MATH_1 | 260 | 264 | PF00917 | 0.549 |
DOC_USP7_MATH_1 | 336 | 340 | PF00917 | 0.486 |
DOC_USP7_MATH_1 | 550 | 554 | PF00917 | 0.717 |
DOC_USP7_MATH_1 | 59 | 63 | PF00917 | 0.704 |
DOC_USP7_MATH_1 | 620 | 624 | PF00917 | 0.447 |
DOC_USP7_MATH_1 | 8 | 12 | PF00917 | 0.623 |
DOC_USP7_UBL2_3 | 1007 | 1011 | PF12436 | 0.447 |
DOC_USP7_UBL2_3 | 451 | 455 | PF12436 | 0.612 |
DOC_USP7_UBL2_3 | 649 | 653 | PF12436 | 0.461 |
DOC_WW_Pin1_4 | 102 | 107 | PF00397 | 0.607 |
DOC_WW_Pin1_4 | 160 | 165 | PF00397 | 0.334 |
DOC_WW_Pin1_4 | 22 | 27 | PF00397 | 0.758 |
DOC_WW_Pin1_4 | 338 | 343 | PF00397 | 0.549 |
DOC_WW_Pin1_4 | 529 | 534 | PF00397 | 0.493 |
DOC_WW_Pin1_4 | 572 | 577 | PF00397 | 0.455 |
DOC_WW_Pin1_4 | 853 | 858 | PF00397 | 0.509 |
DOC_WW_Pin1_4 | 86 | 91 | PF00397 | 0.636 |
LIG_14-3-3_CanoR_1 | 117 | 122 | PF00244 | 0.459 |
LIG_14-3-3_CanoR_1 | 19 | 29 | PF00244 | 0.769 |
LIG_14-3-3_CanoR_1 | 408 | 414 | PF00244 | 0.499 |
LIG_14-3-3_CanoR_1 | 439 | 449 | PF00244 | 0.557 |
LIG_14-3-3_CanoR_1 | 502 | 506 | PF00244 | 0.725 |
LIG_14-3-3_CanoR_1 | 689 | 696 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 845 | 851 | PF00244 | 0.539 |
LIG_14-3-3_CanoR_1 | 929 | 933 | PF00244 | 0.447 |
LIG_14-3-3_CanoR_1 | 937 | 943 | PF00244 | 0.447 |
LIG_APCC_ABBA_1 | 218 | 223 | PF00400 | 0.534 |
LIG_BRCT_BRCA1_1 | 1043 | 1047 | PF00533 | 0.349 |
LIG_BRCT_BRCA1_1 | 598 | 602 | PF00533 | 0.452 |
LIG_BRCT_BRCA1_1 | 956 | 960 | PF00533 | 0.299 |
LIG_BRCT_BRCA1_1 | 976 | 980 | PF00533 | 0.117 |
LIG_Clathr_ClatBox_1 | 49 | 53 | PF01394 | 0.621 |
LIG_CtBP_PxDLS_1 | 397 | 401 | PF00389 | 0.447 |
LIG_CtBP_PxDLS_1 | 432 | 436 | PF00389 | 0.480 |
LIG_deltaCOP1_diTrp_1 | 179 | 184 | PF00928 | 0.594 |
LIG_FHA_1 | 1053 | 1059 | PF00498 | 0.314 |
LIG_FHA_1 | 1066 | 1072 | PF00498 | 0.299 |
LIG_FHA_1 | 23 | 29 | PF00498 | 0.759 |
LIG_FHA_1 | 239 | 245 | PF00498 | 0.452 |
LIG_FHA_1 | 262 | 268 | PF00498 | 0.469 |
LIG_FHA_1 | 292 | 298 | PF00498 | 0.513 |
LIG_FHA_1 | 317 | 323 | PF00498 | 0.510 |
LIG_FHA_1 | 444 | 450 | PF00498 | 0.477 |
LIG_FHA_1 | 470 | 476 | PF00498 | 0.650 |
LIG_FHA_1 | 610 | 616 | PF00498 | 0.534 |
LIG_FHA_1 | 725 | 731 | PF00498 | 0.596 |
LIG_FHA_1 | 775 | 781 | PF00498 | 0.493 |
LIG_FHA_1 | 820 | 826 | PF00498 | 0.483 |
LIG_FHA_1 | 90 | 96 | PF00498 | 0.473 |
LIG_FHA_1 | 933 | 939 | PF00498 | 0.534 |
LIG_FHA_1 | 962 | 968 | PF00498 | 0.258 |
LIG_FHA_2 | 327 | 333 | PF00498 | 0.447 |
LIG_FHA_2 | 541 | 547 | PF00498 | 0.736 |
LIG_FHA_2 | 591 | 597 | PF00498 | 0.488 |
LIG_FHA_2 | 688 | 694 | PF00498 | 0.546 |
LIG_FHA_2 | 733 | 739 | PF00498 | 0.482 |
LIG_GBD_Chelix_1 | 1090 | 1098 | PF00786 | 0.427 |
LIG_Integrin_RGD_1 | 378 | 380 | PF01839 | 0.334 |
LIG_LIR_Apic_2 | 160 | 164 | PF02991 | 0.315 |
LIG_LIR_Gen_1 | 1044 | 1054 | PF02991 | 0.260 |
LIG_LIR_Gen_1 | 266 | 277 | PF02991 | 0.511 |
LIG_LIR_Gen_1 | 368 | 377 | PF02991 | 0.467 |
LIG_LIR_Gen_1 | 380 | 389 | PF02991 | 0.413 |
LIG_LIR_Gen_1 | 612 | 621 | PF02991 | 0.419 |
LIG_LIR_Gen_1 | 838 | 848 | PF02991 | 0.503 |
LIG_LIR_Gen_1 | 954 | 961 | PF02991 | 0.420 |
LIG_LIR_LC3C_4 | 319 | 324 | PF02991 | 0.549 |
LIG_LIR_Nem_3 | 1001 | 1005 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 103 | 107 | PF02991 | 0.635 |
LIG_LIR_Nem_3 | 1044 | 1050 | PF02991 | 0.274 |
LIG_LIR_Nem_3 | 1051 | 1057 | PF02991 | 0.347 |
LIG_LIR_Nem_3 | 1116 | 1121 | PF02991 | 0.266 |
LIG_LIR_Nem_3 | 122 | 127 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 160 | 165 | PF02991 | 0.334 |
LIG_LIR_Nem_3 | 179 | 184 | PF02991 | 0.577 |
LIG_LIR_Nem_3 | 193 | 198 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 266 | 272 | PF02991 | 0.511 |
LIG_LIR_Nem_3 | 368 | 372 | PF02991 | 0.489 |
LIG_LIR_Nem_3 | 593 | 597 | PF02991 | 0.507 |
LIG_LIR_Nem_3 | 612 | 616 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 838 | 843 | PF02991 | 0.499 |
LIG_LIR_Nem_3 | 846 | 851 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 954 | 959 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 966 | 971 | PF02991 | 0.198 |
LIG_LYPXL_yS_3 | 1002 | 1005 | PF13949 | 0.534 |
LIG_NRBOX | 366 | 372 | PF00104 | 0.531 |
LIG_NRBOX | 77 | 83 | PF00104 | 0.598 |
LIG_PCNA_yPIPBox_3 | 401 | 410 | PF02747 | 0.494 |
LIG_PCNA_yPIPBox_3 | 678 | 689 | PF02747 | 0.490 |
LIG_Pex14_1 | 1025 | 1029 | PF04695 | 0.299 |
LIG_Pex14_1 | 255 | 259 | PF04695 | 0.447 |
LIG_Pex14_2 | 100 | 104 | PF04695 | 0.640 |
LIG_Pex14_2 | 1107 | 1111 | PF04695 | 0.283 |
LIG_Pex14_2 | 133 | 137 | PF04695 | 0.438 |
LIG_Pex14_2 | 139 | 143 | PF04695 | 0.287 |
LIG_Pex14_2 | 377 | 381 | PF04695 | 0.472 |
LIG_Pex14_2 | 385 | 389 | PF04695 | 0.467 |
LIG_Pex14_2 | 956 | 960 | PF04695 | 0.315 |
LIG_PTB_Apo_2 | 113 | 120 | PF02174 | 0.458 |
LIG_PTB_Apo_2 | 135 | 142 | PF02174 | 0.291 |
LIG_PTB_Phospho_1 | 113 | 119 | PF10480 | 0.458 |
LIG_PTB_Phospho_1 | 135 | 141 | PF10480 | 0.315 |
LIG_SH2_CRK | 1054 | 1058 | PF00017 | 0.315 |
LIG_SH2_CRK | 6 | 10 | PF00017 | 0.746 |
LIG_SH2_CRK | 613 | 617 | PF00017 | 0.400 |
LIG_SH2_CRK | 848 | 852 | PF00017 | 0.483 |
LIG_SH2_CRK | 949 | 953 | PF00017 | 0.299 |
LIG_SH2_CRK | 976 | 980 | PF00017 | 0.315 |
LIG_SH2_NCK_1 | 949 | 953 | PF00017 | 0.299 |
LIG_SH2_NCK_1 | 976 | 980 | PF00017 | 0.299 |
LIG_SH2_STAP1 | 1054 | 1058 | PF00017 | 0.315 |
LIG_SH2_STAP1 | 269 | 273 | PF00017 | 0.442 |
LIG_SH2_STAP1 | 411 | 415 | PF00017 | 0.473 |
LIG_SH2_STAP1 | 703 | 707 | PF00017 | 0.606 |
LIG_SH2_STAP1 | 848 | 852 | PF00017 | 0.483 |
LIG_SH2_STAP1 | 976 | 980 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 1054 | 1057 | PF00017 | 0.332 |
LIG_SH2_STAT5 | 1141 | 1144 | PF00017 | 0.584 |
LIG_SH2_STAT5 | 119 | 122 | PF00017 | 0.317 |
LIG_SH2_STAT5 | 141 | 144 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 161 | 164 | PF00017 | 0.287 |
LIG_SH2_STAT5 | 269 | 272 | PF00017 | 0.406 |
LIG_SH2_STAT5 | 328 | 331 | PF00017 | 0.508 |
LIG_SH2_STAT5 | 440 | 443 | PF00017 | 0.463 |
LIG_SH2_STAT5 | 482 | 485 | PF00017 | 0.604 |
LIG_SH2_STAT5 | 613 | 616 | PF00017 | 0.496 |
LIG_SH2_STAT5 | 788 | 791 | PF00017 | 0.553 |
LIG_SH2_STAT5 | 832 | 835 | PF00017 | 0.568 |
LIG_SH2_STAT5 | 971 | 974 | PF00017 | 0.299 |
LIG_SH2_STAT5 | 99 | 102 | PF00017 | 0.648 |
LIG_SH3_3 | 104 | 110 | PF00018 | 0.589 |
LIG_SH3_3 | 1098 | 1104 | PF00018 | 0.420 |
LIG_SH3_3 | 33 | 39 | PF00018 | 0.751 |
LIG_SH3_3 | 416 | 422 | PF00018 | 0.617 |
LIG_SH3_3 | 532 | 538 | PF00018 | 0.549 |
LIG_SUMO_SIM_anti_2 | 1060 | 1066 | PF11976 | 0.299 |
LIG_SUMO_SIM_anti_2 | 1088 | 1095 | PF11976 | 0.420 |
LIG_SUMO_SIM_anti_2 | 163 | 169 | PF11976 | 0.270 |
LIG_SUMO_SIM_anti_2 | 216 | 221 | PF11976 | 0.454 |
LIG_SUMO_SIM_anti_2 | 48 | 54 | PF11976 | 0.620 |
LIG_SUMO_SIM_anti_2 | 577 | 583 | PF11976 | 0.534 |
LIG_SUMO_SIM_par_1 | 1099 | 1106 | PF11976 | 0.299 |
LIG_SUMO_SIM_par_1 | 203 | 209 | PF11976 | 0.543 |
LIG_SUMO_SIM_par_1 | 362 | 368 | PF11976 | 0.470 |
LIG_SUMO_SIM_par_1 | 48 | 54 | PF11976 | 0.620 |
LIG_SUMO_SIM_par_1 | 532 | 537 | PF11976 | 0.619 |
LIG_SUMO_SIM_par_1 | 821 | 826 | PF11976 | 0.458 |
LIG_SxIP_EBH_1 | 389 | 401 | PF03271 | 0.534 |
LIG_TRAF2_1 | 13 | 16 | PF00917 | 0.739 |
LIG_TRAF2_1 | 478 | 481 | PF00917 | 0.628 |
LIG_TRAF2_1 | 643 | 646 | PF00917 | 0.529 |
LIG_TYR_ITIM | 1052 | 1057 | PF00017 | 0.315 |
LIG_TYR_ITIM | 267 | 272 | PF00017 | 0.420 |
LIG_TYR_ITIM | 4 | 9 | PF00017 | 0.711 |
LIG_TYR_ITIM | 592 | 597 | PF00017 | 0.420 |
LIG_TYR_ITIM | 947 | 952 | PF00017 | 0.385 |
LIG_TYR_ITSM | 844 | 851 | PF00017 | 0.400 |
LIG_UBA3_1 | 1035 | 1043 | PF00899 | 0.442 |
LIG_UBA3_1 | 1133 | 1140 | PF00899 | 0.442 |
LIG_Vh1_VBS_1 | 1084 | 1102 | PF01044 | 0.442 |
LIG_WRC_WIRS_1 | 121 | 126 | PF05994 | 0.299 |
LIG_WRC_WIRS_1 | 288 | 293 | PF05994 | 0.407 |
LIG_WRC_WIRS_1 | 366 | 371 | PF05994 | 0.385 |
MOD_CDK_SPK_2 | 338 | 343 | PF00069 | 0.442 |
MOD_CDK_SPxxK_3 | 338 | 345 | PF00069 | 0.442 |
MOD_CDK_SPxxK_3 | 853 | 860 | PF00069 | 0.377 |
MOD_CDK_SPxxK_3 | 86 | 93 | PF00069 | 0.413 |
MOD_CK1_1 | 1014 | 1020 | PF00069 | 0.357 |
MOD_CK1_1 | 20 | 26 | PF00069 | 0.687 |
MOD_CK1_1 | 236 | 242 | PF00069 | 0.338 |
MOD_CK1_1 | 263 | 269 | PF00069 | 0.412 |
MOD_CK1_1 | 443 | 449 | PF00069 | 0.425 |
MOD_CK1_1 | 54 | 60 | PF00069 | 0.619 |
MOD_CK1_1 | 566 | 572 | PF00069 | 0.631 |
MOD_CK1_1 | 62 | 68 | PF00069 | 0.534 |
MOD_CK1_1 | 640 | 646 | PF00069 | 0.428 |
MOD_CK1_1 | 835 | 841 | PF00069 | 0.490 |
MOD_CK1_1 | 89 | 95 | PF00069 | 0.537 |
MOD_CK2_1 | 326 | 332 | PF00069 | 0.420 |
MOD_CK2_1 | 540 | 546 | PF00069 | 0.704 |
MOD_CK2_1 | 572 | 578 | PF00069 | 0.286 |
MOD_CK2_1 | 640 | 646 | PF00069 | 0.428 |
MOD_CK2_1 | 687 | 693 | PF00069 | 0.510 |
MOD_CK2_1 | 732 | 738 | PF00069 | 0.359 |
MOD_CMANNOS | 1115 | 1118 | PF00535 | 0.357 |
MOD_Cter_Amidation | 797 | 800 | PF01082 | 0.437 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.687 |
MOD_GlcNHglycan | 208 | 211 | PF01048 | 0.313 |
MOD_GlcNHglycan | 237 | 241 | PF01048 | 0.352 |
MOD_GlcNHglycan | 31 | 34 | PF01048 | 0.720 |
MOD_GlcNHglycan | 334 | 337 | PF01048 | 0.379 |
MOD_GlcNHglycan | 499 | 502 | PF01048 | 0.621 |
MOD_GlcNHglycan | 552 | 555 | PF01048 | 0.735 |
MOD_GlcNHglycan | 639 | 642 | PF01048 | 0.424 |
MOD_GSK3_1 | 1048 | 1055 | PF00069 | 0.306 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.432 |
MOD_GSK3_1 | 1085 | 1092 | PF00069 | 0.413 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.711 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.321 |
MOD_GSK3_1 | 263 | 270 | PF00069 | 0.285 |
MOD_GSK3_1 | 287 | 294 | PF00069 | 0.361 |
MOD_GSK3_1 | 326 | 333 | PF00069 | 0.324 |
MOD_GSK3_1 | 409 | 416 | PF00069 | 0.467 |
MOD_GSK3_1 | 443 | 450 | PF00069 | 0.345 |
MOD_GSK3_1 | 465 | 472 | PF00069 | 0.552 |
MOD_GSK3_1 | 497 | 504 | PF00069 | 0.662 |
MOD_GSK3_1 | 505 | 512 | PF00069 | 0.613 |
MOD_GSK3_1 | 540 | 547 | PF00069 | 0.721 |
MOD_GSK3_1 | 558 | 565 | PF00069 | 0.757 |
MOD_GSK3_1 | 596 | 603 | PF00069 | 0.336 |
MOD_GSK3_1 | 611 | 618 | PF00069 | 0.245 |
MOD_GSK3_1 | 640 | 647 | PF00069 | 0.352 |
MOD_GSK3_1 | 685 | 692 | PF00069 | 0.470 |
MOD_GSK3_1 | 769 | 776 | PF00069 | 0.396 |
MOD_GSK3_1 | 832 | 839 | PF00069 | 0.337 |
MOD_GSK3_1 | 928 | 935 | PF00069 | 0.299 |
MOD_GSK3_1 | 947 | 954 | PF00069 | 0.299 |
MOD_GSK3_1 | 974 | 981 | PF00069 | 0.315 |
MOD_N-GLC_1 | 21 | 26 | PF02516 | 0.740 |
MOD_N-GLC_1 | 261 | 266 | PF02516 | 0.381 |
MOD_N-GLC_1 | 337 | 342 | PF02516 | 0.315 |
MOD_N-GLC_1 | 497 | 502 | PF02516 | 0.702 |
MOD_N-GLC_1 | 529 | 534 | PF02516 | 0.379 |
MOD_N-GLC_1 | 544 | 549 | PF02516 | 0.587 |
MOD_N-GLC_1 | 994 | 999 | PF02516 | 0.442 |
MOD_NEK2_1 | 1111 | 1116 | PF00069 | 0.303 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.313 |
MOD_NEK2_1 | 157 | 162 | PF00069 | 0.306 |
MOD_NEK2_1 | 261 | 266 | PF00069 | 0.315 |
MOD_NEK2_1 | 29 | 34 | PF00069 | 0.717 |
MOD_NEK2_1 | 337 | 342 | PF00069 | 0.315 |
MOD_NEK2_1 | 365 | 370 | PF00069 | 0.361 |
MOD_NEK2_1 | 391 | 396 | PF00069 | 0.437 |
MOD_NEK2_1 | 505 | 510 | PF00069 | 0.543 |
MOD_NEK2_1 | 584 | 589 | PF00069 | 0.312 |
MOD_NEK2_1 | 729 | 734 | PF00069 | 0.470 |
MOD_NEK2_1 | 867 | 872 | PF00069 | 0.530 |
MOD_NEK2_1 | 912 | 917 | PF00069 | 0.315 |
MOD_NEK2_1 | 960 | 965 | PF00069 | 0.347 |
MOD_NEK2_1 | 974 | 979 | PF00069 | 0.299 |
MOD_NEK2_2 | 501 | 506 | PF00069 | 0.688 |
MOD_NEK2_2 | 644 | 649 | PF00069 | 0.389 |
MOD_NEK2_2 | 932 | 937 | PF00069 | 0.315 |
MOD_NEK2_2 | 975 | 980 | PF00069 | 0.299 |
MOD_OFUCOSY | 809 | 814 | PF10250 | 0.609 |
MOD_PIKK_1 | 144 | 150 | PF00454 | 0.299 |
MOD_PIKK_1 | 855 | 861 | PF00454 | 0.383 |
MOD_PIKK_1 | 936 | 942 | PF00454 | 0.315 |
MOD_PK_1 | 658 | 664 | PF00069 | 0.466 |
MOD_PKA_1 | 117 | 123 | PF00069 | 0.315 |
MOD_PKA_1 | 70 | 76 | PF00069 | 0.512 |
MOD_PKA_2 | 117 | 123 | PF00069 | 0.300 |
MOD_PKA_2 | 330 | 336 | PF00069 | 0.413 |
MOD_PKA_2 | 469 | 475 | PF00069 | 0.554 |
MOD_PKA_2 | 501 | 507 | PF00069 | 0.686 |
MOD_PKA_2 | 663 | 669 | PF00069 | 0.415 |
MOD_PKA_2 | 774 | 780 | PF00069 | 0.378 |
MOD_PKA_2 | 867 | 873 | PF00069 | 0.541 |
MOD_PKA_2 | 928 | 934 | PF00069 | 0.299 |
MOD_PKA_2 | 936 | 942 | PF00069 | 0.299 |
MOD_PKB_1 | 633 | 641 | PF00069 | 0.420 |
MOD_Plk_1 | 595 | 601 | PF00069 | 0.388 |
MOD_Plk_1 | 884 | 890 | PF00069 | 0.400 |
MOD_Plk_1 | 910 | 916 | PF00069 | 0.299 |
MOD_Plk_2-3 | 303 | 309 | PF00069 | 0.334 |
MOD_Plk_4 | 1024 | 1030 | PF00069 | 0.334 |
MOD_Plk_4 | 1053 | 1059 | PF00069 | 0.299 |
MOD_Plk_4 | 1089 | 1095 | PF00069 | 0.339 |
MOD_Plk_4 | 120 | 126 | PF00069 | 0.301 |
MOD_Plk_4 | 169 | 175 | PF00069 | 0.315 |
MOD_Plk_4 | 239 | 245 | PF00069 | 0.420 |
MOD_Plk_4 | 318 | 324 | PF00069 | 0.366 |
MOD_Plk_4 | 365 | 371 | PF00069 | 0.354 |
MOD_Plk_4 | 391 | 397 | PF00069 | 0.400 |
MOD_Plk_4 | 462 | 468 | PF00069 | 0.414 |
MOD_Plk_4 | 59 | 65 | PF00069 | 0.610 |
MOD_Plk_4 | 611 | 617 | PF00069 | 0.410 |
MOD_Plk_4 | 658 | 664 | PF00069 | 0.415 |
MOD_Plk_4 | 705 | 711 | PF00069 | 0.459 |
MOD_Plk_4 | 813 | 819 | PF00069 | 0.625 |
MOD_Plk_4 | 846 | 852 | PF00069 | 0.318 |
MOD_Plk_4 | 862 | 868 | PF00069 | 0.371 |
MOD_Plk_4 | 884 | 890 | PF00069 | 0.384 |
MOD_Plk_4 | 947 | 953 | PF00069 | 0.296 |
MOD_Plk_4 | 963 | 969 | PF00069 | 0.311 |
MOD_Plk_4 | 975 | 981 | PF00069 | 0.299 |
MOD_ProDKin_1 | 102 | 108 | PF00069 | 0.520 |
MOD_ProDKin_1 | 160 | 166 | PF00069 | 0.334 |
MOD_ProDKin_1 | 22 | 28 | PF00069 | 0.736 |
MOD_ProDKin_1 | 338 | 344 | PF00069 | 0.442 |
MOD_ProDKin_1 | 529 | 535 | PF00069 | 0.374 |
MOD_ProDKin_1 | 572 | 578 | PF00069 | 0.311 |
MOD_ProDKin_1 | 853 | 859 | PF00069 | 0.382 |
MOD_ProDKin_1 | 86 | 92 | PF00069 | 0.563 |
MOD_SUMO_rev_2 | 176 | 184 | PF00179 | 0.457 |
MOD_SUMO_rev_2 | 250 | 257 | PF00179 | 0.299 |
MOD_SUMO_rev_2 | 622 | 628 | PF00179 | 0.319 |
MOD_SUMO_rev_2 | 899 | 906 | PF00179 | 0.416 |
TRG_DiLeu_BaEn_1 | 1089 | 1094 | PF01217 | 0.420 |
TRG_DiLeu_BaEn_4 | 433 | 439 | PF01217 | 0.359 |
TRG_DiLeu_BaLyEn_6 | 161 | 166 | PF01217 | 0.367 |
TRG_DiLeu_BaLyEn_6 | 775 | 780 | PF01217 | 0.379 |
TRG_DiLeu_BaLyEn_6 | 919 | 924 | PF01217 | 0.299 |
TRG_ENDOCYTIC_2 | 1002 | 1005 | PF00928 | 0.315 |
TRG_ENDOCYTIC_2 | 1006 | 1009 | PF00928 | 0.282 |
TRG_ENDOCYTIC_2 | 1054 | 1057 | PF00928 | 0.332 |
TRG_ENDOCYTIC_2 | 1141 | 1144 | PF00928 | 0.521 |
TRG_ENDOCYTIC_2 | 141 | 144 | PF00928 | 0.315 |
TRG_ENDOCYTIC_2 | 269 | 272 | PF00928 | 0.403 |
TRG_ENDOCYTIC_2 | 594 | 597 | PF00928 | 0.420 |
TRG_ENDOCYTIC_2 | 6 | 9 | PF00928 | 0.718 |
TRG_ENDOCYTIC_2 | 613 | 616 | PF00928 | 0.220 |
TRG_ENDOCYTIC_2 | 848 | 851 | PF00928 | 0.367 |
TRG_ENDOCYTIC_2 | 949 | 952 | PF00928 | 0.299 |
TRG_ENDOCYTIC_2 | 971 | 974 | PF00928 | 0.311 |
TRG_ENDOCYTIC_2 | 976 | 979 | PF00928 | 0.315 |
TRG_ER_diArg_1 | 1 | 3 | PF00400 | 0.710 |
TRG_ER_diArg_1 | 1078 | 1081 | PF00400 | 0.357 |
TRG_ER_diArg_1 | 117 | 119 | PF00400 | 0.334 |
TRG_ER_diArg_1 | 184 | 186 | PF00400 | 0.441 |
TRG_ER_diArg_1 | 437 | 440 | PF00400 | 0.497 |
TRG_ER_diArg_1 | 74 | 76 | PF00400 | 0.572 |
TRG_ER_diArg_1 | 799 | 801 | PF00400 | 0.402 |
TRG_NES_CRM1_1 | 287 | 301 | PF08389 | 0.393 |
TRG_NLS_MonoExtC_3 | 181 | 186 | PF00514 | 0.487 |
TRG_Pf-PMV_PEXEL_1 | 1072 | 1077 | PF00026 | 0.315 |
TRG_Pf-PMV_PEXEL_1 | 346 | 350 | PF00026 | 0.242 |
TRG_Pf-PMV_PEXEL_1 | 439 | 444 | PF00026 | 0.486 |
TRG_Pf-PMV_PEXEL_1 | 689 | 693 | PF00026 | 0.389 |
TRG_Pf-PMV_PEXEL_1 | 76 | 80 | PF00026 | 0.551 |
TRG_Pf-PMV_PEXEL_1 | 799 | 803 | PF00026 | 0.410 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P450 | Leptomonas seymouri | 74% | 98% |
A0A0N1I0X4 | Leptomonas seymouri | 30% | 100% |
A0A0N1PF54 | Leptomonas seymouri | 26% | 89% |
A0A0S4IM76 | Bodo saltans | 54% | 100% |
A0A0S4ITW3 | Bodo saltans | 26% | 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 | 58% | 100% |
A0A3Q8IFQ5 | Leishmania donovani | 27% | 90% |
A0A3Q8INM6 | Leishmania donovani | 94% | 100% |
A0A3R7P4C4 | Trypanosoma rangeli | 29% | 100% |
A0A422NNI9 | Trypanosoma rangeli | 57% | 100% |
A1A4J6 | Bos taurus | 41% | 100% |
A3FIN4 | Mus musculus | 28% | 98% |
A4H7E2 | Leishmania braziliensis | 30% | 100% |
A4H7E4 | Leishmania braziliensis | 30% | 100% |
A4HIF8 | Leishmania braziliensis | 26% | 93% |
A4HVT2 | Leishmania infantum | 30% | 100% |
A4I5Q4 | Leishmania infantum | 27% | 90% |
A4IA89 | Leishmania infantum | 94% | 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) | 29% | 100% |
E9B0Z9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 90% |
E9B5B1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
F1Q4S1 | Danio rerio | 42% | 100% |
G5EBH1 | Caenorhabditis elegans | 40% | 100% |
J9VQQ3 | Cryptococcus neoformans var. grubii serotype A (strain H99 / ATCC 208821 / CBS 10515 / FGSC 9487) | 22% | 82% |
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) | 29% | 92% |
P32660 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 29% | 74% |
P39524 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 29% | 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 | 28% | 96% |
P98199 | Mus musculus | 28% | 96% |
P98200 | Mus musculus | 30% | 100% |
P98204 | Arabidopsis thaliana | 28% | 100% |
P98205 | Arabidopsis thaliana | 30% | 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) | 27% | 72% |
Q148W0 | Mus musculus | 27% | 92% |
Q29449 | Bos taurus | 29% | 100% |
Q4Q767 | Leishmania major | 27% | 90% |
Q4QG01 | Leishmania major | 30% | 100% |
Q5BL50 | Xenopus tropicalis | 29% | 93% |
Q6DFW5 | Mus musculus | 28% | 98% |
Q6VXY9 | Leishmania donovani | 30% | 100% |
Q8NB49 | Homo sapiens | 27% | 100% |
Q8TF62 | Homo sapiens | 29% | 97% |
Q9LI83 | Arabidopsis thaliana | 28% | 96% |
Q9LK90 | Arabidopsis thaliana | 28% | 97% |
Q9LNQ4 | Arabidopsis thaliana | 28% | 95% |
Q9LVK9 | Arabidopsis thaliana | 28% | 93% |
Q9N0Z4 | Oryctolagus cuniculus | 28% | 99% |
Q9NTI2 | Homo sapiens | 30% | 97% |
Q9QZW0 | Mus musculus | 27% | 100% |
Q9SAF5 | Arabidopsis thaliana | 27% | 96% |
Q9SGG3 | Arabidopsis thaliana | 27% | 94% |
Q9SLK6 | Arabidopsis thaliana | 29% | 93% |
Q9SX33 | Arabidopsis thaliana | 27% | 96% |
Q9U280 | Caenorhabditis elegans | 27% | 100% |
Q9XIE6 | Arabidopsis thaliana | 29% | 95% |
Q9Y2G3 | Homo sapiens | 28% | 98% |
Q9Y2Q0 | Homo sapiens | 28% | 99% |
V5BHI7 | Trypanosoma cruzi | 28% | 100% |
V5BV40 | Trypanosoma cruzi | 58% | 100% |
V5DCY9 | Trypanosoma cruzi | 30% | 100% |