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: A4H553
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 | 0.507 |
CLV_C14_Caspase3-7 | 619 | 623 | PF00656 | 0.538 |
CLV_C14_Caspase3-7 | 760 | 764 | PF00656 | 0.581 |
CLV_NRD_NRD_1 | 1172 | 1174 | PF00675 | 0.283 |
CLV_NRD_NRD_1 | 142 | 144 | PF00675 | 0.273 |
CLV_NRD_NRD_1 | 20 | 22 | PF00675 | 0.281 |
CLV_NRD_NRD_1 | 612 | 614 | PF00675 | 0.260 |
CLV_NRD_NRD_1 | 683 | 685 | PF00675 | 0.421 |
CLV_NRD_NRD_1 | 786 | 788 | PF00675 | 0.368 |
CLV_NRD_NRD_1 | 931 | 933 | PF00675 | 0.294 |
CLV_PCSK_FUR_1 | 784 | 788 | PF00082 | 0.405 |
CLV_PCSK_KEX2_1 | 20 | 22 | PF00082 | 0.294 |
CLV_PCSK_KEX2_1 | 274 | 276 | PF00082 | 0.289 |
CLV_PCSK_KEX2_1 | 612 | 614 | PF00082 | 0.260 |
CLV_PCSK_KEX2_1 | 683 | 685 | PF00082 | 0.422 |
CLV_PCSK_KEX2_1 | 745 | 747 | PF00082 | 0.322 |
CLV_PCSK_KEX2_1 | 786 | 788 | PF00082 | 0.430 |
CLV_PCSK_KEX2_1 | 931 | 933 | PF00082 | 0.305 |
CLV_PCSK_PC1ET2_1 | 274 | 276 | PF00082 | 0.267 |
CLV_PCSK_PC1ET2_1 | 745 | 747 | PF00082 | 0.382 |
CLV_PCSK_PC1ET2_1 | 788 | 790 | PF00082 | 0.291 |
CLV_PCSK_PC1ET2_1 | 931 | 933 | PF00082 | 0.396 |
CLV_PCSK_PC7_1 | 16 | 22 | PF00082 | 0.294 |
CLV_PCSK_PC7_1 | 784 | 790 | PF00082 | 0.292 |
CLV_PCSK_SKI1_1 | 1007 | 1011 | PF00082 | 0.332 |
CLV_PCSK_SKI1_1 | 1086 | 1090 | PF00082 | 0.241 |
CLV_PCSK_SKI1_1 | 1176 | 1180 | PF00082 | 0.203 |
CLV_PCSK_SKI1_1 | 274 | 278 | PF00082 | 0.283 |
CLV_PCSK_SKI1_1 | 341 | 345 | PF00082 | 0.203 |
CLV_PCSK_SKI1_1 | 390 | 394 | PF00082 | 0.213 |
CLV_PCSK_SKI1_1 | 438 | 442 | PF00082 | 0.203 |
CLV_PCSK_SKI1_1 | 516 | 520 | PF00082 | 0.399 |
CLV_PCSK_SKI1_1 | 575 | 579 | PF00082 | 0.353 |
CLV_PCSK_SKI1_1 | 600 | 604 | PF00082 | 0.354 |
CLV_PCSK_SKI1_1 | 666 | 670 | PF00082 | 0.321 |
CLV_PCSK_SKI1_1 | 705 | 709 | PF00082 | 0.294 |
CLV_PCSK_SKI1_1 | 775 | 779 | PF00082 | 0.333 |
DEG_SPOP_SBC_1 | 356 | 360 | PF00917 | 0.345 |
DOC_CDC14_PxL_1 | 42 | 50 | PF14671 | 0.496 |
DOC_CYCLIN_RxL_1 | 1027 | 1039 | PF00134 | 0.406 |
DOC_CYCLIN_yCln2_LP_2 | 603 | 609 | PF00134 | 0.577 |
DOC_MAPK_gen_1 | 1173 | 1182 | PF00069 | 0.505 |
DOC_MAPK_gen_1 | 1215 | 1224 | PF00069 | 0.216 |
DOC_MAPK_gen_1 | 254 | 264 | PF00069 | 0.518 |
DOC_MAPK_gen_1 | 337 | 345 | PF00069 | 0.453 |
DOC_MAPK_gen_1 | 367 | 375 | PF00069 | 0.431 |
DOC_MAPK_gen_1 | 434 | 441 | PF00069 | 0.403 |
DOC_MAPK_gen_1 | 597 | 605 | PF00069 | 0.485 |
DOC_MAPK_gen_1 | 931 | 939 | PF00069 | 0.442 |
DOC_MAPK_MEF2A_6 | 1173 | 1182 | PF00069 | 0.505 |
DOC_MAPK_MEF2A_6 | 369 | 377 | PF00069 | 0.403 |
DOC_MAPK_MEF2A_6 | 597 | 605 | PF00069 | 0.488 |
DOC_MAPK_MEF2A_6 | 692 | 700 | PF00069 | 0.535 |
DOC_PP2B_LxvP_1 | 898 | 901 | PF13499 | 0.586 |
DOC_PP4_FxxP_1 | 154 | 157 | PF00568 | 0.453 |
DOC_PP4_FxxP_1 | 481 | 484 | PF00568 | 0.451 |
DOC_PP4_FxxP_1 | 571 | 574 | PF00568 | 0.467 |
DOC_USP7_MATH_1 | 1008 | 1012 | PF00917 | 0.436 |
DOC_USP7_MATH_1 | 1124 | 1128 | PF00917 | 0.328 |
DOC_USP7_MATH_1 | 1193 | 1197 | PF00917 | 0.301 |
DOC_USP7_MATH_1 | 356 | 360 | PF00917 | 0.424 |
DOC_USP7_MATH_1 | 432 | 436 | PF00917 | 0.414 |
DOC_USP7_MATH_1 | 768 | 772 | PF00917 | 0.500 |
DOC_USP7_MATH_1 | 958 | 962 | PF00917 | 0.638 |
DOC_USP7_MATH_1 | 967 | 971 | PF00917 | 0.557 |
DOC_USP7_UBL2_3 | 1053 | 1057 | PF12436 | 0.295 |
DOC_USP7_UBL2_3 | 523 | 527 | PF12436 | 0.542 |
DOC_USP7_UBL2_3 | 704 | 708 | PF12436 | 0.465 |
DOC_USP7_UBL2_3 | 947 | 951 | PF12436 | 0.559 |
DOC_USP7_UBL2_3 | 953 | 957 | PF12436 | 0.511 |
DOC_WW_Pin1_4 | 1194 | 1199 | PF00397 | 0.468 |
DOC_WW_Pin1_4 | 206 | 211 | PF00397 | 0.383 |
DOC_WW_Pin1_4 | 317 | 322 | PF00397 | 0.403 |
DOC_WW_Pin1_4 | 628 | 633 | PF00397 | 0.491 |
DOC_WW_Pin1_4 | 787 | 792 | PF00397 | 0.533 |
DOC_WW_Pin1_4 | 803 | 808 | PF00397 | 0.563 |
DOC_WW_Pin1_4 | 914 | 919 | PF00397 | 0.594 |
LIG_14-3-3_CanoR_1 | 1020 | 1024 | PF00244 | 0.440 |
LIG_14-3-3_CanoR_1 | 103 | 111 | PF00244 | 0.453 |
LIG_14-3-3_CanoR_1 | 1215 | 1224 | PF00244 | 0.257 |
LIG_14-3-3_CanoR_1 | 251 | 257 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 52 | 56 | PF00244 | 0.308 |
LIG_Actin_WH2_2 | 411 | 428 | PF00022 | 0.403 |
LIG_Actin_WH2_2 | 635 | 650 | PF00022 | 0.580 |
LIG_ActinCP_TwfCPI_2 | 154 | 162 | PF01115 | 0.458 |
LIG_AP2alpha_1 | 199 | 203 | PF02296 | 0.530 |
LIG_APCC_ABBA_1 | 1237 | 1242 | PF00400 | 0.577 |
LIG_APCC_ABBA_1 | 124 | 129 | PF00400 | 0.591 |
LIG_APCC_ABBA_1 | 42 | 47 | PF00400 | 0.387 |
LIG_APCC_ABBA_1 | 814 | 819 | PF00400 | 0.414 |
LIG_BIR_III_4 | 1225 | 1229 | PF00653 | 0.255 |
LIG_BRCT_BRCA1_1 | 1066 | 1070 | PF00533 | 0.255 |
LIG_BRCT_BRCA1_1 | 1144 | 1148 | PF00533 | 0.255 |
LIG_BRCT_BRCA1_1 | 1196 | 1200 | PF00533 | 0.344 |
LIG_BRCT_BRCA1_1 | 208 | 212 | PF00533 | 0.383 |
LIG_BRCT_BRCA1_1 | 86 | 90 | PF00533 | 0.456 |
LIG_BRCT_BRCA1_2 | 1196 | 1202 | PF00533 | 0.218 |
LIG_Clathr_ClatBox_1 | 1221 | 1225 | PF01394 | 0.334 |
LIG_Clathr_ClatBox_1 | 283 | 287 | PF01394 | 0.403 |
LIG_Clathr_ClatBox_1 | 539 | 543 | PF01394 | 0.487 |
LIG_CtBP_PxDLS_1 | 456 | 460 | PF00389 | 0.403 |
LIG_deltaCOP1_diTrp_1 | 22 | 30 | PF00928 | 0.457 |
LIG_deltaCOP1_diTrp_1 | 225 | 233 | PF00928 | 0.203 |
LIG_eIF4E_1 | 227 | 233 | PF01652 | 0.214 |
LIG_eIF4E_1 | 43 | 49 | PF01652 | 0.376 |
LIG_FHA_1 | 1 | 7 | PF00498 | 0.580 |
LIG_FHA_1 | 1019 | 1025 | PF00498 | 0.528 |
LIG_FHA_1 | 106 | 112 | PF00498 | 0.479 |
LIG_FHA_1 | 1144 | 1150 | PF00498 | 0.282 |
LIG_FHA_1 | 1156 | 1162 | PF00498 | 0.214 |
LIG_FHA_1 | 1217 | 1223 | PF00498 | 0.383 |
LIG_FHA_1 | 184 | 190 | PF00498 | 0.483 |
LIG_FHA_1 | 278 | 284 | PF00498 | 0.422 |
LIG_FHA_1 | 318 | 324 | PF00498 | 0.425 |
LIG_FHA_1 | 346 | 352 | PF00498 | 0.403 |
LIG_FHA_1 | 446 | 452 | PF00498 | 0.405 |
LIG_FHA_1 | 463 | 469 | PF00498 | 0.414 |
LIG_FHA_1 | 495 | 501 | PF00498 | 0.466 |
LIG_FHA_1 | 52 | 58 | PF00498 | 0.323 |
LIG_FHA_1 | 851 | 857 | PF00498 | 0.510 |
LIG_FHA_2 | 1123 | 1129 | PF00498 | 0.391 |
LIG_FHA_2 | 253 | 259 | PF00498 | 0.548 |
LIG_FHA_2 | 356 | 362 | PF00498 | 0.515 |
LIG_FHA_2 | 377 | 383 | PF00498 | 0.389 |
LIG_FHA_2 | 499 | 505 | PF00498 | 0.467 |
LIG_FHA_2 | 58 | 64 | PF00498 | 0.313 |
LIG_FHA_2 | 667 | 673 | PF00498 | 0.599 |
LIG_FHA_2 | 771 | 777 | PF00498 | 0.608 |
LIG_FHA_2 | 788 | 794 | PF00498 | 0.515 |
LIG_FHA_2 | 828 | 834 | PF00498 | 0.506 |
LIG_GBD_Chelix_1 | 72 | 80 | PF00786 | 0.186 |
LIG_LIR_Apic_2 | 151 | 157 | PF02991 | 0.455 |
LIG_LIR_Apic_2 | 478 | 484 | PF02991 | 0.458 |
LIG_LIR_Apic_2 | 568 | 574 | PF02991 | 0.458 |
LIG_LIR_Gen_1 | 1067 | 1078 | PF02991 | 0.240 |
LIG_LIR_Gen_1 | 1099 | 1109 | PF02991 | 0.161 |
LIG_LIR_Gen_1 | 1130 | 1140 | PF02991 | 0.265 |
LIG_LIR_Gen_1 | 1216 | 1226 | PF02991 | 0.259 |
LIG_LIR_Gen_1 | 198 | 207 | PF02991 | 0.475 |
LIG_LIR_Gen_1 | 22 | 32 | PF02991 | 0.421 |
LIG_LIR_Gen_1 | 244 | 253 | PF02991 | 0.424 |
LIG_LIR_Gen_1 | 47 | 57 | PF02991 | 0.332 |
LIG_LIR_Gen_1 | 60 | 68 | PF02991 | 0.291 |
LIG_LIR_Gen_1 | 78 | 85 | PF02991 | 0.240 |
LIG_LIR_Gen_1 | 917 | 927 | PF02991 | 0.635 |
LIG_LIR_Nem_3 | 1089 | 1095 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 1099 | 1105 | PF02991 | 0.240 |
LIG_LIR_Nem_3 | 1130 | 1136 | PF02991 | 0.269 |
LIG_LIR_Nem_3 | 1216 | 1221 | PF02991 | 0.259 |
LIG_LIR_Nem_3 | 164 | 168 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 198 | 202 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 209 | 214 | PF02991 | 0.240 |
LIG_LIR_Nem_3 | 22 | 27 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 225 | 230 | PF02991 | 0.215 |
LIG_LIR_Nem_3 | 231 | 236 | PF02991 | 0.235 |
LIG_LIR_Nem_3 | 244 | 250 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 405 | 410 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 435 | 440 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 47 | 53 | PF02991 | 0.352 |
LIG_LIR_Nem_3 | 504 | 510 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 60 | 64 | PF02991 | 0.264 |
LIG_LIR_Nem_3 | 78 | 82 | PF02991 | 0.307 |
LIG_LYPXL_S_1 | 44 | 48 | PF13949 | 0.589 |
LIG_LYPXL_yS_3 | 45 | 48 | PF13949 | 0.389 |
LIG_MLH1_MIPbox_1 | 208 | 212 | PF16413 | 0.383 |
LIG_Pex14_1 | 86 | 90 | PF04695 | 0.456 |
LIG_Pex14_2 | 1200 | 1204 | PF04695 | 0.338 |
LIG_Pex14_2 | 1214 | 1218 | PF04695 | 0.219 |
LIG_Pex14_2 | 199 | 203 | PF04695 | 0.505 |
LIG_Pex14_2 | 75 | 79 | PF04695 | 0.260 |
LIG_SH2_CRK | 1030 | 1034 | PF00017 | 0.403 |
LIG_SH2_CRK | 247 | 251 | PF00017 | 0.553 |
LIG_SH2_CRK | 599 | 603 | PF00017 | 0.468 |
LIG_SH2_CRK | 658 | 662 | PF00017 | 0.487 |
LIG_SH2_CRK | 665 | 669 | PF00017 | 0.491 |
LIG_SH2_CRK | 96 | 100 | PF00017 | 0.564 |
LIG_SH2_PTP2 | 699 | 702 | PF00017 | 0.561 |
LIG_SH2_SRC | 1133 | 1136 | PF00017 | 0.362 |
LIG_SH2_SRC | 43 | 46 | PF00017 | 0.493 |
LIG_SH2_STAP1 | 1042 | 1046 | PF00017 | 0.251 |
LIG_SH2_STAT5 | 1109 | 1112 | PF00017 | 0.334 |
LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.580 |
LIG_SH2_STAT5 | 36 | 39 | PF00017 | 0.253 |
LIG_SH2_STAT5 | 423 | 426 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 43 | 46 | PF00017 | 0.311 |
LIG_SH2_STAT5 | 541 | 544 | PF00017 | 0.627 |
LIG_SH2_STAT5 | 55 | 58 | PF00017 | 0.290 |
LIG_SH2_STAT5 | 61 | 64 | PF00017 | 0.271 |
LIG_SH2_STAT5 | 625 | 628 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 699 | 702 | PF00017 | 0.561 |
LIG_SH3_2 | 157 | 162 | PF14604 | 0.460 |
LIG_SH3_3 | 1081 | 1087 | PF00018 | 0.448 |
LIG_SH3_3 | 1088 | 1094 | PF00018 | 0.479 |
LIG_SH3_3 | 154 | 160 | PF00018 | 0.453 |
LIG_SH3_3 | 191 | 197 | PF00018 | 0.485 |
LIG_SH3_3 | 447 | 453 | PF00018 | 0.403 |
LIG_SH3_3 | 615 | 621 | PF00018 | 0.504 |
LIG_SH3_3 | 889 | 895 | PF00018 | 0.597 |
LIG_SH3_3 | 907 | 913 | PF00018 | 0.558 |
LIG_SUMO_SIM_anti_2 | 1186 | 1191 | PF11976 | 0.174 |
LIG_SUMO_SIM_anti_2 | 266 | 271 | PF11976 | 0.452 |
LIG_SUMO_SIM_anti_2 | 287 | 293 | PF11976 | 0.407 |
LIG_SUMO_SIM_par_1 | 1181 | 1186 | PF11976 | 0.223 |
LIG_SUMO_SIM_par_1 | 1219 | 1225 | PF11976 | 0.336 |
LIG_SUMO_SIM_par_1 | 287 | 293 | PF11976 | 0.505 |
LIG_SUMO_SIM_par_1 | 465 | 471 | PF11976 | 0.481 |
LIG_TRAF2_1 | 359 | 362 | PF00917 | 0.505 |
LIG_TYR_ITIM | 663 | 668 | PF00017 | 0.362 |
LIG_TYR_ITIM | 94 | 99 | PF00017 | 0.448 |
LIG_TYR_ITSM | 243 | 250 | PF00017 | 0.429 |
LIG_UBA3_1 | 467 | 472 | PF00899 | 0.255 |
LIG_UBA3_1 | 518 | 527 | PF00899 | 0.411 |
LIG_UBA3_1 | 82 | 89 | PF00899 | 0.318 |
LIG_WRC_WIRS_1 | 76 | 81 | PF05994 | 0.316 |
MOD_CDK_SPxxK_3 | 317 | 324 | PF00069 | 0.240 |
MOD_CK1_1 | 1127 | 1133 | PF00069 | 0.555 |
MOD_CK1_1 | 1155 | 1161 | PF00069 | 0.383 |
MOD_CK1_1 | 231 | 237 | PF00069 | 0.240 |
MOD_CK1_1 | 400 | 406 | PF00069 | 0.279 |
MOD_CK1_1 | 631 | 637 | PF00069 | 0.393 |
MOD_CK1_1 | 675 | 681 | PF00069 | 0.512 |
MOD_CK1_1 | 728 | 734 | PF00069 | 0.320 |
MOD_CK1_1 | 78 | 84 | PF00069 | 0.269 |
MOD_CK1_1 | 806 | 812 | PF00069 | 0.402 |
MOD_CK2_1 | 1193 | 1199 | PF00069 | 0.278 |
MOD_CK2_1 | 355 | 361 | PF00069 | 0.322 |
MOD_CK2_1 | 376 | 382 | PF00069 | 0.327 |
MOD_CK2_1 | 498 | 504 | PF00069 | 0.326 |
MOD_CK2_1 | 666 | 672 | PF00069 | 0.500 |
MOD_CK2_1 | 787 | 793 | PF00069 | 0.386 |
MOD_CK2_1 | 827 | 833 | PF00069 | 0.394 |
MOD_CMANNOS | 23 | 26 | PF00535 | 0.346 |
MOD_Cter_Amidation | 272 | 275 | PF01082 | 0.375 |
MOD_GlcNHglycan | 1154 | 1157 | PF01048 | 0.299 |
MOD_GlcNHglycan | 345 | 348 | PF01048 | 0.246 |
MOD_GlcNHglycan | 38 | 41 | PF01048 | 0.380 |
MOD_GlcNHglycan | 401 | 405 | PF01048 | 0.254 |
MOD_GlcNHglycan | 420 | 423 | PF01048 | 0.283 |
MOD_GlcNHglycan | 618 | 621 | PF01048 | 0.365 |
MOD_GlcNHglycan | 765 | 768 | PF01048 | 0.443 |
MOD_GlcNHglycan | 770 | 773 | PF01048 | 0.368 |
MOD_GlcNHglycan | 870 | 873 | PF01048 | 0.505 |
MOD_GlcNHglycan | 958 | 961 | PF01048 | 0.402 |
MOD_GlcNHglycan | 964 | 967 | PF01048 | 0.406 |
MOD_GSK3_1 | 1003 | 1010 | PF00069 | 0.371 |
MOD_GSK3_1 | 1018 | 1025 | PF00069 | 0.199 |
MOD_GSK3_1 | 1036 | 1043 | PF00069 | 0.240 |
MOD_GSK3_1 | 1138 | 1145 | PF00069 | 0.334 |
MOD_GSK3_1 | 1148 | 1155 | PF00069 | 0.240 |
MOD_GSK3_1 | 1204 | 1211 | PF00069 | 0.422 |
MOD_GSK3_1 | 313 | 320 | PF00069 | 0.249 |
MOD_GSK3_1 | 376 | 383 | PF00069 | 0.224 |
MOD_GSK3_1 | 388 | 395 | PF00069 | 0.223 |
MOD_GSK3_1 | 494 | 501 | PF00069 | 0.295 |
MOD_GSK3_1 | 778 | 785 | PF00069 | 0.451 |
MOD_GSK3_1 | 958 | 965 | PF00069 | 0.567 |
MOD_LATS_1 | 365 | 371 | PF00433 | 0.351 |
MOD_N-GLC_1 | 1143 | 1148 | PF02516 | 0.383 |
MOD_N-GLC_1 | 463 | 468 | PF02516 | 0.255 |
MOD_N-GLC_1 | 712 | 717 | PF02516 | 0.384 |
MOD_NEK2_1 | 1018 | 1023 | PF00069 | 0.287 |
MOD_NEK2_1 | 1071 | 1076 | PF00069 | 0.377 |
MOD_NEK2_1 | 1096 | 1101 | PF00069 | 0.240 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.408 |
MOD_NEK2_1 | 1111 | 1116 | PF00069 | 0.292 |
MOD_NEK2_1 | 1142 | 1147 | PF00069 | 0.249 |
MOD_NEK2_1 | 1148 | 1153 | PF00069 | 0.254 |
MOD_NEK2_1 | 1204 | 1209 | PF00069 | 0.461 |
MOD_NEK2_1 | 241 | 246 | PF00069 | 0.240 |
MOD_NEK2_1 | 343 | 348 | PF00069 | 0.300 |
MOD_NEK2_1 | 388 | 393 | PF00069 | 0.240 |
MOD_NEK2_1 | 418 | 423 | PF00069 | 0.329 |
MOD_NEK2_1 | 439 | 444 | PF00069 | 0.254 |
MOD_NEK2_1 | 457 | 462 | PF00069 | 0.177 |
MOD_NEK2_1 | 468 | 473 | PF00069 | 0.325 |
MOD_NEK2_1 | 494 | 499 | PF00069 | 0.298 |
MOD_NEK2_1 | 607 | 612 | PF00069 | 0.489 |
MOD_NEK2_1 | 638 | 643 | PF00069 | 0.356 |
MOD_NEK2_1 | 75 | 80 | PF00069 | 0.446 |
MOD_NEK2_1 | 778 | 783 | PF00069 | 0.417 |
MOD_NEK2_1 | 904 | 909 | PF00069 | 0.422 |
MOD_NEK2_1 | 937 | 942 | PF00069 | 0.459 |
MOD_NEK2_1 | 962 | 967 | PF00069 | 0.540 |
MOD_NEK2_1 | 973 | 978 | PF00069 | 0.479 |
MOD_NEK2_2 | 228 | 233 | PF00069 | 0.240 |
MOD_NEK2_2 | 566 | 571 | PF00069 | 0.297 |
MOD_PIKK_1 | 1036 | 1042 | PF00454 | 0.377 |
MOD_PIKK_1 | 1216 | 1222 | PF00454 | 0.410 |
MOD_PIKK_1 | 345 | 351 | PF00454 | 0.299 |
MOD_PIKK_1 | 367 | 373 | PF00454 | 0.159 |
MOD_PIKK_1 | 392 | 398 | PF00454 | 0.240 |
MOD_PIKK_1 | 827 | 833 | PF00454 | 0.413 |
MOD_PKA_1 | 274 | 280 | PF00069 | 0.375 |
MOD_PKA_1 | 956 | 962 | PF00069 | 0.402 |
MOD_PKA_2 | 1019 | 1025 | PF00069 | 0.271 |
MOD_PKA_2 | 102 | 108 | PF00069 | 0.262 |
MOD_PKA_2 | 1216 | 1222 | PF00069 | 0.383 |
MOD_PKA_2 | 274 | 280 | PF00069 | 0.334 |
MOD_PKA_2 | 397 | 403 | PF00069 | 0.240 |
MOD_PKA_2 | 51 | 57 | PF00069 | 0.389 |
MOD_PKA_2 | 672 | 678 | PF00069 | 0.590 |
MOD_PKA_2 | 819 | 825 | PF00069 | 0.232 |
MOD_Plk_1 | 1143 | 1149 | PF00069 | 0.383 |
MOD_Plk_1 | 1204 | 1210 | PF00069 | 0.425 |
MOD_Plk_1 | 241 | 247 | PF00069 | 0.240 |
MOD_Plk_1 | 311 | 317 | PF00069 | 0.255 |
MOD_Plk_1 | 330 | 336 | PF00069 | 0.255 |
MOD_Plk_1 | 457 | 463 | PF00069 | 0.240 |
MOD_Plk_1 | 543 | 549 | PF00069 | 0.542 |
MOD_Plk_1 | 566 | 572 | PF00069 | 0.300 |
MOD_Plk_1 | 7 | 13 | PF00069 | 0.337 |
MOD_Plk_1 | 737 | 743 | PF00069 | 0.382 |
MOD_Plk_1 | 994 | 1000 | PF00069 | 0.354 |
MOD_Plk_2-3 | 1122 | 1128 | PF00069 | 0.459 |
MOD_Plk_2-3 | 579 | 585 | PF00069 | 0.474 |
MOD_Plk_4 | 1019 | 1025 | PF00069 | 0.271 |
MOD_Plk_4 | 1042 | 1048 | PF00069 | 0.242 |
MOD_Plk_4 | 1096 | 1102 | PF00069 | 0.240 |
MOD_Plk_4 | 1112 | 1118 | PF00069 | 0.292 |
MOD_Plk_4 | 1138 | 1144 | PF00069 | 0.312 |
MOD_Plk_4 | 1149 | 1155 | PF00069 | 0.240 |
MOD_Plk_4 | 1183 | 1189 | PF00069 | 0.178 |
MOD_Plk_4 | 1233 | 1239 | PF00069 | 0.439 |
MOD_Plk_4 | 22 | 28 | PF00069 | 0.295 |
MOD_Plk_4 | 228 | 234 | PF00069 | 0.240 |
MOD_Plk_4 | 242 | 248 | PF00069 | 0.240 |
MOD_Plk_4 | 446 | 452 | PF00069 | 0.327 |
MOD_Plk_4 | 463 | 469 | PF00069 | 0.159 |
MOD_Plk_4 | 51 | 57 | PF00069 | 0.368 |
MOD_Plk_4 | 535 | 541 | PF00069 | 0.352 |
MOD_Plk_4 | 566 | 572 | PF00069 | 0.396 |
MOD_Plk_4 | 7 | 13 | PF00069 | 0.423 |
MOD_Plk_4 | 737 | 743 | PF00069 | 0.378 |
MOD_Plk_4 | 75 | 81 | PF00069 | 0.269 |
MOD_Plk_4 | 819 | 825 | PF00069 | 0.475 |
MOD_Plk_4 | 958 | 964 | PF00069 | 0.569 |
MOD_Plk_4 | 973 | 979 | PF00069 | 0.465 |
MOD_ProDKin_1 | 1194 | 1200 | PF00069 | 0.467 |
MOD_ProDKin_1 | 206 | 212 | PF00069 | 0.383 |
MOD_ProDKin_1 | 317 | 323 | PF00069 | 0.240 |
MOD_ProDKin_1 | 628 | 634 | PF00069 | 0.362 |
MOD_ProDKin_1 | 787 | 793 | PF00069 | 0.421 |
MOD_ProDKin_1 | 803 | 809 | PF00069 | 0.456 |
MOD_ProDKin_1 | 914 | 920 | PF00069 | 0.508 |
MOD_SUMO_for_1 | 876 | 879 | PF00179 | 0.616 |
MOD_SUMO_rev_2 | 1135 | 1141 | PF00179 | 0.399 |
MOD_SUMO_rev_2 | 511 | 518 | PF00179 | 0.485 |
MOD_SUMO_rev_2 | 567 | 577 | PF00179 | 0.587 |
MOD_SUMO_rev_2 | 619 | 626 | PF00179 | 0.341 |
MOD_SUMO_rev_2 | 891 | 901 | PF00179 | 0.475 |
MOD_SUMO_rev_2 | 950 | 959 | PF00179 | 0.579 |
TRG_DiLeu_BaEn_1 | 1233 | 1238 | PF01217 | 0.444 |
TRG_DiLeu_BaEn_1 | 969 | 974 | PF01217 | 0.408 |
TRG_DiLeu_BaEn_2 | 404 | 410 | PF01217 | 0.240 |
TRG_DiLeu_BaLyEn_6 | 13 | 18 | PF01217 | 0.360 |
TRG_DiLeu_BaLyEn_6 | 90 | 95 | PF01217 | 0.221 |
TRG_ENDOCYTIC_2 | 1030 | 1033 | PF00928 | 0.240 |
TRG_ENDOCYTIC_2 | 1109 | 1112 | PF00928 | 0.240 |
TRG_ENDOCYTIC_2 | 1133 | 1136 | PF00928 | 0.462 |
TRG_ENDOCYTIC_2 | 229 | 232 | PF00928 | 0.255 |
TRG_ENDOCYTIC_2 | 24 | 27 | PF00928 | 0.516 |
TRG_ENDOCYTIC_2 | 247 | 250 | PF00928 | 0.386 |
TRG_ENDOCYTIC_2 | 45 | 48 | PF00928 | 0.437 |
TRG_ENDOCYTIC_2 | 599 | 602 | PF00928 | 0.331 |
TRG_ENDOCYTIC_2 | 61 | 64 | PF00928 | 0.260 |
TRG_ENDOCYTIC_2 | 658 | 661 | PF00928 | 0.372 |
TRG_ENDOCYTIC_2 | 665 | 668 | PF00928 | 0.395 |
TRG_ENDOCYTIC_2 | 96 | 99 | PF00928 | 0.459 |
TRG_ER_diArg_1 | 1214 | 1217 | PF00400 | 0.343 |
TRG_ER_diArg_1 | 434 | 437 | PF00400 | 0.255 |
TRG_ER_diArg_1 | 611 | 613 | PF00400 | 0.338 |
TRG_ER_diArg_1 | 682 | 684 | PF00400 | 0.520 |
TRG_ER_diArg_1 | 784 | 787 | PF00400 | 0.604 |
TRG_ER_diArg_1 | 90 | 93 | PF00400 | 0.495 |
TRG_NLS_MonoExtC_3 | 1172 | 1177 | PF00514 | 0.363 |
TRG_NLS_MonoExtC_3 | 142 | 148 | PF00514 | 0.363 |
TRG_NLS_MonoExtC_3 | 786 | 791 | PF00514 | 0.356 |
TRG_NLS_MonoExtN_4 | 784 | 791 | PF00514 | 0.466 |
TRG_Pf-PMV_PEXEL_1 | 254 | 258 | PF00026 | 0.478 |
TRG_Pf-PMV_PEXEL_1 | 666 | 670 | PF00026 | 0.345 |
TRG_Pf-PMV_PEXEL_1 | 680 | 685 | PF00026 | 0.390 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZI4 | Leptomonas seymouri | 82% | 100% |
A0A0S4INU6 | Bodo saltans | 57% | 100% |
A0A1X0NPJ3 | Trypanosomatidae | 66% | 100% |
A0A3R7N8T2 | Trypanosoma rangeli | 66% | 100% |
A0A3S5H614 | Leishmania donovani | 89% | 100% |
A0A451EJU6 | Leishmania donovani | 21% | 100% |
A4HRZ6 | Leishmania infantum | 21% | 100% |
A4HTD0 | Leishmania infantum | 89% | 100% |
C9ZUI4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 62% | 99% |
E9ALC3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
O14072 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 34% | 100% |
P39986 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 35% | 100% |
Q4QII2 | Leishmania major | 89% | 100% |
Q95Z93 | Leishmania major | 21% | 100% |
Q9EPE9 | Mus musculus | 36% | 100% |
Q9LT02 | Arabidopsis thaliana | 35% | 100% |
V5BNZ8 | Trypanosoma cruzi | 67% | 100% |