Eukaryotic P-ATPase protein, its closest animal relatives (ATP11A) are involved in phospholipid transport.. Localization: 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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 17 |
NetGPI | no | yes: 0, no: 17 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005886 | plasma membrane | 3 | 2 |
GO:0016020 | membrane | 2 | 18 |
GO:0110165 | cellular anatomical entity | 1 | 18 |
Related structures:
AlphaFold database: Q4Q767
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 13 |
GO:0006869 | lipid transport | 5 | 13 |
GO:0009987 | cellular process | 1 | 2 |
GO:0015748 | organophosphate ester transport | 5 | 13 |
GO:0015914 | phospholipid transport | 6 | 13 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0034204 | lipid translocation | 4 | 2 |
GO:0045332 | phospholipid translocation | 5 | 2 |
GO:0051179 | localization | 1 | 13 |
GO:0051234 | establishment of localization | 2 | 13 |
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 | 13 |
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 | 18 |
GO:0000287 | magnesium ion binding | 5 | 13 |
GO:0003824 | catalytic activity | 1 | 17 |
GO:0005215 | transporter activity | 1 | 17 |
GO:0005319 | lipid transporter activity | 2 | 17 |
GO:0005488 | binding | 1 | 18 |
GO:0005524 | ATP binding | 5 | 17 |
GO:0016462 | pyrophosphatase activity | 5 | 17 |
GO:0016787 | hydrolase activity | 2 | 17 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 17 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 17 |
GO:0016887 | ATP hydrolysis activity | 7 | 17 |
GO:0017076 | purine nucleotide binding | 4 | 17 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 17 |
GO:0030554 | adenyl nucleotide binding | 5 | 17 |
GO:0032553 | ribonucleotide binding | 3 | 17 |
GO:0032555 | purine ribonucleotide binding | 4 | 17 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 17 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 17 |
GO:0036094 | small molecule binding | 2 | 18 |
GO:0043167 | ion binding | 2 | 17 |
GO:0043168 | anion binding | 3 | 17 |
GO:0043169 | cation binding | 3 | 13 |
GO:0046872 | metal ion binding | 4 | 13 |
GO:0097159 | organic cyclic compound binding | 2 | 18 |
GO:0097367 | carbohydrate derivative binding | 2 | 17 |
GO:0140303 | intramembrane lipid transporter activity | 3 | 17 |
GO:0140326 | ATPase-coupled intramembrane lipid transporter activity | 2 | 17 |
GO:0140657 | ATP-dependent activity | 1 | 17 |
GO:1901265 | nucleoside phosphate binding | 3 | 18 |
GO:1901363 | heterocyclic compound binding | 2 | 18 |
GO:0004518 | nuclease activity | 4 | 1 |
GO:0004519 | endonuclease activity | 5 | 1 |
GO:0004521 | RNA endonuclease activity | 5 | 1 |
GO:0004526 | ribonuclease P activity | 6 | 1 |
GO:0004540 | RNA nuclease activity | 4 | 1 |
GO:0004549 | tRNA-specific ribonuclease activity | 5 | 1 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 1 |
GO:0016891 | RNA endonuclease activity, producing 5'-phosphomonoesters | 6 | 1 |
GO:0016893 | endonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 5'-phosphomonoesters | 6 | 1 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 1 |
GO:0140101 | catalytic activity, acting on a tRNA | 4 | 1 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 151 | 155 | PF00656 | 0.478 |
CLV_C14_Caspase3-7 | 597 | 601 | PF00656 | 0.368 |
CLV_C14_Caspase3-7 | 836 | 840 | PF00656 | 0.691 |
CLV_C14_Caspase3-7 | 939 | 943 | PF00656 | 0.450 |
CLV_NRD_NRD_1 | 101 | 103 | PF00675 | 0.306 |
CLV_NRD_NRD_1 | 1180 | 1182 | PF00675 | 0.506 |
CLV_NRD_NRD_1 | 1227 | 1229 | PF00675 | 0.361 |
CLV_NRD_NRD_1 | 1235 | 1237 | PF00675 | 0.368 |
CLV_NRD_NRD_1 | 1261 | 1263 | PF00675 | 0.498 |
CLV_NRD_NRD_1 | 177 | 179 | PF00675 | 0.405 |
CLV_NRD_NRD_1 | 2 | 4 | PF00675 | 0.327 |
CLV_NRD_NRD_1 | 279 | 281 | PF00675 | 0.315 |
CLV_NRD_NRD_1 | 391 | 393 | PF00675 | 0.370 |
CLV_NRD_NRD_1 | 472 | 474 | PF00675 | 0.393 |
CLV_NRD_NRD_1 | 518 | 520 | PF00675 | 0.289 |
CLV_NRD_NRD_1 | 538 | 540 | PF00675 | 0.257 |
CLV_NRD_NRD_1 | 589 | 591 | PF00675 | 0.273 |
CLV_NRD_NRD_1 | 650 | 652 | PF00675 | 0.327 |
CLV_PCSK_FUR_1 | 389 | 393 | PF00082 | 0.349 |
CLV_PCSK_FUR_1 | 536 | 540 | PF00082 | 0.322 |
CLV_PCSK_KEX2_1 | 101 | 103 | PF00082 | 0.284 |
CLV_PCSK_KEX2_1 | 1227 | 1229 | PF00082 | 0.342 |
CLV_PCSK_KEX2_1 | 1235 | 1237 | PF00082 | 0.358 |
CLV_PCSK_KEX2_1 | 1239 | 1241 | PF00082 | 0.353 |
CLV_PCSK_KEX2_1 | 1261 | 1263 | PF00082 | 0.498 |
CLV_PCSK_KEX2_1 | 177 | 179 | PF00082 | 0.405 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.303 |
CLV_PCSK_KEX2_1 | 279 | 281 | PF00082 | 0.377 |
CLV_PCSK_KEX2_1 | 391 | 393 | PF00082 | 0.370 |
CLV_PCSK_KEX2_1 | 472 | 474 | PF00082 | 0.366 |
CLV_PCSK_KEX2_1 | 538 | 540 | PF00082 | 0.249 |
CLV_PCSK_KEX2_1 | 589 | 591 | PF00082 | 0.230 |
CLV_PCSK_KEX2_1 | 650 | 652 | PF00082 | 0.363 |
CLV_PCSK_KEX2_1 | 88 | 90 | PF00082 | 0.314 |
CLV_PCSK_PC1ET2_1 | 1239 | 1241 | PF00082 | 0.431 |
CLV_PCSK_PC1ET2_1 | 279 | 281 | PF00082 | 0.343 |
CLV_PCSK_PC1ET2_1 | 88 | 90 | PF00082 | 0.322 |
CLV_PCSK_PC7_1 | 1235 | 1241 | PF00082 | 0.455 |
CLV_PCSK_SKI1_1 | 1006 | 1010 | PF00082 | 0.303 |
CLV_PCSK_SKI1_1 | 101 | 105 | PF00082 | 0.272 |
CLV_PCSK_SKI1_1 | 1058 | 1062 | PF00082 | 0.229 |
CLV_PCSK_SKI1_1 | 1089 | 1093 | PF00082 | 0.294 |
CLV_PCSK_SKI1_1 | 1218 | 1222 | PF00082 | 0.340 |
CLV_PCSK_SKI1_1 | 1230 | 1234 | PF00082 | 0.353 |
CLV_PCSK_SKI1_1 | 346 | 350 | PF00082 | 0.255 |
CLV_PCSK_SKI1_1 | 532 | 536 | PF00082 | 0.241 |
CLV_PCSK_SKI1_1 | 654 | 658 | PF00082 | 0.282 |
CLV_PCSK_SKI1_1 | 661 | 665 | PF00082 | 0.295 |
CLV_PCSK_SKI1_1 | 982 | 986 | PF00082 | 0.226 |
DEG_APCC_DBOX_1 | 1088 | 1096 | PF00400 | 0.398 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.508 |
DEG_ODPH_VHL_1 | 59 | 71 | PF01847 | 0.275 |
DEG_SCF_TRCP1_1 | 1113 | 1119 | PF00400 | 0.277 |
DEG_SPOP_SBC_1 | 1162 | 1166 | PF00917 | 0.386 |
DOC_ANK_TNKS_1 | 1102 | 1109 | PF00023 | 0.148 |
DOC_CKS1_1 | 1212 | 1217 | PF01111 | 0.484 |
DOC_CYCLIN_RxL_1 | 1227 | 1237 | PF00134 | 0.599 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 1146 | 1155 | PF00134 | 0.508 |
DOC_CYCLIN_yCln2_LP_2 | 1155 | 1161 | PF00134 | 0.386 |
DOC_MAPK_gen_1 | 1069 | 1077 | PF00069 | 0.422 |
DOC_MAPK_gen_1 | 1227 | 1233 | PF00069 | 0.628 |
DOC_MAPK_gen_1 | 1235 | 1246 | PF00069 | 0.619 |
DOC_MAPK_gen_1 | 160 | 167 | PF00069 | 0.589 |
DOC_MAPK_gen_1 | 472 | 480 | PF00069 | 0.573 |
DOC_MAPK_gen_1 | 519 | 525 | PF00069 | 0.457 |
DOC_MAPK_gen_1 | 589 | 596 | PF00069 | 0.443 |
DOC_MAPK_gen_1 | 650 | 658 | PF00069 | 0.462 |
DOC_MAPK_gen_1 | 784 | 793 | PF00069 | 0.617 |
DOC_MAPK_gen_1 | 928 | 938 | PF00069 | 0.466 |
DOC_MAPK_JIP1_4 | 41 | 47 | PF00069 | 0.430 |
DOC_MAPK_MEF2A_6 | 589 | 596 | PF00069 | 0.448 |
DOC_MAPK_MEF2A_6 | 665 | 672 | PF00069 | 0.593 |
DOC_MAPK_MEF2A_6 | 752 | 760 | PF00069 | 0.616 |
DOC_MAPK_MEF2A_6 | 931 | 940 | PF00069 | 0.450 |
DOC_PP1_RVXF_1 | 106 | 112 | PF00149 | 0.454 |
DOC_PP1_RVXF_1 | 370 | 377 | PF00149 | 0.543 |
DOC_PP1_RVXF_1 | 601 | 607 | PF00149 | 0.517 |
DOC_PP1_RVXF_1 | 829 | 836 | PF00149 | 0.663 |
DOC_PP1_RVXF_1 | 980 | 987 | PF00149 | 0.410 |
DOC_PP2B_LxvP_1 | 1155 | 1158 | PF13499 | 0.386 |
DOC_PP2B_LxvP_1 | 1199 | 1202 | PF13499 | 0.294 |
DOC_PP2B_LxvP_1 | 329 | 332 | PF13499 | 0.342 |
DOC_PP2B_LxvP_1 | 798 | 801 | PF13499 | 0.646 |
DOC_PP4_FxxP_1 | 1212 | 1215 | PF00568 | 0.607 |
DOC_PP4_FxxP_1 | 39 | 42 | PF00568 | 0.401 |
DOC_USP7_MATH_1 | 110 | 114 | PF00917 | 0.474 |
DOC_USP7_MATH_1 | 230 | 234 | PF00917 | 0.656 |
DOC_USP7_MATH_1 | 336 | 340 | PF00917 | 0.359 |
DOC_USP7_MATH_1 | 393 | 397 | PF00917 | 0.607 |
DOC_USP7_MATH_1 | 489 | 493 | PF00917 | 0.690 |
DOC_USP7_MATH_1 | 584 | 588 | PF00917 | 0.408 |
DOC_USP7_MATH_1 | 623 | 627 | PF00917 | 0.621 |
DOC_USP7_MATH_1 | 676 | 680 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 814 | 818 | PF00917 | 0.639 |
DOC_USP7_MATH_1 | 837 | 841 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 854 | 858 | PF00917 | 0.647 |
DOC_USP7_MATH_1 | 870 | 874 | PF00917 | 0.712 |
DOC_USP7_MATH_1 | 971 | 975 | PF00917 | 0.438 |
DOC_USP7_UBL2_3 | 281 | 285 | PF12436 | 0.564 |
DOC_WW_Pin1_4 | 1144 | 1149 | PF00397 | 0.517 |
DOC_WW_Pin1_4 | 1168 | 1173 | PF00397 | 0.282 |
DOC_WW_Pin1_4 | 1211 | 1216 | PF00397 | 0.486 |
DOC_WW_Pin1_4 | 1249 | 1254 | PF00397 | 0.628 |
DOC_WW_Pin1_4 | 505 | 510 | PF00397 | 0.445 |
DOC_WW_Pin1_4 | 916 | 921 | PF00397 | 0.487 |
LIG_14-3-3_CanoR_1 | 1181 | 1185 | PF00244 | 0.305 |
LIG_14-3-3_CanoR_1 | 1261 | 1267 | PF00244 | 0.664 |
LIG_14-3-3_CanoR_1 | 24 | 28 | PF00244 | 0.413 |
LIG_14-3-3_CanoR_1 | 241 | 251 | PF00244 | 0.564 |
LIG_14-3-3_CanoR_1 | 295 | 302 | PF00244 | 0.517 |
LIG_14-3-3_CanoR_1 | 589 | 593 | PF00244 | 0.442 |
LIG_14-3-3_CanoR_1 | 644 | 648 | PF00244 | 0.499 |
LIG_14-3-3_CanoR_1 | 651 | 657 | PF00244 | 0.480 |
LIG_14-3-3_CanoR_1 | 752 | 760 | PF00244 | 0.498 |
LIG_14-3-3_CanoR_1 | 807 | 816 | PF00244 | 0.637 |
LIG_APCC_ABBA_1 | 635 | 640 | PF00400 | 0.502 |
LIG_BRCT_BRCA1_1 | 357 | 361 | PF00533 | 0.265 |
LIG_CtBP_PxDLS_1 | 522 | 528 | PF00389 | 0.517 |
LIG_EH1_1 | 1085 | 1093 | PF00400 | 0.161 |
LIG_EVH1_1 | 798 | 802 | PF00568 | 0.672 |
LIG_FHA_1 | 1121 | 1127 | PF00498 | 0.232 |
LIG_FHA_1 | 1184 | 1190 | PF00498 | 0.268 |
LIG_FHA_1 | 1206 | 1212 | PF00498 | 0.363 |
LIG_FHA_1 | 141 | 147 | PF00498 | 0.488 |
LIG_FHA_1 | 148 | 154 | PF00498 | 0.472 |
LIG_FHA_1 | 15 | 21 | PF00498 | 0.533 |
LIG_FHA_1 | 177 | 183 | PF00498 | 0.590 |
LIG_FHA_1 | 350 | 356 | PF00498 | 0.289 |
LIG_FHA_1 | 421 | 427 | PF00498 | 0.445 |
LIG_FHA_1 | 463 | 469 | PF00498 | 0.622 |
LIG_FHA_1 | 481 | 487 | PF00498 | 0.524 |
LIG_FHA_1 | 574 | 580 | PF00498 | 0.476 |
LIG_FHA_1 | 589 | 595 | PF00498 | 0.381 |
LIG_FHA_1 | 653 | 659 | PF00498 | 0.476 |
LIG_FHA_1 | 72 | 78 | PF00498 | 0.259 |
LIG_FHA_1 | 828 | 834 | PF00498 | 0.650 |
LIG_FHA_1 | 935 | 941 | PF00498 | 0.451 |
LIG_FHA_2 | 1232 | 1238 | PF00498 | 0.507 |
LIG_FHA_2 | 1250 | 1256 | PF00498 | 0.558 |
LIG_FHA_2 | 166 | 172 | PF00498 | 0.610 |
LIG_FHA_2 | 267 | 273 | PF00498 | 0.433 |
LIG_FHA_2 | 453 | 459 | PF00498 | 0.665 |
LIG_FHA_2 | 662 | 668 | PF00498 | 0.505 |
LIG_FHA_2 | 704 | 710 | PF00498 | 0.474 |
LIG_FHA_2 | 717 | 723 | PF00498 | 0.467 |
LIG_GBD_Chelix_1 | 724 | 732 | PF00786 | 0.214 |
LIG_HCF-1_HBM_1 | 93 | 96 | PF13415 | 0.500 |
LIG_IBAR_NPY_1 | 1064 | 1066 | PF08397 | 0.420 |
LIG_LIR_Apic_2 | 1210 | 1215 | PF02991 | 0.544 |
LIG_LIR_Apic_2 | 324 | 330 | PF02991 | 0.412 |
LIG_LIR_Apic_2 | 37 | 42 | PF02991 | 0.401 |
LIG_LIR_Gen_1 | 1011 | 1020 | PF02991 | 0.272 |
LIG_LIR_Gen_1 | 1028 | 1037 | PF02991 | 0.208 |
LIG_LIR_Gen_1 | 1125 | 1136 | PF02991 | 0.270 |
LIG_LIR_Gen_1 | 1203 | 1212 | PF02991 | 0.161 |
LIG_LIR_Gen_1 | 164 | 175 | PF02991 | 0.516 |
LIG_LIR_Gen_1 | 976 | 986 | PF02991 | 0.418 |
LIG_LIR_LC3C_4 | 1196 | 1201 | PF02991 | 0.400 |
LIG_LIR_LC3C_4 | 17 | 21 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 1011 | 1015 | PF02991 | 0.273 |
LIG_LIR_Nem_3 | 1028 | 1033 | PF02991 | 0.209 |
LIG_LIR_Nem_3 | 1036 | 1041 | PF02991 | 0.262 |
LIG_LIR_Nem_3 | 1047 | 1052 | PF02991 | 0.317 |
LIG_LIR_Nem_3 | 1081 | 1086 | PF02991 | 0.427 |
LIG_LIR_Nem_3 | 1125 | 1131 | PF02991 | 0.285 |
LIG_LIR_Nem_3 | 1173 | 1179 | PF02991 | 0.236 |
LIG_LIR_Nem_3 | 1203 | 1209 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 164 | 170 | PF02991 | 0.630 |
LIG_LIR_Nem_3 | 358 | 362 | PF02991 | 0.337 |
LIG_LIR_Nem_3 | 82 | 87 | PF02991 | 0.519 |
LIG_LIR_Nem_3 | 976 | 981 | PF02991 | 0.418 |
LIG_NRBOX | 1150 | 1156 | PF00104 | 0.396 |
LIG_NRBOX | 980 | 986 | PF00104 | 0.421 |
LIG_PCNA_yPIPBox_3 | 307 | 318 | PF02747 | 0.398 |
LIG_PCNA_yPIPBox_3 | 91 | 104 | PF02747 | 0.576 |
LIG_PDZ_Class_3 | 1274 | 1279 | PF00595 | 0.624 |
LIG_Pex14_1 | 1038 | 1042 | PF04695 | 0.287 |
LIG_Pex14_1 | 1245 | 1249 | PF04695 | 0.654 |
LIG_Pex14_2 | 1029 | 1033 | PF04695 | 0.207 |
LIG_Pex14_2 | 1082 | 1086 | PF04695 | 0.319 |
LIG_PTB_Apo_2 | 1036 | 1043 | PF02174 | 0.246 |
LIG_PTB_Apo_2 | 19 | 26 | PF02174 | 0.418 |
LIG_PTB_Phospho_1 | 1036 | 1042 | PF10480 | 0.275 |
LIG_PTB_Phospho_1 | 19 | 25 | PF10480 | 0.418 |
LIG_RPA_C_Fungi | 109 | 121 | PF08784 | 0.292 |
LIG_SH2_CRK | 1017 | 1021 | PF00017 | 0.349 |
LIG_SH2_CRK | 1042 | 1046 | PF00017 | 0.267 |
LIG_SH2_CRK | 1128 | 1132 | PF00017 | 0.286 |
LIG_SH2_CRK | 1264 | 1268 | PF00017 | 0.698 |
LIG_SH2_NCK_1 | 1017 | 1021 | PF00017 | 0.352 |
LIG_SH2_NCK_1 | 1042 | 1046 | PF00017 | 0.278 |
LIG_SH2_NCK_1 | 1264 | 1268 | PF00017 | 0.407 |
LIG_SH2_SRC | 1111 | 1114 | PF00017 | 0.386 |
LIG_SH2_SRC | 1161 | 1164 | PF00017 | 0.398 |
LIG_SH2_SRC | 84 | 87 | PF00017 | 0.339 |
LIG_SH2_STAP1 | 1128 | 1132 | PF00017 | 0.261 |
LIG_SH2_STAP1 | 1137 | 1141 | PF00017 | 0.263 |
LIG_SH2_STAP1 | 1163 | 1167 | PF00017 | 0.371 |
LIG_SH2_STAP1 | 296 | 300 | PF00017 | 0.259 |
LIG_SH2_STAT3 | 25 | 28 | PF00017 | 0.398 |
LIG_SH2_STAT5 | 1042 | 1045 | PF00017 | 0.302 |
LIG_SH2_STAT5 | 1050 | 1053 | PF00017 | 0.252 |
LIG_SH2_STAT5 | 1066 | 1069 | PF00017 | 0.302 |
LIG_SH2_STAT5 | 1128 | 1131 | PF00017 | 0.308 |
LIG_SH2_STAT5 | 1137 | 1140 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 1161 | 1164 | PF00017 | 0.280 |
LIG_SH2_STAT5 | 1176 | 1179 | PF00017 | 0.352 |
LIG_SH2_STAT5 | 1206 | 1209 | PF00017 | 0.390 |
LIG_SH2_STAT5 | 147 | 150 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 15 | 18 | PF00017 | 0.261 |
LIG_SH2_STAT5 | 25 | 28 | PF00017 | 0.225 |
LIG_SH2_STAT5 | 268 | 271 | PF00017 | 0.308 |
LIG_SH2_STAT5 | 328 | 331 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 417 | 420 | PF00017 | 0.270 |
LIG_SH2_STAT5 | 46 | 49 | PF00017 | 0.257 |
LIG_SH2_STAT5 | 993 | 996 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 998 | 1001 | PF00017 | 0.302 |
LIG_SH3_3 | 338 | 344 | PF00018 | 0.281 |
LIG_SH3_3 | 350 | 356 | PF00018 | 0.204 |
LIG_SH3_3 | 483 | 489 | PF00018 | 0.515 |
LIG_SH3_3 | 55 | 61 | PF00018 | 0.268 |
LIG_SH3_3 | 593 | 599 | PF00018 | 0.453 |
LIG_SH3_3 | 633 | 639 | PF00018 | 0.601 |
LIG_SH3_3 | 796 | 802 | PF00018 | 0.572 |
LIG_SUMO_SIM_anti_2 | 1196 | 1201 | PF11976 | 0.412 |
LIG_SUMO_SIM_anti_2 | 123 | 132 | PF11976 | 0.306 |
LIG_SUMO_SIM_anti_2 | 136 | 141 | PF11976 | 0.254 |
LIG_SUMO_SIM_anti_2 | 483 | 488 | PF11976 | 0.497 |
LIG_SUMO_SIM_anti_2 | 697 | 704 | PF11976 | 0.433 |
LIG_SUMO_SIM_anti_2 | 877 | 883 | PF11976 | 0.391 |
LIG_SUMO_SIM_par_1 | 123 | 132 | PF11976 | 0.343 |
LIG_SUMO_SIM_par_1 | 73 | 78 | PF11976 | 0.384 |
LIG_SUMO_SIM_par_1 | 880 | 885 | PF11976 | 0.371 |
LIG_SUMO_SIM_par_1 | 936 | 942 | PF11976 | 0.291 |
LIG_TYR_ITIM | 1015 | 1020 | PF00017 | 0.352 |
LIG_TYR_ITIM | 1126 | 1131 | PF00017 | 0.275 |
LIG_TYR_ITIM | 1174 | 1179 | PF00017 | 0.367 |
LIG_TYR_ITIM | 1204 | 1209 | PF00017 | 0.358 |
LIG_TYR_ITIM | 326 | 331 | PF00017 | 0.294 |
LIG_WRC_WIRS_1 | 1009 | 1014 | PF05994 | 0.312 |
LIG_WRC_WIRS_1 | 1083 | 1088 | PF05994 | 0.325 |
LIG_WRC_WIRS_1 | 215 | 220 | PF05994 | 0.352 |
MOD_CDK_SPxxK_3 | 1211 | 1218 | PF00069 | 0.347 |
MOD_CDK_SPxxK_3 | 916 | 923 | PF00069 | 0.345 |
MOD_CK1_1 | 1025 | 1031 | PF00069 | 0.266 |
MOD_CK1_1 | 1114 | 1120 | PF00069 | 0.351 |
MOD_CK1_1 | 1166 | 1172 | PF00069 | 0.276 |
MOD_CK1_1 | 1183 | 1189 | PF00069 | 0.427 |
MOD_CK1_1 | 1265 | 1271 | PF00069 | 0.618 |
MOD_CK1_1 | 176 | 182 | PF00069 | 0.519 |
MOD_CK1_1 | 199 | 205 | PF00069 | 0.446 |
MOD_CK1_1 | 23 | 29 | PF00069 | 0.262 |
MOD_CK1_1 | 294 | 300 | PF00069 | 0.333 |
MOD_CK1_1 | 334 | 340 | PF00069 | 0.351 |
MOD_CK1_1 | 420 | 426 | PF00069 | 0.297 |
MOD_CK1_1 | 543 | 549 | PF00069 | 0.461 |
MOD_CK1_1 | 626 | 632 | PF00069 | 0.641 |
MOD_CK1_1 | 698 | 704 | PF00069 | 0.330 |
MOD_CK1_1 | 803 | 809 | PF00069 | 0.644 |
MOD_CK1_1 | 810 | 816 | PF00069 | 0.465 |
MOD_CK1_1 | 838 | 844 | PF00069 | 0.641 |
MOD_CK1_1 | 918 | 924 | PF00069 | 0.379 |
MOD_CK2_1 | 184 | 190 | PF00069 | 0.591 |
MOD_CK2_1 | 404 | 410 | PF00069 | 0.293 |
MOD_CK2_1 | 452 | 458 | PF00069 | 0.586 |
MOD_CK2_1 | 505 | 511 | PF00069 | 0.257 |
MOD_CK2_1 | 541 | 547 | PF00069 | 0.409 |
MOD_CK2_1 | 703 | 709 | PF00069 | 0.337 |
MOD_CK2_1 | 782 | 788 | PF00069 | 0.653 |
MOD_CK2_1 | 854 | 860 | PF00069 | 0.653 |
MOD_CMANNOS | 1245 | 1248 | PF00535 | 0.588 |
MOD_GlcNHglycan | 1024 | 1027 | PF01048 | 0.266 |
MOD_GlcNHglycan | 1113 | 1116 | PF01048 | 0.271 |
MOD_GlcNHglycan | 1190 | 1193 | PF01048 | 0.414 |
MOD_GlcNHglycan | 1264 | 1267 | PF01048 | 0.577 |
MOD_GlcNHglycan | 143 | 146 | PF01048 | 0.453 |
MOD_GlcNHglycan | 211 | 214 | PF01048 | 0.303 |
MOD_GlcNHglycan | 296 | 299 | PF01048 | 0.384 |
MOD_GlcNHglycan | 335 | 339 | PF01048 | 0.519 |
MOD_GlcNHglycan | 492 | 495 | PF01048 | 0.645 |
MOD_GlcNHglycan | 559 | 562 | PF01048 | 0.398 |
MOD_GlcNHglycan | 600 | 603 | PF01048 | 0.450 |
MOD_GlcNHglycan | 628 | 631 | PF01048 | 0.695 |
MOD_GlcNHglycan | 697 | 700 | PF01048 | 0.499 |
MOD_GlcNHglycan | 765 | 768 | PF01048 | 0.512 |
MOD_GlcNHglycan | 809 | 812 | PF01048 | 0.549 |
MOD_GlcNHglycan | 816 | 819 | PF01048 | 0.534 |
MOD_GlcNHglycan | 872 | 875 | PF01048 | 0.577 |
MOD_GlcNHglycan | 995 | 998 | PF01048 | 0.248 |
MOD_GSK3_1 | 1000 | 1007 | PF00069 | 0.249 |
MOD_GSK3_1 | 1025 | 1032 | PF00069 | 0.252 |
MOD_GSK3_1 | 1040 | 1047 | PF00069 | 0.212 |
MOD_GSK3_1 | 1116 | 1123 | PF00069 | 0.349 |
MOD_GSK3_1 | 1131 | 1138 | PF00069 | 0.244 |
MOD_GSK3_1 | 1140 | 1147 | PF00069 | 0.249 |
MOD_GSK3_1 | 1162 | 1169 | PF00069 | 0.292 |
MOD_GSK3_1 | 1207 | 1214 | PF00069 | 0.328 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.462 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.532 |
MOD_GSK3_1 | 266 | 273 | PF00069 | 0.277 |
MOD_GSK3_1 | 376 | 383 | PF00069 | 0.493 |
MOD_GSK3_1 | 420 | 427 | PF00069 | 0.308 |
MOD_GSK3_1 | 575 | 582 | PF00069 | 0.378 |
MOD_GSK3_1 | 584 | 591 | PF00069 | 0.297 |
MOD_GSK3_1 | 617 | 624 | PF00069 | 0.488 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.259 |
MOD_GSK3_1 | 731 | 738 | PF00069 | 0.366 |
MOD_GSK3_1 | 778 | 785 | PF00069 | 0.687 |
MOD_GSK3_1 | 803 | 810 | PF00069 | 0.585 |
MOD_GSK3_1 | 837 | 844 | PF00069 | 0.655 |
MOD_GSK3_1 | 905 | 912 | PF00069 | 0.381 |
MOD_N-GLC_1 | 173 | 178 | PF02516 | 0.633 |
MOD_N-GLC_1 | 318 | 323 | PF02516 | 0.506 |
MOD_N-GLC_1 | 404 | 409 | PF02516 | 0.327 |
MOD_N-GLC_1 | 96 | 101 | PF02516 | 0.546 |
MOD_NEK2_1 | 1004 | 1009 | PF00069 | 0.256 |
MOD_NEK2_1 | 1029 | 1034 | PF00069 | 0.262 |
MOD_NEK2_1 | 1082 | 1087 | PF00069 | 0.342 |
MOD_NEK2_1 | 1091 | 1096 | PF00069 | 0.286 |
MOD_NEK2_1 | 1098 | 1103 | PF00069 | 0.243 |
MOD_NEK2_1 | 1124 | 1129 | PF00069 | 0.293 |
MOD_NEK2_1 | 1131 | 1136 | PF00069 | 0.267 |
MOD_NEK2_1 | 1193 | 1198 | PF00069 | 0.396 |
MOD_NEK2_1 | 1207 | 1212 | PF00069 | 0.333 |
MOD_NEK2_1 | 1231 | 1236 | PF00069 | 0.509 |
MOD_NEK2_1 | 140 | 145 | PF00069 | 0.438 |
MOD_NEK2_1 | 165 | 170 | PF00069 | 0.478 |
MOD_NEK2_1 | 348 | 353 | PF00069 | 0.259 |
MOD_NEK2_1 | 380 | 385 | PF00069 | 0.399 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.237 |
MOD_NEK2_1 | 521 | 526 | PF00069 | 0.303 |
MOD_NEK2_1 | 575 | 580 | PF00069 | 0.235 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.240 |
MOD_NEK2_1 | 936 | 941 | PF00069 | 0.366 |
MOD_NEK2_2 | 1163 | 1168 | PF00069 | 0.400 |
MOD_NEK2_2 | 643 | 648 | PF00069 | 0.324 |
MOD_NEK2_2 | 666 | 671 | PF00069 | 0.522 |
MOD_NEK2_2 | 96 | 101 | PF00069 | 0.553 |
MOD_PIKK_1 | 1131 | 1137 | PF00454 | 0.319 |
MOD_PIKK_1 | 393 | 399 | PF00454 | 0.424 |
MOD_PIKK_1 | 424 | 430 | PF00454 | 0.332 |
MOD_PIKK_1 | 760 | 766 | PF00454 | 0.439 |
MOD_PIKK_1 | 838 | 844 | PF00454 | 0.664 |
MOD_PIKK_1 | 918 | 924 | PF00454 | 0.351 |
MOD_PIKK_1 | 973 | 979 | PF00454 | 0.345 |
MOD_PK_1 | 404 | 410 | PF00069 | 0.349 |
MOD_PK_1 | 909 | 915 | PF00069 | 0.421 |
MOD_PKA_2 | 1180 | 1186 | PF00069 | 0.366 |
MOD_PKA_2 | 176 | 182 | PF00069 | 0.644 |
MOD_PKA_2 | 23 | 29 | PF00069 | 0.259 |
MOD_PKA_2 | 294 | 300 | PF00069 | 0.359 |
MOD_PKA_2 | 588 | 594 | PF00069 | 0.290 |
MOD_PKA_2 | 643 | 649 | PF00069 | 0.318 |
MOD_PKA_2 | 751 | 757 | PF00069 | 0.527 |
MOD_PKA_2 | 758 | 764 | PF00069 | 0.529 |
MOD_PKA_2 | 770 | 776 | PF00069 | 0.548 |
MOD_PKA_2 | 806 | 812 | PF00069 | 0.527 |
MOD_PKB_1 | 902 | 910 | PF00069 | 0.338 |
MOD_Plk_1 | 1120 | 1126 | PF00069 | 0.313 |
MOD_Plk_1 | 1254 | 1260 | PF00069 | 0.540 |
MOD_Plk_1 | 376 | 382 | PF00069 | 0.439 |
MOD_Plk_1 | 404 | 410 | PF00069 | 0.278 |
MOD_Plk_1 | 573 | 579 | PF00069 | 0.392 |
MOD_Plk_1 | 666 | 672 | PF00069 | 0.446 |
MOD_Plk_1 | 676 | 682 | PF00069 | 0.408 |
MOD_Plk_1 | 838 | 844 | PF00069 | 0.687 |
MOD_Plk_1 | 96 | 102 | PF00069 | 0.544 |
MOD_Plk_1 | 971 | 977 | PF00069 | 0.259 |
MOD_Plk_2-3 | 184 | 190 | PF00069 | 0.422 |
MOD_Plk_4 | 1000 | 1006 | PF00069 | 0.254 |
MOD_Plk_4 | 1025 | 1031 | PF00069 | 0.263 |
MOD_Plk_4 | 1033 | 1039 | PF00069 | 0.276 |
MOD_Plk_4 | 1044 | 1050 | PF00069 | 0.190 |
MOD_Plk_4 | 1082 | 1088 | PF00069 | 0.308 |
MOD_Plk_4 | 1135 | 1141 | PF00069 | 0.299 |
MOD_Plk_4 | 1163 | 1169 | PF00069 | 0.331 |
MOD_Plk_4 | 1200 | 1206 | PF00069 | 0.381 |
MOD_Plk_4 | 1207 | 1213 | PF00069 | 0.338 |
MOD_Plk_4 | 1254 | 1260 | PF00069 | 0.446 |
MOD_Plk_4 | 349 | 355 | PF00069 | 0.289 |
MOD_Plk_4 | 376 | 382 | PF00069 | 0.481 |
MOD_Plk_4 | 404 | 410 | PF00069 | 0.304 |
MOD_Plk_4 | 521 | 527 | PF00069 | 0.349 |
MOD_Plk_4 | 54 | 60 | PF00069 | 0.279 |
MOD_Plk_4 | 64 | 70 | PF00069 | 0.229 |
MOD_Plk_4 | 643 | 649 | PF00069 | 0.401 |
MOD_Plk_4 | 666 | 672 | PF00069 | 0.416 |
MOD_Plk_4 | 698 | 704 | PF00069 | 0.447 |
MOD_Plk_4 | 889 | 895 | PF00069 | 0.402 |
MOD_Plk_4 | 909 | 915 | PF00069 | 0.334 |
MOD_ProDKin_1 | 1144 | 1150 | PF00069 | 0.398 |
MOD_ProDKin_1 | 1168 | 1174 | PF00069 | 0.349 |
MOD_ProDKin_1 | 1211 | 1217 | PF00069 | 0.352 |
MOD_ProDKin_1 | 1249 | 1255 | PF00069 | 0.557 |
MOD_ProDKin_1 | 505 | 511 | PF00069 | 0.297 |
MOD_ProDKin_1 | 916 | 922 | PF00069 | 0.350 |
MOD_SUMO_rev_2 | 154 | 161 | PF00179 | 0.401 |
TRG_DiLeu_BaEn_1 | 677 | 682 | PF01217 | 0.306 |
TRG_DiLeu_BaLyEn_6 | 1227 | 1232 | PF01217 | 0.558 |
TRG_DiLeu_BaLyEn_6 | 2 | 7 | PF01217 | 0.289 |
TRG_DiLeu_BaLyEn_6 | 67 | 72 | PF01217 | 0.322 |
TRG_ENDOCYTIC_2 | 1005 | 1008 | PF00928 | 0.274 |
TRG_ENDOCYTIC_2 | 1017 | 1020 | PF00928 | 0.236 |
TRG_ENDOCYTIC_2 | 1128 | 1131 | PF00928 | 0.279 |
TRG_ENDOCYTIC_2 | 1176 | 1179 | PF00928 | 0.340 |
TRG_ENDOCYTIC_2 | 1206 | 1209 | PF00928 | 0.291 |
TRG_ENDOCYTIC_2 | 1238 | 1241 | PF00928 | 0.440 |
TRG_ENDOCYTIC_2 | 328 | 331 | PF00928 | 0.426 |
TRG_ENDOCYTIC_2 | 36 | 39 | PF00928 | 0.279 |
TRG_ENDOCYTIC_2 | 46 | 49 | PF00928 | 0.280 |
TRG_ENDOCYTIC_2 | 84 | 87 | PF00928 | 0.372 |
TRG_ER_diArg_1 | 1 | 3 | PF00400 | 0.357 |
TRG_ER_diArg_1 | 100 | 102 | PF00400 | 0.478 |
TRG_ER_diArg_1 | 1226 | 1228 | PF00400 | 0.441 |
TRG_ER_diArg_1 | 177 | 180 | PF00400 | 0.476 |
TRG_ER_diArg_1 | 389 | 392 | PF00400 | 0.661 |
TRG_ER_diArg_1 | 471 | 473 | PF00400 | 0.527 |
TRG_ER_diArg_1 | 535 | 538 | PF00400 | 0.380 |
TRG_ER_diArg_1 | 899 | 902 | PF00400 | 0.494 |
TRG_NES_CRM1_1 | 695 | 709 | PF08389 | 0.298 |
TRG_NLS_MonoExtC_3 | 278 | 283 | PF00514 | 0.310 |
TRG_NLS_MonoExtC_3 | 87 | 93 | PF00514 | 0.384 |
TRG_Pf-PMV_PEXEL_1 | 102 | 107 | PF00026 | 0.309 |
TRG_Pf-PMV_PEXEL_1 | 33 | 37 | PF00026 | 0.398 |
TRG_Pf-PMV_PEXEL_1 | 5 | 9 | PF00026 | 0.313 |
TRG_Pf-PMV_PEXEL_1 | 673 | 677 | PF00026 | 0.452 |
TRG_Pf-PMV_PEXEL_1 | 831 | 836 | PF00026 | 0.597 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IKQ9 | Leptomonas seymouri | 29% | 85% |
A0A0N1PF54 | Leptomonas seymouri | 61% | 98% |
A0A0S4ITW3 | Bodo saltans | 41% | 92% |
A0A1X0P1Z0 | Trypanosomatidae | 49% | 100% |
A0A1X0PA06 | Trypanosomatidae | 30% | 99% |
A0A3Q8IFQ5 | Leishmania donovani | 93% | 100% |
A0A3Q8INM6 | Leishmania donovani | 28% | 100% |
A0A3R7NV92 | Trypanosoma rangeli | 31% | 100% |
A0A3S5IS27 | Trypanosoma rangeli | 48% | 100% |
A4H7E2 | Leishmania braziliensis | 28% | 100% |
A4H7E4 | Leishmania braziliensis | 28% | 100% |
A4HAY0 | Leishmania braziliensis | 29% | 85% |
A4HIF8 | Leishmania braziliensis | 75% | 100% |
A4HVT2 | Leishmania infantum | 28% | 100% |
A4I5Q4 | Leishmania infantum | 93% | 100% |
A4IA89 | Leishmania infantum | 28% | 100% |
C9ZR23 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
E9APH7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9B0Z9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
E9B5B1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
P57792 | Arabidopsis thaliana | 28% | 100% |
Q4Q2M2 | Leishmania major | 27% | 100% |
Q4QG01 | Leishmania major | 28% | 100% |
Q6VXY9 | Leishmania donovani | 28% | 100% |
Q9LK90 | Arabidopsis thaliana | 28% | 100% |
Q9SX33 | Arabidopsis thaliana | 26% | 100% |
V5BQC7 | Trypanosoma cruzi | 32% | 100% |
V5DCY9 | Trypanosoma cruzi | 47% | 100% |