Homologous to animal ER-localized Ca2+ ATPases. Localization: ER (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: 2 |
Forrest at al. (procyclic) | no | yes: 2 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 12 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 5 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 5 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0005886 | plasma membrane | 3 | 1 |
Related structures:
AlphaFold database: E9B686
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 1 |
GO:0006811 | monoatomic ion transport | 4 | 1 |
GO:0006812 | monoatomic cation transport | 5 | 1 |
GO:0006816 | calcium ion transport | 7 | 1 |
GO:0006873 | intracellular monoatomic ion homeostasis | 4 | 1 |
GO:0006874 | intracellular calcium ion homeostasis | 7 | 1 |
GO:0006875 | obsolete intracellular metal ion homeostasis | 6 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0019725 | cellular homeostasis | 2 | 1 |
GO:0030001 | metal ion transport | 6 | 1 |
GO:0030003 | intracellular monoatomic cation homeostasis | 5 | 1 |
GO:0034220 | monoatomic ion transmembrane transport | 3 | 1 |
GO:0042592 | homeostatic process | 3 | 1 |
GO:0048878 | chemical homeostasis | 4 | 1 |
GO:0050801 | monoatomic ion homeostasis | 5 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0055065 | obsolete metal ion homeostasis | 7 | 1 |
GO:0055074 | calcium ion homeostasis | 8 | 1 |
GO:0055080 | monoatomic cation homeostasis | 6 | 1 |
GO:0055082 | intracellular chemical homeostasis | 3 | 1 |
GO:0055085 | transmembrane transport | 2 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0065008 | regulation of biological quality | 2 | 1 |
GO:0070588 | calcium ion transmembrane transport | 6 | 1 |
GO:0072503 | obsolete cellular divalent inorganic cation homeostasis | 6 | 1 |
GO:0072507 | obsolete divalent inorganic cation homeostasis | 7 | 1 |
GO:0098655 | monoatomic cation transmembrane transport | 4 | 1 |
GO:0098660 | inorganic ion transmembrane transport | 4 | 1 |
GO:0098662 | inorganic cation transmembrane transport | 5 | 1 |
GO:0098771 | inorganic ion homeostasis | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0016462 | pyrophosphatase activity | 5 | 12 |
GO:0016787 | hydrolase activity | 2 | 12 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 12 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 12 |
GO:0016887 | ATP hydrolysis activity | 7 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 12 |
GO:0030554 | adenyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
GO:0005215 | transporter activity | 1 | 2 |
GO:0005388 | P-type calcium transporter activity | 4 | 1 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 2 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 2 |
GO:0015085 | calcium ion transmembrane transporter activity | 6 | 1 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 2 |
GO:0015399 | primary active transmembrane transporter activity | 4 | 2 |
GO:0015662 | P-type ion transporter activity | 4 | 1 |
GO:0019829 | ATPase-coupled monoatomic cation transmembrane transporter activity | 3 | 2 |
GO:0022804 | active transmembrane transporter activity | 3 | 2 |
GO:0022853 | active monoatomic ion transmembrane transporter activity | 4 | 2 |
GO:0022857 | transmembrane transporter activity | 2 | 2 |
GO:0022890 | inorganic cation transmembrane transporter activity | 4 | 2 |
GO:0042626 | ATPase-coupled transmembrane transporter activity | 2 | 2 |
GO:0046873 | metal ion transmembrane transporter activity | 5 | 1 |
GO:0140358 | P-type transmembrane transporter activity | 3 | 1 |
GO:0140657 | ATP-dependent activity | 1 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 222 | 226 | PF00656 | 0.499 |
CLV_C14_Caspase3-7 | 232 | 236 | PF00656 | 0.437 |
CLV_C14_Caspase3-7 | 605 | 609 | PF00656 | 0.522 |
CLV_C14_Caspase3-7 | 825 | 829 | PF00656 | 0.482 |
CLV_NRD_NRD_1 | 1143 | 1145 | PF00675 | 0.359 |
CLV_NRD_NRD_1 | 1221 | 1223 | PF00675 | 0.491 |
CLV_NRD_NRD_1 | 388 | 390 | PF00675 | 0.224 |
CLV_NRD_NRD_1 | 436 | 438 | PF00675 | 0.211 |
CLV_NRD_NRD_1 | 507 | 509 | PF00675 | 0.271 |
CLV_NRD_NRD_1 | 804 | 806 | PF00675 | 0.317 |
CLV_NRD_NRD_1 | 854 | 856 | PF00675 | 0.239 |
CLV_NRD_NRD_1 | 912 | 914 | PF00675 | 0.237 |
CLV_NRD_NRD_1 | 918 | 920 | PF00675 | 0.246 |
CLV_PCSK_KEX2_1 | 1216 | 1218 | PF00082 | 0.438 |
CLV_PCSK_KEX2_1 | 1223 | 1225 | PF00082 | 0.467 |
CLV_PCSK_KEX2_1 | 123 | 125 | PF00082 | 0.348 |
CLV_PCSK_KEX2_1 | 422 | 424 | PF00082 | 0.317 |
CLV_PCSK_KEX2_1 | 498 | 500 | PF00082 | 0.239 |
CLV_PCSK_KEX2_1 | 653 | 655 | PF00082 | 0.215 |
CLV_PCSK_KEX2_1 | 803 | 805 | PF00082 | 0.285 |
CLV_PCSK_KEX2_1 | 854 | 856 | PF00082 | 0.225 |
CLV_PCSK_KEX2_1 | 912 | 914 | PF00082 | 0.237 |
CLV_PCSK_PC1ET2_1 | 1216 | 1218 | PF00082 | 0.476 |
CLV_PCSK_PC1ET2_1 | 1223 | 1225 | PF00082 | 0.493 |
CLV_PCSK_PC1ET2_1 | 123 | 125 | PF00082 | 0.348 |
CLV_PCSK_PC1ET2_1 | 422 | 424 | PF00082 | 0.317 |
CLV_PCSK_PC1ET2_1 | 498 | 500 | PF00082 | 0.257 |
CLV_PCSK_PC1ET2_1 | 653 | 655 | PF00082 | 0.215 |
CLV_PCSK_SKI1_1 | 1080 | 1084 | PF00082 | 0.282 |
CLV_PCSK_SKI1_1 | 1134 | 1138 | PF00082 | 0.262 |
CLV_PCSK_SKI1_1 | 1144 | 1148 | PF00082 | 0.331 |
CLV_PCSK_SKI1_1 | 307 | 311 | PF00082 | 0.215 |
CLV_PCSK_SKI1_1 | 383 | 387 | PF00082 | 0.317 |
CLV_PCSK_SKI1_1 | 419 | 423 | PF00082 | 0.305 |
CLV_PCSK_SKI1_1 | 432 | 436 | PF00082 | 0.300 |
CLV_PCSK_SKI1_1 | 782 | 786 | PF00082 | 0.215 |
DEG_APCC_DBOX_1 | 1143 | 1151 | PF00400 | 0.559 |
DOC_ANK_TNKS_1 | 156 | 163 | PF00023 | 0.667 |
DOC_CYCLIN_yCln2_LP_2 | 1092 | 1098 | PF00134 | 0.266 |
DOC_CYCLIN_yCln2_LP_2 | 807 | 813 | PF00134 | 0.517 |
DOC_MAPK_DCC_7 | 318 | 326 | PF00069 | 0.517 |
DOC_MAPK_gen_1 | 1144 | 1150 | PF00069 | 0.561 |
DOC_MAPK_gen_1 | 197 | 205 | PF00069 | 0.558 |
DOC_MAPK_gen_1 | 437 | 445 | PF00069 | 0.476 |
DOC_MAPK_gen_1 | 508 | 515 | PF00069 | 0.465 |
DOC_MAPK_gen_1 | 538 | 544 | PF00069 | 0.439 |
DOC_MAPK_gen_1 | 662 | 669 | PF00069 | 0.472 |
DOC_MAPK_gen_1 | 919 | 925 | PF00069 | 0.425 |
DOC_MAPK_MEF2A_6 | 113 | 121 | PF00069 | 0.558 |
DOC_MAPK_MEF2A_6 | 255 | 264 | PF00069 | 0.395 |
DOC_MAPK_MEF2A_6 | 318 | 326 | PF00069 | 0.439 |
DOC_MAPK_MEF2A_6 | 508 | 515 | PF00069 | 0.568 |
DOC_PP1_RVXF_1 | 1135 | 1142 | PF00149 | 0.580 |
DOC_PP1_RVXF_1 | 714 | 721 | PF00149 | 0.453 |
DOC_PP2B_LxvP_1 | 1092 | 1095 | PF13499 | 0.340 |
DOC_PP2B_LxvP_1 | 982 | 985 | PF13499 | 0.425 |
DOC_PP2B_PxIxI_1 | 869 | 875 | PF00149 | 0.439 |
DOC_PP4_FxxP_1 | 1206 | 1209 | PF00568 | 0.728 |
DOC_PP4_FxxP_1 | 730 | 733 | PF00568 | 0.425 |
DOC_USP7_MATH_1 | 1067 | 1071 | PF00917 | 0.482 |
DOC_USP7_MATH_1 | 299 | 303 | PF00917 | 0.500 |
DOC_USP7_MATH_1 | 593 | 597 | PF00917 | 0.443 |
DOC_USP7_MATH_1 | 80 | 84 | PF00917 | 0.597 |
DOC_USP7_MATH_1 | 880 | 884 | PF00917 | 0.475 |
DOC_USP7_MATH_1 | 92 | 96 | PF00917 | 0.677 |
DOC_USP7_UBL2_3 | 428 | 432 | PF12436 | 0.517 |
DOC_USP7_UBL2_3 | 534 | 538 | PF12436 | 0.425 |
DOC_WW_Pin1_4 | 187 | 192 | PF00397 | 0.669 |
DOC_WW_Pin1_4 | 32 | 37 | PF00397 | 0.608 |
DOC_WW_Pin1_4 | 463 | 468 | PF00397 | 0.317 |
DOC_WW_Pin1_4 | 838 | 843 | PF00397 | 0.415 |
DOC_WW_Pin1_4 | 866 | 871 | PF00397 | 0.425 |
DOC_WW_Pin1_4 | 950 | 955 | PF00397 | 0.251 |
LIG_14-3-3_CanoR_1 | 1046 | 1054 | PF00244 | 0.229 |
LIG_14-3-3_CanoR_1 | 1188 | 1192 | PF00244 | 0.588 |
LIG_14-3-3_CanoR_1 | 124 | 128 | PF00244 | 0.548 |
LIG_14-3-3_CanoR_1 | 301 | 307 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 56 | 64 | PF00244 | 0.637 |
LIG_14-3-3_CanoR_1 | 79 | 85 | PF00244 | 0.574 |
LIG_14-3-3_CanoR_1 | 912 | 921 | PF00244 | 0.442 |
LIG_14-3-3_CanoR_1 | 976 | 984 | PF00244 | 0.440 |
LIG_Actin_WH2_2 | 1175 | 1190 | PF00022 | 0.583 |
LIG_Actin_WH2_2 | 703 | 718 | PF00022 | 0.415 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.590 |
LIG_BRCT_BRCA1_1 | 1046 | 1050 | PF00533 | 0.267 |
LIG_BRCT_BRCA1_1 | 1089 | 1093 | PF00533 | 0.251 |
LIG_BRCT_BRCA1_1 | 268 | 272 | PF00533 | 0.306 |
LIG_Clathr_ClatBox_1 | 1147 | 1151 | PF01394 | 0.642 |
LIG_Clathr_ClatBox_1 | 211 | 215 | PF01394 | 0.439 |
LIG_CtBP_PxDLS_1 | 573 | 577 | PF00389 | 0.422 |
LIG_deltaCOP1_diTrp_1 | 1040 | 1050 | PF00928 | 0.227 |
LIG_deltaCOP1_diTrp_1 | 1078 | 1083 | PF00928 | 0.415 |
LIG_deltaCOP1_diTrp_1 | 274 | 278 | PF00928 | 0.293 |
LIG_deltaCOP1_diTrp_1 | 956 | 963 | PF00928 | 0.285 |
LIG_eIF4E_1 | 441 | 447 | PF01652 | 0.439 |
LIG_FAT_LD_1 | 439 | 447 | PF03623 | 0.425 |
LIG_FHA_1 | 1130 | 1136 | PF00498 | 0.451 |
LIG_FHA_1 | 257 | 263 | PF00498 | 0.266 |
LIG_FHA_1 | 308 | 314 | PF00498 | 0.488 |
LIG_FHA_1 | 492 | 498 | PF00498 | 0.419 |
LIG_FHA_1 | 52 | 58 | PF00498 | 0.686 |
LIG_FHA_1 | 525 | 531 | PF00498 | 0.425 |
LIG_FHA_1 | 595 | 601 | PF00498 | 0.448 |
LIG_FHA_1 | 681 | 687 | PF00498 | 0.494 |
LIG_FHA_1 | 886 | 892 | PF00498 | 0.489 |
LIG_FHA_1 | 976 | 982 | PF00498 | 0.452 |
LIG_FHA_1 | 991 | 997 | PF00498 | 0.366 |
LIG_FHA_2 | 1170 | 1176 | PF00498 | 0.686 |
LIG_FHA_2 | 527 | 533 | PF00498 | 0.425 |
LIG_FHA_2 | 555 | 561 | PF00498 | 0.503 |
LIG_FHA_2 | 655 | 661 | PF00498 | 0.517 |
LIG_FHA_2 | 694 | 700 | PF00498 | 0.423 |
LIG_GBD_Chelix_1 | 409 | 417 | PF00786 | 0.282 |
LIG_Integrin_isoDGR_2 | 155 | 157 | PF01839 | 0.470 |
LIG_IRF3_LxIS_1 | 936 | 943 | PF10401 | 0.453 |
LIG_LIR_Apic_2 | 1203 | 1209 | PF02991 | 0.722 |
LIG_LIR_Apic_2 | 727 | 733 | PF02991 | 0.461 |
LIG_LIR_Gen_1 | 1165 | 1174 | PF02991 | 0.680 |
LIG_LIR_Gen_1 | 1190 | 1199 | PF02991 | 0.647 |
LIG_LIR_Gen_1 | 206 | 217 | PF02991 | 0.475 |
LIG_LIR_Gen_1 | 245 | 254 | PF02991 | 0.519 |
LIG_LIR_Gen_1 | 274 | 283 | PF02991 | 0.227 |
LIG_LIR_Gen_1 | 637 | 648 | PF02991 | 0.427 |
LIG_LIR_Gen_1 | 818 | 827 | PF02991 | 0.433 |
LIG_LIR_Gen_1 | 828 | 837 | PF02991 | 0.416 |
LIG_LIR_Gen_1 | 898 | 909 | PF02991 | 0.448 |
LIG_LIR_Gen_1 | 956 | 967 | PF02991 | 0.266 |
LIG_LIR_Nem_3 | 1047 | 1053 | PF02991 | 0.255 |
LIG_LIR_Nem_3 | 1090 | 1096 | PF02991 | 0.201 |
LIG_LIR_Nem_3 | 1113 | 1119 | PF02991 | 0.225 |
LIG_LIR_Nem_3 | 1131 | 1136 | PF02991 | 0.266 |
LIG_LIR_Nem_3 | 1165 | 1169 | PF02991 | 0.578 |
LIG_LIR_Nem_3 | 1190 | 1194 | PF02991 | 0.620 |
LIG_LIR_Nem_3 | 198 | 203 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 206 | 212 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 245 | 249 | PF02991 | 0.519 |
LIG_LIR_Nem_3 | 274 | 278 | PF02991 | 0.294 |
LIG_LIR_Nem_3 | 440 | 444 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 637 | 643 | PF02991 | 0.427 |
LIG_LIR_Nem_3 | 750 | 756 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 818 | 822 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 828 | 833 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 898 | 904 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 988 | 994 | PF02991 | 0.465 |
LIG_MYND_3 | 510 | 514 | PF01753 | 0.564 |
LIG_Pex14_1 | 959 | 963 | PF04695 | 0.266 |
LIG_Pex14_2 | 1072 | 1076 | PF04695 | 0.418 |
LIG_Pex14_2 | 283 | 287 | PF04695 | 0.251 |
LIG_PTB_Apo_2 | 1135 | 1142 | PF02174 | 0.488 |
LIG_REV1ctd_RIR_1 | 1218 | 1225 | PF16727 | 0.544 |
LIG_RPA_C_Fungi | 1041 | 1053 | PF08784 | 0.285 |
LIG_SH2_CRK | 1133 | 1137 | PF00017 | 0.266 |
LIG_SH2_CRK | 586 | 590 | PF00017 | 0.224 |
LIG_SH2_CRK | 760 | 764 | PF00017 | 0.266 |
LIG_SH2_GRB2like | 1098 | 1101 | PF00017 | 0.395 |
LIG_SH2_NCK_1 | 465 | 469 | PF00017 | 0.324 |
LIG_SH2_SRC | 1098 | 1101 | PF00017 | 0.285 |
LIG_SH2_SRC | 760 | 763 | PF00017 | 0.266 |
LIG_SH2_STAP1 | 472 | 476 | PF00017 | 0.251 |
LIG_SH2_STAT3 | 34 | 37 | PF00017 | 0.483 |
LIG_SH2_STAT3 | 584 | 587 | PF00017 | 0.286 |
LIG_SH2_STAT5 | 1054 | 1057 | PF00017 | 0.251 |
LIG_SH2_STAT5 | 1062 | 1065 | PF00017 | 0.251 |
LIG_SH2_STAT5 | 1098 | 1101 | PF00017 | 0.251 |
LIG_SH2_STAT5 | 34 | 37 | PF00017 | 0.483 |
LIG_SH2_STAT5 | 444 | 447 | PF00017 | 0.269 |
LIG_SH2_STAT5 | 465 | 468 | PF00017 | 0.395 |
LIG_SH2_STAT5 | 584 | 587 | PF00017 | 0.395 |
LIG_SH2_STAT5 | 668 | 671 | PF00017 | 0.266 |
LIG_SH3_3 | 1061 | 1067 | PF00018 | 0.285 |
LIG_SH3_3 | 759 | 765 | PF00018 | 0.266 |
LIG_SUMO_SIM_anti_2 | 245 | 252 | PF11976 | 0.395 |
LIG_SUMO_SIM_anti_2 | 259 | 265 | PF11976 | 0.273 |
LIG_SUMO_SIM_anti_2 | 334 | 339 | PF11976 | 0.278 |
LIG_SUMO_SIM_anti_2 | 932 | 938 | PF11976 | 0.252 |
LIG_SUMO_SIM_anti_2 | 953 | 959 | PF11976 | 0.266 |
LIG_SUMO_SIM_anti_2 | 993 | 1000 | PF11976 | 0.378 |
LIG_SUMO_SIM_par_1 | 100 | 105 | PF11976 | 0.484 |
LIG_SUMO_SIM_par_1 | 1146 | 1154 | PF11976 | 0.544 |
LIG_SUMO_SIM_par_1 | 245 | 252 | PF11976 | 0.395 |
LIG_SUMO_SIM_par_1 | 263 | 269 | PF11976 | 0.301 |
LIG_SUMO_SIM_par_1 | 334 | 339 | PF11976 | 0.287 |
LIG_SUMO_SIM_par_1 | 676 | 683 | PF11976 | 0.285 |
LIG_SUMO_SIM_par_1 | 691 | 696 | PF11976 | 0.285 |
LIG_TRFH_1 | 950 | 954 | PF08558 | 0.251 |
LIG_TYR_ITIM | 1052 | 1057 | PF00017 | 0.251 |
LIG_UBA3_1 | 1139 | 1145 | PF00899 | 0.548 |
LIG_UBA3_1 | 247 | 255 | PF00899 | 0.274 |
LIG_UBA3_1 | 848 | 857 | PF00899 | 0.266 |
LIG_WRC_WIRS_1 | 1123 | 1128 | PF05994 | 0.286 |
LIG_WRC_WIRS_1 | 1166 | 1171 | PF05994 | 0.610 |
LIG_WRC_WIRS_1 | 14 | 19 | PF05994 | 0.529 |
LIG_WW_3 | 761 | 765 | PF00397 | 0.251 |
MOD_CDK_SPxxK_3 | 838 | 845 | PF00069 | 0.251 |
MOD_CDK_SPxxK_3 | 866 | 873 | PF00069 | 0.266 |
MOD_CK1_1 | 1110 | 1116 | PF00069 | 0.286 |
MOD_CK1_1 | 1190 | 1196 | PF00069 | 0.494 |
MOD_CK1_1 | 1197 | 1203 | PF00069 | 0.519 |
MOD_CK1_1 | 302 | 308 | PF00069 | 0.381 |
MOD_CK1_1 | 427 | 433 | PF00069 | 0.320 |
MOD_CK1_1 | 471 | 477 | PF00069 | 0.277 |
MOD_CK1_1 | 524 | 530 | PF00069 | 0.251 |
MOD_CK1_1 | 58 | 64 | PF00069 | 0.519 |
MOD_CK1_1 | 647 | 653 | PF00069 | 0.286 |
MOD_CK1_1 | 767 | 773 | PF00069 | 0.266 |
MOD_CK1_1 | 794 | 800 | PF00069 | 0.345 |
MOD_CK1_1 | 841 | 847 | PF00069 | 0.251 |
MOD_CK2_1 | 1021 | 1027 | PF00069 | 0.286 |
MOD_CK2_1 | 526 | 532 | PF00069 | 0.283 |
MOD_CK2_1 | 654 | 660 | PF00069 | 0.395 |
MOD_CK2_1 | 950 | 956 | PF00069 | 0.266 |
MOD_Cter_Amidation | 910 | 913 | PF01082 | 0.283 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.501 |
MOD_GlcNHglycan | 1023 | 1026 | PF01048 | 0.341 |
MOD_GlcNHglycan | 104 | 107 | PF01048 | 0.712 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.575 |
MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.761 |
MOD_GlcNHglycan | 268 | 271 | PF01048 | 0.266 |
MOD_GlcNHglycan | 429 | 432 | PF01048 | 0.298 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.551 |
MOD_GlcNHglycan | 882 | 885 | PF01048 | 0.369 |
MOD_GlcNHglycan | 964 | 967 | PF01048 | 0.285 |
MOD_GSK3_1 | 102 | 109 | PF00069 | 0.703 |
MOD_GSK3_1 | 1041 | 1048 | PF00069 | 0.441 |
MOD_GSK3_1 | 1165 | 1172 | PF00069 | 0.609 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.737 |
MOD_GSK3_1 | 1190 | 1197 | PF00069 | 0.509 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.676 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.648 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.515 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.460 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.523 |
MOD_GSK3_1 | 393 | 400 | PF00069 | 0.242 |
MOD_GSK3_1 | 422 | 429 | PF00069 | 0.267 |
MOD_GSK3_1 | 487 | 494 | PF00069 | 0.284 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.549 |
MOD_GSK3_1 | 517 | 524 | PF00069 | 0.291 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.532 |
MOD_GSK3_1 | 680 | 687 | PF00069 | 0.287 |
MOD_GSK3_1 | 782 | 789 | PF00069 | 0.355 |
MOD_N-GLC_1 | 517 | 522 | PF02516 | 0.307 |
MOD_N-GLC_1 | 69 | 74 | PF02516 | 0.535 |
MOD_N-GLC_1 | 866 | 871 | PF02516 | 0.251 |
MOD_NEK2_1 | 1058 | 1063 | PF00069 | 0.310 |
MOD_NEK2_1 | 1107 | 1112 | PF00069 | 0.295 |
MOD_NEK2_1 | 1169 | 1174 | PF00069 | 0.620 |
MOD_NEK2_1 | 1187 | 1192 | PF00069 | 0.478 |
MOD_NEK2_1 | 17 | 22 | PF00069 | 0.502 |
MOD_NEK2_1 | 424 | 429 | PF00069 | 0.467 |
MOD_NEK2_1 | 493 | 498 | PF00069 | 0.251 |
MOD_NEK2_1 | 594 | 599 | PF00069 | 0.265 |
MOD_NEK2_1 | 848 | 853 | PF00069 | 0.389 |
MOD_NEK2_1 | 925 | 930 | PF00069 | 0.266 |
MOD_NEK2_1 | 962 | 967 | PF00069 | 0.266 |
MOD_NEK2_2 | 1067 | 1072 | PF00069 | 0.345 |
MOD_NEK2_2 | 945 | 950 | PF00069 | 0.403 |
MOD_PIKK_1 | 17 | 23 | PF00454 | 0.492 |
MOD_PIKK_1 | 249 | 255 | PF00454 | 0.395 |
MOD_PIKK_1 | 394 | 400 | PF00454 | 0.276 |
MOD_PIKK_1 | 693 | 699 | PF00454 | 0.395 |
MOD_PIKK_1 | 912 | 918 | PF00454 | 0.304 |
MOD_PIKK_1 | 985 | 991 | PF00454 | 0.286 |
MOD_PKA_1 | 1215 | 1221 | PF00069 | 0.520 |
MOD_PKA_1 | 123 | 129 | PF00069 | 0.512 |
MOD_PKA_1 | 422 | 428 | PF00069 | 0.229 |
MOD_PKA_1 | 653 | 659 | PF00069 | 0.251 |
MOD_PKA_1 | 912 | 918 | PF00069 | 0.304 |
MOD_PKA_2 | 1045 | 1051 | PF00069 | 0.248 |
MOD_PKA_2 | 1067 | 1073 | PF00069 | 0.255 |
MOD_PKA_2 | 1187 | 1193 | PF00069 | 0.491 |
MOD_PKA_2 | 123 | 129 | PF00069 | 0.437 |
MOD_PKA_2 | 394 | 400 | PF00069 | 0.251 |
MOD_PKA_2 | 422 | 428 | PF00069 | 0.284 |
MOD_PKA_2 | 55 | 61 | PF00069 | 0.526 |
MOD_PKA_2 | 653 | 659 | PF00069 | 0.280 |
MOD_PKA_2 | 767 | 773 | PF00069 | 0.345 |
MOD_PKA_2 | 78 | 84 | PF00069 | 0.516 |
MOD_PKA_2 | 912 | 918 | PF00069 | 0.304 |
MOD_PKA_2 | 975 | 981 | PF00069 | 0.286 |
MOD_Plk_1 | 299 | 305 | PF00069 | 0.369 |
MOD_Plk_1 | 58 | 64 | PF00069 | 0.507 |
MOD_Plk_1 | 644 | 650 | PF00069 | 0.395 |
MOD_Plk_2-3 | 823 | 829 | PF00069 | 0.297 |
MOD_Plk_2-3 | 975 | 981 | PF00069 | 0.395 |
MOD_Plk_4 | 1067 | 1073 | PF00069 | 0.251 |
MOD_Plk_4 | 1087 | 1093 | PF00069 | 0.124 |
MOD_Plk_4 | 1122 | 1128 | PF00069 | 0.183 |
MOD_Plk_4 | 123 | 129 | PF00069 | 0.473 |
MOD_Plk_4 | 242 | 248 | PF00069 | 0.395 |
MOD_Plk_4 | 595 | 601 | PF00069 | 0.291 |
MOD_Plk_4 | 767 | 773 | PF00069 | 0.305 |
MOD_Plk_4 | 794 | 800 | PF00069 | 0.345 |
MOD_Plk_4 | 900 | 906 | PF00069 | 0.294 |
MOD_Plk_4 | 945 | 951 | PF00069 | 0.381 |
MOD_Plk_4 | 997 | 1003 | PF00069 | 0.283 |
MOD_ProDKin_1 | 187 | 193 | PF00069 | 0.599 |
MOD_ProDKin_1 | 32 | 38 | PF00069 | 0.521 |
MOD_ProDKin_1 | 463 | 469 | PF00069 | 0.395 |
MOD_ProDKin_1 | 838 | 844 | PF00069 | 0.251 |
MOD_ProDKin_1 | 866 | 872 | PF00069 | 0.266 |
MOD_ProDKin_1 | 950 | 956 | PF00069 | 0.251 |
MOD_SUMO_for_1 | 663 | 666 | PF00179 | 0.286 |
MOD_SUMO_rev_2 | 425 | 430 | PF00179 | 0.186 |
MOD_SUMO_rev_2 | 645 | 652 | PF00179 | 0.266 |
MOD_SUMO_rev_2 | 656 | 663 | PF00179 | 0.266 |
MOD_SUMO_rev_2 | 687 | 693 | PF00179 | 0.418 |
MOD_SUMO_rev_2 | 841 | 846 | PF00179 | 0.251 |
TRG_DiLeu_BaEn_1 | 688 | 693 | PF01217 | 0.395 |
TRG_DiLeu_BaEn_1 | 932 | 937 | PF01217 | 0.251 |
TRG_ENDOCYTIC_2 | 1054 | 1057 | PF00928 | 0.251 |
TRG_ENDOCYTIC_2 | 1133 | 1136 | PF00928 | 0.266 |
TRG_ENDOCYTIC_2 | 1166 | 1169 | PF00928 | 0.474 |
TRG_ENDOCYTIC_2 | 14 | 17 | PF00928 | 0.532 |
TRG_ENDOCYTIC_2 | 444 | 447 | PF00928 | 0.266 |
TRG_ENDOCYTIC_2 | 586 | 589 | PF00928 | 0.305 |
TRG_ER_diArg_1 | 1072 | 1075 | PF00400 | 0.324 |
TRG_ER_diArg_1 | 1221 | 1224 | PF00400 | 0.696 |
TRG_ER_diArg_1 | 802 | 805 | PF00400 | 0.324 |
TRG_ER_diArg_1 | 912 | 914 | PF00400 | 0.282 |
TRG_NES_CRM1_1 | 323 | 334 | PF08389 | 0.345 |
TRG_NES_CRM1_1 | 750 | 761 | PF08389 | 0.270 |
TRG_NLS_MonoCore_2 | 1213 | 1218 | PF00514 | 0.566 |
TRG_NLS_MonoExtN_4 | 1214 | 1219 | PF00514 | 0.602 |
TRG_NLS_MonoExtN_4 | 854 | 859 | PF00514 | 0.310 |
TRG_Pf-PMV_PEXEL_1 | 1145 | 1149 | PF00026 | 0.560 |
TRG_Pf-PMV_PEXEL_1 | 135 | 139 | PF00026 | 0.585 |
TRG_Pf-PMV_PEXEL_1 | 157 | 161 | PF00026 | 0.609 |
TRG_Pf-PMV_PEXEL_1 | 583 | 587 | PF00026 | 0.288 |
TRG_Pf-PMV_PEXEL_1 | 782 | 787 | PF00026 | 0.251 |
TRG_Pf-PMV_PEXEL_1 | 805 | 809 | PF00026 | 0.395 |
TRG_Pf-PMV_PEXEL_1 | 912 | 916 | PF00026 | 0.308 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3Y1 | Leptomonas seymouri | 31% | 100% |
A0A0N1HWG6 | Leptomonas seymouri | 28% | 100% |
A0A0N1PFH3 | Leptomonas seymouri | 73% | 100% |
A0A0S4J5A1 | Bodo saltans | 51% | 100% |
A0A0S4JA92 | Bodo saltans | 27% | 100% |
A0A0S4KIG5 | Bodo saltans | 32% | 100% |
A0A0S4KNQ6 | Bodo saltans | 27% | 100% |
A0A1X0NNY6 | Trypanosomatidae | 30% | 100% |
A0A1X0P689 | Trypanosomatidae | 69% | 100% |
A0A381MFJ0 | Leishmania infantum | 27% | 100% |
A0A3R7MRX8 | Trypanosoma rangeli | 63% | 100% |
A0A3S5H5Y9 | Leishmania donovani | 25% | 100% |
A0A3S5ISK9 | Trypanosoma rangeli | 25% | 100% |
A0A3S7WPW0 | Leishmania donovani | 25% | 100% |
A0A3S7WV61 | Leishmania donovani | 27% | 100% |
A0A3S7WV68 | Leishmania donovani | 27% | 100% |
A0A3S7X978 | Leishmania donovani | 96% | 100% |
A0A422NTS7 | Trypanosoma rangeli | 30% | 100% |
A0A451EJU6 | Leishmania donovani | 31% | 100% |
A4H3S2 | Leishmania braziliensis | 31% | 100% |
A4H514 | Leishmania braziliensis | 27% | 100% |
A4H903 | Leishmania braziliensis | 29% | 100% |
A4H9Q5 | Leishmania braziliensis | 27% | 100% |
A4HMM8 | Leishmania braziliensis | 89% | 100% |
A4HRZ6 | Leishmania infantum | 31% | 100% |
A4HT82 | Leishmania infantum | 27% | 100% |
A4HTF0 | Leishmania infantum | 26% | 100% |
A4HY23 | Leishmania infantum | 27% | 100% |
A4IBA6 | Leishmania infantum | 96% | 100% |
A7L9Z8 | Mus musculus | 28% | 100% |
C9ZPL1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
C9ZUN6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
C9ZZN4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 63% | 100% |
E9AF31 | Leishmania major | 95% | 100% |
E9AJY3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E9AL76 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9AL78 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9ART6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
J9VQQ3 | Cryptococcus neoformans var. grubii serotype A (strain H99 / ATCC 208821 / CBS 10515 / FGSC 9487) | 27% | 87% |
O14983 | Homo sapiens | 30% | 100% |
O22218 | Arabidopsis thaliana | 27% | 100% |
O23087 | Arabidopsis thaliana | 32% | 100% |
O34431 | Bacillus subtilis (strain 168) | 34% | 100% |
O43108 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 31% | 100% |
O46674 | Canis lupus familiaris | 30% | 100% |
O55143 | Mus musculus | 30% | 100% |
O59868 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 31% | 100% |
O64806 | Arabidopsis thaliana | 27% | 100% |
O70228 | Mus musculus | 22% | 100% |
O75110 | Homo sapiens | 22% | 100% |
O75185 | Homo sapiens | 29% | 100% |
O77696 | Sus scrofa | 31% | 100% |
O94296 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 23% | 97% |
P04191 | Oryctolagus cuniculus | 30% | 100% |
P05025 | Tetronarce californica | 30% | 100% |
P11507 | Rattus norvegicus | 30% | 100% |
P11607 | Sus scrofa | 30% | 100% |
P13585 | Gallus gallus | 30% | 100% |
P13586 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 28% | 100% |
P13587 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 35% | 100% |
P13607 | Drosophila melanogaster | 29% | 100% |
P16615 | Homo sapiens | 30% | 100% |
P17326 | Artemia franciscana | 28% | 100% |
P18596 | Rattus norvegicus | 31% | 100% |
P20647 | Oryctolagus cuniculus | 30% | 100% |
P22189 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 38% | 100% |
P22700 | Drosophila melanogaster | 31% | 100% |
P28774 | Artemia franciscana | 29% | 100% |
P30714 | Rhinella marina | 29% | 100% |
P35315 | Trypanosoma brucei brucei | 31% | 100% |
P35316 | Artemia franciscana | 28% | 100% |
P37278 | Synechococcus elongatus (strain PCC 7942 / FACHB-805) | 35% | 100% |
P54209 | Dunaliella bioculata | 30% | 100% |
P54210 | Dunaliella acidophila | 24% | 100% |
P54679 | Dictyostelium discoideum | 26% | 100% |
P54707 | Homo sapiens | 28% | 100% |
P57709 | Bos taurus | 29% | 100% |
P63688 | Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) | 30% | 100% |
P70083 | Makaira nigricans | 31% | 100% |
P70704 | Mus musculus | 23% | 100% |
P92939 | Arabidopsis thaliana | 31% | 100% |
P98194 | Homo sapiens | 30% | 100% |
P9WPS8 | Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) | 30% | 100% |
P9WPS9 | Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) | 30% | 100% |
Q00779 | Felis catus | 30% | 100% |
Q01896 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 35% | 100% |
Q03669 | Gallus gallus | 29% | 100% |
Q0VCY0 | Bos taurus | 30% | 100% |
Q12691 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 35% | 100% |
Q292Q0 | Drosophila pseudoobscura pseudoobscura | 30% | 100% |
Q29449 | Bos taurus | 23% | 100% |
Q2QY12 | Oryza sativa subsp. japonica | 28% | 100% |
Q2RAS0 | Oryza sativa subsp. japonica | 26% | 100% |
Q42883 | Solanum lycopersicum | 31% | 100% |
Q4QDN7 | Leishmania major | 27% | 100% |
Q4QDN8 | Leishmania major | 27% | 100% |
Q4QIM6 | Leishmania major | 27% | 100% |
Q4QIM8 | Leishmania major | 27% | 100% |
Q5R5K5 | Pongo abelii | 30% | 100% |
Q64518 | Mus musculus | 31% | 100% |
Q64541 | Rattus norvegicus | 28% | 100% |
Q64566 | Rattus norvegicus | 30% | 100% |
Q64578 | Rattus norvegicus | 30% | 100% |
Q6RWA9 | Taenia solium | 29% | 100% |
Q73E41 | Bacillus cereus (strain ATCC 10987 / NRS 248) | 33% | 100% |
Q7PPA5 | Anopheles gambiae | 30% | 100% |
Q7X8B5 | Oryza sativa subsp. japonica | 27% | 100% |
Q80XR2 | Mus musculus | 30% | 100% |
Q8R429 | Mus musculus | 30% | 100% |
Q8R4C1 | Rattus norvegicus | 29% | 100% |
Q8Y8Q5 | Listeria monocytogenes serovar 1/2a (strain ATCC BAA-679 / EGD-e) | 30% | 100% |
Q92036 | Rhinella marina | 29% | 100% |
Q92105 | Pelophylax lessonae | 30% | 100% |
Q92126 | Xenopus laevis | 26% | 100% |
Q93084 | Homo sapiens | 32% | 100% |
Q95Z93 | Leishmania major | 31% | 100% |
Q9CFU9 | Lactococcus lactis subsp. lactis (strain IL1403) | 29% | 100% |
Q9CTG6 | Mus musculus | 21% | 100% |
Q9HDW7 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 28% | 95% |
Q9LF79 | Arabidopsis thaliana | 31% | 100% |
Q9M2L4 | Arabidopsis thaliana | 26% | 100% |
Q9SY55 | Arabidopsis thaliana | 31% | 100% |
Q9TV52 | Oryctolagus cuniculus | 29% | 100% |
Q9XES1 | Arabidopsis thaliana | 32% | 100% |
Q9YGL9 | Gallus gallus | 30% | 100% |
V5B873 | Trypanosoma cruzi | 26% | 100% |
V5BHZ2 | Trypanosoma cruzi | 67% | 100% |
V5BLM1 | Trypanosoma cruzi | 31% | 100% |