Homologous to other eukaryotic P-type Ca2+ ATPases.. For some reason, this group has heavily expanded in Kinetoplastida.. Localization: Endosomal (by homology) / 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: 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: 18 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 14 |
NetGPI | no | yes: 0, no: 14 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005886 | plasma membrane | 3 | 3 |
GO:0016020 | membrane | 2 | 15 |
GO:0043226 | organelle | 2 | 4 |
GO:0043227 | membrane-bounded organelle | 3 | 4 |
GO:0043229 | intracellular organelle | 3 | 4 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 4 |
GO:0110165 | cellular anatomical entity | 1 | 15 |
GO:0005783 | endoplasmic reticulum | 5 | 1 |
Related structures:
AlphaFold database: Q4Q490
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 | 15 |
GO:0003824 | catalytic activity | 1 | 15 |
GO:0005215 | transporter activity | 1 | 4 |
GO:0005388 | P-type calcium transporter activity | 4 | 4 |
GO:0005488 | binding | 1 | 15 |
GO:0005524 | ATP binding | 5 | 15 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 4 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 4 |
GO:0015085 | calcium ion transmembrane transporter activity | 6 | 4 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 4 |
GO:0015399 | primary active transmembrane transporter activity | 4 | 4 |
GO:0015662 | P-type ion transporter activity | 4 | 4 |
GO:0016462 | pyrophosphatase activity | 5 | 15 |
GO:0016787 | hydrolase activity | 2 | 15 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 15 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 15 |
GO:0016887 | ATP hydrolysis activity | 7 | 15 |
GO:0017076 | purine nucleotide binding | 4 | 15 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 15 |
GO:0019829 | ATPase-coupled monoatomic cation transmembrane transporter activity | 3 | 4 |
GO:0022804 | active transmembrane transporter activity | 3 | 4 |
GO:0022853 | active monoatomic ion transmembrane transporter activity | 4 | 4 |
GO:0022857 | transmembrane transporter activity | 2 | 4 |
GO:0022890 | inorganic cation transmembrane transporter activity | 4 | 4 |
GO:0030554 | adenyl nucleotide binding | 5 | 15 |
GO:0032553 | ribonucleotide binding | 3 | 15 |
GO:0032555 | purine ribonucleotide binding | 4 | 15 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 15 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 15 |
GO:0036094 | small molecule binding | 2 | 15 |
GO:0042626 | ATPase-coupled transmembrane transporter activity | 2 | 4 |
GO:0043167 | ion binding | 2 | 15 |
GO:0043168 | anion binding | 3 | 15 |
GO:0046873 | metal ion transmembrane transporter activity | 5 | 4 |
GO:0097159 | organic cyclic compound binding | 2 | 15 |
GO:0097367 | carbohydrate derivative binding | 2 | 15 |
GO:0140358 | P-type transmembrane transporter activity | 3 | 4 |
GO:0140657 | ATP-dependent activity | 1 | 4 |
GO:1901265 | nucleoside phosphate binding | 3 | 15 |
GO:1901363 | heterocyclic compound binding | 2 | 15 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 176 | 180 | PF00656 | 0.697 |
CLV_C14_Caspase3-7 | 188 | 192 | PF00656 | 0.639 |
CLV_C14_Caspase3-7 | 261 | 265 | PF00656 | 0.448 |
CLV_C14_Caspase3-7 | 772 | 776 | PF00656 | 0.723 |
CLV_NRD_NRD_1 | 1182 | 1184 | PF00675 | 0.405 |
CLV_NRD_NRD_1 | 147 | 149 | PF00675 | 0.409 |
CLV_NRD_NRD_1 | 165 | 167 | PF00675 | 0.361 |
CLV_NRD_NRD_1 | 50 | 52 | PF00675 | 0.320 |
CLV_NRD_NRD_1 | 560 | 562 | PF00675 | 0.363 |
CLV_NRD_NRD_1 | 871 | 873 | PF00675 | 0.251 |
CLV_NRD_NRD_1 | 938 | 940 | PF00675 | 0.285 |
CLV_PCSK_FUR_1 | 1180 | 1184 | PF00082 | 0.377 |
CLV_PCSK_FUR_1 | 558 | 562 | PF00082 | 0.313 |
CLV_PCSK_KEX2_1 | 1165 | 1167 | PF00082 | 0.472 |
CLV_PCSK_KEX2_1 | 1182 | 1184 | PF00082 | 0.417 |
CLV_PCSK_KEX2_1 | 164 | 166 | PF00082 | 0.393 |
CLV_PCSK_KEX2_1 | 5 | 7 | PF00082 | 0.406 |
CLV_PCSK_KEX2_1 | 50 | 52 | PF00082 | 0.322 |
CLV_PCSK_KEX2_1 | 560 | 562 | PF00082 | 0.356 |
CLV_PCSK_KEX2_1 | 864 | 866 | PF00082 | 0.324 |
CLV_PCSK_KEX2_1 | 871 | 873 | PF00082 | 0.279 |
CLV_PCSK_KEX2_1 | 909 | 911 | PF00082 | 0.248 |
CLV_PCSK_PC1ET2_1 | 1165 | 1167 | PF00082 | 0.369 |
CLV_PCSK_PC1ET2_1 | 5 | 7 | PF00082 | 0.404 |
CLV_PCSK_PC1ET2_1 | 864 | 866 | PF00082 | 0.323 |
CLV_PCSK_PC1ET2_1 | 909 | 911 | PF00082 | 0.248 |
CLV_PCSK_SKI1_1 | 1165 | 1169 | PF00082 | 0.367 |
CLV_PCSK_SKI1_1 | 1175 | 1179 | PF00082 | 0.377 |
CLV_PCSK_SKI1_1 | 1183 | 1187 | PF00082 | 0.401 |
CLV_PCSK_SKI1_1 | 165 | 169 | PF00082 | 0.347 |
CLV_PCSK_SKI1_1 | 248 | 252 | PF00082 | 0.323 |
CLV_PCSK_SKI1_1 | 328 | 332 | PF00082 | 0.357 |
CLV_PCSK_SKI1_1 | 377 | 381 | PF00082 | 0.268 |
CLV_PCSK_SKI1_1 | 417 | 421 | PF00082 | 0.311 |
CLV_PCSK_SKI1_1 | 482 | 486 | PF00082 | 0.414 |
CLV_PCSK_SKI1_1 | 864 | 868 | PF00082 | 0.354 |
CLV_PCSK_SKI1_1 | 932 | 936 | PF00082 | 0.278 |
CLV_PCSK_SKI1_1 | 939 | 943 | PF00082 | 0.306 |
CLV_Separin_Metazoa | 155 | 159 | PF03568 | 0.593 |
DEG_APCC_DBOX_1 | 1174 | 1182 | PF00400 | 0.606 |
DEG_APCC_DBOX_1 | 49 | 57 | PF00400 | 0.451 |
DEG_COP1_1 | 1006 | 1017 | PF00400 | 0.506 |
DEG_MDM2_SWIB_1 | 1097 | 1105 | PF02201 | 0.400 |
DEG_SPOP_SBC_1 | 174 | 178 | PF00917 | 0.533 |
DOC_ANK_TNKS_1 | 686 | 693 | PF00023 | 0.570 |
DOC_CKS1_1 | 109 | 114 | PF01111 | 0.451 |
DOC_CYCLIN_RxL_1 | 935 | 947 | PF00134 | 0.519 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 380 | 389 | PF00134 | 0.551 |
DOC_CYCLIN_yCln2_LP_2 | 251 | 257 | PF00134 | 0.513 |
DOC_CYCLIN_yCln2_LP_2 | 578 | 584 | PF00134 | 0.425 |
DOC_MAPK_gen_1 | 863 | 869 | PF00069 | 0.509 |
DOC_MAPK_gen_1 | 909 | 917 | PF00069 | 0.456 |
DOC_MAPK_MEF2A_6 | 115 | 123 | PF00069 | 0.358 |
DOC_MAPK_MEF2A_6 | 971 | 980 | PF00069 | 0.284 |
DOC_PP1_RVXF_1 | 938 | 945 | PF00149 | 0.506 |
DOC_PP2B_LxvP_1 | 198 | 201 | PF13499 | 0.453 |
DOC_PP2B_LxvP_1 | 409 | 412 | PF13499 | 0.575 |
DOC_PP2B_PxIxI_1 | 849 | 855 | PF00149 | 0.564 |
DOC_PP4_FxxP_1 | 461 | 464 | PF00568 | 0.653 |
DOC_USP7_MATH_1 | 101 | 105 | PF00917 | 0.513 |
DOC_USP7_MATH_1 | 174 | 178 | PF00917 | 0.585 |
DOC_USP7_MATH_1 | 234 | 238 | PF00917 | 0.451 |
DOC_USP7_MATH_1 | 452 | 456 | PF00917 | 0.661 |
DOC_USP7_MATH_1 | 563 | 567 | PF00917 | 0.499 |
DOC_USP7_MATH_1 | 618 | 622 | PF00917 | 0.547 |
DOC_USP7_MATH_1 | 76 | 80 | PF00917 | 0.543 |
DOC_USP7_MATH_1 | 770 | 774 | PF00917 | 0.609 |
DOC_USP7_MATH_1 | 960 | 964 | PF00917 | 0.382 |
DOC_WW_Pin1_4 | 1055 | 1060 | PF00397 | 0.229 |
DOC_WW_Pin1_4 | 108 | 113 | PF00397 | 0.438 |
DOC_WW_Pin1_4 | 26 | 31 | PF00397 | 0.650 |
DOC_WW_Pin1_4 | 294 | 299 | PF00397 | 0.516 |
DOC_WW_Pin1_4 | 335 | 340 | PF00397 | 0.477 |
DOC_WW_Pin1_4 | 444 | 449 | PF00397 | 0.723 |
DOC_WW_Pin1_4 | 470 | 475 | PF00397 | 0.772 |
DOC_WW_Pin1_4 | 766 | 771 | PF00397 | 0.788 |
DOC_WW_Pin1_4 | 817 | 822 | PF00397 | 0.663 |
DOC_WW_Pin1_4 | 856 | 861 | PF00397 | 0.557 |
DOC_WW_Pin1_4 | 965 | 970 | PF00397 | 0.381 |
LIG_14-3-3_CanoR_1 | 1063 | 1072 | PF00244 | 0.396 |
LIG_14-3-3_CanoR_1 | 1180 | 1186 | PF00244 | 0.706 |
LIG_14-3-3_CanoR_1 | 164 | 170 | PF00244 | 0.618 |
LIG_14-3-3_CanoR_1 | 454 | 464 | PF00244 | 0.636 |
LIG_14-3-3_CanoR_1 | 543 | 550 | PF00244 | 0.565 |
LIG_14-3-3_CanoR_1 | 561 | 570 | PF00244 | 0.483 |
LIG_14-3-3_CanoR_1 | 605 | 610 | PF00244 | 0.539 |
LIG_14-3-3_CanoR_1 | 633 | 639 | PF00244 | 0.477 |
LIG_14-3-3_CanoR_1 | 726 | 734 | PF00244 | 0.612 |
LIG_14-3-3_CanoR_1 | 837 | 845 | PF00244 | 0.555 |
LIG_14-3-3_CanoR_1 | 865 | 870 | PF00244 | 0.482 |
LIG_14-3-3_CanoR_1 | 910 | 917 | PF00244 | 0.448 |
LIG_Actin_WH2_2 | 365 | 383 | PF00022 | 0.513 |
LIG_AP2alpha_2 | 253 | 255 | PF02296 | 0.448 |
LIG_APCC_ABBA_1 | 493 | 498 | PF00400 | 0.452 |
LIG_BIR_III_4 | 648 | 652 | PF00653 | 0.598 |
LIG_BRCT_BRCA1_1 | 1015 | 1019 | PF00533 | 0.465 |
LIG_BRCT_BRCA1_1 | 694 | 698 | PF00533 | 0.498 |
LIG_deltaCOP1_diTrp_1 | 78 | 83 | PF00928 | 0.496 |
LIG_EH1_1 | 1107 | 1115 | PF00400 | 0.256 |
LIG_EH1_1 | 373 | 381 | PF00400 | 0.448 |
LIG_EVH1_2 | 466 | 470 | PF00568 | 0.646 |
LIG_FHA_1 | 1008 | 1014 | PF00498 | 0.513 |
LIG_FHA_1 | 1024 | 1030 | PF00498 | 0.442 |
LIG_FHA_1 | 1047 | 1053 | PF00498 | 0.270 |
LIG_FHA_1 | 1129 | 1135 | PF00498 | 0.244 |
LIG_FHA_1 | 114 | 120 | PF00498 | 0.440 |
LIG_FHA_1 | 1147 | 1153 | PF00498 | 0.402 |
LIG_FHA_1 | 188 | 194 | PF00498 | 0.673 |
LIG_FHA_1 | 348 | 354 | PF00498 | 0.483 |
LIG_FHA_1 | 367 | 373 | PF00498 | 0.608 |
LIG_FHA_1 | 404 | 410 | PF00498 | 0.572 |
LIG_FHA_1 | 411 | 417 | PF00498 | 0.587 |
LIG_FHA_1 | 423 | 429 | PF00498 | 0.589 |
LIG_FHA_1 | 451 | 457 | PF00498 | 0.683 |
LIG_FHA_1 | 483 | 489 | PF00498 | 0.564 |
LIG_FHA_1 | 605 | 611 | PF00498 | 0.503 |
LIG_FHA_1 | 755 | 761 | PF00498 | 0.650 |
LIG_FHA_1 | 780 | 786 | PF00498 | 0.627 |
LIG_FHA_1 | 840 | 846 | PF00498 | 0.518 |
LIG_FHA_2 | 108 | 114 | PF00498 | 0.491 |
LIG_FHA_2 | 1133 | 1139 | PF00498 | 0.270 |
LIG_FHA_2 | 186 | 192 | PF00498 | 0.718 |
LIG_FHA_2 | 439 | 445 | PF00498 | 0.658 |
LIG_FHA_2 | 533 | 539 | PF00498 | 0.522 |
LIG_FHA_2 | 857 | 863 | PF00498 | 0.529 |
LIG_LIR_Apic_2 | 458 | 464 | PF02991 | 0.638 |
LIG_LIR_Gen_1 | 1025 | 1035 | PF02991 | 0.344 |
LIG_LIR_Gen_1 | 1138 | 1146 | PF02991 | 0.336 |
LIG_LIR_Gen_1 | 151 | 159 | PF02991 | 0.655 |
LIG_LIR_Gen_1 | 220 | 229 | PF02991 | 0.469 |
LIG_LIR_Gen_1 | 321 | 330 | PF02991 | 0.449 |
LIG_LIR_Gen_1 | 78 | 88 | PF02991 | 0.509 |
LIG_LIR_Nem_3 | 1016 | 1021 | PF02991 | 0.518 |
LIG_LIR_Nem_3 | 1138 | 1144 | PF02991 | 0.317 |
LIG_LIR_Nem_3 | 151 | 156 | PF02991 | 0.678 |
LIG_LIR_Nem_3 | 220 | 224 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 321 | 325 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 329 | 334 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 78 | 84 | PF02991 | 0.533 |
LIG_LIR_Nem_3 | 834 | 839 | PF02991 | 0.578 |
LIG_NRBOX | 865 | 871 | PF00104 | 0.595 |
LIG_NRP_CendR_1 | 1191 | 1194 | PF00754 | 0.447 |
LIG_Pex14_1 | 1079 | 1083 | PF04695 | 0.367 |
LIG_Pex14_2 | 1019 | 1023 | PF04695 | 0.376 |
LIG_Pex14_2 | 1097 | 1101 | PF04695 | 0.451 |
LIG_Pex14_2 | 132 | 136 | PF04695 | 0.267 |
LIG_PTB_Apo_2 | 915 | 922 | PF02174 | 0.455 |
LIG_REV1ctd_RIR_1 | 1083 | 1093 | PF16727 | 0.276 |
LIG_SH2_CRK | 1038 | 1042 | PF00017 | 0.251 |
LIG_SH2_CRK | 1141 | 1145 | PF00017 | 0.281 |
LIG_SH2_CRK | 172 | 176 | PF00017 | 0.534 |
LIG_SH2_GRB2like | 609 | 612 | PF00017 | 0.597 |
LIG_SH2_GRB2like | 787 | 790 | PF00017 | 0.655 |
LIG_SH2_SRC | 787 | 790 | PF00017 | 0.650 |
LIG_SH2_STAP1 | 1141 | 1145 | PF00017 | 0.367 |
LIG_SH2_STAP1 | 1163 | 1167 | PF00017 | 0.562 |
LIG_SH2_STAP1 | 22 | 26 | PF00017 | 0.557 |
LIG_SH2_STAP1 | 341 | 345 | PF00017 | 0.474 |
LIG_SH2_STAP1 | 374 | 378 | PF00017 | 0.513 |
LIG_SH2_STAT3 | 147 | 150 | PF00017 | 0.545 |
LIG_SH2_STAT3 | 848 | 851 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 1064 | 1067 | PF00017 | 0.270 |
LIG_SH2_STAT5 | 333 | 336 | PF00017 | 0.535 |
LIG_SH2_STAT5 | 609 | 612 | PF00017 | 0.581 |
LIG_SH2_STAT5 | 634 | 637 | PF00017 | 0.540 |
LIG_SH2_STAT5 | 848 | 851 | PF00017 | 0.522 |
LIG_SH3_3 | 1048 | 1054 | PF00018 | 0.228 |
LIG_SH3_3 | 1056 | 1062 | PF00018 | 0.203 |
LIG_SH3_3 | 355 | 361 | PF00018 | 0.499 |
LIG_SH3_3 | 459 | 465 | PF00018 | 0.716 |
LIG_SH3_3 | 483 | 489 | PF00018 | 0.564 |
LIG_SH3_3 | 612 | 618 | PF00018 | 0.595 |
LIG_SH3_3 | 685 | 691 | PF00018 | 0.564 |
LIG_SH3_3 | 734 | 740 | PF00018 | 0.672 |
LIG_SH3_3 | 746 | 752 | PF00018 | 0.671 |
LIG_SH3_3 | 966 | 972 | PF00018 | 0.284 |
LIG_SH3_3 | 992 | 998 | PF00018 | 0.524 |
LIG_SUMO_SIM_anti_2 | 268 | 274 | PF11976 | 0.513 |
LIG_SUMO_SIM_anti_2 | 350 | 357 | PF11976 | 0.484 |
LIG_SUMO_SIM_anti_2 | 912 | 919 | PF11976 | 0.499 |
LIG_SUMO_SIM_par_1 | 1118 | 1123 | PF11976 | 0.468 |
LIG_SUMO_SIM_par_1 | 356 | 362 | PF11976 | 0.499 |
LIG_SUMO_SIM_par_1 | 364 | 369 | PF11976 | 0.499 |
LIG_SUMO_SIM_par_1 | 703 | 708 | PF11976 | 0.506 |
LIG_SUMO_SIM_par_1 | 912 | 919 | PF11976 | 0.499 |
LIG_TRAF2_1 | 40 | 43 | PF00917 | 0.625 |
LIG_TRAF2_2 | 821 | 826 | PF00917 | 0.619 |
LIG_TYR_ITIM | 1036 | 1041 | PF00017 | 0.256 |
LIG_UBA3_1 | 1177 | 1186 | PF00899 | 0.588 |
LIG_WRC_WIRS_1 | 137 | 142 | PF05994 | 0.208 |
LIG_WRC_WIRS_1 | 319 | 324 | PF05994 | 0.276 |
LIG_WRC_WIRS_1 | 439 | 444 | PF05994 | 0.567 |
LIG_WRC_WIRS_1 | 539 | 544 | PF05994 | 0.343 |
LIG_WRC_WIRS_1 | 954 | 959 | PF05994 | 0.361 |
LIG_WW_2 | 737 | 740 | PF00397 | 0.532 |
MOD_CDC14_SPxK_1 | 968 | 971 | PF00782 | 0.326 |
MOD_CDK_SPK_2 | 1055 | 1060 | PF00069 | 0.208 |
MOD_CDK_SPxK_1 | 965 | 971 | PF00069 | 0.326 |
MOD_CDK_SPxxK_3 | 108 | 115 | PF00069 | 0.452 |
MOD_CDK_SPxxK_3 | 470 | 477 | PF00069 | 0.537 |
MOD_CDK_SPxxK_3 | 856 | 863 | PF00069 | 0.416 |
MOD_CK1_1 | 1007 | 1013 | PF00069 | 0.411 |
MOD_CK1_1 | 1055 | 1061 | PF00069 | 0.287 |
MOD_CK1_1 | 1184 | 1190 | PF00069 | 0.612 |
MOD_CK1_1 | 185 | 191 | PF00069 | 0.565 |
MOD_CK1_1 | 237 | 243 | PF00069 | 0.438 |
MOD_CK1_1 | 258 | 264 | PF00069 | 0.324 |
MOD_CK1_1 | 288 | 294 | PF00069 | 0.367 |
MOD_CK1_1 | 422 | 428 | PF00069 | 0.602 |
MOD_CK1_1 | 455 | 461 | PF00069 | 0.549 |
MOD_CK1_1 | 473 | 479 | PF00069 | 0.653 |
MOD_CK1_1 | 532 | 538 | PF00069 | 0.322 |
MOD_CK1_1 | 565 | 571 | PF00069 | 0.371 |
MOD_CK1_1 | 753 | 759 | PF00069 | 0.645 |
MOD_CK2_1 | 1132 | 1138 | PF00069 | 0.377 |
MOD_CK2_1 | 37 | 43 | PF00069 | 0.666 |
MOD_CK2_1 | 56 | 62 | PF00069 | 0.345 |
MOD_CK2_1 | 766 | 772 | PF00069 | 0.552 |
MOD_CK2_1 | 791 | 797 | PF00069 | 0.569 |
MOD_CK2_1 | 83 | 89 | PF00069 | 0.368 |
MOD_CK2_1 | 837 | 843 | PF00069 | 0.519 |
MOD_Cter_Amidation | 1191 | 1194 | PF01082 | 0.705 |
MOD_GlcNHglycan | 1043 | 1046 | PF01048 | 0.394 |
MOD_GlcNHglycan | 1054 | 1057 | PF01048 | 0.266 |
MOD_GlcNHglycan | 1146 | 1149 | PF01048 | 0.291 |
MOD_GlcNHglycan | 1186 | 1189 | PF01048 | 0.640 |
MOD_GlcNHglycan | 213 | 216 | PF01048 | 0.376 |
MOD_GlcNHglycan | 257 | 260 | PF01048 | 0.284 |
MOD_GlcNHglycan | 264 | 268 | PF01048 | 0.326 |
MOD_GlcNHglycan | 281 | 284 | PF01048 | 0.224 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.595 |
MOD_GlcNHglycan | 421 | 424 | PF01048 | 0.555 |
MOD_GlcNHglycan | 43 | 47 | PF01048 | 0.519 |
MOD_GlcNHglycan | 636 | 639 | PF01048 | 0.514 |
MOD_GlcNHglycan | 730 | 733 | PF01048 | 0.691 |
MOD_GlcNHglycan | 788 | 792 | PF01048 | 0.795 |
MOD_GlcNHglycan | 826 | 829 | PF01048 | 0.663 |
MOD_GlcNHglycan | 874 | 878 | PF01048 | 0.303 |
MOD_GlcNHglycan | 950 | 953 | PF01048 | 0.451 |
MOD_GSK3_1 | 1128 | 1135 | PF00069 | 0.291 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.682 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.645 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.333 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.277 |
MOD_GSK3_1 | 396 | 403 | PF00069 | 0.419 |
MOD_GSK3_1 | 478 | 485 | PF00069 | 0.587 |
MOD_GSK3_1 | 510 | 517 | PF00069 | 0.486 |
MOD_GSK3_1 | 528 | 535 | PF00069 | 0.347 |
MOD_GSK3_1 | 538 | 545 | PF00069 | 0.451 |
MOD_GSK3_1 | 634 | 641 | PF00069 | 0.377 |
MOD_GSK3_1 | 705 | 712 | PF00069 | 0.374 |
MOD_GSK3_1 | 750 | 757 | PF00069 | 0.597 |
MOD_GSK3_1 | 766 | 773 | PF00069 | 0.551 |
MOD_GSK3_1 | 787 | 794 | PF00069 | 0.560 |
MOD_GSK3_1 | 813 | 820 | PF00069 | 0.473 |
MOD_GSK3_1 | 879 | 886 | PF00069 | 0.340 |
MOD_GSK3_1 | 944 | 951 | PF00069 | 0.275 |
MOD_N-GLC_1 | 347 | 352 | PF02516 | 0.284 |
MOD_N-GLC_1 | 513 | 518 | PF02516 | 0.344 |
MOD_N-GLC_1 | 742 | 747 | PF02516 | 0.635 |
MOD_N-GLC_1 | 780 | 785 | PF02516 | 0.741 |
MOD_N-GLC_1 | 817 | 822 | PF02516 | 0.483 |
MOD_N-GLC_1 | 948 | 953 | PF02516 | 0.414 |
MOD_N-GLC_1 | 965 | 970 | PF02516 | 0.313 |
MOD_N-GLC_2 | 37 | 39 | PF02516 | 0.507 |
MOD_NEK2_1 | 1023 | 1028 | PF00069 | 0.337 |
MOD_NEK2_1 | 107 | 112 | PF00069 | 0.493 |
MOD_NEK2_1 | 1144 | 1149 | PF00069 | 0.405 |
MOD_NEK2_1 | 1181 | 1186 | PF00069 | 0.481 |
MOD_NEK2_1 | 136 | 141 | PF00069 | 0.436 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.450 |
MOD_NEK2_1 | 255 | 260 | PF00069 | 0.308 |
MOD_NEK2_1 | 334 | 339 | PF00069 | 0.337 |
MOD_NEK2_1 | 366 | 371 | PF00069 | 0.366 |
MOD_NEK2_1 | 372 | 377 | PF00069 | 0.326 |
MOD_NEK2_1 | 527 | 532 | PF00069 | 0.377 |
MOD_NEK2_1 | 542 | 547 | PF00069 | 0.300 |
MOD_NEK2_1 | 779 | 784 | PF00069 | 0.532 |
MOD_NEK2_1 | 805 | 810 | PF00069 | 0.624 |
MOD_NEK2_1 | 824 | 829 | PF00069 | 0.576 |
MOD_NEK2_1 | 83 | 88 | PF00069 | 0.449 |
MOD_NEK2_1 | 944 | 949 | PF00069 | 0.340 |
MOD_NEK2_1 | 999 | 1004 | PF00069 | 0.349 |
MOD_NEK2_2 | 452 | 457 | PF00069 | 0.529 |
MOD_NEK2_2 | 742 | 747 | PF00069 | 0.591 |
MOD_PIKK_1 | 532 | 538 | PF00454 | 0.256 |
MOD_PIKK_1 | 542 | 548 | PF00454 | 0.256 |
MOD_PIKK_1 | 692 | 698 | PF00454 | 0.347 |
MOD_PIKK_1 | 70 | 76 | PF00454 | 0.279 |
MOD_PKA_1 | 165 | 171 | PF00069 | 0.464 |
MOD_PKA_1 | 909 | 915 | PF00069 | 0.276 |
MOD_PKA_2 | 1161 | 1167 | PF00069 | 0.541 |
MOD_PKA_2 | 1181 | 1187 | PF00069 | 0.610 |
MOD_PKA_2 | 165 | 171 | PF00069 | 0.441 |
MOD_PKA_2 | 510 | 516 | PF00069 | 0.355 |
MOD_PKA_2 | 542 | 548 | PF00069 | 0.357 |
MOD_PKA_2 | 604 | 610 | PF00069 | 0.406 |
MOD_PKA_2 | 62 | 68 | PF00069 | 0.268 |
MOD_PKA_2 | 632 | 638 | PF00069 | 0.534 |
MOD_PKA_2 | 909 | 915 | PF00069 | 0.276 |
MOD_Plk_1 | 234 | 240 | PF00069 | 0.416 |
MOD_Plk_1 | 437 | 443 | PF00069 | 0.502 |
MOD_Plk_1 | 709 | 715 | PF00069 | 0.393 |
MOD_Plk_1 | 742 | 748 | PF00069 | 0.554 |
MOD_Plk_1 | 780 | 786 | PF00069 | 0.735 |
MOD_Plk_2-3 | 438 | 444 | PF00069 | 0.684 |
MOD_Plk_4 | 101 | 107 | PF00069 | 0.372 |
MOD_Plk_4 | 1013 | 1019 | PF00069 | 0.333 |
MOD_Plk_4 | 1101 | 1107 | PF00069 | 0.325 |
MOD_Plk_4 | 1139 | 1145 | PF00069 | 0.419 |
MOD_Plk_4 | 131 | 137 | PF00069 | 0.344 |
MOD_Plk_4 | 165 | 171 | PF00069 | 0.378 |
MOD_Plk_4 | 258 | 264 | PF00069 | 0.350 |
MOD_Plk_4 | 396 | 402 | PF00069 | 0.373 |
MOD_Plk_4 | 430 | 436 | PF00069 | 0.433 |
MOD_Plk_4 | 457 | 463 | PF00069 | 0.497 |
MOD_Plk_4 | 605 | 611 | PF00069 | 0.384 |
MOD_Plk_4 | 76 | 82 | PF00069 | 0.358 |
MOD_Plk_4 | 780 | 786 | PF00069 | 0.530 |
MOD_Plk_4 | 865 | 871 | PF00069 | 0.338 |
MOD_Plk_4 | 925 | 931 | PF00069 | 0.366 |
MOD_ProDKin_1 | 1055 | 1061 | PF00069 | 0.249 |
MOD_ProDKin_1 | 108 | 114 | PF00069 | 0.445 |
MOD_ProDKin_1 | 26 | 32 | PF00069 | 0.569 |
MOD_ProDKin_1 | 294 | 300 | PF00069 | 0.371 |
MOD_ProDKin_1 | 335 | 341 | PF00069 | 0.316 |
MOD_ProDKin_1 | 444 | 450 | PF00069 | 0.659 |
MOD_ProDKin_1 | 470 | 476 | PF00069 | 0.724 |
MOD_ProDKin_1 | 766 | 772 | PF00069 | 0.752 |
MOD_ProDKin_1 | 817 | 823 | PF00069 | 0.575 |
MOD_ProDKin_1 | 856 | 862 | PF00069 | 0.421 |
MOD_ProDKin_1 | 965 | 971 | PF00069 | 0.368 |
MOD_SUMO_rev_2 | 1002 | 1010 | PF00179 | 0.343 |
MOD_SUMO_rev_2 | 648 | 657 | PF00179 | 0.365 |
MOD_SUMO_rev_2 | 8 | 17 | PF00179 | 0.457 |
TRG_DiLeu_BaEn_1 | 268 | 273 | PF01217 | 0.419 |
TRG_DiLeu_BaLyEn_6 | 1086 | 1091 | PF01217 | 0.276 |
TRG_DiLeu_BaLyEn_6 | 1154 | 1159 | PF01217 | 0.287 |
TRG_DiLeu_BaLyEn_6 | 862 | 867 | PF01217 | 0.386 |
TRG_ENDOCYTIC_2 | 1038 | 1041 | PF00928 | 0.414 |
TRG_ENDOCYTIC_2 | 1141 | 1144 | PF00928 | 0.367 |
TRG_ENDOCYTIC_2 | 172 | 175 | PF00928 | 0.404 |
TRG_ER_diArg_1 | 1179 | 1182 | PF00400 | 0.529 |
TRG_ER_diArg_1 | 164 | 166 | PF00400 | 0.482 |
TRG_ER_diArg_1 | 558 | 561 | PF00400 | 0.412 |
TRG_ER_diArg_1 | 590 | 593 | PF00400 | 0.343 |
TRG_ER_diArg_1 | 870 | 872 | PF00400 | 0.369 |
TRG_NES_CRM1_1 | 347 | 362 | PF08389 | 0.361 |
TRG_NES_CRM1_1 | 673 | 685 | PF08389 | 0.328 |
TRG_Pf-PMV_PEXEL_1 | 1166 | 1171 | PF00026 | 0.570 |
TRG_Pf-PMV_PEXEL_1 | 837 | 841 | PF00026 | 0.424 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I8I8 | Leptomonas seymouri | 67% | 98% |
A0A1X0P0Y8 | Trypanosomatidae | 47% | 100% |
A0A3S7WUG2 | Leishmania donovani | 35% | 100% |
A0A3S7X6H3 | Leishmania donovani | 95% | 100% |
A4HLF4 | Leishmania braziliensis | 80% | 100% |
A4HTF0 | Leishmania infantum | 32% | 100% |
A4HXD4 | Leishmania infantum | 35% | 100% |
A4I8W5 | Leishmania infantum | 95% | 100% |
E9AR29 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
E9B3T4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
Q4QED4 | Leishmania major | 36% | 100% |
Q95Z93 | Leishmania major | 25% | 100% |
V5BPC6 | Trypanosoma cruzi | 48% | 100% |