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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0005783 | endoplasmic reticulum | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
Related structures:
AlphaFold database: E9ALC3
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 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:0030003 | intracellular monoatomic cation homeostasis | 5 | 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:0072503 | obsolete cellular divalent inorganic cation homeostasis | 6 | 1 |
GO:0072507 | obsolete divalent inorganic cation homeostasis | 7 | 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:0005215 | transporter activity | 1 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 11 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 12 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 12 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 12 |
GO:0015399 | primary active transmembrane transporter activity | 4 | 12 |
GO:0016462 | pyrophosphatase activity | 5 | 11 |
GO:0016787 | hydrolase activity | 2 | 12 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 11 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 11 |
GO:0016887 | ATP hydrolysis activity | 7 | 11 |
GO:0017076 | purine nucleotide binding | 4 | 11 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 11 |
GO:0019829 | ATPase-coupled monoatomic cation transmembrane transporter activity | 3 | 12 |
GO:0022804 | active transmembrane transporter activity | 3 | 12 |
GO:0022853 | active monoatomic ion transmembrane transporter activity | 4 | 12 |
GO:0022857 | transmembrane transporter activity | 2 | 12 |
GO:0022890 | inorganic cation transmembrane transporter activity | 4 | 12 |
GO:0030554 | adenyl nucleotide binding | 5 | 11 |
GO:0032553 | ribonucleotide binding | 3 | 11 |
GO:0032555 | purine ribonucleotide binding | 4 | 11 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 11 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 11 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0042626 | ATPase-coupled transmembrane transporter activity | 2 | 12 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043168 | anion binding | 3 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 11 |
GO:0140358 | P-type transmembrane transporter activity | 3 | 12 |
GO:0140657 | ATP-dependent activity | 1 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
GO:0015662 | P-type ion transporter activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 511 | 515 | PF00656 | 0.514 |
CLV_C14_Caspase3-7 | 619 | 623 | PF00656 | 0.534 |
CLV_C14_Caspase3-7 | 667 | 671 | PF00656 | 0.529 |
CLV_C14_Caspase3-7 | 759 | 763 | PF00656 | 0.575 |
CLV_NRD_NRD_1 | 1173 | 1175 | PF00675 | 0.284 |
CLV_NRD_NRD_1 | 142 | 144 | PF00675 | 0.273 |
CLV_NRD_NRD_1 | 20 | 22 | PF00675 | 0.277 |
CLV_NRD_NRD_1 | 612 | 614 | PF00675 | 0.256 |
CLV_NRD_NRD_1 | 683 | 685 | PF00675 | 0.410 |
CLV_NRD_NRD_1 | 785 | 787 | PF00675 | 0.346 |
CLV_NRD_NRD_1 | 931 | 933 | PF00675 | 0.311 |
CLV_PCSK_FUR_1 | 783 | 787 | PF00082 | 0.387 |
CLV_PCSK_KEX2_1 | 19 | 21 | PF00082 | 0.289 |
CLV_PCSK_KEX2_1 | 274 | 276 | PF00082 | 0.288 |
CLV_PCSK_KEX2_1 | 426 | 428 | PF00082 | 0.187 |
CLV_PCSK_KEX2_1 | 612 | 614 | PF00082 | 0.256 |
CLV_PCSK_KEX2_1 | 683 | 685 | PF00082 | 0.411 |
CLV_PCSK_KEX2_1 | 745 | 747 | PF00082 | 0.311 |
CLV_PCSK_KEX2_1 | 785 | 787 | PF00082 | 0.408 |
CLV_PCSK_KEX2_1 | 931 | 933 | PF00082 | 0.322 |
CLV_PCSK_PC1ET2_1 | 274 | 276 | PF00082 | 0.267 |
CLV_PCSK_PC1ET2_1 | 426 | 428 | PF00082 | 0.197 |
CLV_PCSK_PC1ET2_1 | 745 | 747 | PF00082 | 0.371 |
CLV_PCSK_PC1ET2_1 | 931 | 933 | PF00082 | 0.413 |
CLV_PCSK_PC7_1 | 16 | 22 | PF00082 | 0.294 |
CLV_PCSK_SKI1_1 | 1008 | 1012 | PF00082 | 0.331 |
CLV_PCSK_SKI1_1 | 1078 | 1082 | PF00082 | 0.300 |
CLV_PCSK_SKI1_1 | 1087 | 1091 | PF00082 | 0.239 |
CLV_PCSK_SKI1_1 | 1177 | 1181 | PF00082 | 0.202 |
CLV_PCSK_SKI1_1 | 274 | 278 | PF00082 | 0.282 |
CLV_PCSK_SKI1_1 | 341 | 345 | PF00082 | 0.202 |
CLV_PCSK_SKI1_1 | 390 | 394 | PF00082 | 0.212 |
CLV_PCSK_SKI1_1 | 438 | 442 | PF00082 | 0.202 |
CLV_PCSK_SKI1_1 | 516 | 520 | PF00082 | 0.400 |
CLV_PCSK_SKI1_1 | 600 | 604 | PF00082 | 0.348 |
CLV_PCSK_SKI1_1 | 666 | 670 | PF00082 | 0.315 |
CLV_PCSK_SKI1_1 | 705 | 709 | PF00082 | 0.292 |
CLV_PCSK_SKI1_1 | 786 | 790 | PF00082 | 0.340 |
CLV_PCSK_SKI1_1 | 937 | 941 | PF00082 | 0.381 |
CLV_PCSK_SKI1_1 | 944 | 948 | PF00082 | 0.328 |
DEG_APCC_DBOX_1 | 1176 | 1184 | PF00400 | 0.422 |
DEG_SCF_FBW7_2 | 915 | 921 | PF00400 | 0.519 |
DOC_CDC14_PxL_1 | 42 | 50 | PF14671 | 0.500 |
DOC_CKS1_1 | 770 | 775 | PF01111 | 0.438 |
DOC_CKS1_1 | 915 | 920 | PF01111 | 0.627 |
DOC_CYCLIN_RxL_1 | 1028 | 1040 | PF00134 | 0.405 |
DOC_CYCLIN_yCln2_LP_2 | 603 | 609 | PF00134 | 0.573 |
DOC_MAPK_DCC_7 | 279 | 288 | PF00069 | 0.492 |
DOC_MAPK_gen_1 | 1174 | 1183 | PF00069 | 0.505 |
DOC_MAPK_gen_1 | 1216 | 1225 | PF00069 | 0.215 |
DOC_MAPK_gen_1 | 254 | 264 | PF00069 | 0.517 |
DOC_MAPK_gen_1 | 337 | 345 | PF00069 | 0.452 |
DOC_MAPK_gen_1 | 367 | 375 | PF00069 | 0.430 |
DOC_MAPK_gen_1 | 434 | 441 | PF00069 | 0.402 |
DOC_MAPK_gen_1 | 597 | 605 | PF00069 | 0.478 |
DOC_MAPK_gen_1 | 673 | 682 | PF00069 | 0.587 |
DOC_MAPK_gen_1 | 689 | 698 | PF00069 | 0.417 |
DOC_MAPK_HePTP_8 | 276 | 288 | PF00069 | 0.492 |
DOC_MAPK_MEF2A_6 | 1174 | 1183 | PF00069 | 0.505 |
DOC_MAPK_MEF2A_6 | 279 | 288 | PF00069 | 0.458 |
DOC_MAPK_MEF2A_6 | 369 | 377 | PF00069 | 0.402 |
DOC_MAPK_MEF2A_6 | 597 | 605 | PF00069 | 0.481 |
DOC_MAPK_MEF2A_6 | 692 | 700 | PF00069 | 0.533 |
DOC_PP1_RVXF_1 | 687 | 694 | PF00149 | 0.455 |
DOC_PP2B_LxvP_1 | 898 | 901 | PF13499 | 0.639 |
DOC_PP4_FxxP_1 | 154 | 157 | PF00568 | 0.455 |
DOC_PP4_FxxP_1 | 481 | 484 | PF00568 | 0.445 |
DOC_USP7_MATH_1 | 1009 | 1013 | PF00917 | 0.435 |
DOC_USP7_MATH_1 | 432 | 436 | PF00917 | 0.413 |
DOC_USP7_MATH_1 | 664 | 668 | PF00917 | 0.500 |
DOC_USP7_UBL2_3 | 1054 | 1058 | PF12436 | 0.293 |
DOC_USP7_UBL2_3 | 523 | 527 | PF12436 | 0.539 |
DOC_USP7_UBL2_3 | 704 | 708 | PF12436 | 0.462 |
DOC_USP7_UBL2_3 | 876 | 880 | PF12436 | 0.648 |
DOC_USP7_UBL2_3 | 933 | 937 | PF12436 | 0.636 |
DOC_USP7_UBL2_3 | 947 | 951 | PF12436 | 0.578 |
DOC_USP7_UBL2_3 | 953 | 957 | PF12436 | 0.542 |
DOC_WW_Pin1_4 | 1195 | 1200 | PF00397 | 0.464 |
DOC_WW_Pin1_4 | 206 | 211 | PF00397 | 0.382 |
DOC_WW_Pin1_4 | 317 | 322 | PF00397 | 0.402 |
DOC_WW_Pin1_4 | 628 | 633 | PF00397 | 0.487 |
DOC_WW_Pin1_4 | 769 | 774 | PF00397 | 0.478 |
DOC_WW_Pin1_4 | 786 | 791 | PF00397 | 0.514 |
DOC_WW_Pin1_4 | 802 | 807 | PF00397 | 0.553 |
DOC_WW_Pin1_4 | 914 | 919 | PF00397 | 0.596 |
LIG_14-3-3_CanoR_1 | 1021 | 1025 | PF00244 | 0.439 |
LIG_14-3-3_CanoR_1 | 1216 | 1225 | PF00244 | 0.257 |
LIG_14-3-3_CanoR_1 | 251 | 257 | PF00244 | 0.503 |
LIG_14-3-3_CanoR_1 | 52 | 56 | PF00244 | 0.318 |
LIG_Actin_WH2_2 | 411 | 428 | PF00022 | 0.402 |
LIG_Actin_WH2_2 | 635 | 650 | PF00022 | 0.581 |
LIG_ActinCP_TwfCPI_2 | 154 | 162 | PF01115 | 0.458 |
LIG_AP2alpha_1 | 199 | 203 | PF02296 | 0.529 |
LIG_APCC_ABBA_1 | 1238 | 1243 | PF00400 | 0.575 |
LIG_APCC_ABBA_1 | 124 | 129 | PF00400 | 0.593 |
LIG_APCC_ABBA_1 | 42 | 47 | PF00400 | 0.389 |
LIG_BIR_III_4 | 1226 | 1230 | PF00653 | 0.254 |
LIG_BIR_III_4 | 185 | 189 | PF00653 | 0.441 |
LIG_BIR_III_4 | 752 | 756 | PF00653 | 0.524 |
LIG_BRCT_BRCA1_1 | 1067 | 1071 | PF00533 | 0.254 |
LIG_BRCT_BRCA1_1 | 1145 | 1149 | PF00533 | 0.254 |
LIG_BRCT_BRCA1_1 | 1197 | 1201 | PF00533 | 0.344 |
LIG_BRCT_BRCA1_1 | 208 | 212 | PF00533 | 0.382 |
LIG_BRCT_BRCA1_1 | 86 | 90 | PF00533 | 0.456 |
LIG_Clathr_ClatBox_1 | 1222 | 1226 | PF01394 | 0.333 |
LIG_Clathr_ClatBox_1 | 283 | 287 | PF01394 | 0.402 |
LIG_Clathr_ClatBox_1 | 539 | 543 | PF01394 | 0.484 |
LIG_CtBP_PxDLS_1 | 456 | 460 | PF00389 | 0.402 |
LIG_deltaCOP1_diTrp_1 | 22 | 30 | PF00928 | 0.457 |
LIG_deltaCOP1_diTrp_1 | 225 | 233 | PF00928 | 0.202 |
LIG_eIF4E_1 | 227 | 233 | PF01652 | 0.213 |
LIG_eIF4E_1 | 43 | 49 | PF01652 | 0.377 |
LIG_FHA_1 | 1 | 7 | PF00498 | 0.584 |
LIG_FHA_1 | 1020 | 1026 | PF00498 | 0.527 |
LIG_FHA_1 | 106 | 112 | PF00498 | 0.471 |
LIG_FHA_1 | 1145 | 1151 | PF00498 | 0.282 |
LIG_FHA_1 | 1157 | 1163 | PF00498 | 0.213 |
LIG_FHA_1 | 1218 | 1224 | PF00498 | 0.382 |
LIG_FHA_1 | 179 | 185 | PF00498 | 0.546 |
LIG_FHA_1 | 278 | 284 | PF00498 | 0.421 |
LIG_FHA_1 | 305 | 311 | PF00498 | 0.393 |
LIG_FHA_1 | 318 | 324 | PF00498 | 0.424 |
LIG_FHA_1 | 346 | 352 | PF00498 | 0.402 |
LIG_FHA_1 | 446 | 452 | PF00498 | 0.404 |
LIG_FHA_1 | 463 | 469 | PF00498 | 0.413 |
LIG_FHA_1 | 495 | 501 | PF00498 | 0.464 |
LIG_FHA_1 | 52 | 58 | PF00498 | 0.333 |
LIG_FHA_1 | 850 | 856 | PF00498 | 0.509 |
LIG_FHA_2 | 1124 | 1130 | PF00498 | 0.409 |
LIG_FHA_2 | 253 | 259 | PF00498 | 0.548 |
LIG_FHA_2 | 357 | 363 | PF00498 | 0.512 |
LIG_FHA_2 | 377 | 383 | PF00498 | 0.389 |
LIG_FHA_2 | 499 | 505 | PF00498 | 0.463 |
LIG_FHA_2 | 58 | 64 | PF00498 | 0.322 |
LIG_FHA_2 | 667 | 673 | PF00498 | 0.590 |
LIG_FHA_2 | 770 | 776 | PF00498 | 0.601 |
LIG_FHA_2 | 787 | 793 | PF00498 | 0.499 |
LIG_FHA_2 | 813 | 819 | PF00498 | 0.475 |
LIG_FHA_2 | 827 | 833 | PF00498 | 0.504 |
LIG_FHA_2 | 950 | 956 | PF00498 | 0.624 |
LIG_LIR_Apic_2 | 151 | 157 | PF02991 | 0.458 |
LIG_LIR_Apic_2 | 478 | 484 | PF02991 | 0.455 |
LIG_LIR_Gen_1 | 1068 | 1079 | PF02991 | 0.239 |
LIG_LIR_Gen_1 | 1131 | 1141 | PF02991 | 0.282 |
LIG_LIR_Gen_1 | 1217 | 1227 | PF02991 | 0.259 |
LIG_LIR_Gen_1 | 198 | 207 | PF02991 | 0.474 |
LIG_LIR_Gen_1 | 22 | 32 | PF02991 | 0.420 |
LIG_LIR_Gen_1 | 234 | 241 | PF02991 | 0.309 |
LIG_LIR_Gen_1 | 244 | 253 | PF02991 | 0.426 |
LIG_LIR_Gen_1 | 47 | 57 | PF02991 | 0.341 |
LIG_LIR_Gen_1 | 60 | 68 | PF02991 | 0.300 |
LIG_LIR_Gen_1 | 78 | 85 | PF02991 | 0.239 |
LIG_LIR_Gen_1 | 917 | 927 | PF02991 | 0.636 |
LIG_LIR_LC3C_4 | 881 | 884 | PF02991 | 0.653 |
LIG_LIR_Nem_3 | 1090 | 1096 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 1100 | 1105 | PF02991 | 0.239 |
LIG_LIR_Nem_3 | 1131 | 1137 | PF02991 | 0.289 |
LIG_LIR_Nem_3 | 1217 | 1222 | PF02991 | 0.259 |
LIG_LIR_Nem_3 | 164 | 168 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 198 | 202 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 209 | 214 | PF02991 | 0.239 |
LIG_LIR_Nem_3 | 22 | 27 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 225 | 230 | PF02991 | 0.211 |
LIG_LIR_Nem_3 | 231 | 236 | PF02991 | 0.235 |
LIG_LIR_Nem_3 | 244 | 250 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 405 | 410 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 435 | 440 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 47 | 53 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 504 | 510 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 60 | 64 | PF02991 | 0.273 |
LIG_LIR_Nem_3 | 78 | 82 | PF02991 | 0.306 |
LIG_LYPXL_S_1 | 44 | 48 | PF13949 | 0.590 |
LIG_LYPXL_yS_3 | 45 | 48 | PF13949 | 0.390 |
LIG_MLH1_MIPbox_1 | 208 | 212 | PF16413 | 0.382 |
LIG_PCNA_yPIPBox_3 | 1085 | 1093 | PF02747 | 0.557 |
LIG_PCNA_yPIPBox_3 | 589 | 602 | PF02747 | 0.454 |
LIG_Pex14_1 | 86 | 90 | PF04695 | 0.456 |
LIG_Pex14_2 | 1201 | 1205 | PF04695 | 0.342 |
LIG_Pex14_2 | 1215 | 1219 | PF04695 | 0.218 |
LIG_Pex14_2 | 199 | 203 | PF04695 | 0.505 |
LIG_Pex14_2 | 75 | 79 | PF04695 | 0.259 |
LIG_SH2_CRK | 1031 | 1035 | PF00017 | 0.402 |
LIG_SH2_CRK | 247 | 251 | PF00017 | 0.553 |
LIG_SH2_CRK | 599 | 603 | PF00017 | 0.461 |
LIG_SH2_CRK | 658 | 662 | PF00017 | 0.481 |
LIG_SH2_CRK | 665 | 669 | PF00017 | 0.486 |
LIG_SH2_CRK | 96 | 100 | PF00017 | 0.562 |
LIG_SH2_PTP2 | 699 | 702 | PF00017 | 0.557 |
LIG_SH2_SRC | 1134 | 1137 | PF00017 | 0.383 |
LIG_SH2_SRC | 43 | 46 | PF00017 | 0.493 |
LIG_SH2_STAP1 | 1043 | 1047 | PF00017 | 0.251 |
LIG_SH2_STAP1 | 528 | 532 | PF00017 | 0.527 |
LIG_SH2_STAT5 | 1110 | 1113 | PF00017 | 0.333 |
LIG_SH2_STAT5 | 168 | 171 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.576 |
LIG_SH2_STAT5 | 36 | 39 | PF00017 | 0.253 |
LIG_SH2_STAT5 | 423 | 426 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 43 | 46 | PF00017 | 0.310 |
LIG_SH2_STAT5 | 541 | 544 | PF00017 | 0.626 |
LIG_SH2_STAT5 | 55 | 58 | PF00017 | 0.302 |
LIG_SH2_STAT5 | 61 | 64 | PF00017 | 0.281 |
LIG_SH2_STAT5 | 625 | 628 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 699 | 702 | PF00017 | 0.557 |
LIG_SH2_STAT5 | 811 | 814 | PF00017 | 0.394 |
LIG_SH3_2 | 157 | 162 | PF14604 | 0.458 |
LIG_SH3_3 | 1089 | 1095 | PF00018 | 0.479 |
LIG_SH3_3 | 154 | 160 | PF00018 | 0.454 |
LIG_SH3_3 | 191 | 197 | PF00018 | 0.483 |
LIG_SH3_3 | 447 | 453 | PF00018 | 0.402 |
LIG_SH3_3 | 615 | 621 | PF00018 | 0.501 |
LIG_SH3_3 | 764 | 770 | PF00018 | 0.533 |
LIG_SH3_3 | 880 | 886 | PF00018 | 0.673 |
LIG_SH3_3 | 889 | 895 | PF00018 | 0.623 |
LIG_SH3_3 | 905 | 911 | PF00018 | 0.577 |
LIG_SH3_3 | 912 | 918 | PF00018 | 0.560 |
LIG_SH3_3 | 958 | 964 | PF00018 | 0.605 |
LIG_SUMO_SIM_anti_2 | 1220 | 1226 | PF11976 | 0.442 |
LIG_SUMO_SIM_anti_2 | 266 | 271 | PF11976 | 0.451 |
LIG_SUMO_SIM_anti_2 | 287 | 293 | PF11976 | 0.406 |
LIG_SUMO_SIM_par_1 | 1220 | 1226 | PF11976 | 0.335 |
LIG_SUMO_SIM_par_1 | 287 | 293 | PF11976 | 0.505 |
LIG_SUMO_SIM_par_1 | 465 | 471 | PF11976 | 0.480 |
LIG_TRAF2_1 | 359 | 362 | PF00917 | 0.505 |
LIG_TYR_ITIM | 663 | 668 | PF00017 | 0.355 |
LIG_TYR_ITIM | 94 | 99 | PF00017 | 0.443 |
LIG_TYR_ITSM | 243 | 250 | PF00017 | 0.429 |
LIG_UBA3_1 | 467 | 472 | PF00899 | 0.254 |
LIG_UBA3_1 | 518 | 527 | PF00899 | 0.410 |
LIG_WRC_WIRS_1 | 76 | 81 | PF05994 | 0.315 |
MOD_CDK_SPK_2 | 786 | 791 | PF00069 | 0.376 |
MOD_CDK_SPxxK_3 | 317 | 324 | PF00069 | 0.239 |
MOD_CK1_1 | 1128 | 1134 | PF00069 | 0.584 |
MOD_CK1_1 | 1156 | 1162 | PF00069 | 0.382 |
MOD_CK1_1 | 1195 | 1201 | PF00069 | 0.464 |
MOD_CK1_1 | 231 | 237 | PF00069 | 0.239 |
MOD_CK1_1 | 400 | 406 | PF00069 | 0.279 |
MOD_CK1_1 | 631 | 637 | PF00069 | 0.390 |
MOD_CK1_1 | 675 | 681 | PF00069 | 0.494 |
MOD_CK1_1 | 728 | 734 | PF00069 | 0.316 |
MOD_CK1_1 | 763 | 769 | PF00069 | 0.417 |
MOD_CK1_1 | 78 | 84 | PF00069 | 0.268 |
MOD_CK1_1 | 805 | 811 | PF00069 | 0.389 |
MOD_CK2_1 | 356 | 362 | PF00069 | 0.320 |
MOD_CK2_1 | 376 | 382 | PF00069 | 0.326 |
MOD_CK2_1 | 498 | 504 | PF00069 | 0.321 |
MOD_CK2_1 | 638 | 644 | PF00069 | 0.395 |
MOD_CK2_1 | 666 | 672 | PF00069 | 0.490 |
MOD_CK2_1 | 786 | 792 | PF00069 | 0.362 |
MOD_CK2_1 | 812 | 818 | PF00069 | 0.340 |
MOD_CK2_1 | 826 | 832 | PF00069 | 0.391 |
MOD_CK2_1 | 978 | 984 | PF00069 | 0.674 |
MOD_CMANNOS | 23 | 26 | PF00535 | 0.342 |
MOD_Cter_Amidation | 272 | 275 | PF01082 | 0.375 |
MOD_GlcNHglycan | 1155 | 1158 | PF01048 | 0.299 |
MOD_GlcNHglycan | 345 | 348 | PF01048 | 0.245 |
MOD_GlcNHglycan | 401 | 405 | PF01048 | 0.254 |
MOD_GlcNHglycan | 420 | 423 | PF01048 | 0.282 |
MOD_GlcNHglycan | 618 | 621 | PF01048 | 0.361 |
MOD_GlcNHglycan | 869 | 872 | PF01048 | 0.503 |
MOD_GSK3_1 | 1004 | 1011 | PF00069 | 0.368 |
MOD_GSK3_1 | 1019 | 1026 | PF00069 | 0.198 |
MOD_GSK3_1 | 1037 | 1044 | PF00069 | 0.239 |
MOD_GSK3_1 | 1074 | 1081 | PF00069 | 0.446 |
MOD_GSK3_1 | 1139 | 1146 | PF00069 | 0.341 |
MOD_GSK3_1 | 1149 | 1156 | PF00069 | 0.239 |
MOD_GSK3_1 | 1205 | 1212 | PF00069 | 0.423 |
MOD_GSK3_1 | 313 | 320 | PF00069 | 0.248 |
MOD_GSK3_1 | 363 | 370 | PF00069 | 0.304 |
MOD_GSK3_1 | 376 | 383 | PF00069 | 0.223 |
MOD_GSK3_1 | 388 | 395 | PF00069 | 0.223 |
MOD_GSK3_1 | 494 | 501 | PF00069 | 0.292 |
MOD_GSK3_1 | 777 | 784 | PF00069 | 0.437 |
MOD_GSK3_1 | 974 | 981 | PF00069 | 0.690 |
MOD_LATS_1 | 365 | 371 | PF00433 | 0.351 |
MOD_N-GLC_1 | 1144 | 1149 | PF02516 | 0.382 |
MOD_N-GLC_1 | 463 | 468 | PF02516 | 0.254 |
MOD_N-GLC_1 | 965 | 970 | PF02516 | 0.537 |
MOD_NEK2_1 | 1019 | 1024 | PF00069 | 0.285 |
MOD_NEK2_1 | 1072 | 1077 | PF00069 | 0.367 |
MOD_NEK2_1 | 1097 | 1102 | PF00069 | 0.239 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.402 |
MOD_NEK2_1 | 1112 | 1117 | PF00069 | 0.297 |
MOD_NEK2_1 | 1143 | 1148 | PF00069 | 0.249 |
MOD_NEK2_1 | 1149 | 1154 | PF00069 | 0.253 |
MOD_NEK2_1 | 1205 | 1210 | PF00069 | 0.463 |
MOD_NEK2_1 | 241 | 246 | PF00069 | 0.239 |
MOD_NEK2_1 | 343 | 348 | PF00069 | 0.299 |
MOD_NEK2_1 | 388 | 393 | PF00069 | 0.239 |
MOD_NEK2_1 | 418 | 423 | PF00069 | 0.328 |
MOD_NEK2_1 | 439 | 444 | PF00069 | 0.253 |
MOD_NEK2_1 | 457 | 462 | PF00069 | 0.176 |
MOD_NEK2_1 | 468 | 473 | PF00069 | 0.321 |
MOD_NEK2_1 | 494 | 499 | PF00069 | 0.296 |
MOD_NEK2_1 | 607 | 612 | PF00069 | 0.485 |
MOD_NEK2_1 | 638 | 643 | PF00069 | 0.358 |
MOD_NEK2_1 | 75 | 80 | PF00069 | 0.446 |
MOD_NEK2_1 | 781 | 786 | PF00069 | 0.452 |
MOD_NEK2_1 | 904 | 909 | PF00069 | 0.446 |
MOD_NEK2_1 | 974 | 979 | PF00069 | 0.473 |
MOD_NEK2_2 | 228 | 233 | PF00069 | 0.239 |
MOD_PIKK_1 | 1037 | 1043 | PF00454 | 0.376 |
MOD_PIKK_1 | 1217 | 1223 | PF00454 | 0.409 |
MOD_PIKK_1 | 345 | 351 | PF00454 | 0.299 |
MOD_PIKK_1 | 392 | 398 | PF00454 | 0.239 |
MOD_PIKK_1 | 826 | 832 | PF00454 | 0.410 |
MOD_PKA_1 | 274 | 280 | PF00069 | 0.375 |
MOD_PKA_2 | 1020 | 1026 | PF00069 | 0.270 |
MOD_PKA_2 | 1217 | 1223 | PF00069 | 0.382 |
MOD_PKA_2 | 274 | 280 | PF00069 | 0.333 |
MOD_PKA_2 | 397 | 403 | PF00069 | 0.239 |
MOD_PKA_2 | 51 | 57 | PF00069 | 0.404 |
MOD_PKA_2 | 672 | 678 | PF00069 | 0.573 |
MOD_PKB_1 | 1085 | 1093 | PF00069 | 0.401 |
MOD_Plk_1 | 1122 | 1128 | PF00069 | 0.268 |
MOD_Plk_1 | 1144 | 1150 | PF00069 | 0.382 |
MOD_Plk_1 | 1205 | 1211 | PF00069 | 0.427 |
MOD_Plk_1 | 241 | 247 | PF00069 | 0.239 |
MOD_Plk_1 | 311 | 317 | PF00069 | 0.254 |
MOD_Plk_1 | 457 | 463 | PF00069 | 0.239 |
MOD_Plk_1 | 543 | 549 | PF00069 | 0.539 |
MOD_Plk_1 | 737 | 743 | PF00069 | 0.373 |
MOD_Plk_1 | 995 | 1001 | PF00069 | 0.353 |
MOD_Plk_2-3 | 1123 | 1129 | PF00069 | 0.481 |
MOD_Plk_4 | 1020 | 1026 | PF00069 | 0.270 |
MOD_Plk_4 | 1043 | 1049 | PF00069 | 0.242 |
MOD_Plk_4 | 1097 | 1103 | PF00069 | 0.239 |
MOD_Plk_4 | 1113 | 1119 | PF00069 | 0.297 |
MOD_Plk_4 | 1139 | 1145 | PF00069 | 0.321 |
MOD_Plk_4 | 1150 | 1156 | PF00069 | 0.239 |
MOD_Plk_4 | 1234 | 1240 | PF00069 | 0.440 |
MOD_Plk_4 | 22 | 28 | PF00069 | 0.289 |
MOD_Plk_4 | 228 | 234 | PF00069 | 0.239 |
MOD_Plk_4 | 242 | 248 | PF00069 | 0.239 |
MOD_Plk_4 | 36 | 42 | PF00069 | 0.326 |
MOD_Plk_4 | 446 | 452 | PF00069 | 0.326 |
MOD_Plk_4 | 463 | 469 | PF00069 | 0.158 |
MOD_Plk_4 | 51 | 57 | PF00069 | 0.383 |
MOD_Plk_4 | 535 | 541 | PF00069 | 0.346 |
MOD_Plk_4 | 675 | 681 | PF00069 | 0.518 |
MOD_Plk_4 | 7 | 13 | PF00069 | 0.415 |
MOD_Plk_4 | 737 | 743 | PF00069 | 0.369 |
MOD_Plk_4 | 75 | 81 | PF00069 | 0.268 |
MOD_Plk_4 | 763 | 769 | PF00069 | 0.472 |
MOD_Plk_4 | 818 | 824 | PF00069 | 0.461 |
MOD_Plk_4 | 974 | 980 | PF00069 | 0.461 |
MOD_ProDKin_1 | 1195 | 1201 | PF00069 | 0.464 |
MOD_ProDKin_1 | 206 | 212 | PF00069 | 0.382 |
MOD_ProDKin_1 | 317 | 323 | PF00069 | 0.239 |
MOD_ProDKin_1 | 628 | 634 | PF00069 | 0.358 |
MOD_ProDKin_1 | 769 | 775 | PF00069 | 0.344 |
MOD_ProDKin_1 | 786 | 792 | PF00069 | 0.397 |
MOD_ProDKin_1 | 802 | 808 | PF00069 | 0.442 |
MOD_ProDKin_1 | 914 | 920 | PF00069 | 0.510 |
MOD_SUMO_for_1 | 875 | 878 | PF00179 | 0.604 |
MOD_SUMO_rev_2 | 1136 | 1142 | PF00179 | 0.407 |
MOD_SUMO_rev_2 | 511 | 518 | PF00179 | 0.489 |
MOD_SUMO_rev_2 | 567 | 577 | PF00179 | 0.568 |
MOD_SUMO_rev_2 | 619 | 626 | PF00179 | 0.336 |
MOD_SUMO_rev_2 | 872 | 882 | PF00179 | 0.585 |
MOD_SUMO_rev_2 | 891 | 901 | PF00179 | 0.526 |
MOD_SUMO_rev_2 | 929 | 939 | PF00179 | 0.597 |
MOD_SUMO_rev_2 | 950 | 959 | PF00179 | 0.621 |
TRG_DiLeu_BaEn_1 | 1234 | 1239 | PF01217 | 0.445 |
TRG_DiLeu_BaEn_1 | 878 | 883 | PF01217 | 0.580 |
TRG_DiLeu_BaEn_2 | 404 | 410 | PF01217 | 0.239 |
TRG_DiLeu_BaLyEn_6 | 13 | 18 | PF01217 | 0.354 |
TRG_ENDOCYTIC_2 | 1031 | 1034 | PF00928 | 0.239 |
TRG_ENDOCYTIC_2 | 1110 | 1113 | PF00928 | 0.239 |
TRG_ENDOCYTIC_2 | 1134 | 1137 | PF00928 | 0.492 |
TRG_ENDOCYTIC_2 | 229 | 232 | PF00928 | 0.254 |
TRG_ENDOCYTIC_2 | 24 | 27 | PF00928 | 0.511 |
TRG_ENDOCYTIC_2 | 247 | 250 | PF00928 | 0.386 |
TRG_ENDOCYTIC_2 | 45 | 48 | PF00928 | 0.439 |
TRG_ENDOCYTIC_2 | 528 | 531 | PF00928 | 0.316 |
TRG_ENDOCYTIC_2 | 599 | 602 | PF00928 | 0.322 |
TRG_ENDOCYTIC_2 | 61 | 64 | PF00928 | 0.275 |
TRG_ENDOCYTIC_2 | 658 | 661 | PF00928 | 0.364 |
TRG_ENDOCYTIC_2 | 665 | 668 | PF00928 | 0.389 |
TRG_ENDOCYTIC_2 | 96 | 99 | PF00928 | 0.456 |
TRG_ER_diArg_1 | 1085 | 1088 | PF00400 | 0.398 |
TRG_ER_diArg_1 | 1215 | 1218 | PF00400 | 0.342 |
TRG_ER_diArg_1 | 18 | 21 | PF00400 | 0.346 |
TRG_ER_diArg_1 | 434 | 437 | PF00400 | 0.254 |
TRG_ER_diArg_1 | 611 | 613 | PF00400 | 0.334 |
TRG_ER_diArg_1 | 682 | 684 | PF00400 | 0.506 |
TRG_ER_diArg_1 | 783 | 786 | PF00400 | 0.580 |
TRG_ER_diArg_1 | 90 | 93 | PF00400 | 0.496 |
TRG_NLS_MonoExtC_3 | 1173 | 1178 | PF00514 | 0.362 |
TRG_NLS_MonoExtC_3 | 142 | 148 | PF00514 | 0.363 |
TRG_Pf-PMV_PEXEL_1 | 254 | 258 | PF00026 | 0.478 |
TRG_Pf-PMV_PEXEL_1 | 427 | 431 | PF00026 | 0.218 |
TRG_Pf-PMV_PEXEL_1 | 666 | 670 | PF00026 | 0.338 |
TRG_Pf-PMV_PEXEL_1 | 944 | 948 | PF00026 | 0.461 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZI4 | Leptomonas seymouri | 82% | 100% |
A0A0S4INU6 | Bodo saltans | 57% | 100% |
A0A1X0NPJ3 | Trypanosomatidae | 67% | 100% |
A0A3R7N8T2 | Trypanosoma rangeli | 67% | 100% |
A0A3S5H614 | Leishmania donovani | 97% | 100% |
A4H553 | Leishmania braziliensis | 89% | 100% |
A4HTD0 | Leishmania infantum | 97% | 100% |
A4HTF0 | Leishmania infantum | 23% | 100% |
C9ZUI4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 63% | 99% |
O14072 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 35% | 100% |
P39986 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 35% | 100% |
P90747 | Caenorhabditis elegans | 36% | 100% |
Q4QII2 | Leishmania major | 95% | 100% |
Q9HD20 | Homo sapiens | 39% | 100% |
Q9LT02 | Arabidopsis thaliana | 35% | 100% |
V5BNZ8 | Trypanosoma cruzi | 67% | 100% |