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: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 12 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 13 |
GO:0110165 | cellular anatomical entity | 1 | 13 |
GO:0005783 | endoplasmic reticulum | 5 | 1 |
GO:0043226 | organelle | 2 | 3 |
GO:0043227 | membrane-bounded organelle | 3 | 3 |
GO:0043229 | intracellular organelle | 3 | 3 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 3 |
GO:0005886 | plasma membrane | 3 | 2 |
Related structures:
AlphaFold database: A0A3S7X6H3
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 | 13 |
GO:0003824 | catalytic activity | 1 | 13 |
GO:0005488 | binding | 1 | 13 |
GO:0005524 | ATP binding | 5 | 13 |
GO:0016462 | pyrophosphatase activity | 5 | 13 |
GO:0016787 | hydrolase activity | 2 | 13 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 13 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 13 |
GO:0016887 | ATP hydrolysis activity | 7 | 13 |
GO:0017076 | purine nucleotide binding | 4 | 13 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 13 |
GO:0030554 | adenyl nucleotide binding | 5 | 13 |
GO:0032553 | ribonucleotide binding | 3 | 13 |
GO:0032555 | purine ribonucleotide binding | 4 | 13 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 13 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 13 |
GO:0036094 | small molecule binding | 2 | 13 |
GO:0043167 | ion binding | 2 | 13 |
GO:0043168 | anion binding | 3 | 13 |
GO:0097159 | organic cyclic compound binding | 2 | 13 |
GO:0097367 | carbohydrate derivative binding | 2 | 13 |
GO:1901265 | nucleoside phosphate binding | 3 | 13 |
GO:1901363 | heterocyclic compound binding | 2 | 13 |
GO:0005215 | transporter activity | 1 | 3 |
GO:0005388 | P-type calcium transporter activity | 4 | 3 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 3 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 3 |
GO:0015085 | calcium ion transmembrane transporter activity | 6 | 3 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 3 |
GO:0015399 | primary active transmembrane transporter activity | 4 | 3 |
GO:0015662 | P-type ion transporter activity | 4 | 3 |
GO:0019829 | ATPase-coupled monoatomic cation transmembrane transporter activity | 3 | 3 |
GO:0022804 | active transmembrane transporter activity | 3 | 3 |
GO:0022853 | active monoatomic ion transmembrane transporter activity | 4 | 3 |
GO:0022857 | transmembrane transporter activity | 2 | 3 |
GO:0022890 | inorganic cation transmembrane transporter activity | 4 | 3 |
GO:0042626 | ATPase-coupled transmembrane transporter activity | 2 | 3 |
GO:0046873 | metal ion transmembrane transporter activity | 5 | 3 |
GO:0140358 | P-type transmembrane transporter activity | 3 | 3 |
GO:0140657 | ATP-dependent activity | 1 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 188 | 192 | PF00656 | 0.607 |
CLV_C14_Caspase3-7 | 261 | 265 | PF00656 | 0.425 |
CLV_C14_Caspase3-7 | 775 | 779 | PF00656 | 0.695 |
CLV_NRD_NRD_1 | 1185 | 1187 | PF00675 | 0.405 |
CLV_NRD_NRD_1 | 147 | 149 | PF00675 | 0.389 |
CLV_NRD_NRD_1 | 165 | 167 | PF00675 | 0.336 |
CLV_NRD_NRD_1 | 481 | 483 | PF00675 | 0.442 |
CLV_NRD_NRD_1 | 50 | 52 | PF00675 | 0.296 |
CLV_NRD_NRD_1 | 560 | 562 | PF00675 | 0.338 |
CLV_NRD_NRD_1 | 723 | 725 | PF00675 | 0.378 |
CLV_NRD_NRD_1 | 874 | 876 | PF00675 | 0.229 |
CLV_NRD_NRD_1 | 941 | 943 | PF00675 | 0.272 |
CLV_PCSK_FUR_1 | 1183 | 1187 | PF00082 | 0.368 |
CLV_PCSK_FUR_1 | 558 | 562 | PF00082 | 0.290 |
CLV_PCSK_KEX2_1 | 1168 | 1170 | PF00082 | 0.383 |
CLV_PCSK_KEX2_1 | 1185 | 1187 | PF00082 | 0.416 |
CLV_PCSK_KEX2_1 | 164 | 166 | PF00082 | 0.370 |
CLV_PCSK_KEX2_1 | 481 | 483 | PF00082 | 0.442 |
CLV_PCSK_KEX2_1 | 5 | 7 | PF00082 | 0.377 |
CLV_PCSK_KEX2_1 | 50 | 52 | PF00082 | 0.299 |
CLV_PCSK_KEX2_1 | 560 | 562 | PF00082 | 0.331 |
CLV_PCSK_KEX2_1 | 723 | 725 | PF00082 | 0.378 |
CLV_PCSK_KEX2_1 | 867 | 869 | PF00082 | 0.301 |
CLV_PCSK_KEX2_1 | 874 | 876 | PF00082 | 0.250 |
CLV_PCSK_KEX2_1 | 912 | 914 | PF00082 | 0.225 |
CLV_PCSK_PC1ET2_1 | 1168 | 1170 | PF00082 | 0.348 |
CLV_PCSK_PC1ET2_1 | 5 | 7 | PF00082 | 0.375 |
CLV_PCSK_PC1ET2_1 | 867 | 869 | PF00082 | 0.300 |
CLV_PCSK_PC1ET2_1 | 912 | 914 | PF00082 | 0.225 |
CLV_PCSK_PC7_1 | 477 | 483 | PF00082 | 0.399 |
CLV_PCSK_SKI1_1 | 1168 | 1172 | PF00082 | 0.353 |
CLV_PCSK_SKI1_1 | 1178 | 1182 | PF00082 | 0.373 |
CLV_PCSK_SKI1_1 | 1186 | 1190 | PF00082 | 0.400 |
CLV_PCSK_SKI1_1 | 165 | 169 | PF00082 | 0.321 |
CLV_PCSK_SKI1_1 | 248 | 252 | PF00082 | 0.300 |
CLV_PCSK_SKI1_1 | 328 | 332 | PF00082 | 0.331 |
CLV_PCSK_SKI1_1 | 377 | 381 | PF00082 | 0.244 |
CLV_PCSK_SKI1_1 | 417 | 421 | PF00082 | 0.287 |
CLV_PCSK_SKI1_1 | 482 | 486 | PF00082 | 0.450 |
CLV_PCSK_SKI1_1 | 867 | 871 | PF00082 | 0.329 |
CLV_PCSK_SKI1_1 | 935 | 939 | PF00082 | 0.270 |
CLV_PCSK_SKI1_1 | 942 | 946 | PF00082 | 0.301 |
CLV_Separin_Metazoa | 1060 | 1064 | PF03568 | 0.300 |
CLV_Separin_Metazoa | 155 | 159 | PF03568 | 0.568 |
DEG_APCC_DBOX_1 | 1177 | 1185 | PF00400 | 0.593 |
DEG_APCC_DBOX_1 | 49 | 57 | PF00400 | 0.429 |
DEG_COP1_1 | 1009 | 1020 | PF00400 | 0.484 |
DEG_COP1_1 | 406 | 414 | PF00400 | 0.447 |
DOC_ANK_TNKS_1 | 689 | 696 | PF00023 | 0.545 |
DOC_CKS1_1 | 109 | 114 | PF01111 | 0.424 |
DOC_CYCLIN_RxL_1 | 1173 | 1182 | PF00134 | 0.545 |
DOC_CYCLIN_RxL_1 | 938 | 950 | PF00134 | 0.493 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 380 | 389 | PF00134 | 0.525 |
DOC_CYCLIN_yCln2_LP_2 | 251 | 257 | PF00134 | 0.490 |
DOC_CYCLIN_yCln2_LP_2 | 578 | 584 | PF00134 | 0.402 |
DOC_MAPK_gen_1 | 481 | 488 | PF00069 | 0.586 |
DOC_MAPK_gen_1 | 63 | 71 | PF00069 | 0.482 |
DOC_MAPK_gen_1 | 866 | 872 | PF00069 | 0.483 |
DOC_MAPK_gen_1 | 912 | 920 | PF00069 | 0.433 |
DOC_MAPK_MEF2A_6 | 115 | 123 | PF00069 | 0.335 |
DOC_MAPK_MEF2A_6 | 481 | 488 | PF00069 | 0.585 |
DOC_MAPK_MEF2A_6 | 974 | 983 | PF00069 | 0.257 |
DOC_PP1_RVXF_1 | 941 | 948 | PF00149 | 0.480 |
DOC_PP2B_LxvP_1 | 198 | 201 | PF13499 | 0.431 |
DOC_PP2B_LxvP_1 | 409 | 412 | PF13499 | 0.551 |
DOC_PP2B_LxvP_1 | 578 | 581 | PF13499 | 0.437 |
DOC_PP2B_PxIxI_1 | 852 | 858 | PF00149 | 0.546 |
DOC_PP4_FxxP_1 | 461 | 464 | PF00568 | 0.651 |
DOC_USP7_MATH_1 | 101 | 105 | PF00917 | 0.488 |
DOC_USP7_MATH_1 | 174 | 178 | PF00917 | 0.551 |
DOC_USP7_MATH_1 | 234 | 238 | PF00917 | 0.429 |
DOC_USP7_MATH_1 | 452 | 456 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 563 | 567 | PF00917 | 0.474 |
DOC_USP7_MATH_1 | 618 | 622 | PF00917 | 0.524 |
DOC_USP7_MATH_1 | 76 | 80 | PF00917 | 0.521 |
DOC_USP7_MATH_1 | 963 | 967 | PF00917 | 0.359 |
DOC_WW_Pin1_4 | 108 | 113 | PF00397 | 0.410 |
DOC_WW_Pin1_4 | 26 | 31 | PF00397 | 0.591 |
DOC_WW_Pin1_4 | 294 | 299 | PF00397 | 0.491 |
DOC_WW_Pin1_4 | 335 | 340 | PF00397 | 0.432 |
DOC_WW_Pin1_4 | 444 | 449 | PF00397 | 0.704 |
DOC_WW_Pin1_4 | 470 | 475 | PF00397 | 0.777 |
DOC_WW_Pin1_4 | 737 | 742 | PF00397 | 0.653 |
DOC_WW_Pin1_4 | 769 | 774 | PF00397 | 0.756 |
DOC_WW_Pin1_4 | 820 | 825 | PF00397 | 0.688 |
DOC_WW_Pin1_4 | 859 | 864 | PF00397 | 0.530 |
DOC_WW_Pin1_4 | 968 | 973 | PF00397 | 0.353 |
LIG_14-3-3_CanoR_1 | 1066 | 1075 | PF00244 | 0.358 |
LIG_14-3-3_CanoR_1 | 1183 | 1189 | PF00244 | 0.611 |
LIG_14-3-3_CanoR_1 | 164 | 170 | PF00244 | 0.589 |
LIG_14-3-3_CanoR_1 | 454 | 464 | PF00244 | 0.612 |
LIG_14-3-3_CanoR_1 | 481 | 487 | PF00244 | 0.626 |
LIG_14-3-3_CanoR_1 | 543 | 550 | PF00244 | 0.542 |
LIG_14-3-3_CanoR_1 | 561 | 570 | PF00244 | 0.457 |
LIG_14-3-3_CanoR_1 | 605 | 610 | PF00244 | 0.515 |
LIG_14-3-3_CanoR_1 | 729 | 737 | PF00244 | 0.583 |
LIG_14-3-3_CanoR_1 | 840 | 848 | PF00244 | 0.532 |
LIG_14-3-3_CanoR_1 | 868 | 873 | PF00244 | 0.460 |
LIG_14-3-3_CanoR_1 | 913 | 920 | PF00244 | 0.425 |
LIG_Actin_WH2_2 | 365 | 383 | PF00022 | 0.490 |
LIG_AP2alpha_2 | 253 | 255 | PF02296 | 0.425 |
LIG_BIR_III_2 | 430 | 434 | PF00653 | 0.561 |
LIG_BIR_III_4 | 648 | 652 | PF00653 | 0.556 |
LIG_BRCT_BRCA1_1 | 1018 | 1022 | PF00533 | 0.448 |
LIG_BRCT_BRCA1_1 | 1096 | 1100 | PF00533 | 0.541 |
LIG_BRCT_BRCA1_1 | 697 | 701 | PF00533 | 0.477 |
LIG_deltaCOP1_diTrp_1 | 78 | 83 | PF00928 | 0.474 |
LIG_EH1_1 | 1110 | 1118 | PF00400 | 0.235 |
LIG_EH1_1 | 373 | 381 | PF00400 | 0.425 |
LIG_EH1_1 | 676 | 684 | PF00400 | 0.507 |
LIG_EVH1_2 | 466 | 470 | PF00568 | 0.636 |
LIG_FHA_1 | 1011 | 1017 | PF00498 | 0.490 |
LIG_FHA_1 | 1027 | 1033 | PF00498 | 0.419 |
LIG_FHA_1 | 1050 | 1056 | PF00498 | 0.240 |
LIG_FHA_1 | 1132 | 1138 | PF00498 | 0.253 |
LIG_FHA_1 | 114 | 120 | PF00498 | 0.413 |
LIG_FHA_1 | 1150 | 1156 | PF00498 | 0.388 |
LIG_FHA_1 | 188 | 194 | PF00498 | 0.640 |
LIG_FHA_1 | 284 | 290 | PF00498 | 0.392 |
LIG_FHA_1 | 348 | 354 | PF00498 | 0.457 |
LIG_FHA_1 | 367 | 373 | PF00498 | 0.584 |
LIG_FHA_1 | 404 | 410 | PF00498 | 0.546 |
LIG_FHA_1 | 411 | 417 | PF00498 | 0.560 |
LIG_FHA_1 | 423 | 429 | PF00498 | 0.568 |
LIG_FHA_1 | 451 | 457 | PF00498 | 0.662 |
LIG_FHA_1 | 483 | 489 | PF00498 | 0.583 |
LIG_FHA_1 | 605 | 611 | PF00498 | 0.480 |
LIG_FHA_1 | 758 | 764 | PF00498 | 0.625 |
LIG_FHA_1 | 772 | 778 | PF00498 | 0.567 |
LIG_FHA_1 | 783 | 789 | PF00498 | 0.599 |
LIG_FHA_1 | 843 | 849 | PF00498 | 0.495 |
LIG_FHA_2 | 108 | 114 | PF00498 | 0.459 |
LIG_FHA_2 | 1136 | 1142 | PF00498 | 0.248 |
LIG_FHA_2 | 186 | 192 | PF00498 | 0.685 |
LIG_FHA_2 | 439 | 445 | PF00498 | 0.637 |
LIG_FHA_2 | 533 | 539 | PF00498 | 0.500 |
LIG_FHA_2 | 860 | 866 | PF00498 | 0.506 |
LIG_LIR_Apic_2 | 458 | 464 | PF02991 | 0.625 |
LIG_LIR_Gen_1 | 1028 | 1038 | PF02991 | 0.317 |
LIG_LIR_Gen_1 | 1079 | 1089 | PF02991 | 0.307 |
LIG_LIR_Gen_1 | 1141 | 1149 | PF02991 | 0.314 |
LIG_LIR_Gen_1 | 151 | 159 | PF02991 | 0.631 |
LIG_LIR_Gen_1 | 220 | 229 | PF02991 | 0.447 |
LIG_LIR_Gen_1 | 321 | 330 | PF02991 | 0.431 |
LIG_LIR_Gen_1 | 676 | 685 | PF02991 | 0.547 |
LIG_LIR_Gen_1 | 78 | 88 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 1019 | 1024 | PF02991 | 0.493 |
LIG_LIR_Nem_3 | 1079 | 1085 | PF02991 | 0.341 |
LIG_LIR_Nem_3 | 1141 | 1147 | PF02991 | 0.295 |
LIG_LIR_Nem_3 | 151 | 156 | PF02991 | 0.651 |
LIG_LIR_Nem_3 | 220 | 224 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 321 | 325 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 329 | 334 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 676 | 680 | PF02991 | 0.577 |
LIG_LIR_Nem_3 | 78 | 84 | PF02991 | 0.508 |
LIG_LIR_Nem_3 | 837 | 842 | PF02991 | 0.557 |
LIG_NRBOX | 16 | 22 | PF00104 | 0.482 |
LIG_NRBOX | 868 | 874 | PF00104 | 0.573 |
LIG_NRP_CendR_1 | 1194 | 1197 | PF00754 | 0.425 |
LIG_Pex14_1 | 1082 | 1086 | PF04695 | 0.345 |
LIG_Pex14_2 | 1022 | 1026 | PF04695 | 0.497 |
LIG_Pex14_2 | 1100 | 1104 | PF04695 | 0.436 |
LIG_Pex14_2 | 132 | 136 | PF04695 | 0.245 |
LIG_PTB_Apo_2 | 918 | 925 | PF02174 | 0.433 |
LIG_REV1ctd_RIR_1 | 1086 | 1096 | PF16727 | 0.254 |
LIG_SH2_CRK | 1041 | 1045 | PF00017 | 0.227 |
LIG_SH2_CRK | 1144 | 1148 | PF00017 | 0.260 |
LIG_SH2_CRK | 172 | 176 | PF00017 | 0.501 |
LIG_SH2_GRB2like | 609 | 612 | PF00017 | 0.575 |
LIG_SH2_GRB2like | 790 | 793 | PF00017 | 0.630 |
LIG_SH2_SRC | 790 | 793 | PF00017 | 0.626 |
LIG_SH2_SRC | 851 | 854 | PF00017 | 0.499 |
LIG_SH2_STAP1 | 1144 | 1148 | PF00017 | 0.260 |
LIG_SH2_STAP1 | 1166 | 1170 | PF00017 | 0.542 |
LIG_SH2_STAP1 | 22 | 26 | PF00017 | 0.508 |
LIG_SH2_STAP1 | 341 | 345 | PF00017 | 0.474 |
LIG_SH2_STAP1 | 374 | 378 | PF00017 | 0.490 |
LIG_SH2_STAT3 | 147 | 150 | PF00017 | 0.525 |
LIG_SH2_STAT5 | 1067 | 1070 | PF00017 | 0.248 |
LIG_SH2_STAT5 | 333 | 336 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 609 | 612 | PF00017 | 0.558 |
LIG_SH2_STAT5 | 634 | 637 | PF00017 | 0.514 |
LIG_SH2_STAT5 | 851 | 854 | PF00017 | 0.504 |
LIG_SH3_2 | 463 | 468 | PF14604 | 0.618 |
LIG_SH3_3 | 1051 | 1057 | PF00018 | 0.274 |
LIG_SH3_3 | 1059 | 1065 | PF00018 | 0.310 |
LIG_SH3_3 | 355 | 361 | PF00018 | 0.474 |
LIG_SH3_3 | 460 | 466 | PF00018 | 0.713 |
LIG_SH3_3 | 483 | 489 | PF00018 | 0.583 |
LIG_SH3_3 | 612 | 618 | PF00018 | 0.572 |
LIG_SH3_3 | 688 | 694 | PF00018 | 0.539 |
LIG_SH3_3 | 749 | 755 | PF00018 | 0.636 |
LIG_SH3_3 | 969 | 975 | PF00018 | 0.257 |
LIG_SH3_3 | 995 | 1001 | PF00018 | 0.498 |
LIG_SH3_CIN85_PxpxPR_1 | 463 | 468 | PF14604 | 0.618 |
LIG_SUMO_SIM_anti_2 | 268 | 274 | PF11976 | 0.486 |
LIG_SUMO_SIM_anti_2 | 350 | 357 | PF11976 | 0.458 |
LIG_SUMO_SIM_anti_2 | 915 | 922 | PF11976 | 0.473 |
LIG_SUMO_SIM_par_1 | 1121 | 1126 | PF11976 | 0.445 |
LIG_SUMO_SIM_par_1 | 356 | 362 | PF11976 | 0.474 |
LIG_SUMO_SIM_par_1 | 364 | 369 | PF11976 | 0.474 |
LIG_SUMO_SIM_par_1 | 406 | 413 | PF11976 | 0.447 |
LIG_SUMO_SIM_par_1 | 706 | 711 | PF11976 | 0.484 |
LIG_SUMO_SIM_par_1 | 915 | 922 | PF11976 | 0.473 |
LIG_TRAF2_1 | 40 | 43 | PF00917 | 0.566 |
LIG_TRAF2_2 | 824 | 829 | PF00917 | 0.651 |
LIG_TYR_ITIM | 1039 | 1044 | PF00017 | 0.235 |
LIG_UBA3_1 | 1180 | 1189 | PF00899 | 0.477 |
LIG_WRC_WIRS_1 | 1077 | 1082 | PF05994 | 0.315 |
LIG_WRC_WIRS_1 | 319 | 324 | PF05994 | 0.254 |
LIG_WRC_WIRS_1 | 439 | 444 | PF05994 | 0.542 |
LIG_WRC_WIRS_1 | 539 | 544 | PF05994 | 0.322 |
LIG_WRC_WIRS_1 | 957 | 962 | PF05994 | 0.334 |
LIG_WW_3 | 1060 | 1064 | PF00397 | 0.203 |
LIG_WW_3 | 465 | 469 | PF00397 | 0.521 |
LIG_WW_3 | 478 | 482 | PF00397 | 0.502 |
MOD_CDC14_SPxK_1 | 971 | 974 | PF00782 | 0.299 |
MOD_CDK_SPxK_1 | 968 | 974 | PF00069 | 0.299 |
MOD_CDK_SPxxK_3 | 108 | 115 | PF00069 | 0.424 |
MOD_CDK_SPxxK_3 | 470 | 477 | PF00069 | 0.557 |
MOD_CDK_SPxxK_3 | 859 | 866 | PF00069 | 0.388 |
MOD_CK1_1 | 1010 | 1016 | PF00069 | 0.389 |
MOD_CK1_1 | 1187 | 1193 | PF00069 | 0.643 |
MOD_CK1_1 | 237 | 243 | PF00069 | 0.412 |
MOD_CK1_1 | 258 | 264 | PF00069 | 0.298 |
MOD_CK1_1 | 288 | 294 | PF00069 | 0.345 |
MOD_CK1_1 | 422 | 428 | PF00069 | 0.583 |
MOD_CK1_1 | 455 | 461 | PF00069 | 0.521 |
MOD_CK1_1 | 473 | 479 | PF00069 | 0.677 |
MOD_CK1_1 | 532 | 538 | PF00069 | 0.300 |
MOD_CK1_1 | 565 | 571 | PF00069 | 0.350 |
MOD_CK1_1 | 756 | 762 | PF00069 | 0.618 |
MOD_CK2_1 | 1135 | 1141 | PF00069 | 0.356 |
MOD_CK2_1 | 37 | 43 | PF00069 | 0.581 |
MOD_CK2_1 | 56 | 62 | PF00069 | 0.320 |
MOD_CK2_1 | 769 | 775 | PF00069 | 0.518 |
MOD_CK2_1 | 794 | 800 | PF00069 | 0.543 |
MOD_CK2_1 | 840 | 846 | PF00069 | 0.498 |
MOD_Cter_Amidation | 1194 | 1197 | PF01082 | 0.676 |
MOD_GlcNHglycan | 1046 | 1049 | PF01048 | 0.404 |
MOD_GlcNHglycan | 1057 | 1060 | PF01048 | 0.295 |
MOD_GlcNHglycan | 1106 | 1109 | PF01048 | 0.231 |
MOD_GlcNHglycan | 1149 | 1152 | PF01048 | 0.285 |
MOD_GlcNHglycan | 1189 | 1192 | PF01048 | 0.691 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.514 |
MOD_GlcNHglycan | 213 | 216 | PF01048 | 0.350 |
MOD_GlcNHglycan | 257 | 260 | PF01048 | 0.262 |
MOD_GlcNHglycan | 264 | 268 | PF01048 | 0.299 |
MOD_GlcNHglycan | 281 | 284 | PF01048 | 0.201 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.526 |
MOD_GlcNHglycan | 421 | 424 | PF01048 | 0.490 |
MOD_GlcNHglycan | 43 | 47 | PF01048 | 0.444 |
MOD_GlcNHglycan | 636 | 639 | PF01048 | 0.484 |
MOD_GlcNHglycan | 733 | 736 | PF01048 | 0.657 |
MOD_GlcNHglycan | 791 | 795 | PF01048 | 0.767 |
MOD_GlcNHglycan | 805 | 808 | PF01048 | 0.524 |
MOD_GlcNHglycan | 829 | 832 | PF01048 | 0.673 |
MOD_GlcNHglycan | 877 | 881 | PF01048 | 0.275 |
MOD_GlcNHglycan | 953 | 956 | PF01048 | 0.235 |
MOD_GSK3_1 | 1131 | 1138 | PF00069 | 0.290 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.649 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.577 |
MOD_GSK3_1 | 279 | 286 | PF00069 | 0.347 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.310 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.256 |
MOD_GSK3_1 | 396 | 403 | PF00069 | 0.384 |
MOD_GSK3_1 | 510 | 517 | PF00069 | 0.460 |
MOD_GSK3_1 | 528 | 535 | PF00069 | 0.307 |
MOD_GSK3_1 | 538 | 545 | PF00069 | 0.420 |
MOD_GSK3_1 | 634 | 641 | PF00069 | 0.348 |
MOD_GSK3_1 | 708 | 715 | PF00069 | 0.358 |
MOD_GSK3_1 | 753 | 760 | PF00069 | 0.566 |
MOD_GSK3_1 | 790 | 797 | PF00069 | 0.535 |
MOD_GSK3_1 | 816 | 823 | PF00069 | 0.500 |
MOD_GSK3_1 | 882 | 889 | PF00069 | 0.314 |
MOD_GSK3_1 | 947 | 954 | PF00069 | 0.279 |
MOD_N-GLC_1 | 347 | 352 | PF02516 | 0.266 |
MOD_N-GLC_1 | 513 | 518 | PF02516 | 0.323 |
MOD_N-GLC_1 | 783 | 788 | PF02516 | 0.710 |
MOD_N-GLC_1 | 820 | 825 | PF02516 | 0.528 |
MOD_N-GLC_1 | 951 | 956 | PF02516 | 0.417 |
MOD_N-GLC_1 | 968 | 973 | PF02516 | 0.287 |
MOD_N-GLC_2 | 37 | 39 | PF02516 | 0.425 |
MOD_NEK2_1 | 1002 | 1007 | PF00069 | 0.328 |
MOD_NEK2_1 | 1026 | 1031 | PF00069 | 0.364 |
MOD_NEK2_1 | 107 | 112 | PF00069 | 0.464 |
MOD_NEK2_1 | 1076 | 1081 | PF00069 | 0.317 |
MOD_NEK2_1 | 1147 | 1152 | PF00069 | 0.308 |
MOD_NEK2_1 | 1184 | 1189 | PF00069 | 0.482 |
MOD_NEK2_1 | 136 | 141 | PF00069 | 0.411 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.425 |
MOD_NEK2_1 | 255 | 260 | PF00069 | 0.286 |
MOD_NEK2_1 | 366 | 371 | PF00069 | 0.340 |
MOD_NEK2_1 | 372 | 377 | PF00069 | 0.300 |
MOD_NEK2_1 | 527 | 532 | PF00069 | 0.357 |
MOD_NEK2_1 | 542 | 547 | PF00069 | 0.269 |
MOD_NEK2_1 | 743 | 748 | PF00069 | 0.703 |
MOD_NEK2_1 | 782 | 787 | PF00069 | 0.500 |
MOD_NEK2_1 | 803 | 808 | PF00069 | 0.634 |
MOD_NEK2_1 | 827 | 832 | PF00069 | 0.608 |
MOD_NEK2_1 | 83 | 88 | PF00069 | 0.426 |
MOD_NEK2_1 | 947 | 952 | PF00069 | 0.336 |
MOD_NEK2_2 | 452 | 457 | PF00069 | 0.499 |
MOD_NEK2_2 | 745 | 750 | PF00069 | 0.544 |
MOD_PIKK_1 | 532 | 538 | PF00454 | 0.235 |
MOD_PIKK_1 | 542 | 548 | PF00454 | 0.235 |
MOD_PIKK_1 | 695 | 701 | PF00454 | 0.327 |
MOD_PIKK_1 | 70 | 76 | PF00454 | 0.253 |
MOD_PKA_1 | 165 | 171 | PF00069 | 0.437 |
MOD_PKA_1 | 912 | 918 | PF00069 | 0.254 |
MOD_PKA_2 | 1164 | 1170 | PF00069 | 0.517 |
MOD_PKA_2 | 1184 | 1190 | PF00069 | 0.458 |
MOD_PKA_2 | 165 | 171 | PF00069 | 0.413 |
MOD_PKA_2 | 510 | 516 | PF00069 | 0.319 |
MOD_PKA_2 | 542 | 548 | PF00069 | 0.334 |
MOD_PKA_2 | 604 | 610 | PF00069 | 0.384 |
MOD_PKA_2 | 62 | 68 | PF00069 | 0.247 |
MOD_PKA_2 | 912 | 918 | PF00069 | 0.254 |
MOD_Plk_1 | 234 | 240 | PF00069 | 0.394 |
MOD_Plk_1 | 283 | 289 | PF00069 | 0.305 |
MOD_Plk_1 | 712 | 718 | PF00069 | 0.382 |
MOD_Plk_1 | 783 | 789 | PF00069 | 0.705 |
MOD_Plk_2-3 | 438 | 444 | PF00069 | 0.634 |
MOD_Plk_4 | 101 | 107 | PF00069 | 0.344 |
MOD_Plk_4 | 1016 | 1022 | PF00069 | 0.307 |
MOD_Plk_4 | 1076 | 1082 | PF00069 | 0.372 |
MOD_Plk_4 | 1142 | 1148 | PF00069 | 0.394 |
MOD_Plk_4 | 131 | 137 | PF00069 | 0.319 |
MOD_Plk_4 | 165 | 171 | PF00069 | 0.351 |
MOD_Plk_4 | 258 | 264 | PF00069 | 0.326 |
MOD_Plk_4 | 396 | 402 | PF00069 | 0.366 |
MOD_Plk_4 | 545 | 551 | PF00069 | 0.237 |
MOD_Plk_4 | 605 | 611 | PF00069 | 0.362 |
MOD_Plk_4 | 76 | 82 | PF00069 | 0.333 |
MOD_Plk_4 | 783 | 789 | PF00069 | 0.500 |
MOD_Plk_4 | 868 | 874 | PF00069 | 0.317 |
MOD_Plk_4 | 928 | 934 | PF00069 | 0.346 |
MOD_ProDKin_1 | 108 | 114 | PF00069 | 0.417 |
MOD_ProDKin_1 | 26 | 32 | PF00069 | 0.503 |
MOD_ProDKin_1 | 294 | 300 | PF00069 | 0.346 |
MOD_ProDKin_1 | 335 | 341 | PF00069 | 0.264 |
MOD_ProDKin_1 | 444 | 450 | PF00069 | 0.645 |
MOD_ProDKin_1 | 470 | 476 | PF00069 | 0.743 |
MOD_ProDKin_1 | 737 | 743 | PF00069 | 0.574 |
MOD_ProDKin_1 | 769 | 775 | PF00069 | 0.717 |
MOD_ProDKin_1 | 820 | 826 | PF00069 | 0.617 |
MOD_ProDKin_1 | 859 | 865 | PF00069 | 0.393 |
MOD_ProDKin_1 | 968 | 974 | PF00069 | 0.344 |
MOD_SUMO_rev_2 | 1005 | 1013 | PF00179 | 0.322 |
MOD_SUMO_rev_2 | 8 | 17 | PF00179 | 0.388 |
TRG_DiLeu_BaEn_1 | 268 | 273 | PF01217 | 0.392 |
TRG_DiLeu_BaLyEn_6 | 1089 | 1094 | PF01217 | 0.254 |
TRG_DiLeu_BaLyEn_6 | 738 | 743 | PF01217 | 0.695 |
TRG_DiLeu_BaLyEn_6 | 865 | 870 | PF01217 | 0.365 |
TRG_ENDOCYTIC_2 | 1041 | 1044 | PF00928 | 0.349 |
TRG_ENDOCYTIC_2 | 1144 | 1147 | PF00928 | 0.260 |
TRG_ENDOCYTIC_2 | 172 | 175 | PF00928 | 0.368 |
TRG_ER_diArg_1 | 1183 | 1186 | PF00400 | 0.522 |
TRG_ER_diArg_1 | 164 | 166 | PF00400 | 0.460 |
TRG_ER_diArg_1 | 480 | 482 | PF00400 | 0.558 |
TRG_ER_diArg_1 | 558 | 561 | PF00400 | 0.387 |
TRG_ER_diArg_1 | 590 | 593 | PF00400 | 0.322 |
TRG_ER_diArg_1 | 873 | 875 | PF00400 | 0.348 |
TRG_NES_CRM1_1 | 347 | 362 | PF08389 | 0.334 |
TRG_Pf-PMV_PEXEL_1 | 1169 | 1174 | PF00026 | 0.454 |
TRG_Pf-PMV_PEXEL_1 | 840 | 844 | PF00026 | 0.402 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I8I8 | Leptomonas seymouri | 68% | 98% |
A0A1X0P0Y8 | Trypanosomatidae | 46% | 100% |
A4H903 | Leishmania braziliensis | 35% | 100% |
A4HLF4 | Leishmania braziliensis | 81% | 100% |
A4HTF0 | Leishmania infantum | 31% | 100% |
A4I8W5 | Leishmania infantum | 100% | 100% |
E9B3T4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
Q4Q490 | Leishmania major | 95% | 100% |
Q4QED4 | Leishmania major | 35% | 100% |
Q5ZKB7 | Gallus gallus | 21% | 99% |
Q95Z93 | Leishmania major | 24% | 100% |
Q9NQ11 | Homo sapiens | 22% | 100% |
V5BPC6 | Trypanosoma cruzi | 47% | 100% |